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Publication date
2016 Apr
Authors
Singh, T Kurki, MI Curtis, D Purcell, SM Crooks, L Mcrae, J Suvisaari, J Chheda, H Blackwood, D Breen, G Pietilainen, O Gerety, SS Ayub, M Blyth, M Cole, T Collier, D Coomber, EL Craddock, N Daly, MJ Danesh, J DiForti, M Foster, A Freimer, NB Geschwind, D Johnstone, M Joss, S Kirov, G Korkko, J Kuismin, O Holmans, P Hultman, CM Iyegbe, C Lonnqvist, J Mannikko, M McCarroll, SA McGuffin, P McIntosh, AM McQuillin, A Moilanen, JS Moore, C Murray, RM Newbury-Ecob, R Ouwehand, W Paunio, T Prigmore, E Rees, E Roberts, D Sambrook, J Sklar, P St Clair, D Veijola, J Walters, JTR Williams, H Sullivan, PF Hurles, ME O'Donovan, MC Palotie, A Owen, MJ Barrett, JC
Group authors
UK 10 K Consortium DDD Study INTERVAL Study Swedish Schizophrenia Study
Author KI Usernames
Hultman, CM|chrhul Sullivan, PF|patrsu
Pubmed ID
26974950
Journal
Nature neuroscience
Doctype
Article
KI Connection
Låg
Mesh SV
Fall-kontrollstudier Finland Genetiska sjukdomsanlag Genetisk associationsundersökning Genetisk variation Histon-lysin-N-metyltransferas Kohortstudier Kvinnlig Manlig Människa Schizofreni Utvecklingsneurologiska störningar
Mesh EN
Case-Control Studies Cohort Studies Finland Genetic Association Studies Genetic Predisposition to Disease Genetic Variation Histone-Lysine N-Methyltransferase Neurodevelopmental Disorders Schizophrenia
First date
2016-04-17T10:59:49.416Z