Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 5 Jun 2009

Conroy Judith, Cochrane Lynne, Anney Richard J L, Sutcliffe James S, Carthy Paula, Dunlop Adam, Mullarkey Marice, O'hici Bronagh, Green Andrew J, Ennis Sean, Gill Michael, Gallagher Louise

Abstract excerpt

Autism (OMIM %209850) is a neurodevelopmental disorder with a strong genetic component. We previously reported a de novo rearrangement of chromosome 2q31 in a patient with autism [Gallagher et al. (2003); J Autism Dev Disord 33(1):105-108]. Further cytogenetic analysis revealed this to be a 46,XY, t(9;2)(q31.1;q32.2q31.3) translocation. Association mapping with microsatellite and SNP markers of this translocated...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Autistic Disorder

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosome Mapping

Share to Chromosomes, Human, Pair 2

Share to Haplotypes

Share to Karyotyping

Share to Microsatellite Repeats

Share to Pedigree

Source

Identifiers

PMID: 18846500
DOI: 10.1002/ajmg.b.30854

Genes

ITGA4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32.PMID 18846500Read ↗

Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample.Semantic proximity Read ↗

Recurrent 16p11.2 microdeletions in autism.Semantic proximity Read ↗

Association and mutation analyses of 16p11.2 autism candidate genes.Semantic proximity Read ↗

Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother.Semantic proximity Read ↗

Association of the alpha4 integrin subunit gene (ITGA4) with autism.Semantic proximity Read ↗

[16p11.2 Microdeletion: first report in Argentina].Semantic proximity Read ↗

Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes.Semantic proximity Read ↗

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism.Semantic proximity Read ↗

Narrowing the critical deletion region for autism spectrum disorders on 16p11.2.Semantic proximity Read ↗

Refinement of chromosome 3p22.3 region and identification of a susceptibility gene for bipolar affective disorder.Semantic proximity Read ↗

Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.Semantic proximity Read ↗

Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.