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Article

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT.

American journal of human genetics - 1 Jun 2005

Barnby Gabrielle, Abbott Aaron, Sykes Nuala, Morris Andrew, Weeks Daniel E, Mott Richard, Lamb Janine, Bailey Anthony J, Monaco Anthony P

Abstract excerpt

Autism is a highly heritable neurodevelopmental disorder whose underlying genetic causes have yet to be identified. To date, there have been eight genome screens for autism, two of which identified a putative susceptibility locus on chromosome 16p. In the present study, 10 positional candidate genes that map to 16p11-13 were examined for coding variants: A2BP1, ABAT, BFAR, CREBBP, EMP2, GRIN2A, MRTF-B, SSTR5,...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 15830322
DOI: 10.1086/430454
PMCID: PMC1196454

Genes

ABAT
CREBBP
BFAR
EMP2
SSTR5
TBX6
UBN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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