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

Sex-specific association of a common variant of the XG gene with autism spectrum disorders.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Oct 2013

Chang Shun-Chiao, Pauls David L, Lange Christoph, Sasanfar Roksana, Santangelo Susan L

Abstract excerpt

Autism spectrum disorders (ASD) are much more common in males than in females. Studies using both linkage and candidate gene association approaches have identified genetic variants specific to families in which all affected cases were male, suggesting that sex may interact with or otherwise influence the expression of specific genes in association with ASD. In this study, we specifically evaluated the...

Read the complete abstract on PubMed

Topics

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

Share to Blood Group Antigens
Share to Cell Adhesion Molecules

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child Development Disorders, Pervasive

Share to IRS2 gene

Share to Genetic Predisposition to Disease

Share to Genome-Wide Association Study

Share to Polymorphism, Single Nucleotide

Share to Sex Characteristics

Source

Identifiers

PMID: 24132906
DOI: 10.1002/ajmg.b.32165

Genes

IRS2
MYO16

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

Sex-specific association of a common variant of the XG gene with autism spectrum disorders.PMID 24132906Read ↗

Chromosome X-wide common variant association study in autism spectrum disorder.Semantic proximity Read ↗

Pleiotropic Mechanisms Indicated for Sex Differences in Autism.Semantic proximity Read ↗

Emerging X-linked genes associated with neurodevelopmental disorders in females.Semantic proximity Read ↗

Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity DisorderSemantic proximity Read ↗

Towards understanding sex differences in autism spectrum disorders.Semantic proximity Read ↗

A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk.Semantic proximity Read ↗

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.Semantic proximity Read ↗

Examining Sex Differences in Autism Heritability.Semantic proximity Read ↗

A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders.Semantic proximity Read ↗

Age-specific DNA methylation alterations in sperm at imprint control regions may contribute to the risk of autism spectrum disorder in offspring.Semantic proximity Read ↗

Autism Spectrum Disorder in Males with Sex Chromosome Aneuploidy: XXY/Klinefelter Syndrome, XYY, and XXYYSemantic proximity Read ↗

Epigenetic Signatures in Family Clusters: Links Between Male Fertility and Autism Risk.Semantic proximity Read ↗

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