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Article

Analysis of reelin as a candidate gene for autism.

Molecular psychiatry - 1 Oct 2003

Bonora E, Beyer K S, Lamb J A, Parr J R, Klauck S M, Benner A, Paolucci M, Abbott A, Ragoussis I, Poustka A, Bailey A J, Monaco A P

Abstract excerpt

Genetic studies indicate that chromosome 7q is likely to contain an autism susceptibility locus (AUTS1). We have followed a positional candidate gene approach to identify relevant gene(s) and report here the analysis of reelin (RELN), a gene located under our peak of linkage. Screening RELN for DNA changes identified novel missense variants absent in a large control group; however, the low frequency of these...

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Topics

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Share to Autistic Disorder
Share to Cell Adhesion Molecules, Neuronal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Extracellular Matrix Proteins

Share to Linkage Disequilibrium

Share to Mutation, Missense

Share to Nerve Tissue Proteins

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Source

Identifiers

PMID: 14515139
DOI: 10.1038/sj.mp.4001310

Genes

RELN

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of reelin as a candidate gene for autism.PMID 14515139Read ↗

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

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

Association of Reelin gene polymorphisms with 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 ↗

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 ↗

Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis.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 analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.Semantic proximity Read ↗

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism.Semantic proximity Read ↗

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

Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network.Semantic proximity Read ↗

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

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