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Article

Common genetic variation in Neuregulin 3 (NRG3) influences risk for schizophrenia and impacts NRG3 expression in human brain.

Proceedings of the National Academy of Sciences of the United States of America - 31 Aug 2010

Kao Wee-Tin, Wang Yanhong, Kleinman Joel E, Lipska Barbara K, Hyde Thomas M, Weinberger Daniel R, Law Amanda J

Abstract excerpt

Structural and polymorphic variations in Neuregulin 3 (NRG3), 10q22-23 are associated with a broad spectrum of neurodevelopmental disorders including developmental delay, cognitive impairment, autism, and schizophrenia. NRG3 is a member of the neuregulin family of EGF proteins and a ligand for th...

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Source

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Identifiers

PMID: 20713722
DOI: 10.1073/pnas.1005410107
PMCID: PMC2932571

Genes

NRG3
EGF
NRG1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20713722-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Common genetic variation in Neuregulin 3 (NRG3) influences risk for schizophrenia and impacts NRG3 expression in human brain.PMID 20713722Read ↗

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