Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Browse by Current Cardiff authors

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Number of items: 287.

Leonenko, Ganna, Richards, Alexander L., Walters, James T., Pocklington, Andrew, Chambert, Kimberly, Al Eissa, Mariam M., Sharp, Sally I., O'Brien, Niamh L., Curtis, David, Bass, Nicholas J., McQuillin, Andrew, Hultman, Christina, Moran, Jennifer L., McCarroll, Steven A., Sklar, Pamela, Neale, Benjamin M., Holmans, Peter A., Owen, Michael J., Sullivan, Patrick F. and O'Donovan, Michael C. 2017. Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 10.1002/ajmg.b.32560

Sims, Rebecca, J, van der Lee, Sven, C, Naj, Adam, Badarinarayan, Nandini, Taniesha, Morgan,, Denning, Nicola, Majounie, Elisa, O'Donovan, Michael, Owen, Michael, Jones, Lesley, Escott-Price, Valentina, Holmans, Peter and Williams, Julie 2017. Rare coding variants in PLCG2, ABI3 and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics 10.1038/ng.3916
Item availability restricted.
file

Holmans, Peter A., Massey, Thomas H. and Jones, Lesley 2017. Genetic modifiers of Mendelian disease: Huntington's disease and the trinucleotide repeat disorders. Human Molecular Genetics , pp. 87-101. 10.1093/hmg/ddx261
Item availability restricted.
file

Weiner, Daniel J, Wigdor, Emilie M, Ripke, Stephan, Walters, Raymond K, Kosmicki, Jack A, Grove, Jakob, Samocha, Kaitlin E, Goldstein, Jacqueline I, Okbay, Aysu, Bybjerg-Grauholm, Jonas, Werge, Thomas, Hougaard, David M, Taylor, Jacob, Bækvad-Hansen, Marie, Dumont, Ashley, Hansen, Christine, Hansen, Thomas F, Howrigan, Daniel, Mattheisen, Manuel, Moran, Jennifer, Mors, Ole, Nordentoft, Merete, Nørgaard-Pedersen, Bent, Poterba, Timothy, Poulsen, Jesper, Stevens, Christine, Anttila, Verneri, Holmans, Peter Alan, Huang, Hailiang, Klei, Lambertus, Lee, Phil H, Medland, Sarah E, Neale, Benjamin, Weiss, Lauren A, Zwaigenbaum, Lonnie, Yu, Timothy W, Wittemeyer, Kerstin, Willsey, A Jeremy, Wijsman, Ellen M, Wassink, Thomas H, Waltes, Regina, Walsh, Christopher A, Wallace, Simon, Vorstman, Jacob A S, Vieland, Veronica J, Vicente, Astrid M, van Engeland, Herman, Tsang, Kathryn, Thompson, Ann P, Szatmari, Peter, Svantesson, Oscar, Steinberg, Stacy, Stefansson, Kari, Stefansson, Hreinn, State, Matthew W, Soorya, Latha, Silagadze, Teimuraz, Scherer, Stephen W, Schellenberg, Gerard D, Sandin, Sven, Saemundsen, Evald, Rouleau, Guy A, Rogé, Bernadette, Roeder, Kathryn, Roberts, Wendy, Reichert, Jennifer, Reichenberg, Abraham, Rehnström, Karola, Regan, Regina, Poustka, Fritz, Poultney, Christopher S, Piven, Joseph, Pinto, Dalila, Pericak-Vance, Margaret A, Pejovic-Milovancevic, Milica, Pedersen, Marianne G, Pedersen, Carsten B, Paterson, Andrew D, Parr, Jeremy R, Pagnamenta, Alistair T, Oliveira, Guiomar, Nurnberger, John I, Nordentoft, Merete, Murtha, Michael T, Mouga, Susana, Mors, Ole, Morrow, Eric M, De Luca, Daniel Moreno, Monaco, Anthony P, Minshew, Nancy, Merikangas, Alison, McMahon, William M, McGrew, Susan G, Mattheisen, Manuel, Martsenkovsky, Igor, Martin, Donna M, Mane, Shrikant M, Magnusson, Pall, Magalhaes, Tiago, Maestrini, Elena, Lowe, Jennifer K, Lord, Catherine, Levitt, Pat, Martin, Christa Lese, Ledbetter, David H, Leboyer, Marion, Le Couteur, Ann S, Ladd-Acosta, Christine, Kolevzon, Alexander, Klauck, Sabine M, Jacob, Suma, Iliadou, Bozenna, Hultman, Christina M, Hertz-Picciotto, Irva, Hendren, Robert, Hansen, Christine S, Haines, Jonathan L, Guter, Stephen J, Grice, Dorothy E, Green, Jonathan M, Green, Andrew, Goldberg, Arthur P, Gillberg, Christopher, Gilbert, John, Gallagher, Louise, Freitag, Christine M, Fombonne, Eric, Folstein, Susan E, Fernandez, Bridget, Fallin, M Daniele, Ercan-Sencicek, A Gulhan, Ennis, Sean, Duque, Frederico, Duketis, Eftichia, Delorme, Richard, De Rubeis, Silvia, De Jonge, Maretha V, Dawson, Geraldine, Cuccaro, Michael L, Correia, Catarina T, Conroy, Judith, Conceição, Inês C, Chiocchetti, Andreas G, Celestino-Soper, Patrícia B S, Casey, Jillian, Cantor, Rita M, Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F, Bölte, Sven, Bolshakova, Nadia, Betancur, Catalina, Bernier, Raphael, Beaudet, Arthur L, Battaglia, Agatino, Bal, Vanessa H, Baird, Gillian, Bailey, Anthony J, Bækvad-Hansen, Marie, Bader, Joel S, Bacchelli, Elena, Anagnostou, Evdokia, Amaral, David, Almeida, Joana, Buxbaum, Joseph D, Chakravarti, Aravinda, Cook, Edwin H, Coon, Hilary, Geschwind, Daniel H, Gill, Michael, Hakonarson, Hakon, Hallmayer, Joachim, Palotie, Aarno, Santangelo, Susan, Sutcliffe, James S, Arking, Dan E, Skuse, David, Devlin, Bernie, Anney, Richard, Sanders, Stephan J, Bishop, Somer, Mortensen, Preben Bo, Børglum, Anders D, Smith, George Davey, Daly, Mark J and Robinson, Elise B 2017. Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. Nature Genetics 49 (7) , pp. 978-985. 10.1038/ng.3863
Item availability restricted.
file

Hendricks, Audrey E., Bochukova, Elena G., Marenne, Gaëlle, Keogh, Julia M., Atanassova, Neli, Bounds, Rebecca, Wheeler, Eleanor, Mistry, Vanisha, Henning, Elana, Körner, Antje, Muddyman, Dawn, McCarthy, Shane, Hinney, Anke, Hebebrand, Johannes, Scott, Robert A., Langenberg, Claudia, Wareham, Nick J., Surendran, Praveen, Howson, Joanna M., Butterworth, Adam S., Danesh, John, Nordestgaard, Børge G, Nielsen, Sune F., Afzal, Shoaib, Papadia, Sofia, Ashford, Sofie, Garg, Sumedha, Millhauser, Glenn L., Palomino, Rafael I., Kwasniewska, Alexandra, Tachmazidou, Ioanna, O'Rahilly, Stephen, Zeggini, Eleftheria, Barroso, Ines, Farooqi, I. Sadaf, UK10K, Consortium, Craddock, Nicholas, Holmans, Peter, O'Donovan, Michael C., Owen, Michael J., Walters, James T. R. and Williams, Hywel J. 2017. Rare variant analysis of human and rodent obesity genes in individuals with severe childhood obesity. Scientific Reports 7 , 4394. 10.1038/s41598-017-03054-8
file

Witt, Stephanie H, Streit, Fabian, Jungkunz, Martin, Frank, Josef, Awasthi, Swapnil, Reinbold, Céline S, Treutlein, Jens, Degenhardt, Franziska, Forstner, Andreas J, Heilmann-Heimbach, Stefanie, Dietl, Lydie, Schwarze, Cornelia E, Schende, Darja l, Strohmaier, Jana, Bethell, Andrew, Craddock, Nicholas, Di Florio, Arianna, Forty, Elizabeth, Fraser, Christine, Hamshere, Marian, Holmans, Peter, Jones, Ian, Kirov, George, O'Donovan, Michael C and Owen, Michael J 2017. Genome-wide association study of borderline personality disorder reveals genetic overlap with the bipolar disorder, schizophrenia and major depression. Translational Psychiatry
file

Hensman Moss, Davina J, Pardinas, Antonio, Langbehn, Douglas, Lo, Kitty, Leavitt, Blair R, Roos, Raymund, Durr, Alexandra, Mead, Simon, Holmans, Peter, Jones, Lesley, Tabrizi, Sarah J, Coleman, A, Santos, R Dar, Decolongon, J, Sturrock, A, Bardinet, E, Ret, C Jauff, Justo, D, Lehericy, S, Marelli, C, Nigaud, K, Valabrègue, R, van den Bogaard, SJA, Dumas, E M, van der Grond, J, t'Hart, EP, Jurgens, C, Witjes-Ane, M-N, Arran, N, Callaghan, J, Stopford, C, Frost, C, Jones, R, Hobbs, N, Lahiri, N, Ordidge, R, Owen, G, Pepple, T, Read, J, Say, M, Wild, E, Patel, A, Fox, N C, Gibbard, C, Malone, I, Crawford, H, Whitehead, D, Keenan, S, Cash, D M, Berna, C, Bechtel, N, Bohlen, S, Man, A Hoff, Kraus, P, Axelson, E, Wang, C, Acharya, T, Lee, S, Monaco, W, Campbell, C, Queller, S, Whitlock, K, Campbell, C, Campbell, M, Frajman, E, Milchman, C, O'Regan, A, Labuschagne, I, Stout, J, Landwehrmeyer, B, Craufurd, D, Scahill, R, Hicks, S, Kennard, C, Johnson, H, Tobin, A, Rosas, HD, Reilmann, R, Borowsky, B, Pourchot, C, Andrews, S C, Bachoud-Lévi, Anne-Catherine, Bentivoglio, Anna Rita, Biunno, Ida, Bonelli, Raphael, Burgunder, Jean-Marc, Dunnett, Stephen, Ferreira, Joaquim, Handley, Olivia, Heiberg, Arvid, Illmann, Torsten, Landwehrmeyer, G. Bernhard, Levey, Jamie, Ramos-Arroyo, Maria A., Nielsen, Jørgen, Koivisto, Susana Pro, Päivärinta, Markku, Roos, Raymund A.C., Sebastián, A Rojo, Tabrizi, Sarah, Vandenberghe, Wim, Verellen-Dumoulin, Christine, Uhrova, Tereza, Wahlström, Jan, Zaremba, Jacek, Baake, Verena, Barth, Katrin, Garde, Monica Bascuñana, Betz, Sabrina, Bos, Reineke, Callaghan, Jenny, Come, Adrien, Guedes, Leonor Correia, Ecker, Daniel, Finisterra, Ana Maria, Fullam, Ruth, Gilling, Mette, Gustafsson, Lena, Handley, Olivia J, Hvalstedt, Carina, Held, Christine, Koppers, Kerstin, Lamanna, Claudia, Laurà, Matilde, Descals, Asunción Martínez, Martinez-Horta, Saül, Mestre, Tiago, Minster, Sara, Monza, Daniela, Mütze, Lisanne, Oehmen, Martin, Orth, Michael, Padieu, Hélène, Paterski, Laurent, Peppa, Nadia, Koivisto, Susana Pro, Di Renzo, Martina, Rialland, Amandine, Røren, Niini, ?a?inková, Pavla, Timewell, Erika, Townhill, Jenny, Cubillo, Patricia Trigo, da Silva, Wildson Vieira, van Walsem, Marleen R, Whalstedt, Carina, Witjes-Ané, Marie-Noelle, Witkowski, Grzegorz, Wright, Abigail, Zielonka, Daniel, Zielonka, Eugeniusz, Zinzi, Paola, Bonelli, Raphael M., Lilek, Sabine, Hecht, Karen, Herranhof, Brigitte, Holl, Anna, Kapfhammer, Hans-Peter, Koppitz, Michael, Magnet, Markus, Müller, Nicole, Otti, Daniela, Painold, Annamaria, Reisinger, Karin, Scheibl, Monika, Schöggl, Helmut, Ullah, Jasmin, Braunwarth, Eva-Maria, Brugger, Florian, Buratti, Lisa, Hametner, Eva-Maria, Hepperger, Caroline, Holas, Christiane, Hotter, Anna, Hussl, Anna, Müller, Christoph, Poewe, Werner, Seppi, Klaus, Sprenger, Fabienne, Wenning, Gregor, Boogaerts, Andrea, Calmeyn, Godelinde, Delvaux, Isabelle, Liessens, Dirk, Somers, Nele, Dupuit, Michel, Minet, Cécile, van Paemel, Dominique, Ribaï, Pascale, Verellen-Dumoulin, Christine, Boogaerts, Andrea, Vandenberghe, Wim, van Reijen, Dimphna, Klempír, Jirí, Majerová, Veronika, Roth, Jan, Stárková, Irena, Hjermind, Lena E., Jacobsen, Oda, Nielsen, Jørgen E., Larsen, Ida Unmack, Vinther-Jensen, Tua, Hiivola, Heli, Hyppönen, Hannele, Martikainen, Kirsti, Tuuha, Katri, Allain, Philippe, Bonneau, Dominique, Bost, Marie, Gohier, Bénédicte, Guérid, Marie-Anne, Olivier, Audrey, Prundean, Adriana, Scherer-Gagou, Clarisse, Verny, Christophe, Babiloni, Blandine, Debruxelles, Sabrina, Duché, Charlotte, Goizet, Cyril, Jameau, Laetitia, Lafoucrière, Danielle, Spampinato, Umberto, Barthélémy, Rekha, De Bruycker, Christelle, Carette, Maryline Cabaret Anne-Sophie, Defebvre, Eric Decorte Luc, Delliaux, Marie, Delval, Arnaud, Destee, Alain, Dujardin, Kathy, Lemaire, Marie-Hélène, Manouvrier, Sylvie, Peter, Mireille, Plomhouse, Lucie, Sablonnière, Bernard, Simonin, Clémence, Thibault-Tanchou, Stéphanie, Vuillaume, Isabelle, Bellonet, Marcellin, Berrissoul, Hassan, Blin, Stéphanie, Courtin, Françoise, Duru, Cécile, Fasquel, Véronique, Godefroy, Olivier, Krystkowiak, Pierre, Mantaux, Béatrice, Roussel, Martine, Wannepain, Sandrine, Azulay, Jean-Philippe, Delfini, Marie, Eusebio, Alexandre, Fluchere, Frédérique, Mundler, Laura, Anheim, Mathieu, Julié, Celine, Boukbiza, Ouhaid Lagha, Longato, Nadine, Rudolf, Gabrielle, Tranchant, Christine, Zimmermann, Marie-Agathe, Kosinski, Christoph Michael, Milkereit, Eva, Probst, Daniela, Reetz, Kathrin, Sass, Christian, Schiefer, Johannes, Schlangen, Christiane, Werner, Cornelius J., Gelderblom, Harald, Priller, Josef, Prüß, Harald, Spruth, Eike Jakob, Ellrichmann, Gisa, Herrmann, Lennard, Hoffmann, Rainer, Kaminski, Barbara, Kotz, Peter, Prehn, Christian, Saft, Carsten, Lange, Herwig, Maiwald, Robert, Löhle, Matthias, Maass, Antonia, Schmidt, Simone, Bosredon, Cecile, Storch, Alexander, Wolz, Annett, Wolz, Martin, Capetian, Philipp, Lambeck, Johann, Zucker, Birgit, Boelmans, Kai, Ganos, Christos, Heinicke, Walburgis, Hidding, Ute, Lewerenz, Jan, Münchau, Alexander, Orth, Michael, Schmalfeld, Jenny, Stubbe, Lars, Zittel, Simone, Diercks, Gabriele, Dressler, Dirk, Gorzolla, Heike, Schrader, Christoph, Tacik, Pawel, Ribbat, Michael, Longinus, Bernhard, Bürk, Katrin, Möller, Jens Carsten, Rissling, Ida, Mühlau, Mark, Peinemann, Alexander, Städtler, Michael, Weindl, Adolf, Winkelmann, Juliane, Ziegler, Cornelia, Bechtel, Natalie, Beckmann, Heike, Bohlen, Stefan, Hölzner, Eva, Lange, Herwig, Reilmann, Ralf, Rohm, Stefanie, Rumpf, Silke, Schepers, Sigrun, Weber, Natalia, Dose, Matthias, Leythäuser, Gabriele, Marquard, Ralf, Raab, Tina, Wiedemann, Alexandra, Barth, Katrin, Buck, Andrea, Connemann, Julia, Ecker, Daniel, Geitner, Carolin, Held, Christine, Kesse, Andrea, Landwehrmeyer, Bernhard, Lang, Christina, Lewerenz, Jan, Lezius, Franziska, Nepper, Solveig, Niess, Anke, Orth, Michael, Schneider, Ariane, Schwenk, Daniela, Süßmuth, Sigurd, Trautmann, Sonja, Weydt, Patrick, Cormio, Claudia, Sciruicchio, Vittorio, Serpino, Claudia, de Tommaso, Marina, Capellari, Sabina, Cortelli, Pietro, Galassi, Roberto, Rizzo, Giovanni, Poda, Roberto, Scaglione, Cesa, Bertini, Elisabetta, Ghelli, Elena, Ginestroni, Andrea, Massaro, Francesca, Mechi, Claudia, Paganini, Marco, Piacentini, Silvia, Pradella, Silvia, Romoli, Anna Maria, Sorbi, Sandro, Abbruzzese, Giovanni, di Poggio, Monica Bandettini, Ferrandes, Giovanna, Mandich, Paola, Marchese, Roberta, Albanese, Alberto, Di Bella, Daniela, Castaldo, Anna, Di Donato, Stefano, Gellera, Cinzia, Genitrini, Silvia, Mariotti, Caterina, Monza, Daniela, Nanetti, Lorenzo, Paridi, Dominga, Soliveri, Paola, Tomasello, Chiara, De Michele, Giuseppe, Di Maio, Luigi, Massarelli, Marco, Peluso, Silvio, Roca, Alessandro, Russo, Cinzia Valeria, Salvatore, Elena, Sorrentino, Pierpaolo, Amico, Enrico, Favellato, Mariagrazia, Griguoli, Annamaria, Mazzante, Irene, Petrollini, Martina, Squitieri, Ferdinando, D'Alessio, Barbara, Esposito, Chiara, Bentivoglio, Rita, Frontali, Marina, Guidubaldi, Arianna, Ialongo, Tamara, Jacopini, Gioia, Piano, Carla, Romano, Silvia, Soleti, Francesco, Spadaro, Maria, Zinzi, Paola, van Hout, Monique S.E., Verhoeven, Marloes E., van Vugt, Jeroen P.P., de Weert, A. Marit, Bolwijn, J.J.W., Dekker, M., Kremer, B., Leenders, K.L., van Oostrom, J.C.H., van den Bogaard, Simon J.A., Bos, Reineke, Dumas, Eve M., 't Hart, Ellen P., Roos, Raymund A.C., Kremer, Berry, Verstappen, C.C.P., Aaserud, Olaf, C, Jan Frich, Heiberg, Arvid, van Walsem, Marleen R, Wehus, Ragnhild, Bjørgo, Kathrine, Fannemel, Madeleine, Gørvell, Per F., Lorentzen, Eirin, Koivisto, Susana Pro, Retterstøl, Lars, Stokke, Bodil, Bjørnevoll, Inga, Sando, Sigrid Botne, Dziadkiewicz, Artur, Nowak, Malgorzata, Robowski, Piotr, Sitek, Emilia, Slawek, Jaroslaw, Soltan, Witold, Szinwelski, Michal, Blaszcyk, Magdalena, Boczarska-Jedynak, Magdalena, Ciach-Wysocka, Ewelina, Gorzkowska, Agnieszka, Jasinska-Myga, Barbara, Klodowska-Duda, Gabriela, Opala, Gregorz, Stompel, Daniel, Banaszkiewicz, Krzysztof, Bocwinska, Dorota, Bojakowska-Jaremek, Kamila, Dec, Malgorzata, Krawczyk, Malgorzata, Rudzinska, Monika, Szczygiel, Elzbieta, Szczudlik, Andrzej, Wasielewska, Anna, Wójcik, Magdalena, Bryl, Anna, Ciesielska, Anna, Klimberg, Aneta, Marcinkowski, Jerzy, Samara, Husam, Sempolowicz, Justyna, Zielonka, Daniel, Gogol, Anna, Janik, Piotr, Kwiecinski, Hubert, Jamrozik, Zygmunt, Antczak, Jakub, Jachinska, Katarzyna, Krysa, Wioletta, Rakowicz, Maryla, Richter, Przemyslaw, Rola, Rafal, Ryglewicz, Danuta, Sienkiewicz-Jarosz, Halina, Stepniak, Iwona, Sulek, Anna, Witkowski, Grzegorz, Zaremba, Jacek, Zdzienicka, Elzbieta, Zieora-Jakutowicz, Karolina, Ferreira, Joaquim J, Coelho, Miguel, Guedes, Leonor Correia, Mendes, Tiago, Mestre, Tiago, Valadas, Anabela, Andrade, Carlos, Gago, Miguel, Garrett, Carolina, Guerra, Maria Rosália, Herrera, Carmen Durán, Garcia, Patrocinio Moreno, Barbera, Miquel Aguilar, Guia, Dolors Badenes, Hernanz, Laura Casas, Catena, Judit López, Ferrer, Pilar Quiléz, Sebastián, Ana Rojo, Carruesco, Gemma Tome, Bas, Jordi, Busquets, Núria, Calopa, Matilde, Robert, Misericordia Floriach, Viladrich, Celia Mareca, Idiago, Jesús Miguel Ruiz, Riballo, Antonio Villa, Cubo, Esther, Polo, Cecilia Gil, Mariscal, Natividad, Rivadeneyra, Perez Jessica, Barrero, Francisco, Morales, Blas, Fenollar, María, García, Rocío García-Ramos, Ortega, Paloma, Villanueva, Clara, Alegre, Javier, Bascuñana, Mónica, Caldentey, Juan Garcia, Ventura, Marta Fatás, Ribas, Guillermo García, de Yébenes, Justo García, Moreno, José Luis López-Sendón, Cubillo, Patricia Trigo, Alegre, Javier, Frech, Fernando Alonso, de Yébenes, Justo García, Ruíz, Pedro J García, Martínez-Descals, Asunción, Guerrero, Rosa, Artiga, María José Saiz, Sánchez, Vicenta, Perea, María Fuensanta Noguera, Fortuna, Lorenza, Manzanares, Salvadora, Reinante, Gema, Torres, María Martirio Antequera, Moreau, Laura Vivancos, González González, Sonia, Guisasola, Luis Menéndez, Salvador, Carlos, Martín, Esther Suaréz San, Ramirez, Inés Legarda, Gorospe, Aranzazú, Lopera, Mónica Rodriguez, Arques, Penelope Navas, Rodríguez, María José Torres, Pastor, Barbara Vives, Gaston, Itziar, Martinez-Jaurrieta, Maria Dolores, Ramos-Arroyo, Maria A., Moreno, Jose Manuel Garcia, Lucena, Carolina Mendez, Damas, Fatima, Cortegana, Hermoso Eva Pacheco, Peña, José Chacón, Redondo, Luis, Carrillo, Fátima, Teresa Cáceres, María, Mir, Pablo, Suarez, María José Lama, Vargas-González, Laura, Bosca, Maria E., Brugada, Francisco Castera, Burguera, Juan Andres, Campos, Anabel, Vilaplana, Garcia Carmen Peiró, Berglund, Peter, Constantinescu, Radu, Fredlund, Gunnel, Høsterey-Ugander, Ulrika, Linnsand, Petra, Neleborn-Lingefjärd, Liselotte, Wahlström, Jan, Wentzel, Magnus, Loutfi, Ghada, Olofsson, Carina, Stattin, Eva-Lena, Westman, Laila, Wikström, Birgitta, Burgunder, Jean-Marc, Stebler, Yanik, Kaelin, Alain, Romero, Irene, Schüpbach, Michael, Weber Zaugg, Sabine, Hauer, Maria, Gonzenbach, Roman, Jung, Hans H., Mihaylova, Violeta, Petersen, Jens, Jack, Roisin, Matheson, Kirsty, Miedzybrodzka, Zosia, Rae, Daniela, Simpson, Sheila A, Summers, Fiona, Ure, Alexandra, Vaughan, Vivien, Akhtar, Shahbana, Crooks, Jenny, Curtis, Adrienne, de Souza, Jenny, Piedad, John, Rickards, Hugh, Wright, Jan, Coulthard, Elizabeth, Gethin, Louise, Hayward, Beverley, Sieradzan, Kasia, Wright, Abigail, Armstrong, Matthew, Barker, Roger A., O'Keefe, Deidre, Di Pietro, Anna, Fisher, Kate, Goodman, Anna, Hill, Susan, Kershaw, Ann, Mason, Sarah, Paterson, Nicole, Raymond, Lucy, Swain, Rachel, Guzman, Natalie Valle, Busse, Monica, Butcher, Cynthia, Callaghan, Jenny, Dunnett, Stephen, Clenaghan, Catherine, Fullam, Ruth, Handley, Olivia, Hunt, Sarah, Jones, Lesley, Jones, Una, Khalil, Hanan, Minster, Sara, Owen, Michael, Price, Kathleen, Rosser, Anne, Townhill, Jenny, Edwards, Maureen, Ho, Carrie, Hughes, Teresa, McGill, Marie, Pearson, Pauline, Porteous, Mary, Smith, Paul, Brockie, Peter, Foster, Jillian, Johns, Nicola, McKenzie, Sue, Rothery, Jean, Thomas, Gareth, Yates, Shona, Burrows, Liz, Chu, Carol, Fletcher, Amy, Gallantrae, Deena, Hamer, Stephanie, Harding, Alison, Klöppel, Stefan, Kraus, Alison, Laver, Fiona, Lewis, Monica, Longthorpe, Mandy, Markova, Ivana, Raman, Ashok, Robertson, Nicola, Silva, Mark, Thomson, Aileen, Wild, Sue, Yardumian, Pam, Chu, Carol, Evans, Carole, Gallentrae, Deena, Hamer, Stephanie, Kraus, Alison, Markova, Ivana, Raman, Ashok, Chu, Carol, Hamer, Stephanie, Hobson, Emma, Jamieson, Stuart, Kraus, Alison, Markova, Ivana, Raman, Ashok, Musgrave, Hannah, Rowett, Liz, Toscano, Jean, Wild, Sue, Yardumian, Pam, Bourne, Colin, Clapton, Jackie, Clayton, Carole, Dipple, Heather, Freire-Patino, Dawn, Grant, Janet, Gross, Diana, Hallam, Caroline, Middleton, Julia, Murch, Ann, Thompson, Catherine, Alusi, Sundus, Davies, Rhys, Foy, Kevin, Gerrans, Emily, Pate, Louise, Andrews, Thomasin, Dougherty, Andrew, Golding, Charlotte, Kavalier, Fred, Laing, Hana, Lashwood, Alison, Robertson, Dene, Ruddy, Deborah, Santhouse, Alastair, Whaite, Anna, Andrews, Thomasin, Bruno, Stefania, Doherty, Karen, Golding, Charlotte, Haider, Salman, Hensman, Davina, Lahiri, Nayana, Lewis, Monica, Novak, Marianne, Patel, Aakta, Robertson, Nicola, Rosser, Elisabeth, Tabrizi, Sarah, Taylor, Rachel, Warner, Thomas, Wild, Edward, Arran, Natalie, Bek, Judith, Callaghan, Jenny, Craufurd, David, Fullam, Ruth, Hare, Marianne, Howard, Liz, Huson, Susan, Johnson, Liz, Jones, Mary, Murphy, Helen, Oughton, Emma, Partington-Jones, Lucy, Rogers, Dawn, Sollom, Andrea, Snowden, Julie, Stopford, Cheryl, Thompson, Jennifer, Trender-Gerhard, Iris, Verstraelen, Nichola, Westmoreland, Leann, Armstrong, Richard, Dixon, Kathryn, Nemeth, Andrea H, Siuda, Gill, Valentine, Ruth, Harrison, David, Hughes, Max, Parkinson, Andrew, Soltysiak, Beverley, Bandmann, Oliver, Bradbury, Alyson, Gill, Paul, Fairtlough, Helen, Fillingham, Kay, Foustanos, Isabella, Kazoka, Mbombe, O'Donovan, Kirsty, Peppa, Nadia, Taylor, Cat, Tidswell, Katherine, Quarrell, Oliver, Burgunder, Jean-Marc, Lau, Puay Ngoh, Pica, Emmanul and Tan, Louis 2017. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study. The Lancet Neurology 10.1016/S1474-4422(17)30161-8
Item availability restricted.
file

Holmans, Peter 2017. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Molecular Autism 8 (21) 10.1186/s13229-017-0137-9
file

McLaughlin, Russell L., Schijven, Dick, van Rheenen, Wouter, van Eijk, Kristel R., O'Brien, Margaret, Kahn, René S., Ophoff, Roel A., Goris, An, Bradley, Daniel G., Al-Chalabi, Ammar, van den Berg, Leonard H., Luykx, Jurjen J., Hardiman, Orla, Veldink, Jan H., Shatunov, Aleksey, Dekker, Annelot M., Diekstra, Frank P., Pulit, Sara L., van der Spek, Rick A. A., van Doormaal, Perry T. C., Sproviero, William, Jones, Ashley R., Nicholson, Garth A., Rowe, Dominic B., Pamphlett, Roger, Kiernan, Matthew C., Bauer, Denis, Kahlke, Tim, Williams, Kelly, Eftimov, Filip, Fogh, Isabella, Ticozzi, Nicola, Lin, Kuang, Millecamps, Stéphanie, Salachas, François, Meininger, Vincent, de Carvalho, Mamede, Pinto, Susana, Mora, Jesus S., Rojas-García, Ricardo, Polak, Meraida, Chandran, Siddharthan, Colville, Shuna, Swingler, Robert, Morrison, Karen E., Shaw, Pamela J., Hardy, John, Orrell, Richard W., Pittman, Alan, Sidle, Katie, Fratta, Pietro, Malaspina, Andrea, Petri, Susanne, Abdulla, Susanna, Drepper, Carsten, Sendtner, Michael, Meyer, Thomas, Wiedau-Pazos, Martina, Lomen-Hoerth, Catherine, Van Deerlin, Vivianna M., Trojanowski, John Q., Elman, Lauren, McCluskey, Leo, Basak, Nazli, Meitinger, Thomas, Lichtner, Peter, Blagojevic-Radivojkov, Milena, Andres, Christian R., Maurel, Cindy, Bensimon, Gilbert, Landwehrmeyer, Bernhard, Brice, Alexis, Payan, Christine A. M., Saker-Delye, Safa, Dürr, Alexandra, Wood, Nicholas, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Rietschel, Marcella, Cichon, Sven, Nöuthen, Markus M., Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean- François, Uitterlinden, Andre G., Rivadeneira, Fernando, Estrada, Karol, Hofman, Albert, Curtis, Charles, van der Kooi, Anneke J., de Visser, Marianne, Weber, Markus, Shaw, Christopher E., Smith, Bradley N., Pansarasa, Orietta, Cereda, Cristina, Del Bo, Roberto, Comi, Giacomo P., D'Alfonso, Sandra, Bertolin, Cinzia, Sorarù, Gianni, Mazzini, Letizia, Pensato, Viviana, Gellera, Cinzia, Tiloca, Cinzia, Ratti, Antonia, Calvo, Andrea, Moglia, Cristina, Brunetti, Maura, Arcuti, Simon, Capozzo, Rosa, Zecca, Chiara, Lunetta, Christian, Penco, Silvana, Riva, Nilo, Padovani, Alessandro, Filosto, Massimiliano, Blair, Ian, Leigh, P Nigel, Casale, Federico, Chio, Adriano, Beghi, Ettore, Pupillo, Elisabetta, Tortelli, Rosanna, Logroscino, Giancarlo, Powell, John, Ludolph, Albert C., Weishaupt, Jochen H., Robberecht, Wim, Van Damme, Philip, Brown, Robert H., Glass, Jonathan, Landers, John E., Andersen, Peter M., Corcia, Philippe, Vourc'h, Patrick, Silani, Vincenzo, van Es, Michael A., Pasterkamp, R Jeroen, Lewis, Cathryn M., Breen, Gerome, Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T. R., Farh, Kai-How, Holmans, Peter, Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Pers, Tune H., Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Begemann, Martin, Belliveau, Richard A., Bene, Judit, Bergen, Sarah E., Bevilacqua, Elizabeth, Bigdeli, Tim B., Black, Donald W., Bruggeman, Richard, Buccola, Nancy G., Buckner, Randy L., Byerley, William, Cahn, Wiepke, Cai, Guiqing, Campion, Dominique, Cantor, Rita M., Carr, Vaughan J., Carrera, Noa, Catts, Stanley V., Chambert, Kimberley D., Chan, Raymond C. K., Chan, Ronald Y. L., Chen, Eric Y. H., Cheng, Wei, Cheung, Eric F. C., Chong, Siow Ann, Cloninger, C Robert, Cohen, David, Cohen, Nadine, Cormican, Paul, Craddock, Nick, Crowley, James J., Curtis, David, Davidson, Michael, Davis, Kenneth L., Degenhardt, Franziska, Del Favero, Jurgen, Demontis, Ditte, Dikeos, Dimitris, Dinan, Timothy, Djurovic, Srdjan, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Dudbridge, Frank, Durmishi, Naser, Eichhammer, Peter, Eriksson, Johan, Escott-Price, Valentina, Essioux, Laurent, Fanous, Ayman H., Farrell, Martilias S., Frank, Josef, Franke, Lude, Freedman, Robert, Freimer, Nelson B., Friedl, Marion, Friedman, Joseph I., Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Giegling, Ina, Giusti-Rodríguez, Paola, Godard, Stephanie, Goldstein, Jacqueline I., Golimbet, Vera, Gopal, Srihari, Gratten, Jacob, de Haan, Lieuwe, Hammer, Christian, Hamshere, Marian L, Hansen, Mark, Hansen, Thomas, Haroutunian, Vahram, Hartmann, Annette M., Henskens, Frans A., Herms, Stefan, Hirschhorn, Joel N., Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V., Hougaard, David M., Ikeda, Masashi, Joa, Inge, Julià, Antonio, Kalaydjieva, Luba, Karachanak-Yankova, Sena, Karjalainen, Juha, Kavanagh, David, Keller, Matthew C., Kennedy, James L., Khrunin, Andrey, Kim, Yunjung, Klovins, Janis, Knowles, James A., Konte, Bettina, Kucinskas, Vaidutis, Kucinskiene, Zita Ausrele, Kuzelova-Ptackova, Hana, Kähler, Anna K., Laurent, Claudine, Lee, Jimmy, Lee, S Hong, Legge, Sophie E, Lerer, Bernard, Li, Miaoxin, Li, Tao, Liang, Kung-Yee, Lieberman, Jeffrey, Limborska, Svetlana, Loughland, Carmel M., Lubinski, Jan, Lönnqvist, Jouko, Macek, Milan, Magnusson, Patrik K. E., Maher, Brion S., Maier, Wolfgang, Mallet, Jacques, Marsal, Sara, Mattheisen, Manuel, Mattingsdal, Morten, McCarley, Robert W., McDonald, Colm, McIntosh, Andrew M., Meier, Sandra, Meijer, Carin J., Melegh, Bela, Melle, Ingrid, Mesholam-Gately, Raquelle I., Metspalu, Andres, Michie, Patricia T., Milani, Lili, Milanova, Vihra, Mokrab, Younes, Morris, Derek W., Mors, Ole, Murphy, Kieran C., Murray, Robin M., Myin-Germeys, Inez, Müller-Myhsok, Bertram, Nelis, Mari, Nenadic, Igor, Nertney, Deborah A., Nestadt, Gerald, Nicodemus, Kristin K., Nikitina-Zake, Liene, Nisenbaum, Laura, Nordin, Annelie, O'Callaghan, Eadbhard, O'Dushlaine, Colm, O'Neill, F Anthony, Oh, Sang-Yun, Olincy, Ann, Olsen, Line, Van Os, Jim, Pantelis, Christos, Papadimitriou, George N., Papiol, Sergi, Parkhomenko, Elena, Pato, Michele T., Paunio, Tiina, Pejovic-Milovancevic, Milica, Perkins, Diana O., Pietiläinen, Olli, Pimm, Jonathan, Pocklington, Andrew J, Price, Alkes, Pulver, Ann E., Purcell, Shaun M., Quested, Digby, Rasmussen, Henrik B., Reichenberg, Abraham, Reimers, Mark A., Richards, Alexander L., Roffman, Joshua L., Roussos, Panos, Ruderfer, Douglas M., Salomaa, Veikko, Sanders, Alan R., Schall, Ulrich, Schubert, Christian R., Schulze, Thomas G., Schwab, Sibylle G., Scolnick, Edward M., Scott, Rodney J., Seidman, Larry J., Shi, Jianxin, Sigurdsson, Engilbert, Silagadze, Teimuraz, Silverman, Jeremy M., Sim, Kang, Slominsky, Petr, Smoller, Jordan W., So, Hon-Cheong, Spencer, Chris C. A., Stahl, Eli A., Stefansson, Hreinn, Steinberg, Stacy, Stogmann, Elisabeth, Straub, Richard E., Strengman, Eric, Strohmaier, Jana, Stroup, T Scott, Subramaniam, Mythily, Suvisaari, Jaana, Svrakic, Dragan M., Szatkiewicz, Jin P., Söderman, Erik, Thirumalai, Srinivas, Toncheva, Draga, Tosato, Sarah, Veijola, Juha, Waddington, John, Walsh, Dermot, Wang, Dai, Wang, Qiang, Webb, Bradley T., Weiser, Mark, Wildenauer, Dieter B., Williams, Nigel M., Williams, Stephanie, Witt, Stephanie H., Wolen, Aaron R., Wong, Emily H. M., Wormley, Brandon K., Xi, Hualin Simon, Zai, Clement C., Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R., Stefansson, Kari, Visscher, Peter M., Adolfsson, Rolf, Andreassen, Ole A., Blackwood, Douglas H. R., Bramon, Elvira, Buxbaum, Joseph D., Børglum, Anders D., Darvasi, Ariel, Domenici, Enrico, Ehrenreich, Hannelore, Esko, Tõnu, Gejman, Pablo V., Gill, Michael, Gurling, Hugh, Hultman, Christina M., Iwata, Nakao, Jablensky, Assen V., Jönsson, Erik G., Kendler, Kenneth S., Kirov, George, Knight, Jo, Lencz, Todd, Levinson, Douglas F., Li, Qingqin S., Liu, Jianjun, Malhotra, Anil K., McCarroll, Steven A., McQuillin, Andrew, Moran, Jennifer L., Mortensen, Preben B., Mowry, Bryan J., Owen, Michael J, Palotie, Aarno, Pato, Carlos N., Petryshen, Tracey L., Posthuma, Danielle, Riley, Brien P., Rujescu, Dan, Sham, Pak C., Sklar, Pamela, St Clair, David, Weinberger, Daniel R., Wendland, Jens R., Werge, Thomas, Daly, Mark J., Sullivan, Patrick F. and O'Donovan, Michael C 2017. Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Nature Communications 8 , 14774. 10.1038/ncomms14774
file

Hensman Moss, Davina J., Flower, Michael D., Lo, Kitty K., Miller, James R. C., van Ommen, Gert-Jan B., 't Hoen, Peter A. C., Stone, Timothy C., Guinee, Amelia, Langbehn, Douglas R., Jones, Lesley, Plagnol, Vincent, van Roon-Mom, Willeke M. C., Holmans, Peter and Tabrizi, Sarah J. 2017. Huntington's disease blood and brain show a common gene expression pattern and share an immune signature with Alzheimer's disease. Scientific Reports 7 , 44849. 10.1038/srep44849
Item availability restricted.
file

