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Article

Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder.

Translational psychiatry - 28 May 2013

Vardarajan B N, Eran A, Jung J-Y, Kunkel L M, Wall D P

Abstract excerpt

Autism spectrum disorder (ASD) is a neurodevelopmental condition that results in behavioral, social and communication impairments. ASD has a substantial genetic component, with 88-95% trait concordance among monozygotic twins. Efforts to elucidate the causes of ASD have uncovered hundreds of susceptibility loci and candidate genes. However, owing to its polygenic nature and clinical heterogeneity, only a few of...

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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: 23715297
DOI: 10.1038/tp.2013.38
PMCID: PMC3669925

Genes

CADPS2
CNTN4
NTRK3
SUMF1

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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