Neuropsychological effects of the CSMD1 genome‐wide associated schizophrenia risk variant rs10503253 von Donohoe, G., Walters, J., Hargreaves, A., Rose, E.J., Morris, D.W., Fahey, C., Bellini, S., Cummins, E., Giegling, I., Hartmann, A.M., Möller, H.‐J., Muglia, P., Owen, M.J., Gill, M., O'Donovan, M.C., Tropea, D., Rujescu, D., Corvin, A.

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Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia von Carroll, L.S., Williams, H.J., Walters, J., Kirov, G., O'Donovan, M.C., Owen, M.J.

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Evaluating historical candidate genes for schizophrenia von Farrell, M S, Werge, T, Sklar, P, Owen, M J, Ophoff, R A, O'Donovan, M C, Corvin, A, Cichon, S, Sullivan, P F

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Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia von Ruderfer, D M, Fanous, A H, Ripke, S, McQuillin, A, Amdur, R L, Gejman, P V, O'Donovan, M C, Andreassen, O A, Djurovic, S, Hultman, C M, Kelsoe, J R, Jamain, S, Landén, M, Leboyer, M, Nimgaonkar, V, Nurnberger, J, Smoller, J W, Craddock, N, Corvin, A, Sullivan, P F, Holmans, P, Sklar, P, Kendler, K S

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P.4.016 Follow-up of schizophrenia genome-wide association studies implicates the MHC region in cognition von Walters, J, O'Donovan, M.C, Giegling, I, Rujescu, D, Owen, M.J

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De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia von Kirov, G, Pocklington, A J, Holmans, P, Ivanov, D, Ikeda, M, Ruderfer, D, Moran, J, Chambert, K, Toncheva, D, Georgieva, L, Grozeva, D, Fjodorova, M, Wollerton, R, Rees, E, Nikolov, I, 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, M C, Owen, M J

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Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction von Ayalew, M, Le-Niculescu, H, Levey, D F, Jain, N, Changala, B, Patel, S D, Winiger, E, Breier, A, Shekhar, A, Amdur, R, Koller, D, Nurnberger, J I, Corvin, A, Geyer, M, Tsuang, M T, Salomon, D, Schork, N J, Fanous, A H, O'Donovan, M C, Niculescu, A B

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Common alleles contribute to schizophrenia in CNV carriers von Tansey, K E, Rees, E, Linden, D E, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, P, Kirov, G, Walters, J, Owen, M J, O'Donovan, M C

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Copy number variation in bipolar disorder von Green, E K, Rees, E, Walters, J T R, Smith, K-G, Forty, L, Grozeva, D, Moran, J L, Sklar, P, Ripke, S, Chambert, K D, Genovese, G, McCarroll, S A, Jones, I, Jones, L, Owen, M J, O'Donovan, M C, Craddock, N, Kirov, G

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Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk von Moskvina, V, Craddock, N, Holmans, P, Nikolov, I, Pahwa, J S, Green, E, Owen, M J, O'Donovan, M C

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Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC von Hamshere, M L, Walters, J T R, Smith, R, Richards, A L, Green, E, Grozeva, D, Jones, I, Forty, L, Jones, L, Gordon-Smith, K, Riley, B, O'Neill, T, Kendler, K S, Sklar, P, Purcell, S, Kranz, J, Morris, D, Gill, M, Holmans, P, Craddock, N, Corvin, A, Owen, M J, O'Donovan, M C

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Copy number variation in schizophrenia in Sweden von 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, E, Kirov, G, O'Donovan, M C, Owen, M J, Walters, J, Scolnick, E, Sklar, P, Purcell, S, Hultman, C M, McCarroll, S A, Sullivan, P F

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The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia von Green, E K, Grozeva, D, Jones, I, Jones, L, Kirov, G, Caesar, S, Gordon-Smith, K, Fraser, C, Forty, L, Russell, E, Hamshere, M L, Moskvina, V, Nikolov, I, Farmer, A, McGuffin, P, Holmans, P A, Owen, M J, O'Donovan, M C, Craddock, N

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Schizophrenia genetics: emerging themes for a complex disorder von Kavanagh, D H, Tansey, K E, O'Donovan, M C, Owen, M J

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Association analysis of the glial cell line-derived neurotrophic factor ( GDNF ) gene in schizophrenia von Williams, H.J, Norton, N, Peirce, T, Dwyer, S, Williams, N.M, Moskvina, V, Owen, M.J, O'Donovan, M.C

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Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci von Andreassen, O A, Harbo, H F, Wang, Y, Thompson, W K, Schork, A J, Mattingsdal, M, Zuber, V, Bettella, F, Ripke, S, Kelsoe, J R, Kendler, K S, O'Donovan, M C, Sklar, P, McEvoy, L K, Desikan, R S, Lie, B A, Djurovic, S, Dale, A M

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Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia von Lips, E S, Cornelisse, L N, Toonen, R F, Min, J L, Hultman, C M, Holmans, P A, O'Donovan, M C, Purcell, S M, Smit, A B, Verhage, M, Sullivan, P F, Visscher, P M, Posthuma, D

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An examination of MUTED as a schizophrenia susceptibility gene von Gerrish, A, Williams, H, Moskvina, V, Owen, M.J, O'Donovan, M.C, Williams, N.M

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Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case–control sample von Green, E K, Hamshere, M, Forty, L, Gordon-Smith, K, Fraser, C, Russell, E, Grozeva, D, Kirov, G, Holmans, P, Moran, J L, Purcell, S, Sklar, P, Owen, M J, O'Donovan, M C, Jones, L, Jones, I R, Craddock, N

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Genome-wide analysis of over 106000 individuals identifies 9 neuroticism-associated loci von Smith, D.J, Escott-Price, V, Davies, G, Bailey, M.E.S, Colodro-Conde, L, Ward, J, Vedernikov, A, Marioni, R, Cullen, B, Lyall, D, Hagenaars, S.P, Liewald, D.C.M, Luciano, M, Gale, C.R, Ritchie, S.J, Hayward, C, Nicholl, B, Bulik-Sullivan, B, Adams, M, Couvy-Duchesne, B, Graham, N, Mackay, D, Evans, J, Smith, B.H, Porteous, D.J, Medland, S.E, Ma, Holmans, P, McIntosh, A.M, Pell, J.P, Deary, I.J, O'Donovan, M.C

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