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Number of items: 282.

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
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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
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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
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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
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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
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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,

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

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
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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
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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
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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
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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
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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
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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
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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

Kirov, George, Owen, L., Ballard, Hazel, Leighton, A., Hannigan, K., Llewellyn, D., Escott-Price, Valentina and Atkins, M. 2016. Evaluation of cumulative cognitive deficits from electroconvulsive therapy. British Journal of Psychiatry 208 (3) , pp. 266-270. 10.1192/bjp.bp.114.158261

Bigdeli, Tim B., Ripke, Stephan, Bacanu, Silviu-Alin, Lee, Sang Hong, Wray, Naomi R., Gejman, Pablo V., Rietschel, Marcella, Cichon, Sven, St Clair, David, Corvin, Aiden, Kirov, George, McQuillin, Andrew, Gurling, Hugh, Rujescu, Dan, Andreassen, Ole A., Werge, Thomas, Blackwood, Douglas H.R., Pato, Carlos N., Pato, Michele T., Malhotra, Anil K., O'Donovan, Michael Conlon, Kendler, Kenneth S. and Fanous, Ayman H. 2016. Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics , n/a. 10.1002/ajmg.b.32402

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

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

Green, E. K., Rees, Elliott, Walters, James Tynan Rhys, Smith, K-G, Forty, Elizabeth, Grozeva, D., Moran, J. L., Sklar, P., Ripke, S., Chambert, K. D., Genovese, G., McCarroll, S. A., Jones, Ian Richard, Jones, L., Owen, Michael John, O'Donovan, Michael Conlon, Craddock, Nicholas John and Kirov, George 2016. Copy number variation in bipolar disorder. Molecular Psychiatry 21 (1) , pp. 89-93. 10.1038/mp.2014.174
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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

Escott-Price, Valentina, Kirov, George, Rees, Elliott, Isles, Anthony Roger, Owen, Michael John and O'Donovan, Michael Conlon 2015. No evidence for enrichment in schizophrenia for common allelic associations at imprinted loci. Plos One 10 (12) , e0144172. 10.1371/journal.pone.0144172
file

Kirov, George 2015. CNVs in neuropsychiatric disorders. Human Molecular Genetics 24 (R1) , R45-R49. 10.1093/hmg/ddv253

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

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

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

Kirov, George, Rees, Elliott and Walters, James Tynan Rhys 2015. What a psychiatrist needs to know about copy number variants. BJPscyh Advances 21 (3) , pp. 157-163. 10.1192/apt.bp.113.012039

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

Carroll, Liam S., Woolf, Rebecca, Ibrahim, Yousef, Williams, Hywel J., Dwyer, Sarah, Walters, James Tynan, Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2015. Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation. Psychiatric Genetics , p. 1. 10.1097/YPG.0000000000000110

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

Peall, Kathryn J., Kurian, Manju A., Wardle, Mark, Waite, Adrian, Hedderly, Tammy, Lin, Jean-Pierre, Smith, Martin, Whone, Alan, Pall, Hardev, White, Cathy, Lux, Andrew, Jardine, Philip E., Lynch, Bryan, Kirov, George, O'Riordan, Sean, Samuel, Michael, Lynch, Timothy, King, Mary D., Chinnery, Patrick F., Warner, Thomas T., Blake, Derek, Owen, Michael John and Morris, Huw 2014. SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype. Journal of Neurology 261 (12) , pp. 2296-2304. 10.1007/s00415-014-7488-3

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

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

Rees, Elliott, Walters, James Tynan Rhys, Owen, Michael John and Kirov, George 2014. Authors' reply [Letter]. British Journal of Psychiatry 205 (1) , p. 78. 10.1192/bjp.205.1.78

Szatkiewicz, J. P., O'Dushlaine, C., Chen, G., Chambert, K., Moran, J. L., Neale, B. M., Fromer, M., Ruderfer, D., Akterin, S., Bergen, S. E., Kähler, A., Magnusson, P. K. E., Kim, Y., Crowley, J..J., Rees, Elliott, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John, Walters, James Tynan Rhys, Scolnick, E., Sklar, P., Purcell, S., Hultman, C. M., McCarroll, S. A. and Sullivan, P. F. 2014. Copy number variation in schizophrenia in Sweden. Molecular Psychiatry 19 (7) , pp. 762-773. 10.1038/mp.2014.40

Morris, D. W., Pearson, R. D., Cormican, P., Kenny, E. M., O'Dushlaine, C. T., Perreault, L.-P. L., Giannoulatou, E., Tropea, D., Maher, B. S., Wormley, B., Kelleher, E., Fahey, C., Molinos, I., Bellini, S., Pirinen, M., Strange, A., Freeman, C., Thiselton, D. L., Elves, R. L., Regan, R., Ennis, S., Dinan, T. G., McDonald, C., Murphy, K. C., O'Callaghan, E., Waddington, J. L., Walsh, D., O'Donovan, Michael Conlon, Grozeva, Detelina, Craddock, Nicholas John, Stone, J., Scolnick, E., Purcell, S., Sklar, P., Coe, B., Eichler, E. E., Ophoff, R., Buizer, J., Szatkiewicz, J., Hultman, C., Sullivan, P., Gurling, H., Mcquillin, A., St Clair, D., Rees, Elliott, Kirov, George, Walters, James Tynan Rhys, Blackwood, D., Johnstone, M., Donohoe, G., O'Neill, F. A., Kendler, K. S., Gill, M., Riley, B. P., Spencer, C. C. A. and Corvin, A. 2014. An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis. Human Molecular Genetics 23 (12) , pp. 3316-3326. 10.1093/hmg/ddu025

Mulle, Jennifer Gladys, Pulver, Ann E., McGrath, John A., Wolyniec, Paula S., Dodd, Anne F., Cutler, David J., Sebat, Jonathan, Malhotra, Dheeraj, Nestadt, Gerald, Conrad, Donald F., Hurles, Matthew, Barnes, Chris P., Ikeda, Masashi, Iwata, Nakao, Levinson, Douglas F., Gejman, Pablo V., Sanders, Alan R., Duan, Jubao, Mitchell, Adele A., Peter, Inga, Sklar, Pamela, O?Dushlaine, Colm T., Grozeva, Detelina, O'Donovan, Michael Conlon, Owen, Michael John, Hultman, Christina M., Kähler, Anna K., Sullivan, Patrick F., Kirov, George and Warren, Stephen T. 2014. Reciprocal duplication of the Williams-Beuren Syndrome deletion on chromosome 7q11.23 is associated with schizophrenia. Biological Psychiatry 75 (5) , pp. 371-7. 10.1016/j.biopsych.2013.05.040

Rees, Elliott, Walters, James Tynan Rhys, Chambert, K. D., O'Dushlaine, C., Szatkiewicz, J., Richards, Alexander, Georgieva, Lyudmila, Mahoney-Davies, Gerwyn, Legge, Sophie E., Moran, J. L., Genovese, G., Levinson, D., Morris, D. W., Cormican, P., Kendler, K. S., O'Neill, F. A., Riley, B., Gill, M., Corvin, A., Sklar, P., Hultman, C., Pato, C., Pato, M., Sullivan, P. F., Gejman, P. V., McCarroll, S. A., O'Donovan, Michael Conlon, Owen, Michael John and Kirov, George 2014. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Human Molecular Genetics 23 (6) , pp. 1669-1676. 10.1093/hmg/ddt540
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Hoeffding, Louise Kristine Enggaard, Hansen, Thomas, Ingason, Andrés, Doung, Linh, Thygesen, Johan H., Møller, Rikke S., Tommerup, Niels, Kirov, George, Rujescu, Dan, Larsen, Lars A., Werge, Thomas and Kirov, George 2014. Sequence analysis of 17NRXN1deletions. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165 (1) , pp. 52-61. 10.1002/ajmg.b.32204

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

Rees, Elliott, Walters, James Tynan Rhys, Georgieva, Lyudmila, Isles, Anthony Roger, Chambert, K. D., Richards, Alexander, Mahoney-Davies, Gerwyn, Legge, Sophie E., Moran, J. L., McCarroll, S. A., O'Donovan, Michael Conlon, Owen, Michael John and Kirov, George 2014. Analysis of copy number variations at 15 schizophrenia-associated loci. British Journal of Psychiatry 204 (2) , pp. 108-114. 10.1192/bjp.bp.113.131052
file

Grozeva, Detelina, Kirov, George, Conrad, Donald F, Barnes, Chris P, Hurles, Matthew, Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas John 2013. Reduced burden of very large and rare CNVs in bipolar affective disorder. Bipolar Disorders 15 (8) , pp. 893-8. 10.1111/bdi.12125

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

Rees, Elliott, Kirov, George, Sanders, A., Walters, James Tynan Rhys, Chambert, K. D., Shi, J., Szatkiewicz, J., O'Dushlaine, C., Richards, Alexander L., Green, Elaine Karen, Jones, Ian Richard, Davies, Geraint, Legge, Sophie E., Moran, J. L., Pato, C., Pato, M., Genovese, G., Levinson, D., Duan, J., Moy, W., Göring, H. H. H., Morris, D., Cormican, P., Kendler, K. S., O'Neill, F. A., Riley, B., Gill, M., Corvin, A., Craddock, Nicholas John, Sklar, P., Hultman, C., Sullivan, P. F., Gejman, P. V., McCarroll, S. A., O'Donovan, Michael Conlon and Owen, Michael John 2013. Evidence that duplications of 22q11.2 protect against schizophrenia. Molecular Psychiatry n/a 10.1038/mp.2013.156
file

Ruderfer, D., Chambert, K., Moran, J., Talkowski, M., Chen, E., Gigek, C., Gusella, J., Blackwood, D., Corvin, A., Gurling, H., Hultman, C., Kirov, George, Magnusson, P., O'Donovan, Michael Conlon, Owen, Michael John, Pato, C., St Clair, D., Sullivan, P., Purcell, S., Sklar, P. and Ernst, C. 2013. Mosaic copy number variation in schizophrenia. European Journal of Human Genetics 21 (9) , pp. 1007-1011. 10.1038/ejhg.2012.287

