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

A Pooled Genome-Wide Association Study of Asperger Syndrome.

PloS one - 1 Jan 2015

Warrier Varun, Chakrabarti Bhismadev, Murphy Laura, Chan Allen, Craig Ian, Mallya Uma, Lakatošová Silvia, Rehnstrom Karola, Peltonen Leena, Wheelwright Sally, Allison Carrie, Fisher Simon E, Baron-Cohen Simon

Abstract excerpt

Asperger Syndrome (AS) is a neurodevelopmental condition characterized by impairments in social interaction and communication, alongside the presence of unusually repetitive, restricted interests and stereotyped behaviour. Individuals with AS have no delay in cognitive and language development. It is a subset of Autism Spectrum Conditions (ASC), which are highly heritable and has a population prevalence of...

Read the complete abstract on PubMed

Topics

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

Share to Case-Control Studies
Share to Gene Frequency

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Genome, Human

Share to Genome-Wide Association Study

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 26176695
DOI: 10.1371/journal.pone.0131202
PMCID: PMC4503355

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

A Pooled Genome-Wide Association Study of Asperger Syndrome.PMID 26176695Read ↗

Variants in several genomic regions associated with asperger disorder.Semantic proximity Read ↗

Genome-wide scan for loci of Asperger syndrome.Semantic proximity Read ↗

Deleterious coding variation associated with autism is shared across ancestries.Semantic proximity Read ↗

The genetics of Autism Spectrum Disorders--a guide for clinicians.Semantic proximity Read ↗

Autism genetics: strategies, challenges, and opportunities.Semantic proximity Read ↗

Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.Semantic proximity Read ↗

Closing the Gap in Autism Genetics: Population-Specific Variants and the Imperative for Global Inclusion.Semantic proximity Read ↗

Common DNA methylation alterations in multiple brain regions in autism.Semantic proximity Read ↗

Comprehensive Genetic Analysis of Non-syndromic Autism Spectrum Disorder in Clinical Settings.Semantic proximity Read ↗

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.Semantic proximity Read ↗

A genome-wide scan for common alleles affecting risk for autism.Semantic proximity Read ↗

A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples.Semantic proximity Read ↗

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