Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

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

期刊名称Nature Neuroscience
作者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
印刷ISSN1097-6256
电子ISSN1546-1726
文件大小734.69KB
发表时间2016-3-14
DOI10.1038/nn.4267

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Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders