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Article

No association between polymorphisms of WNT2 and schizophrenia in a Korean population.

BMC medical genetics - 24 May 2010

Kim Hak-Jae, Park Jin Kyung, Kim Su Kang, Kang Sung Wook, Kim Jong Woo, Park Hyun-Kyung, Cho Ah-Rang, Song Ji Young, Chung Joo-Ho

Abstract excerpt

BACKGROUND: Wingless-type MMTV integration site family member 2 (WNT2) has a potentially important role in neuronal development; however, there has yet to be an investigation into the association between single nucleotide polymorphisms (SNPs) of WNT2 and schizophrenia. This study aimed to determine whether certain SNPs of WNT2 were associated with schizophrenia in a Korean population. METHODS: e genotyped 7...

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Identifiers

PMID: 20492734
DOI: 10.1186/1471-2350-11-78
PMCID: PMC2887425

Genes

WNT2

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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