Bowles, Kathryn R., Stone, Timothy C., Holmans, Peter Alan, Allen, Nicholas Denby, Dunnett, Stephen Bruce and Jones, Lesley 2017. SMAD transcription factors are altered in cell models of HD and regulate HTT expression. Cellular Signalling 31 , pp. 1-14. 10.1016/j.cellsig.2016.12.005
file

Marshall, Christian R., Howrigan, Daniel P., Merico, Daniele, Holmans, Peter Alan, Carrera, Noa, Craddock, Nicholas, Escott-Price, Valentina, Georgieva, Lyudmila, Kavanagh, David, Legge, Sophie, Pocklington, Andrew, Richards, Alexander, Ruderfer, Douglas M, Williams, Nigel, Kirov, George, Owen, Michael, Walters, James and O’Donovan, Michael Conlon 2017. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nature Genetics 49 (1) , pp. 27-35. 10.1038/ng.3725
Item availability restricted.
file

Chao, Michael J., Gillis, Tammy, Atwal, Ranjit S., Srinidhi Mysore, Jayalakshmi, Arjomand, Jamshid, Harold, Denise, Holmans, Peter Alan, Jones, Lesley, Orth, Michael, Myers, Richard H., Kwak, Seung, Wheeler, Vanessa C., MacDonald, Marcy E., Gusella, James F. and Lee, Jong-Min 2017. Haplotype-based stratification of Huntington's disease. European Journal of Human Genetics
Item availability restricted.
file

Rees, Elliott, Kendall, Kimberley, Pardinas, Antonio, Legge, Sophie E., Pocklington, Andrew, Escott-Price, Valentina, MacCabe, James H., Collier, David A., Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John, Walters, James Tynan Rhys and Kirov, George 2016. Analysis of intellectual disability copy number variants for association with schizophrenia. JAMA Psychiatry 73 (9) , pp. 963-969. 10.1001/jamapsychiatry.2016.1831

Mooney, Michael A., McWeeney, Shannon K., Faraone, Stephen, Hinney, Anke, Hebebrand, Johannes, Nigg, Joel T., Wilmot, Beth, Thapar, Anita, Martin, Joanna, O'Donovan, Michael Conlon, Owen, Michael John, Williams, Nigel Melville, Anney, Richard, Langley, Kate, Holmans, Peter Alan and German ADHD GWAS Group, 2016. Pathway analysis in attention deficit hyperactivity disorder: an ensemble approach. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 (6) , pp. 815-826. 10.1002/ajmg.b.32446

Thapar, Anita, Martin, Joanna, Mick, E., Arias Vasquez, A., Langley, Kate, Scherer, S.W., Schacher, R., Crosbie, J., Williams, Nigel Melville, Franke, B., Elia, J., Glessner, J., Hakonarson, H., Owen, Michael John, Faraone, S.V., O'Donovan, Michael Conlon and Holmans, Peter Alan 2016. Psychiatric gene discoveries shape evidence on ADHD's biology. Molecular Psychiatry 21 (9) , pp. 1202-1207. 10.1038/mp.2015.163
file

Pardinas, Antonio, Holmans, Peter, Pocklington, Andrew, Escott-Price, Valentina, Stephan, Ripke,, Carrera, Noa, E, Legge, Sophie, Sophie, Bishop,, Darren, Cameron,, Hamshere, Marian, Jun, Han,, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, H, MacCabe, James, A, McCarroll, Stephen, T, Baune, Bernhard, Gerome, Breen,, M, Byrne, Enda, Udo, Dannlowski,, C, Eley, Thalia, Caroline, Hayward,, G, Martin, Nicholas, M, McIntosh, Andrew, Robert, Plomin,, J, Porteous, David, R, Wray, Naomi, Consortium, ,the GERADI, A, Collier, David, Dan, Rujescu,, Kirov, George, Owen, Michael, O'Donovan, Michael and Walters, James 2016. Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection. bioRxiv 10.1101/068593
file

Tansey, Katherine, Rees, Elliott, Linden, David Edmund Johannes, Ripke, S., Chambert, D., Moran, J. L., McCarroll, S. A., Holmans, Peter Alan, Kirov, George, Walters, James Tynan Rhys, Owen, Michael John and O'Donovan, Michael Conlon 2016. Common alleles contribute to schizophrenia in CNV carriers. Molecular Psychiatry 21 (8) , pp. 1085-1089. 10.1038/mp.2015.143
file

Miller, James RC, Lo, Kitty K, Andre, Ralph, Moss, Davina J Hensman, Träger, Ulrike, Stone, Timothy C., Jones, Lesley, Holmans, Peter, Plagnol, Vincent and Tabrizi, Sarah J 2016. RNA-Seq of Huntington's Disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activation. Human Molecular Genetics 25 (14) , pp. 2893-2904. 10.1093/hmg/ddw142
file

Legge, Sophie E., Hamshere, Marian Lindsay, Ripke, S., Pardinas, Antonio, Goldstein, J. I., Rees, Elliott, Richards, Alexander, Leonenko, Ganna M., Jorskog, L. F., Goldstein, Jacqueline I., Jarskog, L Fredrik, Hilliard, Chris, Alfirevic, Ana, Duncan, Laramie, Fourches, Denie, Huang, Hailiang, Lek, Monkol, Neale, Benjamin M, Ripke, Stephan, Shianna, Kevin, Szatkiewicz, Jin P, Tropsha, Alexander, van den Oord, Edwin JCG, Cascorbi, Ingolf, Dettling, Michael, Gazit, Ephraim, Goff, Donald C, Holden, Arthur L, Kelly, Deanna L, Malhotra, Anil K, Nielsen, Jimmi, Pirmohamed, Munir, Rujescu, Dan, Werge, Thomas, Levy, Deborah L, Josiassen, Richard C, Kennedy, James L, Lieberman, Jeffrey A, Daly, Mark J, Sullivan, Patrick F, Chambert, K. D., Collier, D. A., Genovese, G., Giegling, I., Holmans, Peter Alan, Jonasdottir, A., Kirov, George, McCarroll, S. A., MacCabe, J. H., Mantripragada, Kiran Kumar, Moran, J. L., Neale, B. M., Stefansson, H., Rujescu, D., Daly, M. J., Sullivan, P. F., Owen, Michael John, O'Donovan, Michael Conlon and Walters, James Tynan Rhys 2016. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Molecular Psychiatry 10.1038/mp.2016.97
file

Smith, Daniel J., Escott-Price, Valentina, Davies, Gail, Bailey, Mark E. S., Colodro-Conde, Lucia, Ward, Joey, Vedernikov, Alexey, Marioni, Riccardo, Cullen, Breda, Lyall, Donals, Hagenaars, Saskia P., Liewald, David C. M., Luciano, Michelle, Gale, Catharine R., Ritchie, Stuart J., Hayward, Caroline, Nicholl, Barbara, Bulik-Sullivan, Brendan, Adams, Mark, Couvy-Duchesne, Baptiste, Graham, Nicholas, Mackay, Daniel, Evans, Jonathan, Smith, Blair H., Porteous, David J., Medland, Sarah, Martin, Nick G., Holmans, Peter Alan, McIntosh, Andrew M., Pell, Jill P., Deary, Ian and O'Donovan, Michael Conlon 2016. Genome-wide analysis of over 106,000 individuals identifies 9 neuroticism-associated loci. Molecular Psychiatry 21 (6) , pp. 749-757. 10.1038/mp.2016.49
file

Bettencourt, Conceicao, Hensman-Moss, Davina J., Flower, Michael, Wiethoff, Sarah, Brice, Alexis, Goizet, Cyril, Stevanin, Giovanni, Koutis, Georgios, Karadima, Georgia, Panos, Marios, Yescas-Gomez, Petra, Garcia-Velazquez, Lizbeth Esmeralda, Alonso-Vilatela, Maria Elisa, Lima, Manuela, Raposo, Mafalda, Traynor, Bryan, Sweeney, Mary, Wood, Nicholas, Guinti, Paola, Holmans, Peter Alan, Durr, Alexandra, Houlden, Henry, Tabrizi, Sarah J. and Jones, Lesley 2016. DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases. Annals of Neurology 79 (6) , pp. 983-990. 10.1002/ana.24656
filefile

Han, Jun, Walters, James, Kirov, George, Pocklington, Andrew, Escott-Price, Valentina, Owen, Michael John, Holmans, Peter Alan, O'Donovan, Michael Conlon and Rees, Elliott 2016. Gender differences in CNV burden do not confound schizophrenia CNV associations. Scientific Reports 6 , 25986. 10.1038/srep25986
file

Fry, Andrew Evan, Rees, Elliott, Thompson, Rose, Mantripragada, Kiran, Blake, Penny, Jones, Glyn, Morgan, Sian, Jose, Sian, Mugalaasi, Hood, Archer, Hayley, McCann, Emma, Clarke, Angus John, Taylor, Clare, Davies, Sally, Gibbon, Frances, Te Water Naude, Johann, Hartley, Louise, Thomas, Gareth, White, Catharine, Natarajan, Jaya, Thomas, Rhys H., Drew, Cheney, Chung, Seo-Kyung, Rees, Mark I., Holmans, Peter Alan, Owen, Michael John, Kirov, George, Pilz, Daniela T. and Kerr, Michael Patrick 2016. Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy. BMC Medical Genetics 17 , 34. 10.1186/s12881-016-0294-2
file

Singh, Tarjinder, Kurki, Mitja I, Curtis, David, Purcell, Shaun M, Crooks, Lucy, McRae, Jeremy, Suvisaari, Jaana, Chheda, Himanshu, Blackwood, Douglas, Breen, Gerome, Pietiläinen, Olli, Gerety, Sebastian S., Ayub, Muhammad, Blyth, Moira, Cole, Trevor, Collier, David, Coomber, Eve L, Craddock, Nicholas, Daly, Mark J, Danesh, John, DiForti, Marta, Foster, Alison, Freimer, Nelson B., Geschwind, Daniel, Johnstone, Mandy, Joss, Shelagh, Kirov, George, Körkkö, Jarmo, Kuismin, Outi, Holmans, Peter, Hultman, Christina M., Iyegbe, Conrad, Lönnqvist, Jouko, Männikkö, Minna, McCarroll, Steve A., McGuffin, Peter, McIntosh, Andrew M., McQuillin, Andrew, Moilanen, Jukka S., Moore, Carmel, Murray, Robin M., Newbury-Ecob, Ruth, Ouwehand, Willem, Paunio, Tiina, Prigmore, Elena, Rees, Elliott, Roberts, David, Sambrook, Jennifer, Sklar, Pamela, Clair, David St, Veijola, Juha, Walters, James Tynan Rhys, Williams, Hywel, Sullivan, Patrick F, Hurles, Matthew E., O'Donovan, Michael Conlon, Palotie, Aarno, Owen, Michael John and Barrett, Jeffrey C. 2016. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. Nature Neuroscience 19 (4) , pp. 571-577. 10.1038/nn.4267

Keum, Jae Whan, Shin, Aram, Gillis, Tammy, Mysore, Jayalakshmi Srinidhi, Elneel, Kawther Abu, Lucente, Diane, Hadzi, Tiffany, Holmans, Peter Alan, Jones, Lesley, Orth, Michael, Kwak, Seung, MacDonald, Marcy, Gusella, James F. and Lee, Jong-Min 2016. The HTT CAG expansion mutation determines age at death but not disease duration in Huntington’s Disease. American Journal of Human Genetics 98 (2) , pp. 287-298.
file

Keum, Jae Whan, Shin, Aram, Gillis, Tammy, Mysore, Jayalakshmi Srinidhi, Abu Elneel, Kawther, Lucente, Diane, Hadzi, Tiffany, Holmans, Peter, Jones, Lesley, Orth, Michael, Kwak, Seung, MacDonald, Marcy E., Gusella, James F. and Lee, Jong-Min 2016. The HTT CAG-Expansion mutation determines age at death but not disease duration in Huntington disease. The American Journal of Human Genetics 98 (2) , pp. 287-298. 10.1016/j.ajhg.2015.12.018

Franke, Barbara, Stein, Jason L, Ripke, Stephan, Anttila, Verneri, Hibar, Derrek P, van Hulzen, Kimm J E, Arias-Vasquez, Alejandro, Smoller, Jordan W, Nichols, Thomas E, Neale, Michael C, McIntosh, Andrew M, Lee, Phil, McMahon, Francis J, Meyer-Lindenberg, Andreas, Mattheisen, Manuel, Andreassen, Ole A, Gruber, Oliver, Sachdev, Perminder S, Roiz-Santiañez, Roberto, Saykin, Andrew J, Ehrlich, Stefan, Mather, Karen A, Turner, Jessica A, Schwarz, Emanuel, Thalamuthu, Anbupalam, Yao, Yin, Ho, Yvonne Y W, Martin, Nicholas G, Wright, Margaret J, Ripke, Stephan, Neale, Benjamin M, Corvin, Aiden, Walters, James Tynan Rhys, Farh, Kai-How, Holmans, Peter Alan, Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A, Huang, Hailiang, Pers, Tune H, Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A, Begemann, Martin, Belliveau, Richard A, Bene, Judit, Bergen, Sarah E, Bevilacqua, Elizabeth, Bigdeli, Tim B, Black, Donald W, Bruggeman, Richard, Buccola, Nancy G, Buckner, Randy L, Byerley, William F, Cahn, Wiepke, Cai, Guiqing, Cairns, Murray J, Campion, Dominique, Cantor, Rita M, Carr, Vaughan J, Carrera, Noa, Catts, Stanley V, Chambert, Kimberley D, Chan, Raymond C K, Chen, Eric Y H, Chen, Ronald Y L, Cheng, Wei, Cheung, Eric F C, Chong, Siow Ann, Cloninger, C Robert, Cohen, David, Cohen, Nadine, Cormican, Paul, Craddock, Nicholas, Crespo-Facorro, Benedicto, Crowley, James J, Curtis, David, Davidson, Michael, Davis, Kenneth L, Degenhardt, Franziska, Del Favero, Jurgen, DeLisi, Lynn E, Demontis, Ditte, Dikeos, Dimitris, Dinan, Timothy, Djurovic, Srdjan, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Dudbridge, Frank, Eichhammer, Peter, Eriksson, Johan, Escott-Price, Valentina, Essioux, Laurent, Fanous, Ayman H, Farrell, Martilias S, Frank, Josef, Franke, Lude, Freedman, Robert, Freimer, Nelson B, Friedman, Joseph I, Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Gershon, Elliot S, Giegling, Ina, Giusti-Rodríguez, Paola, Godard, Stephanie, Goldstein, Jacqueline I, Gopal, Srihari, Gratten, Jacob, de Haan, Lieuwe, Hammer, Christian, Hamshere, Marian Lindsay, Hansen, Mark, Hansen, Thomas, Haroutunian, Vahram, Hartmann, Annette M, Henskens, Frans A, Herms, Stefan L, Hirschhorn, Joel N, Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V, Hougaard, David M, Ikeda, Masashi, Joa, Inge, Julià, Antonio, Kähler, Anna K, Kahn, René S, Kalaydjieva, Luba, Karachanak-Yankova, Sena, Karjalainen, Juha, Kavanagh, David, Keller, Matthew C, Kelly, Brian J, Kennedy, James L, Khrunin, Andrey, Kim, Yunjung, Klovins, Janis, Knowles, James A, Konte, Bettina, Kucinskas, Vaidutis, Kucinskiene, Zita Ausrele, Kuzelova-Ptackova, Hana, Laurent, Claudine, Lee, S Hong, Keong, Jimmy Lee Chee, Legge, Sophie E., Lerer, Bernard, Li, Miaoxin, Li, Tao, Liang, Kung-Yee, Lieberman, Jeffrey, Limborska, Svetlana, Lönnqvist, Jouko, Loughland, Carmel M, Lubinski, Jan, Macek, Milan, Magnusson, Patrik K E, Maher, Brion S, Maier, Wolfgang, Mallet, Jacques, Marsal, Sara, Mattheisen, Manuel, Mattingsdal, Morten, McCarley, Robert W, McDonald, Colm, McIntosh, Andrew M, Meier, Sandra, Meijer, Carin J, Melegh, Bela, Melle, Ingrid, Mesholam-Gately, Raquelle I, Metspalu, Andres, Michie, Patricia T, Milani, Lili, Milanova, Vihra, Mokrab, Younes, Morris, Derek W, Mors, Ole, Müller-Myhsok, Bertram, Murphy, Kieran C, Murray, Robin M, Myin-Germeys, Inez, Nelis, Mari, Nenadic, Igor, Nertney, Deborah A, Nestadt, Gerald, Nicodemus, Kristin K, Nikitina-Zake, Liene, Nisenbaum, Laura, Nordin, Annelie, O'Callaghan, Eadbhard, O'Dushlaine, Colm, O'Neill, F Anthony, Oh, Sang-Yun, Olincy, Ann, Olsen, Line, Van Os, Jim, Pantelis, Christos, Papadimitriou, George N, Papiol, Sergi, Parkhomenko, Elena, Pato, Michele T, Paunio, Tiina, Perkins, Diana O, Pietiläinen, Olli, Pimm, Jonathan, Pocklington, Andrew, Powell, John, Price, Alkes, Pulver, Ann E, Purcell, Shaun M, Quested, Digby, Rasmussen, Henrik B, Reichenberg, Abraham, Reimers, Mark A, Richards, Alexander, Roffman, Joshua L, Roussos, Panos, Ruderfer, Douglas M., Salomaa, Veikko, Sanders, Alan R, Schall, Ulrich, Schubert, Christian R, Schulze, Thomas G, Schwab, Sibylle G, Scolnick, Edward M, Scott, Rodney J, Seidman, Larry J, Shi, Jianxin, Silverman, Jeremy M, Sim, Kang, Slominsky, Petr, Smoller, Jordan W, So, Hon-Cheong, Söderman, Erik, Spencer, Chris C A, Stahl, Eli A, Stogmann, Elisabeth, Straub, Richard E, Strengman, Eric, Strohmaier, Jana, Stroup, T Scott, Subramaniam, Mythily, Suvisaari, Jaana, Svrakic, Dragan M, Szatkiewicz, Jin P, Thirumalai, Srinivas, Toncheva, Draga, Tooney, Paul A, Veijola, Juha, Waddington, John, Walsh, Dermot, Wang, Dai, Wang, Qiang, Webb, Bradley T, Weiser, Mark, Wildenauer, Dieter B, Williams, Nigel Melville, Williams, Stephanie, Witt, Stephanie H, Wolen, Aaron R, Wong, Emily H M, Wormley, Brandon K, Wu, Jing Qin, Xi, Hualin Simon, Zai, Clement C, Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R, Visscher, Peter M, Adolfsson, Rolf, Andreassen, Ole A, Blackwood, Douglas H R, Børglum, Anders D, Bramon, Elvira, Buxbaum, Joseph D, Cichon, Sven, Darvasi, Ariel, Domenici, Enrico, Ehrenreich, Hannelore, Esko, Tõnu, Gejman, Pablo V, Gill, Michael, Gurling, Hugh, Hultman, Christina M, Iwata, Nakao, Jablensky, Assen V, Jönsson, Erik G, Kendler, Kenneth S, Kirov, George, Knight, Jo, Lencz, Todd, Levinson, Douglas F, Li, Qingqin S, Liu, Jianjun, Malhotra, Anil K, McCarroll, Steven A, McQuillin, Andrew, Moran, Jennifer L, Mortensen, Preben B, Mowry, Bryan J, Nöthen, Markus M, Ophoff, Roel A, Owen, Michael John, Palotie, Aarno, Pato, Carlos N, Petryshen, Tracey L, Posthuma, Danielle, Rietschel, Marcella, Riley, Brien P, Rujescu, Dan, Sham, Pak C, Sklar, Pamela, St Clair, David, Weinberger, Daniel R, Wendland, Jens R, Werge, Thomas, Daly, Mark J, Sullivan, Patrick F, O'Donovan, Michael C, Hibar, Derrek P, Stein, Jason L, Renteria, Miguel E, Arias-Vasquez, Alejandro, Desrivières, Sylvane, Jahanshad, Neda, Toro, Roberto, Wittfeld, Katharina, Abramovic, Lucija, Andersson, Micael, Aribisala, Benjamin S, Armstrong, Nicola J, Bernard, Manon, Bohlken, Marc M, Boks, Marco P, Bralten, Janita, Brown, Andrew A, Chakravarty, M Mallar, Chen, Qiang, Ching, Christopher R K, Cuellar-Partida, Gabriel, den Braber, Anouk, Giddaluru, Sudheer, Goldman, Aaron L, Grimm, Oliver, Guadalupe, Tulio, Hass, Johanna, Woldehawariat, Girma, Holmes, Avram J, Hoogman, Martine, Janowitz, Deborah, Jia, Tianye, Kim, Sungeun, Klein, Marieke, Kraemer, Bernd, Lee, Phil, Loohuis, Loes M Olde, Luciano, Michelle, Macare, Christine, Mather, Karen A, Mattheisen, Manuel, Milaneschi, Yuri, Nho, Kwangsik, Papmeyer, Martina, Ramasamy, Adaikalavan, Risacher, Shannon L, Roiz-Santiañez, Roberto, Rose, Emma J, Salami, Alireza, Sämann, Philipp G, Schmaal, Lianne, Schork, Andrew J, Shin, Jean, Strike, Lachlan T, Teumer, Alexander, van Donkelaar, Marjolein M J, van Eijk, Kristel R, Walters, Raymond K, Westlye, Lars T, Whelan, Christopher D, Winkler, Anderson M, Zwiers, Marcel P, Alhusaini, Saud, Athanasiu, Lavinia, Ehrlich, Stefan, Hakobjan, Marina M H, Hartberg, Cecilie B, Haukvik, Unn, Heister, Angelien J G A M, Höhn, David, Kasperaviciute, Dalia, Liewald, David C M, Lopez, Lorna M, Makkinje, Remco R R, Matarin, Mar, Naber, Marlies A M, McKay, David R, Needham, Margaret, Nugent, Allison C, Pütz, Benno, Royle, Natalie A, Shen, Li, Sprooten, Emma, Trabzuni, Daniah, van der Marel, Saskia S L, van Hulzen, Kimm J E, Walton, Esther, Wolf, Christiane, Almasy, Laura, Ames, David, Arepalli, Sampath, Assareh, Amelia A, Bastin, Mark E, Brodaty, Henry, Bulayeva, Kazima B, Carless, Melanie A, Cichon, Sven, Corvin, Aiden, Curran, Joanne E, Czisch, Michael, de Zubicaray, Greig I, Dillman, Allissa, Duggirala, Ravi, Dyer, Thomas D, Erk, Susanne, Fedko, Iryna O, Ferrucci, Luigi, Foroud, Tatiana M, Fox, Peter T, Fukunaga, Masaki, Gibbs, Raphael, Göring, Harald H H, Green, Robert C, Guelfi, Sebastian, Hansell, Narelle K, Hartman, Catharina A, Hegenscheid, Katrin, Heinz, Andreas, Hernandez, Dena G, Heslenfeld, Dirk J, Hoekstra, Pieter J, Holsboer, Florian, Homuth, Georg, Hottenga, Jouke-Jan, Ikeda, Masashi, Jack, Clifford R, Jenkinson, Mark, Johnson, Robert, Kanai, Ryota, Keil, Maria, Kent, Jack W, Kochunov, Peter, Kwok, John B, Lawrie, Stephen M, Liu, Xinmin, Longo, Dan L, McMahon, Katie L, Meisenzahl, Eva, Melle, Ingrid, Mohnke, Sebastian, Montgomery, Grant W, Mostert, Jeanette C, Mühleisen, Thomas W, Nalls, Michael A, Nichols, Thomas E, Nilsson, Lars G, Nöthen, Markus M, Ohi, Kazutaka, Olvera, Rene L, Perez-Iglesias, Rocio, Pike, G Bruce, Potkin, Steven G, Reinvang, Ivar, Reppermund, Simone, Rietschel, Marcella, Romanczuk-Seiferth, Nina, Rosen, Glenn D, Rujescu, Dan, Schnell, Knut, Schofield, Peter R, Smith, Colin, Steen, Vidar M, Sussmann, Jessika E, Thalamuthu, Anbupalam, Toga, Arthur W, Traynor, Bryan, Troncoso, Juan, Turner, Jessica A, Hernández, Maria C Valdés, Ent, Dennis van 't, van der Brug, Marcel, van der Wee, Nic J A, van Tol, Marie-Jose, Veltman, Dick J, Wassink, Thomas H, Westman, Eric, Zielke, Ronald H, Zonderman, Alan, Ashbrook, David G, Hager, Reinmar, Lu, Lu, McMahon, Francis J, Morris, Derek W, Williams, Robert W, Brunner, Han G, Buckner, Randy L, Buitelaar, Jan K, Cahn, Wiepke, Calhoun, Vince D, Cavalleri, Gianpiero L, Crespo-Facorro, Benedicto, Dale, Anders M, Davies, Gareth E, Delanty, Norman, Depondt, Chantal, Djurovic, Srdjan, Drevets, Wayne C, Espeseth, Thomas, Gollub, Randy L, Ho, Beng-Choon, Hoffmann, Wolfgang, Hosten, Norbert, Kahn, René S, LeHellard, Stephanie, Meyer-Lindenberg, Andreas, Müller-Myhsok, Bertram, Nauck, Matthias, Nyberg, Lars, Pandolfo, Massimo, Penninx, Brenda W J H, Roffman, Joshua L, Sisodiya, Sanjay M, Smoller, Jordan W, van Bokhoven, Hans, van Haren, Neeltje E M, Völzke, Henry, Walter, Henrik, Weiner, Michael W, Wen, Wei, White, Tonya, Agartz, Ingrid, Andreassen, Ole A, Blangero, John, Boomsma, Dorret I, Brouwer, Rachel M, Cannon, Dara M, Cookson, Mark R, de Geus, Eco J C, Deary, Ian J, Donohoe, Gary, Fernández, Guillén, Fisher, Simon E, Francks, Clyde, Glahn, David C, Grabe, Hans J, Gruber, Oliver, Hardy, John, Hashimoto, Ryota, Hulshoff Pol, Hilleke E, Jönsson, Erik G, Kloszewska, Iwona, Lovestone, Simon, Mattay, Venkata S, Mecocci, Patrizia, McDonald, Colm, McIntosh, Andrew M, Ophoff, Roel A, Paus, Tomas, Pausova, Zdenka, Ryten, Mina, Sachdev, Perminder S, Saykin, Andrew J, Simmons, Andy, Singleton, Andrew, Soininen, Hilkka, Wardlaw, Joanna M, Weale, Michael E, Weinberger, Daniel R, Adams, Hieab H H, Launer, Lenore J, Seiler, Stephan, Schmidt, Reinhold, Chauhan, Ganesh, Satizabal, Claudia L, Becker, James T, Yanek, Lisa, van der Lee, Sven J, Ebling, Maritza, Fischl, Bruce, Longstreth, W T, Greve, Douglas, Schmidt, Helena, Nyquist, Paul, Vinke, Louis N, van Duijn, Cornelia M, Luting, Xue, Mazoyer, Bernard, Bis, Joshua C, Gudnason, Vilmundur, Seshadri, Sudha, Ikram, M Arfan, Martin, Nicholas G, Wright, Margaret J, Schumann, Gunter, Franke, Barbara, Thompson, Paul M, Medland, Sarah E, O'Donovan, Michael Conlon, Thompson, Paul M, Neale, Benjamin M, Medland, Sarah E and Sullivan, Patrick F 2016. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept. Nature Neuroscience 19 (3) , pp. 420-431. 10.1038/nn.4228

Jones, Hannah J., Stergiakouli, Evie, Tansey, Katherine E., Hubbard, Leon, Heron, Jon, Cannon, Mary, Holmans, Peter Alan, Lewis, Glyn, Linden, David Edmund Johannes, Jones, Peter B., Davey Smith, George, O'Donovan, Michael Conlon, Owen, Michael John, Walters, James Tynan Rhys and Zammit, Stanley 2016. Phenotypic manifestation of genetic risk for schizophrenia during adolescence in the general population. JAMA Psychiatry 10.1001/jamapsychiatry.2015.3058

Singh, Tarjinder, Kurki, Mitja I., Curtis, David, Purcell, Shaun M., Crooks, Lucy, McRae, Jeremy, Suvisaari, Jaana, Chheda, Himanshu, Blackwood, Douglas, Breen, Gerome, Pietilainen, Olli, Gerety, Sebastian S., Ayub, Muhammad, Blyth, Moira, Cole, Trevor, Collier, David, Coomber, Eve L., Craddock, Nicholas John, Daly, Mark J., Danesh, John, DiForti, Marta, Foster, Alison, Freimer, Nelson B., Geschwind, Daniel, Johnstone, Mandy, Joss, Shelagh, Kirov, George, Korkko, Jarmo, Kuismin, Outi, Holmans, Peter Alan, Hultman, Christina M., Iyegbe, Conrad, Lonnqvist, Jouko, Mannikko, Minna, McCaroll, Steve A., McGuffin, Peter, McIntosh, Andrew M., McQuillin, Andrew, Moilanen, Jukka S., Moore, Carmel, Murray, Robin M., Newbury-Ecob, Ruth, Ouwehand, Willem, Paunio, Tiina, Prigmore, Elena, Rees, Elliott, Roberts, David, Sambrook, Jennifer, Sklar, Pamela, St Clair, David, Vejola, Juha, Walters, James Tynan Rhys, Williams, Hywel, Swedish Schizophrenia Study, , INTERVAL Study, , DDD Study, , UK10K Consortium, , Sullivan, Patrick F., Hurles, Matthew E., O'Donovan, Michael Conlon, Palotie, Aarno, Owen, Michael John and Barrett, Jeffrey C. 2016. Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders. bioRxiv 10.1101/036384

Deming, Yuetiva, Xia, Jian, Cai, Yefei, Lord, Jenny, Holmans, Peter Alan, Bertelsen, Sarah, Holtzman, David, Morris, John C., Bales, Kelly, Pickering, Eve H., Kauwe, John, Goate, Alison and Cruchaga, Carlos 2016. A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin. Neurobiology of Aging 37 , 208.e1-208.e9. 10.1016/j.neurobiolaging.2015.09.009

Richards, Alexander, Leonenko, Ganna M, Walters, James Tynan Rhys, Kavanagh, D, Rees, Elliott, Evans, Anna, Chambert, K. D., Moran, J. L., Goldstein, J., Neale, B. M., McCarroll, S. A., Pocklington, Andrew, Holmans, Peter Alan, Owen, Michael John and O'Donovan, Michael Conlon 2016. Exome arrays capture polygenic rare variant contributions to schizophrenia. Human Molecular Genetics 25 (5) , pp. 1001-1007. 10.1093/hmg/ddv620
file

Bayram-Weston, Zubeyde, Stone, Timothy C., Giles, Peter James, Elliston, Linda Anne, Janghra, Narinder, Higgs, Gemma, Holmans, Peter Alan, Dunnett, Stephen Bruce, Brooks, Simon Philip and Jones, Lesley 2015. Similar striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntington's disease are not reflected in mutant Huntingtin inclusion prevalence. BMC Genomics 16 (1) , 1079. 10.1186/s12864-015-2251-4
file

Tansey, K E, Rees, Elliott, Linden, David Edmun Johannes, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, Peter Alan, Kirov, George, Walters, James Tynan Rhys, Owen, Michael John and O'Donovan, Michael Conlon 2015. Common alleles contribute to schizophrenia in CNV carriers [Erratum]. Molecular Psychiatry 10.1038/mp.2015.170

Kun-Rodrigues, Celia, Ganos, Christos, Guerreiro, Rita, Schneider, Susanne A., Schulte, Claudia, Lesage, Suzanne, Darwent, Lee, Holmans, Peter Alan, Singleton, Andrew, Bhatia, Kailash and Bras, Jose 2015. A systematic screening to identifyde novomutations causing sporadic early-onset Parkinson's disease. Human Molecular Genetics 24 (23) , pp. 6711-20. 10.1093/hmg/ddv376

Escott-Price, Valentina, Sims, Rebecca, Bannister, Christian, Harold, Denise, Vronskaya, Maria, Majounie, Elisa, Badarinarayan, Nandini, Morgan, Kevin, Passmore, Peter, Holmes, Clive, Powell, John, Brayne, Carol, Gill, Michael, Mead, Simon, Goate, Alison, Cruchaga, Carlos, Lambert, Jean-Charles, van Duijn, Cornelia, Maier, Wolfgang, Ramirez, Alfredo, Holmans, Peter Alan, Jones, Lesley, Hardy, John, Seshadri, Sudha, Schellenberg, Gerard D., Amouyel, Philippe and Williams, Julie 2015. Common polygenic variation enhances risk prediction for Alzheimer's disease. Brain 138 (12) , pp. 3673-3684. 10.1093/brain/awv268

Walter, Klaudia, Min, Josine L., Huang, Jie, Crooks, Lucy, Memari, Yasin, McCarthy, Shane, Perry, John R. B., Xu, ChangJiang, Futema, Marta, Lawson, Daniel, Iotchkova, Valentina, Schiffels, Stephan, Hendricks, Audrey E., Danecek, Petr, Li, Rui, Floyd, James, Wain, Louise V., Barroso, Inês, Humphries, Steve E., Hurles, Matthew E., Zeggini, Eleftheria, Barrett, Jeffrey C., Plagnol, Vincent, Brent Richards, J., Greenwood, Celia M. T., Timpson, Nicholas J., Durbin, Richard, Soranzo, Nicole, Bala, Senduran, Clapham, Peter, Coates, Guy, Cox, Tony, Daly, Allan, Danecek, Petr, Du, Yuanping, Durbin, Richard, Edkins, Sarah, Ellis, Peter, Flicek, Paul, Guo, Xiaosen, Guo, Xueqin, Huang, Liren, Jackson, David K., Joyce, Chris, Keane, Thomas, Kolb-Kokocinski, Anja, Langford, Cordelia, Li, Yingrui, Liang, Jieqin, Lin, Hong, Liu, Ryan, Maslen, John, McCarthy, Shane, Muddyman, Dawn, Quail, Michael A., Stalker, Jim, Sun, Jianping, Tian, Jing, Wang, Guangbiao, Wang, Jun, Wang, Yu, Wong, Kim, Zhang, Pingbo, Barroso, Inês, Birney, Ewan, Boustred, Chris, Chen, Lu, Clement, Gail, Cocca, Massimiliano, Danecek, Petr, Davey Smith, George, Day, Ian N. M., Day-Williams, Aaron, Down, Thomas, Dunham, Ian, Durbin, Richard, Evans, David M., Gaunt, Tom R., Geihs, Matthias, Greenwood, Celia M. T., Hart, Deborah, Hendricks, Audrey E., Howie, Bryan, Huang, Jie, Hubbard, Tim, Hysi, Pirro, Iotchkova, Valentina, Jamshidi, Yalda, Karczewski, Konrad J., Kemp, John P., Lachance, Genevieve, Lawson, Daniel, Lek, Monkol, Lopes, Margarida, MacArthur, Daniel G., Marchini, Jonathan, Mangino, Massimo, Mathieson, Iain, McCarthy, Shane, Memari, Yasin, Metrustry, Sarah, Min, Josine L., Moayyeri, Alireza, Muddyman, Dawn, Northstone, Kate, Panoutsopoulou, Kalliope, Paternoster, Lavinia, Perry, John R. B., Quaye, Lydia, Brent Richards, J., Ring, Susan, Ritchie, Graham R. S., Schiffels, Stephan, Shihab, Hashem A., Shin, So-Youn, Small, Kerrin S., Soler Artigas, María, Soranzo, Nicole, Southam, Lorraine, Spector, Timothy D., St Pourcain, Beate, Surdulescu, Gabriela, Tachmazidou, Ioanna, Timpson, Nicholas J., Tobin, Martin D., Valdes, Ana M., Visscher, Peter M., Wain, Louise V., Walter, Klaudia, Ward, Kirsten, Wilson, Scott G., Wong, Kim, Yang, Jian, Zeggini, Eleftheria, Zhang, Feng, Zheng, Hou-Feng, Anney, Richard, Ayub, Muhammad, Barrett, Jeffrey C., Blackwood, Douglas, Bolton, Patrick F., Breen, Gerome, Collier, David A., Craddock, Nicholas John, Crooks, Lucy, Curran, Sarah, Curtis, David, Durbin, Richard, Gallagher, Louise, Geschwind, Daniel, Gurling, Hugh, Holmans, Peter Alan, Lee, Irene, Lönnqvist, Jouko, McCarthy, Shane, McGuffin, Peter, McIntosh, Andrew M., McKechanie, Andrew G., McQuillin, Andrew, Morris, James, Muddyman, Dawn, O'Donovan, Michael Conlon, Owen, Michael John, Palotie, Aarno, Parr, Jeremy R., Paunio, Tiina, Pietilainen, Olli, Rehnström, Karola, Sharp, Sally I., Skuse, David, St Clair, David, Suvisaari, Jaana, Walters, James Tynan Rhys, Williams, Hywel J., Barroso, Inês, Bochukova, Elena, Bounds, Rebecca, Dominiczak, Anna, Durbin, Richard, Farooqi, I. Sadaf, Hendricks, Audrey E., Keogh, Julia, Marenne, Gaëlle, McCarthy, Shane, Morris, Andrew, Muddyman, Dawn, O'Rahilly, Stephen, Porteous, David J., Smith, Blair H., Tachmazidou, Ioanna, Wheeler, Eleanor, Zeggini, Eleftheria, Al Turki, Saeed, Anderson, Carl A., Antony, Dinu, Barroso, Inês, Beales, Phil, Bentham, Jamie, Bhattacharya, Shoumo, Calissano, Mattia, Carss, Keren, Chatterjee, Krishna, Cirak, Sebahattin, Cosgrove, Catherine, Durbin, Richard, Fitzpatrick, David R., Floyd, James, Reghan Foley, A., Franklin, Christopher S., Futema, Marta, Grozeva, Detelina, Humphries, Steve E., Hurles, Matthew E., McCarthy, Shane, Mitchison, Hannah M., Muddyman, Dawn, Muntoni, Francesco, O'Rahilly, Stephen, Onoufriadis, Alexandros, Parker, Victoria, Payne, Felicity, Plagnol, Vincent, Lucy Raymond, F., Roberts, Nicola, Savage, David B., Scambler, Peter, Schmidts, Miriam, Schoenmakers, Nadia, Semple, Robert K., Serra, Eva, Spasic-Boskovic, Olivera, Stevens, Elizabeth, van Kogelenberg, Margriet, Vijayarangakannan, Parthiban, Walter, Klaudia, Williamson, Kathleen A., Wilson, Crispian, Whyte, Tamieka, Ciampi, Antonio, Greenwood, Celia M. T., Hendricks, Audrey E., Li, Rui, Metrustry, Sarah, Oualkacha, Karim, Tachmazidou, Ioanna, Xu, ChangJiang, Zeggini, Eleftheria, Bobrow, Martin, Bolton, Patrick F., Durbin, Richard, Fitzpatrick, David R., Griffin, Heather, Hurles, Matthew E., Kaye, Jane, Kennedy, Karen, Kent, Alastair, Muddyman, Dawn, Muntoni, Francesco, Lucy Raymond, F., Semple, Robert K., Smee, Carol, Spector, Timothy D., Timpson, Nicholas J., Charlton, Ruth, Ekong, Rosemary, Futema, Marta, Humphries, Steve E., Khawaja, Farrah, Lopes, Luis R., Migone, Nicola, Payne, Stewart J., Plagnol, Vincent, Pollitt, Rebecca C., Povey, Sue, Ridout, Cheryl K., Robinson, Rachel L., Scott, Richard H., Shaw, Adam, Syrris, Petros, Taylor, Rohan, Vandersteen, Anthony M., Barrett, Jeffrey C., Barroso, Inês, Davey Smith, George, Durbin, Richard, Farooqi, I. Sadaf, Fitzpatrick, David R., Hurles, Matthew E., Kaye, Jane, Kennedy, Karen, Langford, Cordelia, McCarthy, Shane, Muddyman, Dawn, Owen, Michael J., Palotie, Aarno, Brent Richards, J., Soranzo, Nicole, Spector, Timothy D., Stalker, Jim, Timpson, Nicholas J., Zeggini, Eleftheria, Amuzu, Antoinette, Pablo Casas, Juan, Chambers, John C., Cocca, Massimiliano, Dedoussis, George, Gambaro, Giovanni, Gasparini, Paolo, Gaunt, Tom R., Huang, Jie, Iotchkova, Valentina, Isaacs, Aaron, Johnson, Jon, Kleber, Marcus E., Kooner, Jaspal S., Langenberg, Claudia, Luan, Jian'an, Malerba, Giovanni, März, Winfried, Matchan, Angela, Min, Josine L., Morris, Richard, Nordestgaard, Børge G., Benn, Marianne, Ring, Susan, Scott, Robert A., Soranzo, Nicole, Southam, Lorraine, Timpson, Nicholas J., Toniolo, Daniela, Traglia, Michela, Tybjaerg-Hansen, Anne, van Duijn, Cornelia M., van Leeuwen, Elisabeth M., Varbo, Anette, Whincup, Peter, Zaza, Gianluigi, Zeggini, Eleftheria and Zhang, Weihua 2015. The UK10K project identifies rare variants in health and disease. Nature 526 , pp. 82-90.

