Browse by Current Cardiff authors

Peall, Kathryn J., Lorentzos, M.S., Heyman, I., Tijssen, M.A.J., Owen, Michael J., Dale, R.C. and Kurian, M.A. 2017. A review of psychiatric co-morbidity described in genetic and immune mediated movement disorders. Neuroscience & Biobehavioral Reviews 80 , pp. 23-35. 10.1016/j.neubiorev.2017.05.014 Item availability restricted.

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.

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

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

Chawner, Samuel, Doherty, Joanne L., Moss, Hayley, Niarchou, Maria, Walters, James, Owen, Michael J. and Van Den Bree, Marianne Bernadette 2017. Case-control study finds no evidence that 22q11.2 Deletion Syndrome is associated with cognitive deterioration. British Journal of Psychiatry Item availability restricted.

Singh, Tarjinder, Walters, James, Johnstone, Mandy, Curtis, David, Suvisaari, Jaana, Torniainen, Minna, Rees, Elliott, Iyegbe, Conrad, Blackwood, Douglas, McIntosh, Andrew M., Kirov, George, Geschwind, Daniel, Murray, Robin M, Di Forti, Marta, Bramon, Elvira, Gandal, Michael, Hultman, Christina M., Sklar, Pamela, Palotie, Aarno, Patrick F., Sullivan, O'Donovan, Michael C., Owen, Michael and Barrett, Jeffrey C. 2017. The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. Nature Genetics Item availability restricted.

Bigdeli, T B, Ripke, S, Peterson, R E, Trzaskowski, M, Bacanu, S-A, Abdellaoui, A, Andlauer, T F M, Beekman, A T F, Berger, K, Blackwood, D H R, Boomsma, D I, Breen, G, Buttenschøn, H N, Byrne, E M, Cichon, S, Clarke, T-K, Couvy-Duchesne, B, Craddock, Nicholas, de Geus, E J C, Degenhardt, F, Dunn, E C, Edwards, A C, Fanous, A H, Forstner, A J, Frank, J, Gill, M, Gordon, S D, Grabe, H J, Hamilton, S P, Hardiman, O, Hayward, C, Heath, A C, Henders, A K, Herms, S, Hickie, I B, Hoffmann, P, Homuth, G, Hottenga, J-J, Ising, M, Jansen, R, Kloiber, S, Knowles, J A, Lang, M, Li, Q S, Lucae, S, MacIntyre, D J, Madden, P A F, Martin, N G, McGrath, P J, McGuffin, P, McIntosh, A M, Medland, S E, Mehta, D, Middeldorp, C M, Milaneschi, Y, Montgomery, G W, Mors, O, Müller-Myhsok, B, Nauck, M, Nyholt, D R, Nöthen, M M, Owen, Michael, Penninx, B W J H, Pergadia, M L, Perlis, R H, Peyrot, W J, Porteous, D J, Potash, J B, Rice, J P, Rietschel, M, Riley, B P, Rivera, M, Schoevers, R, Schulze, T G, Shi, J, Shyn, S I, Smit, J H, Smoller, J W, Streit, F, Strohmaier, J, Teumer, A, Treutlein, J, Van der Auwera, S, van Grootheest, G, van Hemert, A M, Völzke, H, Webb, B T, Weissman, M M, Wellmann, J, Willemsen, G, Witt, S H, Levinson, D F, Lewis, C M, Wray, N R, Flint, J, Sullivan, P F and Kendler, K S 2017. Genetic effects influencing risk for major depressive disorder in China and Europe. Translational Psychiatry 7 (3) , e1074. 10.1038/tp.2016.292

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

Clifton, Nicholas, Pocklington, Andrew, Scholz, B., Rees, Elliott, Walters, James, Kirov, George, O'Donovan, Michael, Owen, Michael, Wilkinson, Lawrence, Thomas, Kerrie and Hall, Jeremy 2017. Schizophrenia copy number variants and associative learning. Molecular Psychiatry 22 (2) , pp. 178-182. 10.1038/mp.2016.227

Cosgrove, D, Harold, D, Mothersill, O, Anney, Richard, Hill, Martin, Bray, Nicholas, Blokland, G, Petryshen, T, Donnelly, Peter, Bates, Lesley, Barroso, Ines, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Deloukas, Panos, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S, Mathew, Christopher G, Palmer, Colin N A, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas W, Spencer, Chris C A, Band, Gavin, Bellenguez, Céline, Freeman, Colin, Hellenthal, Garrett, Giannoulatou, Eleni, Hopkins, Lucinda, Pirinen, Matti, Pearson, Richard, Strange, Amy, Su, Zhan, Vukcevic, Damjan, Langford, Cordelia, Hunt, Sarah E, Edkins, Sarah, Gwilliam, Rhian, Blackburn, Hannah, Bumpstead, Suzannah J, Dronov, Serge, Gillman, Matthew, Gray, Emma, Hammond, Naomi, Jayakumar, Alagurevathi, McCann, Owen T, Liddle, Jennifer, Potter, Simon C, Ravindrarajah, Radhi, Ricketts, Michelle, Waller, Matthew, Weston, PaulWeston, Widaa, SaraWidaa, Whittaker, Pamela, Richards, Alexander, Mantripragada, Kiran, Owen, Michael, O'Donovan, Michael, Gill, M, Corvin, A, Morris, D W and Donohoe, G 2017. MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls. Translational Psychiatry 7 (1) , e1012. 10.1038/tp.2016.286

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.

