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Hong-Hee Won
Hong-Hee Won
Associate Professor, SAIHST, Sungkyunkwan University
Dirección de correo verificada de broadinstitute.org - Página principal
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Analysis of protein-coding genetic variation in 60,706 humans
M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ...
Nature 536 (7616), 285-291, 2016
107052016
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
Nature genetics 47 (10), 1121-1130, 2015
25412015
Modeling linkage disequilibrium increases accuracy of polygenic risk scores
BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ...
The american journal of human genetics 97 (4), 576-592, 2015
14312015
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
N Mullins, AJ Forstner, KS O’Connell, B Coombes, JRI Coleman, Z Qiao, ...
Nature genetics 53 (6), 817-829, 2021
10062021
Diagnostic yield and clinical utility of sequencing familial hypercholesterolemia genes in patients with severe hypercholesterolemia
AV Khera, HH Won, GM Peloso, KS Lawson, TM Bartz, X Deng, ...
Journal of the American College of Cardiology 67 (22), 2578-2589, 2016
9652016
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, P Angelica Merlini, ...
Nature 518 (7537), 102-106, 2015
7782015
Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease
Myocardial Infarction Genetics Consortium Investigators
New England Journal of Medicine 371 (22), 2072-2082, 2014
4772014
Machine learning in DNA microarray analysis for cancer classification
SB Cho, HH Won
Proceedings of the First Asia-Pacific Bioinformatics Conference on …, 2003
4242003
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators
New England Journal of Medicine 374 (12), 1134-1144, 2016
4142016
Improving polygenic prediction in ancestrally diverse populations
Y Ruan, YF Lin, YCA Feng, CY Chen, M Lam, Z Guo, L He, A Sawa, ...
Nature genetics 54 (5), 573-580, 2022
3982022
Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity
D Saleheen, P Natarajan, IM Armean, W Zhao, A Rasheed, SA Khetarpal, ...
Nature 544 (7649), 235-239, 2017
3302017
Systematic evaluation of pleiotropy identifies 6 further loci associated with coronary artery disease
TR Webb, J Erdmann, KE Stirrups, NO Stitziel, NGD Masca, H Jansen, ...
Journal of the American College of Cardiology 69 (7), 823-836, 2017
2602017
Phenotypic characterization of genetically lowered human lipoprotein (a) levels
CA Emdin, AV Khera, P Natarajan, D Klarin, HH Won, GM Peloso, ...
Journal of the American College of Cardiology 68 (25), 2761-2772, 2016
2312016
SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians
A Miyashita, A Koike, G Jun, LS Wang, S Takahashi, E Matsubara, ...
PloS one 8 (4), e58618, 2013
2262013
Association between adiposity and cardiovascular outcomes: an umbrella review and meta-analysis of observational and Mendelian randomization studies
MS Kim, WJ Kim, AV Khera, JY Kim, DK Yon, SW Lee, JI Shin, HH Won
European heart journal 42 (34), 3388-3403, 2021
2072021
Physical activity and the risk of SARS-CoV-2 infection, severe COVID-19 illness and COVID-19 related mortality in South Korea: a nationwide cohort study
SW Lee, J Lee, SY Moon, HY Jin, JM Yang, S Ogino, M Song, SH Hong, ...
British journal of sports medicine 56 (16), 901-912, 2022
2022022
Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection
D Adlam, TM Olson, N Combaret, JC Kovacic, SE Iismaa, A Al-Hussaini, ...
Journal of the American College of Cardiology 73 (1), 58-66, 2019
1972019
Association of rare and common variation in the lipoprotein lipase gene with coronary artery disease
AV Khera, HH Won, GM Peloso, C O’Dushlaine, D Liu, NO Stitziel, ...
Jama 317 (9), 937-946, 2017
1912017
Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors
N Mullins, JE Kang, AI Campos, JRI Coleman, AC Edwards, H Galfalvy, ...
Biological psychiatry 91 (3), 313-327, 2022
1782022
Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing …
HJ Kim, KM Sohn, ME Shy, KM Krajewski, M Hwang, JH Park, SY Jang, ...
The American Journal of Human Genetics 81 (3), 552-558, 2007
1622007
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