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Genome-wide association analysis identifies 13 new risk loci for schizophrenia
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Differences in depressive symptom profile between males and females
The effect of a genetic variant at the schizophrenia associated AS3MT/BORCS7 locus on striatal dopamine function: A PET imaging study
