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Article

Identification of candidate intergenic risk loci in autism spectrum disorder.

BMC genomics - 24 Jul 2013

Walker Susan, Scherer Stephen W

Abstract excerpt

BACKGROUND: Copy number variations (CNVs) and DNA sequence alterations affecting specific neuronal genes are established risk factors for Autism Spectrum Disorder (ASD). In what is largely considered a genetic condition, so far, these mutations account for ~20% of individuals having an ASD diagnosis. However, non-coding genomic sequence also contains functional elements introducing additional disease risk loci...

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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: 23879678
DOI: 10.1186/1471-2164-14-499
PMCID: PMC3734099

Genes

CDH8
MOCS1
NRXN1
ZHX2

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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