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

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

Molecular psychiatry - 1 Jan 2002

Bonora E, Bacchelli E, Levy E R, Blasi F, Marlow A, Monaco A P, Maestrini E

Abstract excerpt

Genetic studies indicate that chromosome 7q is likely to contain an autism susceptibility locus (AUTS1). We have followed a positional candidate gene approach to identify the relevant gene and report the analysis of four adjacent genes localised to a 800 kb region in 7q32 that contains an imprint...

Read the complete abstract on PubMed

Topics

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

Share to Autistic Disorder
Share to Carboxypeptidases
Share to Chromosomes, Human, Pair 7

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Coatomer Protein

Share to DNA Methylation

Share to DNA Replication

Share to Genomic Imprinting

Share to Proteins

Source

Identifiers

PMID: 11920156
DOI: 10.1038/sj.mp.4001004

Genes

COPG2
CPA1
CPA5
MEST

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-11920156-2026-09-01.1. 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

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region.PMID 11920156Read ↗

The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome.Semantic proximity Read ↗

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

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

Mutations in the TSGA14 gene in families with autism spectrum disorders.Semantic proximity Read ↗

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

3p interstitial deletion including PRICKLE2 in identical twins with autistic features.Semantic proximity Read ↗

Screening individuals with intellectual disability, autism and Tourette's syndrome for KCNK9 mutations and aberrant DNA methylation within the 8q24 imprinted cluster.Semantic proximity Read ↗

Strategies for autism candidate gene analysis.Semantic proximity Read ↗

CMIP haploinsufficiency in two patients with autism spectrum disorder and co-occurring gastrointestinal issues.Semantic proximity Read ↗

Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.Semantic proximity Read ↗

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

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