H
Hyun Sub Cheong
Researcher at Sogang University
Publications - 158
Citations - 4053
Hyun Sub Cheong is an academic researcher from Sogang University. The author has contributed to research in topics: Single-nucleotide polymorphism & Haplotype. The author has an hindex of 32, co-authored 158 publications receiving 3685 citations. Previous affiliations of Hyun Sub Cheong include New Generation University College & Soonchunhyang University.
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Journal ArticleDOI
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.
Daniel F. Gudbjartsson,Unnur S. Bjornsdottir,Unnur S. Bjornsdottir,Eva Halapi,Anna Helgadottir,Patrick Sulem,Gudrun M. Jonsdottir,Gudmar Thorleifsson,Hafdis T. Helgadottir,Valgerdur Steinthorsdottir,Hreinn Stefansson,Carolyn Williams,Jennie Hui,John Beilby,Nicole M. Warrington,Alan L. James,Alan L. James,Lyle J. Palmer,Gerard H. Koppelman,Andrea Heinzmann,Marcus Krueger,H. Marike Boezen,Amanda Wheatley,Janine Altmüller,Hyoung Doo Shin,Soo-Taek Uh,Hyun Sub Cheong,Brynja Jonsdottir,David Gislason,Choon-Sik Park,Linda M. Rasmussen,Celeste Porsbjerg,Jakob Werner Hansen,Vibeke Backer,Thomas Werge,Christer Janson,Ulla-Britt Jönsson,Maggie C.Y. Ng,Juliana C.N. Chan,Wing-Yee So,Ronald C.W. Ma,Svati H. Shah,Christopher B. Granger,Arshed A. Quyyumi,Allan I. Levey,Viola Vaccarino,Muredach P. Reilly,Daniel J. Rader,Michael J.A. Williams,Andre M. van Rij,Gregory T. Jones,Elisabetta Trabetti,Giovanni Malerba,Pier Franco Pignatti,Attilio Boner,Lydia Pescollderungg,Domenico Girelli,Oliviero Olivieri,Nicola Martinelli,Bjorn R. Ludviksson,Dora Ludviksdottir,Gudmundur I. Eyjolfsson,David O. Arnar,Gudmundur Thorgeirsson,Klaus A. Deichmann,Philip J. Thompson,Matthias Wjst,Ian P. Hall,Dirkje S. Postma,Thorarinn Gislason,Jeffrey R. Gulcher,Augustine Kong,Ingileif Jonsdottir,Ingileif Jonsdottir,Unnur Thorsteinsdottir,Unnur Thorsteinsdottir,Kari Stefansson,Kari Stefansson +77 more
TL;DR: A genome-wide association scan for sequence variants affecting eosinophil counts in blood of 9,392 Icelanders found that a nonsynonymous SNP at 12q24, in SH2B3, associated significantly with myocardial infarction in six different populations.
Journal ArticleDOI
Identification of copy number variations and common deletion polymorphisms in cattle
Joon Seol Bae,Hyun Sub Cheong,Lyoung Hyo Kim,Suk NamGung,Tae Joon Park,Ji-Yong Chun,Jason Yongha Kim,Charisse Flerida A. Pasaje,Jin Sol Lee,Hyoung Doo Shin +9 more
TL;DR: A map of bovine CNVs is described to contribute to animal breeding and protection from diseases with the aid of genomic information and provide important resources for future bovines genome research.
Journal ArticleDOI
A sequence variant on 17q21 is associated with age at onset and severity of asthma
Eva Halapi,Daniel F. Gudbjartsson,Gudrun M. Jonsdottir,Unnur S. Bjornsdottir,Unnur S. Bjornsdottir,Gudmar Thorleifsson,Hafdis T. Helgadottir,Carolyn Williams,Gerard H. Koppelman,Andrea Heinzmann,H. Marike Boezen,Aslaug Jonasdottir,Thorarinn Blondal,Sigurjon A. Gudjonsson,Adalbjorg Jonasdottir,Theodora Thorlacius,Amanda P. Henry,Janine Altmueller,Marcus Krueger,Hyoung Doo Shin,Soo-Taek Uh,Hyun Sub Cheong,Brynja Jonsdottir,Bjorn R. Ludviksson,Dora Ludviksdottir,David Gislason,Choon-Sik Park,Klaus A. Deichmann,Philip J. Thompson,Matthias Wjst,Ian P. Hall,Dirkje S. Postma,Thorarinn Gislason,Augustine Kong,Ingileif Jonsdottir,Ingileif Jonsdottir,Unnur Thorsteinsdottir,Unnur Thorsteinsdottir,Kari Stefansson,Kari Stefansson +39 more
TL;DR: The contribution of rs7216389-T to the development of asthma is unlikely to operate only through an impact on the expression of ORMDL3 or GSDMB genes, as other sequence variants showing a weaker association with asthma compared with that of rs 7216389 were more strongly associated with the expression with both genes.
Journal ArticleDOI
Extended genetic effects of ADH cluster genes on the risk of alcohol dependence: from GWAS to replication
Byung Lae Park,Jee Wook Kim,Hyun Sub Cheong,Lyoung Hyo Kim,Boung Chul Lee,Cheong Hoon Seo,Tae-Cheon Kang,Young-Woo Nam,Goon-Bo Kim,Hyoung Doo Shin,Ihn-Geun Choi +10 more
TL;DR: The present study used GWAS and replication studies in a Korean cohort with AD to identify new candidate genes and suggested that ADH1Brs1229984 (H47R) might be the sole functional genetic marker across the ADH gene cluster.
Journal ArticleDOI
Frequent Amplification of CENPF, GMNN and CDK13 Genes in Hepatocellular Carcinomas
Hye Eun Kim,Dae Ghon Kim,Kyungjin Lee,Jang Geun Son,Min Young Song,Young-Mi Park,Jae-Jung Kim,Sung Won Cho,Sung Gil Chi,Hyun Sub Cheong,Hyoung Doo Shin,Sang Wook Lee,Jong-Keuk Lee +12 more
TL;DR: The results suggest that coincidently amplified CDK13, GMNN, and CENPF genes can play a role as common cancer-driver genes in human cancers.