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

Lionel, A. C., Vaags, A. K., Sato, D., Gazzellone, M. J., Mitchell, E. B., Chen, H. Y., Costain, G., Walker, S., Egger, G., Thiruvahindrapuram, B., Merico, D., Prasad, A., Anagnostou, E., Fombonne, E., Zwaigenbaum, L., Roberts, W., Szatmari, P., Fernandez, B. A., Georgieva, Lyudmila, Brzustowicz, L. M., Roetzer, K., Kaschnitz, W., Vincent, J. B., Windpassinger, C., Marshall, C. R., Trifiletti, R. R., Kirmani, S., Kirov, George, Petek, E., Hodge, J. C., Bassett, A. S. and Scherer, S. W. 2013. Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures. Human Molecular Genetics 22 (10) , pp. 2055-2066. 10.1093/hmg/ddt056

Kronenberg, Florian, Huertas-Vazquez, Adriana, Nelson, Christopher P., Guo, Xiuqing, Reinier, Kyndaron, Uy-Evanado, Audrey, Teodorescu, Carmen, Ayala, Jo, Jerger, Katherine, Chugh, Harpriya, WTCCC+, , Braund, Peter S., Deloukas, Panos, Hall, Alistair S., Balmforth, Anthony J., Jones, Michelle, Taylor, Kent D., Pulit, Sara L., Newton-Cheh, Christopher, Gunson, Karen, Jui, Jonathan, Rotter, Jerome I., Albert, Christine M., Samani, Nilesh J., Chugh, Sumeet S., Craddock, Nicholas John, Dunajewski, Katherine, Forty, Elizabeth, Green, Elaine, Grozeva, Detelina, Jones, Ian Richard, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John and Robertson, Neil 2013. Novel Loci Associated with Increased Risk of Sudden Cardiac Death in the Context of Coronary Artery Disease [Article]. PLoS ONE 8 (4) , e59905. 10.1371/journal.pone.0059905

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

Guha, Saurav, Rees, Elliott, Darvasi, Ariel, Ivanov, Dobril, Ikeda, Masashi, Bergen, Sarah E., Magnusson, Patrik K., Cormican, Paul, Morris, Derek, Gill, Michael, Cichon, Sven, Rosenfeld, Jeffrey A., Lee, Annette, Gregersen, Peter K., Kane, John M., Malhotra, Anil K., Rietschel, Marcella, Nöthen, Markus M., Degenhardt, Franziska, Priebe, Lutz, Breuer, René, Strohmaier, Jana, Ruderfer, Douglas M., Moran, Jennifer L., Chambert, Kimberly D., Sanders, Alan R., Shi, Jianxin, Kendler, Kenneth, Riley, Brien, O’Neill,, Tony, Walsh, Dermot, Malhotra, Dheeraj, Corvin, Aiden, Purcell, Shaun, Sklar, Pamela, Iwata, Nakao, Hultman, Christina M., Sullivan, Patrick F., Sebat, Jonathan, McCarthy, Shane, Gejman, Pablo V., Levinson, Douglas F., Owen, Michael John, O'Donovan, Michael Conlon, Lencz, Todd and Kirov, George 2013. Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry 70 (3) , pp. 253-260. 10.1001/2013.jamapsychiatry.71

Williams, Hywel John, Monks, Stephen, Murphy, Kieran C., Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2013. Schizophrenia two-hit hypothesis in velo-cardio facial syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 (2) , pp. 177-182. 10.1002/ajmg.b.32129

Betcheva, Elitza T., Yosifova, Adelina G., Mushiroda, Taisei, Kubo, Michiaki, Takahashi, Atsushi, Karachanak, Sena K., Zaharieva, Irina T., Hadjidekova, Savina P., Dimova, Ivanka I., Vazharova, Radoslava V., Stoyanov, Drozdstoy S., Milanova, Vihra K., Tolev, Todor, Kirov, George, Kamatani, Naoyuki, Toncheva, Draga I. and Nakamura, Yusuke 2013. Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene [Article]. Psychiatric Genetics 23 (1) , pp. 11-19. 10.1097/YPG.0b013e3283586343

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

Betcheva, E., Yosifova, A., Mushiroda, T., Kubo, M., Takahashi, A., Karachanak, S., Zaharieva, I., Hadjidekova, S., Dimova, I., Vazharova, R., Stoyanov, D., Milanova, V., Tolev, T., Kirov, George, Kamatani, N., Toncheva, D. and Nakamura, Y. 2013. Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene. Psychiatric Genetics 23 (1) , pp. 11-19. 10.1097/YPG.0b013e3283586343

Kim, Y., Ripke, Stephan, Kirov, George, Sklar, Pamela, Purcell, Shaun M., Owen, Michael John, O'Donovan, Michael Conlon and Sullivan, Patrick F. 2013. Non-random mating, parent-of-origin, and maternal-fetal incompatibility effects in schizophrenia. Schizophrenia Research 143 (1) , pp. 11-17. 10.1016/j.schres.2012.11.002

Peall, Kathryn J., Smith, Daniel J., Kurian, Manju A., Wardle, Mark, Waite, Adrian James, Hedderly, Tammy, Lin, Jean-Pierre, Smith, Martin, Whone, Alan, Pall, Hardev, White, Cathy, Lux, Andrew, Jardine, Philip, Bajaj, Narinder, Lynch, Bryan, Kirov, George, O'Riordan, Sean, Samuel, Michael, Lynch, Timothy, King, Mary D., Chinnery, Patrick F., Warner, Thomas T., Blake, Derek J., Owen, Michael John and Morris, Huw Rees 2013. SGCE mutations cause psychiatric disorders: clinical and genetic characterization. Brain 136 (1) , pp. 294-303. 10.1093/brain/aws308

Peall, K., Smith, D., Kurian, M., Wardle, M., Waite, A., Hedderly, T., Lin, J., Smith, M., Whone, A., Pall, H., White, C., Lux, A., Jardine, P., Bajaj, N., Lynch, B., Kirov, George, O'Riordan, S., Samuel, M., Lynch, T., King, M., Chinnery, P., Warner, T., Blake, D., Owen, Michael John and Morris, H. 2013. Are psychiatric symptoms a core phenotype of myoclonus dystonia syndrome caused by SGCE mutations? Journal of Neurology, Neurosurgery & Psychiatry 84 (9) , e1. 10.1136/jnnp-2013-306103.24

Kirov, George, Rees, Elliott, Walters, James Tynan Rhys, Escott-Price, Valentina, Georgieva, Lyudmila, Richards, Alexander, Chambert, Kimberly D., Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Steven A., O'Donovan, Michael Conlon and Owen, Michael John 2013. The penetrance of copy number variations for schizophrenia and developmental delay. Biological Psychiatry 75 (5) , pp. 378-385. 10.1016/j.biopsych.2013.07.022
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Aberg, Karolina A., Liu, Youfang, Bukszár, Jozsef, McClay, Joseph L., Khachane, Amit N., Andreassen, Ole A., Blackwood, Douglas, Corvin, Aiden, Djurovic, Srdjan, Gurling, Hugh, Ophoff, Roel, Pato, Carlos N., Pato, Michele T., Riley, Brien, Webb, Todd, Kendler, Kenneth, O'Donovan, Michael Conlon, Craddock, Nicholas John, Kirov, George, Owen, Michael John, Rujescu, Dan, St Clair, David, Werge, Thomas, Hultman, Christina M., Delisi, Lynn E., Sullivan, Patrick and van den Oord, Edwin J. 2013. A comprehensive family-based replication study of schizophrenia genes. JAMA Psychiatry 70 (6) , pp. 573-581. 10.1001/jamapsychiatry.2013.288

Cooper, J. D., Simmonds, M. J., Walker, N. M., Burren, O., Brand, O. J., Guo, H., Wallace, C., Stevens, H., Coleman, G., Franklyn, J. A., Todd, J. A., Gough, S. C. L., Craddock, Nicholas John, Dunajewski, K., Forty, Elizabeth, Green, E., Grozeva, D., Jones, Ian Richard, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John and Robertson, Neil 2012. Seven newly identified loci for autoimmune thyroid disease. Human Molecular Genetics 21 (23) , pp. 5202-5208. 10.1093/hmg/dds357

Jostins, Luke, Ripke, Stephan, Weersma, Rinse K., Duerr, Richard H., McGovern, Dermot P., Hui, Ken Y., Lee, James C., Philip Schumm, L., Sharma, Yashoda, Anderson, Carl A., Essers, Jonah, Mitrovic, Mitja, Ning, Kaida, Cleynen, Isabelle, Theatre, Emilie, Spain, Sarah L., Raychaudhuri, Soumya, Goyette, Philippe, Wei, Zhi, Abraham, Clara, Achkar, Jean-Paul, Ahmad, Tariq, Amininejad, Leila, Ananthakrishnan, Ashwin N., Andersen, Vibeke, Andrews, Jane M., Baidoo, Leonard, Balschun, Tobias, Bampton, Peter A., Bitton, Alain, Boucher, Gabrielle, Brand, Stephan, Büning, Carsten, Cohain, Ariella, Cichon, Sven, D?Amato, Mauro, De Jong, Dirk, Devaney, Kathy L., Dubinsky, Marla, Edwards, Cathryn, Ellinghaus, David, Ferguson, Lynnette R., Franchimont, Denis, Fransen, Karin, Gearry, Richard, Georges, Michel, Gieger, Christian, Glas, Jürgen, Haritunians, Talin, Hart, Ailsa, Hawkey, Chris, Hedl, Matija, Hu, Xinli, Karlsen, Tom H., Kupcinskas, Limas, Kugathasan, Subra, Latiano, Anna, Laukens, Debby, Lawrance, Ian C., Lees, Charlie W., Louis, Edouard, Mahy, Gillian, Mansfield, John, Morgan, Angharad R., Mowat, Craig, Newman, William, Palmieri, Orazio, Ponsioen, Cyriel Y., Potocnik, Uros, Prescott, Natalie J., Regueiro, Miguel, Rotter, Jerome I., Russell, Richard K., Sanderson, Jeremy D., Sans, Miquel, Satsangi, Jack, Schreiber, Stefan, Simms, Lisa A., Sventoraityte, Jurgita, Targan, Stephan R., Taylor, Kent D., Tremelling, Mark, Verspaget, Hein W., De Vos, Martine, Wijmenga, Cisca, Wilson, David C., Winkelmann, Juliane, Xavier, Ramnik J., Zeissig, Sebastian, Zhang, Bin, Zhang, Clarence K., Zhao, Hongyu, Silverberg, Mark S., Annese, Vito, Hakonarson, Hakon, Brant, Steven R., Radford-Smith, Graham, Mathew, Christopher G., Rioux, John D., Schadt, Eric E., Daly, Mark J., Franke, Andre, Parkes, Miles, Vermeire, Severine, Barrett, Jeffrey C., Cho, Judy H, Craddock, Nicholas John, Dunajewski, Katherine, Forty, Elizabeth, Green, Elaine, Grozeva, Detelina, Jones, Ian Richard, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John and Robertson, Neil 2012. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature 491 (7422) , pp. 119-124. 10.1038/nature11582

