Alon Keinan

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Goncalo AbecasisUniversity of Michigan School of Public HealthVerified email at umich.edu
Feng GaoSenior Applied Scientist at AmazonVerified email at amazon.com
Kaixiong YeAssistant Professor, University of GeorgiaVerified email at uga.edu
Adam Auton23andMeVerified email at 23andme.com
Mark DePristoBigHat BiosciencesVerified email at bighatbio.com
Leonardo ArbizaCornell UniversityVerified email at cornell.edu
Isaac MeilijsonTel Aviv UniversityVerified email at math.tau.ac.il
Nick PattersonStaff scientist, Broad InstituteVerified email at broadinstitute.org
Zhenglong GuCornell UniversityVerified email at cornell.edu
Claus C. HilgetagProfessor & Director, Department of Computational Neuroscience, University Medical Center EppendorfVerified email at uke.de
Ran BlekhmanAssociate Professor, University of ChicagoVerified email at uchicago.edu
Julia GoodrichGraduate Student, Cornell UniversityVerified email at cornell.edu
Jordana T BellKing's College LondonVerified email at kcl.ac.uk
Dirk GeversJanssen Human Microbiome InstituteVerified email at its.jnj.com
gil atzmonUniversity of HaifaVerified email at univ.haifa.ac.il
Mark GersteinProfessor of Biomedical Informatics, Yale UniversityVerified email at yale.edu
Adam SiepelSimons Center for Quantitative Biology, Cold Spring Harbor LaboratoryVerified email at cshl.edu
Qasim AyubWellcome Trust Sanger InstituteVerified email at sanger.ac.uk
David N. CooperProfessor of Human Molecular Genetics, Cardiff University, UKVerified email at cardiff.ac.uk
Elodie GazaveCornell UniversityVerified email at cornell.edu

Alon Keinan

Associate Professor of Computational Biology, Cornell University

Verified email at cornell.edu - Homepage

computational genomics population genetics statistical genetics deep learning human genetics


Title Sort by citations Sort by year Sort by title	Cited by Cited by	Year
A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015	15312	2015
The Variant Call Format and VCFtools P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ... Bioinformatics, 2011	13330	2011
A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010	8819	2010
An integrated map of genetic variation from 1,092 human genomes. GR Abecasis, A Auton, LD Brooks, MA DePristo, RM Durbin, ... Nature 491 (7422), 56, 2012	8345*	2012
Integrating common and rare genetic variation in diverse human populations International HapMap 3 Consortium Nature 467 (7311), 52, 2010	3212	2010
An integrated map of structural variation in 2,504 human genomes PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ... Nature 526 (7571), 75-81, 2015	2431	2015
A systematic survey of loss-of-function variants in human protein-coding genes DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ... Science 335 (6070), 823-828, 2012	1391	2012
Mapping copy number variation by population-scale genome sequencing RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ... Nature 470 (7332), 59-65, 2011	1295	2011
Auton A, Brooks LD, Durbin RM, Garrison EP, Kang HM, Korbel JO, Marchini JL, McCarthy S, McVean GA, Abecasis GR. A Global Reference for Human Genetic Variation Genomes Project Consortium Nature 526 (7571), 68-74, 2015	969	2015
Diversity of human copy number variation and multicopy genes PH Sudmant, JO Kitzman, F Antonacci, C Alkan, M Malig, A Tsalenko, ... Science 330 (6004), 641-646, 2010	800	2010
Host genetic variation impacts microbiome composition across human body sites R Blekhman, JK Goodrich, K Huang, Q Sun, R Bukowski, JT Bell, ... Genome biology 16, 1-12, 2015	768	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	719	2011
Recent explosive human population growth has resulted in an excess of rare genetic variants A Keinan, AG Clark science 336 (6082), 740-743, 2012	648	2012
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel O Delaneau, J Marchini Nature communications 5 (1), 3934, 2014	452	2014
Integrative annotation of variants from 1092 humans: application to cancer genomics E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ... Science 342 (6154), 1235587, 2013	423	2013
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences GD Poznik, Y Xue, FL Mendez, TF Willems, A Massaia, MA Wilson Sayres, ... Nature genetics 48 (6), 593-599, 2016	362	2016
The 1000 Genomes Project: data management and community access L Clarke, X Zheng-Bradley, R Smith, E Kulesha, C Xiao, I Toneva, ... Nature methods 9 (5), 459-462, 2012	354	2012
The Mobile Element Locator Tool (MELT): population-scale mobile element discovery and biology EJ Gardner, VK Lam, DN Harris, NT Chuang, EC Scott, WS Pittard, ... Genome research 27 (11), 1916-1929, 2017	343	2017
Measurement of the human allele frequency spectrum demonstrates greater genetic drift in East Asians than in Europeans A Keinan, JC Mullikin, N Patterson, D Reich Nature genetics 39 (10), 1251-1255, 2007	324	2007
Deleterious-and disease-allele prevalence in healthy individuals: insights from current predictions, mutation databases, and population-scale resequencing Y Xue, Y Chen, Q Ayub, N Huang, EV Ball, M Mort, AD Phillips, K Shaw, ... The American Journal of Human Genetics 91 (6), 1022-1032, 2012	317	2012

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