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

Multiple rare variants in the etiology of autism spectrum disorders.

Dialogues in clinical neuroscience - 1 Jan 2009

Buxbaum Joseph D

Abstract excerpt

Recent studies in autism spectrum disorders (ASDs) support an important role for multiple rare variants in these conditions. This is a clinically important finding, as, with the demonstration that a significant proportion of ASDs are the result of rare, etiological genetic variants, it becomes possible to make use of genetic testing to supplement behavioral analyses for an earlier diagnosis. As it appears that...

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 Brain Chemistry
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Genetic Testing

Share to Genetic Variation

Share to Inheritance Patterns

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 19432386
PMCID: PMC3181906

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Multiple rare variants in the etiology of autism spectrum disorders.PMID 19432386Read ↗

Genetic research in autism spectrum disorders.Semantic proximity Read ↗

Autism spectrum disorder in the genetics clinic: a review.Semantic proximity Read ↗

The genetics of autism: key issues, recent findings, and clinical implications.Semantic proximity Read ↗

Genetic contributions to autism spectrum disorder.Semantic proximity Read ↗

A systematic review of common genetic variation and biological pathways in autism spectrum disorder.Semantic proximity Read ↗

The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders.Semantic proximity Read ↗

Diagnosis and management of autism spectrum disorder in the era of genomics: rare disorders can pave the way for targeted treatments.Semantic proximity Read ↗

Functional significance of rare neuroligin 1 variants found in autism.Semantic proximity Read ↗

Recent Advances in Understanding the Genetic Architecture of Autism.Semantic proximity Read ↗

Rare structural variation of synapse and neurotransmission genes in autism.Semantic proximity Read ↗

Unraveling the Genetic and Molecular Architecture of Autism Spectrum Disorder: Implications for Clinical Genetics and Genomic Diagnostics.Semantic proximity Read ↗

DE NOVO MUTATIONS IN AUTISM IMPLICATE THE SYNAPTIC ELIMINATION NETWORK.Semantic proximity Read ↗

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