Kendall, Kimberley, Kirov, George and Owen, Michael 2017. Schizophrenia Genetics. In: Benjamin, Sadock,, Virginia, Sadock, and Pedro, Ruiz, eds. Kaplan and Sadock?s Comprehensive Textbook of Psychiatry, Wolters Kluwer,

Whitton, Laura, Cosgrove, Donna, Clarkson, Christopher, Harold, Denise, Kendall, Kimberley, Richards, Alexander, Mantripragada, Kiran, Owen, Michael John, O'Donovan, Michael Conlon, Walters, James, Hartmann, Annette, Konte, Betina, Rujescu, Dan, Gill, Michael, Corvin, Aiden, Rea, Stephen, Donohoe, Gary and Morris, Derek W. 2016. Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 (8) , pp. 1170-1179. 10.1002/ajmg.b.32503

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

Kendall, Kimberley, Rees, Elliott, Escott-Price, Valentina, Einon, Mark, Thomas, Rhys, Hewitt, Jonathan, O'Donovan, Michael Conlon, Owen, Michael John, Walters, James Tynan Rhys and Kirov, George 2016. Cognitive performance among carriers of pathogenic copy number variants: analysis of 152,000 UK Biobank subjects. Biological Psychiatry 10.1016/j.biopsych.2016.08.014

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

Howes, Oliver D., McCutcheon, Robert, Owen, Michael and Murray, Robin M. 2016. The role of genes, stress, and dopamine in the development of schizophrenia. Biological psychiatry 81 (1) , pp. 9-20. 10.1016/j.biopsych.2016.07.014

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

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

Millan, Mark J., Andrieux, Annie, Bartzokis, George, Cadenhead, Kristin, Dazzan, Paola, Fusar-Poli, Paolo, Gallinat, Jürgen, Giedd, Jay, Grayson, Dennis R., Heinrichs, Markus, Kahn, René, Krebs, Marie-Odile, Leboyer, Marion, Lewis, David, Marin, Oscar, Marin, Philippe, Meyer-Lindenberg, Andreas, McGorry, Patrick, McGuire, Philip, Owen, Michael John, Patterson, Paul, Sawa, Akira, Spedding, Michael, Uhlhaas, Peter, Vaccarino, Flora, Wahlestedt, Claes and Weinberger, Daniel 2016. Altering the course of schizophrenia: progress and perspectives. Nature Reviews Drug Discovery 18 (7) , pp. 485-515. 10.1038/nrd.2016.28

Legge, Sophie, Hamshere, Marian Lindsay, Hayes, Richard D., Downs, Johnny, O'Donovan, Michael Conlon, Owen, Michael John, Walters, James Tynan Rhys and McCabe, James H. 2016. Reasons for discontinuing clozapine: a cohort study of patients commencing treatment. Schizophrenia Research 174 , pp. 113-119. 10.1016/j.schres.2016.05.002

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

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

Isles, Anthony Roger, Ingason, Andrés, Lowther, Chelsea, Walters, James Tynan Rhys, Gawlick, Micha, Stöber, Gerald, Rees, Elliott, Martin, Joanna, Little, Rosie B., Potter, Harry, Georgieva, Lyudmila, Pizzo, Lucilla, Ozaki, Norio, Aleksic, Branko, Kushima, Itaru, Ikeda, Masashi, Iwata, Nakao, Levinson, Douglas F., Gejman, Pablo V., Shi, Jianxin, Sanders, Alan R., Duan, Jubao, Willis, Joseph, Sisodiya, Sanjay, Costain, Gregory, Werge, Thomas M., Degenhardt, Franziska, Giegling, Ina, Rujescu, Dan, Hreidarsson, Stefan J., Saemundsen, Evald, Ahn, Joo Wook, Ogilvie, Caroline, Girirajan, Santhosh D., Stefansson, Hreinn, Stefansson, Kari, O'Donovan, Michael Conlon, Owen, Michael John, Bassett, Anne and Kirov, George 2016. Parental origin of interstitial duplications at 15q11.2-q13.3 in schizophrenia and neurodevelopmental disorders. PLoS Genetics 12 (5) , e1005993. 10.1371/journal.pgen.1005993

Walters, James Tynan Rhys and Owen, Michael John 2016. Genome-wide significant associations for cannabis dependence severity. JAMA Psychiatry 73 (5) , pp. 443-444. 10.1001/jamapsychiatry.2016.0046

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Owen, Michael John, O'Donovan, Michael Conlon, Thapar, Anita and Craddock, Nicholas John 2011. Neurodevelopmental hypothesis of schizophrenia. British Journal of Psychiatry 198 (3) , pp. 173-175. 10.1192/bjp.bp.110.084384

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

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

Ruderfer, D. M., Kirov, George, Chambert, K., Moran, J. L., Owen, Michael John, O'Donovan, Michael Conlon, Sklar, P. and Purcell, S. M. 2011. A family-based study of common polygenic variation and risk of schizophrenia [Letter]. Molecular Psychiatry 16 (9) , pp. 887-888. 10.1038/mp.2011.34

Rivera, M., Cohen-Woods, S., Kapur, K., Breen, G., Ng, M. Y., Butler, A. W., Craddock, Nicholas John, Gill, M., Korszun, A., Maier, W., Mors, O., Owen, Michael John, Preisig, M., Bergmann, S., Tozzi, F., Rice, J., Rietschel, M., Rucker, J., Schosser, A., Aitchison, K. J., Uher, R., Craig, I. W., Lewis, C. M., Farmer, A. E. and McGuffin, P. 2011. Depressive disorder moderates the effect of the FTO gene on body mass index. Molecular Psychiatry 17 (6) , pp. 604-611. 10.1038/mp.2011.45