Vilhjálmsson, Bjarni J., Yang, Jian, Finucane, Hilary K., Gusev, Alexander, Lindström, Sara, Ripke, Stephan, Genovese, Giulio, Loh, Po-Ru, Bhatia, Gaurav, Do, Ron, Hayeck, Tristan, Won, Hong-Hee, Kathiresan, Sekar, Pato, Michele, Pato, Carlos, Tamimi, Rulla, Stahl, Eli, Zaitlen, Noah, Pasaniuc, Bogdan, Belbin, Gillian, Kenny, Eimear E., Schierup, Mikkel H., De Jager, Philip, Patsopoulos, Nikolaos A., McCarroll, Steve, Daly, Mark, Purcell, Shaun, Chasman, Daniel, Neale, Benjamin, Goddard, Michael, Visscher, Peter M., Kraft, Peter, Patterson, Nick, Price, Alkes L., Holmans, Peter Alan, Escott-Price, Valentina, Hamshere, Marian Lindsay and O'Donovan, Michael Conlon 2015. Modeling linkage disequilibrium increases accuracy of polygenic risk scores. American Journal of Human Genetics 97 (4) , pp. 576-592. 10.1016/j.ajhg.2015.09.001

Huang, Jie, Howie, Bryan, McCarthy, Shane, Memari, Yasin, Walter, Klaudia, Min, Josine L., Danecek, Petr, Malerba, Giovanni, Trabetti, Elisabetta, Zheng, Hou-Feng, Al Turki, Saeed, Amuzu, Antoinette, Anderson, Carl A., Anney, Richard, Antony, Dinu, Artigas, María Soler, Ayub, Muhammad, Bala, Senduran, Barrett, Jeffrey C., Barroso, Inês, Beales, Phil, Benn, Marianne, Bentham, Jamie, Bhattacharya, Shoumo, Birney, Ewan, Blackwood, Douglas, Bobrow, Martin, Bochukova, Elena, Bolton, Patrick F., Bounds, Rebecca, Boustred, Chris, Breen, Gerome, Calissano, Mattia, Carss, Keren, Pablo Casas, Juan, Chambers, John C., Charlton, Ruth, Chatterjee, Krishna, Chen, Lu, Ciampi, Antonio, Cirak, Sebahattin, Clapham, Peter, Clement, Gail, Coates, Guy, Cocca, Massimiliano, Collier, David A., Cosgrove, Catherine, Cox, Tony, Craddock, Nicholas John, Crooks, Lucy, Curran, Sarah, Curtis, David, Daly, Allan, Day, Ian N. M., Day-Williams, Aaron, Dedoussis, George, Down, Thomas, Du, Yuanping, van Duijn, Cornelia M., Dunham, Ian, Edkins, Sarah, Ekong, Rosemary, Ellis, Peter, Evans, David M., Farooqi, I. Sadaf, Fitzpatrick, David R., Flicek, Paul, Floyd, James, Foley, A. Reghan, Franklin, Christopher S., Futema, Marta, Gallagher, Louise, Gasparini, Paolo, Gaunt, Tom R., Geihs, Matthias, Geschwind, Daniel, Greenwood, Celia, Griffin, Heather, Grozeva, Detelina, Guo, Xiaosen, Guo, Xueqin, Gurling, Hugh, Hart, Deborah, Hendricks, Audrey E., Holmans, Peter Alan, Huang, Liren, Hubbard, Tim, Humphries, Steve E., Hurles, Matthew E., Hysi, Pirro, Iotchkova, Valentina, Isaacs, Aaron, Jackson, David K., Jamshidi, Yalda, Johnson, Jon, Joyce, Chris, Karczewski, Konrad J., Kaye, Jane, Keane, Thomas, Kemp, John P., Kennedy, Karen, Kent, Alastair, Keogh, Julia, Khawaja, Farrah, Kleber, Marcus E., van Kogelenberg, Margriet, Kolb-Kokocinski, Anja, Kooner, Jaspal S., Lachance, Genevieve, Langenberg, Claudia, Langford, Cordelia, Lawson, Daniel, Lee, Irene, van Leeuwen, Elisabeth M., Lek, Monkol, Li, Rui, Li, Yingrui, Liang, Jieqin, Lin, Hong, Liu, Ryan, Lönnqvist, Jouko, Lopes, Luis R., Lopes, Margarida, Luan, Jian'an, MacArthur, Daniel G., Mangino, Massimo, Marenne, Gaëlle, März, Winfried, Maslen, John, Matchan, Angela, Mathieson, Iain, McGuffin, Peter, McIntosh, Andrew M., McKechanie, Andrew G., McQuillin, Andrew, Metrustry, Sarah, Migone, Nicola, Mitchison, Hannah M., Moayyeri, Alireza, Morris, James, Morris, Richard, Muddyman, Dawn, Muntoni, Francesco, Nordestgaard, Børge G., Northstone, Kate, O'Donovan, Michael Conlon, O'Rahilly, Stephen, Onoufriadis, Alexandros, Oualkacha, Karim, Owen, Michael John, Palotie, Aarno, Panoutsopoulou, Kalliope, Parker, Victoria, Parr, Jeremy R., Paternoster, Lavinia, Paunio, Tiina, Payne, Felicity, Payne, Stewart J., Perry, John R. B., Pietilainen, Olli, Plagnol, Vincent, Pollitt, Rebecca C., Povey, Sue, Quail, Michael A., Quaye, Lydia, Raymond, Lucy, Rehnström, Karola, Ridout, Cheryl K., Ring, Susan, Ritchie, Graham R. S., Roberts, Nicola, Robinson, Rachel L., Savage, David B., Scambler, Peter, Schiffels, Stephan, Schmidts, Miriam, Schoenmakers, Nadia, Scott, Richard H., Scott, Robert A., Semple, Robert K., Serra, Eva, Sharp, Sally I., Shaw, Adam, Shihab, Hashem A., Shin, So-Youn, Skuse, David, Small, Kerrin S., Smee, Carol, Smith, George Davey, Southam, Lorraine, Spasic-Boskovic, Olivera, Spector, Timothy D., St Clair, David, St Pourcain, Beate, Stalker, Jim, Stevens, Elizabeth, Sun, Jianping, Surdulescu, Gabriela, Suvisaari, Jaana, Syrris, Petros, Tachmazidou, Ioanna, Taylor, Rohan, Tian, Jing, Tobin, Martin D., Toniolo, Daniela, Traglia, Michela, Tybjaerg-Hansen, Anne, Valdes, Ana M., Vandersteen, Anthony M., Varbo, Anette, Vijayarangakannan, Parthiban, Visscher, Peter M., Wain, Louise V., Walters, James Tynan Rhys, Wang, Guangbiao, Wang, Jun, Wang, Yu, Ward, Kirsten, Wheeler, Eleanor, Whincup, Peter, Whyte, Tamieka, Williams, Hywel J., Williamson, Kathleen A., Wilson, Crispian, Wilson, Scott G., Wong, Kim, Xu, ChangJiang, Yang, Jian, Zaza, Gianluigi, Zeggini, Eleftheria, Zhang, Feng, Zhang, Pingbo, Zhang, Weihua, Gambaro, Giovanni, Richards, J. Brent, Durbin, Richard, Timpson, Nicholas J., Marchini, Jonathan and Soranzo, Nicole 2015. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel. Nature Communications 6 , 8111. 10.1038/ncomms9111

Lee, S Hong, Byrne, Enda M, Hultman, Christina M, Kähler, Anna, Vinkhuyzen, Anna AE, Ripke, Stephan, Andreassen, Ole A, Frisell, Thomas, Gusev, Alexander, Hu, Xinli, Karlsson, Robert, Mantzioris, Vasilis X, McGrath, John J, Mehta, Divya, Stahl, Eli A, Zhao, Qiongyi, Kendler, Kenneth S, Sullivan, Patrick F, Price, Alkes L, O'Donovan, Michael Conlon, Okada, Yukinori, Mowry, Bryan J, Raychaudhuri, Soumya, Wray, Naomi R, Byerley, William, Cahn, Wiepke, Cantor, Rita M, Cichon, Sven, Cormican, Paul, Curtis, David, Djurovic, Srdjan, Escott-Price, Valentina, Gejman, Pablo V, Georgieva, Lyudmila, Giegling, Ina, Hansen, Thomas F, Ingason, Andrés, Kim, Yunjung, Konte, Bettina, Lee, Phil H, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek W, Nöthen, Markus M, O'Dushlaine, Colm, Olincy, Ann, Olsen, Line, Pato, Carlos N, Pato, Michele T, Pickard, Benjamin S, Posthuma, Danielle, Rasmussen, Henrik B, Rietschel, Marcella, Rujescu, Dan, Schulze, Thomas G, Silverman, Jeremy M, Thirumalai, Srinivasa, Werge, Thomas, Agartz, Ingrid, Amin, Farooq, Azevedo, Maria H, Bass, Nicholas, Black, Donald W, Blackwood, Douglas H R, Bruggeman, Richard, Buccola, Nancy G, Choudhury, Khalid, Cloninger, Robert C, Corvin, Aiden, Craddock, Nicholas John, Daly, Mark J, Datta, Susmita, Donohoe, Gary J, Duan, Jubao, Dudbridge, Frank, Fanous, Ayman, Freedman, Robert, Freimer, Nelson B, Friedl, Marion, Gill, Michael, Gurling, Hugh, De Haan, Lieuwe, Hamshere, Marian Lindsay, Hartmann, Annette M, Holmans, Peter Alan, Kahn, René S, Keller, Matthew C, Kenny, Elaine, Kirov, George, Krabbendam, Lydia, Krasucki, Robert, Lawrence, Jacob, Lencz, Todd, Levinson, Douglas F, Lieberman, Jeffrey A, Lin, Dan-Yu, Linszen, Don H, Magnusson, Patrik KE, Maier, Wolfgang, Malhotra, Anil K, Mattheisen, Manuel, Mattingsdal, Morten, McCarroll, Steven A, Medeiros, Helena, Melle, Ingrid, Milanova, Vihra, Myin-Germeys, Inez, Neale, Benjamin M, Ophoff, Roel A, Owen, Michael John, Pimm, Jonathan, Purcell, Shaun M, Puri, Vinay, Quested, Digby J, Rossin, Lizzy, Ruderfer, Douglas, Sanders, Alan R, Shi, Jianxin, Sklar, Pamela, St. Clair, David, Scott Stroup, T, Van Os, Jim, Visscher, Peter M, Wiersma, Durk, Zammit, Stanley, Louis Bridges, S, Choi, Hyon K, Coenen, Marieke JH, de Vries, Niek, Dieud, Philippe, Greenberg, Jeffrey D, Huizinga, Tom WJ, Padyukov, Leonid, Siminovitch, Katherine A, Tak, Paul P, Worthington, Jane, De Jager, Philip L, Denny, Joshua C, Gregersen, Peter K, Klareskog, Lars, Mariette, Xavier, Plenge, Robert M, van Laar, Mart and van Riel, Piet 2015. New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology , pii: dyv136. 10.1093/ije/dyv136

Leonpacher, A. K., Liebers, D., Pirooznia, M., Jancic, D., MacKinnon, D. F., Mondimore, F. M., Schweizer, B., Potash, J. B., Zandi, P. P., NIMH Genetics Initiative Bipolar Disorder Consortium, , Goes, F. S. and Holmans, Peter Alan 2015. Distinguishing bipolar from unipolar depression: the importance of clinical symptoms and illness features. Psychological Medicine 45 (11) , pp. 2437-2446. 10.1017/S0033291715000446

Lee, J. M., Wheeler, V. C., Chao, M. J., Vonsattel, P., Pinto, R. M., Lucente, D., Abu-Elmeel, K., Ramos, E. M., Mysore, J. S., Gillis, T., MacDonald, M. E., Gusella, J. F., Harold, Denise, Stone, Timothy C., Escott-Price, Valentina, Han, Jun, Vedernikov, Alexey, Holmans, Peter Alan, Jones, Lesley, Kwak, S., Mahmoudi, M., Orth, M., Landwehmeyer, G. B., Paulsen, J. S., Dorsey, R., Shoulson, I. and Myers, R. H. 2015. Identification of Genetic Factors that Modify Clinical Onset of Huntington's Disease. Cell 162 (3) , pp. 516-26. 10.1016/j.cell.2015.07.003

Rees, Elliott, Kirov, George, Walters, James Tynan Rhys, Richards, Alexander, Howrigan, D., Kavanagh, D. H., Pocklington, Andrew, Fromer, M., Ruderfer, D..M., Georgieva, Lyudmila, Carrera, Noa, Gormley, P., Palta, P., Williams, H., Dwyer, S., Johnson, J. S., Roussos, P., Barker, D. D., Banks, E., Milanova, V., Rose, S .A., Chambert, K., Mahajan, M, Scolnick, E. M., Moran, J. L., Tsuang, M. T., Glatt, S. J., Chen, W. J., Hwu, H.-G., Faraone, Stephen V., Roe, Cheri A., Chandler, Sharon D., Liu, Chih-Min, Liu, Chen-Chung, Yeh, Ling-Ling, Ouyang, Wen-Chen, Chan, Hung-Yu, Chen, Chun-Ying, Neale, B. M., Palotie, A., Sklar, P., Purcell, S. M., McCarroll, S .A., Holmans, Peter Alan, Owen, Michael John and O'Donovan, Michael Conlon 2015. Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia. Translational Psychiatry 5 (7) , e607. 10.1038/tp.2015.99
file

Østergaard, Søren D., Mukherjee, Shubhabrata, Sharp, Stephen J., Proitsi, Petroula, Lotta, Luca A., Day, Felix, Perry, John R. B., Boehme, Kevin L., Walter, Stefan, Kauwe, John S., Gibbons, Laura E., Alzheimer's Disease Genetics Consortium, , EPIC-InterAct Consortium, , Larson, Eric B., Powell, John F., Langenberg, Claudia, Crane, Paul K., Wareham, Nicholas J., Scott, Robert A., Sims, Rebecca, Gerrish, Amy, Hamshere, Marian Linsday, Escott-Price, Valentina, Badarinarayan, Nandini, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Julie 2015. Associations between potentially modifiable risk factors and Alzheimer disease: A mendelian randomization study. Public Library of Science Medicine 12 (6) , e1001841. 10.1371/journal.pmed.1001841

Schmidts, Miriam, Hou, Yuqing, Cortés, Claudio R., Mans, Dorus A., Huber, Celine, Boldt, Karsten, Patel, Mitali, van Reeuwijk, Jeroen, Plaza, Jean-Marc, van Beersum, Sylvia E. C., Yap, Zhi Min, Letteboer, Stef J. F., Taylor, S. Paige, Herridge, Warren, Johnson, Colin A., Scambler, Peter J., Ueffing, Marius, Kayserili, Hulya, Krakow, Deborah, King, Stephen M., Beales, Philip L., Al-Gazali, Lihadh, Wicking, Carol, Cormier-Daire, Valerie, Roepman, Ronald, Mitchison, Hannah M., Witman, George B., Al-Turki, Saeed, Anderson, Carl, Anney, Richard, Antony, Dinu, Asimit, Jennifer, Ayub, Mohammad, Barrett, Jeff, Barroso, Inês, Bentham, Jamie, Bhattacharya, Shoumo, Blackwood, Douglas, Bobrow, Martin, Bochukova, Elena, Bolton, Patrick, Boustred, Chris, Breen, Gerome, Brion, Marie-Jo, Brown, Andrew, Calissano, Mattia, Carss, Keren, Chatterjee, Krishna, Chen, Lu, Cirak, Sebhattin, Clapham, Peter, Clement, Gail, Coates, Guy, Collier, David, Cosgrove, Catherine, Cox, Tony, Craddock, Nicholas John, Crooks, Lucy, Curran, Sarah, Daly, Allan, Danecek, Petr, Smith, George Davey, Day-Williams, Aaron, Day, Ian, Durbin, Richard, Edkins, Sarah, Ellis, Peter, Evans, David, Farooqi, I. Sadaf, Fatemifar, Ghazaleh, Fitzpatrick, David, Flicek, Paul, Floyd, Jamie, Foley, A. Reghan, Franklin, Chris, Futema, Marta, Gallagher, Louise, Gaunt, Tom, Geschwind, Daniel, Greenwood, Celia, Grozeva, Detelina, Guo, Xiaosen, Gurling, Hugh, Hart, Deborah, Hendricks, Audrey, Holmans, Peter Alan, Huang, Jie, Humphries, Steve E., Hurles, Matt, Hysi, Pirro, Jackson, David, Jamshidi, Yalda, Jewell, David, Chris, Joyce, Kaye, Jane, Keane, Thomas, Kemp, John, Kennedy, Karen, Kent, Alastair, Kolb-Kokocinski, Anja, Lachance, Genevieve, Langford, Cordelia, Lee, Irene, Li, Rui, Li, Yingrui, Ryan, Liu, Lönnqvist, Jouko, Lopes, Margarida, MacArthur, Daniel G., Massimo, Mangino, Marchini, Jonathan, Maslen, John, McCarthy, Shane, McGuffin, Peter, McIntosh, Andrew, McKechanie, Andrew, McQuillin, Andrew, Memari, Yasin, Metrustry, Sarah, Min, Josine, Moayyeri, Alireza, Morris, James, Muddyman, Dawn, Muntoni, Francesco, Northstone, Kate, O'Donovan, Michael Conlon, O?Rahilly, Stephen, Onoufriadis, Alexandros, Oualkacha, Karim, Owen, Michael John, Palotie, Aarno, Panoutsopoulou, Kalliope, Parker, Victoria, Parr, Jeremy, Paternoster, Lavinia, Paunio, Tiina, Payne, Felicity, Perry, John, Pietilainen, Olli, Plagnol, Vincent, Quail, Michael A., Quaye, Lydia, Raymond, Lucy, Rehnström, Karola, Brent Richards, J., Ring, Sue, Ritchie, Graham R S, Savage, David B., Schoenmakers, Nadia, Semple, Robert K., Serra, Eva, Shihab, Hashem, Shin, So-Youn, Skuse, David, Small, Kerrin, Smee, Carol, Soler, Artigas María, Soranzo, Nicole, Southam, Lorraine, Spector, Tim, St Pourcain, Beate, St. Clair, David, Stalker, Jim, Surdulescu, Gabriela, Suvisaari, Jaana, Tachmazidou, Ioanna, Tian, Jing, Timpson, Nic, Tobin, Martin, Valdes, Ana, van Kogelenberg, Margriet, Vijayarangakannan, Parthiban, Wain, Louise, Walter, Klaudia, Wang, Jun, Ward, Kirsten, Wheeler, Ellie, Whittall, Ros, Williams, Hywel, Williamson, Kathy, Wilson, Scott G., Wong, Kim, Whyte, Tamieka, ChangJiang, Xu, Zeggini, Eleftheria, Zhang, Feng and Zheng, Hou-Feng 2015. TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport. Nature Communications 6 , 7074. 10.1038/ncomms8074

Pocklington, Andrew, Rees, Elliott, Walters, James Tynan Rhys, Han, Jun, Kavanagh, David H., Chambert, Kimberly D., Holmans, Peter Alan, Moran, Jennifer L., McCarroll, Steven A., Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2015. Novel findings from CNVs implicate inhibitory and excitatory signaling complexes in schizophrenia. Neuron 86 (5) , pp. 1203-1214. 10.1016/j.neuron.2015.04.022
file

Jones, Lesley, Lambert, J-C., Wang, L-S., Choi, S-H., Harold, Denise, Vedernikov, Alexey, Escott-Price, Valentina, Stone, Timothy C., Richards, Alexander, Bellenguez, C., Ibrahim-Verbaas, C. A., Naj, A. C., Sims, Rebecca, Gerrish, Amy, Jun, G., DeStefano, A. L., Bis, J. C., Beecham, G. W., Grenier-Boley, B., Russo, G., Thornton-Wells, T. A., Denning, Nicola, Smith, A. V., Chouraki, V., Thomas, Charlene, Ikram, M. A., Zelenika, D., Vardarajan, B. N., Kamatani, Y., Lin, C-F., Schmidt, H., Kunkle, B. W., Dunstan, Melanie, Ruiz, A., Bihoreau, M-T., Reitz, C., Pasquier, F., Hollingworth, P., Hanon, O., Fitzpatrick, A. L., Buxbaum, J. D., Campion, D., Crane, P. K., Becker, T., Gudnason, V., Cruchaga, C., Craig, D., Amin, N., Berr, C., Lopez, O. L., De Jager, P. L., Deramecourt, V., Johnston, J. A., Evans, D., Lovestone, S., Letteneur, L., Kornhuber, J., Tarraga, L., Rubinsztein, D. C., Eiriksdottir, G., Sleegers, K., Goate, A. M., Fievet, N., Heuntelman, M. J., Gill, M., Emilsson, V., Brown, K., Kamboh, M. I., Keller, L., Barberger-Gateau, P., McGuinness, B., Larson, E. B., Myers, A. J., Dufoil, C., Todd, S., Wallon, D., Love, S., Kehoe, P., Rogaeva, E., Gallacher, J., St George-Hyslop, P., Clarimon, J., Lleo, A., Bayer, Antony, Tsuang, D. W., Yu, L., Tsolaki, M., Bossu, P., Spalletta, G., Proitsi, P., Collinge, J., Sorbi, S., Sanchez Garcia, F., Fox, N., Hardy, J., Deniz Naranjo, M. C., Razquin, C., Bosco, P., Clarke, R., Brayne, C., Galimberti, D., Mancuso, M., Moebus, S., Mecocci, P., del Zompo, M., Maier, W., Hampel, H., Pilotto, A., Bullido, M., Panza, F., Caffarra, P., Nacmias, B., Gilbert, J. R., Mayhaus, M., Jessen, F., Dichgans, M., Lannfelt, L., Hakonarson, H., Pichier, S., Carrasquillo, M. M., Ingelsson, M., Beekly, D., Alavarez, V., Zou, F., Valadares, O., Younkin, S. G., Coto, E., Hamilton-Nelson, K. L., Mateo, I., Owen, Michael John, Faber, K. M., Jonsson, P. V., Combarros, O., O'Donovan, Michael Conlon, Cantwell, L. B., Soininen, H., Blacker, D., Mead, S., Mosley Jr., T. H., Bennett, D. A., Harris, T. B., Fratiglioni, L., Holmes, C., de Bruijn, R. F. A. G., Passmore, P., Montine, T. J., Bettens, K., Rotter, J. I., Brice, A., Morgan, K., Faroud, T. M., Kukull, W. A., Hannequin, D., Powell, J. F., Nalls, M. A., Ritchie, K., Lunetta, K. L., Kauwe, J. S. K., Boenwinkle, E., Riemenschneider, M., Boada, M., Hiltunen, M., Martin, E. R., Pastor, P., Schmidt, R., Rujescu, D., Dartigues, J-F., Mayeaux, R., Tzourio, C., Hofman, A., Nothen, M. M., Graff, C., Psaty, B. W., Haines, J. L., Lathrop, M., Pericak-Vance, M. A., Launer, L. J., Farren, L. A., van Duijn, C. M., Van Broeckhoven, C., Ramirez, A., Schellenberg, G. D., Seshadri, S., Amouye, P., Williams, Julie and Holmans, Peter Alan 2015. Convergent genetic and expression data implicate immunity in Alzheimer's disease. Alzheimer's & Dementia 11 (6) , pp. 658-671. 10.1016/j.jalz.2014.05.1757

Hosp, Fabian, Vossfeldt, Hannes, Heinig, Matthias, Vasiljevic, Djordje, Arumughan, Anup, Wyler, Emanuel, Landthaler, Markus, Hubner, Norbert, Wanker, Erich E., Lannfelt, Lars, Ingelsson, Martin, Lalowski, Maciej, Voigt, Aaron, Selbach, Matthias, Owen, Michael John, O'Donovan, Michael Conlon, Escott-Price, Valentina, Holmans, Peter Alan, Williams, Julie and Hamshere, Marian Lindsay 2015. Quantitative interaction proteomics of neurodegenerative disease proteins. Cell Reports 11 (7) , pp. 1134-46. 10.1016/j.celrep.2015.04.030

Taylor, Peter N., Porcu, Eleonora, Chew, Shelby, Campbell, Purdey J., Traglia, Michela, Brown, Suzanne J., Mullin, Benjamin H., Shihab, Hashem A., Min, Josine, Walter, Klaudia, Memari, Yasin, Huang, Jie, Barnes, Michael R., Beilby, John P., Charoen, Pimphen, Danecek, Petr, Dudbridge, Frank, Forgetta, Vincenzo, Greenwood, Celia, Grundberg, Elin, Johnson, Andrew D., Hui, Jennie, Lim, Ee M., McCarthy, Shane, Muddyman, Dawn, Panicker, Vijay, Perry, John R.B., Bell, Jordana T., Yuan, Wei, Relton, Caroline, Gaunt, Tom, Schlessinger, David, Abecasis, Goncalo, Cucca, Francesco, Surdulescu, Gabriela L., Woltersdorf, Wolfram, Zeggini, Eleftheria, Zheng, Hou-Feng, Toniolo, Daniela, Dayan, Colin M., Naitza, Silvia, Walsh, John P., Spector, Tim, Davey Smith, George, Durbin, Richard, Brent Richards, J., Sanna, Serena, Soranzo, Nicole, Timpson, Nicholas J., Wilson, Scott G., Turki, Saeed Al, Anderson, Carl, Anney, Richard, Antony, Dinu, Artigas, Maria Soler, Ayub, Muhammad, Balasubramaniam, Senduran, Barrett, Jeffrey C., Barroso, Inês, Beales, Phil, Bentham, Jamie, Bhattacharya, Shoumo, Birney, Ewan, Blackwood, Douglas, Bobrow, Martin, Bochukova, Elena, Bolton, Patrick, Bounds, Rebecca, Boustred, Chris, Breen, Gerome, Calissano, Mattia, Carss, Keren, Chatterjee, Krishna, Chen, Lu, Ciampi, Antonio, Cirak, Sebhattin, Clapham, Peter, Clement, Gail, Coates, Guy, Collier, David, Cosgrove, Catherine, Cox, Tony, Craddock, Nicholas John, Crooks, Lucy, Curran, Sarah, Curtis, David, Daly, Allan, Day-Williams, Aaron, Day, Ian N.M., Down, Thomas, Du, Yuanping, Dunham, Ian, Edkins, Sarah, Ellis, Peter, Evans, David, Faroogi, Sadaf, Fatemifar, Ghazaleh, Fitzpatrick, David R., Flicek, Paul, Flyod, James, Foley, A. Reghan, Franklin, Christopher S., Futema, Marta, Gallagher, Louise, Geihs, Matthias, Geschwind, Daniel, Griffin, Heather, Grozeva, Detelina, Guo, Xueqin, Guo, Xiaosen, Gurling, Hugh, Hart, Deborah, Hendricks, Audrey, Holmans, Peter Alan, Howie, Bryan, Huang, Liren, Hubbard, Tim, Humphries, Steve E., Hurles, Matthew E., Hysi, Pirro, Jackson, David K., Jamshidi, Yalda, Jing, Tian, Joyce, Chris, Kaye, Jane, Keane, Thomas, Keogh, Julia, Kemp, John, Kennedy, Karen, Kolb-Kokocinski, Anja, Lachance, Genevieve, Langford, Cordelia, Lawson, Daniel, Lee, Irene, Lek, Monkol, Liang, Jieqin, Lin, Hong, Li, Rui, Li, Yingrui, Liu, Ryan, Lönnqvist, Jouko, Lopes, Margarida, Lotchkova, Valentina, MacArthur, Daniel, Marchini, Jonathan, Maslen, John, Massimo, Mangino, Mathieson, Iain, Marenne, Gaëlle, McGuffin, Peter, McIntosh, Andrew, McKechanie, Andrew G., McQuillin, Andrew, Metrustry, Sarah, Mitchison, Hannah, Moayyeri, Alireza, Morris, James, Muntoni, Francesco, Northstone, Kate, O'Donovan, Michael Conlon, Onoufriadis, Alexandros, O'Rahilly, Stephen, Oualkacha, Karim, Owen, Michael John, Palotie, Aarno, Panoutsopoulou, Kalliope, Parker, Victoria, Parr, Jeremy R., Paternoster, Lavinia, Paunio, Tiina, Payne, Felicity, Pietilainen, Olli, Plagnol, Vincent, Quaye, Lydia, Quai, Michael A., Raymond, Lucy, Rehnström, Karola, Richards, Brent, Ring, Susan, Ritchie, Graham R.S., Roberts, Nicola, Savage, David B., Scambler, Peter, Schiffels, Stephen, Schmidts, Miriam, Schoenmakers, Nadia, Semple, Robert K., Serra, Eva, Sharp, Sally I., Shin, So-Youn, Skuse, David, Small, Kerrin, Southam, Lorraine, Spasic-Boskovic, Olivera, Clair, David St, Stalker, Jim, Stevens, Elizabeth, Pourcian, Beate St, Sun, Jianping, Suvisaari, Jaana, Tachmazidou, Ionna, Tobin, Martin D., Valdes, Ana, Kogelenberg, Margriet Van, Vijayarangakannan, Parthiban, Visscher, Peter M., Wain, Louise V., Walters, James Tynan Rhys, Wang, Guangbiao, Wang, Jun, Wang, Yu, Ward, Kirsten, Wheeler, Elanor, Whyte, Tamieka, Williams, Hywel, Williamson, Kathleen A., Wilson, Crispian, Wong, Kim, Xu, ChangJiang, Yang, Jian, Zhang, Fend and Zhang, Pingbo 2015. Whole-genome sequence-based analysis of thyroid function. Nature Communications 6 , p. 5681. 10.1038/ncomms6681

Maier, Robert, Moser, Gerhard, Chen, Guo-Bo, Ripke, Stephan, Coryell, William, Potash, James B., Scheftner, William A., Shi, Jianxin, Weissman, Myrna M., Hultman, Christina M., Landén, Mikael, Levinson, Douglas F., Kendler, Kenneth S., Smoller, Jordan W., Wray, Naomi R., Lee, S. Hong, Fraser, Christine, Hamshere, Marian Lindsay, Holmans, Peter Alan, Jones, Ian Richard, Jones, Leslie, Kirov, George, Lewis, Catrin, O'Donovan, Michael Conlon and Owen, Michael John 2015. Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder. The American Journal of Human Genetics 96 (2) , pp. 283-294. 10.1016/j.ajhg.2014.12.006

Bulik-Sullivan, Brendan K, Loh, Po-Ru, Finucane, Hilary K, Ripke, Stephan, Yang, Jian, Schizophrenia Working Group of the Psychiatric Genetics Consorti, , Patterson, Nick, Daly, Mark J., Price, Alkes L., Neale, Benjamin M., Holmans, Peter Alan, Escott-Price, Valentina, Kirov, George and O'Donovan, Michael Conlon 2015. LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Nature Genetics 47 (3) , pp. 291-295. 10.1038/ng.3211

O'Dushlaine, Colm, Rossin, Lizzy, Lee, Phil H, Duncan, Laramie, Parikshak, Neelroop N, Newhouse, Stephen, Ripke, Stephan, Neale, Benjamin M, Purcell, Shaun M, Posthuma, Danielle, Nurnberger, John I, Lee, S Hong, Faraone, Stephen V, Perlis, Roy H, Mowry, Bryan J, Thapar, Anita, Goddard, Michael E, Witte, John S, Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A, Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E, Asherson, Philip, Azevedo, Maria H, Backlund, Lena, Badner, Judith A, Bailey, Anthony J, Banaschewski, Tobias, Barchas, Jack D, Barnes, Michael R, Barrett, Thomas B, Bass, Nicholas, Battaglia, Agatino, Bauer, Michael, Bayés, Mònica, Bellivier, Frank, Bergen, Sarah E, Berrettini, Wade, Betancur, Catalina, Bettecken, Thomas, Biederman, Joseph, Binder, Elisabeth B, Black, Donald W, Blackwood, Douglas H R, Bloss, Cinnamon S, Boehnke, Michael, Boomsma, Dorret I, Breuer, René, Bruggeman, Richard, Cormican, Paul, Buccola, Nancy G, Buitelaar, Jan K, Bunney, William E, Buxbaum, Joseph D, Byerley, William F, Byrne, Enda M, Caesar, Sian, Cahn, Wiepke, Cantor, Rita M, Casas, Miguel, Chakravarti, Aravinda, Chambert, Kimberly, Choudhury, Khalid, Cichon, Sven, Mattheisen, Manuel, Cloninger, C Robert, Collier, David A, Cook, Edwin H, Coon, Hilary, Cormand, Bru, Corvin, Aiden, Coryell, William H, Craig, David W, Craig, Ian W, Crosbie, Jennifer, Cuccaro, Michael L, Curtis, David, Czamara, Darina, Datta, Susmita, Dawson, Geraldine, Day, Richard, De Geus, Eco J, Degenhardt, Franziska, Djurovic, Srdjan, Donohoe, Gary J, Doyle, Alysa E, Duan, Jubao, Dudbridge, Frank, Duketis, Eftichia, Ebstein, Richard P, Edenberg, Howard J, Elia, Josephine, Ennis, Sean, Etain, Bruno, Fanous, Ayman, Farmer, Anne E, Ferrier, I Nicol, Flickinger, Matthew, Fombonne, Eric, Foroud, Tatiana, Frank, Josef, Franke, Barbara, Fraser, Christine, Freedman, Robert, Freimer, Nelson B, Freitag, Christine M, Friedl, Marion, Frisén, Louise, Gallagher, Louise, Gejman, Pablo V, Georgieva, Lyudmila, Gershon, Elliot S, Giegling, Ina, Gill, Michael, Gordon, Scott D, Gordon-Smith, Katherine, Green, Elaine K, Greenwood, Tiffany A, Grice, Dorothy E, Gross, Magdalena, Grozeva, Detelina, Guan, Weihua, Gurling, Hugh, De Haan, Lieuwe, Haines, Jonathan L, Hakonarson, Hakon, Hallmayer, Joachim, Hamilton, Steven P, Hamshere, Marian Lindsay, Hansen, Thomas F, Hartmann, Annette M, Hautzinger, Martin, Heath, Andrew C, Henders, Anjali K, Herms, Stefan, Hickie, Ian B, Hipolito, Maria, Hoefels, Susanne, Holsboer, Florian, Hoogendijk, Witte J, Hottenga, Jouke-Jan, Hultman, Christina M, Hus, Vanessa, Ingason, Andrés, Ising, Marcus, Jamain, Stéphane, Jones, Edward G, Jones, Ian Richard, Jones, Lisa, Tzeng, Jung-Ying, Kähler, Anna K, Kahn, René S, Kandaswamy, Radhika, Keller, Matthew C, Kennedy, James L, Kenny, Elaine, Kent, Lindsey, Kim, Yunjung, Kirov, George, Klauck, Sabine M, Klei, Lambertus, Knowles, James A, Kohli, Martin A, Koller, Daniel L, Konte, Bettina, Korszun, Ania, Krabbendam, Lydia, Krasucki, Robert, Kuntsi, Jonna, Kwan, Phoenix, Landén, Mikael, Längström, Niklas, Lathrop, Mark, Lawrence, Jacob, Lawson, William B, Leboyer, Marion, Ledbetter, David H, Lencz, Todd, Lesch, Klaus-Peter, Levinson, Douglas F, Lewis, Cathryn M, Li, Jun, Lichtenstein, Paul, Lieberman, Jeffrey A, Lin, Dan-Yu, Linszen, Don H, Liu, Chunyu, Lohoff, Falk W, Loo, Sandra K, Lord, Catherine, Lowe, Jennifer K, Lucae, Susanne, MacIntyre, Donald J, Madden, Pamela A F, Maestrini, Elena, Magnusson, Patrik K E, Mahon, Pamela B, Maier, Wolfgang, Malhotra, Anil K, Mane, Shrikant M, Martin, Christa L, Martin, Nicholas G, Matthews, Keith, Mattingsdal, Morten, McCarroll, Steven A, McGhee, Kevin A, McGough, James J, McGrath, Patrick J, McGuffin, Peter, McInnis, Melvin G, McIntosh, Andrew, McKinney, Rebecca, McLean, Alan W, McMahon, Francis J, McMahon, William M, McQuillin, Andrew, Medeiros, Helena, Medland, Sarah E, Meier, Sandra, Melle, Ingrid, Meng, Fan, Meyer, Jobst, Middeldorp, Christel M, Middleton, Lefkos, Milanova, Vihra, Miranda, Ana, Monaco, Anthony P, Montgomery, Grant W, Moran, Jennifer L, Moreno-De-Luca, Daniel, Morken, Gunnar, Morris, Derek W, Morrow, Eric M, Escott-Price, Valentina, Muglia, Pierandrea, Mühleisen, Thomas W, Muir, Walter J, Müller-Myhsok, Bertram, Murtha, Michael, Myers, Richard M, Myin-Germeys, Inez, Neale, Michael C, Nelson, Stan F, Nievergelt, Caroline M, Nikolov, Ivan, Nimgaonkar, Vishwajit, Nolen, Willem A, Nöthen, Markus M, Nwulia, Evaristus A, Nyholt, Dale R, Oades, Robert D, Olincy, Ann, Oliveira, Guiomar, Olsen, Line, Ophoff, Roel A, Osby, Urban, Owen, Michael John, Palotie, Aarno, Parr, Jeremy R, Paterson, Andrew D, Pato, Carlos N, Pato, Michele T, Penninx, Brenda W, Pergadia, Michele L, Pericak-Vance, Margaret A, Pickard, Benjamin S, Pimm, Jonathan, Piven, Joseph, Potash, James B, Poustka, Fritz, Propping, Peter, Puri, Vinay, Quested, Digby J, Quinn, Emma M, Ramos-Quiroga, Josep Antoni, Rasmussen, Henrik B, Raychaudhuri, Soumya, Rehnström, Karola, Reif, Andreas, Ribasés, Marta, Rice, John P, Rietschel, Marcella, Roeder, Kathryn, Roeyers, Herbert, Rothenberger, Aribert, Rouleau, Guy, Ruderfer, Douglas, Rujescu, Dan, Sanders, Alan R, Sanders, Stephan J, Santangelo, Susan L, Sergeant, Joseph A, Schachar, Russell, Schalling, Martin, Schatzberg, Alan F, Scheftner, William A, Schellenberg, Gerard D, Scherer, Stephen W, Schork, Nicholas J, Schulze, Thomas G, Schumacher, Johannes, Schwarz, Markus, Scolnick, Edward, Scott, Laura J, Shi, Jianxin, Shilling, Paul D, Shyn, Stanley I, Silverman, Jeremy M, Slager, Susan L, Smalley, Susan L, Smit, Johannes H, Smith, Erin N, Sonuga-Barke, Edmund J S, Clair, David St., State, Matthew, Steffens, Michael, Steinhausen, Hans-Christoph, Strauss, John S, Strohmaier, Jana, Stroup, T Scott, Sutcliffe, James S, Szatmari, Peter, Szelinger, Szabocls, Thirumalai, Srinivasa, Thompson, Robert C, Todorov, Alexandre A, Tozzi, Federica, Treutlein, Jens, Uhr, Manfred, van den Oord, Edwin J C G, Van Grootheest, Gerard, Van Os, Jim, Vicente, Astrid M, Vieland, Veronica J, Vincent, John B, Visscher, Peter M, Walsh, Christopher A, Wassink, Thomas H, Watson, Stanley J, Weissman, Myrna M, Werge, Thomas, Wienker, Thomas F, Wijsman, Ellen M, Willemsen, Gonneke, Williams, Nigel, Willsey, A Jeremy, Witt, Stephanie H, Xu, Wei, Young, Allan H, Yu, Timothy W, Zammit, Stanley, Zandi, Peter P, Zhang, Peng, Zitman, Frans G, Zöllner, Sebastian, Devlin, Bernie, Kelsoe, John R, Sklar, Pamela, Daly, Mark J, O'Donovan, Michael Conlon, Craddock, Nicholas John, Kendler, Kenneth S, A Weiss, Lauren, Wray, Naomi R, Zhao, Zhaoming, Geschwind, Daniel H, Sullivan, Patrick F, Smoller, Jordan W, Holmans, Peter Alan and Breen, Gerome 2015. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nature Neuroscience 18 (2) , pp. 199-209. 10.1038/nn.3922

