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Article

Rare structural variation of synapse and neurotransmission genes in autism.

Molecular psychiatry - 1 Apr 2012

Gai X, Xie H M, Perin J C, Takahashi N, Murphy K, Wenocur A S, D'arcy M, O'Hara R J, Goldmuntz E, Grice D E, Shaikh T H, Hakonarson H, Buxbaum J D, Elia J, White P S

Abstract excerpt

Autism spectrum disorders (ASDs) comprise a constellation of highly heritable neuropsychiatric disorders. Genome-wide studies of autistic individuals have implicated numerous minor risk alleles but few common variants, suggesting a complex genetic model with many contributing loci. To assess commonality of biological function among rare risk alleles, we compared functional knowledge of genes overlapping inherited...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 21358714
DOI: 10.1038/mp.2011.10
PMCID: PMC3314176

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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