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Article

A genome-wide association study of copy-number variation identifies putative loci associated with osteoarthritis in Koreans.

BMC musculoskeletal disorders - 4 Apr 2015

Moon Sanghoon, Keam Bhumsuk, Hwang Mi Yeong, Lee Young, Park Suyeon, Oh Ji Hee, Kim Yeon-Jung, Lee Heun-Sik, Kim Nam Hee, Kim Young Jin, Kim Dong-Hyun, Han Bok-Ghee, Kim Bong-Jo, Lee Juyoung

Abstract excerpt

BACKGROUND: OA is a complex disease caused by environmental and genetic risk factors. The purpose of this study is to identify candidate copy number variations (CNVs) associated with OA. METHODS: We performed a genome-wide association study of CNV to identify potential loci that confer susceptibility to or protection from OA. CNV genotyping was conducted using NimbleGen HD2 3 × 720K comparative hybridization...

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Identifiers

PMID: 25880085
DOI: 10.1186/s12891-015-0531-4
PMCID: PMC4395893

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TNKS

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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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