Ratings
0
Nobody has rated this yet. Be the first!
Works
7
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia
Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1).
Age-at-onset in bipolar-I disorder: mixture analysis of 1369 cases identifies three distinct clinical sub-groups
