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Dong Mun Shin
Observed names:
DONG MUN SHIN,
Dong M. Shin,
Shin, Dong Mun
Institutions:
Emory University,
Korea National Institute of Health
Observed institutions:
Emory University,
Chungbuk National University,
Korea National Institute of Health,
Korea Disease Control and Prevention Agency
ORCID:
0009-0001-4772-7843
Observed ORCID:
0009-0001-4772-7843
OpenAlex ID:
A5050371536
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
2022
·
Anubha Mahajan
, Cassandra N. Spracklen
, et al.
·
Nature Genetics
·
736
PDF
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
2024
·
Ken Suzuki
, Konstantinos Hatzikotoulas
, et al.
·
Nature
·
689
PDF
Identification of type 2 diabetes loci in 433,540 East Asian individuals
2020
·
Cassandra N. Spracklen
, Momoko Horikoshi
, et al.
·
Nature
·
460
PDF
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits
2019
·
Sanghoon Moon
, Young Jin Kim
, et al.
·
Scientific Reports
·
292
PDF
The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians
2022
·
Young Jin Kim
, Sanghoon Moon
, et al.
·
Nature Communications
·
63
PDF
GEN2VCF: a converter for human genome imputation output format to VCF format
2020
·
Dong Mun Shin
, Mi Yeong Hwang
, et al.
·
Genes & Genomics
·
9
PDF
Uncovering potential causal genes for undiagnosed congenital anomalies using an in-house pipeline for trio-based whole-genome sequencing
2025
·
Jeong-Min Kim
, Hye-Won Cho
, et al.
·
Human Genomics
·
6
PDF
Development of an MHC imputation panel highlights independent contributions of HLA amino acid residues and C4 copy number variations to SLE risk
2025
·
Chae-Yeon Yu
, Dong Mun Shin
, et al.
·
Annals of the Rheumatic Diseases
·
3
PDF
Accelerating genetic diagnosis in the NICU: neonatologist-driven rapid whole genome sequencing
2026
·
Hye-Won Cho
, Jeong-Min Kim
, et al.
·
Scientific Reports
·
1
PDF
Unraveling the cellular characteristics of cardiomyopathy with rare variant-driven gene signatures using multi-omics analysis
2025
·
Ha-Eun Jeong
, Kyung-Hyun Kim
, et al.
·
Scientific Reports
·
1
Two novel genetic variants in the WFDC2 gene from patients with bronchiectasis
2025
·
Jeong-Min Kim
, Soojin Hwang
, et al.
·
Respiratory Research
·
1
PDF
Deep Learning-Based Spatial Profiling Identifies MET-Associated Immune Exclusion and Therapeutic Vulnerability Underlying Racial Disparities in Head and Neck Cancer
2026
·
Xinyu Cui
, Fanghui Chen
, et al.
·
Research Square
PDF
Identification of novel MYO19 variants in neonatal hypertrophic cardiomyopathy: a familial analysis revealing oligogenic contributors to disease severity
2025
·
Hye-Won Cho
, Hyeseon Kim
, et al.
·
Orphanet Journal of Rare Diseases
PDF
Replication of Previously Type 2 Diabetes Associated Loci in 35,000 Samples of Korean Population
2018
·
YOUNG JIN KIM
, MI YEONG HWANG
, et al.
·
Diabetes
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Works count:
20
Citation count:
2,261
H-index:
6
I10-index:
5
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