Correia, Kevin, Harold, Denise, Kim, Kyung-Hee, Holmans, Peter Alan, Jones, Lesley, Orth, Michael, Myers, Richard H., Kwak, Seung, Wheeler, Vanessa C., MacDonald, Marcy E., Gusella, James F. and Lee, Jong-Min 2015. The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease. Journal of Huntington's Disease 4 (3) , pp. 279-284. 10.3233/JHD-150169

Georgieva, Lyudmila, Rees, Elliott, Moran, Jennifer L., Chambert, Kimberly D., Milanova, Vihra, Craddock, Nicholas John, Purcell, Shaun, Sklar, Pamela, McCarroll, Steven, Holmans, Peter, O'Donovan, Michael Conlon, Owen, Michael John and Kirov, George 2014. De novo CNVs in bipolar affective disorder and schizophrenia. Human Molecular Genetics 23 (24) , pp. 6677-6683. 10.1093/hmg/ddu379
file

Gusev, Alexander, Lee, S. Hong, Trynka, Gosia, Finucane, Hilary, Vilhjálmsson, Bjarni J., Xu, Han, Zang, Chongzhi, Ripke, Stephan, Bulik-Sullivan, Brendan, Stahl, Eli, Kähler, Anna K., Hultman, Christina M., Purcell, Shaun M., McCarroll, Steven A., Daly, Mark, Pasaniuc, Bogdan, Sullivan, Patrick F., Neale, Benjamin M., Wray, Naomi R., Raychaudhuri, Soumya, Price, Alkes L., Escott-Price, Valentina, Carrera, Noa, Hamshere, Marian Lindsay, Holmans, Peter ALan, Kirov, George, Legge, Sophie, Li, Meng, O'Donovan, Michael Conlon, Owen, Michael John, Pocklington, Andrew, Richards, Alexander, Walters, James Tynan Rhys and Williams, Nigel Melville 2014. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. American Journal of Human Genetics 95 (5) , pp. 535-552. 10.1016/j.ajhg.2014.10.004

Ruderfer, Doug, Lim, Elaine T, Genovese, Giulio, Moran, Jennifer L, Hultman, Christina M, Sullivan, Patrick F, McCarroll, Steven A, Holmans, Peter Alan, Sklar, Pamela and Purcell, Shaun M 2014. No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia. European Journal of Human Genetics 23 (4) , p. 555. 10.1038/ejhg.2014.228

Timpson, Nicholas J., Walter, Klaudia, Min, Josine L., Tachmazidou, Ioanna, Malerba, Giovanni, Shin, So-Youn, Chen, Lu, Futema, Marta, Southam, Lorraine, Iotchkova, Valentina, Cocca, Massimiliano, Huang, Jie, Memari, Yasin, McCarthy, Shane, Danecek, Petr, Muddyman, Dawn, Mangino, Massimo, Menni, Cristina, Perry, John R. B., Ring, Susan M., Gaye, Amadou, Dedoussis, George, Farmaki, Aliki-Eleni, Burton, Paul, Talmud, Philippa J., Gambaro, Giovanni, Spector, Tim D., Smith, George Davey, Durbin, Richard, Richards, J Brent, Humphries, Steve E., Zeggini, Eleftheria, Soranzo, Nicole, Al Turki, Saeed, Anderson, Carl, Anney, Richard, Antony, Dinu, Soler Artigas, Maria, Ayub, Muhammad, Balasubramaniam, Senduran, Barrett, Jeffrey C., Barroso, Inês, Beales, Phil, Bentham, Jamie, Bhattacharya, Shoumo, Birney, Ewan, Blackwood, Douglas, Bobrow, Martin, Bochukova, Elena, Bolton, Patrick, Bounds, Rebecca, Boustred, Chris, Breen, Gerome, Calissano, Mattia, Carss, Keren, Chatterjee, Krishna, Chen, Lu, Ciampi, Antonio, Cirak, Sebhattin, Clapham, Peter, Clement, Gail, Coates, Guy, Collier, David, Cosgrove, Catherine, Cox, Tony, Craddock, Nicholas John, Crooks, Lucy, Curran, Sarah, Curtis, David, Daly, Allan, Danecek, Petr, Davey Smith, George, Day-Williams, Aaron, Day, Ian N. M., Down, Thomas, Du, Yuanping, Dunham, Ian, Durbin, Richard, Edkins, Sarah, Ellis, Peter, Evans, David, Faroogi, Sadaf, Fatemifar, Ghazaleh, Fitzpatrick, David R., Flicek, Paul, Flyod, James, Foley, A Reghan, Franklin, Christopher S, Futema, Marta, Gallagher, Louise, Gaunt, Tom, Geihs, Matthias, Geschwind, Daniel, Greenwood, Celia, Griffin, Heather, Grozeva, Detelina, Guo, Xueqin, Guo, Xiaosen, Gurling, Hugh, Hart, Deborah, Hendricks, Audrey, Holmans, Peter Alan, Howie, Bryan, Huang, Jie, Huang, Liren, Hubbard, Tim, Humphries, Steve E., Hurles, Matthew E., Hysi, Pirro, Jackson, David K., Jamshidi, Yalda, Jing, Tian, Joyce, Chris, Kaye, Jane, Keane, Thomas, Keogh, Julia, Kemp, John, Kennedy, Karen, Kolb-Kokocinski, Anja, Lachance, Genevieve, Langford, Cordelia, Lawson, Daniel, Lee, Irene, Lek, Monkol, Liang, Jieqin, Lin, Hong, Li, Rui, Li, Yingrui, Liu, Ryan, Lönnqvist, Jouko, Lopes, Margarida, Lotchkova, Valentina, MacArthur, Daniel, Marchini, Jonathan, Maslen, John, Massimo, Mangino, Mathieson, Iain, Marenne, Gaëlle, McCarthy, Shane, McGuffin, Peter, McIntosh, Andrew, McKechanie, Andrew G., McQuillin, Andrew, Memari, Yasin, Metrustry, Sarah, Min, Josine, Mitchison, Hannah, Moayyeri, Alireza, Morris, James, Muddyman, Dawn, Muntoni, Francesco, Northstone, Kate, O'Donovan, Michael Conlon, Onoufriadis, Alexandros, O'Rahilly, Stephen, Oualkacha, Karim, Owen, Michael John, Palotie, Aarno, Panoutsopoulou, Kalliope, Parker, Victoria, Parr, Jeremy R., Paternoster, Lavinia, Paunio, Tiina, Payne, Felicity, Perry, John, Pietilainen, Olli, Plagnol, Vincent, Quaye, Lydia, Quail, Michael A., Raymond, Lucy, Rehnström, Karola, Richards, Brent, Ring, Susan, Ritchie, Graham R. S., Roberts, Nicola, Savage, David B., Scambler, Peter, Schiffels, Stephen, Schmidts, Miriam, Schoenmakers, Nadia, Semple, Robert K., Serra, Eva, Sharp, Sally I., Shihab, Hasheem, Shin, So-Youn, Skuse, David, Small, Kerrin, Soranzo, Nicole, Southam, Lorraine, Spasic-Boskovic, Olivera, Spector, Tim, St Clair, David, Stalker, Jim, Stevens, Elizabeth, St Pourcian, Beate, Sun, Jianping, Surdulescu, Gabriela, Suvisaari, Jaana, Tachmazidou, Ionna, Timpson, Nicholas, Tobin, Martin D., Valdes, Ana, Van Kogelenberg, Margriet, Vijayarangakannan, Parthiban, Visscher, Peter M., Wain, Louise V., Walter, Klaudia, Walters, James Tynan Rhys, Wang, Guangbiao, Wang, Jun, Wang, Yu, Ward, Kirsten, Wheeler, Elanor, Whyte, Tamieka, Williams, Hywel, Williamson, Kathleen A., Wilson, Crispian, Wilson, Scott G., Wong, Kim, Xu, ChangJiang, Yang, Jian, Zeggini, Eleftheria, Zhang, Fend, Zhang, Pingbo and Zheng, Hou-Feng 2014. A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans. Nature Communications 5 , 4871. 10.1038/ncomms5871

Ruderfer, D. M., Fanous, A. H., Ripke, S., McQuillin, A., Amdur, R. L., Gejman, P. V., O'Donovan, Michael Conlon, Andreassen, O. A., Djurovic, S., Hultman, C. M., Kelsoe, J. R., Jamain, S., Landén, M., Leboyer, M., Nimgaonkar, V., Nurnberger, J., Smoller, J. W., Craddock, Nicholas John, Corvin, A., Sullivan, P. F., Holmans, Peter Alan, Sklar, P. and Kendler, K. S. 2014. Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia. Molecular Psychiatry 19 (9) , pp. 1017-24. 10.1038/mp.2013.138

Munafò, Marcus, Noble, Simon, Browne, William J., Brunner, Dani, Button, Katherine, Ferreira, Joaquim, Holmans, Peter, Langbehn, Douglas, Lewis, Glyn, Lindquist, Martin, Tilling, Kate, Wagenmakers, Eric-Jan and Blumenstein, Robi 2014. Scientific rigor and the art of motorcycle maintenance. Nature Biotechnology 32 (9) , pp. 871-873. 10.1038/nbt.3004

Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James Tynan Rhys, Farh, Kai-How, Holmans, Peter A., Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Pers, Tune H., Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Begemann, Martin, Belliveau Jr, Richard A., Bene, Judit, Bergen, Sarah E., Bevilacqua, Elizabeth, Bigdeli, Tim B., Black, Donald W., Bruggeman, Richard, Buccola, Nancy G., Buckner, Randy L., Byerley, William, Cahn, Wiepke, Cai, Guiqing, Campion, Dominique, Cantor, Rita M., Carr, Vaughan J., Carrera, Noa, Catts, Stanley V., Chambert, Kimberly D., Chan, Raymond C. K., Chen, Ronald Y. L., Chen, Eric Y. H., Cheng, Wei, Cheung, Eric F. C., Ann Chong, Siow, Robert Cloninger, C., Cohen, David, Cohen, Nadine, Cormican, Paul, Craddock, Nicholas John, Crowley, James J., Curtis, David, Davidson, Michael, Davis, Kenneth L., Degenhardt, Franziska, Del Favero, Jurgen, Demontis, Ditte, Dikeos, Dimitris, Dinan, Timothy, Djurovic, Srdjan, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Dudbridge, Frank, Durmishi, Naser, Eichhammer, Peter, Eriksson, Johan, Escott-Price, Valentina, Essioux, Laurent, Fanous, Ayman H., Farrell, Martilias S., Frank, Josef, Franke, Lude, Freedman, Robert, Freimer, Nelson B., Friedl, Marion, Friedman, Joseph I., Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Giegling, Ina, Giusti-Rodríguez, Paola, Godard, Stephanie, Goldstein, Jacqueline I., Golimbet, Vera, Gopal, Srihari, Gratten, Jacob, de Haan, Lieuwe, Hammer, Christian, Hamshere, Marian Lindsay, Hansen, Mark, Hansen, Thomas, Haroutunian, Vahram, Hartmann, Annette M., Henskens, Frans A., Herms, Stefan, Hirschhorn, Joel N., Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V., Hougaard, David M., Ikeda, Masashi, Joa, Inge, Julià, Antonio, Kahn, René S., Kalaydjieva, Luba, Karachanak-Yankova, Sena, Karjalainen, Juha, Kavanagh, David, Keller, Matthew C., Kennedy, James L., Khrunin, Andrey, Kim, Yunjung, Klovins, Janis, Knowles, James A., Konte, Bettina, Kucinskas, Vaidutis, Ausrele Kucinskiene, Zita, Kuzelova-Ptackova, Hana, Kähler, Anna K., Laurent, Claudine, Lee Chee Keong, Jimmy, Hong Lee, S., Legge, Sophie E., Lerer, Bernard, Li, Miaoxin, Li, Tao, Liang, Kung-Yee, Lieberman, Jeffrey, Limborska, Svetlana, Loughland, Carmel M., Lubinski, Jan, Lönnqvist, Jouko, Macek Jr, Milan, Magnusson, Patrik K. E., Maher, Brion S., Maier, Wolfgang, Mallet, Jacques, Marsal, Sara, Mattheisen, Manuel, Mattingsdal, Morten, McCarley, Robert W., McDonald, Colm, McIntosh, Andrew M., Meier, Sandra, Meijer, Carin J., Melegh, Bela, Melle, Ingrid, Mesholam-Gately, Raquelle I., Metspalu, Andres, Michie, Patricia T., Milani, Lili, Milanova, Vihra, Mokrab, Younes, Morris, Derek W., Mors, Ole, Murphy, Kieran C., Murray, Robin M., Myin-Germeys, Inez, Müller-Myhsok, Bertram, Nelis, Mari, Nenadic, Igor, Nertney, Deborah A., Nestadt, Gerald, Nicodemus, Kristin K., Nikitina-Zake, Liene, Nisenbaum, Laura, Nordin, Annelie, O'Callaghan, Eadbhard, O'Dushlaine, Colm, O'Neill, F. Anthony, Oh, Sang-Yun, Olincy, Ann, Olsen, Line, Van Os, Jim, Endophenotypes International Consortium, Psychosis, Pantelis, Christos, Papadimitriou, George N., Papiol, Sergi, Parkhomenko, Elena, Pato, Michele T., Paunio, Tiina, Pejovic-Milovancevic, Milica, Perkins, Diana O., Pietiläinen, Olli, Pimm, Jonathan, Pocklington, Andrew, Powell, John, Price, Alkes, Pulver, Ann E., Purcell, Shaun M., Quested, Digby, Rasmussen, Henrik B., Reichenberg, Abraham, Reimers, Mark A., Richards, Alexander, Roffman, Joshua L., Roussos, Panos, Ruderfer, Douglas, Salomaa, Veikko, Sanders, Alan R., Schall, Ulrich, Schubert, Christian R., Schulze, Thomas G., Schwab, Sibylle G., Scolnick, Edward M., Scott, Rodney J., Seidman, Larry J., Shi, Jianxin, Sigurdsson, Engilbert, Silagadze, Teimuraz, Silverman, Jeremy M., Sim, Kang, Slominsky, Petr, Smoller, Jordan W., So, Hon-Cheong, Spencer, ChrisC. A., Stahl, Eli A., Stefansson, Hreinn, Steinberg, Stacy, Stogmann, Elisabeth, Straub, Richard E., Strengman, Eric, Strohmaier, Jana, Scott Stroup, T., Subramaniam, Mythily, Suvisaari, Jaana, Svrakic, Dragan M., Szatkiewicz, Jin P., Söderman, Erik, Thirumalai, Srinivas, Toncheva, Draga, Tosato, Sarah, Veijola, Juha, Waddington, John, Walsh, Dermot, Wang, Dai, Wang, Qiang, Webb, Bradley T., Weiser, Mark, Wildenauer, Dieter B., Williams, Nigel Melville, Williams, Stephanie, Witt, Stephanie H., Wolen, Aaron R., Wong, Emily H. M., Wormley, Brandon K., Simon Xi, Hualin, Zai, Clement C., Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R., Stefansson, Kari, Visscher, Peter M., Trust Case-Control Consortium, Wellcome, Adolfsson, Rolf, Andreassen, Ole A., Blackwood, Douglas H. R., Bramon, Elvira, Buxbaum, Joseph D., Børglum, Anders D., Cichon, Sven, Darvasi, Ariel, Domenici, Enrico, Ehrenreich, Hannelore, Esko, Tõnu, Gejman, Pablo V., Gill, Michael, Gurling, Hugh, Hultman, Christina M., Iwata, Nakao, Jablensky, Assen V., Jönsson, Erik G., Kendler, Kenneth S., Kirov, George, Knight, Jo, Lencz, Todd, Levinson, Douglas F., Li, Qingqin S., Liu, Jianjun, Malhotra, Anil K., McCarroll, Steven A., McQuillin, Andrew, Moran, Jennifer L., Mortensen, Preben B., Mowry, Bryan J., Nöthen, Markus M., Ophoff, Roel A., Owen, Michael John, Palotie, Aarno, Pato, Carlos N., Petryshen, Tracey L., Posthuma, Danielle, Rietschel, Marcella, Riley, Brien P., Rujescu, Dan, Sham, Pak C., Sklar, Pamela, St Clair, David, Weinberger, Daniel R., Wendland, Jens R., Werge, Thomas, Daly, Mark J., Sullivan, Patrick F., O’Donovan, Michael Conlon, Holmans, Peter and Li, Meng 2014. Biological insights from 108 schizophrenia-associated genetic loci. Nature 511 (7510) , pp. 421-427. 10.1038/nature13595

Erk, Susanne, Meyer-Lindenberg, Andreas, Linden, David Edmund Johannes, Lancaster, Thomas, Mohnke, Sebastian, Grimm, Oliver, Degenhardt, Franziska, Holmans, Peter Alan, Pocklington, Andrew, Schmierer, Phöbe, Haddad, Leila, Mühleisen, Thomas W., Mattheisen, Manuel, Witt, Stephanie H., Romanczuk-Seiferth, Nina, Tost, Heike, Schott, Björn H., Cichon, Sven, Nöthen, Markus M., Rietschel, Marcella, Heinz, Andreas and Walter, Henrik 2014. Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects. NeuroImage 94 , pp. 147-154. 10.1016/j.neuroimage.2014.03.007

Craddock, Nicholas John, Holmans, Peter Alan, Humphreys, Isla, Li, Meng, O'Donovan, Michael Conlon, Owen, Michael John, Richards, Alexander and Williams, Nigel Melville 2014. Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations. Schizophrenia Bulletin 40 (4) , pp. 729-736. 10.1093/schbul/sbu069

Martin, Joanna, Cooper, Miriam, Hamshere, Marian Lindsay, Pocklington, Andrew, Scherer, Stephen W., Kent, Lindsey, Gill, Michael, Owen, Michael John, Williams, Nigel Melville, O'Donovan, Michael Conlon, Thapar, Anita and Holmans, Peter Alan 2014. Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants. Journal of the American Academy of Child & Adolescent Psychiatry 53 (7) , pp. 761-770. 10.1016/j.jaac.2014.03.004
file

Escott-Price, Valentina, Bellenguez, Céline, Wang, Li-San, Choi, Seung-Hoan, Harold, Denise, Jones, Lesley, Holmans, Peter Alan, Gerrish, Amy, Vedernikov, Alexey, Richards, Alexander, DeStefano, Anita L., Lambert, Jean-Charles, Ibrahim-Verbaas, Carla A., Naj, Adam C., Sims, Rebecca, Jun, Gyungah, Bis, Joshua C., Beecham, Gary W., Grenier-Boley, Benjamin, Russo, Giancarlo, Thornton-Wells, Tricia A., Denning, Nicola, Smith, Albert V., Chouraki, Vincent, Thomas, Charlene, Ikram, M. Arfan, Zelenika, Diana, Vardarajan, Badri N., Kamatani, Yoichiro, Lin, Chiao-Feng, Schmidt, Helena, Kunkle, Brian, Dunstan, Melanie, Vronskaya, Maria, Johnson, Andrew D., Ruiz, Agustin, Bihoreau, Marie-Thérèse, Reitz, Christiane, Pasquier, Florence, Hollingworth, Paul, Hanon, Olivier, Fitzpatrick, Annette L., Buxbaum, Joseph D., Campion, Dominique, Crane, Paul K., Baldwin, Clinton, Becker, Tim, Gudnason, Vilmundur, Cruchaga, Carlos, Craig, David, Amin, Najaf, Berr, Claudine, Lopez, Oscar L., De Jager, Philip L., Deramecourt, Vincent, Johnston, Janet A., Evans, Denis, Lovestone, Simon, Letenneur, Luc, Hernández, Isabel, Rubinsztein, David C., Eiriksdottir, Gudny, Sleegers, Kristel, Goate, Alison M., Fiévet, Nathalie, Huentelman, Matthew J., Gill, Michael, Brown, Kristelle, Kamboh, M. Ilyas, Keller, Lina, Barberger-Gateau, Pascale, McGuinness, Bernadette, Larson, Eric B., Myers, Amanda J., Dufouil, Carole, Todd, Stephen, Wallon, David, Love, Seth, Rogaeva, Ekaterina, Gallacher, John, George-Hyslop, Peter St, Clarimon, Jordi, Lleo, Alberto, Bayer, Antony James, Tsuang, Debby W., Yu, Lei, Tsolaki, Magda, Bossù, Paola, Spalletta, Gianfranco, Proitsi, Petra, Collinge, John, Sorbi, Sandro, Garcia, Florentino Sanchez, Fox, Nick C., Hardy, John, Naranjo, Maria Candida Deniz, Bosco, Paolo, Clarke, Robert, Brayne, Carol, Galimberti, Daniela, Scarpini, Elio, Bonuccelli, Ubaldo, Mancuso, Michelangelo, Siciliano, Gabriele, Moebus, Susanne, Mecocci, Patrizia, Zompo, Maria Del, Maier, Wolfgang, Hampel, Harald, Pilotto, Alberto, Frank-García, Ana, Panza, Francesco, Solfrizzi, Vincenzo, Caffarra, Paolo, Nacmias, Benedetta, Perry, William, Mayhaus, Manuel, Lannfelt, Lars, Hakonarson, Hakon, Pichler, Sabrina, Carrasquillo, Minerva M., Ingelsson, Martin, Beekly, Duane, Alvarez, Victoria, Zou, Fanggeng, Valladares, Otto, Younkin, Steven G., Coto, Eliecer, Hamilton-Nelson, Kara L., Gu, Wei, Razquin, Cristina, Pastor, Pau, Mateo, Ignacio, Owen, Michael John, Faber, Kelley M., Jonsson, Palmi V., Combarros, Onofre, O'Donovan, Michael Conlon, Cantwell, Laura B., Soininen, Hilkka, Blacker, Deborah, Mead, Simon, Mosley, Thomas H., Bennett, David A., Harris, Tamara B., Fratiglioni, Laura, Holmes, Clive, de Bruijn, Renee F. A. G., Passmore, Peter, Montine, Thomas J., Bettens, Karolien, Rotter, Jerome I., Brice, Alexis, Morgan, Kevin, Foroud, Tatiana M., Kukull, Walter A., Hannequin, Didier, Powell, John F., Nalls, Michael A., Ritchie, Karen, Lunetta, Kathryn L., Kauwe, John S. K., Boerwinkle, Eric, Riemenschneider, Matthias, Boada, Mercè, Hiltunen, Mikko, Martin, Eden R., Schmidt, Reinhold, Rujescu, Dan, Dartigues, Jean-François, Mayeux, Richard, Tzourio, Christophe, Hofman, Albert, Nöthen, Markus M., Graff, Caroline, Psaty, Bruce M., Haines, Jonathan L., Lathrop, Mark, Pericak-Vance, Margaret A., Launer, Lenore J., Van Broeckhoven, Christine, Farrer, Lindsay A., van Duijn, Cornelia M., Ramirez, Alfredo, Seshadri, Sudha, Schellenberg, Gerard D., Amouyel, Philippe and Williams, Julie 2014. Gene-wide analysis detects two new susceptibility genes for Alzheimer's Disease. PLoS ONE 9 (6) , e94661. 10.1371/journal.pone.0094661
file

Liu, Guiyou, Yao, Lifen, Liu, Jiafeng, Jiang, Yongshuai, Ma, Guoda, Chen, Zugen, Zhao, Bin, Li, Keshen, Chapman, Jade, Denning, Nicola, Escott-Price, Valentina, Gerrish, Amy, Hamshere, Marian Lindsay, Harold, Denise, Hollingworth, Paul, Holmans, Peter Alan, O'Donovan, Michael Conlon and Owen, Michael John 2014. Cardiovascular disease contributes to Alzheimer's disease: evidence from large-scale genome-wide association studies. Neurobiology of Aging 35 (4) , pp. 786-92. 10.1016/j.neurobiolaging.2013.10.084

Duncan, Laramie E., Holmans, Peter Alan, Lee, Phil H., O'Dushlaine, Colm T., Kirby, Andrew W., Smoller, Jordan W., Öngür, Dost and Cohen, Bruce M. 2014. Pathway analyses implicate glial cells in schizophrenia. PLoS ONE 9 (2) , e89441. 10.1371/journal.pone.0089441
file

Fromer, Menachem, Pocklington, Andrew, Kavanagh, David, Williams, Hywel John, Dwyer, Sarah, Gormley, Padhraig, Georgieva, Lyudmila, Rees, Elliott, Palta, Priit, Ruderfer, Douglas, Carrera, Noa, Humphreys, Isla, Johnson, Jessica S., Roussos, Panos, Barker, Douglas D., Banks, Eric, Milanova, Vihra, Grant, Seth G., Hannon, Eilis, Rose, Samuel A., Chambert, Kimberly, Mahajan, Milind, Scolnick, Edward M., Moran, Jennifer L., Kirov, George, Palotie, Aarno, McCarroll, Steven A., Holmans, Peter Alan, Sklar, Pamela, Owen, Michael John, Purcell, Shaun M. and O'Donovan, Michael Conlon 2014. De novo mutations in schizophrenia implicate synaptic networks. Nature 506 (7487) , pp. 179-184. 10.1038/nature12929

van Scheltinga, A. F. Terwisscha, Bakker, S. C., van Haren, N. E. M., Derks, E. M., Buizer-Voskamp, J. E., Cahn, W., Ripke, S., Ophoff, R. A., Kahn, R. S., Craddock, Nicholas John, Escott-Price, Valentina, Georgieva, Lyudmila, Hamshere, Marian Lindsay, Holmans, Peter Alan, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John, Ruderfer, Doug, Williams, Hywel, Williams, Nigel Melville and Zammit, Stanley 2013. Schizophrenia genetic variants are not associated with intelligence. Psychological Medicine 43 (12) , pp. 2563-2570. 10.1017/S0033291713000196

Green, Elaine Karen, Hamshere, Marian Lindsay, Forty, Elizabeth, Gordon-Smith, K., Fraser, Christine, Russell, Elen Elizabeth, Grozeva, Detelina Valentinova, Kirov, George, Holmans, Peter Alan, Moran, J. L., Purcell, S., Sklar, P., Owen, Michael John, O'Donovan, Michael Conlon, Jones, L., Jones, Ian Richard and Craddock, Nicholas John 2013. Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample. Molecular Psychiatry 18 (12) , pp. 1302-1307. 10.1038/mp.2012.142

Lambert, Jean-Charles, Ibrahim-Verbaas, Carla A., Harold, Denise, Naj, Adam C., Sims, Rebecca, Bellenguez, Céline, Jun, Gyungah, DeStefano, Anita L., Bis, Joshua C., Beecham, Gary W., Grenier-Boley, Benjamin, Russo, Giancarlo, Thornton-Wells, Tricia A., Denning, Nicola, Smith, Albert V., Chouraki, Vincent, Thomas, Charlene, Ikram, M. Arfan, Zelenika, Diana, Vardarajan, Badri N., Kamatani, Yoichiro, Lin, Chiao-Feng, Gerrish, Amy, Schmidt, Helena, Kunkle, Brian, Dunstan, Melanie, Ruiz, Agustin, Bihoreau, Marie-Thérèse, Choi, Seung-Hoan, Reitz, Christiane, Pasquier, Florence, Hollingworth, Paul, Ramirez, Alfredo, Hanon, Olivier, Fitzpatrick, Annette L., Buxbaum, Joseph D., Campion, Dominique, Crane, Paul K, Baldwin, Clinton, Becker, Tim, Gudnason, Vilmundur, Cruchaga, Carlos, Craig, David, Amin, Najaf, Berr, Claudine, Lopez, Oscar L., De Jager, Philip L., Deramecourt, Vincent, Johnston, Janet A., Evans, Denis, Lovestone, Simon, Letenneur, Luc, Morón, Francisco J., Rubinsztein, David C., Eiriksdottir, Gudny, Sleegers, Kristel, Goate, Alison M., Fiévet, Nathalie, Huentelman, Matthew J., Gill, Michael, Brown, Kristelle, Kamboh, M Ilyas, Keller, Lina, Barberger-Gateau, Pascale, McGuinness, Bernadette, Larson, Eric B., Green, Robert, Myers, Amanda J., Dufouil, Carole, Todd, Stephen, Wallon, David, Love, Seth, Rogaeva, Ekaterina, Gallacher, John Edward, St George-Hyslop, Peter, Clarimon, Jordi, Lleo, Alberto, Bayer, Antony James, Tsuang, Debby W., Yu, Lei, Tsolaki, Magda, Bossù, Paola, Spalletta, Gianfranco, Proitsi, Petroula, Collinge, John, Sorbi, Sandro, Sanchez-Garcia, Florentino, Fox, Nick C., Hardy, John, Naranjo, Maria Candida Deniz, Bosco, Paolo, Clarke, Robert, Brayne, Carol, Galimberti, Daniela, Mancuso, Michelangelo, Matthews, Fiona, Moebus, Susanne, Mecocci, Patrizia, Del Zompo, Maria, Maier, Wolfgang, Hampel, Harald, Pilotto, Alberto, Bullido, Maria, Panza, Francesco, Caffarra, Paolo, Nacmias, Benedetta, Gilbert, John R., Mayhaus, Manuel, Lannfelt, Lars, Hakonarson, Hakon, Pichler, Sabrina, Carrasquillo, Minerva M., Ingelsson, Martin, Beekly, Duane, Alvarez, Victoria, Zou, Fanggeng, Valladares, Otto, Younkin, Steven G., Coto, Eliecer, Hamilton-Nelson, Kara L., Gu, Wei, Razquin, Cristina, Pastor, Pau, Mateo, Ignacio, Owen, Michael John, Faber, Kelley M., Jonsson, Palmi V., Combarros, Onofre, O'Donovan, Michael Conlon, Cantwell, Laura B., Soininen, Hilkka, Blacker, Deborah, Mead, Simon, Mosley, Thomas H., Bennett, David A., Harris, Tamara B., Fratiglioni, Laura, Holmes, Clive, de Bruijn, Renee F. A. G., Passmore, Peter, Montine, Thomas J., Bettens, Karolien, Rotter, Jerome I., Brice, Alexis, Morgan, Kevin, Foroud, Tatiana M., Kukull, Walter A., Hannequin, Didier, Powell, John F., Nalls, Michael A., Ritchie, Karen, Lunetta, Kathryn L., Kauwe, John S. K., Boerwinkle, Eric, Riemenschneider, Matthias, Boada, Mercè, Hiltunen, Mikko, Martin, Eden R, Schmidt, Reinhold, Rujescu, Dan, Wang, Li-San, Dartigues, Jean-François, Mayeux, Richard, Tzourio, Christophe, Hofman, Albert, Nöthen, Markus M., Graff, Caroline, Psaty, Bruce M., Jones, Lesley, Haines, Jonathan L., Holmans, Peter Alan, Lathrop, Mark, Pericak-Vance, Margaret A., Launer, Lenore J., Farrer, Lindsay A., van Duijn, Cornelia M., Van Broeckhoven, Christine, Escott-Price, Valentina, Seshadri, Sudha, Williams, Julie, Schellenberg, Gerard D. and Amouyel, Philippe 2013. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease [Letter]. Nature Genetics 45 (12) , pp. 1452-1458. 10.1038/ng.2802

Lee, S., Ripke, S., Neale, B., Faraone, S., Purcell, S., Perlis, R., Mowry, B., Thapar, Anita, Goddard, M., Witte, J., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen, O., Anjorin, A., Anney, Richard, Anttila, V., Arking, D., Asherson, P., Azevedo, M., Backlund, L., Badner, J., Bailey, A., Banaschewski, T., Barchas, J., Barnes, M., Barrett, T., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen, S., Berrettini, W., Betancur, C., Bettecken, T., Biederman, J., Binder, E., Black, D., Blackwood, D., Bloss, C., Boehnke, M., Boomsma, D., Breen, G., Breuer, R., Bruggeman, R., Cormican, P., Buccola, N., Buitelaar, J., Bunney, W., Buxbaum, J., Byerley, W., Byrne, E., Caesar, S., Cahn, W., Cantor, R., Casas, M., Chakravarti, A., Chambert, K., Choudhury, K., Cichon, S., Cloninger, C., Collier, D., Cook, E., Coon, H., Cormand, B., Corvin, A., Coryell, W., Craig, D., Craig, I., Crosbie, J., Cuccaro, M., Curtis, D., Czamara, D., Datta, S., Dawson, G., Day, R., De Geus, E., Degenhardt, F., Djurovic, S., Donohoe, G., Doyle, A., Duan, J., Dudbridge, F., Duketis, E., Ebstein, R., Edenberg, H., Elia, J., Ennis, S., Etain, B., Fanous, A., Farmer, A., Ferrier, I., Flickinger, M., Fombonne, E., Foroud, T., Frank, J., Franke, B., Fraser, Christine, Freedman, R., Freimer, N., Freitag, C., Friedl, M., Frisén, L., Gallagher, L., Gejman, P., Georgieva, Lyudmila, Gershon, E., Geschwind, D., Giegling, I., Gill, M., Gordon, S., Gordon-Smith, K., Green, E., Greenwood, T., Grice, D., Gross, M., Grozeva, D., Guan, W., Gurling, H., De Haan, L., Haines, J., Hakonarson, H., Hallmayer, J., Hamilton, S., Hamshere, Marian Lindsay, Hansen, T., Hartmann, A., Hautzinger, M., Heath, A., Henders, A., Herms, S., Hickie, I., Hipolito, M., Hoefels, S., Holmans, Peter Alan, Holsboer, F., Hoogendijk, W., Hottenga, J., Hultman, C., Hus, V., Ingason, A., Ising, M., Jamain, S., Jones, E., Jones, Ian Richard, Jones, L., Tzeng, J., Kähler, A., Kahn, R., Kandaswamy, R., Keller, M., Kennedy, J., Kenny, E., Kent, L., Kim, Y., Kirov, George, Klauck, S., Klei, L., Knowles, J., Kohli, M., Koller, D., Konte, B., Korszun, A., Krabbendam, L., Krasucki, R., Kuntsi, J., Kwan, P., Landén, M., Långström, N., Lathrop, M., Lawrence, J., Lawson, W., Leboyer, M., Ledbetter, D., Lee, P., Lencz, T., Lesch, K., Levinson, D., Lewis, C., Li, J., Lichtenstein, P., Lieberman, J., Lin, D., Linszen, D., Liu, C., Lohoff, F., Loo, S., Lord, C., Lowe, J., Lucae, S., MacIntyre, D., Madden, P., Maestrini, E., Magnusson, P., Mahon, P., Maier, W., Malhotra, A., Mane, S., Martin, C., Martin, N., Mattheisen, M., Matthews, K., Mattingsdal, M., McCarroll, S., McGhee, K., McGough, J., McGrath, P., McGuffin, P., McInnis, M., McIntosh, A., McKinney, R., McLean, A., McMahon, F., McMahon, W., McQuillin, A., Medeiros, H., Medland, S., Meier, S., Melle, I., Meng, F., Meyer, J., Middeldorp, C., Middleton, L., Milanova, V., Miranda, A., Monaco, A., Montgomery, G., Moran, J., Moreno-De-Luca, D., Morken, G., Morris, D., Morrow, E., Moskvina, V., Muglia, P., Mühleisen, T., Muir, W., Müller-Myhsok, B., Murtha, M., Myers, R., Myin-Germeys, I., Neale, M., Nelson, S., Nievergelt, C., Nikolov, I., Nimgaonkar, V., Nolen, W., Nöthen, M., Nurnberger, J., Nwulia, E., Nyholt, D., O'Dushlaine, C., Oades, R., Olincy, A., Oliveira, G., Olsen, L., Ophoff, R., Osby, U., Owen, Michael John, Palotie, A., Parr, J., Paterson, A., Pato, C., Pato, M., Penninx, B., Pergadia, M., Pericak-Vance, M., Pickard, B., Pimm, J., Piven, J., Posthuma, D., Potash, J., Poustka, F., Propping, P., Puri, V., Quested, D., Quinn, E., Ramos-Quiroga, J., Rasmussen, H., Raychaudhuri, S., Rehnström, K., Reif, A., Ribasés, M., Rice, J., Rietschel, M., Roeder, K., Roeyers, H., Rossin, L., Rothenberger, A., Rouleau, G., Ruderfer, D., Rujescu, D., Sanders, A., Sanders, S., Santangelo, S., Sergeant, J., Schachar, R., Schalling, M., Schatzberg, A., Scheftner, W., Schellenberg, G., Scherer, S., Schork, N., Schulze, T., Schumacher, J., Schwarz, M., Scolnick, E., Scott, L., Shi, J., Shilling, P., Shyn, S., Silverman, J., Slager, S., Smalley, S., Smit, J., Smith, E., Sonuga-Barke, E., St. Clair, D., State, M., Steffens, M., Steinhausen, H., Strauss, J., Strohmaier, J., Stroup, T., Sutcliffe, J., Szatmari, P., Szelinger, S., Thirumalai, S., Thompson, R., Todorov, A., Tozzi, F., Treutlein, J., Uhr, M., van den Oord, E., Van Grootheest, G., Van Os, J., Vicente, A., Vieland, V., Vincent, J., Visscher, P., Walsh, C., Wassink, T., Watson, S., Weissman, M., Werge, T., Wienker, T., Wijsman, E., Willemsen, G., Williams, Nigel Melville, Willsey, A., Witt, S., Xu, W., Young, A., Yu, T., Zammit, Stanley, Zandi, P., Zhang, P., Zitman, F., Zöllner, S., Devlin, B., Kelsoe, J., Sklar, P., Daly, M., O'Donovan, Michael Conlon, Craddock, Nicholas John, Sullivan, P., Smoller, J., Kendler, K., Wray, N. and Escott-Price, Valentina 2013. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics 45 (9) , pp. 984-994. 10.1038/ng.2711

