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BMC Bioinformatics|April 20, 2017
On the association analysis of CNV data: a fast and robust family-based association methodMeiling Liu, Sanghoon Moon, Longfei Wang, et al.
Genomics|June 3, 2014
Genome-wide copy number variation study reveals KCNIP1 as a modulator of insulin secretionHeun-Sik Lee, Sanghoon Moon, Jun Ho Yun, et al.
Genomics|November 14, 2012
Gene-based copy number variation study reveals a microdeletion at 12q24 that influences height in the Korean populationYun Kyoung Kim, Sanghoon Moon, Mi Yeong Hwang, et al.
BMC Medical Genetics|June 7, 2014
Identification of a genetic variant at 2q12.1 associated with blood pressure in East Asians by genome-wide scan including gene-environment interactionsYun Kyoung Kim, Youngdoe Kim, Mi Yeong Hwang, et al.
Genomics|December 24, 2014
Combinatorial approach to estimate copy number genotype using whole-exome sequencing dataMi Yeong Hwang, Sanghoon Moon, Lyong Heo, et al.
Oncology Letters|December 2, 2015
MicroRNA-650 in a copy number-variable region regulates the production of interleukin 6 in human osteosarcoma cellsJun Ho Yun, Sanghoon Moon, Heun-Sik Lee, et al.
Biomed Research International|June 12, 2015
Influence of Genetic Variants in EGF and Other Genes on Hematological Traits in Korean Populations by a Genome-Wide ApproachYun Kyoung Kim, Ji Hee Oh, Young Jin Kim, et al.
Molecular Therapy Oncolytics|August 30, 2019
Programmable Nuclease-Based Integration into Novel Extragenic Genomic Safe Harbor Identified from Korean Population-Based CNV AnalysisEun-Seo Lee, Sanghoon Moon, Kwaku Dad Abu-Bonsrah, et al.
Human Molecular Genetics|January 19, 2022
Phenome-wide association study of the major histocompatibility complex region in the Korean population identifies novel association signalsChanwoo Kim, Young Jin Kim, Wanson Choi, et al.
BMC Musculoskeletal Disorders|April 17, 2015
A genome-wide association study of copy-number variation identifies putative loci associated with osteoarthritis in KoreansSanghoon Moon, Bhumsuk Keam, Mi Yeong Hwang, et al.
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