Manuel A. Rivas - Google Scholar Citations

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Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteVerified email at atgu.mgh.harvard.edu
Aaron McKennaGeisel School of Medicine, Dartmouth CollegeVerified email at dartmouth.edu
Mark DePristoGoogle Inc.Verified email at google.com
Benjamin NealeAssistant Professor, Analytic and Translational Genetics Unit, Massachusetts General HospitalVerified email at broadinstitute.org
Tuuli LappalainenNew York Genome Center & Columbia UniversityVerified email at nygenome.org
Sekar KathiresanAssociate Professor of Medicine, Harvard Medical SchoolVerified email at partners.org
Daniel G MacArthurAnalytic and Translational Genetics Unit, Massachusetts General HospitalVerified email at atgu.mgh.harvard.edu
Matti PirinenUniversity of HelsinkiVerified email at helsinki.fi
Kyle Jeffrie GaultonAssistant Professor, University of California San DiegoVerified email at ucsd.edu
Chris CotsapasYale School of MedicineVerified email at broadinstitute.org
Emmanouil DermitzakisProfessor of Genetics, University of Geneva Medical School / Director, Health 2030 Genome CenterVerified email at unige.ch
Shaun PurcellBrigham & Women's Hospital, BostonVerified email at bwh.harvard.edu
Benjamin F. VoightAssociate Professor, Dept. of Systems Pharmacology and Translational Therapeutics, Dept. of GeneticsVerified email at pennmedicine.upenn.edu
Kathryn RoederProfessor of Statistics, Carnegie Mellon UniversityVerified email at andrew.cmu.edu
Bernie DevlinUniversity of Pittsburgh School of MedicineVerified email at upmc.edu
Loukas MoutsianasWHRI, QMUL & Genomics EnglandVerified email at qmul.ac.uk
Noah A ZaitlenAssociate Professor at UCLAVerified email at ucla.edu
Vamsi MoothaMassachusetts General Hospital, Harvard Medical SchoolVerified email at hms.harvard.edu
Sarah E CalvoBroad Institute, Massachusetts General Hospital, Harvard Medical SchoolVerified email at broadinstitute.org
Peter HumburgStatistician, Macquarie UniversityVerified email at mq.edu.au

Manuel A. Rivas

Assistant Professor, Department of Biomedical Data Science, Stanford University

Verified email at stanford.edu - Homepage

Human Genetics Statistics Therapeutics Sequencing Biobanks and Integrated Health care systems


Title	Cited by	Year
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, 2011	6776	2011
A map of human genome variation from population-scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010	6673	2010
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, 2016	5330	2016
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, 2013	2619	2013
The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans GTEx Consortium Science 348 (6235), 648-660, 2015	2049	2015
Transcriptome and genome sequencing uncovers functional variation in humans T Lappalainen, M Sammeth, MR Friedländer, P AC‘t Hoen, J Monlong, ... Nature 501 (7468), 506, 2013	1243	2013
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, 2011	642	2011
The genetic architecture of type 2 diabetes C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ... Nature 536 (7614), 41, 2016	601	2016
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	564	2011
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	454	2011
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, PA Merlini, A Kiezun, ... Nature 518 (7537), 102, 2015	433	2015
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, 2010	311	2010
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, 2017	274	2017
Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines E Choy, R Yelensky, S Bonakdar, RM Plenge, R Saxena, PL De Jager, ... PLoS genetics 4 (11), e1000287, 2008	228	2008
Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer E Ruark, K Snape, P Humburg, C Loveday, I Bajrami, R Brough, ... Nature 493 (7432), 406, 2013	193	2013
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	174	2014
Effect of predicted protein-truncating genetic variants on the human transcriptome MA Rivas, M Pirinen, DF Conrad, M Lek, EK Tsang, KJ Karczewski, ... Science 348 (6235), 666-669, 2015	157	2015
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, 2017	136	2017
Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis M Beaudoin, P Goyette, G Boucher, KS Lo, MA Rivas, C Stevens, ... PLoS genetics 9 (9), e1003723, 2013	132	2013
Choice of transcripts and software has a large effect on variant annotation DJ McCarthy, P Humburg, A Kanapin, MA Rivas, K Gaulton, JB Cazier, ... Genome medicine 6 (3), 26, 2014	130	2014

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