Honghuang Lin

Процитировано

	Все	Начиная с 2018 г.
Статистика цитирования	14450	10938
h-индекс	55	46
i10-индекс	145	126

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Emelia J. BenjaminThe Framingham Heart Study, Boston UniversityПодтвержден адрес электронной почты в домене bu.edu
Patrick T. Ellinor, MD, PhDBroad Institute of MIT and Harvard, Massachusetts General Hospital, Harvard Medical SchoolПодтвержден адрес электронной почты в домене mgh.harvard.edu
Daniel LevyNational Heart, Lung, and Blood InstituteПодтвержден адрес электронной почты в домене nih.gov
Yu Zong ChenProfessor Department of Pharmacy National University of SingaporeПодтвержден адрес электронной почты в домене nus.edu.sg
Leo, Lianyi HanNational Center for Biotechnology InformationПодтвержден адрес электронной почты в домене ncbi.nlm.nih.gov
Hailei Zhangbroad instituteПодтвержден адрес электронной почты в домене broadinstitute.org
Juan CuiAssociate Professor of Computer Science, University of Nebraska-LincolnПодтвержден адрес электронной почты в домене unl.edu
Guang Lan ZhangCS Department, MET, Boston University; Dana-Farber Cancer Institute, Harvard Medical SchoolПодтвержден адрес электронной почты в домене bu.edu
Ming-Huei ChenPopulation Sciences Branch, National Heart, Lung and Blood InstituteПодтвержден адрес электронной почты в домене nih.gov
L Adrienne CupplesProfessor of BiostatisticsПодтвержден адрес электронной почты в домене bu.edu
Jennifer BrodyUniversity of WashingtonПодтвержден адрес электронной почты в домене uw.edu
Surajit RayUniversity of GlasgowПодтвержден адрес электронной почты в домене math.bu.edu
Chun Wei YapNational Healthcare GroupПодтвержден адрес электронной почты в домене nhg.com.sg
Mohammad Asif KhanProfessor, University of Doha for Science and Technology, QatarПодтвержден адрес электронной почты в домене udst.edu.qa
Tin Wee TanAssociate Professor, Dept of Biochemistry, National University of SingaporeПодтвержден адрес электронной почты в домене bic.nus.edu.sg

Honghuang Lin

Professor, University of Massachusetts Medical School

Подтвержден адрес электронной почты в домене umassmed.edu - Главная страница

Bioinformatics genomics machine learning


Название По числу цитат По году По названию	Процитировано Процитировано	Год
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	1677	2019
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	792	2017
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	640	2012
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	580	2017
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	481	2018
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	429	2016
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	429*	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	401	2016
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	363	2006
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	349	2020
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	321	2011
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	281	2018
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	281	2016
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	275	2018
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	275	2017
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	271	2008
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), 1-15, 2016	259	2016
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	224	2014
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	208	2018
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation JC Bis, X Jian, BW Kunkle, Y Chen, KL Hamilton-Nelson, WS Bush, ... Molecular psychiatry 25 (8), 1859-1875, 2020	206	2020

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