Williams, Hywel John, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2012. Absence of de novo point mutations in exons of GRIN2B in a large schizophrenia trio sample [Letter]. Schizophrenia Research 141 (2-3) , pp. 274-276. 10.1016/j.schres.2012.08.024

Fromer, Menachem, Moran, Jennifer L., Chambert, Kimberly, Banks, Eric, Bergen, Sarah E., Ruderfer, Douglas M., Handsaker, Robert E., McCarroll, Steven A., O'Donovan, Michael Conlon, Owen, Michael John, Kirov, George, Sullivan, Patrick F., Hultman, Christina M., Sklar, Pamela and Purcell, Shaun M. 2012. Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. American Journal of Human Genetics 91 (4) , pp. 597-607. 10.1016/j.ajhg.2012.08.005

Badner, J. A., Koller, D., Foroud, T., Edenberg, H., Nurnberger, J. I., Zandi, P. P., Willour, V. L., McMahon, F. J., Potash, J. B., Hamshere, Marian Lindsay, Grozeva, Detelina Valentinova, Green, Elaine Karen, Kirov, George, Jones, Ian Richard, Jones, L., Craddock, Nicholas John, Morris, D., Segurado, R., Gill, M., Sadovnick, D., Remick, R., Keck, P., Kelsoe, J., Ayub, M., MacLean, A., Blackwood, D., Liu, C.-Y., Gershon, E. S., McMahon, W., Lyon, G. J., Robinson, R., Ross, J. and Byerley, W. 2012. Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms. Molecular Psychiatry 17 (8) , pp. 818-826. 10.1038/mp.2011.89

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
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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
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Rees, Elliott, Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2012. De Novo mutation in schizophrenia. Schizophrenia Bulletin 38 (3) , pp. 377-381. 10.1093/schbul/sbs047

Kirov, George and Miller, Geoffrey 2012. Creativity and mental disorder. British Journal of Psychiatry 200 (4) , p. 347. 10.1192/bjp.200.4.347a

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
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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

Werge, Thomas, Ingason, Andrés, Kirov, George, Rujescu, Dan and Sigurdsson, Engilbert 2012. Response to Boot et al. [Letter]. American Journal of Psychiatry 169 (1) , p. 97. 10.1176/appi.ajp.2011.11091382r

Grozeva, Detelina Valentinova, Conrad, Donald F., Barnes, Chris P., Hurles, Matthew, Owen, Michael John, O'Donovan, Michael Conlon, Craddock, Nicholas John and Kirov, George 2012. Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia. Schizophrenia Research 135 (1-3) , pp. 1-7. 10.1016/j.schres.2011.11.004

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
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Forstbauer, Lina M., Brockschmidt, Felix F., Escott-Price, Valentina, Herold, Christine, Redler, Silke, Herzog, Alexandra, Hillmer, Axel M., Meesters, Christian, Heilmann, Stefanie, Albert, Florian, Alblas, Margrieta, Hanneken, Sandra, Eigelshoven, Sibylle, Giehl, Kathrin A., Jagielska, Dagny, Blume-Peytavi, Ulrike, Bartels, Natalie Garcia, Kuhn, Jennifer, Hennies, Hans Christian, Goebeler, Matthias, Jung, Andreas, Peitsch, Wiebke K., Kortüm, Anne-Katrin, Moll, Ingrid, Kruse, Roland, Lutz, Gerhard, Wolff, Hans, Blaumeiser, Bettina, Böhm, Markus, Kirov, George, Becker, Tim, Nöthen, Markus M. and Betz, Regina C. 2012. Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata. European Journal of Human Genetics 20 (3) , pp. 326-332. 10.1038/ejhg.2011.185

Rees, Elliott, Escott-Price, Valentina, Owen, Michael John, O'Donovan, Michael Conlon and Kirov, George 2011. De novo rates and selection of schizophrenia-associated copy number variants. Biological Psychiatry 70 (12) , pp. 1109-1114. 10.1016/j.biopsych.2011.07.011

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.

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

Ingason, Andres, Kirov, George, Giegling, Ina, Hansen, Thomas, Isles, Anthony Roger, Jakobsen, Klaus D., Kristinsson, Kari T., le Roux, Louise, Gustafsson, Omar, Craddock, Nicholas John, Moller, Hans-Jurgen, McQuillin, Andrew, Muglia, Pierandrea, Cichon, Sven, Rietschel, Marcella, Ophoff, Roel A., Djurovic, Srdjan, Andreassen, Ole A., Pietilainen, Ollie P. H., Peltonen, Leena, Dempster, Emma, Collier, David A., St. Clair, David, Rasmussen, Henrik B., Glenthoj, Birte Y., Kiemeney, Lambertus A., Franke, Barbara, Tosato, Sarah, Bonetto, Chiara, Saemundsen, Evald, Hreidarsson, Stefan J., Nothen, Markis M., Gurling, Hugh, O'Donovan, Michael Conlon, Owen, Michael John, Sigurdsson, Engilbert, Petursson, Hannes, Stefansson, Hreinn, Rujescu, Dan, Stefansson, Kari and Werge, Thomas 2011. Maternally derived microduplications at 15q11-q13: Implication of imprinted genes in psychotic illness. American Journal of Psychiatry 168 (4) , pp. 408-417. 10.1176/appi.ajp.2010.09111660

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

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

Green, Elaine Karen, Grozeva, Detelina Valentinova, Sims, Rebecca, Raybould, Rachel, Forty, Elizabeth, Gordon-Smith, K., Russell, Elen, St. Clair, D., Young, A.H., Ferrier, I.N., Kirov, George, Jones, Ian Richard, Jones, L., Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas John 2011. DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (4) , pp. 490-492. 10.1002/ajmg.b.31187

Smith, Rhodri L., Knight, Deborah, Williams, Hywel John, Dwyer, Sarah Lynne, Richards, Alexander, Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2011. Analysis of neurogranin (NRGN) in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (5) , pp. 532-535. 10.1002/ajmg.b.31191

Carroll, Liam Stuart, Williams, Hywel John, Walters, James Tynan Rhys, Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2011. Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 844-849. 10.1002/ajmg.b.31231

Yosifova, A., Mushiroda, T., Kubo, M., Takahashi, A., Kamatani, Y., Kamatani, N., Stoianov, D., Vazharova, R., Karachanak, S., Zaharieva, I., Dimova, I., Hadjidekova, S., Milanova, V., Madjirova, N., Gerdjikov, I., Tolev, T., Poryazova, N., O'Donovan, Michael Conlon, Owen, Michael John, Kirov, George, Toncheva, D. and Nakamura, Y. 2011. Genome-wide association study on bipolar disorder in the Bulgarian population. Genes, Brain and Behavior 10 (7) , pp. 789-797. 10.1111/j.1601-183X.2011.00721.x

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
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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

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

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

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

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

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

Kirov, George 2010. The role of copy number variation in schizophrenia. Expert Review of Neurotherapeutics 10 (1) , pp. 25-32. 10.1586/ern.09.133

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

Kirov, George 2010. Lithium plus valproate combination therapy versus monotherapy for relapse prevention in bipolar I disorder (BALANCE): a randomised open-label trial. The Lancet 375 (9712) , pp. 385-395. 10.1016/S0140-6736(09)61828-6

Tredget, John, Kirov, Anna and Kirov, George 2010. Effects of chronic lithium treatment on renal function. Journal of affective disorders 126 (3) , pp. 436-440. 10.1016/j.jad.2010.04.018

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

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

O'Dushlaine, Colm T., Morris, Derek, Escott-Price, Valentina, Kirov, George, Gill, Michael, Corvin, Aiden, Wilson, James F. and Cavalleri, Gianpiero L. 2010. Population structure and genome-wide patterns of variation in Ireland and Britain. European Journal of Human Genetics 18 (11) , pp. 1248-1254. 10.1038/ejhg.2010.87

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

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

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

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
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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

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

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

Hamshere, Marian Lindsay, Gordon-Smith, Katherine, Forty, Elizabeth, Jones, Lisa, Caesar, Sian, Fraser, Christine, Hyde, Sally, Tredget, John, Kirov, George, Jones, Ian Richard, Craddock, Nicholas John and Smith, Daniel J. 2009. Age-at-onset in bipolar-I disorder: mixture analysis of 1369 cases identifies three distinct clinical sub-groups. Journal of affective disorders 116 (1-2) , pp. 23-29. 10.1016/j.jad.2008.10.021

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

Kirov, George and Owen, Michael John 2009. Genetics of schizophrenia. In: Sadock, Benjamin J., Sadock, Virginia A. and Ruiz, Pedro eds. Kaplan and Sadock’s Comprehensive Textbook of Psychiatry. 9th ed., Vol. 1. Philadelphia: Lippincott Williams and Wilkins, pp. 1462-1474.

