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He Zhang
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GSDS 2.0: an upgraded gene feature visualization server
B Hu, J Jin, AY Guo, H Zhang, J Luo, G Gao
Bioinformatics 31 (8), 1296-1297, 2015
36622015
A reference panel of 64,976 haplotypes for genotype imputation
S McCarthy, S Das, W Kretzschmar, O Delaneau, AR Wood, A Teumer, ...
Nature genetics, 2016
3184*2016
PlantTFDB 3.0: a portal for the functional and evolutionary study of plant transcription factors
J Jin, H Zhang, L Kong, G Gao, J Luo
Nucleic acids research 42 (D1), D1182-D1187, 2014
9632014
Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
TG and HDL Working Group of the Exome Sequencing Project, National Heart ...
New England Journal of Medicine 371 (1), 22-31, 2014
8662014
Targeting renal cell carcinoma with a HIF-2 antagonist
W Chen, H Hill, A Christie, MS Kim, E Holloman, A Pavia-Jimenez, ...
Nature 539 (7627), 112-117, 2016
7102016
Exome-wide association study of plasma lipids in> 300,000 individuals
DJ Liu, GM Peloso, H Yu, AS Butterworth, X Wang, A Mahajan, ...
Nature genetics 49 (12), 1758-1766, 2017
5822017
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
4182016
PlantTFDB 2.0: update and improvement of the comprehensive plant transcription factor database
H Zhang, J Jin, L Tang, Y Zhao, X Gu, G Gao, J Luo
Nucleic acids research 39 (suppl_1), D1114-D1117, 2011
3862011
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
P Surendran, F Drenos, R Young, H Warren, JP Cook, AK Manning, ...
Nature genetics 48 (10), 1151-1161, 2016
3392016
Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk
OL Holmen, H Zhang, Y Fan, DH Hovelson, EM Schmidt, W Zhou, Y Guo, ...
Nature genetics 46 (4), 345-351, 2014
3342014
PlantTFDB: a comprehensive plant transcription factor database
AY Guo, X Chen, G Gao, H Zhang, QH Zhu, XC Liu, YF Zhong, X Gu, K He, ...
Nucleic Acids Research 36 (suppl_1), D966-D969, 2007
2922007
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
2632017
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
2452014
Meta-analysis of gene-level tests for rare variant association
DJ Liu, GM Peloso, X Zhan, OL Holmen, M Zawistowski, S Feng, ...
Nature genetics 46 (2), 200-204, 2014
2432014
A ubiquitin ligase mediates target-directed microRNA decay independently of tailing and trimming
J Han, CA LaVigne, BT Jones, H Zhang, F Gillett, JT Mendell
Science 370 (6523), eabc9546, 2020
1902020
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
P Surendran, EV Feofanova, N Lahrouchi, I Ntalla, S Karthikeyan, J Cook, ...
Nature genetics 52 (12), 1314-1332, 2020
1592020
Exome chip meta-analysis identifies novel loci and East Asian–specific coding variants that contribute to lipid levels and coronary artery disease
X Lu, GM Peloso, DJ Liu, Y Wu, H Zhang, W Zhou, J Li, CS Tang, ...
Nature genetics 49 (12), 1722-1730, 2017
1482017
PUMILIO hyperactivity drives premature aging of Norad-deficient mice
F Kopp, MM Elguindy, ME Yalvac, H Zhang, B Chen, FA Gillett, S Lee, ...
eLife 8, e42650, 2019
1002019
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese
CS Tang, H Zhang, CYY Cheung, M Xu, JCY Ho, W Zhou, SS Cherny, ...
Nature communications 6 (1), 10206, 2015
1002015
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations
SK Ganesh, DI Chasman, MG Larson, X Guo, G Verwoert, JC Bis, X Gu, ...
The American Journal of Human Genetics 95 (1), 49-65, 2014
952014
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