Rietschel, M., Mattheisen, M., Degenhardt, F., Kahn, René S, Linszen, Don H., Os, Jim van, Wiersma, Durk, Bruggeman, Richard, Cahn, Wiepke, de Haan, Lieuwe, Krabbendam, Lydia, Myin-Germeys, Inez, Mühleisen, T. W., Kirsch, P., Esslinger, C., Herms, S., Demontis, D., Steffens, M., Strohmaier, J., Haenisch, B., Breuer, R., Czerski, P. M., Giegling, I., Strengman, E., Schmael, C., Mors, O., Mortensen, P. B., Hougaard, D. M., Ørntoft, T., Kapelski, P., Priebe, L., Basmanav, F. B., Forstner, A. J., Hoffmann, P., Meier, S., Nikitopoulos, J., Moebus, S., Alexander, M., Mössner, R., Wichmann, H.-E., Schreiber, S., Rivandeneira, F., Hofman, A., Uitterlinden, A. G., Wienker, T. F., Schumacher, J., Hauser, J., Maier, W., Cantor, R. M., Erk, S.., Schulze, T. G., Stefansson, Hreinn, Steinberg, Stacy, Gustafsson, Omar, Sigurdsson, Engilbert, Petursson, Hannes, Kong, Augustine, Stefansson, Kari, Pietiläinen, Olli P. H., Tuulio-Henriksson, Annamari, Paunio, Tiina, Lonnqvist, Jouko, Suvisaari, Jaana, Peltonen, Leena, Ruggeri, Mirella, Tosato, Sarah, Walshe, Muriel, Murray, Robin, Collier, David A., St. Clair, David, Hansen, Thomas, Ingason, Andres, Jakobsen, Klaus D., Duong, Linh, Werge, Thomas, Melle, Ingrid, Andreassen, Ole A., Djurovic, Srdjan, Bitter, István, Réthelyi, János M., Abramova, Lilia, Kaleda, Vasily, Golimbet, Vera, Jönsson, Erik G., Terenius, Lars, Agartz, Ingrid, Winkel, Ruud van, Kenis, Gunter, Hert, Marc De, Veldink, Jan, Wiuf, Carsten, Didriksen, Michael, Craddock, Nicholas John, Owen, Michael John, O'Donovan, Michael Conlon, Børglum, A. D., Rujescu, D., Walter, H., Meyer-Lindenberg, A., Nöthen, M. M., Ophoff, R. A. and Cichon, S. 2011. Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Molecular Psychiatry , pp. 1-12. 10.1038/mp.2011.80

Langley, Kate, Heron, Jon, O'Donovan, Michael Conlon, Owen, Michael John and Thapar, Anita 2010. Genotype link with extreme antisocial behavior: The contribution of cognitive pathways. Archives of General Psychiatry 67 (12) , pp. 1317-1323. 10.1001/archgenpsychiatry.2010.163

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

Nishikawa, Keizo, Nakashima, Tomoki, Takeda, Shu, Isogai, Masashi, Hamada, Michito, Kimura, Ayako, Kodama, Tatsuhiko, Yamaguchi, Akira, Owen, Michael John, Takahashi, Satoru and Takayanagi, Hiroshi 2010. Maf promotes osteoblast differentiation in mice by mediating the age-related switch in mesenchymal cell differentiation. The Journal of Clinical Investigation 120 (10) , pp. 3455-3465. 10.1172/JCI42528

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

Zammit, Stanley, Owen, Michael John and Lewis, G. 2010. Misconceptions about gene-environment interactions in psychiatry. Evidence Based Mental Health 13 (3) , pp. 65-68. 10.1136/ebmh.13.3.65

Walters, James Tynan Rhys, Corvin, A., Owen, Michael John, Williams, Hywel John, Dragovic, M., Quinn, E. M., Judge, R., Smith, Daniel J., Norton, Nadine, Giegling, I., Hartmann, A. M., Moller, H.-J., Muglia, P., Escott-Price, Valentina, Dwyer, Sarah Lynne, O'Donoghue, T., Morar, B., Cooper, M., Chandler, D., Jablensky, A., Gill, M., Kaladjieva, L., Morris, D. W., O'Donovan, Michael Conlon, Rujescu, D. and Donohoe, G. 2010. Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia. Archives of General Psychiatry 67 (7) , pp. 692-700. 10.1001/archgenpsychiatry.2010.81

Seshadri, Sudha, Fitzpatrick, Annette L., Ikram, M. Arfan, DeStefano, Anita L., Gudnason, Vilmunder, Boada, Merce, Bis, Joshua C., Smith, Albert V., Carrasquillo, Minerva M., Lambert, Jean Charles, Harold, Denise, Schrijvers, Elizabeth M. C., Ramirez-Lorca, Reposo, Debette, Stephanie, Longstreth, W. T., Janssens, A. Cecile J. W., Pankratz, V. Shane, Dartigues, Jean Francois, Hollingworth, Paul, Aspelund, Thor, Hernandez, Isabel, Beiser, Alexa, Kuller, Lewis H., Koudstaal, Peter J., Dickson, Dennis W., Tzourio, Christope, Abraham, Richard Alun, Antunez, Carmen, Du, Yangchun, Rotter, Jerome I., Aulchenko, Yurii S., Harris, Tamara B., Petersen, Ronald C., Berr, Claudine, Owen, Michael John, Lopez-Arrieta, Jesus, Vardarajan, Bardi N., Becker, James T., Rivadeneira, Fernando, Nalls, Michael A., Graff-Radford, Neill R., Campion, Dominique, Auerbach, Sanford, Rice, Kenneth, Hofman, Albert, Jonsson, Palmi V., Schmidt, Helena, Lathrop, Mark, Mosley, Thomas H., Au, Rhoda, Psaty, Bruce M., Uitterlinden, Andre G., Farrer, Lindsay A., Lumley, Thomas, Ruiz, Agustin, Williams, Julie, Amouyel, Philippe, Younkin, Steve G., Wolf, Philip A., Launer, Lenore J., Lopez, Oscar L., van Duijn, Cornelia M. and Breteler, Monique M. B. 2010. Genome-wide analysis of genetic loci associated with Alzheimer Disease. JAMA - The Journal of the American Medical Association 303 (18) , pp. 1832-1840. 10.1001/jama.2010.574

