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Article

RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.

Biological psychiatry - 1 Nov 2008

Liu Yu-Li, Fann Cathy Shen-Jang, Liu Chih-Min, Chen Wei J, Wu Jer-Yuarn, Hung Shuen-Iu, Chen Chun-Houh, Jou Yuh-Shan, Liu Shi-Kai, Hwang Tzung-Jeng, Hsieh Ming H, Chang Chien Ching, Yang Wei-Chih, Lin Jin-Jia, Chou Frank Huang-Chih, Faraone Stephen V, Tsuang Ming T, Hwu Hai-Gwo

Abstract excerpt

BACKGROUND: In a previous linkage study of schizophrenia that included Taiwanese samples, the marker D22S278 (22q12.3) was significantly linked to schizophrenia (p = .001). METHODS: We conducted fine mapping of the implicated genomic region, with 47 validated single nucleotide polymorphism (SNP) markers around 1 Mb of D22S278, in a Taiwanese sample of 218 pedigrees with at least 2 siblings affected with...

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Source

Identifiers

PMID: 18571626
DOI: 10.1016/j.biopsych.2008.04.035

Genes

CACNG2
MYH9
RASD2
APOL5

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.

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