Author details

Full Name

Mi Yeong Hwang

Affiliation

ORCID

Career Start Year

2013

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35043955	Phenome-wide association study of the major histocompatibility complex region in the Korean population identifies novel association signals.	Human Molecular Genetics	2022
35589828	Shared genetic architectures of subjective well-being in East Asian and European ancestry populations.	Nat Hum Behav	2022
36333282	The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians.	Nature Communications	2022
35609976	Biological insights into systemic lupus erythematosus through an immune cell-specific transcriptome-wide association study.	Ann Rheum Dis	2022
36506321	Analyzing the Korean reference genome with meta-imputation increased the imputation accuracy and spectrum of rare variants in the Korean population.		2022
35012284	Validation and genetic heritability estimation of known type 2 diabetes related variants in the Korean population.		2021
34108472	Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.	Nat Commun	2021
33272962	Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus.	Ann Rheum Dis	2021
32723749	Genome-wide association study in a Korean population identifies six novel susceptibility loci for rheumatoid arthritis.	Annals of the Rheumatic Diseases	2020
32803703	GEN2VCF: a converter for human genome imputation output format to VCF format.	Genes and Genomics	2020
31463366	Programmable Nuclease-Based Integration into Novel Extragenic Genomic Safe Harbor Identified from Korean Population-Based CNV Analysis.	Molecular Therapy - Oncolytics	2019
31896248	Recapitulation of previously reported associations for type 2 diabetes and metabolic traits in the 126K East Asians.		2019
31087446	Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups.	Genetic Epidemiology	2019
31118516	Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.	Nature	2019
30718733	The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits.	Scientific Reports	2019
29941447	Nonsynonymous Variants in <i>PAX4</i> and <i>GLP1R</i> Are Associated With Type 2 Diabetes in an East Asian Population.	Diabetes	2018
30487518	Interethnic analyses of blood pressure loci in populations of East Asian and European descent.	Nat Commun	2018
28100915	Whole-exome sequencing study reveals common copy number variants in protocadherin genes associated with childhood obesity in Koreans.	International Journal of Obesity	2017
28420343	On the association analysis of CNV data: a fast and robust family-based association method.	BMC Bioinformatics	2017
28334899	Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.	Hum Mol Genet	2017
28978046	Positive correlation of cg16672562 methylation with obesity-related traits in childhood obesity, and its independence with underlying <i>HIF3A</i> (hypoxia-inducible factor 3a) genetic background.	Oncotarget	2017
28154514	Identification of a Copy Number Variation on Chromosome 20q13.12 Associated with Osteoporotic Fractures in the Korean Population.		2016
26833210	Evaluation of pleiotropic effects among common genetic loci identified for cardio-metabolic traits in a Korean population.	Cardiovascular Diabetology	2016
26064965	Influence of Genetic Variants in EGF and Other Genes on Hematological Traits in Korean Populations by a Genome-Wide Approach.	BioMed Research International	2015
25880085	A genome-wide association study of copy-number variation identifies putative loci associated with osteoarthritis in Koreans.	BMC Musculoskelet Disord	2015
25535679	Combinatorial approach to estimate copy number genotype using whole-exome sequencing data.	Genomics	2015
26622897	MicroRNA-650 in a copy number-variable region regulates the production of interleukin 6 in human osteosarcoma cells.	Oncology Letters	2015
24886904	Genome-wide copy number variation study reveals KCNIP1 as a modulator of insulin secretion.	Genomics	2014
24903457	Identification of a genetic variant at 2q12.1 associated with blood pressure in East Asians by genome-wide scan including gene-environment interactions.	BMC Medical Genetics	2014
23626002	KGVDB: a population-based genomic map of CNVs tagged by SNPs in Koreans.		2013
23147675	Gene-based copy number variation study reveals a microdeletion at 12q24 that influences height in the Korean population.	Genomics	2013