The influence of risk factors on the onset and outcome of psychosis: What we learned from the GAP study von Murray, R.M., Mondelli, V., Stilo, S.A., Trotta, A., Sideli, L., Ajnakina, O., Ferraro, L., Vassos, E., Iyegbe, C., Schoeler, T., Bhattacharyya, S., Marques, T.R., Dazzan, P., Lopez-Morinigo, J., Colizzi, M., O'Connor, J., Falcone, M.A., Quattrone, D., Rodriguez, V., Tripoli, G., La Barbera, D., La Cascia, C., Alameda, L., Trotta, G., Morgan, C., Gaughran, F., David, A., Di Forti, M.

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Clinical correlates of vitamin D deficiency in established psychosis von Lally, J, Gardner-Sood, P, Firdosi, M, Iyegbe, C, Stubbs, B, Greenwood, K, Murray, R, Smith, S, Howes, O, Gaughran, F

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Protein kinase B (AKT1) genotype mediates sensitivity to cannabis-induced impairments in psychomotor control von Bhattacharyya, S., Iyegbe, C., Atakan, Z., Martin-Santos, R., Crippa, J. A., Xu, X., Williams, S., Brammer, M., Rubia, K., Prata, D., Collier, D. A., McGuire, P. K.

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Differences in cannabis-related experiences between patients with a first episode of psychosis and controls von Bianconi, F., Bonomo, M., Marconi, A., Kolliakou, A., Stilo, S. A., Iyegbe, C., Gurillo Muñoz, P., Homayoun, S., Mondelli, V., Luzi, S., Dazzan, P., Prata, D., La Cascia, C., O'Connor, J., David, A., Morgan, C., Murray, R. M., Lynskey, M., Di Forti, M.

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Associations between psychosis endophenotypes across brain functional, structural, and cognitive domains von Blakey, R., Ranlund, S., Zartaloudi, E., Cahn, W., Calafato, S., Colizzi, M., Crespo-Facorro, B., Daniel, C., Díez-Revuelta, Á., Di Forti, M., Iyegbe, C., Jablensky, A., Jones, R., Hall, M.-H., Kahn, R., Kalaydjieva, L., Kravariti, E., Lin, K., McDonald, C., McIntosh, A. M., Picchioni, M., Powell, J., Presman, A., Rujescu, D., Schulze, K., Shaikh, M., Thygesen, J. H., Toulopoulou, T., Van Haren, N., Van Os, J., Walshe, M., Murray, R. M., Bramon, E.

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Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations von Peterson, Roseann E., Kuchenbaecker, Karoline, Walters, Raymond K., Chen, Chia-Yen, Popejoy, Alice B., Periyasamy, Sathish, Lam, Max, Iyegbe, Conrad, Strawbridge, Rona J., Brick, Leslie, Carey, Caitlin E., Martin, Alicia R., Meyers, Jacquelyn L., Su, Jinni, Chen, Junfang, Edwards, Alexis C., Kalungi, Allan, Koen, Nastassja, Majara, Lerato, Schwarz, Emanuel, Smoller, Jordan W., Stahl, Eli A., Sullivan, Patrick F., Vassos, Evangelos, Mowry, Bryan, Prieto, Miguel L., Cuellar-Barboza, Alfredo, Bigdeli, Tim B., Edenberg, Howard J., Huang, Hailiang, Duncan, Laramie E.

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Associations between the schizophrenia susceptibility gene ZNF804A and clinical outcomes in psychosis von Wickramasinghe, A, Tulloch, A D, Hayes, R D, Chang, C-K, Broadbent, M, Di Forti, M, Murray, R M, Iyegbe, C, Stewart, R

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The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability von Singh, Tarjinder, Walters, James T R, Johnstone, Mandy, Curtis, David, Suvisaari, Jaana, Torniainen, Minna, Rees, Elliott, Iyegbe, Conrad, Blackwood, Douglas, McIntosh, Andrew M, Kirov, Georg, Geschwind, Daniel, Murray, Robin M, Di Forti, Marta, Bramon, Elvira, Gandal, Michael, Hultman, Christina M, Sklar, Pamela, Palotie, Aarno, Sullivan, Patrick F, O'Donovan, Michael C, Owen, Michael J, Barrett, Jeffrey C

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Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders von 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, Nick, Daly, Mark J, Danesh, John, DiForti, Marta, Foster, Alison, Freimer, Nelson B, Geschwind, Daniel, Johnstone, Mandy, Joss, Shelagh, Kirov, Georg, 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 T R, Williams, Hywel, Sullivan, Patrick F, Hurles, Matthew E, O'Donovan, Michael C, Palotie, Aarno, Owen, Michael J, Barrett, Jeffrey C

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Precision Medicine Approaches to Vascular Disease von Miller, Clint L., Kontorovich, Amy R., Hao, Ke, Ma, Lijiang, Iyegbe, Conrad, Björkegren, Johan L.M., Kovacic, Jason C.

