Manuel A. Rivas

인용

	전체	2020년 이후
서지정보	65897	32946
h-index	62	55
i10-index	117	108

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Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad Instituteatgu.mgh.harvard.edu의 이메일 확인됨
Aaron McKennaGeisel School of Medicine, Dartmouth Collegedartmouth.edu의 이메일 확인됨
Mark DePristoBigHat Biosciencesbighatbio.com의 이메일 확인됨
Matti PirinenUniversity of Helsinkihelsinki.fi의 이메일 확인됨
Benjamin NealeMassachusetts General Hospital; Broad Institute; Harvard Medical Schoolbroadinstitute.org의 이메일 확인됨
Tuuli LappalainenSciLifeLab, KTH Royal Institute of Technology & New York Genome Centernygenome.org의 이메일 확인됨
Kyle Jeffrie GaultonWinkler Endowed Chair in Type 1 Diabetes; Associate Professor of Pediatrics, UCSDucsd.edu의 이메일 확인됨
Chris CotsapasYale School of Medicinebroadinstitute.org의 이메일 확인됨
Noah A ZaitlenProfessor at UCLAucla.edu의 이메일 확인됨
Loukas MoutsianasGenomics Englandgenomicsengland.co.uk의 이메일 확인됨
Shaun PurcellSleep & Neurogenetics Lab, Brigham & Women's Hospital, Bostonbwh.harvard.edu의 이메일 확인됨
Benjamin F. VoightAssociate Professor, Dept. of Systems Pharmacology and Translational Therapeutics, Dept. of Geneticspennmedicine.upenn.edu의 이메일 확인됨
Kathryn RoederProfessor of Statistics, Carnegie Mellon Universityandrew.cmu.edu의 이메일 확인됨
Bernie DevlinUniversity of Pittsburgh School of Medicineupmc.edu의 이메일 확인됨
Vamsi MoothaMassachusetts General Hospital, Harvard Medical School, HHMIhms.harvard.edu의 이메일 확인됨
Sarah E CalvoBroad Institute, Massachusetts General Hospital, Harvard Medical Schoolbroadinstitute.org의 이메일 확인됨
Eleazar EskinUniversity of California, Los Angelescs.ucla.edu의 이메일 확인됨
Hyun Min KangProfessor of Biostatistics, University of Michigan, Ann Arborumich.edu의 이메일 확인됨
Eun Yong KangMachine Learning, Microsoftmicrosoft.com의 이메일 확인됨
Buhm HanDepartment of Biomedical Sciences, Seoul National University College of Medicinesnu.ac.kr의 이메일 확인됨

팔로우

Manuel A. Rivas

Assistant Professor, Department of Biomedical Data Science, Stanford University

stanford.edu의 이메일 확인됨 - 홈페이지

Human Genetics Statistics & Optimization Therapeutics AI Biobanks


제목 서지정보순 정렬 연도순 정렬 제목순 정렬	인용 인용	연도
A framework for variation discovery and genotyping using next-generation DNA sequencing data MA DePristo, E Banks, R Poplin, KV Garimella, JR Maguire, C Hartl, ... Nature genetics 43 (5), 491-498, 2011	12259	2011
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	10696	2016
A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010	8978	2010
The genotype-tissue expression (GTEx) project J Lonsdale, J Thomas, M Salvatore, R Phillips, E Lo, S Shad, R Hasz, ... Nature genetics 45 (6), 580-585, 2013	8393	2013
The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans GTEx Consortium, KG Ardlie, DS Deluca, AV Segrè, TJ Sullivan, ... Science 348 (6235), 648-660, 2015	4848	2015
Transcriptome and genome sequencing uncovers functional variation in humans T Lappalainen, M Sammeth, MR Friedländer, PAC ‘t Hoen, J Monlong, ... Nature 501 (7468), 506-511, 2013	2131	2013
A cross-population atlas of genetic associations for 220 human phenotypes S Sakaue, M Kanai, Y Tanigawa, J Karjalainen, M Kurki, S Koshiba, ... Nature genetics 53 (10), 1415-1424, 2021	1351	2021
The genetic architecture of type 2 diabetes C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ... Nature 536 (7614), 41-47, 2016	1305	2016
Landscape of X chromosome inactivation across human tissues T Tukiainen, AC Villani, A Yen, MA Rivas, JL Marshall, R Satija, M Aguirre, ... Nature 550 (7675), 244-248, 2017	975	2017
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease MA Rivas, M Beaudoin, A Gardet, C Stevens, Y Sharma, CK Zhang, ... Nature genetics 43 (11), 1066-1073, 2011	907	2011
Mapping the human genetic architecture of COVID-19 Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ... Nature 600 (7889), 472-477, 2021	839	2021
Opportunities and challenges for transcriptome-wide association studies M Wainberg, N Sinnott-Armstrong, N Mancuso, AN Barbeira, DA Knowles, ... Nature genetics 51 (4), 592-599, 2019	806	2019
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	785	2015
Demographic history and rare allele sharing among human populations S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ... Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011	739	2011
Testing for an unusual distribution of rare variants BM Neale, MA Rivas, BF Voight, D Altshuler, B Devlin, M Orho-Melander, ... PLoS genetics 7 (3), e1001322, 2011	737	2011
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	686	2017
Genetics of 35 blood and urine biomarkers in the UK Biobank N Sinnott-Armstrong, Y Tanigawa, D Amar, N Mars, C Benner, M Aguirre, ... Nature genetics 53 (2), 185-194, 2021	628	2021
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency SE Calvo, EJ Tucker, AG Compton, DM Kirby, G Crawford, NP Burtt, ... Nature genetics 42 (10), 851-858, 2010	430	2010
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease KY Hui, H Fernandez-Hernandez, J Hu, A Schaffner, N Pankratz, NY Hsu, ... Science translational medicine 10 (423), eaai7795, 2018	389	2018
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	375	2018

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