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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, 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

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Item Type: Article
Date Type: Published Online
Status: Published
Schools: Medicine
Subjects: R Medicine > R Medicine (General)
Publisher: Nature Publishing Group
ISSN: 1097-6256
Date of First Compliant Deposit: 25 May 2018
Date of Acceptance: 11 February 2016
Last Modified: 24 Jan 2019 23:53
URI: http://orca.cf.ac.uk/id/eprint/90087

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