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Article

Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese population.

Schizophrenia bulletin - 1 May 2013

Zhao Qian, Li Tao, Zhao XinZhi, Huang Ke, Wang Ti, Li ZhiQiang, Ji Jue, Zeng Zhen, Zhang Zhao, Li Kan, Feng GuoYin, St Clair David, He Lin, Shi YongYong

Abstract excerpt

BACKGROUND: Rare copy number variations (CNVs) were involved in the etiology of neuropsychiatric disorders, and some of them appeared to be shared risk factors for several different diseases. One of those promising loci is the CNV at 15q11.2, including 4 genes, TUBGCP5, CYFIP1, NIPA2, and NIPA1. Several studies showed that microdeletions at this locus were significant associated with schizophrenia. In the current...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 22317777
DOI: 10.1093/schbul/sbr197
PMCID: PMC3627771

Genes

CYFIP1
NIPA1
NIPA2
TUBGCP5

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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