Mutation screening and association analysis of six candidate genes for autism on chromosome 7q.

doi:10.1038/sj.ejhg.5201315

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

Community

Back to search

Article

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q.

European journal of human genetics : EJHG - 1 Feb 2005

Bonora Elena, Lamb Janine A, Barnby Gabrielle, Sykes Nuala, Moberly Thomas, Beyer Kim S, Klauck Sabine M, Poustka Firtz, Bacchelli Elena, Blasi Francesca, Maestrini Elena, Battaglia Agatino, Haracopos Demetrios, Pedersen Lennart, Isager Torben, Eriksen Gunna, Viskum Birgitte, Sorensen Ester-Ulsted, Brondum-Nielsen Karen, Cotterill Rodney, Engeland Herman von, Jonge Maretha de, Kemner Chantal, Steggehuis Karlijn, Scherpenisse Margret, Rutter Michael, Bolton Patrick F, Parr Jeremy R, Poustka Annemarie, Bailey Anthony J, Monaco Anthony P

Abstract excerpt

Genetic studies have provided evidence for an autism susceptibility locus (AUTS1) on chromosome 7q. Screening for mutations in six genes mapping to 7q, CUTL1, SRPK2, SYPL, LAMB1, NRCAM and PTPRZ1 in 48 unrelated individuals with autism led to the identification of several new coding variants in the genes CUTL1, LAMB1 and PTPRZ1. Analysis of genetic variants provided evidence for association with autism for one of...

Read the complete abstract on PubMed

Topics

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

Share to Autistic Disorder

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cell Adhesion Molecules

Share to Chromosomes, Human, Pair 7

Share to Gene Expression Regulation

Share to Lamin Type B

Share to Promoter Regions, Genetic

Share to Quantitative Trait Loci

Share to Untranslated Regions

Source

Open in PubMed

Identifiers

PMID: 15523497
DOI: 10.1038/sj.ejhg.5201315

Genes

LAMB1
NRCAM
PTPRZ1
SRPK2

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

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q.PMID 15523497Read ↗

Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes.Semantic proximity Read ↗

Construction of a physical map of an autism susceptibility region in 7q32.3-q33.Semantic proximity Read ↗

Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual.Semantic proximity Read ↗

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region.Semantic proximity Read ↗

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

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

Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.Semantic proximity Read ↗

A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints.Semantic proximity Read ↗

Defining the autism minimum candidate gene region on chromosome 7.Semantic proximity Read ↗

Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility.Semantic proximity Read ↗

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.Semantic proximity Read ↗

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.Semantic proximity Read ↗

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