Craddock, Nicholas John, Hurles, Matthew E., Cardin, Niall, Pearson, Richard D., Plagnol, Vincent, Robson, Samuel, Vukcevic, Damjan, Barnes, Chris, Conrad, Donald F., Giannoulatou, Eleni, Holmes, Chris, Marchini, Jonathan L., Stirrups, Kathy, Tobin, Martin D., Wain, Louise V., Yau, Chris, Aerts, Jan, Ahmad, Tariq, Daniel Andrews, T., Arbury, Hazel, Attwood, Anthony, Auton, Adam, Ball, Stephen G., Balmforth, Anthony J., Barrett, Jeffrey C., Barroso, Inês, Barton, Anne, Bennett, Amanda J., Bhaskar, Sanjeev, Blaszczyk, Katarzyna, Bowes, John, Brand, Oliver J., Braund, Peter S., Bredin, Francesca, Breen, Gerome, Brown, Morris J., Bruce, Ian N., Bull, Jaswinder, Burren, Oliver S., Burton, John, Byrnes, Jake, Caesar, Sian, Clee, Chris M., Coffey, Alison J., Connell, John M. C., Cooper, Jason D., Dominiczak, Anna F., Downes, Kate, Drummond, Hazel E., Dudakia, Darshna, Dunham, Andrew, Ebbs, Bernadette, Eccles, Diana, Edkins, Sarah, Edwards, Cathryn, Elliot, Anna, Emery, Paul, Evans, David M., Evans, Gareth, Eyre, Steve, Farmer, Anne, Nicol Ferrier, I., Feuk, Lars, Fitzgerald, Tomas, Flynn, Edward, Forbes, Alistair, Forty, Elizabeth, Franklyn, Jayne A., Freathy, Rachel M., Gibbs, Polly, Gilbert, Paul, Gokumen, Omer, Gordon-Smith, Katherine, Gray, Emma, Green, Elaine Karen, Groves, Chris J., Grozeva, Detelina Valentinova, Gwilliam, Rhian, Hall, Anita, Hammond, Naomi, Hardy, Matt, Harrison, Pile, Hassanali, Neelam, Hebaishi, Husam, Hines, Sarah, Hinks, Anne, Hitman, Graham A, Hocking, Lynne, Howard, Eleanor, Howard, Philip, Howson, Joanna M. M., Hughes, Debbie, Hunt, Sarah, Isaacs, John D., Jain, Mahim, Jewell, Derek P., Johnson, Toby, Jolley, Jennifer D., Jones, Ian Richard, Jones, Lisa A., Kirov, George, Langford, Cordelia F., Lango-Allen, Hana, Mark Lathrop, G., Lee, James, Lee, Kate L., Lees, Charlie, Lewis, Kevin, Lindgren, Cecilia M., Maisuria-Armer, Meeta, Maller, Julian, Mansfield, John, Martin, Paul, Massey, Dunecan C. O., McArdle, Wendy L., McGuffin, Peter, McLay, Kirsten E., Mentzer, Alex, Mimmack, Michael L., Morgan, Ann E., Morris, Andrew P., Mowat, Craig, Myers, Simon, Newman, William, Nimmo, Elaine R., O'Donovan, Michael Conlon, Onipinla, Abiodun, Onyiah, Ifejinelo, Ovington, Nigel R., Owen, Michael John, Palin, Kimmo, Parnell, Kirstie, Pernet, David, Perry, John R. B., Phillips, Anne, Pinto, Dalila, Prescott, Natalie J., Prokopenko, Inga, Quail, Michael A., Rafelt, Suzanne, Rayner, Nigel W., Redon, Richard, Reid, David M., Renwick, Anthony, Ring, Susan M., Robertson, Neil, Russell, Elen, St Clair, David, Sambrook, Jennifer G., Sanderson, Jeremy D., Schuilenburg, Helen, Scott, Carol E., Scott, Richard, Seal, Sheila, Shaw-Hawkins, Sue, Shields, Beverley M., Simmonds, Matthew J., Smyth, Debbie J., Somaskantharajah, Elilan, Spanova, Katarina, Steer, Sophia, Stephens, Jonathan, Stevens, Helen E., Stone, Millicent A., Su, Zhan, Symmons, Deborah P. M., Thompson, John R., Thomson, Wendy, Travers, Mary E., Turnbull, Clare, Valsesia, Armand, Walker, Mark, Walker, Neil M., Wallace, Chris, Warren-Perry, Margaret, Watkins, Nicholas A., Webster, John, Weedon, Michael N., Wilson, Anthony G., Woodburn, Matthew, Wordsworth, B. Paul, Young, Allan H., Zeggini, Eleftheria, Carter, Nigel P., Frayling, Timothy M., Lee, Charles, McVean, Gil, Munroe, Patricia B., Palotie, Aarno, Sawcer, Stephen J., Scherer, Stephen W., Strachan, David P., Tyler-Smith, Chris, Brown, Matthew A., Burton, Paul R., Caulfield, Mark J., Compston, Alastair, Farrall, Martin, Gough, Stephen C. L., Hall, Alistair S., Hattersley, Andrew T., Hill, Adrian V. S., Mathew, Christopher G., Pembrey, Marcus, Satsangi, Jack, Stratton, Michael R., Worthington, Jane, Deloukas, Panos, Duncanson, Audrey, Kwiatkowski, Dominic P., McCarthy, Mark I., Ouwehand, Willem H., Parkes, Miles, Rahman, Nazneen, Todd, John A., Samani, Nilesh J. and Donnelly, Peter 2010. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature 464 (7289) , pp. 713-720. 10.1038/nature08979

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

Langley, Kate, Fowler, Tom Alan, Ford, Tamsin, Thapar, Ajay Kumar, van den Bree, Marianne Bernadette, Harold, Gordon Thomas, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2010. Adolescent clinical outcomes for young people with attention-deficit hyperactivity disorder. British Journal of Psychiatry 196 (3) , pp. 235-240. 10.1192/bjp.bp.109.066274

Ikeda, Masashi, Tomita, Yasuyuki, Mouri, Akihiro, Koga, Minori, Okochi, Tomo, Yoshimura, Reiji, Yamanouchi, Yoshio, Kinoshita, Yoko, Hashimoto, Ryota, Williams, Hywel John, Takeda, Masatoshi, Nakamura, Jun, Nabeshima, Toshitaka, Owen, Michael John, O'Donovan, Michael Conlon, Honda, Hiroyuki, Arinami, Tadao, Ozaki, Norio and Iwata, Nakao 2010. Identification of novel candidate genes for treatment response to risperidone and susceptibility for schizophrenia: integrated analysis among pharmacogenomics, mouse expression, and genetic case-control association approaches. Biological psychiatry 67 (3) , pp. 263-269. 10.1016/j.biopsych.2009.08.030