Ripke, S., O'Dushlaine, C., Chambert, K., Moran, J., Kähler, A., Akterin, S., Bergen, S., Collins, A., Crowley, J., Fromer, M., Kim, Y., Lee, S., Magnusson, P., Sanchez, N., Stahl, E., Williams, S., Wray, N., Xia, K., Bettella, F., Borglum, A., Bulik-Sullivan, B., Cormican, P., Craddock, Nicholas John, de Leeuw, C., Durmishi, N., Gill, M., Golimbet, V., Hamshere, Marian Lindsay, Holmans, Peter Alan, Hougaard, D., Kendler, K., Lin, K., Morris, D., Mors, O., Mortensen, P., Neale, B., O'Neill, F., Owen, Michael John, Milovancevic, M., Posthuma, D., Powell, J., Richards, Alexander, Riley, B., Ruderfer, D., Rujescu, D., Sigurdsson, E., Silagadze, T., Smit, A., Stefansson, H., Steinberg, S., Suvisaari, J., Tosato, S., Verhage, M., Walters, James Tynan Rhys, Levinson, D., Gejman, P., Kendler, K., Laurent, C., Mowry, B., O'Donovan, Michael Conlon, Owen, Michael John, Pulver, A., Riley, B., Schwab, S., Wildenauer, D., Dudbridge, F., Holmans, Peter Alan, Shi, J., Albus, M., Alexander, M., Campion, D., Cohen, D., Dikeos, D., Duan, J., Eichhammer, P., Godard, S., Hansen, M., Lerer, F., Liang, K., Maier, W., Mallet, J., Nertney, D., Nestadt, G., Norton, N., O'Neill, F., Papadimitriou, G., Ribble, R., Sanders, A., Silverman, J., Walsh, D., Williams, Nigel Melville, Wormley, B., Arranz, M., Bakker, S., Bender, S., Bramon, E., Collier, D., Crespo-Facorro, B., Hall, Jeremy, Iyegbe, C., Jablensky, A., Kahn, R., Kalaydjieva, L., Lawrie, S., Lewis, C., Lin, K., Linszen, D., Mata, I., McIntosh, A., Murray, R., Ophoff, R., Powell, John, Rujescu, D., Van Os, J., Walshe, M., Weisbrod, M., Wiersma, D., Donnelly, P., Barroso, I., Blackwell, J., Bramon, E., Brown, M., Casas, J., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H., Mathew, C., Palmer, C., Plomin, R., Rautanen, A., Sawcer, S., Trembath, R., Viswanathan, A., Wood, N., Spencer, C., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Donnelly, P., Langford, C., Hunt, S., Edkins, Sarah, Gwilliam, R., Blackburn, H., Bumpstead, S., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., McCann, O., Liddle, J., Potter, S., Ravindrarajah, R., Ricketts, M., Tashakkori-Ghanbaria, A., Waller, M., Weston, P., Widaa, S., Whittaker, P., Barroso, I., Deloukas, P., Mathew, C., Blackwell, J., Brown, M., Corvin, Aiden P, McCarthy, Mark I, Spencer, Chris C A, Bramon, Elvira, Corvin, Aiden P, O'Donovan, Michael C, Stefansson, Kari, Scolnick, Edward, Purcell, Shaun, McCarroll, Steven A, Sklar, Pamela, Hultman, Christina M and Sullivan, Patrick F 2013. Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nature Genetics 45 (10) , pp. 1150-1159. 10.1038/ng.2742

Hamshere, Marian Lindsay, Stergiakouli, Evangelia, Langley, Kate, Martin, Joanna, Holmans, Peter Alan, Kent, L., Owen, Michael John, Gill, M., Thapar, Anita, O'Donovan, Michael Conlon and Craddock, Nicholas John 2013. Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia. British Journal of Psychiatry 203 (2) , pp. 107-111. 10.1192/bjp.bp.112.117432
file

Hamshere, Marian Lindsay, Langley, Kate, Martin, Joanna, Agha, Sharifah Shameem, Stergiakouli, Evangelia, Anney, Richard, Buitelaar, Jan, Faraone, Stephen V., Lesch, Klaus-Peter, Neale, Benjamin M., Franke, Barbara, Sonuga-Barke, Edmund, Asherson, Philip, Merwood, Andrew, Kuntsi, Jonna, Medland, Sarah E., Ripke, Stephan, Steinhausen, Hans-Christoph, Freitag, Christine, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Meyer, Jobst, Palmason, Haukur, Vasquez, Alejandro Arias, Lambregts-Rommelse, Nanda, Roeyers, Herbert, Biederman, Joseph, Doyle, Alysa E., Hakonarson, Hakon, Rothenberger, Aribert, Banaschewski, Tobias, Oades, Robert D., McGough, James J., Kent, Lindsey, Williams, Nigel Melville, Owen, Michael John, Holmans, Peter Alan, O'Donovan, Michael Conlon and Thapar, Anita 2013. High loading of polygenic risk for ADHD in children with comorbid aggression. American Journal of Psychiatry 170 (8) , pp. 909-916. 10.1176/appi.ajp.2013.12081129

Yang, Li, Neale, Benjamin M., Liu, Lu, Lee, S. Hong, Wray, Naomi R., Ji, Ning, Li, Haimei, Qian, Qiujin, Wang, Dongliang, Li, Jun, Faraone, Stephen V., Wang, Yufeng, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John, Thapar, Anita and Williams, Nigel Melville 2013. Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: Genome-wide association study of both common and rare variants. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 (5) , pp. 419-430. 10.1002/ajmg.b.32169

Hamshere, Marian Lindsay, Walters, James Tynan Rhys, Smith, Rhodri, Richards, Alexander, Green, Elaine Karen, Grozeva, Detelina Valentinova, Jones, Ian Richard, Forty, Elizabeth, Jones, L., Gordon-Smith, Katherine, Riley, B., O'Neill, T., Kendler, K. S., Sklar, P., Purcell, S, Kranz, J., Morris, D., Gill, M., Holmans, Peter Alan, Craddock, Nicholas John, Corvin, A., Owen, Michael John and O'Donovan, Michael Conlon 2013. Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC. Molecular Psychiatry 18 (6) , pp. 708-712. 10.1038/mp.2012.67

Zou, Fanggeng, Belbin, Olivia, Carrasquillo, Minerva M., Culley, Oliver J., Hunter, Talisha A., Ma, Li, Bisceglio, Gina D., Allen, Mariet, Dickson, Dennis W., Graff-Radford, Neill R., Petersen, Ronald C., Morgan, Kevin, Younkin, Steven G., Chapman, Jade, Denning, Nicola, Escott-Price, Valentina, Gerrish, Amy, Hamshere, Marian Lindsay, Harold, Denise, Hollingworth, Paul, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John, Pahwa, Jaspreet, Sims, Rebecca, Thomas, Charlene and Williams, Julie 2013. Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's Disease pathology. PLoS ONE 8 (5) , e64802. 10.1371/journal.pone.0064802
file

Terwisscha van Scheltinga, Afke F., Bakker, Steven C., van Haren, Neeltje E.M., Derks, Eske M., Buizer-Voskamp, Jacobine E., Boos, Heleen B.M., Cahn, Wiepke, Hulshoff Pol, Hilleke E., Ripke, Stephan, Ophoff, Roel A., Kahn, René S., Craddock, Nicholas John, Dwyer, Sarah, Escott-Price, Valentina, Georgieva, Lyudmila, Hamshere, Marian Lindsay, Holmans, Peter Alan, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John, Ruderfer, Doug, Williams, Nigel Melville and Zammit, Stanley 2013. Genetic schizophrenia risk variants jointly modulate total brain and white matter volume. Biological Psychiatry 73 (6) , pp. 525-531. 10.1016/j.biopsych.2012.08.017

Holmans, Peter Alan, Escott-Price, Valentina, Jones, Lesley, Sharma, Manu, Vedernikov, Alexey, Buchel, Finja, Sadd, Mohamad, Bras, Jose M., Bettella, Francesco, Nicolaou, Nayia, Simón-Sánchez, Javier, Mittag, Florian, Gibbs, J. Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W., Martinez, Maria, Singleton, Andrew B., Nalls, Michael A., Hardy, John, Morris, Huw Rees and Williams, Nigel Melville 2013. A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease. Human Molecular Genetics 22 (5) , pp. 1039-1049. 10.1093/hmg/dds492

Chapman, J., Rees, Elliott, Harold, Denise, Ivanov, Dobril, Gerrish, Amy, Sims, Rebecca, Hollingworth, P, Stretton, A., Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon, Williams, Julie and Kirov, George 2013. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Human Molecular Genetics 22 (4) , pp. 816-824. 10.1093/hmg/dds476

Escott-Price, Valentina, Harold, Denise, Russo, Giancarlo, Vedernikov, Alexey, Sharma, Manu, Saad, Mohamad, Holmans, Peter Alan, Bras, Jose M., Bettella, Francesco, Keller, Margaux F., Nicolaou, Nayia, Simón-Sánchez, Javier, Gibbs, J. Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Peter, Martinez, Maria, Singleton, Andrew B., Nalls, Michael A., Hardy, John, Owen, Michael John, O’Donovan, Michael Conlon, Williams, Julie, Morris, Huw and Williams, Nigel Melville 2013. Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk. JAMA Neurology 70 (10) , pp. 1268-1276. 10.1001/jamaneurol.2013.448

Eyre, Steve, Bowes, John, Diogo, Dorothée, Lee, Annette, Barton, Anne, Martin, Paul, Zhernakova, Alexandra, Stahl, Eli, Viatte, Sebastien, McAllister, Kate, Amos, Christopher I, Padyukov, Leonid, Toes, Rene E M, Huizinga, Tom W J, Wijmenga, Cisca, Trynka, Gosia, Franke, Lude, Westra, Harm-Jan, Alfredsson, Lars, Hu, Xinli, Sandor, Cynthia, de Bakker, Paul I W, Davila, Sonia, Khor, Chiea Chuen, Heng, Khai Koon, Andrews, Robert, Edkins, Sarah, Hunt, Sarah E, Langford, Cordelia, Symmons, Deborah, Concannon, Pat, Onengut-Gumuscu, Suna, Rich, Stephen S, Deloukas, Panos, Gonzalez-Gay, Miguel A, Rodriguez-Rodriguez, Luis, Ärlsetig, Lisbeth, Martin, Javier, Rantapää-Dahlqvist, Solbritt, Plenge, Robert M, Raychaudhuri, Soumya, Klareskog, Lars, Gregersen, Peter K, Worthington, Jane, Craddock, Nicholas John, Dunajewski, Katherine, Escott-Price, Valentina, Fraser, Christine, Green, Elaine, Grozeva, Detelina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Jones, Ian Richard, O'Donovan, Michael Conlon and Owen, Michael John 2012. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nature Genetics 44 (12) , pp. 1336-1340. 10.1038/ng.2462

Hollingworth, Paul, Sweet, R., Sims, Rebecca, Harold, Denise, Russo, Giancarlo, Abraham, Richard Alun, Stretton, Alexandra, Denning, Nicola, Gerrish, Amy, Chapman, Jade Alice, Ivanov, Dobril Kirilov, Escott-Price, Valentina, Lovestone, S., Priotsi, P., Lupton, M., Brayne, C., Gill, M., Lawlor, B., Lynch, A., Craig, D., McGuinness, B., Johnston, J., Holmes, C., Livingston, G., Bass, N. J., Gurling, H., McQuillin, A., Holmans, Peter Alan, Jones, Lesley, Devlin, B., Klei, L., Barmada, M. M., Demirci, F. Y., DeKosky, S. T., Lopez, O. L., Passmore, P., Owen, Michael John, O'Donovan, Michael Conlon, Mayeux, R., Kamboh, M. I. and Williams, Julie 2012. Genome-wide association study of Alzheimer's disease with psychotic symptoms. Molecular Psychiatry 17 (12) , pp. 1316-1327. 10.1038/mp.2011.125

Keller, Marguax F., Saad, Mohamad, Bras, Jose, Bettella, Francesco, Nicolaou, Nayia, Simon-Sanchez, Javier, Mittag, Florian, Buchel, Finja, Sharma, Manu, Gibbs, J. Raphael, Schulte, Claudia, Escott-Price, Valentina, Durr, Alexandra, Holmans, Peter Alan, Kilarski, Laura, Guerreiro, Rita, Hernandez, Dena G., Brice, Alexis, Ylikotila, Pauli, Stefansson, Hreinn, Majamaa, Kari, Morris, Huw Rees, Williams, Nigel Melville, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W., Hardy, John, Martinez, Maria, Singleton, Andrew B. and Nalls, Michael A. 2012. Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Human Molecular Genetics 21 (22) , pp. 4996-5009. 10.1093/hmg/dds335

Goes, F. S., Hamshere, Marian Lindsay, Seifuddin, F., Pirooznia, M., Belmonte-Mahon, P., Breuer, R., Schulze, T., Nöthen, M., Cichon, S., Rietschel, M., Holmans, Peter Alan, Zandi, P. P., Craddock, Nicholas John and Potash, J. B. 2012. Genome-wide association of mood-incongruent psychotic bipolar disorder. Translational Psychiatry 2 (10) , e180. 10.1038/tp.2012.106

Tansey, Katherine E., Guipponi, Michel, Perroud, Nader, Bondolfi, Guido, Domenici, Enrico, Evans, David, Hall, Stephanie K., Hauser, Joanna, Henigsberg, Neven, Hu, Xiaolan, Jerman, Borut, Maier, Wolfgang, Mors, Ole, O'Donovan, Michael Conlon, Peters, Tim J., Placentino, Anna, Rietschel, Marcella, Souery, Daniel, Aitchison, Katherine J., Craig, Ian, Farmer, Anne, Wendland, Jens R., Malafosse, Alain, Holmans, Peter Alan, Lewis, Glyn, Lewis, Cathryn M., Stensbøl, Tine Bryan, Kapur, Shitij, McGuffin, Peter and Uher, Rudolf 2012. Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis. Plos Medicine 9 (10) , e1001326. 10.1371/journal.pmed.1001326
file

Hamilton, Gillian, Harris, Sarah E., Davies, Gail, Liewald, David C., Tenesa, Albert, Payton, Antony, Horan, Michael A., Ollier, William E.R., Pendleton, Neil, Starr, John M., Porteous, David, Deary, Ian J., Denning, Nicola, Escott-Price, Valentina, Gerrish, Amy, Hamshere, Marian Lindsay, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John, Sims, Rebecca, Thomas, Charlene and Williams, Julie 2012. The role of ECE1 variants in cognitive ability in old age and Alzheimer's disease risk. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 159B (6) , pp. 696-709. 10.1002/ajmg.b.32073

Levinson, Douglas F., Shi, Jianxin, Wang, Kai, Oh, Sang, Riley, Brien, Pulver, Ann E., Wildenauer, Dieter B., Laurent, Claudine, Mowry, Bryan J., Gejman, Pablo V., Owen, Michael John, Kendler, Kenneth S., Nestadt, Gerald, Schwab, Sibylle G., Mallet, Jacques, Nertney, Deborah, Sanders, Alan R., Williams, Nigel Melville, Wormley, Brandon, Lasseter, Virginia K., Albus, Margot, Godard-Bauché, Stephanie, Alexander, Madeline, Duan, Jubao, O'Donovan, Michael Conlon, Walsh, Dermot, O'Neill, Anthony, Papadimitriou, George N., Dikeos, Dimitris, Maier, Wolfgang, Lerer, Bernard, Campion, Dominique, Cohen, David, Jay, Maurice, Fanous, Ayman, Eichhammer, Peter, Silverman, Jeremy M., Norton, Nadine, Zhang, Nancy, Hakonarson, Hakon, Gao, Cynthia, Citri, Ami, Hansen, Mark, Ripke, Stephan, Dudbridge, Frank and Holmans, Peter Alan 2012. Genome-wide association study of multiplex schizophrenia pedigrees. American Journal of Psychiatry 169 (9) , pp. 963-973. 10.1176/appi.ajp.2012.11091423

Shi, Hui, Belbin, Olivia, Medway, Christopher, Brown, Kristelle, Kalsheker, Noor, Carrasquillo, Minerva, Proitsi, Petroula, Powell, John, Lovestone, Simon, Goate, Alison, Younkin, Steven, Passmore, Peter, Morgan, Kevin, Chapman, Jade, Denning, Nicola, Escott-Price, Valentina, Gerrish, Amy, Hamshere, Marian Lindsay, Harold, Denise, Hollingworth, Paul, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John, Pahwa, Jaspreet, Sims, Rebecca, Thomas, Charlene and Williams, Julie 2012. Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS). Neurobiology of Aging 33 (8) , 1849.e5. 10.1016/j.neurobiolaging.2012.02.014

Hamilton, Gillian, Killick, Richard, Lambert, Jean-Charles, Amouyel, Philippe, Carrasquillo, Minerva M., Pankratz, V. Shane, Graff-Radford, Neill R., Dickson, Dennis W., Petersen, Ronald C., Younkin, Steven G., Powell, John F., Wade-Martins, Richard, Chapman, Jade, Denning, Nicola, Escott-Price, Valentina, Gerrish, Amy, Hamshere, Marian Lindsay, Harold, Denise, Hollingworth, Paul, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John, Pahwa, Jaspreet, Russo, Giancarlo, Sims, Rebecca, Thomas, Charlene and Williams, Julie 2012. Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus. Neurobiology of Aging 33 (8) , 1848.e1. 10.1016/j.neurobiolaging.2012.02.005

Escott-Price, Valentina, Schmidt, Karl Michael, Vedernikov, Alexey, Owen, Michael John, Craddock, Nicholas John, Holmans, Peter Alan and O'Donovan, Michael Conlon 2012. Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis. European Journal of Human Genetics 20 (8) , pp. 890-896. 10.1038/ejhg.2012.8

Le Foll, Bernard, Chen, Jingchun, Brunzell, Darlene H., Jackson, Kia, van der Vaart, Andrew, Ma, Jennie Z., Payne, Thomas J., Sherva, Richard, Farrer, Lindsay A., Gejman, Pablo, Levinson, Douglas F., Holmans, Peter Alan, Aggen, Steven H., Damaj, Imad, Kuo, Po-Hsiu, Webb, Bradley T., Anton, Raymond, Kranzler, Henry R., Gelernter, Joel, Li, Ming D., Kendler, Kenneth S. and Chen, Xiangning 2012. Correction: ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure. PLoS ONE 7 (8) 10.1371/annotation/071abcbd-6f0c-4c4b-9507-dae42450457e

Jia, Peilin, Wang, Lily, Fanous, Ayman H., Pato, Carlos N., Edwards, Todd L., Zhao, Zhongming, Craddock, Nicholas John, Holmans, Peter Alan, Kirov, George, O'Donovan, Michael Conlon and Williams, Nigel Melville 2012. Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia. PLoS Computational Biology 8 (7) , e1002587. 10.1371/journal.pcbi.1002587
file

Goes, F. S., McCusker, M. G., Bienvenu, O. J., MacKinnon, D. F., Mondimore, F. M., Schweizer, B., DePaulo, J. R., Potash, J. B. and Holmans, Peter Alan 2012. Co-morbid anxiety disorders in bipolar disorder and major depression: familial aggregation and clinical characteristics of co-morbid panic disorder, social phobia, specific phobia and obsessive-compulsive disorder. Psychological Medicine 42 (07) , pp. 1449-1459. 10.1017/S0033291711002637

Derks, Eske M., Vorstman, Jacob A. S., Ripke, Stephan, Kahn, Rene S., Ophoff, Roel A., Craddock, Nicholas John, Escott-Price, Valentina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John and Zammit, Stanley 2012. Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: A polygenic risk score analysis. PLoS ONE 7 (6) , e37852. 10.1371/journal.pone.0037852
file

Sabunciyan, Sarven, Aryee, Martin J., Irizarry, Rafael A., Rongione, Michael, Webster, Maree J., Kaufman, Walter E., Murakami, Peter, Lessard, Andree, Yolken, Robert H., Feinberg, Andrew P., Potash, James B., Consortium, GenRED and Holmans, Peter Alan 2012. Genome-Wide DNA methylation scan in major depressive disorder. PLoS ONE 7 (4) , e34451. 10.1371/journal.pone.0034451
file

Hudson, G., Sims, Rebecca, Harold, Denise, Chapman, Jade Alice, Hollingworth, Paul, Gerrish, Amy, Russo, Giancarlo, Hamshere, Marian Lindsay, Escott-Price, Valentina, Denning, Nicola, Thomas, Charlene, Stretton, Alexandra, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John, Williams, Julie and Chinnery, P. F. 2012. No consistent evidence for association between mtDNA variants and Alzheimer disease. Neurology 78 (14) , pp. 1038-1042. 10.1212/WNL.0b013e31824e8f1d

Keller, Matthew C., Simonson, Matthew A., Ripke, Stephan, Neale, Ben M., Gejman, Pablo V., Howrigan, Daniel P., Lee, Sang Hong, Lencz, Todd, Levinson, Douglas F., Sullivan, Patrick F., Kirov, George, O'Donovan, Michael Conlon, Holmans, Peter Alan, Georgieva, Lyudmila, Nikolov, Ivan, Williams, Hywel John, Owen, Michael John, Craddock, Nicholas John, Hamshere, Marian Lindsay, Escott-Price, Valentina, Dwyer, Sarah Lynne and Zammit, Stanley 2012. Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. Plos Genetics 8 (4) , e1002656. 10.1371/journal.pgen.1002656
file

Simón-Sánchez, Javier, Kilarski, Laura, Nalls, Michael A., Martinez, Maria, Schulte, Claudia, Holmans, Peter Alan, Gasser, Thomas, Hardy, John, Singleton, Andrew B., Wood, Nicholas W., Brice, Alexis, Heutink, Peter, Williams, Nigel Melville and Morris, Huw Rees 2012. Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's Disease. PLoS ONE 7 (3) , e28787. 10.1371/journal.pone.0028787
file

Jia, P., Wang, L., Fanous, A. H., Chen, X., Kendler, K. S., Zhao, Z., Craddock, Nicholas John, Georgieva, Lyudmila, Holmans, Peter Alan, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John, Ruderfer, D.M., Williams, H. and Williams, Nigel Melville 2012. A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia. Journal of Medical Genetics 49 (2) , pp. 96-103. 10.1136/jmedgenet-2011-100397

Richards, Alexander, Jones, Lesley, Escott-Price, Valentina, Kirov, George, Gejman, P. V., Levinson, D. F., Sanders, A. R., Molecular Genetics of Schizophrenia Collaboration (MGS), , International Schizophrenia Consortium (ISC), , Purcell, S., Visscher, P. M., Craddock, Nicholas John, Owen, Michael John, Holmans, Peter Alan and O'Donovan, Michael Conlon 2012. Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Molecular Psychiatry 17 (2) , pp. 193-201. 10.1038/mp.2011.11

Stergiakouli, Evangelia, Hamshere, Marian Lindsay, Holmans, Peter Alan, Langley, Kate, Zaharieva, Irina, Hawi, Ziarah, Kent, Lindsey, Gill, Michael, Williams, Nigel Melville, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2012. Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. American Journal of Psychiatry 169 (2) , pp. 186-194. 10.1176/appi.ajp.2011.11040551
file

Williams, Nigel Melville, Franke, Barbara, Mick, Eric, Anney, Richard, Freitag, Christine M., Gill, Michael, Thapar, Anita, O'Donovan, Michael Conlon, Owen, Michael John, Holmans, Peter Alan, Kent, Lindsey, Middleton, Frank, Zhang-James, Yanli, Liu, Lu, Meyer, Jobst, Nguyen, Thuy Trang, Romanos, Jasmin, Romanos, Marcel, Seitz, Christiane, Renner, Tobias J., Walitza, Susanne, Warnke, Andreas, Palmason, Haukur, Buitelaar, Jan, Rommelse, Nanda, Vasquez, Alejandro Arias, Hawi, Ziarih, Langley, Kate, Sergeant, Joseph, Steinhausen, Hans-Christoph, Roeyers, Herbert, Biederman, Joseph, Zaharieva, Irina, Hakonarson, Hakon, Elia, Josephine, Lionel, Anath C., Crosbie, Jennifer, Marshall, Christian R., Schachar, Russell, Scherer, Stephen W., Todorov, Alexandre, Smalley, Susan L., Loo, Sandra, Nelson, Stanley, Shtir, Corina, Asherson, Philip, Reif, Andreas, Lesch, Klaus-Peter and Faraone, Stephen V. 2012. Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. American Journal of Psychiatry 169 (2) , pp. 195-204. 10.1176/appi.ajp.2011.11060822
file

Gerrish, Amy, Russo, Giancarlo, Richards, Alexander, Escott-Price, Valentina, Ivanov, Dobril Kirilov, Harold, Denise, Sims, Rebecca, Abraham, Richard Alun, Hollingworth, Paul, Chapman, Jade Alice, Hamshere, Marian Lindsay, Pahwa, Jaspreet Singh, Dowzell, Kimberley Frances, Williams, Amy, Denning, Nicola, Thomas, Charlene, Stretton, Alexandra, Morgan, Angharad Rhys, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuinness, Bernadette, Todd, Stephen, Johnston, Janet A., Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Kölsch, Heike, Heun, Reinhard, Schürmann, Britta, van den Bussche, Hendrik, Heuser, Isabella, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Hüll, Michael, Rujescu, Dan, Goate, Alison M., Kauwe, John S. K., Cruchaga, Carlos, Nowotny, Petra, Morris, John C., Mayo, Kevin, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panagiotis, Davies, Gail, Harris, Sarah E., Starr, John M., Deary, Ian J., Al-Chalabi, Ammar, Shaw, Christopher E., Tsolaki, Magda, Singleton, Andrew B., Guerreiro, Rita, Mühleisen, Thomas W., Nöthen, Markus M., Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H-Erich, Carrasquillo, Minerva M, Pankratz, V. Shane, Younkin, Steven G., Jones, Lesley, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Julie 2012. The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's Disease. Journal of Alzheimer's Disease 28 (2) , pp. 377-387. 10.3233/JAD-2011-110824

Kirov, George, Pocklington, Andrew, Holmans, Peter Alan, Ivanov, Dobril Kirilov, Ikeda, M., Ruderfer, D., Moran, J., Chambert, K., Toncheva, D., Georgieva, Lyudmila, Grozeva, Detelina Valentinova, Fjodorova, Marija, Wollerton, Rebecca Louise, Rees, Elliott, Nikolov, Ivan, van de Lagemaat, L. N., Bayés, À., Fernandez, E., Olason, P. I., Böttcher, Y., Komiyama, N. H., Collins, M. O., Choudhary, J., Stefansson, K., Stefansson, H., Grant, S. G. N., Purcell, S., Sklar, P., O'Donovan, Michael Conlon and Owen, Michael John 2012. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. Molecular Psychiatry 17 (2) , pp. 142-153. 10.1038/mp.2011.154
file

Chen, Jingchun, Brunzell, Darlene H., Jackson, Kia, van der Vaart, Andrew, Ma, Jennie Z., Payne, Thomas J., Sherva, Richard, Farrer, Lindsay A., Gejman, Pablo, Levinson, Douglas F., Holmans, Peter Alan, Aggen, Steven H., Damaj, Imad, Kuo, Po-Hsiu, Webb, Bradley T., Anton, Raymond, Kranzler, Henry R., Gelernter, Joel, Li, Ming D., Kendler, Kenneth S. and Chen, Xiangning 2011. ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure. PLoS ONE 6 (12) , e28790. 10.1371/journal.pone.0028790
file

Cardno, A. G., Holmans, Peter Andrew, Rees, M. I., Jones, L. A., McCarthy, G. M., Hamshere, Marian Lindsay, Williams, Nigel Melville, Norton, N., Williams, H. J., Fenton, I., Murphy, K. C., Sanders, R. D., Gray, M. Y., O'Donovan, Michael Conlon, McGuffin, P. and Owen, Michael John 2011. A genomewide linkage study of age at onset in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (8) , pp. 929-940. 10.1002/ajmg.1404

Hinney, Anke, Scherag, André, Jarick, Ivonne, Albayrak, Özgür, Pütter, Carolin, Pechlivanis, Sonali, Dauvermann, Maria R., Beck, Sebastian, Weber, Heike, Scherag, Susann, Nguyen, Trang T., Volckmar, Anna-Lena, Knoll, Nadja, Faraone, Stephen V., Neale, Benjamin M., Franke, Barbara, Cichon, Sven, Hoffmann, Per, Nöthen, Markus M., Schreiber, Stefan, Jöckel, Karl-Heinz, Wichmann, H.-Erich, Freitag, Christine, Lempp, Thomas, Meyer, Jobst, Gilsbach, Susanne, Herpertz-Dahlmann, Beate, Sinzig, Judith, Lehmkuhl, Gerd, Renner, Tobias J., Warnke, Andreas, Romanos, Marcel, Lesch, Klaus-Peter, Reif, Andreas, Schimmelmann, Benno G., Hebebrand, Johannes, Holmans, Peter Alan, Langley, Kate, O'Donovan, Michael Conlon, Owen, Michael John, Thapar, Anita and Williams, Nigel Melville 2011. Genome-wide association study in German patients with attention deficit/hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (8) , pp. 888-897. 10.1002/ajmg.b.31246

Ripke, Stephan, Sanders, Alan R., Kendler, Kenneth S., Levinson, Douglas F., Sklar, Pamela, Holmans, Peter Alan, Lin, Dan-Yu, Duan, Jubao, Ophoff, Roel A., Andreassen, Ole A., Scolnick, Edward, Cichon, Sven, St. Clair, David, Corvin, Aiden, Gurling, Hugh, Werge, Thomas, Rujescu, Dan, Blackwood, Douglas H. R., Pato, Carlos N., Malhotra, Anil K., Purcell, Shaun, Dudbridge, Frank, Neale, Benjamin M., Rossin, Lizzy, Visscher, Peter M., Posthuma, Danielle, Ruderfer, Douglas M., Fanous, Ayman, Stefansson, Hreinn, Steinberg, Stacy, Mowry, Bryan J., Golimbet, Vera, De Hert, Marc, Jönsson, Erik G., Bitter, István, Pietiläinen, Olli P. H., Collier, David A., Tosato, Sarah, Agartz, Ingrid, Albus, Margot, Alexander, Madeline, Amdur, Richard L., Amin, Farooq, Bass, Nicholas, Bergen, Sarah E., Black, Donald W., Børglum, Anders D., Brown, Matthew A., Bruggeman, Richard, Buccola, Nancy G., Byerley, William F., Cahn, Wiepke, Cantor, Rita M., Carr, Vaughan J., Catts, Stanley V., Choudhury, Khalid, Cloninger, C Robert, Cormican, Paul, Craddock, Nicholas John, Danoy, Patrick A., Datta, Susmita, de Haan, Lieuwe, Demontis, Ditte, Dikeos, Dimitris, Djurovic, Srdjan, Donnelly, Peter, Donohoe, Gary, Duong, Linh, Dwyer, Sarah Lynne, Fink-Jensen, Anders, Freedman, Robert, Freimer, Nelson B., Friedl, Marion, Georgieva, Lyudmila, Giegling, Ina, Gill, Michael, Glenthøj, Birte, Godard, Stephanie, Hamshere, Marian Lindsay, Hansen, Mark, Hansen, Thomas, Hartmann, Annette M., Henskens, Frans A., Hougaard, David M., Hultman, Christina M., Ingason, Andrés, Jablensky, Assen V., Jakobsen, Klaus D., Jay, Maurice, Jürgens, Gesche, Kahn, René S., Keller, Matthew C., Kenis, Gunter, Kenny, Elaine, Kim, Yunjung, Kirov, George, Konnerth, Heike, Konte, Bettina, Krabbendam, Lydia, Krasucki, Robert, Lasseter, Virginia K., Laurent, Claudine, Lawrence, Jacob, Lencz, Todd, Lerer, F. Bernard, Liang, Kung-Yee, Lichtenstein, Paul, Lieberman, Jeffrey A., Linszen, Don H., Lönnqvist, Jouko, Loughland, Carmel M., Maclean, Alan W., Maher, Brion S., Maier, Wolfgang, Mallet, Jacques, Malloy, Pat, Mattheisen, Manuel, Mattingsdal, Morten, McGhee, Kevin A., McGrath, John J., McIntosh, Andrew, McLean, Duncan E., McQuillin, Andrew, Melle, Ingrid, Michie, Patricia T., Milanova, Vihra, Morris, Derek W., Mors, Ole, Mortensen, Preben B., Escott-Price, Valentina, Muglia, Pierandrea, Myin-Germeys, Inez, Nertney, Deborah A., Nestadt, Gerald, Nielsen, Jimmi, Nikolov, Ivan, Nordentoft, Merete, Norton, Nadine, Nöthen, Markus M., O'Dushlaine, Colm T., Olincy, Ann, Olsen, Line, O'Neill, F. Anthony, Ørntoft, Torben F., Owen, Michael John, Pantelis, Christos, Papadimitriou, George, Pato, Michele T., Peltonen, Leena, Petursson, Hannes, Pickard, Ben, Pimm, Jonathan, Pulver, Ann E., Puri, Vinay, Quested, Digby, Quinn, Emma M., Rasmussen, Henrik B., Réthelyi, János M., Ribble, Robert, Rietschel, Marcella, Riley, Brien P., Ruggeri, Mirella, Schall, Ulrich, Schulze, Thomas G., Schwab, Sibylle G., Scott, Rodney J., Shi, Jianxin, Sigurdsson, Engilbert, Silverman, Jeremy M., Spencer, Chris C. A., Stefansson, Kari, Strange, Amy, Strengman, Eric, Stroup, T. Scott, Suvisaari, Jaana, Terenius, Lars, Thirumalai, Srinivasa, Thygesen, Johan H., Timm, Sally, Toncheva, Draga, van den Oord, Edwin, van Os, Jim, van Winkel, Ruud, Veldink, Jan, Walsh, Dermot, Wang, August G., Wiersma, Durk, Wildenauer, Dieter B., Williams, Hywel John, Williams, Nigel Melville, Wormley, Brandon, Zammit, Stanley, Sullivan, Patrick F., O'Donovan, Michael Conlon, Daly, Mark J. and Gejman, Pablo V. 2011. Genome-wide association study identifies five new schizophrenia loci [Letter]. Nature Genetics 43 (10) , pp. 969-976. 10.1038/ng.940

Sklar, Pamela, Ripke, Stephan, Scott, Laura J., Andreassen, Ole A., Cichon, Sven, Craddock, Nicholas John, Edenberg, Howard J., Nurnberger, John I., Rietschel, Marcella, Blackwood, Douglas, Corvin, Aiden, Flickinger, Matthew, Guan, Weihua, Mattingsdal, Morten, McQuillin, Andrew, Kwan, Phoenix, Wienker, Thomas F., Daly, Mark, Dudbridge, Frank, Holmans, Peter Alan, Lin, Danyu, Burmeister, Margit, Greenwood, Tiffany A., Hamshere, Marian Lindsay, Muglia, Pierandrea, Smith, Erin N., Zandi, Peter P., Nievergelt, Caroline M., McKinney, Rebecca, Shilling, Paul D., Schork, Nicholas J., Bloss, Cinnamon S., Foroud, Tatiana, Koller, Daniel L., Gershon, Elliot S., Liu, Chunyu, Badner, Judith A., Scheftner, William A., Lawson, William B., Nwulia, Evaristus A., Hipolito, Maria, Coryell, William, Rice, John, Byerley, William, McMahon, Francis J., Schulze, Thomas G., Berrettini, Wade, Lohoff, Falk W., Potash, James B., Mahon, Pamela B., McInnis, Melvin G., Zöllner, Sebastian, Zhang, Peng, Craig, David W., Szelinger, Szabocls, Barrett, Thomas B., Breuer, René, Meier, Sandra, Strohmaier, Jana, Witt, Stephanie H., Tozzi, Federica, Farmer, Anne, McGuffin, Peter, Strauss, John, Xu, Wei, Kennedy, James L., Vincent, John B., Matthews, Keith, Day, Richard, Ferreira, Manuel A., O'Dushlaine, Colm, Perlis, Roy, Raychaudhuri, Soumya, Ruderfer, Douglas, Hyoun, Phil L., Smoller, Jordan W., Li, Jun, Absher, Devin, Thompson, Robert C., Meng, Fan Guo, Schatzberg, Alan F., Bunney, William E., Barchas, Jack D., Jones, Edward G., Watson, Stanley J., Myers, Richard M., Akil, Huda, Boehnke, Michael, Chambert, Kim, Moran, Jennifer, Scolnick, Ed, Djurovic, Srdjan, Melle, Ingrid, Morken, Gunnar, Gill, Michael, Morris, Derek, Quinn, Emma, Mühleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Schumacher, Johannes, Maier, Wolfgang, Steffens, Michael, Propping, Peter, Nöthen, Markus M., Anjorin, Adebayo, Bass, Nick, Gurling, Hugh, Kandaswamy, Radhika, Lawrence, Jacob, McGhee, Kevin, McIntosh, Andrew, McLean, Alan W., Muir, Walter J., Pickard, Benjamin S., Breen, Gerome, St. Clair, David, Caesar, Sian, Gordon-Smith, Katherine, Jones, Lisa, Fraser, Christine, Green, Elaine Karen, Grozeva, Detelina Valentinova, Jones, Ian Richard, Kirov, George, Escott-Price, Valentina, Nikolov, Ivan, O'Donovan, Michael Conlon, Owen, Michael John, Collier, David A., Elkin, Amanda, Williamson, Richard, Young, Allan H., Ferrier, I. Nicol, Stefansson, Kari, Stefansson, Hreinn, Þorgeirsson, Þorgeir, Steinberg, Stacy, Gustafsson, Ómar, Bergen, Sarah E., Nimgaonkar, Vishwajit, Hultman, Christina, Landén, Mikael, Lichtenstein, Paul, Sullivan, Patrick, Schalling, Martin, Osby, Urban, Backlund, Lena, Frisén, Louise, Langstrom, Niklas, Jamain, Stéphane, Leboyer, Marion, Etain, Bruno, Bellivier, Frank, Petursson, Hannes, Sigur∂sson, Engilbert, Müller-Mysok, Bertram, Lucae, Susanne, Schwarz, Markus, Schofield, Peter R., Martin, Nick, Montgomery, Grant W., Lathrop, Mark, Óskarsson, Högni, Bauer, Michael, Wright, Adam, Mitchell, Philip B., Hautzinger, Martin, Reif, Andreas, Kelsoe, John R. and Purcell, Shaun M. 2011. Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 [Letter]. Nature Genetics 43 (10) , pp. 977-983. 10.1038/ng.943

Chen, J., Lee, G., Fanous, A. H., Zhao, Z., Jia, P., O'Neill, A., Walsh, D., Kendler, K. S., Chen, X., International Schizophrenia Consortium, , Craddock, Nicholas John, Georgieva, Lyudmila, Holmans, Peter Alan, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John, Ruderfer, Doug, Williams, Hywel and Williams, Nigel Melville 2011. Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia. Schizophrenia Research 131 (1-3) , pp. 43-51.

