Ontology highlight
ABSTRACT:
SUBMITTER: Steinberg S
PROVIDER: S-EPMC3298077 | biostudies-literature | 2011 Oct
REPOSITORIES: biostudies-literature
Human molecular genetics 20110726 20
Common sequence variants have recently joined rare structural polymorphisms as genetic factors with strong evidence for association with schizophrenia. Here we extend our previous genome-wide association study and meta-analysis (totalling 7 946 cases and 19 036 controls) by examining an expanded set of variants using an enlarged follow-up sample (up to 10 260 cases and 23 500 controls). In addition to previously reported alleles in the major histocompatibility complex region, near neurogranin (N ...[more]