Resequencing and association analysis of OXTR with autism spectrum disorder in a Japanese population.

doi:10.1111/pcn.12205

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Article

Resequencing and association analysis of OXTR with autism spectrum disorder in a Japanese population.

Psychiatry and clinical neurosciences - 1 Mar 2015

Egawa Jun, Watanabe Yuichiro, Shibuya Masako, Endo Taro, Sugimoto Atsunori, Igeta Hirofumi, Nunokawa Ayako, Inoue Emiko, Someya Toshiyuki

Abstract excerpt

AIMS: The oxytocin receptor (OXTR) is implicated in the pathophysiology of autism spectrum disorder (ASD). A recent study found a rare non-synonymous OXTR gene variation, rs35062132 (R376G), associated with ASD in a Japanese population. In order to investigate the association between rare non-synonymous OXTR variations and ASD, we resequenced OXTR and performed association analysis with ASD in a Japanese...

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Source

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Identifiers

PMID: 24836510
DOI: 10.1111/pcn.12205

Genes

OXTR

Variants

rs35062132

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.

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