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Article

Investigation of OLIG2 as a candidate gene for schizophrenia and autism spectrum disorder.

Nagoya journal of medical science - 1 May 2022

Furuta Sho, Aleksic Branko, Nawa Yoshihiro, Kimura Hiroki, Kushima Itaru, Ishizuka Kanako, Kato Hidekazu, Toyama Miho, Arioka Yuko, Mori Daisuke, Morikawa Mako, Inada Toshiya, Ozaki Norio

Abstract excerpt

A number of genomic mutations that are thought to be strongly involved in the development of schizophrenia (SCZ) and autism spectrum disorder (ASD) have been identified. Abnormalities involving oligodendrocytes have been reported in SCZ, and as a related gene, oligodendrocyte lineage transcription factor 2 (OLIG2) has been reported to be strongly associated with SCZ. In this study, based on the common...

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Identifiers

PMID: 35967956
DOI: 10.18999/nagjms.84.2.260
PMCID: PMC9350582

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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.

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