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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 12, 2024. (Total: 234319Documents)
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Query Trace: Learning and SETD1A[original query]
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Nature neuroscience 2016 Mar .
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, St Clair David, 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
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