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

[Autism, chromosome 15 and the GAbaergic dysfunction hypothesis].

Investigacion clinica - 1 Dec 2007

Solís-Añez Ernesto, Delgado-Luengo Wilmer, Hernández María Luisa

Abstract excerpt

Autism is a complex neurodevelopmental disorder characterized by impairment of social interaction, language, communication, and stereotyped, repetitive behavior. Genetic predisposition to autism has been demonstrated from families and twin studies. Despite recent advances in identifying some susc...

Read the complete abstract on PubMed

Topics

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

Share to Angelman Syndrome
Share to Autistic Disorder
Share to Chromosome Deletion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 15

Share to Diseases in Twins

Share to gamma-Aminobutyric Acid

Share to Protein Subunits

Share to Receptors, GABA-A

Source

Identifiers

PMID: 18271397

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18271397-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Autism, chromosome 15 and the GAbaergic dysfunction hypothesis].PMID 18271397Read ↗

Meta-Analysis of the Association between GABA Receptor Polymorphisms and Autism Spectrum Disorder (ASD).Semantic proximity Read ↗

No evidence for significant association between GABA receptor genes in chromosome 15q11-q13 and autism in a Japanese population.Semantic proximity Read ↗

Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population.Semantic proximity Read ↗

Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism.Semantic proximity Read ↗

Association of GABRG3, GABRB3, HTR2A gene variants with autism spectrum disorder.Semantic proximity Read ↗

Gamma-Aminobutyric Acid Type A Receptor Variants are Associated with Autism Spectrum Disorders.Semantic proximity Read ↗

A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism.Semantic proximity Read ↗

GABAA receptor subunit gene polymorphisms predict symptom-based and developmental deficits in Chinese Han children and adolescents with autistic spectrum disorders.Semantic proximity Read ↗

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism.Semantic proximity Read ↗

Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.Semantic proximity Read ↗

Shared susceptibility region on chromosome 15 between autism and catatonia.Semantic proximity Read ↗

Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder.Semantic proximity Read ↗

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