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

Sanghoon Moon,Bhumsuk Keam,Mi Yeong Hwang,Young Hee Lee,Suyeon Park,Ji Hee Oh,Yeonjung Kim,Heun-Sik Lee,Namhee Kim,Young-Jin Kim,Dong-Hyun Kim,Bok-Ghee Han,Bong-Jo Kim,Ju Young Lee

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

2015

Sanghoon Moon
Bhumsuk Keam
Mi Yeong Hwang
Young Hee Lee
Suyeon Park
Ji Hee Oh
Yeonjung Kim
Heun-Sik Lee
Namhee Kim
Young-Jin Kim
Dong-Hyun Kim
Bok-Ghee Han
Bong-Jo Kim
Ju Young Lee

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.

Keywords:

Physical medicine and rehabilitation
Disease
Genetics
Locus (genetics)
Case-control study
Copy-number variation
Genome-wide association study
Genotype
Pathology
Medicine
gene deletion
genetic risk
complex disease

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