Kirov, George, Rujescu, Dan, Ingason, Andres, Collier, David A,, O'Donovan, Michael Conlon and Owen, Michael John 2009. Neurexin 1 (NRXN1) deletions in Schizophrenia. Schizophrenia Bulletin 35 (5) , pp. 851-854. 10.1093/schbul/sbp079

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

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

Kirov, George, Creaby, Mary, Khalid, Najeeb and Atkins, Maria 2009. Four years of successful maintenance electroconvulsive therapy [Letter]. The Journal of ECT 25 (3) , pp. 219-220. 10.1097/YCT.0b013e3181937f3d

Betcheva, Elitza T., Mushiroda, Taisei, Takahashi, Atsushi, Kubo, Michiaki, Karachanak, Sena K., Zaharieva, Irina T., Vazharova, Radoslava V., Dimova, Ivanka I., Milanova, Vihra K., Tolev, Todor, Kirov, George, Owen, Michael John, O'Donovan, Michael Conlon, Kamatani, Naoyuki, Nakamura, Yusuke and Toncheva, Draga I. 2009. Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population. Journal of Human Genetics 54 (2) , pp. 98-107. 10.1038/jhg.2008.14

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

Abraham, Richard, Escott-Price, Valentina, Sims, Rebecca, Hollingworth, Paul, Morgan, Angharad, Georgieva, Lyudmila, Dowzell, Kimberley, Cichon, Sven, Hillmer, Axel M, O'Donovan, Michael Conlon, Williams, Julie, Owen, Michael John and Kirov, George 2008. A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. BMC Medical Genomics 1 (1) , p. 44. 10.1186/1755-8794-1-44

Georgieva, Lyudmila, Dimitrova, Albena, Ivanov, Dobril Kirilov, Nikolov, Ivan, Williams, Nigel Melville, Grozeva, Detelina Valentinova, Zaharieva, Irina Takova, Toncheva, Draga, Owen, Michael John, Kirov, George and O'Donovan, Michael Conlon 2008. Support for Neuregulin 1 as a susceptibility gene for Bipolar disorder and schizophrenia. Biological psychiatry 64 (5) , pp. 419-427. 10.1016/j.biopsych.2008.03.025

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

Zaharieva, Irina, Georgieva, Lyudmila, Nikolov, Ivan, Kirov, George, Owen, Michael John, O'Donovan, Michael Conlon and Toncheva, Draga 2008. Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotyping. BMC Psychiatry 8 (1) , p. 11. 10.1186/1471-244X-8-11

Kirov, George, Gumus, Dilihan, Chen, Wei, Norton, Nadine, Georgieva, Lyudmila, Sari, Murat, O'Donovan, Michael Conlon, Erdogan, Fikret, Owen, Michael John, Ropers, Hans-Hilger and Ullmann, Reinhard 2008. Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Human Molecular Genetics 17 (3) , pp. 458-465. 10.1093/hmg/ddm323

Kirov, George, Zaharieva, I., Georgieva, Lyudmila, Escott-Price, Valentina, Nikolov, Ivan, Cichon, S., Hillmer, A., Toncheva, D., Owen, Michael John and O'Donovan, Michael Conlon 2008. A genome-wide association study in 574 schizophrenia trios using DNA pooling. Molecular Psychiatry 14 (8) , pp. 796-803. 10.1038/mp.2008.33

Kirov, George, Ebmeier, K. P., Scott, A. I. F., Atkins, M., Khalid, N., Carrick, L., Stanfield, A., O'Carroll, R. E., Husain, M. M. and Lisanby, S. H. 2008. Quick recovery of orientation after magnetic seizure therapy for major depressive disorder. The British Journal of Psychiatry 193 (2) , pp. 152-155. 10.1192/bjp.bp.107.044362

Khalid, Najeeb, Atkins, Maria, Tredget, John, Giles, Maureen, Champney-Smith, Karen and Kirov, George 2008. The effectiveness of electroconvulsive therapy in treatment-resistant depression. The Journal of ECT 24 (2) , pp. 141-145. 10.1097/YCT.0b013e318157ac58

O'Donovan, Michael Conlon, Kirov, George and Owen, Michael John 2008. Phenotypic variations on the theme of CNVs. Nature Genetics 40 (12) , pp. 1392-1393. 10.1038/ng1208-1392

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

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

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

Williams, Nigel Melville, Glaser, Beate, Norton, Nadine, Williams, Hywel John, Pierce, Timothy, Escott-Price, Valentina, Monks, Stephen, Del Favero, Jurgen, Goossens, Dirk, Rujescu, Dan, Kirov, George, Craddock, Nicholas John, Murphy, Kieran Christopher, O'Donovan, Michael Conlon and Owen, Michael John 2007. Strong evidence that GNB1L is associated with schizophrenia. Human Molecular Genetics 17 (4) , pp. 555-566. 10.1093/hmg/ddm330

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

Sisodiya, S., Cross, J. H., Blumcke, I., Chadwick, D., Craig, J., Crino, P. B., Debenham, P., Delanty, N., Elmslie, F., Gardiner, M., Golden, J., Goldstein, D., Greenberg, D. A., Guerrini, R., Hanna, M., Harris, J., Harrison, P., Johnson, M. R., Kirov, George, Kullman, D. M., Makoff, A., Marini, C. and Nabbout, R. N. 2007. Genetics of epilepsy: epilepsy research foundation workshop report. Epileptic Disorders 9 (2) , pp. 194-236.

Nicholas, B, Rudrasingham, V, Nash, S, Kirov, George, Owen, Michael John and Wimpory, D C 2007. Association of Per1 and Npas2 with autistic disorder: support for the clock genes/social timing hypothesis. Molecular Psychiatry 12 (6) , pp. 581-592. 10.1038/sj.mp.4001953

Bell, Vaughan, Reddy, Venu, Halligan, Peter, Kirov, George and Ellis, Hadyn Douglas 2007. Relative suppression of magical thinking: A transcranial magnetic stimulation study. Cortex 43 (4) , pp. 551-557.

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

Gunnell, D., Lewis, S., Wilkinson, J., Georgieva, Lyudmila, Davey, G. Smith, Day, I.N.M., Holly, J.M.P., O'Donovan, Michael Conlon, Owen, Michael John, Kirov, George and Zammit, Stanley 2007. IGF1, growth pathway polymorphisms and schizophrenia: A pooling study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144B (1) , pp. 117-120. 10.1002/ajmg.b.30396

Talkowski, M. E., Kirov, George, Bamne, M., Georgieva, Lyudmila, Torres, G., Mansour, H., Chowdari, K. V., Milanova, V., Wood, J., McClain, L., Prasad, K., Shirts, B., Zhang, J., O'Donovan, Michael Conlon, Owen, Michael John, Devlin, B. and Nimgaonkar, V. L. 2007. A network of dopaminergic gene variations implicated as risk factors for schizophrenia. Human Molecular Genetics 17 (5) , pp. 747-758. 10.1093/hmg/ddm347

Bell, Vaughan, Reddy, Venu, Halligan, Peter, Kirov, George and Ellis, Hadyn D. 2007. Relative Suppression of Magical Thinking: A Transcranial Magnetic Stimulation Study. Cortex 43 (4) , pp. 551-557. 10.1016/S0010-9452(08)70249-1

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

Glaser, Beate, Escott-Price, Valentina, Kirov, George, Murphy, Kieran C., Williams, Hywel, Williams Melville, Nigel, Owen, Michael John and O'Donovan, Michael Conlon 2006. Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility. Schizophrenia Research 87 (1-3) , p. 21. 10.1016/j.schres.2006.05.024

Khalid, Najeeb, Atkins, Maria and Kirov, George 2006. The effects of etomidate on seizure duration and electrical stimulus dose in seizure-resistant patients during electroconvulsive therapy. The Journal of ECT 22 (3) , pp. 184-88. 10.1097/01.yct.0000235931.24032.15

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

Talkowski, Michael E., Seltman, Howard, Bassett, Anne S., Brzustowicz, Linda M., Chen, Xiangning, Chowdari, Kodavali V., Collier, David A., Cordeiro, Quirino, Corvin, Aiden P., Deshpande, Smita N., Egan, Michael F., Gill, Michael, Kendler, Kenneth S., Kirov, George, Heston, Leonard L., Levitt, Pat, Lewis, David A., Li, Tao, Mirnics, Karoly, Morris, Derek W., Norton, Nadine, O'Donovan, Michael Conlon, Owen, Michael John, Richard, Christian, Semwal, Prachi, Sobell, Janet L., St Clair, David, Straub, Richard E., Thelma, B.K., Vallada, Homero, Weinberger, Daniel R., Williams, Nigel Melville, Wood, Joel, Zhang, Feng, Devlin, Bernie and Nimgaonkar, Vishwajit L. 2006. Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biological psychiatry 60 (2) , pp. 152-162. 10.1016/j.biopsych.2006.02.015

Williams, Nigel Melville, Green, Elaine Karen, Dwyer, Sarah Lynne, Macgregor, Stuart, Norton, Nadine, Williams, Hywel John, Raybould, Rachel, Grozeva, Detelina Valentinova, Hamshere, Marian Lindsay, Zammit, Stanley, Jones, Lisa Anne, Cardno, Alastair George, Kirov, George, Jones, Ian Richard, O'Donovan, Michael Conlon, Owen, Michael John and Craddock, Nicholas John 2006. Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder. Archives of General Psychiatry 63 (4) , pp. 366-373. 10.1001/archpsyc.63.4.366

Kirov, George, Nikolov, Ivan, Georgieva, Lyudmila, Escott-Price, Valentina, Owen, Michael John and O'Donovan, Michael Conlon 2006. Pooled DNA genotyping on Affymetrix SNP genotyping arrays. BMC Genomics 7 (1) , pp. 27-37. 10.1186/1471-2164-7-27
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Kirov, George and Markov, G. 2006. Abdominal compartment syndrome. Khirurgiia 6 , pp. 46-51.

