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Identification of Loci at 1q21 and 16q23 That Affect Susceptibility to Inflammatory Bowel Disease in Koreans

Cited 28 time in Web of Science Cited 31 time in Scopus
Authors

Yang, Suk-Kyun; Hong, Myunghee; Oh, Hyunjung; Low, Hui-Qi; Jung, Seulgi; Ahn, Seonjoo; Kim, Youngjin; Baek, Jiwon; Lee, Cue Hyunkyu; Kim, Eunji; Kim, Kyung Mo; Ye, Byong Duk; Kim, Kyung-Jo; Park, Sang Hyoung; Lee, Ho-Su; Lee, Inchul; Shin, Hyoung Doo; Han, Buhm; McGovern, Dermot P. B.; Liu, Jianjun; Song, Kyuyoung

Issue Date
2016-12
Publisher
W. B. Saunders Co., Ltd.
Citation
Gastroenterology, Vol.151 No.6, pp.1096-1099.e3
Abstract
Recent genome-wide association studies have identified more than 200 regions that affect susceptibility to inflammatory bowel disease (IBD). However, identified common variants account for only a fraction of IBD heritability and largely have been identified in populations of European ancestry. We performed a genome-wide association study of susceptibility loci in Korean individuals, comprising a total of 1505 IBD patients and 4041 controls. We identified 2 new susceptibility loci for IBD at genome-wide significance: rs3766920 near PYGO2-SHC1 at 1q21 and rs16953946 in CDYL2 at 16q23. In addition, we confirmed associations, in Koreans, with 28 established IBD loci (P < 2.16 3 10(-4)). Our findings support the complementary value of genetic studies in different populations.
ISSN
0016-5085
URI
https://hdl.handle.net/10371/191569
DOI
https://doi.org/10.1053/j.gastro.2016.08.025
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  • College of Medicine
  • Department of Medicine
Research Area Bioinformatics, Genomics, Statistical Genetics, Computational Biology, Human Leukocyte Antigen

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