Escott-Price, Valentina, Craddock, Nicholas John, Müller-Myhsok, Bertram, Kam-Thong, Tony, Green, Elaine Karen, Holmans, Peter Alan, Owen, Michael John and O'Donovan, Michael Conlon 2011. An examination of single nucleotide polymorphism selection prioritization strategies for tests of gene-gene interaction. Biological Psychiatry 70 (2) , pp. 198-203. 10.1016/j.biopsych.2011.01.034

Hollingworth, Paul, Harold, Denise, Sims, Rebecca, Gerrish, Amy, Lambert, Jean-Charles, Carrasquillo, Minerva M., Abraham, Richard Alun, Hamshere, Marian Lindsay, Pahwa, Jaspreet Singh, Escott-Price, Valentina, Dowzell, Kimberley Frances, Denning, Nicola, Stretton, Alexandra, Thomas, Charlene, Richards, Alexander, Ivanov, Dobril Kirilov, Widdowson, Caroline Susan, Chapman, Jade Alice, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuinness, Bernadette, Todd, Stephen, Holmes, Clive, Mann, David, Smith, A David, Beaumont, Helen, Warden, Donald, Wilcock, Gordon, Love, Seth, Kehoe, Patrick G., Hooper, Nigel M., Vardy, Emma R. L. C., Hardy, John, Mead, Simon, Fox, Nick C, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Rüther, Eckart, Schürmann, Britta, Heun, Reiner, Kölsch, Heike, van den Bussche, Hendrik, Heuser, Isabella, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Gallacher, John Edward, Hüll, Michael, Rujescu, Dan, Giegling, Ina, Goate, Alison M., Kauwe, John S. K., Cruchaga, Carlos, Nowotny, Petra, Morris, John C., Mayo, Kevin, Sleegers, Kristel, Bettens, Karolien, Engelborghs, Sebastiaan, De Deyn, Peter P, Van Broeckhoven, Christine, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panagiotis, Al-Chalabi, Ammar, Shaw, Christopher E., Tsolaki, Magda, Singleton, Andrew B., Guerreiro, Rita, Mühleisen, Thomas W., Nöthen, Markus M., Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H-Erich, Pankratz, V. Shane, Sando, Sigrid B., Aasly, Jan O., Barcikowska, Maria, Wszolek, Zbigniew K., Dickson, Dennis W., Graff-Radford, Neill R., Petersen, Ronald C., van Duijn, Cornelia M., Breteler, Monique M. B., Ikram, M. Arfan, DeStefano, Anita L., Fitzpatrick, Annette L., Lopez, Oscar, Launer, Lenore J., Seshadri, Sudha, Berr, Claudine, Campion, Dominique, Epelbaum, Jacques, Dartigues, Jean-François, Tzourio, Christophe, Alpérovitch, Annick, Lathrop, Mark, Feulner, Thomas M., Friedrich, Patricia, Riehle, Caterina, Krawczak, Michael, Schreiber, Stefan, Mayhaus, Manuel, Nicolhaus, S., Wagenpfeil, Stefan, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, Snædal, Jon, Björnsson, Sigurbjörn, Jonsson, Palmi V., Chouraki, Vincent, Genier-Boley, Benjamin, Hiltunen, Mikko, Soininen, Hilkka, Combarros, Onofre, Zelenika, Diana, Delepine, Marc, Bullido, Maria J., Pasquier, Florence, Mateo, Ignacio, Frank-Garcia, Ana, Porcellini, Elisa, Hanon, Olivier, Coto, Eliecer, Alvarez, Victoria, Bosco, Paolo, Siciliano, Gabriele, Mancuso, Michelangelo, Panza, Francesco, Solfrizzi, Vincenzo, Nacmias, Benedetta, Sorbi, Sandro, Bossù, Paola, Piccardi, Paola, Arosio, Beatrice, Annoni, Giorgio, Seripa, Davide, Pilotto, Alberto, Scarpini, Elio, Galimberti, Daniela, Brice, Alexis, Hannequin, Didier, Licastro, Federico, Jones, Lesley, Holmans, Peter Alan, Jonsson, Thorlakur, Riemenschneider, Matthias, Morgan, Kevin, Younkin, Steven G., Owen, Michael John, O'Donovan, Michael Conlon, Amouyel, Philippe and Williams, Julie 2011. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nature Genetics 43 (5) , pp. 429-435. 10.1038/ng.803

Williams, Hywel John, Norton, Nadine, Dwyer, Sarah Lynne, Escott-Price, Valentina, Nikolov, Ivan, Carroll, Liam, Georgieva, Lyudmila, Williams, Nigel Melville, Morris, D. W., Quinn, E. M., Giegling, I., Ikeda, Masashi, Wood, J., Lencz, T., Hultman, C., Lichtenstein, P., Thiselton, D., Maher, B. S., Molecular Genetics of Schizophrenia Collaboration (MGS), , International Schizophrenia Consortium (ISC), , SGENE-plus, , GROUP, , Malhotra, A. K., Riley, B., Kendler, K. S., Gill, M., Sullivan, P., Sklar, P., Purcell, S., Nimgaonkar, V. L., Kirov, George, Corvin, A., Holmans, Peter ALan, Rujescu, D., Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 2011. Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder. Molecular Psychiatry 16 (4) , pp. 429-441. 10.1038/mp.2010.36

O'Dushlaine, C, Kenny, E, Heron, E, Donohoe, G, Gill, M, Morris, D, Corvin, A, O'Donovan, Michael Conlon, Kirov, George, Craddock, Nicholas John, Holmans, Peter Alan, Williams, Nigel Melville, Georgieva, Lyudmila and Owen, Michael John 2011. Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility. Molecular Psychiatry 16 (3) , pp. 286-292. 10.1038/mp.2010.7

Peterson, Roseann E., Maes, Hermine H., Holmans, Peter Alan, Sanders, Alan R., Levinson, Douglas F., Shi, Jianxin, Kendler, Kenneth S., Gejman, Pablo V. and Webb, Bradley T. 2011. Genetic risk sum score comprised of common polygenic variation is associated with body mass index. Human Genetics 129 (2) , pp. 221-230. 10.1007/s00439-010-0917-1

Reilly, Muredach P, Li, Mingyao, He, Jing, Ferguson, Jane F, Stylianou, Ioannis M, Mehta, Nehal N, Burnett, Mary Susan, Devaney, Joseph M, Knouff, Christopher W, Thompson, John R, Horne, Benjamin D, Stewart, Alexandre FR, Assimes, Themistocles L, Wild, Philipp S, Allayee, Hooman, Nitschke, Patrick Linsel, Patel, Riyaz S, Martinelli, Nicola, Girelli, Domenico, Quyyumi, Arshed A, Anderson, Jeffrey L, Erdmann, Jeanette, Hall, Alistair S, Schunkert, Heribert, Quertermous, Thomas, Blankenberg, Stefan, Hazen, Stanley L, Roberts, Robert, Kathiresan, Sekar, Samani, Nilesh J, Epstein, Stephen E, Rader, Daniel J, Craddock, Nicholas John, Escott-Price, Valentina, Fraser, Christine, Green, Elaine, Grozeva, Detelina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2011. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. The Lancet 377 (9763) , pp. 383-392. 10.1016/S0140-6736(10)61996-4

Williams, Hywel John, Craddock, Nicholas John, Russo, Giancarlo, Hamshere, Marian Lindsay, Escott-Price, Valentina, Dwyer, Sarah Lynne, Smith, Rhodri L., Green, Elaine Karen, Grozeva, Detelina Valentinova, Holmans, Peter Alan, Owen, Michael John and O'Donovan, Michael Conlon 2011. Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries. Human Molecular Genetics 20 (2) , pp. 387-391. 10.1093/hmg/ddq471

Sims, Rebecca, Dwyer, Sarah Lynne, Harold, Denise, Gerrish, Amy, Hollingworth, Paul, Chapman, Jade Alice, Denning, Nicola, Abraham, Richard Alun, Ivanov, Dobril Kirilov, Pahwa, Jaspreet Singh, Escott-Price, Valentina, Dowzell, Kimberley Frances, Thomas, Charlene, Stretton, Alexandra, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuiness, Bernadette, Todd, Stephen, Johnston, Janet A., Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Jones, Lesley, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Julie 2011. No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 764-771. 10.1002/ajmg.b.31216

Hamshere, Marian Lindsay, Holmans, Peter Alan, McCarthy, Geraldine, Jones, Lisa, Murphy, Kieran C., Sanders, Robert D., Gray, Marion Y., Zammit, Stanley, Williams, Nigel Melville, Norton, Nadine, Williams, Hywel John, McGuffin, Peter, O'Donovan, Michael Conlon, Craddock, Nicholas John, Owen, Michael John and Cardno, Alastair G. 2011. Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (8) , pp. 929-940. 10.1002/ajmg.b.31240

Escott-Price, Valentina, O'Dushlaine, Colm, Purcell, Shaun, Craddock, Nicholas John, Holmans, Peter Alan and O'Donovan, Michael Conlon 2011. Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study. Genetic Epidemiology 35 (8) , pp. 861-866. 10.1002/gepi.20636

Dudbridge, Frank, Holmans, Peter Alan and Wilson, Scott G. 2011. A flexible model for association analysis in sibships with missing genotype data. Annals of Human Genetics 75 (3) , pp. 428-438. 10.1111/j.1469-1809.2010.00636.x

Kendler, Kenneth S., Kalsi, Gursharan, Holmans, Peter Alan, Sanders, Alan R., Aggen, Steven H., Dick, Danielle M., Aliev, Fazil, Shi, Jianxin, Levinson, Douglas F. and Gejman, Pablo V. 2011. Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample. Alcoholism-Clinical and Experimental Research 35 (5) , pp. 963-975. 10.1111/j.1530-0277.2010.01427.x

Levinson, D. F., Duan, J., Oh, S., Wang, K., Sanders, A. R., Shi, J., Zhang, N., Mowry, B. J., Olincy, A., Amin, F., Cloninger, C. R., Silverman, J. M., Buccola, N. G., Byerley, W. F., Black, D. W., Kendler, K. S., Freedman, R., Dudbridge, F., Pe'er, I., Hakonarson, H., Bergen, S. E., Fanous, A. H., Holmans, Peter Alan and Gejman, P. V. 2011. Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. American Journal of Psychiatry 168 (3) , pp. 302-316. 10.1176/appi.ajp.2010.10060876

Bridges, Michael, Heron, Elizabeth A., O'Dushlaine, Colm, Segurado, Ricardo, Morris, Derek, Corvin, Aiden, Gill, Michael, Pinto, Carlos, O'Donovan, Michael Conlon, Kirov, George, Craddock, Nicholas John, Holmans, Peter Alan, Williams, Nigel Melville, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine, Williams, Hywel John, Toncheva, Draga, Milanova, Vihra and Owen, Michael John 2011. Genetic classification of populations using supervised learning. PLoS ONE 6 (5) , e14802. 10.1371/journal.pone.0014802
file

Hamshere, Marian Lindsay, O'Donovan, Michael Conlon, Jones, Ian Richard, Jones, L., Kirov, George, Green, Elaine Karen, Escott-Price, Valentina, Grozeva, Detelina Valentinova, Bass, N., McQuillin, A., Gurling, H., St Clair, D., Young, A. H., Ferrier, I. N., Farmer, Anne, McGuffin, Peter, Sklar, P., Purcell, S., Holmans, Peter Alan, Owen, Michael John and Craddock, Nicholas John 2011. Polygenic dissection of the bipolar phenotype. British Journal of Psychiatry 198 (4) , pp. 284-288. 10.1192/bjp.bp.110.087866

Lips, E. S., Cornelisse, L. N., Toonen, R. F., Min, J. L., Hultman, C. M., Holmans, Peter Alan, O'Donovan, Michael Conlon, Purcell, S. M., Smit, A. B., Verhage, M, Sullivan, P. F., Visscher, P. M. and Posthuma, D 2011. Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. Molecular Psychiatry , pp. 1-11. 10.1038/mp.2011.117

Langley, Kate, Martin, Joanna, Agha, Sharifah Shameem, Davies, Charlotte, Stergiakouli, Evangelia, Holmans, Peter Alan, Williams, Nigel Melville, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2011. Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants. British Journal of Psychiatry 199 (5) , pp. 398-403. 10.1192/bjp.bp.111.092130

Carroll, Liam Stuart, Williams, Nigel Melville, Escott-Price, Valentina, Russell, Elen, Norton, Nadine, Williams, Hywel John, Peirce, Timothy Rowan, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Grozeva, Detelina Valentinova, Greene, E., Farmer, A., McGuffin, P., Morris, D. W., Corvin, A., Gill, M., Rujescu, D., Sham, P., Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, Craddock, Nicholas John, O'Donovan, Michael Conlon and Owen, Michael John 2010. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha. Molecular Psychiatry 15 (11) , pp. 1101-1111. 10.1038/mp.2009.96

Craddock, Nicholas John, Jones, Lesley, Jones, Ian Richard, Kirov, George, Green, Elaine Karen, Grozeva, Detelina Valentinova, Escott-Price, Valentina, Nikolov, Ivan, Hamshere, Marian Lindsay, Vukcevic, D., Caesar, S., Gordon-Smith, Katherine, Fraser, Christine, Russell, E., Norton, Nadine, Breen, G., St Clair, D., Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A, McGuffin, P., Holmans, Peter Alan, Donnelly, Peter, Owen, Michael John and O'Donovan, Michael Conlon 2010. Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype [Corrigendum]. Molecular Psychiatry 15 (11) , p. 1121. 10.1038/mp.2010.62

Williams, Nigel Melville, Zaharieva, Irina, Martin, Andrew Kenneth, Langley, Kate, Mantripragada, Kiran Kumar, Fossdal, Ragnheidur, Stefansson, Hreinn, Stefansson, Kari, Magnusson, Pall, Gudmundsson, Olafur O., Gustafsson, Omar, Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2010. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. The Lancet 376 (9750) , pp. 1401-1408. 10.1016/S0140-6736(10)61109-9

Green, Elaine Karen, Grozeva, Detelina Valentinova, Jones, Ian Richard, Jones, L., Kirov, George, Caesar, S, Gordon-Smith, K., Fraser, Christine, Forty, Elizabeth, Russell, Elen Elizabeth, Hamshere, Marian Lindsay, Escott-Price, Valentina, Nikolov, Ivan, Farmer, A., McGuffin, P., Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas John 2010. The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia. Molecular Psychiatry 15 (10) , pp. 1016-1022. 10.1038/mp.2009.49

Allison, David B., Raychaudhuri, Soumya, Korn, Joshua M., McCarroll, Steven A., Altshuler, David, Sklar, Pamela, Purcell, Shaun, Daly, Mark J., O'Donovan, Michael Conlon, Kirov, George, Craddock, Nicholas John, Holmans, Peter Alan, Williams, Nigel Melville, Georgieva, Lyudmila and Owen, Michael John 2010. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genetics 6 (9) , e1001097. 10.1371/journal.pgen.1001097

Grozeva, Detelina Valentinova, Kirov, George, Ivanov, Dobril Kirilov, Jones, Ian Richard, Jones, Lisa, Green, Elaine Karen, St Clair, David M., Young, Allan H., Ferrier, Nicol, Farmer, Anne E., McGuffin, Peter, Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas John 2010. Rare copy number variants: A point of rarity in genetic risk for bipolar disorder and schizophrenia. Archives of General Psychiatry 67 (4) , pp. 318-327. 10.1001/archgenpsychiatry.2010.25

Craddock, Nicholas John, Jones, L, Jones, Ian Richard, Kirov, George, Green, Elaine Karen, Grozeva, Detelina Valentinova, Escott-Price, Valentina, Nikolov, Ivan, Hamshere, Marian Lindsay, Vukcevic, D., Caesar, S., Gordon-Smith, Katherine, Fraser, Christine, Russell, Elen Elizabeth, Norton, Nadine, Breen, G., St Clair, D., Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Holmans, Peter Alan, Donnelly, P., Owen, Michael John and O'Donovan, Michael Conlon 2010. Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype. Molecular Psychiatry 15 (2) , pp. 146-153. 10.1038/mp.2008.66

Green, Elaine Karen, Grozeva, Detelina Valentinova, Escott-Price, Valentina, Hamshere, Marian Lindsay, Jones, Ian Richard, Jones, Lisa, Forty, Elizabeth, Caesar, Sian, Gordon-Smith, Katherine, Fraser, Christine, Russell, Elen, St Clair, David, Young, Allan H., Ferrier, Nicol, Farmer, Anne, McGuffin, Peter, Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas John 2010. Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (7) , pp. 1347-1349. 10.1002/ajmg.b.31108

Dwyer, Sarah Lynne, Williams, Hywel, Holmans, Peter Alan, Escott-Price, Valentina, Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 2010. No evidence that rare coding variants in ZNF804A confer risk of schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (8) , pp. 1411-1416. 10.1002/ajmg.b.31117

Holmans, Peter Alan 2010. Statistical methods for pathway analysis of genome-wide data for association with complex genetic traits. In: Moore, Jason H. and Dunlap, Jay C. eds. Computational Methods for Genetics of Complex Traits, Advances in Genetics, vol. 72. San Diego, CA: Academic Press, pp. 141-179. (10.1016/B978-0-12-380862-2.00007-2)

Neale, Benjamin M., Medland, Sarah, Ripke, Stephan, Anney, Richard, Asherson, Philip, Buitelaar, Jan, Franke, Barbara, Gill, Michael, Kent, Lindsey, Holmans, Peter Alan, Middleton, Frank, Thapar, Anita, Lesch, Klaus-Peter, Daly, Mark, Nguyen, Thuy Trang, Schäfer, Helmut, Steinhausen, Hans-Christoph, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Walitza, Susanne, Freitag, Christine, Meyer, Jobst, Palmason, Haukur, Rothenberger, Aribert, Hawi, Ziarih, Sergeant, Joseph, Roeyers, Herbert, Mick, Eric and Biederman, Joseph 2010. Case-control genome-wide association study of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child & Adolescent Psychiatry 49 (9) , pp. 906-920. 10.1016/j.jaac.2010.06.007

Neale, Benjamin M., Medland, Sarah E., Ripke, Stephan, Asherson, Philip, Franke, Barbara, Lesch, Klaus-Peter, Faraone, Stephen V., Nguyen, Thuy Trang, Schäfer, Helmut, Holmans, Peter Alan, Daly, Mark, Steinhausen, Hans-Christoph, Freitag, Christine, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Walitza, Susanne, Warnke, Andreas, Meyer, Jobst, Palmason, Haukur, Buitelaar, Jan, Vasquez, Alejandro Arias, Lambregts-Rommelse, Nanda, Gill, Michael, Anney, Richard, Langley, Kate, O'Donovan, Michael Conlon, Williams, Nigel Melville, Owen, Michael John, Thapar, Anita, Kent, Lindsey, Sergeant, Joseph, Roeyers, Herbert, Mick, Eric, Biederman, Joseph, Doyle, Alysa, Smalley, Susan, Loo, Sandra, Hakonarson, Hakon, Elia, Josephine, Todorov, Alexandre, Ana, Miranda, Mulas, Fernando, Ebstein, Richard P., Rothenberger, Aribert, Banaschewski, Tobias, Oades, Richard D., Sonuga-Barke, Edmund, McGough, James, Nisenbaum, Laura, Middleton, Frank, Hu, Xiaolan and Nelson, Stan 2010. Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child & Adolescent Psychiatry 49 (9) , pp. 884-897. 10.1016/j.jaac.2010.06.008

Escott-Price, Valentina, Smith, Michael, Ivanov, Dobril, Blackwood, Douglas, StClair, David, Hultman, Christina, Toncheva, Draga, Gill, Michael, Corvin, Aiden, O'Dushlaine, Colm, Morris, Derek W., Wray, Naomi R., Sullivan, Patrick, Pato, Carlos, Pato, Michele T., Sklar, Pamela, Purcell, Shaun, Holmans, Peter Alan, O'Donovan, Michael Conolon, Owen, Michael John and Kirov, George 2010. Genetic differences between five European populations. Human Heredity 70 (2) , pp. 141-149. 10.1159/000313854

Liu, Y., Blackwood, D. H., Caesar, S., de Geus, E. J. C., Farmer, A., Ferreira, M. A. R., Ferrier, I. N., Fraser, Christine, Gordon-Smith, K., Green, Elaine Karen, Grozeva, Detelina Valentinova, Gurling, H. M., Hamshere, Marian Lindsay, Heutink, P., Holmans, Peter Alan, Hoogendijk, W. J., Hottenga, J. J., Jones, L., Jones, Ian Richard, Kirov, George, Lin, D., McGuffin, P., Escott-Price, Valentina, Nolen, W. A., Perlis, R. H., Posthuma, D., Scolnick, E. M., Smit, A. B., Smit, J. H., Smoller, J. W., St Clair, D., van Dyck, R., Verhage, M., Willemsen, G., Young, A. H., Zandbelt, T., Boomsma, D. I., Craddock, Nicholas John, O'Donovan, Michael Conlon, Owen, Michael John, Penninx, B. W. J. H., Purcell, S., Sklar, P. and Sullivan, P. F. 2010. Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder [Letter]. Molecular Psychiatry 16 (1) , pp. 2-4. 10.1038/mp.2009.107

Shi, J, Potash, J. B., Knowles, J. A., Weissman, M. M., Coryell, W, Scheftner, W. A., Lawson, W. B., DePaulo, J. R., Gejman, P. V., Sanders, A.R., Johnson, J. K., Adams, P, Chaudhury, S, Jancic, D, Evgrafov, O, Zvinyatskovskiy, A, Ertman, N, Gladis, M, Neimanas, K, Goodell, M, Hale, N, Ney, N, Verma, R, Mirel, D, Holmans, Peter Alan and Levinson, D. F. 2010. Genome-wide association study of recurrent early-onset major depressive disorder. Molecular Psychiatry 16 (2) , pp. 193-201. 10.1038/mp.2009.124

Jones, Lesley, Holmans, Peter Alan, Hamshere, Marian Lindsay, Harold, Denise, Escott-Price, Valentina, Ivanov, Dobril Kirilov, Pocklington, Andrew, Abraham, Richard Alun, Hollingworth, Paul, Sims, Rebecca, Gerrish, Amy, Pahwa, Jaspreet Singh, Denning, Nicola, Stretton, Alexandra, Morgan, Angharad Rhys, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuinness, Bernadette, Todd, Stephen, Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Schürmann, Britta, Heun, Reinhard, Kölsch, Heike, van den Bussche, Hendrik, Heuser, Isabella, Peters, Oliver, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Hüll, Michael, Rujescu, Dan, Goate, Alison M., Kauwe, John S. K., Cruchaga, Carlos, Nowotny, Petra, Mayo, Kevin, Morris, John C., Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panos, Al-Chalabi, Ammar, Shaw, Christopher E., Singleton, Andrew B., Guerreiro, Rita, Mühleisen, Thomas W., Nöthen, Markus M., Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H.-Erich, Rüther, Eckhard, Carrasquillo, Minerva M., Pankratz, V. Shane, Younkin, Steven G., Hardy, John, O'Donovan, Michael Conlon, Williams, Julie and Owen, Michael John 2010. Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease. Plos One 5 (11) , e13950. 10.1371/journal.pone.0013950
file

Harold, Denise, Abraham, Richard Alun, Hollingworth, Paul, Sims, Rebecca, Gerrish, Amy, Hamshere, Marian Lindsay, Pahwa, Jaspreet Singh, Escott-Price, Valentina, Dowzell, Kimberley Frances, Williams, Amy, Denning, Nicola, Thomas, Charlene, Stretton, Alexandra, Morgan, Angharad Rhys, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuinness, Bernadette, Todd, Stephen, Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Schürmann, Britta, van den Bussche, Hendrik, Heuser, Isabella, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Hüll, Michael, Rujescu, Dan, Goate, Alison M., Kauwe, John S. K., Cruchaga, Carlos, Nowotny, Petra, Morris, John C., Mayo, Kevin, Sleegers, Kristel, Bettens, Karolien, Engelborghs, Sebastiaan, De Deyn, Peter P., Van Broeckhoven, Christine, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panagiotis, Al-Chalabi, Ammar, Shaw, Christopher E., Tsolaki, Magda, Singleton, Andrew B., Guerreiro, Rita, Mühleisen, Thomas W., Nöthen, Markus M., Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H.-Erich, Carrasquillo, Minerva M., Pankratz, V. Shane, Younkin, Steven G., Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Julie 2009. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease [Letter]. Nature Genetics 41 (10) , pp. 1088-1093. 10.1038/ng.440

Shi, Jianxin, Levinson, Douglas F., Duan, Jubao, Sanders, Alan R., Zheng, Yonglan, Pe'er, Itsik, Dudbridge, Frank, Holmans, Peter Alan, Whittemore, Alice S., Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Crowe, Raymond R., Oksenberg, Jorge R., Mirel, Daniel B., Kendler, Kenneth S., Freedman, Robert and Gejman, Pablo V. 2009. Common variants on chromosome 6p22.1 are associated with schizophrenia [Letter]. Nature 460 (7256) , pp. 753-757. 10.1038/nature08192

Ng, M Y M, Levinson, D F, Faraone, S V, Suarez, B K, DeLisi, L E, Arinami, T, Riley, B, Paunio, T, Pulver, A E, Irmansyah, , Holmans, Peter Alan, Escamilla, M, Wildenauer, D B, Williams, Nigel Melville, Laurent, C, Mowry, B J, Brzustowicz, L M, Maziade, M, Sklar, P, Garver, D L, Abecasis, G R, Lerer, B, Fallin, M D, Gurling, H M D, Gejman, P V, Lindholm, E, Moises, H W, Byerley, W, Wijsman, E M, Forabosco, P, Tsuang, M T, Hwu, H-G, Okazaki, Y, Kendler, K S, Wormley, B, Fanous, A, Walsh, D, O'Neill, F A, Peltonen, L, Nestadt, G, Lasseter, V K, Liang, K Y, Papadimitriou, G M, Dikeos, D G, Schwab, S G, Owen, Michael John, O'Donovan, Michael Conlon, Norton, N, Hare, E, Raventos, H, Nicolini, H, Albus, M, Maier, W, Nimgaonkar, V L, Terenius, L, Mallet, J, Jay, M, Godard, S, Nertney, D, Alexander, M, Crowe, R R, Silverman, J M, Bassett, A S, Roy, M-A, Mérette, C, Pato, C N, Pato, M T, Roos, J Louw, Kohn, Y, Amann-Zalcenstein, D, Kalsi, G, McQuillin, A, Curtis, D, Brynjolfson, J, Sigmundsson, T, Petursson, H, Sanders, A R, Duan, J, Jazin, E, Myles-Worsley, M, Karayiorgou, M and Lewis, C M 2009. Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Molecular Psychiatry 14 (8) , pp. 774-785. 10.1038/mp.2008.135

Holmans, Peter Alan, Riley, B., Pulver, A. E., Owen, Michael John, Wildenauer, D. B., Gejman, P. V., Mowry, B. J., Laurent, C., Kendler, K. S., Nestadt, G., Williams, Nigel Melville, Schwab, S. G., Sanders, A. R., Nertney, D., Mallet, J., Wormley, B., Lasseter, V. K., O'Donovan, Michael Conlon, Duan, J., Albus, M., Alexander, M., Godard, S., Ribble, R., Liang, K. Y., Norton, Nadine, Maier, W., Papadimitriou, G., Walsh, D., Jay, M., O'Neill, A., Lerer, F. B., Dikeos, D., Crowe, R. R., Silverman, J. M. and Levinson, D. F. 2009. Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms. Molecular Psychiatry 14 (8) , pp. 786-795. 10.1038/mp.2009.11

Orozco, G., Hinks, A., Eyre, S., Ke, X., Gibbons, L. J., Bowes, J., Flynn, E., Martin, P., Wilson, A. G., Bax, D. E., Morgan, A. W., Emery, P., Steer, S., Hocking, L., Reid, D. M., Wordsworth, P., Harrison, P., Thomson, W., Barton, A., Worthington, J., Fraser, Christine, Green, Elaine, Grozeva, Detelina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, Escott-Price, Valentina, Nikolov, Ivan, O'Donovan, Michael Conlon, Owen, Michael John and Craddock, Nicholas John 2009. Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23. Human Molecular Genetics 18 (14) , pp. 2693-2699. 10.1093/hmg/ddp193

Holmans, Peter Alan, Green, Elaine Karen, Pahwa, Jaspreet Singh, Ferreira, Manuel A.R., Purcell, Shaun M., Sklar, Pamela, The Wellcome Trust Case-Control Consortium, , Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas Johon 2009. Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder. American Journal of Human Genetics 85 (1) , pp. 13-24. 10.1016/j.ajhg.2009.05.011

Webster, Jennifer A., Gibbs, J. Raphael, Clarke, Jennifer, Ray, Monika, Zhang, Weixiong, Holmans, Peter Alan, Rohrer, Kristen, Zhao, Alice, Marlowe, Lauren, Kaleem, Mona, McCorquodale, Donald S., Cuello, Cindy, Leung, Doris, Bryden, Leslie, Nath, Priti, Zismann, Victoria L., Joshipura, Keta, Huentelman, Matthew J., Hu-Lince, Diane, Coon, Keith D., Craig, David W., Pearson, John V., NACC-Neuropathology Group, , Heward, Chrsitopher B., Reiman, Eria M., Stephan, Dietrich, Hardy, John and Myers, Amanda J. 2009. Genetic control of human brain transcript expression in Alzheimer Disease. American Journal of Human Genetics 84 (4) , pp. 445-458. 10.1016/j.ajhg.2009.03.011

Escott-Price, Valentina, Craddock, Nicholas John, Holmans, Peter Alan, Nikolov, Ivan, Pahwa, Jaspreet Singh, Green, Elaine Karen, Wellcome Trust Case Control Consortium, , Owen, Michael John and O'Donovan, Michael Conlon 2009. Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk. Molecular Psychiatry 14 (3) , pp. 252-260. 10.1038/mp.2008.133

Glaser, Beate and Holmans, Peter Alan 2009. Comparison of methods for combining case-control and family-based association studies. Human Heredity 68 (2) , pp. 106-116. 10.1159/000212503

O'Donovan, Michael Conlon, Norton, Nadine, Williams, Hywel John, Peirce, Timothy Rowan, Escott-Price, Valentina, Nikolov, Ivan, Hamshere, Marian Lindsay, Carroll, Liam Stuart, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Holmans, Peter Alan, Marchini, J. L., Spencer, C. C. A., Howie, B., Leung, H.T., Giegling, I., Hartmann, A. M., Möller, H.J., Morris, D. W., Shi, Y., Feng, G., Hoffmann, P., Propping, P., Vasilescu, C., Maier, W., Rietschel, M., Zammit, Stanley, Schumacher, J., Quinn, E. M., Schulze, T. G., Iwata, N., Ikeda, M., Darvasi, A., Shifman, S., He, L., Duan, J., Sanders, A. R., Levinson, D. F., Adolfsson, R., Ösby, U., Terenius, L, Jönsson, E. G., Cichon, S., Nöthen, M. M., Gill, M., Corvin, A. P., Rujescu, D., Gejman, P. V., Kirov, George, Craddock, Nicholas John, Williams, Nigel Melville and Owen, Michael John 2009. Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2. Molecular Psychiatry 14 (1) , pp. 30-36. 10.1038/mp.2008.108

Langley, Kate, Fowler, T. A., Grady, D. L., Moyzis, R. K., Holmans, Peter Alan, van den Bree, Marianne Bernadette, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2009. Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder. European Child & Adolescent Psychiatry 18 (1) , pp. 26-32. 10.1007/s00787-008-0698-4

Kirov, George, Grozeva, Detelina Valentinova, Norton, Nadine, Ivanov, Dobril Kirilov, Mantripragada, Kiran Kumar, Holmans, Peter Alan, Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 2009. Support for the involvement of large copy number variants in the pathogenesis of schizophrenia. Human Molecular Genetics 18 (8) , pp. 1497-1503. 10.1093/hmg/ddp043

Hamshere, Marian Lindsay, Schulze, Thomas G., Schumacher, Johannes, Corvin, Aiden, Owen, Michael John, Jamra, Rami Abou, Propping, Peter, Maier, Wolfgang, Orozco y Diaz, Guillermo, Mayoral, Fermin, Rivas, Fabio, Jones, Ian Richard, Jones, Lisa, Kirov, George, Gill, Michael, Holmans, Peter Alan, Nöthen, Markus M., Cichon, Sven, Rietschel, Marcella and Craddock, Nicholas John 2009. Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31. Bipolar Disorders 11 (6) , pp. 610-620. 10.1111/j.1399-5618.2009.00736.x

Shyn, S. I., Shi, J., Kraft, J. B., Potash, J. B., Knowles, J. A., Weissman, M. M., Garriock, H. A., Yokoyama, J. S., McGrath, P. J., Peters, E. J., Scheftner, W. A., Coryell, W., Lawson, W. B., Jancic, D., Gejman, P. V., Sanders, A. R., Holmans, Peter Alan, Slager, S. L., Levinson, D. F. and Hamilton, S. P. 2009. Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. Molecular Psychiatry 16 (2) , pp. 202-215. 10.1038/mp.2009.125

Mahon, P. B., Payne, J. L., MacKinnon, D. F., Mondimore, F. M., Goes, F. S., Schweizer, B., Jancic, D., Coryell, W. H., Holmans, Peter Alan, Shi, J., Knowles, J. A., Scheftner, W. A., Weissman, M. M., Levinson, D. F., DePaulo, J. R., Zandi, P. P. and Potash, J. B. 2009. Genome-wide linkage and follow-up association study of postpartum mood symptoms. American Journal of Psychiatry 166 (11) , pp. 1229-1237. 10.1176/appi.ajp.2009.09030417

Hamshere, Marian Lindsay, Green, Elaine Karen, Jones, Ian Richard, Jones, L., Escott-Price, Valentina, Kirov, George, Grozeva, Detelina Valentinova, Nikolov, Ivan, Vukcevic, D., Caesar, S., Gordon-Smith, K., Fraser, Christine, Russell, Elen, Breen, G., St Clair, D., Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas John 2009. Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept. British Journal of Psychiatry 195 (1) , pp. 23-29. 10.1192/bjp.bp.108.061424

Harold, Denise, Abraham, Richard Alun, Hollingworth, Paul, Sims, Rebecca, Gerrish, Amy, Hamshere, Marian Lindsay, Pahwa, Jaspreet Singh, Escott-Price, Valentina, Dowzell, Kimberley Frances, Williams, Amy, Denning, Nicola, Thomas, Charlene, Stretton, Alexandra, Morgan, Angharad Rhys, Lovestone, Simom, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuinness, Bernadette, Todd, Stephen, Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Schürmann, Britta, van den Bussche, Hendrik, Heuser, Isabella, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich,, Lutz, Hampel, Harald, Hüll, Michael, Rujescu, Dan, Goate, Alison M., Kauwe, John S. K., Cruchaga, Carlos, Nowotny, Petra, Morris, John C., Mayo, Kevin, Sleegers, Kristel, Bettens, Karolien, Engelborghs, Sebastiaan, De Deyn, Peter P., Van Broeckhoven, Christine, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panagiotis, Al-Chalabi, Ammar, Shaw, Christopher E., Tsolaki, Magda, Singleton, Andrew B., Guerreiro, Rita, Mühleisen, Thomas W., Nöthen, Markus M., Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H-Erich, Carrasquillo, Minerva M., Pankratz, V. Shane, Younkin, Steven G., Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Julie 2009. Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease [Corrigendum]. Nature Genetics 41 (10) , p. 1156. 10.1038/ng1009-1156d

Purcell, Shaun M., Wray, Naomi R., Stone, Jennifer L., Visscher, Peter M., O'Donovan, Michael Conlon, Sullivan, Patrick F., Sklar, Pamela, Ruderfer, Douglas M., McQuillin, Andrew, Morris, Derek W., O'Dushlaine, Colm T., Corvin, Aiden, Holmans, Peter Alan, Macgregor, Stuart, Gurling, Hugh, Blackwood, Douglas H. R., Craddock, Nicholas John, Gill, Michael, Hultman, Christina M., Kirov, George, Lichtenstein, Paul, Muir, Walter J., Owen, Michael John, Pato, Carlos N., Scolnick, Edward M., St Clair, David, Williams, Nigel Melville, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine, Williams, Hywel John, Toncheva, Draga, Milanova, Vihra, Thelander, Emma F., Kenny, Elaine, Quinn, Emma M., Choudhury, Khalid, Datta, Susmita, Pimm, Jonathan, Thirumalai, Srinivasa, Puri, Vinay, Krasucki, Robert, Lawrence, Jacob, Quested, Digby, Bass, Nicholas, Crombie, Caroline, Fraser, Gillian, Leh Kuan, Soh, Walker, Nicholas, McGhee, Kevin A., Pickard, Ben, Malloy, Pat, Maclean, Alan W., Van Beck, Margaret, Pato, Michele T., Medeiros, Helena, Middleton, Frank, Carvalho, Celia, Morley, Christopher, Fanous, Ayman, Conti, David, Knowles, James A., Paz Ferreira, Carlos, Macedo, Antonio, Helena Azevedo, M., Kirby, Andrew N., Ferreira, Manuel A. R., Daly, Mark J., Chambert, Kimberly, Kuruvilla, Finny, Gabriel, Stacey B., Ardlie, Kristin, Moran, Jennifer L. and Daly, Mark J. 2009. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460 (7256) , pp. 748-752. 10.1038/nature08185

Barton, Anne, Thomson, Wendy, Ke, Xiayi, Eyre, Steve, Hinks, Anne, Bowes, John, Plant, Darren, Gibbons, Laura J, Wilson, Anthony G, Bax, Deborah E, Morgan, Ann W, Emery, Paul, Steer, Sophia, Hocking, Lynne, Reid, David M, Wordsworth, Paul, Harrison, Pille, Worthington, Jane, Craddock, Nicholas John, Fraser, Christine, Green, Elaine, Grozeva, Detelina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, Escott-Price, Valentina, Nikolov, Ivan, O'Donovan, Michael Conlon and Owen, Michael John 2008. Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13. Nature Genetics 40 (10) , pp. 1156-1159. 10.1038/ng.218

O'Donovan, Michael Conlon, Craddock, Nicholas John, Norton, Nadine, Williams, Hywel John, Peirce, Timothy Rowan, Escott-Price, Valentina, Nikolov, Ivan, Hamshere, Marian Lindsay, Carroll, Liam Stuart, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Holmans, Peter Alan, Marchini, Jonathan L, Spencer, Chris C A, Howie, Bryan, Leung, Hin-Tak, Hartmann, Annette M, Möller, Hans-Jürgen, Morris, Derek W, Shi, YongYong, Feng, GuoYin, Hoffmann, Per, Propping, Peter, Vasilescu, Catalina, Maier, Wolfgang, Rietschel, Marcella, Zammit, Stanley, Schumacher, Johannes, Quinn, Emma M, Schulze, Thomas G, Williams, Nigel Melville, Giegling, Ina, Iwata, Nakao, Ikeda, Masashi, Darvasi, Ariel, Shifman, Sagiv, He, Lin, Duan, Jubao, Sanders, Alan R, Levinson, Douglas F, Gejman, Pablo V, Gejman, Pablo V, Sanders, Alan R, Duan, Jubao, Levinson, Douglas F, Buccola, Nancy G, Mowry, Bryan J, Freedman, Robert, Amin, Farooq, Black, Donald W, Silverman, Jeremy M, Byerley, William F, Cloninger, C Robert, Cichon, Sven, Nöthen, Markus M, Gill, Michael, Corvin, Aiden, Rujescu, Dan, Kirov, George and Owen, Michael John 2008. Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nature Genetics 40 (9) , pp. 1053-1055. 10.1038/ng.201

Ferreira, Manuel A R, O'Donovan, Michael Conlon, Meng, Yan A, Jones, Ian Richard, Ruderfer, Douglas M., Jones, Lisa, Fan, Jinbo, Kirov, George, Perlis, Roy H., Green, Elaine Karen, Smoller, Jordan W., Grozeva, Detelina Valentina, Stone, Jennifer, Nikolov, Ivan, Chambert, Kimberly, Hamshere, Marian Lindsay, Nimgaonkar, Vishwajit L., Escott-Price, Valentina, Thase, Michael E., Caesar, Sian, Sachs, Gary S., Franklin, Jennifer, Gordon-Smith, Katherine, Ardlie, Kristin G, Gabriel, Stacey B, Fraser, Christine, Blumenstiel, Brendan, Defelice, Matthew, Breen, Gerome, Gill, Michael, Morris, Derek W., Elkin, Amanda, Muir, Walter J, McGhee, Kevin A., Williamson, Richard, MacIntyre, Donald J.., MacLean, Alan W., St Clair, David, Robinson, Michelle, Van Beck, Margaret, Pereira, Ana C. P., Kandaswamy, Radhika, McQuillin, Andrew, Collier, David A., Bass, Nicholas J., Young, Allan H, Lawrence, Jacob, Nicol Ferrier, I., Anjorin, Adebayo, Farmer, Anne, Curtis, David, Scolnick, Edward M., McGuffin, Peter, Daly, Mark J, Corvin, Aiden P, Holmans, Peter Alan, Blackwood, Douglas H, Gurling, Hugh M, Owen, Michael John, Purcell, Shaun M., Sklar, Pamela and Craddock, Nicholas John 2008. Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. Nature Genetics 40 (9) , pp. 1056-1058. 10.1038/ng.209

Barton, A., Thomson, W., Ke, X., Eyre, S., Hinks, A., Bowes, J., Gibbons, L., Plant, D., Wilson, A. G., Marinou, I., Morgan, A., Emery, P., Steer, S., Hocking, L., Reid, D. M., Wordsworth, P., Harrison, P., Worthington, J., Fraser, Christine, Green, Elaine, Grozeva, Detelina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, Escott-Price, Valentina, Nikolov, Ivan, O'Donovan, Michael Conlon, Owen, Michael John and Craddock, Nicholas John 2008. Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility. Human Molecular Genetics 17 (15) , pp. 2274-2279. 10.1093/hmg/ddn128