Ikeda, Masashi, Aleksic, Branko, Kirov, George, Kinoshita, Yoko, Yamanouchi, Yoshio, Kitajima, Tsuyoshi, Kawashima, Kunihiro, Okochi, Tomo, Kishi, Taro, Zaharieva, Irina Takova, Owen, Michael John, O'Donovan, Michael Conlon, Ozaki, Norio and Iwata, Nakao 2010. Copy number variation in schizophrenia in the Japanese population. Biological Psychiatry 67 (3) , pp. 283-286. 10.1016/j.biopsych.2009.08.034

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

Schosser, A., Ng, M. Y., Butler, A. W., Uher, R., Cohen-Woods, S., Craddock, Nicholas John, Owen, Michael John, Aitchison, K. J., Breen, G., Craig, I., Farmer, A. E., Lewis, C. M. and McGuffin, P. 2010. Genome wide association scan of co-morbid anxiety in major depressive disorder (MDD) [Abstract]. International Journal of Psychiatry in Clinical Practice 14 (S1) , p. 37.

Owen, Michael John, Craddock, Nicholas John and O'Donovan, Michael Conlon 2010. Suggestion of roles for both common and rare risk variants in genome-wide studies of schizophrenia. Archives of General Psychiatry 67 (7) , pp. 667-673. 10.1001/archgenpsychiatry.2010.69

Ikeda, Masashi, Williams, Nigel Melville, Williams, Hywel John, Smith, Rhodri, Monks, Stephen, Owen, Michael John, Murphy, Kieran C. and O'Donovan, Michael Conlon 2010. Failure to confirm association between PIK4CA and psychosis in 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (4) , pp. 980-982. 10.1002/ajmg.b.31060

Cohen-Woods, Sarah, Craig, Ian, Gaysina, Darya, Gray, Joanna, Gunasinghe, Cerisse, Craddock, Nicholas John, Elkin, Amanda, Jones, Lisa, Kennedy, James, King, Nicole, Korszun, Ania, Knight, Jo, Owen, Michael John, Parikh, Sagar, Strauss, John, Sterne, Abram, Tozzi, Federica, Perry, Julia, Muglia, Pierandrea, Vincent, John, McGuffin, Peter and Farmer, Anne 2010. The Bipolar Association Case-Control Study (BACCS) and meta-analysis: No association with the 5,10-Methylenetetrahydrofolate reductase gene and bipolar disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (7) , pp. 1298-1304. 10.1002/ajmg.b.31101

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

Talkowski, Michael E., McCann, Kathleen L., Chen, Michael, McClain, Lora, Bamne, Mikhil, Wood, Joel, Chowdari, Kodavali V., Watson, Annie, Prasad, Konasale M., Kirov, George, Georgieva, Lyudmila, Toncheva, Draga, Mansour, Hader, Lewis, David A., Owen, Michael John, O'Donovan, Michael Conlon, Papasaikas, Panagiotis, Sullivan, Patrick, Ruderfer, Douglas, Yao, Jeffrey K., Leonard, Sherry, Thomas, Pramod, Miyajima, Fabio, Quinn, John, Lopez, A. Javier and Nimgaonkar, Vishwajit L. 2010. Fine-mapping reveals novel alternative splicing of the dopamine transporter. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (8) , pp. 1434-1447. 10.1002/ajmg.b.31125

Butler, Amy W., Breen, Gerome, Tozzi, Federica, Craddock, Nicholas John, Gill, Mike, Korszun, Ania, Maier, Wolfgang, Middleton, Lefkos T., Mors, Ole, Owen, Michael John, Perry, Julia, Preisig, Martin, Rice, John P., Rietschel, Marcella, Jones, Lisa, Farmer, Anne E., Lewis, Cathryn M. and McGuffin, Peter 2010. A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (8) , pp. 1465-1473. 10.1002/ajmg.b.31127

Hollingworth, Paul, Harold, Denise, Jones, Lesley, Owen, Michael John and Williams, Julie 2010. Alzheimer's disease genetics: current knowledge and future challenges. International Journal of Geriatric Psychiatry 26 (8) , pp. 793-802. 10.1002/gps.2628

Lupton, Michelle K, Stahl, Daniel, Archer, Nicola, Foy, Catherine, Poppe, Michaela, Lovestone, Simon, Hollingworth, Paul, Williams, Julie, Owen, Michael John, Dowzell, Kimberley Frances, Abraham, Richard Alun, Sims, Rebecca, Brayne, Carol, Rubinsztein, David, Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn and Powell, John F 2010. Education, occupation and retirement age effects on the age of onset of Alzheimer's disease. International Journal of Geriatric Psychiatry 25 (1) , pp. 30-36. 10.1002/gps.2294

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

Blake, Derek J., Forrest, Marc, Chapman, Ria M., Tinsley, Caroline L., O'Donovan, Michael Conlon and Owen, Michael John 2010. TCF4, Schizophrenia, and Pitt-Hopkins Syndrome. Schizophrenia Bulletin 36 (3) , pp. 443-447. 10.1093/schbul/sbq035

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

Craddock, Nicholas John and Owen, Michael John 2010. Authors' reply:. British Journal of Psychiatry 196 (6) , pp. 495-496. 10.1192/bjp.196.6.495a

Craddock, Nicholas John and Owen, Michael John 2010. Molecular genetics and the relationship between epilepsy and psychosis [Letter]. British Journal of Psychiatry 197 (1) , pp. 75-76. 10.1192/bjp.197.1.75a

