Gil McVean

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Adam Auton23andMeAdresse e-mail validée de 23andme.com
Richard DurbinDept of Genetics, University of CambridgeAdresse e-mail validée de cam.ac.uk
Simon MyersLecturer in Bioinformatics, Oxford UniversityAdresse e-mail validée de stats.ox.ac.uk
Zamin IqbalProfessor of Algorithmic and Microbial Genomics, University of BathAdresse e-mail validée de bath.ac.uk
Goncalo AbecasisUniversity of Michigan School of Public HealthAdresse e-mail validée de umich.edu
Gerton LunterFull Professor, Groningen UniversityAdresse e-mail validée de umcg.nl
Adrián CortésGSKAdresse e-mail validée de gsk.com
Andrew WilkieUniversity of OxfordAdresse e-mail validée de imm.ox.ac.uk
Alexander T DiltheyInstitute of Medical Microbiology, University Hospital of DusseldorfAdresse e-mail validée de med.uni-duesseldorf.de
Colin FreemanWellcome Centre for Human Genetics, University of OxfordAdresse e-mail validée de well.ox.ac.uk
Mark DePristoBigHat BiosciencesAdresse e-mail validée de bighatbio.com
Anne GorielyUniversity of OxfordAdresse e-mail validée de imm.ox.ac.uk
Damjan VukcevicMonash UniversityAdresse e-mail validée de monash.edu
Laurence D HurstUniversity of BathAdresse e-mail validée de bath.ac.uk
Isaac TurnerCurativeAdresse e-mail validée de curative.com
Jerome KelleherBig Data Institute, University of OxfordAdresse e-mail validée de well.ox.ac.uk
Allan MotyerUniversity of MelbourneAdresse e-mail validée de unimelb.edu.au
Iain MathiesonUniversity of PennsylvaniaAdresse e-mail validée de mail.med.upenn.edu
Oliver VennStaff Scientist, GRAILAdresse e-mail validée de grailbio.com
Bontrop R.E.BPRCAdresse e-mail validée de bprc.nl

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Gil McVean

Professor of Statistical Genetics, University of Oxford

Adresse e-mail validée de bdi.ox.ac.uk

Genomics Evolutionary Biology Population Genetics


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
The variant call format and VCFtools P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ... Bioinformatics 27 (15), 2156-2158, 2011	13549	2011
A map of human genome variation from population-scale sequencing The 1000 Genomes Project Consortium Nature 467 (7319), 1061-1073, 2010	8859	2010
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	8373	2012
The UK Biobank resource with deep phenotyping and genomic data C Bycroft, C Freeman, D Petkova, G Band, LT Elliott, K Sharp, A Motyer, ... Nature 562 (7726), 203-209, 2018	6502	2018
A haplotype map of the human genome International HapMap Consortium Altshuler David altshuler@ molbio. mgh ... Nature 437 (7063), 1299-1320, 2005	6182*	2005
A second generation human haplotype map of over 3.1 million SNPs International HapMap Consortium Nature 449 (7164), 851, 2007	5417	2007
Integrating common and rare genetic variation in diverse human populations International HapMap 3 Consortium Nature 467 (7311), 52, 2010	3230	2010
Detecting novel associations in large data sets DN Reshef, YA Reshef, HK Finucane, SR Grossman, G McVean, ... science 334 (6062), 1518-1524, 2011	3225	2011
A new multipoint method for genome-wide association studies by imputation of genotypes J Marchini, B Howie, S Myers, G McVean, P Donnelly Nature genetics 39 (7), 906-913, 2007	3129	2007
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis Nature 476 (7359), 214-219, 2011	3044	2011
Genome-wide detection and characterization of positive selection in human populations PC Sabeti, P Varilly, B Fry, J Lohmueller, E Hostetter, C Cotsapas, X Xie, ... Nature 449 (7164), 913-918, 2007	2277	2007
A fine-scale map of recombination rates and hotspots across the human genome S Myers, L Bottolo, C Freeman, G McVean, P Donnelly Science 310 (5746), 321-324, 2005	1483*	2005
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis International IBD Genetics Consortium (IIBDGC), C Agliardi, L Alfredsson, ... Nature genetics 45 (11), 1353-1360, 2013	1361	2013
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	1301	2011
The genetic architecture of type 2 diabetes C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ... Nature 536 (7614), 41-47, 2016	1269	2016
The fine-scale structure of recombination rate variation in the human genome GAT McVean, SR Myers, S Hunt, P Deloukas, DR Bentley, P Donnelly Science 304 (5670), 581-584, 2004	1143	2004
Integrating mapping-, assembly-and haplotype-based approaches for calling variants in clinical sequencing applications A Rimmer, H Phan, I Mathieson, Z Iqbal, SRF Twigg, WGS500 Consortium, ... Nature genetics 46 (8), 912-918, 2014	1133	2014
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas C Palles, JB Cazier, KM Howarth, E Domingo, AM Jones, P Broderick, ... Nature genetics 45 (2), 136-144, 2013	1108	2013
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility Australo-Anglo-American Spondyloarthritis Consortium (TASC), ... Nature genetics 43 (8), 761-767, 2011	985	2011
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls Nature 464 (7289), 713-720, 2010	943	2010

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