Loos, Ruth J F, Lindgren, Cecilia M, Li, Shengxu, Wheeler, Eleanor, Zhao, Jing Hua, Prokopenko, Inga, Inouye, Michael, Freathy, Rachel M, Attwood, Antony P, Beckmann, Jacques S, Berndt, Sonja I, Jacobs, Kevin B, Chanock, Stephen J, Hayes, Richard B, Bergmann, Sven, Bennett, Amanda J, Bingham, Sheila A, Bochud, Murielle, Brown, Morris, Cauchi, Stéphane, Connell, John M, Cooper, Cyrus, Smith, George Davey, Day, Ian, Dina, Christian, De, Subhajyoti, Dermitzakis, Emmanouil T, Doney, Alex S F, Elliott, Katherine S, Elliott, Paul, Evans, David M, Sadaf Farooqi, I, Froguel, Philippe, Ghori, Jilur, Groves, Christopher J, Gwilliam, Rhian, Hadley, David, Hall, Alistair S, Hattersley, Andrew T, Hebebrand, Johannes, Heid, Iris M, Lamina, Claudia, Gieger, Christian, Illig, Thomas, Meitinger, Thomas, Wichmann, H-Erich, Herrera, Blanca, Hinney, Anke, Hunt, Sarah E, Jarvelin, Marjo-Riitta, Johnson, Toby, Jolley, Jennifer D M, Karpe, Fredrik, Keniry, Andrew, Khaw, Kay-Tee, Luben, Robert N, Mangino, Massimo, Marchini, Jonathan, McArdle, Wendy L, McGinnis, Ralph, Meyre, David, Munroe, Patricia B, Morris, Andrew D, Ness, Andrew R, Neville, Matthew J, Nica, Alexandra C, Ong, Ken K, O'Rahilly, Stephen, Owen, Katharine R, Palmer, Colin N A, Papadakis, Konstantinos, Potter, Simon, Pouta, Anneli, Qi, Lu, Kraft, Peter, Hankinson, Susan E, Hunter, David J, Hu, Frank B, Randall, Joshua C, Rayner, Nigel W, Ring, Susan M, Sandhu, Manjinder S, Scherag, André, Sims, Matthew A, Song, Kijoung, Soranzo, Nicole, Speliotes, Elizabeth K, Lyon, Helen N, Voight, Benjamin F, Ridderstrale, Martin, Groop, Leif, Syddall, Holly E, Teichmann, Sarah A, Timpson, Nicholas J, Tobias, Jonathan H, Uda, Manuela, Scheet, Paul, Sanna, Serena, Abecasis, Goncalo R, Albai, Giuseppe, Nagaraja, Ramaiah, Schlessinger, David, Ganz Vogel, Carla I, Wallace, Chris, Waterworth, Dawn M, Weedon, Michael N, Willer, Cristen J, Jackson, Anne U, Tuomilehto, Jaakko, Collins, Francis S, Boehnke, Michael, Mohlke, Karen L, Wraight, Vicki L, Yuan, Xin, Zeggini, Eleftheria, Hirschhorn, Joel N, Strachan, David P, Ouwehand, Willem H, Caulfield, Mark J, Samani, Nilesh J, Frayling, Timothy M, Vollenweider, Peter, Waeber, Gerard, Mooser, Vincent, Deloukas, Panos, McCarthy, Mark I, Wareham, Nicholas J, Barroso, Inês, Fraser, Christine, Green, Elaine, Grozeva, Detelina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, Escott-Price, Valentina, Nikolov, Ivan, O'Donovan, Michael Conlon, Owen, Michael John and Craddock, Nicholas John 2008. Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nature Genetics 40 (6) , pp. 768-775. 10.1038/ng.140

Fisher, Sheila A, Tremelling, Mark, Anderson, Carl A, Gwilliam, Rhian, Bumpstead, Suzannah, Prescott, Natalie J, Nimmo, Elaine R, Massey, Dunecan, Berzuini, Carlo, Johnson, Christopher, Barrett, Jeffrey C, Cummings, Fraser R, Drummond, Hazel, Lees, Charlie W, Onnie, Clive M, Hanson, Catherine E, Blaszczyk, Katarzyna, Inouye, Mike, Ewels, Philip, Ravindrarajah, Radhi, Keniry, Andrew, Hunt, Sarah, Carter, Martyn, Watkins, Nick, Ouwehand, Willem, Lewis, Cathryn M, Cardon, Lon, Lobo, Alan, Forbes, Alastair, Sanderson, Jeremy, Jewell, Derek P, Mansfield, John C, Deloukas, Panos, Mathew, Christopher G, Parkes, Miles, Satsangi, Jack, Fraser, Christine, Green, Elaine, Grozeva, Detelina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, Escott-Price, Valentina, Nikolov, Ivan, O'Donovan, Michael Conlon, Owen, Michael John and Craddock, Nicholas John 2008. Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease. Nature Genetics 40 (6) , pp. 710-712. 10.1038/ng.145

Verma, Ranjana, Holmans, Peter Alan, Knowles, James A., Grover, Deepak, Evgrafov, Oleg V., Crowe, Raymond R., Scheftner, William A., Weissman, Myrna M., DePaulo, J. Raymond, Potash, James B. and Levinson, Douglas F. 2008. Linkage disequilibrium mapping of a chromosome 15q25-26 major depression linkage region and sequencing of NTRK3. Biological psychiatry 63 (12) , pp. 1185-1189. 10.1016/j.biopsych.2008.02.005

Hodges, Angela Kaye, Hughes, Gareth, Brooks, Simon Philip, Elliston, Linda Anne, Holmans, Peter Alan, Dunnett, Stephen Bruce and Jones, Lesley 2008. Brain gene expression correlates with changes in behavior in the R6/1 mouse model of Huntington's disease. Genes, Brain and Behavior 7 (3) , pp. 288-299. 10.1111/j.1601-183X.2007.00350.x

Langley, Kate, Turic, Dragana, Rice, Frances, Holmans, Peter, van den Bree, Marianne Bernadette, Craddock, Nicholas John, Kent, L., Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2008. Testing for gene × environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (1) , pp. 49-53. 10.1002/ajmg.b.30571

Blom, Elin S., Holmans, Peter Alan, Arepalli, Sampath, Adighibe, Omanma, Hamshere, Marian Lindsay, Gatz, Margaret, Pedersen, Nancy L., Bergem, A. L. Mina, Owen, Michael John, Hollingworth, Paul, Goate, Alison, Williams, Julie, Lannfelt, Lars, Hardy, John, Wavrant-De Vrièze, Fabienne and Glaser, Anna 2008. Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13? American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (6) , pp. 778-783. 10.1002/ajmg.b.30681

Irmansyah, , Schwab, S. G., Heriani, , Handoko, H. Y., Kusumawardhani, A., Widyawati, I., Amir, N., Nasrun, M. W. S., Holmans, Peter Alan, Knapp, M. and Wildenauer, D. B. 2008. Genome-wide scan in 124 Indonesian sib-pair families with Schizophrenia reveals genome-wide significant linkage to a locus on chromosome 3p26-21. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (7) , pp. 1245-1252. 10.1002/ajmg.b.30763

Li, Y., Grupe, A., Rowland, C., Holmans, Peter Alan, Segurado, Ricardo, Abraham, Richard Alun, Jones, Lesley, Catanese, J., Ross, D., Mayo, K., Martinez, M., Hollingworth, Paul, Goate, A., Cairns, N. J., Racette, B. A., Perlmutter, J. S., O'Donovan, Michael Conlon, Morris, J. C., Brayne, C., Rubinsztein, D. C., Lovestone, S., Thal, L. J., Owen, Michael John and Williams, Julie 2008. Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease. Human Molecular Genetics 17 (5) , pp. 759-767. 10.1093/hmg/ddm348

Bray, Nicholas John, Holmans, Peter Alan, van den Bree, Marianne Bernadette, Jones, Lesley, Elliston, Linda Anne, Hughes, Gareth, Richards, Alexander, Williams, Nigel Melville, Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 2008. Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1. Human Molecular Genetics 17 (8) , pp. 1169-1174. 10.1093/hmg/ddn006

Stone, Jennifer L., O'Donovan, Michael Conlon, Gurling, Hugh, Kirov, George, Blackwood, Douglas H. R., Corvin, Aiden, Craddock, Nicholas John, Gill, Michael, Hultman, Christina M., Lichtenstein, Paul, McQuillin, Andrew, Pato, Carlos N., Ruderfer, Douglas M., Owen, Michael John, St Clair, David, Sullivan, Patrick F., Sklar, Pamela, Purcell, Shaun M., Korn, Joshua, Macgregor, Stuart, Morris, Derek W., O'Dushlaine, Colm T., Daly, Mark J., Visscher, Peter M., Holmans, Peter Alan, Scolnick, Edward M., Williams, Nigel Melville, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine, Williams, Hywel John, Toncheva, Draga, Milanova, Vihra, Thelander, Emma F., Kenny, Elaine, Waddington, John L., Choudhury, Khalid, Datta, Susmita, Pimm, Jonathan, Thirumalai, Srinivasa, Puri, Vinay, Krasucki, Robert, Lawrence, Jacob, Quested, Digby, Bass, Nicholas, Curtis, David, Crombie, Caroline, Fraser, Gillian, Leh Kwan, Soh, Walker, Nicholas, Muir, Walter J., McGhee, Kevin A., Pickard, Ben, Malloy, Pat, Maclean, Alan W., Van Beck, Margaret, Pato, Michele T., Medeiros, Helena, Middleton, Frank, Carvalho, Celia, Morley, Christopher, Fanous, Ayman, Conti, David, Knowles, James A., Paz Ferreira, Carlos, Macedo, Antonio, Azevedo, M. Helena, McCarroll, Steve A., Daly, Mark, Chambert, Kimberly, Gates, Casey, Gabriel, Stacey B., Mahon, Scott and Ardlie, Kristen 2008. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455 (7210) , pp. 237-241. 10.1038/nature07239

Richards, Alexander L., Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John and Jones, Lesley 2008. A comparison of four clustering methods for brain expression microarray data. BMC Bioinformatics 9 , 490. 10.1186/1471-2105-9-490
file

Glaser, Beate, Nikolov, Ivan, Chubb, D., Hamshere, Marian Lindsay, Segurado, Ricardo, Escott-Price, Valentina and Holmans, Peter Alan 2007. Analyses of single marker and pairwise effects of candidate loci for rheumatoid arthritis using logistic regression and random forests [Conference Proceedings]. BMC Proceedings 1 (S1) , S54-S54.

Segurado, Ricardo, Hamshere, Marian Lindsay, Glaser, Beate, Nikolov, Ivan, Escott-Price, Valentina and Holmans, Peter Alan 2007. Combining linkage data sets for meta-analysis and mega-analysis: the GAW15 rheumatoid arthritis data set [Conference Proceedings]. BMC Proceedings 1 (S1) , S104-S104.

Hamshere, Marian Lindsay, Segurado, Ricardo, Escott-Price, Valentina, Nikolov, Ivan, Glaser, Beate and Holmans, Peter Alan 2007. Large-scale linkage analysis of 1302 affected relative pairs with rheumatoid arthritis [Conference Proceedings]. BMC Proceedings 1 (S1) , S100-S100.

Nejentsev, Sergey, Howson, Joanna M. M., Walker, Neil M., Szeszko, Jeffrey, Field, Sarah F., Stevens, Helen E., Reynolds, Pamela, Hardy, Matthew, King, Erna, Masters, Jennifer, Hulme, John, Maier, Lisa M., Smyth, Deborah, Bailey, Rebecca, Cooper, Jason D., Ribas, Gloria, Campbell, R. Duncan, Clayton, David G., Todd, John A., Burton, Paul R., Clayton, David G., Cardon, Lon R., Craddock, Nicholas John, Deloukas, Panos, Duncanson, Audrey, Kwiatkowski, Dominic P., McCarthy, Mark I., Ouwehand, Willem H., Samani, Nilesh J., Todd, John A., Donnelly, Peter, Barrett, Jeffrey C., Burton, Paul R., Davison, Dan, Donnelly, Peter, Easton, Doug, Evans, David, Leung, Hin-Tak, Marchini, Jonathan L., Morris, Andrew P., Spencer, Chris C. A., Tobin, Martin D., Cardon, Lon R., Clayton, David G., Attwood, Antony P., Boorman, James P., Cant, Barbara, Everson, Ursula, Hussey, Judith M., Jolley, Jennifer D., Knight, Alexandra S., Koch, Kerstin, Meech, Elizabeth, Nutland, Sarah, Prowse, Christopher V., Stevens, Helen E., Taylor, Niall C., Walters, Graham R., Walker, Neil M., Watkins, Nicholas A., Winzer, Thilo, Todd, John A., Ouwehand, Willem H., Jones, Richard W., McArdle, Wendy L., Ring, Susan M., Strachan, David P., Pembrey, Marcus, Breen, Gerome, St Clair, David, Caesar, Sian, Gordon-Smith, Katherine, Jones, Lisa, Fraser, Christine, Green, Elaine, Grozeva, Detelina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, Escott-Price, Valentina, Nikolov, Ivan, O'Donovan, Michael Conlon, Owen, Michael John, Craddock, Nicholas John, Collier, David A., Elkin, Amanda, Farmer, Anne, Williamson, Richard, McGuffin, Peter, Young, Allan H., Nicol Ferrier, I., Ball, Stephen G., Balmforth, Anthony J., Barrett, Jennifer H., Bishop, D. Timothy, Iles, Mark M., Maqbool, Azhar, Yuldasheva, Nadira, Hall, Alistair S., Braund, Peter S., Burton, Paul R., Dixon, Richard J., Mangino, Massimo, Stevens, Suzanne, Tobin, Martin D., Thompson, John R., Samani, Nilesh J., Bredin, Francesca, Tremelling, Mark, Parkes, Miles, Drummond, Hazel, Lees, Charles W., Nimmo, Elaine R., Satsangi, Jack, Fisher, Sheila A., Forbes, Alastair, Lewis, Cathryn M., Onnie, Clive M., Prescott, Natalie J., Sanderson, Jeremy, Mathew, Christopher G., Barbour, Jamie, Khalid Mohiuddin, M., Todhunter, Catherine E., Mansfield, John C., Ahmad, Tariq, Cummings, Fraser R., Jewell, Derek P., Webster, John, Brown, Morris J., Clayton, David G., Lathrop, G. Mark, Connell, John, Dominiczak, Anna, Samani, Nilesh J., Braga, Carolina A., Burke, Beverley, Dobson, Richard, Gungadoo, Johannie, Lee, Kate L., Munroe, Patricia B., Newhouse, Stephen J., Onipinla, Abiodun, Wallace, Chris, Xue, Mingzhan, Caulfield, Mark, Farrall, Martin, Barton, Anne, Bruce, Ian N., Donovan, Hannah, Eyre, Steve, Gilbert, Paul D., Hider, Samantha L., Hinks, Anne M., John, Sally L., Potter, Catherine, Silman, Alan J., Symmons, Deborah P. M., Thomson, Wendy, Worthington, Jane, Clayton, David G., Dunger, David B., Nutland, Sarah, Stevens, Helen E., Walker, Neil M., Widmer, Barry, Todd, John A., Frayling, Timothy M., Freathy, Rachel M., Lango, Hana, Perry, John R. B., Shields, Beverley M., Weedon, Michael N., Hattersley, Andrew T., Hitman, Graham A., Walker, Mark, Elliott, Kate S., Groves, Christopher J., Lindgren, Cecilia M., Rayner, Nigel W., Timpson, Nicholas J., Zeggini, Eleftheria, McCarthy, Mark I., Newport, Melanie, Sirugo, Giorgio, Lyons, Emily, Vannberg, Fredrik, Hill, Adrian V. S., Bradbury, Linda A., Farrar, Claire, Pointon, Jennifer J., Wordsworth, Paul, Brown, Matthew A., Franklyn, Jayne A., Heward, Joanne M., Simmonds, Matthew J., Gough, Stephen C. L., Seal, Sheila, Stratton, Michael R., Rahman, Nazneen, Ban, Maria, Goris, An, Sawcer, Stephen J., Compston, Alastair, Conway, David, Jallow, Muminatou, Newport, Melanie, Sirugo, Giorgio, Rockett, Kirk A., Kwiatkowski, Dominic P., Bryan, Claire, Bumpstead, Suzannah J., Chaney, Amy, Downes, Kate, Ghori, Jilur, Gwilliam, Rhian, Hunt, Sarah E., Inouye, Michael, Keniry, Andrew, King, Emma, McGinnis, Ralph, Potter, Simon, Ravindrarajah, Rathi, Whittaker, Pamela, Withers, David, Deloukas, Panos, Leung, Hin-Tak, Nutland, Sarah, Stevens, Helen E., Walker, Neil M., Todd, John A., Easton, Doug, Clayton, David G., Burton, Paul R., Tobin, Martin D., Barrett, Jeffrey C., Evans, David, Morris, Andrew P., Cardon, Lon R., Cardin, Niall J., Davison, Dan, Ferreira, Teresa, Pereira-Gale, Joanne, Hallgrimsdóttir, Ingeleif B., Howie, Bryan N., Marchini, Jonathan L., Spencer, Chris C. A., Su, Zhan, Ying Teo, Yik, Vukcevic, Damjan, Donnelly, Peter, Bentley, David, Brown, Matthew A., Cardon, Lon R., Caulfield, Mark, Clayton, David G., Compston, Alistair, Craddock, Nick, Deloukas, Panos, Donnelly, Peter, Farrall, Martin, Gough, Stephen C. L., Hall, Alistair S., Hattersley, Andrew T., Hill, Adrian V. S., Kwiatkowski, Dominic P., Mathew, Christopher G., McCarthy, Mark I., Ouwehand, Willem H., Parkes, Miles, Pembrey, Marcus, Rahman, Nazneen, Samani, Nilesh J., Stratton, Michael R., Todd, John A. and Worthington, Jane 2007. Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A. Nature 450 (7171) , pp. 887-892. 10.1038/nature06406

Verma, Ranjana, Cutler, David J., Holmans, Peter Alan, Knowles, James A., Crowe, Raymond R., Scheftner, William A., Weissman, Myrna M., DePaulo, J. Raymond, Levinson, Douglas F. and Potash, James B. 2007. Investigating the role ofp11 (S100A10) sequence variation in susceptibility to major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144B (8) , pp. 1079-1082. 10.1002/ajmg.b.30514

Thomson, Wendy, Barton, Anne, Ke, Xiayi, Eyre, Steve, Hinks, Anne, Bowes, John, Donn, Rachelle, Symmons, Deborah, Hider, Samantha, Bruce, Ian N, Wilson, Anthony G, Marinou, Ioanna, Morgan, Ann, Emery, Paul, Carter, Angela, Steer, Sophia, Hocking, Lynne, Reid, David M, Wordsworth, Paul, Harrison, Pille, Strachan, David, Worthington, Jane, Fraser, Christine, Green, Elaine K., Grozeva, Detelina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, Escott-Price, Valentina, Nikolov, Ivan, O'Donovan, Michael Conlon, Owen, Michael John and Craddock, Nicholas John 2007. Rheumatoid arthritis association at 6q23. Nature Genetics 39 (12) , pp. 1431-1433. 10.1038/ng.2007.32

Myers, Amanda J, Gibbs, J Raphael, Webster, Jennifer A, Rohrer, Kristen, Zhao, Alice, Marlowe, Lauren, Kaleem, Mona, Leung, Doris, Bryden, Leslie, Nath, Priti, Zismann, Victoria L, Joshipura, Keta, Huentelman, Matthew J, Hu-Lince, Diane, Coon, Keith D, Craig, David W, Pearson, John V, Holmans, Peter Alan, Heward, Christopher B, Reiman, Eric M, Stephan, Dietrich and Hardy, John 2007. A survey of genetic human cortical gene expression. Nature Genetics 39 (12) , pp. 1494-1499. 10.1038/ng.2007.16

Strand, A. D., Baquet, Z. C., Aragaki, A. K., Holmans, Peter Alan, Yang, L., Cleren, C., Beal, M. F., Jones, Lesley, Kooperberg, C., Olson, J. M. and Jones, K. R. 2007. Expression profiling of Huntington's disease models suggests that brain-derived neurotrophic factor depletion plays a major role in striatal degeneration. Journal of Neuroscience 27 (43) , pp. 11758-11768. 10.1523/JNEUROSCI.2461-07.2007

Hollingworth, Paul, Hamshere, Marian Lindsay, Holmans, Peter Alan, O'Donovan, Michael Conlon, Sims, Rebecca, Powell, J., Lovestone, S., Myers, A., DeVrieze, F.W., Hardy, J., Goate, A., Owen, Michael John and Williams, Julie 2007. Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144B (7) , pp. 841-848. 10.1002/ajmg.b.30515

Hamshere, Marian Lindsay, Holmans, Peter Alan, Avramopoulos, Dimitrios, Bassett, Susan S., Blacker, Deborah, Bertram, Lars, Wiener, Howard, Rochberg, Nan, Tanzi, Rudolph E., Myers, Amanda, Wavrant-De Vrièze, Fabienne, Go, Rodney, Fallin, Daniele, Lovestone, Simon, Hardy, John, Goate, Alison, O'Donovan, Michael Conlon, Williams, Julie and Owen, Michael John 2007. Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. Human Molecular Genetics Advanc , pp. 1-34. 10.1093/hmg/ddm224

Jones, Ian Richard, Hamshere, Marian Lindsay, Nangle, Jeanne-Marrie, Bennett, Philip, Green, Elaine Karen, Heron, Jess, Segurado, Ricardo, Lambert, David, Holmans, Peter Alan, Corvin, Aiden, Owen, Michael John, Jones, Lisa Anne, Gill, Michael and Craddock, Nicholas John 2007. Bipolar affective puerperal psychosis: genome-wide significant evidence for linkage to chromosome 16. American journal of psychiatry 164 (7) , pp. 1099-1104. 10.1176/appi.ajp.164.7.1099

Langley, Kate, Holmans, Peter Alan, van den Bree, Marianne Bernadette and Thapar, Anita 2007. Effects of low birth weight, maternal smoking in pregnancy and social class on the phenotypic manifestation of Attention Deficit Hyperactivity Disorder and associated antisocial behaviour: investigation in a clinical sample. BMC Psychiatry 7 (1) , p. 26. 10.1186/1471-244X-7-26

Burton, Paul R., Clayton, David G., Cardon, Lon R., Craddock, Nicholas John, Deloukas, Panos, Duncanson, Audrey, Kwiatkowski, Dominic P., McCarthy, Mark I., Ouwehand, Willem H., Samani, Nilesh J., Todd, John A., Donnelly, Peter, Barrett, Jeffrey C., Burton, Paul R., Davison, Dan, Donnelly, Peter, Easton, Doug, Evans, David, Leung, Hin-Tak, Marchini, Jonathan L., Morris, Andrew P., Spencer, Chris C. A., Tobin, Martin D., Cardon, Lon R., Clayton, David G., Attwood, Antony P., Boorman, James P., Cant, Barbara, Everson, Ursula, Hussey, Judith M., Jolley, Jennifer D., Knight, Alexandra S., Koch, Kerstin, Meech, Elizabeth, Nutland, Sarah, Prowse, Christopher V., Stevens, Helen E., Taylor, Niall C., Walters, Graham R., Walker, Neil M., Watkins, Nicholas A., Winzer, Thilo, Todd, John A., Ouwehand, Willem H., Jones, Richard W., McArdle, Wendy L., Ring, Susan M., Strachan, David P., Pembrey, Marcus, Breen, Gerome, St Clair, David, Caesar, Sian, Gordon-Smith, Katherine, Jones, Lisa, Fraser, Christine, Green, Elaine K., Grozeva, Detelina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, Escott-Price, Valentina, Nikolov, Ivan, O'Donovan, Michael Conlon, Owen, Michael John, Craddock, Nick, Collier, David A., Elkin, Amanda, Farmer, Anne, Williamson, Richard, McGuffin, Peter, Young, Allan H., Ferrier, I. Nicol, Ball, Stephen G., Balmforth, Anthony J., Barrett, Jennifer H., Bishop, D. Timothy, Iles, Mark M., Maqbool, Azhar, Yuldasheva, Nadira, Hall, Alistair S., Braund, Peter S., Burton, Paul R., Dixon, Richard J., Mangino, Massimo, Stevens, Suzanne, Tobin, Martin D., Thompson, John R., Samani, Nilesh J., Bredin, Francesca, Tremelling, Mark, Parkes, Miles, Drummond, Hazel, Lees, Charles W., Nimmo, Elaine R., Satsangi, Jack, Fisher, Sheila A., Forbes, Alastair, Lewis, Cathryn M., Onnie, Clive M., Prescott, Natalie J., Sanderson, Jeremy, Mathew, Christopher G., Barbour, Jamie, Mohiuddin, M. Khalid, Todhunter, Catherine E., Mansfield, John C., Ahmad, Tariq, Cummings, Fraser R., Jewell, Derek P., Webster, John, Brown, Morris J., Clayton, David G., Lathrop, G. Mark, Connell, John, Dominiczak, Anna, Samani, Nilesh J., Marcano, Carolina A. Braga, Burke, Beverley, Dobson, Richard, Gungadoo, Johannie, Lee, Kate L., Munroe, Patricia B., Newhouse, Stephen J., Onipinla, Abiodun, Wallace, Chris, Xue, Mingzhan, Caulfield, Mark, Farrall, Martin, Barton, Anne, and Genomics (BRAGGS), The Biologics in RA Genetics, Bruce, Ian N., Donovan, Hannah, Eyre, Steve, Gilbert, Paul D., Hider, Samantha L., Hinks, Anne M., John, Sally L., Potter, Catherine, Silman, Alan J., Symmons, Deborah P. M., Thomson, Wendy, Worthington, Jane, Clayton, David G., Dunger, David B., Nutland, Sarah, Stevens, Helen E., Walker, Neil M., Widmer, Barry, Todd, John A., Frayling, Timothy M., Freathy, Rachel M., Lango, Hana, Perry, John R. B., Shields, Beverley M., Weedon, Michael N., Hattersley, Andrew T., Hitman, Graham A., Walker, Mark, Elliott, Kate S., Groves, Christopher J., Lindgren, Cecilia M., Rayner, Nigel W., Timpson, Nicholas J., Zeggini, Eleftheria, McCarthy, Mark I., Newport, Melanie, Sirugo, Giorgio, Lyons, Emily, Vannberg, Fredrik, Hill, Adrian V. S., Bradbury, Linda A., Farrar, Claire, Pointon, Jennifer J., Wordsworth, Paul, Brown, Matthew A., Franklyn, Jayne A., Heward, Joanne M., Simmonds, Matthew J., Gough, Stephen C. L., Seal, Sheila, Susceptibility Collaboration (UK), Breast Cancer, Stratton, Michael R., Rahman, Nazneen, Ban, Maria, Goris, An, Sawcer, Stephen J., Compston, Alastair, Conway, David, Jallow, Muminatou, Newport, Melanie, Sirugo, Giorgio, Rockett, Kirk A., Kwiatkowski, Dominic P., Bumpstead, Suzannah J., Chaney, Amy, Downes, Kate, Ghori, Mohammed J. R., Gwilliam, Rhian, Hunt, Sarah E., Inouye, Michael, Keniry, Andrew, King, Emma, McGinnis, Ralph, Potter, Simon, Ravindrarajah, Rathi, Whittaker, Pamela, Widden, Claire, Withers, David, Deloukas, Panos, Leung, Hin-Tak, Nutland, Sarah, Stevens, Helen E., Walker, Neil M., Todd, John A., Easton, Doug, Clayton, David G., Burton, Paul R., Tobin, Martin D., Barrett, Jeffrey C., Evans, David, Morris, Andrew P., Cardon, Lon R., Cardin, Niall J., Davison, Dan, Ferreira, Teresa, Pereira-Gale, Joanne, Hallgrimsdóttir, Ingileif B., Howie, Bryan N., Marchini, Jonathan L., Spencer, Chris C. A., Su, Zhan, Teo, Yik Ying, Vukcevic, Damjan, Donnelly, Peter, Bentley, David, Brown, Matthew A., Cardon, Lon R., Caulfield, Mark, Clayton, David G., Compston, Alistair, Craddock, Nick, Deloukas, Panos, Donnelly, Peter, Farrall, Martin, Gough, Stephen C. L., Hall, Alistair S., Hattersley, Andrew T., Hill, Adrian V. S., Kwiatkowski, Dominic P., Mathew, Christopher G., McCarthy, Mark I., Ouwehand, Willem H., Parkes, Miles, Pembrey, Marcus, Rahman, Nazneen, Samani, Nilesh J., Stratton, Michael R., Todd, John A. and Worthington, Jane 2007. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447 (7145) , pp. 661-678. 10.1038/nature05911

Strand, Andrew D., Aragaki, Aaron K., Baquet, Zachary C., Hodges, Angela, Cunningham, Philip, Holmans, Peter Alan, Jones, Kevin R., Jones, Lesley, Kooperberg, Charles and Olson, James M. 2007. Conservation of regional gene expression in mouse and human brain. PLOS Genetics 3 (4) , e59. 10.1371/journal.pgen.0030059

O'Donovan, Michael Conlon, Holmans, Peter Alan, Zammit, Stanley, Williams, Nigel Melvillle, Escott-Price, Valentina, Kirov, George, Craddock, Nicholas John, Bray, Nicholas John and Owen, Michael John 2007. Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia [Conference Abstract]. Schizophrenia bulletin 33 (2) , pp. 311-312. 10.1093/schbul/sbm004

Levinson, D. F., Evgrafov, O. V., Knowles, J. A., Potash, J. B., Weissman, M. M., Scheftner, W. A., Depaulo, J. R. Jr., Crowe, R. R., Murphy-Eberenz, K., Marta, D. H., McInnis, M. G., Adams, P., Gladis, M., Miller, E. B., Thomas, J. and Holmans, Peter Alan 2007. Genetics of recurrent early-onset major depression (GenRED): significant linkage on chromosome 15q25-q26 after fine mapping with single nucleotide polymorphism markers. American Journal of Psychiatry 164 (2) , pp. 259-264.

Holmans, Peter Alan, Weissman, M. M., Zubenko, G. S., Scheftner, W. A., Crowe, R. R., Depaulo, J. R. Jr., Knowles, J. A., Zubenko, W. N., Murphy-Eberenz, K., Marta, D.H., Boutelle, S., McInnis, M. G., Adams, P., Gladis, M., Steele, J., Miller, E. B., Potash, J. B., Mackinnon, D. F. and Levinson, D. F. 2007. Genetics of recurrent early-onset major depression (GenRED): final genome scan report. American Journal of Psychiatry 164 (2) , pp. 248-258.

Holmans, Peter Alan, Weissman, Myrna M., Zubenko, George S., Scheftner, William A., Crowe, Raymond R., DePaulo, J. Raymond Jr., Knowles, James A., Zubenko, Wendy N., Murphy-Eberenz, Kathleen, Marta, Diana H., Boutelle, Sandra, McInnis, Melvin G., Adams, Philip, Gladis, Madeline, Steele, Jo, Miller, Erin B., Potash, James B., MacKinnon, Dean F. and Levinson, Douglas F. 2007. Genetics of recurrent early-onset major depression (GenRED): final genome scan report. American Journal of Psychiatry 164 (2) , pp. 248-258. 10.1176/appi.ajp.164.2.248

Grupe, Andrew, Abraham, Richard Alun, Li, Yonghong, Rowland, Charles, Hollingworth, Paul, Morgan, Angharad Rhys, Jehu, Luke, Segurado, Ricardo, Stone, David, Schadt, Eric, Karnoub, Maha, Nowotny, Petra, Tacey, Kristina, Catanese, Joseph, Sninsky, John, Brayne, Carol, Rubinsztein, David, Gill, Michael, Lawlor, Brian, Lovestone, Simo, Holmans, Peter Alan, O'Donovan, Michael Conlon, Morris, John C., Thal, Leon, Goate, Alison, Owen, Michael John and Williams, Julie 2007. Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants. Human Molecular Genetics 16 (8) , pp. 865-873. 10.1093/hmg/ddm031

Ghosh, Saurabh, Babron, Marie-Claude, Group 10, , Hamshere, Marian Lindsay and Holmans, Peter Alan 2007. Linkage analyses of rheumatoid arthritis and related quantitative phenotypes: the GAW15 experience. Genetic Epidemiology 31 (S1) , S86-S95. 10.1002/gepi.20284

Martin, Lisa J., Woo, Jessica G., Avery, Christy L., Chen, Huann-Sheng, North, Kari E., Group 15, and Holmans, Peter Alan 2007. Multiple testing in the genomics era: Findings from Genetic Analysis Workshop 15, Group 15. Genetic Epidemiology 31 (S1) , S124-S131. 10.1002/gepi.20289

Thapar, Anita, Harold, Gordon Thomas, Holmans, Peter Alan, Rice, Frances, Langley, Kate, Aggleton, John Patrick, Fowler, Tom, van den Bree, Marianne Bernadette, Owen, Michael John and O'Donovan, Michael Conlon 2007. Promoting Measured Genes and Measured Environments: On the Importance of Careful Statistical Analyses and Biological Relevance—Reply [Letter]. Archives of General Psychiatry 64 (3) , pp. 378-379. 10.1001/archpsyc.64.3.378-b

Burton, Paul R., Clayton, David G., Cardon, Lon R., Craddock, Nicholas John, Deloukas, Panos, Duncanson, Audrey, Kwiatkowski, Dominic P., McCarthy, Mark I., Ouwehand, Willem H., Samani, Nilesh J., Todd, John A., Donnelly (Chair), Peter, Barrett, Jeffrey C., Burton, Paul R., Davison, Dan, Donnelly, Peter, Easton, Doug, Evans, David M., Leung, Hin-Tak, Marchini, Jonathan L., Morris, Andrew P., Spencer, Chris C. A., Tobin, Martin D., Cardon, Lon R., Clayton, David G., Attwood, Antony P., Boorman, James P., Cant, Barbara, Everson, Ursula, Hussey, Judith M., Jolley, Jennifer D., Knight, Alexandra S., Koch, Kerstin, Meech, Elizabeth, Nutland, Sarah, Prowse, Christopher V., Stevens, Helen E., Taylor, Niall C., Walters, Graham R., Walker, Neil M., Watkins, Nicholas A., Winzer, Thilo, Todd, John A., Ouwehand, Willem H., Jones, Richard W., McArdle, Wendy L., Ring, Susan M., Strachan, David P., Pembrey, Marcus, Breen, Gerome, Clair, David St, Caesar, Sian, Gordon-Smith, Katharine, Jones, Lisa, Fraser, Christine, Green, Elaine K., Grozeva, Detelina, Hamshere, Marian Lindsay, Holmans, Peter A., Jones, Ian Richard, Kirov, George, Moskivina, Valentina, Nikolov, Ivan, O'Donovan, Michael Conlon, Owen, Michael John, Craddock, Nicholas, Collier, David A., Elkin, Amanda, Farmer, Anne, Williamson, Richard, McGuffin, Peter, Young, Allan H., Ferrier, I. Nicol, Ball, Stephen G., Balmforth, Anthony J., Barrett, Jennifer H., Bishop, Timothy D., Iles, Mark M., Maqbool, Azhar, Yuldasheva, Nadira, Hall, Alistair S., Braund, Peter S., Burton, Paul R., Dixon, Richard J., Mangino, Massimo, Stevens, Suzanne, Tobin, Martin D., Thompson, John R., Samani, Nilesh J., Bredin, Francesca, Tremelling, Mark, Parkes, Miles, Drummond, Hazel, Lees, Charles W., Nimmo, Elaine R., Satsangi, Jack, Fisher, Sheila A., Forbes, Alastair, Lewis, Cathryn M., Onnie, Clive M., Prescott, Natalie J., Sanderson, Jeremy, Matthew, Christopher G., Barbour, Jamie, Mohiuddin, M. Khalid, Todhunter, Catherine E., Mansfield, John C., Ahmad, Tariq, Cummings, Fraser R., Jewell, Derek P., Webster, John, Brown, Morris J., Clayton, David G., Lathrop, Mark G., Connell, John, Dominiczak, Anna, Samani, Nilesh J., Marcano, Carolina A Braga, Burke, Beverley, Dobson, Richard, Gungadoo, Johannie, Lee, Kate L., Munroe, Patricia B., Newhouse, Stephen J., Onipinla, Abiodun, Wallace, Chris, Xue, Mingzhan, Caulfield, Mark, Farrall, Martin, Barton, Anne, Bruce, Ian N., Donovan, Hannah, Eyre, Steve, Gilbert, Paul D., Hilder, Samantha L., Hinks, Anne M., John, Sally L., Potter, Catherine, Silman, Alan J., Symmons, Deborah P. M., Thomson, Wendy, Worthington, Jane, Clayton, David G., Dunger, David B., Nutland, Sarah, Stevens, Helen E., Walker, Neil M., Widmer, Barry, Todd, John A., Frayling, Timothy M., Freathy, Rachel M., Lango, Hana, Perry, John R. B., Shields, Beverley M., Weedon, Michael N., Hattersley, Andrew T., Hitman, Graham A., Walker, Mark, Elliott, Kate S., Groves, Christopher J., Lindgren, Cecilia M., Rayner, Nigel W., Timpson, Nicolas J., Zeggini, Eleftheria, McCarthy, Mark I., Newport, Melanie, Sirugo, Giorgio, Lyons, Emily, Vannberg, Fredrik, Hill, Adrian V. S., Bradbury, Linda A., Farrar, Claire, Pointon, Jennifer J., Wordsworth, Paul, Brown, Matthew A., Franklyn, Jayne A., Heward, Joanne M., Simmonds, Matthew J., Gough, Stephen C. L., Seal, Sheila, Stratton, Michael R., Rahman, Nazneen, Ban, Maria, Goris, An, Sawcer, Stephen J., Compston, Alastair, Conway, David, Jallow, Muminatou, Newport, Melanie, Sirugo, Giorgio, Rockett, Kirk A., Kwiatkowski, Dominic P., Bumpstead, Suzannah J., Chaney, Amy, Downes, Kate, Ghori, Mohammed J. R., Gwilliam, Rhian, Hunt, Sarah E., Inouye, Michael, Keniry, Andrew, King, Emma, McGinnis, Ralph, Potter, Simon, Ravindrarajah, Rathi, Whittaker, Pamela, Widden, Claire, Withers, David, Deloukas, Panos, Leung, Hin-Tak, Nutland, Sarah, Stevens, Helen E., Walker, Neil M., Todd, John A., Easton, Doug, Clayton, David G., Burton, Paul R., Tobin, Martin D., Barrett, Jeffrey C., Evans, David M., Morris, Andrew P., Cardon, Lon R., Cardin, Niall J., Davison, Dan, Ferreira, Teresa, Pereira-Gale, Joanne, Hallgrimsdóttir, Ingeleif B., Howie, Bryan N., Marchini, Jonathan L., Spencer, Chris C. A., Su, Zhan, Teo, Yik Ying, Vukcevic, Damjan, Donnelly, Peter, Bentley, David, Brown, Matthew A., Cardon, Lon R., Caulfield, Mark, Clayton, David G., Compston, Alastair, Craddock, Nick, Deloukas, Panos, Donnelly, Peter, Farrall, Martin, Gough, Stephen C. L., Hall, Alistair S., Hattersley, Andrew T., Hill, Adrian V. S., Kwiatkowski, Dominic P., Matthew, Christopher G., McCarthy, Mark I., Ouwehand, Willem H., Parkes, Miles, Pembrey, Marcus, Rahman, Nazneen, Samani, Nilesh J., Stratton, Michael R., Todd, John A., Worthington, Jane, Mitchell, Sarah L., Newby, Paul R., Brand, Oliver J., Carr-Smith, Jackie, Pearce, Simon H. S., Gough, Stephen C. L., McGinnis, R., Keniry, A., Deloukas, P., Reveille, John D., Zhou, Xiaodong, Bradbury, Linda A., Sims, Anne-Marie, Dowling, Alison, Taylor, Jacqueline, Doan, Tracy, Cardon, Lon R., Davis, John C., Pointon, Jennifer J., Savage, Laurie, Ward, Michael M., Learch, Thomas L., Weisman, Michael H., Wordsworth, Paul and Brown, Matthew A. 2007. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nature Genetics 39 (11) , pp. 1329-1337. 10.1038/ng.2007.17

Bray, Nicholas John, Holmans, Peter Alan, van Den Bree, Marianne Bernadette, Williams, Nigel Melville, Jones, Lesley, Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 2006. Cis- and trans-acting loci influence expression of DTNBP1, a susceptibility gene for schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (7) , pp. 723-724.

