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Article

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

Molecular psychiatry - 1 Jan 2002

Krebs M O, Betancur C, Leroy S, Bourdel M C, Gillberg C, Leboyer M

Abstract excerpt

Autism is a complex neurodevelopmental disorder with severe cognitive and communication disabilities, that has a strong genetic predisposition. Reelin, a protein involved in neuronal migration during development, is encoded by a gene located on 7q22, within the candidate region on 7q showing increased allele sharing in previous genome scans. A case/control and family-based association study recently reported a...

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Identifiers

PMID: 12192627
DOI: 10.1038/sj.mp.4001071
PMCID: PMC1913931

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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Absence of association between a polymorphic GGC repeat in the 5' untranslated region of the reelin gene and autism.PMID 12192627Read ↗

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

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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 Reelin gene polymorphisms with autism.Semantic proximity Read ↗

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

Association analysis of polymorphic CGG repeat in 5' UTR of the reelin and VLDLR genes with schizophrenia.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 polymorphisms in the Indian population: a possible paternal 5'UTR-CGG-repeat-allele effect on autism.Semantic proximity Read ↗

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

Population-based and family-based association study of 5'UTR polymorphism of the reelin gene and schizophrenia.Semantic proximity Read ↗

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

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