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Article

No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.

American journal of medical genetics - 8 Aug 2002

Devlin Bernie, Bennett Pamela, Cook Edwin H, Dawson Geraldine, Gonen David, Grigorenko Elena L, McMahon William, Pauls David, Smith Moyra, Spence M Anne, Schellenberg Gerard D

Abstract excerpt

A recent study by Ingram et al. [2000b: Teratology 62:393-405] suggests a (His)73(Arg) polymorphism (A:G) in HOXA1 contributes substantially to a liability for autism. Using 68 individuals diagnosed with Autism Spectrum Disorders, they found a significant dearth of G homozygotes and biased transm...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 12210285
DOI: 10.1002/ajmg.10603

Genes

HOXA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12210285-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.PMID 12210285Read ↗

Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders.Semantic proximity Read ↗

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An integrated meta-analysis of two variants in HOXA1/HOXB1 and their effect on the risk of autism spectrum disorders.Semantic proximity Read ↗

Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders.Semantic proximity Read ↗

Maternal genetic liability to autism spectrum disorders and pregnancy outcomes.Semantic proximity Read ↗

Autism and the X chromosome: no linkage to microsatellite loci detected using the affected sibling pair method.Semantic proximity Read ↗

No association between allelic variants of HOXA1/HOXB1 and autism.Semantic proximity Read ↗

Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families.Semantic proximity Read ↗

Allelic variation within the putative autism spectrum disorder risk gene homeobox A1 and cerebellar maturation in typically developing children and adolescents.Semantic proximity Read ↗

The HOXA1 A218G polymorphism and autism: lack of association in white and black patients from the South Carolina Autism Project.Semantic proximity Read ↗

No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set.Semantic proximity Read ↗

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