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Article

Translational Study of Copy Number Variations in Schizophrenia.

International journal of molecular sciences - 31 Dec 2021

Cheng Min-Chih, Chien Wei-Hsien, Huang Yu-Shu, Fang Ting-Hsuan, Chen Chia-Hsiang

Abstract excerpt

Rare copy number variations (CNVs) are part of the genetics of schizophrenia; they are highly heterogeneous and personalized. The CNV Analysis Group of the Psychiatric Genomic Consortium (PGC) conducted a large-scale analysis and discovered that recurrent CNVs at eight genetic loci were pathogenic to schizophrenia, including 1q21.1, 2p16.3 (NRXN1), 3q29, 7q11.23, 15q13.3, distal 16p11.2, proximal 16p11.2, and...

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Identifiers

PMID: 35008879
DOI: 10.3390/ijms23010457
PMCID: PMC8745588

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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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