Craddock, Nicholas John and Owen, Michael John 2010. Data and clinical utility should be the drivers of changes to psychiatric classification [Letter]. British Journal of Psychiatry 197 (2) , p. 158. 10.1192/bjp.197.2.158

Lewis, Cathryn M., Ng, Mandy Y., Butler, Amy W., Cohen-Woods, Sarah, Uher, Rudolf, Pirlo, Katrina, Weale, Michael E., Schosser, Alexandra, Paredes, Ursula M, Rivera, Margarita, Craddock, Nicholas John, Owen, Michael John, Jones, Lisa, Jones, Ian Richard, Korszun, Ania, Aitchison, Katherine J., Shi, Jianxin, Quinn, John P., MacKenzie, Alasdair, Vollenweider, Peter, Waeber, Gerard, Heath, Simon, Lathrop, Mark, Muglia, Pierandrea, Barnes, Michael R., Whittaker, John C., Tozzi, Frederica, Holsboer, Florian, Preisig, Martin, Farmer, Anne E., Breen, Gerome, Craig, Ian W. and McGuffin, Peter 2010. Genome-wide association study of major recurrent depression in the U.K. population. American Journal of Psychiatry 167 (8) , pp. 949-957. 10.1176/appi.ajp.2010.09091380

Cruchaga, Carlos, Kauwe, John S. K., Mayo, Kevin, Spiegel, Noah, Bertelsen, Sarah, Nowotny, Petra, Shah, Aarti R., Abraham, Richard, Hollingworth, Paul, Harold, Denise, Owen, Michael John, Williams, Julie, Lovestone, Simon, Peskind, Elaine R., Li, Ge, Leverenz, James B., Galasko, Douglas, Morris, John C., Fagan, Anne M., Holtzman, David M. and Goate, Alison M. 2010. SNPS associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease. PLoS Genetics 6 (9) , e1001101. 10.1371/journal.pgen.1001101

Baig, Shabnam, Joseph, Sally A., Tayler, Hannah, Abraham, Richard Alun, Owen, Michael John, Williams, Julie, Kehoe, Patrick G. and Love, Seth 2010. Distribution and expression of picalm in alzheimer disease. Journal of Neuropathology and Experimental Neurology 69 (10) , pp. 1071-1077. 10.1097/NEN.0b013e3181f52e01

Craddock, Nicholas John and Owen, Michael John 2010. The Kraepelinian dichotomy - going, going... but still not gone (Reappraisal). British Journal of Psychiatry 196 (2) , pp. 92-95. 10.1192/bjp.bp.109.073429

Chen, X., Lee, G., Maher, B. S., Fanous, A. H., Chen, J., Zhao, Z., Guo, A., van den Oord, E., Sullivan, P. F., Shi, J., Levinson, D. F., Gejman, P. V., Sanders, A., Duan, J., Owen, Michael John, Craddock, Nicholas John, O'Donovan, Michael Conlon, Blackman, Janet, Lewis, D., Kirov, George, Qin, W., Schwab, S., Wildenauer, D., Chowdari, K., Nimgaonkar, V., Straub, R. E., Weinberger, D. R., O'Neill, F. A., Walsh, D., Bronstein, M., Darvasi, A., Lencz, T., Malhotra, A. K., Rujescu, D., Giegling, I., Werge, T., Hansen, T., Ingason, A., Nöethen, M. M., Rietschel, M., Cichon, S., Djurovic, S., Andreassen, O. A., Cantor, R. M., Ophoff, R., Corvin, A., Morris, D. W., Gill, M., Pato, C. N., Pato, M. T., Macedo, A., Gurling, H. M. D., McQuillin, A., Pimm, J., Hultman, C., Lichtenstein, P., Sklar, P., Purcell, S. M., Scolnick, E., St Clair, D., Blackwood, D. H. R. and Kendler, K. S. 2010. GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia. Molecular Psychiatry 16 (11) , pp. 1117-1129. 10.1038/mp.2010.96

Craddock, Nicholas John and Owen, Michael John 2010. Molecular genetics and the kraepelinian dichotomy: one disorder, two disorders, or do we need to start thinking afresh? Psychiatric Annals 40 (2) , pp. 88-91. 10.3928/00485718-20100127-04

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

Fowler, Tom Alan, Langley, Kate, Rice, Frances, van den Bree, Marianne Bernadette, Ross, Kenny, Wilkinson, Lawrence Stephen, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2009. Psychopathy trait scores in adolescents with childhood ADHD: the contribution of genotypes affecting MAOA, 5HTT and COMT activity. Psychiatric Genetics 19 (6) , pp. 312-319. 10.1097/YPG.0b013e3283328df4

Hayesmoore, Jesse B. G., Bray, Nicholas John, Cross, William C., Owen, Michael John, O'Donovan, Michael Conlon and Morris, Huw Rees 2009. The effect of age and the H1c MAPT haplotype on MAPT expression in human brain. Neurobiology of Aging 30 (10) , pp. 1652-1656. 10.1016/j.neurobiolaging.2007.12.017

Carroll, Liam S. and Owen, Michael John 2009. Genetic overlap between autism, schizophrenia and bipolar disorder [Review]. Genome Medicine 1 (10) , p. 102. 10.1186/gm102

Liu, Yang, Chen, Gang, Norton, Nadine, Liu, Wenmin, Zhu, Haining, Zhou, Peng, Luan, Meng, Yang, Shulin, Chen, Xing, Carroll, Liam, Williams, Nigel Melville, O'Donovan, Michael Conlon, Kirov, George and Owen, Michael John 2009. Whole genome association study in a homogenous population in Shandong Peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia. Journal of Biomedicine and Biotechnology , 536918. 10.1155/2009/536918

Donohoe, Gary, Walters, James Tynan Rhys, Morris, Derek W., Quinn, Emma M., Róisín, Judge, Norton, Nadine, Giegling, Ina, Hartmann, Annette M., Möller, Hans-Jürgen, Muglia, Pierandrea, Williams, Hywel John, Escott-Price, Valentina, Peel, Rosemary, O’Donoghue, Theresa, Owen, Michael John, O'Donovan, Michael Conlon, Gill, Michael and Rujescu, Dan 2009. Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects. Archives of General Psychiatry 66 (10) , pp. 1045-1054. 10.1001/archgenpsychiatry.2009.139

