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Genetic Epidemiology|January 22, 2011
On optimal pooling designs to identify rare variants through massive resequencingJoon Sang Lee, Murim Choi, Xiting Yan, et al.
Differentiation; Research in Biological Diversity|August 19, 2006
Morphogenesis of the trachea and esophagus: current players and new roles for noggin and BmpsJianwen Que, Murim Choi, Joshua W Ziel, et al.
Circulation Research|January 16, 2007
The bone morphogenetic protein antagonist noggin regulates mammalian cardiac morphogenesisMurim Choi, Rolf W Stottmann, Yu-Ping Yang, et al.
The Journal of Investigative Dermatology|February 26, 2025
Comprehensive Profiling of Genetic and Nongenetic Factors that Influence Skin Traits in Asian Women from 4 CountriesHyunchae Moon, Minsoo Kim, Hyungtai Sim, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 26, 2019
Oncogenic effects of germline variants in lysosomal storage disease genesJunghoon Shin, Daeyoon Kim, Hyung-Lae Kim, et al.
Annals of Clinical and Laboratory Science|March 2, 2016
Rare Korean Cases of Very-long-chain Acyl-CoA Dehydrogenase Deficiency with a Novel Recurrent MutationJung Min Ko, Jieun Seo, Murim Choi, et al.
American Journal of Medical Genetics. Part A|May 28, 2016
GM3 synthase deficiency due to ST3GAL5 variants in two Korean female siblings: Masquerading as Rett syndrome-like phenotypeJin Sook Lee, Yongjin Yoo, Byung Chan Lim, et al.
The Journal of Clinical Endocrinology and Metabolism|June 29, 2012
Identification of somatic mutations in parathyroid tumors using whole-exome sequencingM Kyle Cromer, Lee F Starker, Murim Choi, et al.
Gene|May 5, 2015
Alpha-thalassemia X-linked intellectual disability syndrome identified by whole exome sequencing in two boys with white matter changes and developmental retardationJin Sook Lee, Sangmoon Lee, Byung Chan Lim, et al.
Elife|December 6, 2024
Increased inflammatory signature in myeloid cells of non-small cell lung cancer patients with high clonal hematopoiesis burdenHyungtai Sim, Hyun Jung Park, Geun-Ho Park, et al.
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