Georgieva, Lyudmila, Escott-Price, Valentina, Peirce, Timothy Rowan, Norton, Nadine, Bray, Nicholas John, Jones, Lesley, Holmans, Peter Alan, Macgregor, Stuart, Zammit, Stanley, Wilkinson, Jennifer Camilla, Williams, Hywel John, Nikolov, Ivan, Williams, Nigel Melville, Ivanov, Dobril Kirilov, Davis, Kenneth L., Haroutunian, Vahram, Buxbaum, Joseph D., Craddock, Nicholas John, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2006. Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia. Proceedings of the National Academy of Sciences of the United States of America (PNAS) ISSN 1091-6490 103 (33) , pp. 12469-12474. 10.1073/pnas.0603029103

Escott-Price, Valentina, Craddock, Nicholas John, Holmans, Peter Alan, Owen, Michael John and O'Donovan, Michael Conlon 2006. Effects of differential genotyping error rate on the Type 1 error probability of case-control studies. Human heredity 61 (1) , pp. 55-64. 10.1159/000092553

Hodges, Angela Kaye, Strand, Andrew D., Aragaki, Aaron K., Kuhn, Alexandre, Sengstag, Thierry, Hughes, Gareth, Elliston, Linda Anne, Hartog, Catherine, Goldstein, Darlene R., Thu, Doris, Hollingsworth, Zane R., Collin, Francois, Synek, Beth, Holmans, Peter Alan, Young, Anne B., Wexler, Nancy S., Delorenzi, Mauro, Kooperberg, Charles, Augood, Sarah J., Faull, Richard L. M., Olson, James M., Jones, Lesley and Luthi-Carter, Ruth 2006. Regional and cellular gene expression changes in human Huntington's disease brain. Human Molecular Genetics 15 (6) , pp. 965-977. 10.1093/hmg/ddl013

Smemo, S1, Nowotny, P., Hinrichs, A. L., Kauwe, J. S., Cherny, S., Erickson, K, Myers, A. J., Kaleem, M., Marlowe, L., Gibson, A. M., Hollingworth, P., O'Donovan, Michael Conlon, Morris, C. M., Holmans, Peter Alan, Lovestone, S., Morris, J. C., Thal, L., Li, Y., Grupe, A., Hardy, J., Owen, Michael John, Williams, J. and Goate, A. 2006. Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease. Annals of Neurology 59 (1) , pp. 21-26. 10.1002/ana.20673

Grupe, Andrew, Li, Yonghong, Rowland, Charles, Nowotny, Petra, Hinrichs, Anthony L., Smemo, Scott, Kauwe, John S. K., Maxwell, Taylor J., Cherny, Sara, Doil, Lisa, Tacey, Kristina, Luchene, Ryan van, Myers, Amanda, Wavrant-De Vrièze, Fabienne, Kaleem, Mona, Hollingworth, Paul, Jehu, Luke, Foy, Catherine, Archer, Nicola, Hamilton, Gillian, Holmans, Peter Alan, Morris, Chris M., Catanese, Joseph, Sninsky, John, White, Thomas J., Powell, John, Hardy, John, O'Donovan, Michael Conlon, Lovestone, Simon, Jones, Lesley, Morris, John C., Thal, Leon, Owen, Michael John, Williams, Julie and Goate, Alison 2006. A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. The American Journal of Human Genetics 78 (1) , pp. 78-88.

Hamshere, Marian Lindsay, Williams, Nigel Melville, Norton, Nadine, Williams, H., Cardno, Alastair G., Zammit, Stanley, Jones, L. A., Murphy, K. C., Sanders, Rebecca, McCarthy, G., Gray, M. Y., Jones, G., Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John and Craddock, Nicholas John 2006. Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes. Journal of Medical Genetics 43 (7) , pp. 563-567. 10.1136/jmg.2005.035345

Macgregor, Stuart, Craddock, Nicholas John and Holmans, Peter Alan 2006. Use of phenotypic covariates in association analysis by sequential addition of cases. European Journal of Human Genetics 14 (5) , pp. 529-534. 10.1038/sj.ejhg.5201604

Hamshere, Marian Lindsay, MacGregor, S., Escott-Price, Valentina, Nikolov, I. N. and Holmans, Peter Alan 2005. Covariate linkage analysis of GAW14 simulated data incorporating subclinical phenotype, sex, population, parent-of-origin, and interaction. BMC Genetics 6 (1) , S45. 10.1186/1471-2156-6-S1-S45

Levinson, D. F. and Holmans, Peter Alan 2005. The effect of linkage disequilibrium on linkage analysis of incomplete pedigrees. BMC Genetics 6 (1) , S6-S6. 10.1186/1471-2156-6-S1-S6

Hamshere, Marian Lindsay, Bennett, Philip, Williams, Nigel Melville, Segurado, Ricardo, Cardno, Alastair George, Norton, Nadine, Lambert, David, Williams, Hywel John, Kirov, George, Corvin, Aiden, Holmans, Peter Alan, Jones, Lisa Anne, Jones, Ian Richard, Gill, Michael, O'Donovan, Michael Conlon, Owen, Michael John and Craddock, Nicholas John 2005. Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13. Archives of general psychiatry 62 (10) , pp. 1081-1088. 10.1001/archpsyc.62.10.1081

Hodges, A., Strand, A. D., Aragaki, A. K., Sengstag, T., Hughes, G., Elliston, Linda Anne, Hartog, C., Goldstein, D. R., Thu, D., Hollingsworth, Z. R., Collin, F., Synek, B., Holmans, Peter Alan, Young, A. B., Wexler, N. S., Delorenzi, M., Kooperberg, C., Augood, S. J., Faull, R. L. M., Olson, J. M., Luthi-Carter, R. and Jones, Lesley 2005. Regional specificity of transcriptional changes in early grade Huntington's disease brain. Journal of Neurology, Neurosurgery and Psychiatry 76 , A16-A16.

Hughes, G. P., Brooks, Simon P., Hodges, A. H., Holmans, Peter Alan, Thomas, J. M., Goldstein, D., Dunnett, Stephen Bruce and Jones, Lesley 2005. Integrating behaviour and brain gene expression in Huntington's disease transgenic mouse models. Journal of Neurology, Neurosurgery and Psychiatry 76 , A41-A41.

Nowotny, P., Hinrichs, A. L., Smemo, S., Kauwe, J. S., Maxwell, T., Holmans, Peter Alan, Hamshere, Marian Lindsay, Turic, D., Jehu, L., Hollingworth, P., Moore, P., Bryden, L., Myers, A., Doil, L. M., Tacey, K. M., Gibson, A. M., McKeith, I. G., Perry, R. H., Morris, C. M., Thal, L., Morris, J. C., O'Donovan, Michael Conlon, Lovestone, S. and Grupe, A. 2005. Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 136B (1) , pp. 62-68. 10.1002/ajmg.b.30186

Holmans, Peter Alan, Hamshere, Marian Lindsay, Hollingworth, P., Rice, Frances, Tunstall, N., Jones, S., Moore, P., Wavrant DeVrieze, F., Myers, A., Crook, R., Compton, D., Marshall, H., Meyer, D., Shears, S., Booth, J., Ramic, D., Williams, Nigel Melville, Norton, N., Abraham, R., Kehoe, P., Williams, H., Rudrasingham, V., O'Donovan, Michael Conlon, Jones, Lesley, Hardy, J., Goate, A., Lovestone, S., Owen, Michael John and Williams, Julie 2005. Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 135B (1) , pp. 24-32. 10.1002/ajmg.b.30114

Lambert, D., Middle, F., Hamshere, Marian Lindsay, Segurado, Ricardo, Raybould, Rachel, Corvin, A., Green, Elaine Karen, O'Mahony, E., Nikolov, Ivan, Mulcahy, T., Haque, S., Bort, S., Bennett, P., Norton, Nadine, Owen, Michael John, Kirov, George, Lendon, C., Jones, Lisa Anne, Jones, Ian Richard, Holmans, Peter Alan, Gill, M. and Craddock, Nicholas John 2005. Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22. Molecular psychiatry 10 (9) , pp. 831-841. 10.1038/sj.mp.4001684

Escott-Price, Valentina, Norton, Nadine, Williams, Nigel Melville, Holmans, Peter Alan, Owen, Michael John and O'Donovan, Michael Conlon 2005. Streamlined analysis of pooled genotype data in SNP-based association studies. Genetic Epidemiology 28 (3) , pp. 273-282. 10.1002/gepi.20062

Li, Y., Hollingworth, P., Moore, P., Foy, C., Archer, N., Powell, J., Nowotny, P., Holmans, Peter Alan, O'Donovan, Michael Conlon, Tacey, K., Doil, L., van Luchene, R., Garcia, V., Rowland, V., Lau, K., Cantanese, J., Sninsky, J., Hardy, J., Thal, L., Morris, J. C., Goate, A., Lovestone, S., Owen, Michael John, Williams, Julie and Grupe, A. 2005. Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease. Human Mutation 25 (3) , pp. 270-277. 10.1002/humu.20138

Seaman, S. R. and Holmans, Peter Alan 2005. Effect of genotyping error on type-I error rate of affected sib pair studies with genotyped parents. Human Heredity 59 (3) , pp. 157-164. 10.1159/000085939

Cope, Natalie Alexandra, Harold, Denise, Hill, Gary Trevor, Escott-Price, Valentina, Stevenson, Jim, Holmans, Peter Alan, Owen, Michael John, O’Donovan, Michael Conlon and Williams, Julie 2005. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. American Journal of Human Genetics 76 (4) , pp. 581-591. 10.1086/429131

Escott-Price, Valentina, Holmans, Peter Alan, Schmidt, Karl Michael and Craddock, Nicholas John 2005. Design of Case-controls Studies with Unscreened Controls. Annals of Human Genetics 69 (5) , pp. 566-576. 10.1111/j.1529-8817.2005.00175.x

Li, Yonghong, Nowotny, Petra, Holmans, Peter Alan, Smemo, Scott, Kauwe, John S. K., Hinrichs, Anthony L., Tacey, Kristina, Doil, Lisa, Luchene, Ryan van, Garcia, Veronica, Rowland, Charles, Schrodi, Steve, Leong, Diane, Gogic, Goran, Chan, Joanne, Cravchik, Anibal, Ross, David, Lau, Kit, Kwok, Shirley, Chang, Sheng-Yung, Catanese, Joseph, Sninsky, John, White, Thomas J., Hardy, John, Powell, John, Lovestone, Simon, Morris, John C., Thal, Leon, Owen, Michael John, Williams, Julie, Goate, Alison and Grupe, Andrew 2004. Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family. Proceedings of the National Academy of Sciences 101 (44) , pp. 15688-15693. 10.1073/pnas.0403535101

Li, Yonghong, Tacey, Kristina, Doil, Lisa, Luchene, Ryan van, Garcia, Veronica, Rowland, Charles, Schrodi, Steve, Leong, Diane, Lau, Kit, Catanese, Joe, Sninsky, John, Nowotny, Petra, Holmans, Peter, Hardy, John, Powell, John, Lovestone, Simon, Thal, Leon, Owen, Michael John, Williams, Julie, Goate, Alison and Grupe, Andrew 2004. Association of ABCA1 with late-onset Alzheimer?s disease is not observed in a case-control study. Neuroscience Letters 366 (3) , pp. 268-271. 10.1016/j.neulet.2004.05.047

Mowry, B J, Holmans, Peter Alan, Pulver, A E, Gejman, P V, Riley, B, Williams, Nigel Melville, Laurent, C, Schwab, S G, Wildenauer, D B, Bauché, S, Owen, Michael John, Wormley, B, Sanders, A R, Nestadt, G, Liang, K Y, Duan, J, Ribble, R, Norton, N, Soubigou, S, Maier, W, Ewen-White, K R, deMarchi, N, Carpenter, B, Walsh, D, Williams, H, Jay, M, Albus, M, Nertney, D A, Papadimitriou, G, O'Neill, A, O'Donovan, Michael Conlon, Deleuze, J-F, Lerer, F B, Dikeos, D, Kendler, K S, Mallet, J, Silverman, J M, Crowe, R R and Levinson, D F 2004. Multicenter linkage study of schizophrenia loci on chromosome 22q. Molecular Psychiatry 9 (8) , pp. 784-795. 10.1038/sj.mp.4001481

Holmans, Peter Alan, Zubenko, George S., Crowe, Raymond R., DePaulo, J. Raymond Jr., Scheftner, William A., Weissman, Myrna M., Zubenko, Wendy N., Boutelle, Sandra, Murphy-Eberenz, Kathleen, MacKinnon, Dean, McInnis, Melvin G., Marta, Diana H., Adams, Philip, Knowles, James A., Gladis, Madeline, Thomas, Jo, Chellis, Jennifer, Miller, Erin and Levinson, Douglas F. 2004. Genomewide significant linkage to recurrent, early-onset major depressive disorder on chromosome 15q. The American Journal of Human Genetics 74 (6) , pp. 1154-1167. 10.1086/421333

Bernardinelli, L., Berzuini, C., Seaman, S. and Holmans, Peter Alan 2004. Bayesian trio models for association in the presence of genotyping errors. Genetic Epidemiology 26 (1) , pp. 70-80. 10.1002/gepi.10291

Myers, Amanda J., Marshall, Helen, Holmans, Peter Alan, Compton, Danielle, Crook, Richard J.P., Mander, Adrian P., Nowotny, Petra, Smemo, Scott, Dunstan, Melanie, Jehu, Luke, Wang, Jen C., Hamshere, Marian Lindsay, Morris, John C., Norton, Joanne, Chakraventy, Sumi, Tunstall, Nigel, Lovestone, Simon, Petersen, Ronald, O'Donovan, Michael Conlon, Jones, Lesley, Williams, Julie, Owen, Michael John, Hardy, John and Goate, Alison 2004. Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD. American Journal of Medical Genetics 124B (1) , pp. 29-37. 10.1002/ajmg.b.20036

Busby, Victoria, Goossens, Steven, Nowotny, Petra, Hamilton, Gillian, Smemo, Scott, Harold, Denise, Turic, Dragana, Jehu, Luke, Myers, Amanda, Womick, Meredith, Woo, Daniel, Compton, Danielle, Doil, Lisa M., Tacey, Kristina M., Lau, Kit F., Al-Saraj, Safa, Killick, Richard, Pickering-Brown, Stuart, Moore, Pamela, Hollingworth, Paul, Archer, Nicola, Foy, Catherine, Walter, Sarah, Lovestone, Simon, O'Donovan, Michael Conlon, Owen, Michael John, Jones, Lesley, Williams, Julie and Holmans, Peter Alan 2004. Alpha-T-Catenin Is Expressed in Human Brain and Interacts With the Wnt Signaling Pathway But Is Not Responsible for Linkage to Chromosome 10 in Alzheimer's Disease. Neuromolecular Medicine 5 (2) , pp. 133-146. 10.1385/NMM:5:2:133

Williams, Nigel Melville, Norton, Nadine, Williams, Hywel John, Ekholm, B., Hamshere, Marian Lindsay, Lindblom, Y., Chowdari, K. V., Cardno, Alastair George, Zammit, Stanley, Jones, Lisa Anne, Murphy, Kieran Christopher, Sanders, Robert David, McCarthy, Geraldine MaryTeresa, Gray, Marion Yvonne, Jones, G., Holmans, Peter Alan, Nimgaonkar, V., Adolfson, R., Osby, U., Terenius, L., Sedvall, G., O'Donovan, Michael Conlon and Owen, Michael John 2003. A systematic genomewide linkage study in 353 sib pairs with schizophrenia. The American journal of human genetics 73 (6) , pp. 1355-1367. 10.1086/380206

Hensiek, A.E., Roxburgh, R., Smilie, B., Coraddu, F., Åkesson, E., Holmans, Peter Alan, Sawcer, S.J. and Compston, D.A.S. 2003. Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis. Journal of Neuroimmunology 143 (1-2) , pp. 25-30. 10.1016/j.jneuroim.2003.08.007

Levinson, Douglas F., Zubenko, George S., Crowe, Raymond R., DePaulo, Raymond J., Scheftner, William S., Weissman, Myrna M., Holmans, Peter Alan, Zubenko, Wendy N., Boutelle, Sandra, Murphy-Eberenz, Kathleen, MacKinnon, Dean, McInnis, Melvin G., Marta, Diana H., Adams, Philip, Sassoon, Stephanie, Knowles, James A., Thomas, Jo and Chellis, Jennifer 2003. Genetics of recurrent early-onset depression (GenRED): Design and preliminary clinical characteristics of a repository sample for genetic linkage studies. American Journal of Medical Genetics 119B (1) , pp. 118-130. 10.1002/ajmg.b.20009

Rice, K. M. and Holmans, Peter Alan 2003. Allowing for Genotyping Error in Analysis of Unmatched Case-Control Studies. Annals of Human Genetics 67 (2) , pp. 165-174. 10.1046/j.1469-1809.2003.00020.x

McInnis, M G, Lan, T-H, Willour, V L, McMahon, F J, Simpson, S G, Addington, A M, MacKinnon, D F, Potash, J B, Mahoney, A T, Chellis, J, Huo, Y, Swift-Scanlan, T, Chen, H, Koskela, R, Colin Stine, O, Jamison, K R, Holmans, Peter Alan, Folstein, S E, Ranade, K, Friddle, C, Botstein, D, Marr, T, Beaty, T H, Zandi, P and Raymond DePaulo, J 2003. Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12. Molecular Psychiatry 8 (3) , pp. 288-298. 10.1038/sj.mp.4001277

Levinson, D.F., Holmans, Peter Alan, Laurent, C., Mallet, J., Riley, B., Kendler, K.S., Pulver, A.E., Gejman, P.V., Sanders, A.R., Schwab, S.G., Wildenauer, D.B., Owen, Michael John and Mowry, B.J. 2002. Is schizophrenia linked to chromosome 1q? Response. Science 298 (5602) , pp. 2277-2279.

Richards, A. J., Morgan, J., Bearcroft, P. W. P., Pickering, E., Owen, Michael John, Holmans, Peter Alan, Williams, Nigel Melville, Tysoe, C., Pope, F. M., Snaed, M. P. and Hughes, H. 2002. Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule. Journal of Medical Genetics 39 (9) , pp. 661-665. 10.1136/jmg.39.9.661

Akesson, E, Oturai, A, Berg, J, Fredrikson, S, Andersen, O, Harbo, H F, Laaksonen, M, Myhr, K M, Nyland, H I, Ryder, L P, Sandberg-Wollheim, M, Sorensen, P S, Spurkland, A, Svejgaard, A, Holmans, Peter, Compston, A, Hillert, J and Sawcer, S 2002. A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis. Genes and Immunity 3 (5) , pp. 279-285. 10.1038/sj.gene.6363866

Levinson, Douglas. F., Holmans, Peter Alan, Laurent, Claudine, Riley, Brien, Pulver, Ann E., Gejman, Pablo V., Schwab, Sibylle G., Williams, Nigel Melville, Owen, Michael John, Wildenauer, Dieter B., Sanders, Alan R., Nestadt, Gerald, Mowry, Brian J., Wormley, Brandon, Bauche, Stephanie, Soubigou, Stephane, Ribble, Robert, Nertney, Deborah A., Liang, Kung Yee, Martinolich, Laura, Maier, Wolfgang, Norton, Nadine, Williams, Hywel John, Albus, Margot, Carpenter, Eric B., DeMarchi, Nicola, Ewen-White, Kelly R., Walsh, Dermot, Jay, Maurice, Deleuze, Jean-Francois, O'Neill, Anthony F., Papadimitriou, George, Weilbaecher, Ann, Lerer, Bernard, O'Donovan, Michael Conlon, Dikeos, Dimitris, Silverman, Jeremy M., Kendler, Kenneth S., Mallet, Jacques, Crowe, Raymond R. and Walters, Marilyn 2002. No major schizophrenia locus detected on chromosome 1q in a large multicenter sample. Science 296 (5568) , pp. 739-741. 10.1126/science.1069914

Myers, Amanda, Wavrant De-Vrieze, Fabienne, Holmans, Peter Alan, Hamshere, Marian Lindsay, Crook, Richard, Compton, Danielle, Marshall, Helen, Meyer, David, Shears, Shantia, Booth, Jeremy, Ramic, Dzanan, Knowles, Heather, Morris, John C., Williams, Nigel Melville, Norton, Nadine, Abraham, Richard, Kehoe, Pat, Williams, Hywel, Rudrasingham, Varuni, Rice, Frances, Giles, Peter, Tunstall, Nigel, Jones, Lesley, Lovestone, Simon, Williams, Julie, Owen, Michael John, Hardy, John and Goate, Alison 2002. Full genome screen for Alzheimer disease: Stage II analysis. American Journal of Medical Genetics 114 (2) , pp. 235-244. 10.1002/ajmg.10183

Holmans, Peter Alan 2002. Detecting gene-gene interactions using affected sib pair analysis with covariates. Human Heredity 53 (2) , pp. 92-102. 10.1159/000057987

Bennett, P., Segurado, R., Jones, Ian Richard, Bort, S., McCandless, F., Lambert, D., Heron, J., Comerford, C., Middle, F., Corvin, A., Pelios, G., Kirov, George, Larsen, B., Mulcahy, T., Williams, Nigel Melville, O'Connell, R., O'Mahony, E., Payne, A., Owen, Michael John, Holmans, Peter Alan, Craddock, Nicholas John and Gill, M. 2002. The Wellcome trust UK-Irish bipolar affective disorder sibling-pair genome screen: first stage report. Molecular Psychiatry 7 (2) , pp. 189-200. 10.1038/sj.mp.4000957

Holmans, Peter Alan 2001. Likelihood-ratio affected sib-pair tests applied to multiply affected sibships: issues of power and type I error rate. Genetic Epidemiology 20 (1) , pp. 44-56. 10.1002/1098-2272(200101)

Myers, A., Holmans, Peter Alan, Marshall, H., Kwon, J., Meyer, D., Ramic, D., Shears, S., Booth, J., DeVrieze, F. W., Crook, R., Hamshere, Marian Lindsay, Abraham, R., Tunstall, N., Rice, Frances, Carty, S., Lillystone, S., Kehoe, P., Rudrasingham, V., Jones, Lesley, Lovestone, S., Perez-Tur, J., Williams, Julie, Owen, Michael John, Hardy, J. and Goate, A. M. 2000. Susceptibility locus for Alzheimer's disease on chromosome 10. Science 290 (5500) , pp. 2304-2305. 10.1126/science.290.5500.2304

Levinson, D. F., Holmans, Peter Alan, Straub, R. E., Owen, Michael John, Wildenauer, D. B., Gejman, P. V., Pulver, A. E., Laurent, C., Kendler, K. S., Walsh, D., Norton, N., Williams, Nigel Melville, Schwab, S. G., Lerer, B., Mowry, B. J., Sanders, A. R., Antonarakis, S. E., Blouin, J. L., DeLeuze, J. F. and Mallet, J. 2000. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. American Journal of Human Genetics 67 (3) , pp. 652-663. 10.1086/303041

Murphy, K. C., Williams, Nigel Melville, Cardno, A. G., Jones, L. A., Holmans, Peter Alan, Thompson, P., Thonas, N., McGuffin, P. and Owen, Michael John 2000. Chromosome 22q, velo-cardio-facial syndrome (VCFS) and schizophrenia. Journal of Medical Genetics 37 , S58-S58.

Bandmann, O., Vaughan, J. R., Holmans, Peter Alan, Marsden, C. D. and Wood, N. W. 2000. Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease. Movement Disorders 15 (1) , pp. 30-35. 10.1002/1531-8257(200001)15:13.0.CO;2-V

Neuman, R. J., Saccone, N. L., Holmans, Peter Alan, Rice, J. P. and Sun, L. 2000. Clustering methods applied to allele sharing data. Genetic Epidemiology 19 (1) , pp. 57-63. 10.1002/1098-2272(2000)19:1+<::AID-GEPI9>3.0.CO;2-D

Williams, Nigel Melville, Rees, M. I., Holmans, Peter Alan, Norton, N., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., McCarthy, G., Gray, M. Y., Fenton, I., McGuffin, P. and Owen, Michael John 1999. A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs. Human Molecular Genetics 8 (9) , pp. 1729-1739. 10.1093/hmg/8.9.1729

Wavrant-De Vrieze, F., Crook, R., Holmans, Peter Alan, Kehoe, P., Owen, Michael John, Williams, Julie, Roehl, K., Laliiri, D. K., Shears, S., Booth, J., Wu, W., Goate, A., Chartier-Harlin, M. C., Hardy, J. and Perez-Tur, J. 1999. Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease. Neuroscience Letters 269 (2) , pp. 67-70.

Hateboer, N., Lazarou, L. P., Williams, A. J., Holmans, Peter Alan and Ravine, D. 1999. Familial phenotype differences in PKD11. Kidney International 56 (1) , pp. 34-40. 10.1046/j.1523-1755.1999.00541.x

Rees, M. I., Fenton, I., Williams, Nigel Melville, Holmans, Peter Alan, Norton, N., Cardno, A., Asherson, P., Spurlock, G., Vallada, H., Dawson, E., Li, M. W., Collier, D. A., Powell, J. F., Nanko, S., Gill, M., McGuffin, P. and Owen, Michael John 1999. Autosome search for schizophrenia susceptibility genes in multiply affected families. Molecular Psychiatry 4 (4) , pp. 353-359. 10.1038/sj.mp.4000521

Wavrant-DeVrieze, F., Rudrasingham, V., Lambert, J. C., Chakraverty, S., Kehoe, P., Crook, R., Amouyel, P., Wu, W., Holmans, Peter Alan, Rice, Frances, Perez-Tur, J., Frigard, B., Morric, J. C., Carty, S., Cottel, D., Tunstall, N., Lovestone, S., Petersen, R. C., Chartier-Harlin, M. C., Goate, A., Owen, Michael John, Williams, Julie and Hardy, J. 1999. No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease. Neuroscience Letters 262 (2) , pp. 137-139. 10.1016/S0304-3940(99)00035-X

Kehoe, P., Wavrant-De Vrieze, F., Crook, R., Wu, W. S., Holmans, Peter Alan, Fenton, I., Williams, Nigel Melville, Lovestone, S., Perez-Tur, J., Hutton, M., Chartier-Harlin, M. C., Shears, S., Roehl, K., Booth, J., Van Voorst, W., Ramic, D., Williams, Julie, Goate, A., Hardy, J. and Owen, Michael John 1999. A full genome scan for late onset Alzheimer's disease. Human Molecular Genetics 8 (2) , pp. 237-245. 10.1093/hmg/8.2.237

Bandmann, O., Vaughan, J., Holmans, Peter Alan, Marsden, C. D. and Wood, N. W. 1999. Toxins, genetics, and Parkinson's disease: the role of N-acetyltransferase 2. Advances in Neurology -New York- Raven Press- 80 , pp. 199-204.

Holmans, Peter Alan 1998. Affected sib-pair methods for detecting linkage to dichotomous traits: review of the methodology. Human biology 70 (6) , pp. 1025-1040.

Kehoe, P. G., Williams, H., Holmans, Peter Alan, Wilcock, G., Cairns, N. J., Neal, J. and Owen, Michael John 1998. The butyrylcholinesterase K variant and susceptibility to Alzheimer's disease. Journal of Medical Genetics 35 (12) , pp. 1034-1035. 10.1136/jmg.35.12.1034

Bandmann, O., Valente, E. M., Holmans, Peter Alan, Surtees, R. A., Walters, J. H., Wevers, R. A., Marsden, C. D. and Wood, N. W. 1998. Dopa-responsive dystonia: a clinical and molecular genetic study. Annals of Neurology 44 (4) , pp. 649-656. 10.1002/ana.410440411

Wu, W. S., Holmans, Peter Alan, Wavrant-DeVrieze, F., Shears, S., Kehoe, P., Crook, R., Booth, J., Williams, Nigel Melville, Perez-Tur, J., Roehl, K., Fenton, I., Chartier-Harlin, M. C., Lovestone, S., Williams, Julie, Hutton, M., Hardy, J., Owen, Michael John and Goate, A. 1998. Genetic studies on chromosome 12 in late-onset Alzheimer disease. JAMA - The Journal of the American Medical Association 280 (7) , pp. 619-622. 10.1001/jama.280.7.619

Daniels, J., Holmans, Peter Alan, Williams, Nigel Melville, Turic, D., McGuffin, P., Plomin, R. and Owen, Michael John 1998. A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies. American Journal of Human Genetics 62 (5) , pp. 1189-1197. 10.1086/301816

Williams, Julie, Spurlock, G., Holmans, Peter Alan, Mant, R., Murphy, K., Jones, L., Cardno, A., Asherson, P., Blackwood, D., Muir, W., Meszaros, K., Aschauer, H., Mallet, J., Laurent, C., Pekkarinen, P., Seppala, J., Stefanis, C. N., Papadimitriou, G. N., Macciardi, F., Verga, M., Pato, C., Azevedo, H., Crocq, M. A., Gurling, H. and Owen, Michael John 1998. A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia. Molecular Psychiatry 3 (2) , pp. 141-149.

Holmans, Peter Alan and Craddock, Nicholas John 1998. Efficient strategies for genome scanning with affected sib pairs - Reply. American Journal of Human Genetics 62 (1) , pp. 205-207. 10.1086/301683

Hateboer, N., Lazarou, L., Holmans, Peter Alan, Williams, A. J. and Ravine, D. 1998. Inter-family variability of phenotype in autosomal dominant polycystic kidney disease type 1. European Journal of Human Genetics 6 (1) , p. 71.

Murphy, K. C., Williams, Nigel Melville, Cardno, A. G., Jones, L. A., Holmans, Peter Alan, McGuffin, P. and Owen, Michael John 1998. A linkage study of chromosome 22q in SIB-pairs with schizophrenia. Schizophrenia Research 29 (1-2) , pp. 131-132. 10.1016/S0920-9964(97)88632-X

Spurlock, G., Heils, A., Holmans, Peter Alan, Williams, J., D'Souza, U. M., Cardno, A., Murphy, K. C., Jones, L., Buckland, Paul Robert, McGuffin, P., Lesch, K. .P and Owen, Michael John 1998. A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter. Molecular Psychiatry 3 (1) , pp. 42-49. 10.1038/sj.mp.4000342

Bandmann, O., Vaughan, J., Holmans, Peter Alan, Marsden, C. D. and Wood, N. W. 1997. Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease. The Lancet 350 (9085) , pp. 1136-1139. 10.1016/S0140-6736(97)03495-8

Hateboer, N., Torra, R., Estivill, E., Bogdanova, N., Davies, F., Lazarou, L., vonDijk, M., Breuning, M., SaggarMalik, A., Jeffery, S., SanMillan, J. L., Martinez, I., Walker, R., Holmans, Peter Alan and Ravine, D. 1997. PKD2: The phenotype defined. Kidney International 52 (4) , p. 1122.

Baboolal, K., Ravine, D., Daniels, J., Williams, Nigel Melville, Holmans, Peter Alan, Coles, G. A. and Williams, J. D. 1997. Association of the angiotensin I converting enzyme gene deletion polymorphism with early onset of ESRF in PKD1 adult polycystic kidney disease. Kidney International 52 (3) , pp. 607-613. 10.1038/ki.1997.373

Hateboer, N., Dijk, M., Torra, R., Bogdanova, N., Davies, F., Lazarou, L., Breuning, M., SaggarMalik, A. K., Jeffery, S., Millan, J. L. S., Martinez, I., Walker, R., Holmans, Peter Alan, Ravine, D. and Coles, G. A. 1997. Phenotype PKD2 vs. PKD1; results from the European concerted action. Journal of the American Society of Nephrology 8 , A1722-A1722.

Rees, M., Norton, N., Jones, Ian Richard, McCandless, F., Scourfield, J., Holmans, Peter Alan, Moorhead, S., Feldman, E., Sadler, S., Cole, T., Redman, K., Farmer, A., McGuffin, P., Owen, Michael John and Craddock, Nicholas John 1997. Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT). Molecular Psychiatry 2 (5) , pp. 398-402. 10.1038/sj.mp.4000256

Owen, Michael John, Holmans, Peter Alan and McGuffin, P. 1997. Association studies in psychiatric genetics. Molecular Psychiatry 2 (4) , pp. 270-273. 10.1038/sj.mp.4000292

Daniels, J. K., Spurlock, G., Williams, Nigel Melville, Cardno, A. G., Jones, L. A., Murphy, K. C., Asherson, P., Holmans, Peter Alan, Fenton, I., McGuffin, P. and Owen, Michael John 1997. Linkage study of chromosome 6p in sib-pairs with schizophrenia. American Journal of Medical Genetics 74 (3) , pp. 319-323. 10.1002/(SICI)1096-8628(19970531)74:3<319::AID-AJMG14>3.0.CO;2-R

Holmans, Peter Alan and Craddock, Nicholas John 1997. Efficient strategies for genome scanning using maximum-likelihood affected-sib-pair analysis. American Journal of Human Genetics 60 (3) , pp. 657-666.

Levinson, D. F., Wildenauer, D. B., Schwab, S. G., Albus, M., Hallmayer, J., Lerer, B., Maier, W., Blackwood, D., Muir, W., StClair, D., Morris, S., Moises, H. W., Yang, L., Kristbjarnarson, H., Helgason, T., Wiese, C., Collier, D. A., Holmans, Peter Alan, Daniels, J., Rees, M., Asherson, P., Roberts, Q., Cardno, A., Arranz, M. J., Vallada, H., McGuffin, D., Owen, Michael John, Pulver, A. E., Antonarakis, S. E., Babb, R., Blouin, J. L., DeMarchi, N., Dombroski, B., Housman, D., Karayiorgou, M., Ott, J., Kasch, L., Kazazian, H., Lasseter, V. K., Loetscher, E., Luebbert, H., Nestadt, G., Ton, C., Wolyniec, P. S., Laurent, C., deChaldee, M., Thibaut, F., Jay, M., Samolyk, D., Petit, M., Campion, D., Mallet, J., Straub, R. E., MacLean, C. J., Easter, S. M., ONeill, F. A., Walsh, D., Kendler, K. S., Gejman, P. V., Cao, Q. H., Gershon, E., Badner, J., Beshah, E., Zhang, J., Riley, B. P., Rajagopalan, S., MogudiCarter, M., Jenkins, T., Williamson, R., DeLisi, L. E., Garner, C., Kelly, M., LeDuc, C., Cardon, L., Lichter, J., Harris, T., Loftus, J., Shields, G., Comasi, M., Vita, A., Smith, A., Dann, J., Joslyn, G., Gurling, H., Kalsi, G., Brynjolfsson, J., Curtis, D., Sigmundsson, T., Butler, R., Read, T., Murphy, P., Chen, A. C. H., Petursson, H., Byerley, B., Hoff, M., Holik, J., Nancarrow, D. J., Crowe, R. R., Andreasen, N., Silverman, J. M., Mohs, R. C., Siever, L. J., Endicott, J., Sharpe, L., Walters, M. K., Lennon, D. P., Hayward, N. K., Sandkuijl, L. A., Mowry, B. J., Aschauer, H. N., Meszaros, K., Lenzinger, E., Fuchs, K., Heiden, A. M., Kruglyak, L., Daly, M. J. and Matise, T. C. 1996. Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8. American Journal of Medical Genetics 67 (6) , pp. 580-594. 10.1002/(SICI)1096-8628(19961122)67:6<580::AID-AJMG11>3.0.CO;2-P

Kehoe, P., Williams, Julie, Holmans, Peter Alan, Liddell, M., Lovestone, S., Holmes, C., Powell, J., Neal, J., Wilcock, G. and Owen, Michael John 1996. Association between a PS-1 intronic polymorphism and late onset Alzheimer's disease. NeuroReport 7 (13) , pp. 2155-2158. 10.1097/00001756-199609020-00019

Asherson, P., Mant, R., Holmans, Peter Alan, Williams, Julie, Cardno, A., Murphy, K., Jones, L., Collier, D., McGuffin, P. and Owen, Michael John 1996. Linkage, association and mutational analysis of the dopamine D3 receptor gene in schizophrenia. Molecular Psychiatry 1 (2) , pp. 125-132.

Craddock, Nicholas John, Daniels, J., Holmans, Peter Alan, Williams, Nigel Melville and Owen, Michael John 1996. Increasing the efficiency of genomic searches for linkage in complex disorders by DNA pooling of affected sib-pairs. Molecular Psychiatry 1 (1) , pp. 59-64.

Gill, M., Vallada, H., Collier, D., Sham, P., Holmans, Peter Alan, Murray, R., McGuffin, P., Nanko, S., Owen, Michael John, Antonarakis, S., Housman, D., Kazazian, H., Nestadt, G., Pulver, A. E., Straub, R. E., MacLean, C. J., Walsh, D., Kendler, K. S., DeLisi, L., Polymeropoulos, M., Coon, H., Byerley, W., Lofthouse, R., Gershon, E. and Read, C. M. 1996. A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). American Journal of Medical Genetics 67 (1) , pp. 40-45. 10.1002/(SICI)1096-8628(19960216)67:1<40::AID-AJMG6>3.0.CO;2-W

Cardno, Alastair, Holmans, Peter Alan, Harvey, I., Williams, M. B., Owen, Michael John and McGuffin, P. 1996. Factor-derived subsyndromes of schizophrenia and familial morbid risks. Schizophrenia Research 18 (2-3) , IVA2-IVA2.

Roberts, A. G., Whatley, S. D., Daniels, J., Holmans, Peter Alan, Fenton, I., Owen, Michael John, Thompson, P., Long, C. and Elder, G. H. 1995. Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23. Human Molecular Genetics 4 (12) , pp. 2387-2390. 10.1093/hmg/4.12.2387

Holmans, Peter Alan and Clayton, D. 1995. Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers. American Journal of Human Genetics 57 (5) , pp. 1221-1232.

Wood, N. W., Sawcer, S. J., Kellar-Wood, H. F., Holmans, Peter Alan, Clayton, D., Robertson, Neil and Compston, D. A. 1995. The T-cell receptor beta locus and susceptibility to multiple sclerosis. Neurology 45 (10) , pp. 1859-1863. 10.1212/WNL.45.10.1859

Wood, N. W., Sawcer, S. J., Kellar-Wood, H. F., Holmans, Peter Alan, Clayton, D., Robertson, Neil and Compston, D. A. 1995. Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region. Journal of Neurology 242 (10) , pp. 677-682. 10.1007/BF00866919

Kellar-Wood, H. F., Wood, N. W., Holmans, Peter Alan, Clayton, D., Robertson, Neil and Compston, D. A. 1995. Multiple sclerosis and the HLA-D region: linkage and association studies. Journal of Neuroimmunology 58 (2) , pp. 183-190. 10.1016/0165-5728(95)00015-T

Holmans, Peter Alan, McGuffin, P. and Clayton, D. 1995. Genome scan for association and linkage. Genetic Epidemiology 12 (6) , pp. 613-618. 10.1002/gepi.1370120615

Robertson, Neil, Wood, N., Holmans, Peter Alan, Kellar-Wood, H. F., Sawcer, S. and Wood, N. W. 1995. Strategies for the identification of susceptibility genes in multiple sclerosis [Editorial]. The International Ms Journal 2 , pp. 19-28.

Wood, N. W., Holmans, Peter Alan, Clayton, D., Robertson, Neil Patrick and Compston, D. A. 1994. No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairs. Journal of Neurology, Neurosurgery & Psychiatry 57 (10) , pp. 1191-1194. 10.1136/jnnp.57.10.1191

Eoli, M., Wood, N.W., Kellar-Wood, H.F., Holmans, Peter Alan, Clayton, D. and Compston, D.A.S. 1994. No linkage between multiple sclerosis and the T cell receptor alpha chain locus. Journal of the Neurological Sciences 124 (1) , p. 32. 10.1016/0022-510X(94)90007-8

Holmans, Peter Alan 1993. Asymptotic properties of affected-sib-pair linkage analysis. American journal of human genetics 52 (2) , pp. 362-374.

This list was generated on Wed Aug 23 07:00:54 2017 BST.