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Article

Analysis of the RELN gene as a genetic risk factor for autism.

Molecular psychiatry - 1 Jun 2005

Skaar D A, Shao Y, Haines J L, Stenger J E, Jaworski J, Martin E R, DeLong G R, Moore J H, McCauley J L, Sutcliffe J S, Ashley-Koch A E, Cuccaro M L, Folstein S E, Gilbert J R, Pericak-Vance M A

Abstract excerpt

Several genome-wide screens have indicated the presence of an autism susceptibility locus within the distal long arm of chromosome 7 (7q). Mapping at 7q22 within this region is the candidate gene reelin (RELN). RELN encodes a signaling protein that plays a pivotal role in the migration of several neuronal cell types and in the development of neural connections. Given these neurodevelopmental functions, recent...

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Source

Identifiers

PMID: 15558079
DOI: 10.1038/sj.mp.4001614

Genes

RELN
PSMC2

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

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of the RELN gene as a genetic risk factor for autism.PMID 15558079Read ↗

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

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

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

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

Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk.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 ↗

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

Two single-nucleotide polymorphisms of the RELN gene and symptom-based and developmental deficits among children and adolescents with autistic spectrum disorders in the Tianjin, China.Semantic proximity Read ↗

Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.Semantic proximity Read ↗

Association and gene-gene interactions study of reelin signaling pathway related genes with autism in the Han Chinese population.Semantic proximity Read ↗

A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.Semantic proximity Read ↗

The association analysis of RELN and GRM8 genes with autistic spectrum disorder in Chinese Han population.Semantic proximity Read ↗

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