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Precision Medicine Approaches to Vascular Disease: JACC Focus Seminar 2/5 von Miller, Clint L, Kontorovich, Amy R, Hao, Ke, Ma, Lijiang, Iyegbe, Conrad, Björkegren, Johan L M, Kovacic, Jason C

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Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study von Thygesen, Johan H., Presman, Amelia, Harju-Seppänen, Jasmine, Irizar, Haritz, Jones, Rebecca, Kuchenbaecker, Karoline, Lin, Kuang, Alizadeh, Behrooz Z., Austin-Zimmerman, Isabelle, Bartels-Velthuis, Agna, Bhat, Anjali, Bruggeman, Richard, Cahn, Wiepke, Calafato, Stella, Crespo-Facorro, Benedicto, de Haan, Liewe, de Zwarte, Sonja M. C., Di Forti, Marta, Díez-Revuelta, Álvaro, Hall, Jeremy, Hall, Mei-Hua, Iyegbe, Conrad, Jablensky, Assen, Kahn, Rene, Kalaydjieva, Luba, Kravariti, Eugenia, Lawrie, Stephen, Luykx, Jurjen J., Mata, Igancio, McDonald, Colm, McIntosh, Andrew M., McQuillin, Andrew, Muir, Rebecca, Ophoff, Roel, Picchioni, Marco, Prata, Diana P., Ranlund, Siri, Rujescu, Dan, Rutten, Bart P. F., Schulze, Katja, Shaikh, Madiha, Schirmbeck, Frederike, Simons, Claudia J. P., Toulopoulou, Timothea, van Amelsvoort, Therese, van Haren, Neeltje, van Os, Jim, van Winkel, Ruud, Vassos, Evangelos, Walshe, Muriel, Weisbrod, Matthias, Zartaloudi, Eirini, Bell, Vaughan, Powell, John, Lewis, Cathryn M., Murray, Robin M., Bramon, Elvira

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Genome-Wide Association Study of Obsessive-Compulsive Symptoms including 33,943 individuals from the general population von Strom, Nora I., Burton, Christie L., Iyegbe, Conrad, Silzer, Talisa, Antonyan, Lilit, Pool, René, Lemire, Mathieu, Crowley, James J., Hottenga, Jouke-Jan, Ivanov, Volen Z., Larsson, Henrik, Lichtenstein, Paul, Magnusson, Patrik, Rück, Christian, Schachar, Russell, Wu, Hei Man, Cath, Danielle, Crosbie, Jennifer, Mataix-Cols, David, Boomsma, Dorret I., Mattheisen, Manuel, Meier, Sandra M., Smit, Dirk J. A., Arnold, Paul D.

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Meta-analysis of genome-wide association studies of hoarding symptoms in 27,537 individuals von Strom, Nora I, Smit, Dirk J A, Silzer, Talisa, Iyegbe, Conrad, Burton, Christie L, Pool, René, Lemire, Mathieu, Crowley, James J, Hottenga, Jouke-Jan, Ivanov, Volen Z, Larsson, Henrik, Lichtenstein, Paul, Magnusson, Patrik, Rück, Christian, Schachar, Russell J, Wu, Hei Man, Meier, Sandra M, Crosbie, Jennifer, Arnold, Paul D, Mattheisen, Manuel, Boomsma, Dorret I, Mataix-Cols, David, Cath, Danielle

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Associations between psychosis endophenotypes across brain functional, structural, and cognitive domains von Blakey, R, Ranlund, S, Zartaloudi, E, Cahn, W, Calafato, S, Colizzi, M, Crespo-Facorro, B, Daniel, C, Díez-Revuelta, Á, Di Forti, M, Iyegbe, C, Jablensky, A, Jones, R, Hall, M.-H, Kahn, R, Kalaydjieva, L, Kravariti, E, Lin, K, McDonald, C, McIntosh, A. M, Picchioni, M, Powell, J, Presman, A, Rujescu, D, Schulze, K, Shaikh, M, Thygesen, J. H, Toulopoulou, T, Van Haren, N, Van Os, J, Walshe, M, Murray, R. M, Bramon, E,

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GENOME-WIDE ASSOCIATION STUDY OF OBSESSIVE-COMPULSIVE SYMPTOMS AND HOARDING SYMPTOMS IN THE GENERAL POPULATION von Strom, NI, Smit, DJA, Silzer, T, Iyegbe, C, Lemire, M, Burton, C, Hottenga, JJ, Pool, R, Boomsma, DI, Crosbie, J, Mataix-Cols, D, Mattheisen, M, Meier, SM, Cath, D, Arnold, PD

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An Examination of Polygenic Score Risk Prediction in Individuals With First-Episode Psychosis von Vassos, E, Di Forti, M, Coleman, J, Iyegbe, C, Prata, D, Euesden, J, O'Reilly, P, Curtis, C, Kolliakou, A, Patel, H, Newhouse, S, Traylor, M, Ajnakina, O, Mondelli, V, Marques, TR, Gardner-Sood, P, Aitchison, KJ, Powell, J, Atakan, Z, Greenwood, KE, Smith, S, Ismail, K, Pariante, C, Gaughran, F, Dazzan, P, Markus, HS, David, AS, Lewis, CM, Murray, RM, Breen, G

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Variant Creutzfeldt-Jakob disease is not associated with individual abilities to metabolise organophosphates von GAROFALO, O, MCFARLANE, EH, IYEGBE, C, WHATLEY, S A, CAMPBELL, I C, KOPP, N, WILL, R G

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Role of environmental confounding in the association between FKBP5 and first-episode psychosis von Ajnakina, O, Borges, S, Di Forti, M, Patel, Y, Xu, X, Green, P, Stilo, SA, Kolliakou, A, Sood, P, Marques, TR, David, AS, Prata, D, Dazzan, P, Powell, J, Pariante, C, Mondelli, V, Morgan, C, Murray, RM, Fisher, HL, Iyegbe, C

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Relationship Between Serum NMDA Receptor Antibodies and Response to Antipsychotic Treatment in First-Episode Psychosis von Pollak, TA, Vincent, A, Iyegbe, C, Coutinho, E, Jacobson, L, Rujescu, D, Stone, J, Jezequel, J, Rogemond, V, Jamain, S, Groc, L, David, A, Egerton, A, Kahn, RS, Honnorat, J, Dazzan, P, Leboyer, M, McGuire, P

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