Bakhsh, Ameen, Kirov, George, Gregory, John Welbourn, Williams, E. D. and Ludgate, Marian Elizabeth 2006. A new form of familial multi-nodular goitre with progression to differentiated thyroid cancer. Endocrine-Related Cancer 13 (2) , pp. 475-483. 10.1677/erc.1.01138

Norton, Nadine, Escott-Price, Valentina, Morris, Derek W., Bray, Nicholas John, Zammit, Stanley, Williams, Nigel Melville, Williams, Hywel John, Preece, Anna Charlotte, Dwyer, Sarah, Wilkinson, Jennifer C., Spurlock, Gillian, Kirov, George, Buckland, Paul Robert, Waddington, John L., Gill, Michael, Corvin, Aiden P., Owen, Michael John and O'Donovan, Michael John 2006. Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (1) , pp. 96-101. 10.1002/ajmg.b.30236

Lambert, D., Middle, F., Hamshere, Marian Lindsay, Segurado, R., Raybould, Rachel, Corvin, A., Green, E., O'Mahony, E., Nikolov, I., Mulcahy, T., Haque, S., Bort, S., Bennett, P., Norton, N., Owen, Michael John, Kirov, George, Lendon, C, Jones, L, Jones, I, Holmans, P, Gill, M and Craddock, Nicholas John 2006. 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 - Corrigendum. Molecular Psychiatry 11 (12) , pp. 1140-1143. 10.1038/sj.mp.4001917

Green, E. K., Norton, N., Peirce, T., Grozeva, D., Kirov, George, Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas John 2006. Evidence that a DISC1 frame-shift deletion associated with psychosis in a single family may not be a pathogenic mutation. Molecular Psychiatry 11 (9) , pp. 798-799. 10.1038/sj.mp.4001853

Blair, I. P., Chetcuti, A. F., Badenhop, R. F., Scimone, A., Moses, M. J., Adams, L. J., Craddock, Nicholas John, Green, E., Kirov, George, Owen, Michael John, Kwok, J. B. J., Donald, J. A., Mitchell, P. B. and Schofield, P. R. 2006. Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele. Molecular Psychiatry 11 (4) , pp. 372-383. 10.1038/sj.mp.4001784

Green, Elaine K., Baybould, Rachel, MacGregor, Stuart, Hyde, Sally, Young, Allan H., O'Donovan, Michael Conlon, Owen, Michael John, Kirov, George, Jones, Lisa, Jones, Ian Richard and Craddock, Nicholas John 2006. Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder: case-control study of over 3000 individuals from the UK. British Journal of Psychiatry 188 (1) , pp. 21-25. 10.1192/bjp.bp.105.009969

Lazarus, John Henry, Kirov, George and Harris, Brian Benjamin 2006. Effect of lithium on the thyroid and endocrine glands. In: Müller-Oerlinghausen, Bruno, Bauer, Michael and Grof, Paul eds. Lithium in Neuropsychiatry : The Comprehensive Guide, Abingdon: Informa UK, pp. 259-270. (10.3109/9780203007051.022)

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

Williams, H. J., Glaser, B., Williams, Nigel Melville, Norton, N., Zammit, Stanley, MacGregor, S., Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2005. No association between schizophrenia and polymorphisms in COMT in two large samples. American Journal of Psychiatry 162 (9) , pp. 1736-1738. 10.1176/appi.ajp.162.9.1736

Kirov, George, Tredget, John, John, R., Owen, Michael John and Lazarus, J. H. 2005. A cross-sectional and a prospective study of thyroid disorders in lithium-treated patients. Journal of affective disorders 87 (2-3) , pp. 313-317. 10.1016/j.jad.2005.03.010

Glaser, B1, Schumacher, J., Williams, H. J., Jamra, R. A., Ianakiev, N., Milev, R., Ohlraun, S., Schulze, T. G., Czerski, P. M., Hauser, J., Jonsson, E. G., Sedvall, G. C., Klopp, N., Illig, T., Becker, T., Propping, P., Williams, Nigel Melville, Cichon, S., Kirov, George, Rietschel, M., Murphy, K. C., O'Donovan, Michael Conlon, Nothen, M. M. and Owen, Michael John 2005. No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples. Biological psychiatry 58 (1) , pp. 78-80.

Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2005. Finding schizophrenia genes. The Journal of Clinical Investigation 115 (6) , pp. 1440-1448. 10.1172/JCI24759

Green, Elaine Karen, Raybould, Rachel, Macgregor, Stuart, Gordon-Smith, Katherine Mary, Heron, Jess, Hyde, Sally, Grozeva, Detelina Valentinova, Hamshere, Marian Lindsay, Williams, Nigel Melville, Owen, Michael John, O'Donovan, Michael Conlon, Jones, Lisa Anne, Jones, Ian Richard, Kirov, George and Craddock, Nicholas John 2005. Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder. Archives of general psychiatry 62 (6) , pp. 642-648. 10.1001/archpsyc.62.6.642

Tredget, John, Kirov, George and Dunn, E. 2005. Transcranial magnetic stimulation for patients with depression. Nursing Standard 19 (37) , pp. 49-50. 10.7748/ns2005.05.19.37.49.c3876

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

Tredget, John and Kirov, George 2005. Add-on topiramate reduces weight in overweight patients with affective disorders: a clinical case series. BMC Psychiatry 5 , p. 19. 10.1186/1471-244X-5-19

Kirov, George, Tredget, John, Dunn, E., Escott-Price, Valentina, Beer, R. and Khalid, N. 2005. Underpowered repetitive transcranial magnetic stimulation might not be an effective antidepressant treatment. Journal of Clinical Psychiatry 66 (4) , p. 543.

Glaser, B., Kirov, George, Green, E., Craddock, Nicholas John and Owen, Michael John 2005. Linkage disequilibrium mapping of bipolar affective disorder at 12q23-q24 provides evidence for association at CUX2 and FLJ32356. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 132B (1) , pp. 38-45. 10.1002/ajmg.b.30081

Dimitrova, A., Milanova, V., Krastev, S., Nikolov, I., Toncheva, D., Owen, Michael John and Kirov, George 2005. Association study of myo-inositol monophosphatase 2 (IMPA2) polymorphisms with bipolar affective disorder and response to lithium treatment. The Pharmacogenomics Journal 5 (1) , pp. 35-41. 10.1038/sj.tpj.6500273

Glaser, B., Kirov, George, Bray, Nicholas John, Green, E., O'Donovan, Michael Conlon, Craddock, Nicholas John and Owen, Michael John 2005. Identification of a potential Bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4. Molecular Psychiatry 10 (10) , pp. 920-927. 10.1038/sj.mp.4001689

Raybould, Rachel, Green, Elaine K., MacGregor, Stuart, Gordon-Smith, Katherine, Heron, Jess, Hyde, Sally, Caesar, Sian, Nikolov, Ivan, Williams, Nigel Melville, Jones, Lisa, O'Donovan, Michael Conlon, Owen, Michael John, Jones, Ian Richard, Kirov, George and Craddock, Nicholas John 2005. Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1). Biological psychiatry 57 (7) , pp. 696-701. 10.1016/j.biopsych.2005.01.018

Green, E., Elvidge, G., Jacobsen, N., Glaser, B., Jones, Ian Richard, O'Donovan, Michael Conlon, Kirov, George, Owen, Michael John and Craddock, Nicholas John 2005. Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-q24 region in two pedigrees with bipolar disorder and Darier's disease. American Journal of Psychiatry 162 (1) , pp. 35-42. 10.1176/appi.ajp.162.1.35

Farbrother, Jane Elizabeth, Kirov, George, Owen, Michael John and Guggenheim, Jeremy Andrew 2004. Family aggregation of high myopia: estimation of the sibling recurrence risk ratio. Investigative Ophthalmology and Visual Science 45 (9) , pp. 2873-2878. 10.1167/iovs.03-1155
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Farbrother, Jane Elizabeth, Kirov, George, Owen, Michael John, Pong-Wong, Ricardo, Haley, Chris S. and Guggenheim, Jeremy Andrew 2004. Linkage analysis of the genetic loci for high myopia on chromosomes 18p, 12q and 17q in 51 UK families. Investigative Ophthalmology and Visual Science 45 (9) , pp. 2879-2885. 10.1167/iovs.03-1156
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Norton, N, Escott-Price, Valentina, Morris, DW, Bray, Nicholas John, Zammit, Stanley, Williams, Nigel Melville, Williams, HJ, Preece, Anna, Dwyer, SL, Wilkinson, JC, Kirov, George, Buckland, Paul Robert, Waddington, JL, Gill, M, Corvin, AP, Owen, Michael John and O'Donovan, Michael Conlon 2004. Interaction between neuregulin 1 and its receptor ERBB4 increases susceptibility to schizophrenia [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 18.

Craddock, Nicholas John, Jones, Ian Richard, Kirov, George and Jones, L. 2004. The Bipolar Affective Disorder Dimension Scale (BADDS)--a dimensional scale for rating lifetime psychopathology in bipolar spectrum disorders. BMC Psychiatry 4 , p. 19. 10.1186/1471-244X-4-19

Turic, D., Langley, Kate, Kirov, George, Owen, Michael John, Thapar, Anita and O'Donovan, Michael Conlon 2004. Direct analysis of the genes encoding G proteins G alpha T2, G alpha o, G alpha Z in ADHD. American Journal of Medical Genetics 127B (1) , pp. 68-72. 10.1002/ajmg.b.20173

Kirov, George, Ivanov, Dobril Kirilov, Williams, Nigel Melville, Preece, Anna Charlotte, Nikolov, Ivan, Milev, Radoi, Koleva, Svetlinka, Dimitrova, Albena, Toncheva, Draga, O'Donovan, Michael Conlon and Owen, Michael John 2004. Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria. Biological psychiatry 55 (10) , pp. 971-975. 10.1016/j.biopsych.2004.01.025

Williams, Nigel Melville, Preece, Anna, Mortis, DW, Spurlock, Gillian, Bray, Nicholas John, Stephens, M, Norton, N, Williams, H, Clement, M, Dwyer, S, Curran, C, Wilkinson, J, Escott-Price, Valentina, Waddington, JL, Gill, M, Corvin, AP, Zammit, Stanley, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2004. Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1). Archives of General Psychiatry 61 (4) , pp. 336-344. 10.1001/archpsyc.61.4.336

Williams, Nigel Melville, Preece, Anna Charlotte, Spurlock, Gillian, Norton, Nadine, Williams, Hywel John, McCreadie, Robin G, Buckland, Paul Robert, Sharkey, Val, Chowdari, Kodavali V., Zammit, Stanley, Nimgaonkar, Vishwajit, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2004. Support for RGS4 as a susceptibility gene for schizophrenia. Biological Psychiatry 55 (2) , pp. 192-195. 10.1016/j.biopsych.2003.11.002

