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Honghuang Lin
Honghuang Lin
在 umassmed.edu 的电子邮件经过验证 - 首页
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Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ...
Nature genetics 51 (3), 414-430, 2019
21302019
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373-1384, 2017
8882017
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
PT Ellinor, KL Lunetta, CM Albert, NL Glazer, MD Ritchie, AV Smith, ...
Nature genetics 44 (6), 670-675, 2012
6692012
Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186-190, 2017
6302017
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
5942018
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
S Shah, A Henry, C Roselli, H Lin, G Sveinbjörnsson, G Fatemifar, ...
Nature communications 11 (1), 163, 2020
5132020
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
C Pattaro, A Teumer, M Gorski, AY Chu, M Li, V Mijatovic, M Garnaas, ...
Nature communications 7 (1), 10023, 2016
4682016
Evaluation of MHC class I peptide binding prediction servers: applications for vaccine research
HH Lin, S Ray, S Tongchusak, EL Reinherz, V Brusic
BMC immunology 9, 1-13, 2008
4482008
Evaluation of MHC-II peptide binding prediction servers: applications for vaccine research
H Lin, G Zhang, S Tongchusak, E Reinherz, V Brusic
BMC Bioinformatics 9, S22, 2008
448*2008
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
GB Ehret, T Ferreira, DI Chasman, AU Jackson, EM Schmidt, T Johnson, ...
Nature genetics 48 (10), 1171-1184, 2016
4272016
PROFEAT: a web server for computing structural and physicochemical features of proteins and peptides from amino acid sequence
ZR Li, HH Lin, LY Han, L Jiang, X Chen, YZ Chen
Nucleic acids research 34 (suppl_2), W32-W37, 2006
3802006
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
3502018
Atrial fibrillation: current knowledge and future directions in epidemiology and genomics
JW Magnani, M Rienstra, H Lin, MF Sinner, SA Lubitz, DD McManus, ...
Circulation 124 (18), 1982-1993, 2011
3362011
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
3182018
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
3132016
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
3122017
DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases
S Ligthart, C Marzi, S Aslibekyan, MM Mendelson, KN Conneely, ...
Genome biology 17, 1-15, 2016
2872016
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
2722022
Genetic predisposition, clinical risk factor burden, and lifetime risk of atrial fibrillation
LC Weng, SR Preis, OL Hulme, MG Larson, SH Choi, B Wang, L Trinquart, ...
Circulation 137 (10), 1027-1038, 2018
2442018
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
2352014
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