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

McCarthy, Shane E., Makarov, Vladimir, Kirov, George, Addington, Anjene M., McClellan, Jon, Yoon, Seungtai, Perkins, Diana O., Dickel, Diane E., Kusenda, Mary, Krastoshevsky, Olga, Krause, Verena, Kumar, Ravinesh A., Grozeva, Detelina Valentinova, Malhotra, Dheeraj, Walsh, Tom, Zackai, Elaine H., Kaplan, Paige, Ganesh, Jaya, Krantz, Ian D., Spinner, Nancy B., Roccanova, Patricia, Bhandari, Abhishek, Pavon, Kevin, Lakshmi, B., Leotta, Anthony, Kendall, Jude, Lee, Yoon-ha, Vacic, Vladimir, Gary, Sydney, Iakoucheva, Lilia M., Crow, Timothy J., Christian, Susan L., Lieberman, Jeffrey A., Stroup, T. Scott, Lehtimäki, Terho, Puura, Kaija, Haldeman-Englert, Chad, Pearl, Justin, Goodell, Meredith, Willour, Virginia L., DeRosse, Pamela, Steele, Jo, Kassem, Layla, Wolff, Jessica, Chitkara, Nisha, McMahon, Francis J., Malhotra, Anil K., Potash, James B., Schulze, Thomas G., Nöthen, Markus M., Cichon, Sven, Rietschel, Marcella, Leibenluft, Ellen, Kustanovich, Vlad, Lajonchere, Clara M., Sutcliffe, James S., Skuse, David, Gill, Michael, Gallagher, Louise, Mendell, Nancy R., Craddock, Nicholas John, Owen, Michael John, O'Donovan, Michael Conlon, Shaikh, Tamim H., Susser, Ezra, DeLisi, Lynn E., Sullivan, Patrick F., Deutsch, Curtis K., Rapoport, Judith, Levy, Deborah L., King, Mary-Claire and Sebat, Jonathan 2009. Microduplications of 16p11.2 are associated with schizophrenia. Nature Genetics 41 (11) , pp. 1223-1227. 10.1038/ng.474

Metlapally, Ravikanth, Li, Yi-Ju, Tran-Viet, Khanh-Nhat, Abbott, Diana, Czaja, Gregory R., Malecaze, Francois, Calvas, Patrick, Mackey, David, Rosenberg, Thomas, Paget, Sandrine, Zayats, Tetyana, Owen, Michael John, Guggenheim, Jeremy Andrew and Young, Terri L. 2009. COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus. Investigative Ophthalmology and Visual Science 50 (9) , pp. 4080-4086. 10.1167/iovs.08-3346

Ball, H. A., Samaan, Z., Brewster, S., Craddock, Nicholas John, Gill, M., Korszun, A., Maier, W., Middleton, L., Mors, O., Owen, Michael John, Perry, Jonathan, Preisig, M., Rice, J., Rietschel, M., Jones, L., Jones, Ian Richard, Farmer, A. E. and McGuffin, P. 2009. Depression, migraine with aura and migraine without aura: their familiality and interrelatedness. Cephalagia 29 (8) , pp. 848-854. 10.1111/j.1468-2982.2008.01808.x

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

Li, Yi-Ju, Guggenheim, Jeremy Andrew, Bulusu, Anuradha, Metlapally, Ravikanth, Abbott, Diana, Malecaze, Francois, Calvas, Patrick, Rosenberg, Thomas, Paget, Sandrine, Creer, Rosalind C., Kirov, George, Owen, Michael John, Zhao, Bei, White, Tristan, Mackey, David A. and Young, Terri L. 2009. An international collaborative family-based whole-genome linkage scan for high-grade myopia. Investigative Ophthalmology & Visual Science 50 (7) , pp. 3116-3127. 10.1167/iovs.08-2781

O'Donovan, Michael Conlon, Craddock, Nicholas John and Owen, Michael John 2009. Genetics of psychosis; insights from views across the genome. Human Genetics 126 (1) , pp. 3-12. 10.1007/s00439-009-0703-0

Owen, Michael John 2009. Will schizophrenia become a graveyard for molecular geneticists? Psychological Medicine 22 (02) , pp. 289-293. 10.1017/S0033291700030221

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

Williams, Hywel, Owen, Michael John and O'Donovan, Michael Conlon 2009. Schizophrenia genetics: new insights from new approaches. British Medical Bulletin 91 (1) , pp. 61-74. 10.1093/bmb/ldp017

Owen, Michael John and Craddock, Nicholas John 2009. Diagnosis of functional psychoses: time to face the future [Comment]. The Lancet 373 (9659) , pp. 190-191. 10.1016/S0140-6736(09)60053-2

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

O'Donovan, Michael Conlon, Craddock, Nicholas John and Owen, Michael John 2009. Strong evidence for multiple psychosis susceptibility genes - a rejoinder to Crow [Letter]. Psychological Medicine 39 (1) , pp. 170-171. 10.1017/S0033291708004583

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

Morgan, Angharad Rhys, Hollingworth, Paul, Abraham, Richard Alun, Lovestone, S., Brayne, C., Rubinsztein, D. C., Lynch, A., Lawlor, B., Gill, M., O'Donovan, Michael Conlon, Owen, Michael John and Williams, J. 2009. Association analysis of dynamin-binding protein (DNMBP) on chromosome 10q with late onset Alzheimer's disease in a large caucasian UK sample. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (1) , pp. 61-64. 10.1002/ajmg.b.30768