Williams, Nigel Melville, Preece, Anna Charlotte, Morris, D. W., Spurlock, Gillian, Bray, Nicholas John, Stephens, Mark Keith, Norton, Nadine, Williams, Hywel John, Clement, Mathew, Dwyer, Sarah Lynne, Curran, Catherine, Wilkinson, Jennifer Camilla, Escott-Price, Valentina, Waddington, J. L., Gill, M., Corvin, A. P., Zammit, Stanley, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2004. Identification in two independent samples of a novel schizophrenia risk haplotype of the dystobrevin binding protein gene (DTNBP1). Archives of general psychiatry 61 (4) , pp. 336-344. 10.1001/archpsyc.61.4.336

Cichon, Sven, Buervenich, Silvia, Kirov, George, Akula, Nirmala, Dimitrova, Albena, Green, Elaine, Schumacher, Johannes, Klopp, Norman, Becker, Tim, Ohlraun, Stephanie, Schulze, Thomas G, Tullius, Monja, Gross, Magdalena M, Jones, Lisa, Krastev, Stefan, Nikolov, Ivan, Hamshere, Marian Lindsay, Jones, Ian Richard, Czerski, Piotr M., Leszczynska-Rodziewicz, Anna, Kapelski, Pawel, Van Den Bogaert, Ann, Illig, Thomas, Hauser, Joanna, Maier, Wolfgang, Berrettini, Wade, Byerley, William, Coryell, William, Gershon, Elliot S., Kelsoe, John R., McInnis, Melvin G., Murphy, Dennis L., Nurnberger, John I., Reich, Theodore, Scheftner, William, O'Donovan, Michael Conlon, Propping, Peter, Owen, Michael John, Rietschel, Marcella, Nöthen, Markus M., McMahon, Francis J. and Craddock, Nicholas John 2004. Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin. Nature Genetics 36 (8) , pp. 783-784. 10.1038/ng0804-783

Ivanov, Dobril Kirilov, Kirov, George, Norton, Nadine, Williams, Hywel John, Williams, Nigel Melville, Nikolov, Ivan, Tzwetkova, R., Stambolova, S. M., Murphy, Kieran Christopher, Toncheva, Draga, Thapar, Anita, O'Donovan, Michael Conlon and Owen, Michael John 2003. Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis. The British Journal of Psychiatry 183 (5) , pp. 409-413. 10.1192/bjp.183.5.409

Kirov, George, Georgieva, Lyudmila, Williams, Nigel Melville, Nikolov, Ivan, Norton, Nadine, Toncheva, Draga, O'Donovan, Michael Conlon and Owen, Michael John 2003. Variation in the protocadherin - A gene cluster? Genomics 82 (4) , pp. 433-440. 10.1016/S0888-7543(03)00167-8

Williams, H.J., Williams, Nigel Melville, Spurlock, G., Norton, N., Zammit, Stanley, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2003. Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia. American Journal of Medical Genetics 120B (1) , pp. 42-46. 10.1002/ajmg.b.20049

Williams, H J, Williams, Nigel Melville, Spurlock, G, Norton, N, Ivanov, D, McCreadie, R G, Preece, A, Sharkey, V, Jones, S, Zammit, Stanley, Nikolov, I, Kehaiov, I, Thapar, Anita, Murphy, K C, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2003. Association between PRODH and schizophrenia is not confirmed. Molecular Psychiatry 8 (7) , pp. 644-645. 10.1038/sj.mp.4001276

Kirov, George and Korszun, A. 2003. The antidepressant debate should move on. British Journal of Psychiatry 182 (6) , p. 551. 10.1192/bjp.182.6.551

Georgieva, Lyudmila, Nikolov, Ivan, Poriazova, Nadezhda, Jones, Gaynor, Toncheva, Draga, Kirov, George and Owen, Michael John 2003. Genetic variation in the seven-pass transmembrane cadherin CELSR1. Psychiatric Genetics 13 (2) , pp. 103-106. 10.1097/01.ypg.0000057486.14812.03

Kirov, George, Georgieva, Lyudmila, Nikolov, Ivan, Zammit, Stanley, Jones, Gaynor, Poriazova, Nadezhda, Tolev, Todor, Owen, Richard, Jones, Sue and Owen, Michael John 2003. Association analysis of the HOPA12bp polymorphism in schizophrenia and manic depressive illness. American Journal of Medical Genetics 118B (1) , pp. 16-19. 10.1002/ajmg.b.10065

Farbrother, Jane Elizabeth, Kirov, George, Owen, Michael John and Guggenheim, Jeremy Andrew 2003. Linkage analysis of 18p, 12q and 17q high myopia loci in 51 UK families. Investigative ophthalmology & visual science 44 (E-Abst)

Børglum, A.D., Kirov, George, Craddock, Nicholas John, Mors, O., Muir, W., Murray, V., McKee, I., Collier, D.A., Ewald, H., Owen, Michael John, Blackwood, D. and Kruse, T. A. 2003. Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder. American Journal of Medical Genetics 117B (1) , pp. 18-22. 10.1002/ajmg.b.10030

Bray, Nicholas John, Kirov, George, Owen, RJ, Jacobsen, NJ, Georgieva, Lyudmila, Williams, HJ, Norton, N, Spurlock, Gillian, Jones, S, Zammit, Stanley, O'Donovan, Michael Conlon and Owen, Michael John 2002. Screening the protocadherin 8 (PCDH8) gene in schizophrenia [Conference Abstract]. American Journal of Medical Genetics 114 (7) , p. 844.

Dimitrova, Albena, Georgieva, Lyudmila, Nikolov, Ivan, Poriazova, Nadejda, Krastev, Stefan, Toncheva, Draga, Owen, Michael John and Kirov, George 2002. Major psychiatric disorders and the serotonin transporter gene (SLC6A4): family-based association studies. Psychiatric Genetics 12 (3) , pp. 137-141. 10.1097/00041444-200209000-00004

Bray, Nicholas John, Kirov, George, Owen, R. J., Jacobsen, N. J., Georgieva, Lyudmila, Williams, H. J., Norton, N., Spurlock, Gillian, Jones, S., Zammit, Stanley, O'Donovan, Michael Conlon and Owen, Michael John 2002. Screening the human protocadherin 8 (PCDH8) gene in schizophrenia. Genes, Brain and Behavior 1 (3) , pp. 187-191. 10.1034/j.1601-183X.2002.10307.x

Norton, Nadine, Kirov, George, Zammit, Stanley, Jones, Gaynor, Jones, Susan, Owen, Richard, Krawczak, Michael, Williams, Nigel Melville, O'Donovan, Michael Conlon and Owen, Michael John 2002. Schizophrenia and functional polymorphisms in the MAOA and COMT genes: No evidence for association or epistasis. American Journal of Medical Genetics 114 (5) , pp. 491-496. 10.1002/ajmg.10517

Georgieva, Lyudmila, Dimitrova, A., Nikolov, I., Koleva, S., Tsvetkova, R., Owen, Michael John, Toncheva, D. and Kirov, George 2002. Dopamine transporter gene (DAT1) VNTR polymorphism in major psychiatric disorders: family-based association study in the Bulgarian population. Acta Psychiatrica Scandinavica 105 (5) , pp. 396-399. 10.1034/j.1600-0447.2002.1o174.x

Norton, Nadine, Williams, Nigel Melville, Williams, Hywel J., Spurlock, Gillian, Kirov, George, Morris, Derek W., Hoogendoorn, Bastiaan, Owen, Michael John and O'Donovan, Michael Conlon 2002. Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools. Human Genetics 110 (5) , pp. 471-478. 10.1007/s00439-002-0706-6

Kirov, George 2002. Use of a lithium analyzer machine in a mood disorders clinics. Journal of affective disorders 68 (1) , p. 120.

Williams, Nigel Melville, Spurlock, Gillian, Norton, Nadine, Williams, Hywel John, Hamshere, Marian Lindsay, Krawczak, Michael, Kirov, George, Nikolov, Ivan, Georgieva, Lyudmila, Jones, S., Cardno, Alastair George, O'Donovan, Michael Conlon and Owen, Michael John 2002. Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach. Molecular Psychiatry 7 (10) , pp. 1092-1100. 10.1038/sj.mp.4001188

Sklar, P., Gabriel, S. B., McInnis, M. G., Bennett, P., Lim, Y-M, Tsan, G., Schaffner, S., Kirov, George, Jones, Ian Richard, Owen, Michael John, Craddock, Nicholas John, DePaulo, J. R. and Lander, E. S. 2002. Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Molecular Psychiatry 7 (6) , p. 579. 10.1038/sj.mp.4001058

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

O'Mahony, E., Corvin, A., O'Connell, R., Comerford, C., Larsen, B., Jones, Ian Richard, McCandless, F., Kirov, George, Cardno, A. G., Craddock, Nicholas John and Gill, M. 2002. Sibling pairs with affective disorders: resemblance of demographic and clinical features. Psychological Medicine 32 (1) , pp. 55-61. 10.1017/S0033291701004986

Kirov, George, Lowry, C. A., Stephens, M., Oldfield, S., O'Donovan, Michael Conlon, Lightman, S. L. and Owen, Michael John 2001. Screening ABCG1, the human homologue of the Drosophila white gene, for polymorphisms and association with bipolar affective disorder. Molecular Psychiatry 6 (6) , pp. 671-677. 10.1038/sj.mp.4000899

Stephens, M, Kirov, George and Owen, Michael John 2001. ADARB1, a brain specific member of the RNA-specific adenosine deaminase family and bipolar affective disorder. American Journal of Medical Genetics 105 (7) , p. 622.

Kirov, George, Stehens, M. and Owen, Michael John 2001. Screening of three candidate genes in the bipolar candidate region on chromosome 21q22.3. American Journal of Medical Genetics 105 (7) , p. 612.

Williams, H., Kirov, George, Meyer, J., Lesch, K. P. and Owen, Michael John 2001. Further analysis of KIAA0027 in schizophrenic patients. American Journal of Medical Genetics 105 (7) , p. 561.

