312 0

Full metadata record

DC FieldValueLanguage
dc.contributor.author김태환-
dc.date.accessioned2017-10-30T02:48:09Z-
dc.date.available2017-10-30T02:48:09Z-
dc.date.issued2016-01-
dc.identifier.citationINFLAMMATORY BOWEL DISEASES, v. 22, NO 1, Page. 13-19en_US
dc.identifier.issn1078-0998-
dc.identifier.issn1536-4844-
dc.identifier.urihttp://pt.wkhealth.com/pt/re/lwwgateway/landingpage.htm;jsessionid=ZxnDLvn3s0pCQjb5Pt4wWfM02slyvTF7H2Lmw8MPZv9hw3l6nH0x!2045564855!181195628!8091!-1?sid=WKPTLP:landingpage&an=00054725-201601000-00002-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/30316-
dc.description.abstractBackground: Recent genetic association studies identified more than 160 susceptibility loci for inflammatory bowel disease in Caucasian populations, but studies in Asian populations are limited. We have previously reported 3 loci associated with Korean ulcerative colitis (UC). Methods: Using the Immunochip custom single nucleotide polymorphisms (SNP) array designed for dense genotyping of 186 known disease loci from 12 immune-mediated diseases, we analyzed 705 patients with UC and 1178 controls for 536,821 SNPs (89,057 genotyped and 447,764 imputed) in the discovery stage followed by replication in additional 980 affected individuals and 2694 controls in a Korean population. Results: We confirmed the associations of 10 known UC risk loci in Koreans: rs76418789 in IL23R (combined P = 1.25 x 10(-8)), rs4728142 in IRF5 (combined P = 3.17 x 10(-8)), rs1830610 near JAK2 (combined P = 2.28 x 10(-9)), rs1555791 near TNFRSF14 (combined P = 1.62 x 10(-6)), rs880790 between IL10-IL19 (combined P = 3.73 x 10(-6)), rs10185424 between IL1R2-IL1R1 (combined P = 1.54 x 10(-4)), rs6478108 in TNFSF15 (combined P = 9.28 x 10(-5)), rs861857 between UBE2L3-YDJC (combined P = 3.05 x 10(-5)), rs1801274 in FCGR2A (discovery P = 1.54 x 10(-4)), and rs17085007 between GPR12-USP12 (discovery P = 3.64 x 10(-4)). The percentage of phenotype variance explained by the 13 risk loci (including 3 previously reported loci) was 5.61% in Koreans (on the liability scale, population prevalence = 0.0308%). Conclusions: Our study increased the number of UC susceptibility loci in Koreans to 13 and highlighted the extensive sharing of genetic risk across populations of UC.en_US
dc.description.sponsorshipSupported by a Mid-career Researcher Program grant through NRF (National Research Foundation of Korea) to K. Song ( 2014R1A2A1A09005824) funded by the Ministry of Science, Information & Communication Technology and Future Planning and a Korean Health Technology R&D Project grant to S.-K. Yang (A120176) from the Ministry of Health & Welfare, the Republic of Korea.en_US
dc.language.isoenen_US
dc.publisherLIPPINCOTT WILLIAMS & WILKINSen_US
dc.subjectulcerative colitisen_US
dc.subjectgeneticsen_US
dc.subjectImmunochipen_US
dc.subjectKoreanen_US
dc.titleIdentification of Ten Additional Susceptibility Loci for Ulcerative Colitis Through Immunochip Analysis in Koreansen_US
dc.typeArticleen_US
dc.relation.no1-
dc.relation.volume22-
dc.identifier.doi10.1097/MIB.0000000000000584-
dc.relation.page13-19-
dc.relation.journalINFLAMMATORY BOWEL DISEASES-
dc.contributor.googleauthorYe, Byong Duk-
dc.contributor.googleauthorChoi, Hyunchul-
dc.contributor.googleauthorHong, Myunghee-
dc.contributor.googleauthorYun, Woo Jin-
dc.contributor.googleauthorLow, Hui-Qi-
dc.contributor.googleauthorHaritunians, Talin-
dc.contributor.googleauthorKim, Kyung-Jo-
dc.contributor.googleauthorPark, Sang Hyoung-
dc.contributor.googleauthorLee, Inchul-
dc.contributor.googleauthorKim, Tae-Hwan-
dc.relation.code2016000123-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidthkim-
Appears in Collections:
COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML


qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE