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

著者: Swedish Schizophrenia Study, Tarjinder Singh, INTERVAL Study, DDD Study, Mitja Kurki, David Curtis, Shaun Purcell, Lucy Crooks, Jeremy F. McRae, Jaana Suvisaari, Himanshu Chheda, Douglas Blackwood, Gerome Breen, Olli Pietiläinen, Sebastian S. Gerety, Muhammad Ayub, Moira Blyth, Trevor Cole, David Collier, Eve L. Coomber, Nick Craddock, Mark J. Daly, John Danesh, Marta Di Forti, Alison Foster, Nelson B. Freimer, Daniel H. Geschwind, Mandy Johnstone, Shelagh Joss, George Kirov, Jarmo Körkkö, Outi Kuismin, Peter Holmans, Christina M. Hultman, Conrad Iyegbe, Jouko Lönnqvist, Minna Männikkö, Steve McCarroll, Peter McGuffin, Andrew M. McIntosh, Andrew McQuillin, Jukka S. Moilanen, Carmel Moore, Robin Murray, Ruth Newbury‐Ecob, Willem H. Ouwehand, Tiina Paunio, Elena Prigmore, Elliott Rees, David J. Roberts, Jennifer Sambrook, Pamela Sklar, David St Clair, Juha Veijola, James Walters, Hywel Williams, Patrick F. Sullivan, Matthew E. Hurles, Michael O‘Donovan, Aarno Palotie, Michael J. Owen, Jeffrey C. Barrett - Nature Neuroscience 2016 被引用: 476