Bowen, Timothy, Ashworth, Lindsay, Kirov, George, Guy, Carol, Jones, Ian Richard, McCandless, Fiona, Craddock, Nicholas John, O'Donovan, Michael Conlon and Owen, Michael John 2000. No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorder. Bipolar Disorders 2 (4) , pp. 328-331. 10.1034/j.1399-5618.2000.020406.x

Kirov, George, Stephens, M. and Owen, Michael John 2000. Examining the 4p16 region for association with bipolar disorder using DNA pooling. American Journal of Medical Genetics 96 (4) , p. 548.

O'Mahony, E., Corvin, A., O'Connell, R., Comerford, C., Larsen, B., Jones, Ian Richard, McCandless, F., Kirov, George, Craddock, Nicholas John and Gill, M. J. 2000. Clinical similarities in siblings with bipolar disorder. American Journal of Medical Genetics 96 (4) , p. 514.

Kirov, George, Nikolov, I., Milanova, V., Roglev, M. and Jivkov, L. 2000. Comparison between clinical and demographic characteristics of bipolar patients collected in two different countries. American Journal of Medical Genetics 96 (4) , p. 506.

Guggenheim, J. A., Kirov, George and Hodson, S. A. 2000. The heritability of high myopia: a reanalysis of Goldschmidt's data. Journal of Medical Genetics 37 (3) , pp. 227-231. 10.1136/jmg.37.3.227

Kirov, George, Stephens, M., Williams, Nigel Melville, O'Donovan, Michael Conlon and Owen, Michael John 2000. Automated genotyping of single-nucleotide polymorphisms by extension of fluorescently labelled primers: analysis of individual and pooled DNA samples. Balkan Journal of Medical Genetics 3 , pp. 23-28.

Kirov, George, Williams, Nigel Melville, Sham, P., Craddock, Nicholas John and Owen, Michael John 2000. Pooled genotyping of microsatellite markers in parent-offspring trios. Genome Research 10 (1) , pp. 105-115.

Hoogendoorn, Bastiaan, Norton, Nadine, Kirov, George, Williams, Nigel Melville, Hamshere, Marian Lindsay, Spurlock, Gillian, Austin, Jehannine, Stephens, Mark, Buckland, Paul Robert, Owen, Michael John and O'Donovan, Michael Conlon 2000. Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools. Human Genetics 107 (5) , pp. 488-493. 10.1007/s004390000397

Kirov, George, Norton, N., Jones, Ian Richard, McCandless, F., Craddock, Nicholas John and Owen, Michael John 1999. A functional polymorphism in the promoter of monoamine oxidase A gene and bipolar affective disorder. International Journal of Neuropsychopharmacology 2 (4) , pp. 293-298. 10.1017/s1461145799001601

Borglum, A. D., Bruun, T. G., Kjeldsen, T. E., Ewald, H., Mors, O., Kirov, George, Russ, C, Freeman, B., Collier, D. A. and Kruse, T. A. 1999. Two novel variants in the DOPA decarboxylase gene: association with bipolar affective disorder. Molecular Psychiatry 4 (6) , pp. 545-551. 10.1038/sj.mp.4000559

Kirov, George, Jones, Ian Richard, McCandless, F., Craddock, Nicholas John and Owen, Michael John 1999. Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5. Molecular Psychiatry 4 (6) , pp. 558-565.

Kirov, George and Owen, Michael John 1999. Identification of new microsatellite markers on chromosome 4p16. American Journal of Human Genetics 65 (4) , A257-A257.

Bowen, Timothy, Kirov, George, Gill, M., Spurlock, Gillian, Vallada, H. P., Murray, R. M., McGuffin, P., Collier, D. A., Owen, Michael John and Craddock, Nicholas John 1999. Linkage studies of bipolar disorder with chromosome 18 markers. American Journal of Medical Genetics 15 (88) , pp. 503-509. 10.1002/(SICI)1096-8628(19991015)88:5<503::AID-AJMG13>3.0.CO;2-U

Petouni, M., Bolonna, A. A., Arranz, M. J., Martinez, M. J., Collier, D. A., Kirov, George and Kerwin, R. W. 1999. Association study between genetic variants in the alpha- adrenergic receptor genes and bipolar affective disorder. Molecular Psychiatry 4 , S112-S112.

Borglum, A. D., Bruun, T. G., Hampson, M., Kjeldsen, T. E., Lodge, P., Ewald, H., Mors, O., Kirov, George, Muir, W., Murray, V., Russ, C., Freeman, B., Blackwood, D., Collier, D. A. and Kruse, T. A. 1999. Association study of the DOPA decarboxylase gene in bipolar affective disorder and schizophrenia. Molecular Psychiatry 4 , S103-S104.

Birkett, J. T. P., Kirov, George, Arranz, M. J., Murray, R. M., Collier, D. A. and Kerwin, R. W. 1999. Association between a 2030-G/A substitution in the human myo-inositol monophosphatase gene (IMPA) and bipolar disorder and schizophrenia. Molecular Psychiatry 4 , S103-S103.

Williams, Nigel Melville, Bowen, Timothy, Kirov, George, Williams, H., Hoogendorn, B., Asherson, P. and Owen, Michael John 1999. Polymorphism screening and association studies of the Wolfram syndrome gene in schizophrenia. Molecular Psychiatry 4 (supp1) , S42-S42.

Kirov, George, Rees, M., Jones, Ian Richard, McCandless, F, Owen, Michael John and Craddock, Nicholas John 1999. Bipolar disorder and the serotonin transporter gene: a family-based association study. Psychological Medicine -London- 29 (5) , pp. 1249-1254. 10.1017/s003329179900882x

Kirov, George and Murray, R. M. 1999. Ethnic differences in the presentation of bipolar affective disorder. European Psychiatry 14 (4) , pp. 199-204.

Li, T., Liu, X., Sham, P. C., Aitchison, K. J., Cai, G., Arranz, M. J., Deng, H., Liu, J., Kirov, George, Murray, R. M. and Collier, D. A. 1999. Association analysis between dopamine receptor genes and bipolar affective disorder. Psychiatry Research 86 (3) , pp. 193-201. 10.1016/S0165-1781(99)00034-7

Bolonna, A. A., Markoff, A. J., Munro, J., Kirov, George and Kerwin, R. W. 1999. An investigation of a structural polymorphism in the mGluR7 gene in association with schizophrenia. Schizophrenia Research 36 (1-3) , p. 99.

Kirov, George, Owen, Michael John, Jones, I., McCandless, F. and Craddock, Nicholas John 1999. Tryptophan hydroxylase gene and manic-depressive illness [letter]. Archives of General Psychiatry 56 (1) , pp. 98-99. 10.1001/archpsyc.56.1.98

Kirov, George, Jones, Ian Richard, McCandless, F., Craddock, Nicholas John and Owen, Michael John 1998. Family-based association studies of candidate genes in bipolar disorder. American Journal of Medical Genetics 81 (6) , pp. 476-477.

Williams, Nigel Melville, Kirov, George, Craddock, Nicholas John and Owen, Michael John 1998. Screening the critical region on chromosome 4p with DNA pooling for association with bipolar disorder. American Journal of Medical Genetics 81 (6) , p. 486.

Birkett, J. T. P., Kirov, George, Powell, J., Murray, R. M., Kerwin, R. W. and Collier, D. A. 1998. No association between a variable number of tandem repeat (VNTR) in the 3 ' untranslated region of the dopamine transporter gene (DAT1) and bipolar affective disorder. American Journal of Medical Genetics 81 (6) , pp. 500-501.

Kaneva, R., Milanova, V., Onchev, G., Stoyanova, V., Chakarova, C. H., Nikolova, A., Hallmayer, J., Belemezova, M., Milenska, T., Kirov, George, Kremensky, I., Kalaydjieva, L. and Jablensky, A. 1998. A linkage study of affective disorders in two Bulgarian Gypsy families: results for candidate regions on chromosomes 18 and 21. Psychiatric Genetics 8 (4) , pp. 245-249. 10.1097/00041444-199808040-00008

Arranz, M. J., Munro, J., Sham, P., Kirov, George, Murray, R. M., Collier, D. A. and Kerwin, R. W. 1998. Meta-analysis of studies on genetic variation in 5-HT2A receptors and clozapine response. Schizophrenia Research 32 (2) , pp. 93-99. 10.1016/S0920-9964(98)00032-2

Kirov, George 1998. Thyroid disorders in lithium-treated patients. Journal of affective disorders 50 (1) , pp. 33-40.

Kirov, George, Murphy, K. C., Arranz, M. J., Jones, Ian Richard, McCandless, F., Kunugi, H., Murray, R. M., McGuffin, P., Collier, D. A., Owen, Michael John and Craddock, Nicholas John 1998. Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder. Molecular Psychiatry 3 (4) , pp. 342-345. 10.1038/sj.mp.4000385

Kemp, R., Kirov, George, Everitt, B., Hayward, P. and David, A. 1998. Randomised controlled trial of compliance therapy. 18-month follow-up. British Journal of Psychiatry 172 , pp. 413-419. 10.1192/bjp.172.5.413

Healey, A., Knapp, M., Astin, J., Beecham, J., Kemp, R., Kirov, George and David, A 1998. Cost-effectiveness evaluation of compliance therapy for people with psychosis. British Journal of Psychiatry 172 , pp. 420-424. 10.1192/bjp.172.5.420

Holmes, C., Russ, C., Kirov, George, Aitchison, K. J., Powell, J. F., Collier, D. A. and Lovestone, S. 1998. Apolipoprotein E: depressive illness, depressive symptoms, and Alzheimer's disease. Biological psychiatry 43 (3) , pp. 159-164. 10.1016/S0006-3223(97)00326-0

Padareva, V., Djoumaliisky, S., Touleshkov, N. and Kirov, George 1998. Modification of blowing agent system based on sodium bicarbonate with activated natural zeolite. Journal of Materials Science Letters 17 (2) , pp. 107-109.

Kirov, George, Kemp, R., Kirov, K. and David, A. S. 1998. Religious faith after psychotic illness. Psychopathology 31 (5) , pp. 234-245. 10.1159/000029045

Arranz, M. J., Munro, J., Owen, Michael John, Spurlock, G., Sham, P. C., Zhao, J., Kirov, George, Collier, D. A. and Kerwin, R. W. 1998. Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine. Molecular Psychiatry 3 (1) , pp. 61-66. 10.1038/sj.mp.4000348

David, A. S., Kemp, R., Kirov, George, Everitt, B. and Hayward, P. 1998. Improving insight and compliance: Predictions and consequences. Schizophrenia Research 29 (1-2) , pp. 34-35. 10.1016/S0920-9964(97)88375-2

Arranz, M. J., Munro, J., Collier, D. A., Kirov, George and Kerwin, R. W. 1998. Genetic variation in the 5-HT3 receptor gene: No association with schizophrenia or drug response. Schizophrenia Research 29 (1-2) , pp. 127-128.

Arranz, M. J., Munro, J., Li, T., Collier, D. A., Kirov, George and Kerwin, R. W. 1998. A polymorphism in the promoter region of the dopamine D2 receptor gene (DRD2) and drug response: Association studies. Schizophrenia Research 29 (1-2) , p. 127.

Vallada, H. P., Vasques, L., Curtis, D, Zatz, M., Kirov, George, Lauriano, V., Gentil, V., Murray, R. M., McGuffin, P., Owen, Michael John, Gill, M., Craddock, Nicholas John and Collier, D. A. 1998. Linkage analysis between bipolar affective disorder and markers on chromosome X. Psychiatric Genetics 8 (3) , pp. 183-186. 10.1097/00041444-199800830-00008

Dawson, E., Kirov, George, Hutchison, G., Murray, R. and Powell, J. F. 1997. The brain cannabinoid receptor gene and bipolar affective disorders. American Journal of Medical Genetics 74 (6) , pp. 613-614.

Arranz, M. J., Munro, J., Kirov, George, Kerwin, R. W. and Collier, D. A. 1997. Novel polymorphisms detected in the 5-HT3 receptor gene: Association studies with schizophrenia and clozapine response. American Journal of Medical Genetics 74 (6) , p. 615.

Craddock, Nicholas John, Jones, Ian Richard, McCandless, F., Kirov, George and Cardno, A. G. 1997. Dimensional classification for use in biological studies of bipolar disorder. American Journal of Medical Genetics 74 (6) , p. 588.

Bolonna, A. A., Makoff, A. J., Collier, D. A., Kirov, George, Arranz, M. J. and Kerwin, R. W. 1997. Analysis of the NMDA receptor in schizophrenia. American Journal of Medical Genetics 74 (6) , p. 631.

Vallada, H. P., Vasques, L., Curtis, D., Kirov, George, Gentil, V., Zatz, M., Murray, R. M., McGuffin, P., Owen, Michael John, Gill, M., Craddock, Nicholas John and Collier, D. A. 1997. Linkage studies in bipolar affective disorder with markers on chromosome Xq25-27. American Journal of Medical Genetics 74 (6) , pp. 679-680.

Kunugi, H., Vallada, H. P., Hoda, F., Kirov, George, Gill, M., Aitchison, K. J., Ball, D., Arranz, M. J., Murray, R. M. and Collier, D. A. 1997. No evidence for an association of affective disorders with high- or low-activity allele of catechol-o-methyltransferase gene. Biological psychiatry 42 (4) , pp. 282-285. 10.1016/S0006-3223(96)00366-6

Kirov, George, Murray, R. M., Seth, R. V. and Feeney, S. 1997. Observations on switching patients with schizophrenia to risperidone treatment. Risperidone Switching Study Group. Acta Psychiatrica Scandinavica 95 (5) , pp. 439-443. 10.1111/j.1600-0447.1997.tb09659.x

Arranz, M. J., Erdmann, J., Kirov, George, Rietschel, M., Sodhi, M., Albus, M., Ball, D., Maier, W., Davies, N., Franzek, E., Abusaad, I., Weigelt, B., Murray, R., Shimron-Abarbanell, D., Kerwin, R., Propping, P., Sham, P., Nothen, N. M. and Collier, D. M. 1997. 5-HT2A receptor and bipolar affective disorder: association studies in affected patients. Neuroscience Letters 224 (2) , pp. 95-98. 10.1016/S0304-3940(97)13456-5

Kirov, George and Murray, R. 1997. The molecular genetics of schizophrenia: progress so far. Molecular Medicine Today 3 (3) , pp. 124-130. 10.1016/S1357-4310(96)10060-5

Arranz, M.J., Munro, J., Sham, P., Zhao, J., Kirov, George, Sodhi, M., Spurlock, G., Owen, Michael John, Collier, D.A. and Kerwin, R. 1997. Polymorphisms in the 5-HT2A receptor gene and promoter region associated with clozapine response. Schizophrenia Research 24 (1-2) , p. 90. 10.1016/S0920-9964(97)82243-8

Sodhi, Monsheel S., Kirov, George, Aitchison, Katherine J., Arranz, Maria J., Collier, David A. and Kerwin, Robert W. 1997. Allelic variation of the 5-HT2C receptor in psychosis. Schizophrenia Research 24 (1-2) , p. 90. 10.1016/S0920-9964(97)82246-3

Bolonna, A.A., Makoff, A.J., Collier, D.A., Kirov, George, Munro, J., Arranz, M.J. and Kerwin, R.W. 1997. An investigation of the GLUR6 receptor gene (GRIK2) in schizophrenia. Schizophrenia Research 24 (1-2) , p. 93. 10.1016/S0920-9964(97)82252-9

Li, T., Holmes, C., Sham, P. C., Vallada, H., Birkett, J., Kirov, George, Lesch, K. P., Powell, J., Lovestone, S. and Collier, D. 1997. Allelic functional variation of serotonin transporter expression is a susceptibility factor for late onset Alzheimer's disease. NeuroReport 8 (3) , pp. 683-686. 10.1097/00001756-199702100-00021

Collier, D. A., Stober, G., Li, T., Heils, A., Catalano, M., Di Bella, D., Arranz, M. J., Murray, R. M., Vallada, H. P., Bengel, D., Muller, C. R., Roberts, G. W., Smeraldi, E., Kirov, George, Sham, P. and Lesch, K. P. 1996. A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders. Molecular Psychiatry 1 (6) , pp. 453-460.

Vallada, H., Craddock, Nicholas John, Vasques, L., Curtis, D., Kirov, George, Lauriano, V., Gentil, V., Passos-Beuno, R., Murray, R. M., Zatz, M., McGuffin, P., Powell, J. F., Gill, M., Owen, Michael John and Collier, D. A. 1996. Linkage studies in bipolar affective disorder with markers on chromosome 21. Journal of affective disorders 41 (3) , pp. 217-221. 10.1016/s0165-0327(96)00055-9

Arranz, M. J., Collier, D. A., Munro, J., Sham, P., Kirov, George, Sodhi, M., Roberts, G., Price, J. and Kerwin, R. W. 1996. Analysis of a structural polymorphism in the 5-HT2A receptor and clinical response to clozapine. Neuroscience Letters 217 (2-3) , pp. 177-178. 10.1016/0304-3940(96)13094-9

Collier, D. A., Arranz, M. J., Sham, P., Battersby, S., Vallada, H., Gill, P., Aitchison, K. J., Sodhi, M., Li, T., Roberts, G. W., Smith, B., Morton, J., Murray, R. M., Smith, D. and Kirov, George 1996. The serotonin transporter is a potential susceptibility factor for bipolar affective disorder. NeuroReport 7 (10) , pp. 1675-1679. 10.1097/00001756-199607080-00030

Kirov, George, Jones, P. B., Harvey, I., Lewis, S. W., Toone, B. K., Rifkin, L., Sham, P. and Murray, R. M. 1996. Do obstetric complications cause the earlier age at onset in male than female schizophrenics? Schizophrenia Research 20 (1-2) , pp. 117-124. 10.1016/0920-9964(95)00063-1

Arranz, M.J., Kirov, George, Sodhi, M.S., Ball, D.M., Kerwin, R.W. and Collier, D.A. 1996. 5-HT2A polymorphisms and mental disorders. Schizophrenia Research 18 (2-3) , p. 164. 10.1016/0920-9964(96)85523-X

Sodhi, M. S., Kirov, George, Arranz, M. J., Ball, D. M., Aitchison, K. J., Kerwin, R. W. and Collier, D. A. 1996. Association between psychoses and allelic variation in the 5-HT2C receptor gene. Schizophrenia Research 18 (2-3) , IXB2.

Kemp, R., Kirov, George, Hayward, P. and David, A. 1996. A randomised controlled trial of compliance therapy in psychosis: Follow-up results and predictors of outcome. Schizophrenia Research 18 (2-3) , p. 135. 10.1016/0920-9964(96)85452-1

Kirov, George, Jones, P. and Murray, R. 1994. Disappearance of gender differences in age at onset in schizophrenics with a familial loading. Acta Psychiatrica Scandinavica 90 (3) , pp. 236-237. 10.1111/j.1600-0447.1994.tb01583.x

Kirov, George, Jones, P. and Lewis, S.W. 1994. Prevalence of Delusional Misidentification Syndromes. Psychopathology 27 (3-5) , pp. 148-149. 10.1159/000284862

Kirov, George, Birch, John, Steadman, Philip and Ramsey, Greig 1994. Plasma magnesium levels in a population of psychiatric patients: correlations with symptoms. Neuropsychobiology 30 (2-3) , pp. 73-78. 10.1159/000119139

Kirov, George 1990. Slowly progressive schizophrenia. British Journal of Psychiatry 157 , p. 457.

Kirov, George and Tsachev, Kamen N. 1990. Magnesium, Schizophrenia and Manic-Depressive Disease. Neuropsychobiology 23 (2) , pp. 79-81. 10.1159/000119431

Nikolova, S., Vinarova, M., Kirov, George and Bradvarova, I. 1987. [In vitro research on the interaction of natural zeolites with diploid cells from the human embryonic lung]. Problemi Na Khigienata 12 , pp. 133-141.

This list was generated on Wed Aug 23 06:56:54 2017 BST.