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

Author:

Singh Tarjinder, ,Kurki Mitja I,Curtis David,Purcell Shaun MORCID,Crooks Lucy,McRae Jeremy,Suvisaari Jaana,Chheda Himanshu,Blackwood DouglasORCID,Breen Gerome,Pietiläinen Olli,Gerety Sebastian S,Ayub Muhammad,Blyth Moira,Cole Trevor,Collier David,Coomber Eve L,Craddock Nick,Daly Mark JORCID,Danesh John,DiForti Marta,Foster Alison,Freimer Nelson BORCID,Geschwind Daniel,Johnstone Mandy,Joss Shelagh,Kirov Georg,Körkkö Jarmo,Kuismin Outi,Holmans PeterORCID,Hultman Christina M,Iyegbe Conrad,Lönnqvist Jouko,Männikkö Minna,McCarroll Steve A,McGuffin Peter,McIntosh Andrew MORCID,McQuillin AndrewORCID,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 HywelORCID,Sullivan Patrick F,Hurles Matthew E,O'Donovan Michael CORCID,Palotie Aarno,Owen Michael J,Barrett Jeffrey CORCID, , ,

Publisher

Springer Science and Business Media LLC

Subject

General Neuroscience

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