Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders
Authors
Tarjinder Singh,
Mitja KurkiDavid Curtis,
Shaun Purcell,
Lucy Crooks,
Jeremy McRae,
Jaana Suvisaari,
Himanshu Chheda,
Douglas Blackwood,
Gerome Breen,
Olli Pietiläinen,
Sebastian Gerety,
Muhammad Ayub,
Moira Blyth,
Trevor Cole,
David Collier,
Eve Coomber,
Nick Craddock,
Mark Daly,
John Danesh,
Marta DiForti,
Alison Foster,
Nelson Freimer,
Daniel Geschwind,
Mandy Johnstone,
Shelagh Joss,
Georg Kirov,
Jarmo Körkkö,
Outi Kuismin,
Peter Holmans,
Christina Hultman,
Conrad Iyegbe,
Jouko Lönnqvist,
Minna Männikkö,
Steve McCarroll,
Peter McGuffin,
Y Zeng,
Andrew McQuillin,
Jukka Moilanen,
Carmel Moore,
Robin Murray,
Ruth Newbury-Ecob,
Willem Ouwehand,
Tiina Paunio,
Elena Prigmore,
Elliott Rees,
David Roberts,
Jennifer Sambrook,
Pamela Sklar,
David Clair,
Juha Veijola,
James Walters,
Hywel Williams,
Swedish Study,
INTERVAL Study,
DDD Study,
UK10K Consortium,
Patrick Sullivan,
Matthew Hurles,
Michael O'Donovan,
Aarno Palotie,
Michael Owen,
Jeffrey Barrett,
John Blangero,
Marta Forti,
George Kirov,
Steven McCarroll,
Andrew McIntosh,
Ruth Newbury‐Ecob,
Jennifer Couper,
Michael O’Donovan +69 authors
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