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jie huang
jie huang
Research Professor in Global Health, Peking University
在 pku.edu.cn 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
Nature genetics 47 (10), 1121-1130, 2015
24112015
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13742018
An atlas of genetic influences on human blood metabolites
SY Shin, EB Fauman, AK Petersen, J Krumsiek, R Santos, J Huang, ...
Nature genetics 46 (6), 543-550, 2014
13132014
The UK10K project identifies rare variants in health and disease
Statistics group Ciampi Antonio 8 Greenwood Celia MT (co-chair) 7 8 14 19 ...
Nature 526 (7571), 82-90, 2015
10892015
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
7632015
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
P Gormley, V Anttila, BS Winsvold, P Palta, T Esko, TH Pers, KH Farh, ...
Nature genetics 48 (8), 856-866, 2016
7382016
A general approach for haplotype phasing across the full spectrum of relatedness
J O'Connell, D Gurdasani, O Delaneau, N Pirastu, S Ulivi, M Cocca, ...
PLoS genetics 10 (4), e1004234, 2014
6442014
Multi-ethnic genome-wide association study for atrial fibrillation
C Roselli, MD Chaffin, LC Weng, S Aeschbacher, G Ahlberg, CM Albert, ...
Nature genetics 50 (9), 1225-1233, 2018
6192018
Genetics of blood lipids among~ 300,000 multi-ethnic participants of the Million Veteran Program
D Klarin, SM Damrauer, K Cho, YV Sun, TM Teslovich, J Honerlaw, ...
Nature genetics 50 (11), 1514-1523, 2018
5712018
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture
HF Zheng, V Forgetta, YH Hsu, K Estrada, A Rosello‐Diez, PJ Leo, ...
Nature 526 (7571), 112-117, 2015
5482015
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
M Vujkovic, JM Keaton, JA Lynch, DR Miller, J Zhou, C Tcheandjieu, ...
Nature genetics 52 (7), 680-691, 2020
5382020
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
E Wheeler, A Leong, CT Liu, MF Hivert, RJ Strawbridge, C Podmore, M Li, ...
PLoS medicine 14 (9), e1002383, 2017
4132017
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
J Huang, B Howie, S McCarthy, Y Memari, K Walter, JL Min, P Danecek, ...
Nature communications 6 (1), 8111, 2015
4122015
Genome analyses of> 200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders
S Ligthart, A Vaez, U Võsa, MG Stathopoulou, PS De Vries, BP Prins, ...
The American Journal of Human Genetics 103 (5), 691-706, 2018
3622018
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
3572022
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
IE Christophersen, M Rienstra, C Roselli, X Yin, B Geelhoed, J Barnard, ...
Nature genetics 49 (6), 946-952, 2017
3292017
Uric acid and cardiovascular events: a Mendelian randomization study
ME Kleber, G Delgado, TB Grammer, G Silbernagel, J Huang, BK Krämer, ...
Journal of the American Society of Nephrology 26 (11), 2831-2838, 2015
3122015
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers
C Sidore, F Busonero, A Maschio, E Porcu, S Naitza, M Zoledziewska, ...
Nature genetics 47 (11), 1272-1281, 2015
2922015
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ...
The American Journal of Human Genetics 94 (2), 233-245, 2014
2402014
Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression
J Huang, RH Perlis, PH Lee, AJ Rush, M Fava, GS Sachs, J Lieberman, ...
American Journal of Psychiatry 167 (10), 1254-1263, 2010
2372010
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