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Article

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Apr 2004

Li Jun, Nguyen Loan, Gleason Christopher, Lotspeich Linda, Spiker Donna, Risch Neil, Myers Richard M

Abstract excerpt

Autism is a pervasive neurodevelopmental disorder characterized by deficits in language development and social interaction, as well as stereotypical, repetitive behaviors. The etiology of autism is largely unknown. Family and twin studies have provided compelling evidence for a strong genetic com...

Read the complete abstract on PubMed

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15048648
DOI: 10.1002/ajmg.b.20122

Genes

WNT2
RELN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-15048648-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism.PMID 15048648Read ↗

Analysis of the RELN gene as a genetic risk factor for autism.Semantic proximity Read ↗

No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population.Semantic proximity Read ↗

Association of Allelic Variants of the Reelin Gene with Autistic Spectrum Disorder: A Systematic Review and Meta-Analysis of Candidate Gene Association Studies.Semantic proximity Read ↗

Evidence supporting WNT2 as an autism susceptibility gene.Semantic proximity Read ↗

Analysis of reelin as a candidate gene for autism.Semantic proximity Read ↗

Absence of association between a polymorphic GGC repeat in the 5' untranslated region of the reelin gene and autism.Semantic proximity Read ↗

Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis.Semantic proximity Read ↗

Reelin gene alleles and susceptibility to autism spectrum disorders.Semantic proximity Read ↗

Three autism candidate genes: a synthesis of human genetic analysis with other disciplines.Semantic proximity Read ↗

Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.Semantic proximity Read ↗

Association between autism and variants in the wingless-type MMTV integration site family member 2 ( WNT2) gene.Semantic proximity Read ↗

RELN gene polymorphisms and susceptibility to autism in Chinese Han population.Semantic proximity Read ↗

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