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Article

Unraveling autism.

American journal of human genetics - 1 Jan 2008

Stephan Dietrich A

Abstract excerpt

In this issue of AJHG, Alarcón et al.,(1) Arking et al.,(2) and Bakkaloglu et al.(3) identify a series of functional variants in the CNTNAP2 gene that unequivocally implicate this gene as causing Type 1 autism in the general population.

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Topics

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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: 18179879
DOI: 10.1016/j.ajhg.2007.12.003
PMCID: PMC2253980

Genes

CNTNAP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18179879-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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Unraveling autism.PMID 18179879Read ↗

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.Semantic proximity Read ↗

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Defining the contribution of CNTNAP2 to autism susceptibility.Semantic proximity Read ↗

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The new genetics of autism: a translational opportunity?Semantic proximity Read ↗

The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population.Semantic proximity Read ↗

No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.Semantic proximity Read ↗

Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder.Semantic proximity Read ↗

A surprising METamorphosis: autism genetics finds a common functional variant.Semantic proximity Read ↗

CNTNAP2 gene polymorphisms in autism spectrum disorder and language impairment among Bangladeshi children: a case-control study combined with a meta-analysis.Semantic proximity Read ↗

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.Semantic proximity Read ↗

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