Talkowski, Michael E., McClain, Lora, Allen, Trina, Bradford, L. DiAnne, Calkins, Monica, Edwards, Neil, Georgieva, Lyudmila, Go, Rodney, Gur, Ruben, Gur, Raquel, Kirov, George, Chowdari, Kodavali, Kwentus, Joseph, Lyons, Paul, Mansour, Hader, McEvoy, Joseph, O'Donovan, Michael Conlon, O'Jile, Judith, Owen, Michael John, Santos, Alberto, Savage, Robert, Toncheva, Draga, Vockley, Gerard, Wood, Joel, Devlin, Bernie and Nimgaonkar, Vishwajit L. 2009. Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (4) , pp. 560-569. 10.1002/ajmg.b.30862

Carroll, Liam Stuart, Kendall, Kimberley, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Nigel Melville 2009. Evidence that putative ADHD low risk alleles atSNAP25may increase the risk of schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (7) , pp. 893-899. 10.1002/ajmg.b.30915

Green, Elaine Karen, Grozeva, Detelina Valentinova, Raybould, Rachel, Elvidge, Gareth, Macgregor, Stuart, Craig, Ian, Farmer, Anne, McGuffin, Peter, Forty, Elizabeth, Jones, Lisa, Jones, Ian Richard, O'Donovan, Michael Conlon, Owen, Michael John, Kirov, George and Craddock, Nicholas John 2009. P2RX7: A bipolar and unipolar disorder candidate susceptibility gene? American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (8) , pp. 1063-1069. 10.1002/ajmg.b.30931

Abraham, Richard Alun, Sims, Rebecca, Carroll, Liam Stuart, Hollingworth, Paul, O'Donovan, Michael Conlon, Williams, Julie and Owen, Michael John 2009. An association study of common variation at theMAPTlocus with late-onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (8) , pp. 1152-1155. 10.1002/ajmg.b.30951

Schosser, A., Cohen-Woods, S., Gaysina, D., Chow, P. C., Martucci, L., Farmer, A., Korszun, A., Gunashinghe, C., Gray, J., Jones, L., Craddock, Nicholas John, Owen, Michael John, Craig, I. W. and McGuffin, P. 2009. NRG1gene in recurrent major depression: No association in a large-scale case-control association study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (1) , pp. 141-147. 10.1002/ajmg.b.30965

Dwyer, Sarah Lynne, Carroll, Liam Stuart, Mantripragada, Kiran Kumar, Owen, Michael John, O'Donovan, Michael Conlon and Williams, Nigel Melville 2009. Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (3) , pp. 766-774. 10.1002/ajmg.b.31045

Kauwe, J. S. K., Bertelsen, S., Mayo, K., Cruchaga, C., Abraham, Richard Alun, Hollingworth, Paul, Harold, Denise, Owen, Michael John, Williams, Julie, Lovestone, S., Morris, J. C. and Goate, A. M. 2009. Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (4) , pp. 955-959. 10.1002/ajmg.b.31053

O'Donovan, Michael Conlon and Owen, Michael John 2009. Genetics and the brain: many pathways to enlightenment [Editorial]. Human Genetics 126 (1) , pp. 1-2. 10.1007/s00439-009-0705-y

Azuma, Rayna, Daly, Eileen M., Campbell, Linda E., Stevens, Angela F., Deeley, Quinton, Giampietro, Vincent, Brammer, Michael J., Glaser, Beate, Ambery, Fiona Z., Morris, Robin G., Williams, Steven C. R., Owen, Michael John, Murphy, Declan G. M. and Murphy, Kieran C. 2009. Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study. Journal of Neurodevelopmental Disorders 1 (1) , pp. 46-60. 10.1007/s11689-009-9008-9

Smith, Daniel J., Owen, Michael John and Craddock, Nicholas John 2009. Bipolar disorder and unipolar depression: what is the genetic relationship? In: Pariante, Carmine M., Nesse, Randolph M., Nutt, David and Wolpert, Lewis eds. Understanding Depression: a Translational Approach, Oxford: Oxford University Press, pp. 67-76.

Owen, Michael John, Williams, Hywel John and O'Donovan, Michael Conlon 2009. Schizophrenia genetics: advancing on two fronts. Current Opinion in Genetics & Development 19 (3) , pp. 266-270. 10.1016/j.gde.2009.02.008

Gerrish, Amy, Williams, Hywel John, Escott-Price, Valentina, Owen, Michael John, O'Donovan, Michael Conlon and Williams, Nigel Melville 2009. An examination of MUTED as a schizophrenia susceptibility gene [Letter]. Schizophrenia Research 107 (1) , pp. 110-111. 10.1016/j.schres.2008.08.011

Sims, Rebecca, Hollingworth, Paul, Escott-Price, Valentina, Dowzell, K., O'Donovan, Michael Conlon, Powell, J., Lovestone, S., Brayne, C., Rubinsztein, D., Owen, Michael John, Williams, John David and Abraham, Richard Alun 2009. Evidence that variation in the oligodendrocyte lineage transcription factor 2 (OLIG2) gene is associated with psychosis in Alzheimer's disease. Neuroscience Letters 461 (1) , pp. 54-59. 10.1016/j.neulet.2009.05.051

Yosifova, Adelina, Mushiroda, Taisei, Stoianov, Drozdstoi, Vazharova, Radoslava, Dimova, Ivanka, Karachanak, Sena, Zaharieva, Irina, Milanova, Vihra, Madjirova, Nadejda, Gerdjikov, Ivan, Tolev, Todor, Velkova, Stoyanka, Kirov, George, Owen, Michael John, O'Donovan, Michael Conlon, Toncheva, Draga and Nakamura, Yusuke 2009. Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian population. Journal of Affective Disorders 117 (1-2) , pp. 87-97. 10.1016/j.jad.2008.12.021

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

Cohen-Woods, S., Gaysina, D., Craddock, Nicholas John, Farmer, A., Gray, J., Gunasinghe, C., Hoda, F., Jones, L., Knight, J., Korszun, A., Owen, Michael John, Sterne, A., Craig, I. W. and McGuffin, P. 2009. Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder. Human Molecular Genetics 18 (8) , pp. 1504-1509. 10.1093/hmg/ddp051

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