Gil McVean

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Adam Auton23andMeDirección de correo verificada de 23andme.com
Richard DurbinDept of Genetics, University of CambridgeDirección de correo verificada de cam.ac.uk
Simon MyersLecturer in Bioinformatics, Oxford UniversityDirección de correo verificada de stats.ox.ac.uk
Zamin IqbalProfessor of Algorithmic and Microbial Genomics, University of BathDirección de correo verificada de bath.ac.uk
Goncalo AbecasisUniversity of Michigan School of Public HealthDirección de correo verificada de umich.edu
Gerton LunterFull Professor, Groningen UniversityDirección de correo verificada de umcg.nl
Adrián CortésGSKDirección de correo verificada de gsk.com
Andrew WilkieUniversity of OxfordDirección de correo verificada de imm.ox.ac.uk
Alexander T DiltheyInstitute of Medical Microbiology, University Hospital of DusseldorfDirección de correo verificada de med.uni-duesseldorf.de
Colin FreemanWellcome Centre for Human Genetics, University of OxfordDirección de correo verificada de well.ox.ac.uk
Mark DePristoBigHat BiosciencesDirección de correo verificada de bighatbio.com
Anne GorielyUniversity of OxfordDirección de correo verificada de imm.ox.ac.uk
Damjan VukcevicMonash UniversityDirección de correo verificada de monash.edu
Laurence D HurstUniversity of BathDirección de correo verificada de bath.ac.uk
Isaac TurnerCurativeDirección de correo verificada de curative.com
Jerome KelleherBig Data Institute, University of OxfordDirección de correo verificada de well.ox.ac.uk
Allan MotyerUniversity of MelbourneDirección de correo verificada de unimelb.edu.au
Iain MathiesonUniversity of PennsylvaniaDirección de correo verificada de mail.med.upenn.edu
Oliver VennStaff Scientist, GRAILDirección de correo verificada de grailbio.com
Bontrop R.E.BPRCDirección de correo verificada de bprc.nl

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Gil McVean

Professor of Statistical Genetics, University of Oxford

Dirección de correo verificada de bdi.ox.ac.uk

Genomics Evolutionary Biology Population Genetics


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
The variant call format and VCFtools P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ... Bioinformatics 27 (15), 2156-2158, 2011	13397	2011
A map of human genome variation from population-scale sequencing The 1000 Genomes Project Consortium Nature 467 (7319), 1061-1073, 2010	8835	2010
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	8360	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	6394	2018
A haplotype map of the human genome International HapMap Consortium Altshuler David altshuler@ molbio. mgh ... Nature 437 (7063), 1299-1320, 2005	6170*	2005
A second generation human haplotype map of over 3.1 million SNPs International HapMap Consortium Nature 449 (7164), 851, 2007	5412	2007
Integrating common and rare genetic variation in diverse human populations International HapMap 3 Consortium Nature 467 (7311), 52, 2010	3218	2010
Detecting novel associations in large data sets DN Reshef, YA Reshef, HK Finucane, SR Grossman, G McVean, ... science 334 (6062), 1518-1524, 2011	3203	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	3126	2007
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis Nature 476 (7359), 214-219, 2011	3037	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	2266	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	1478*	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	1359	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	1296	2011
The genetic architecture of type 2 diabetes C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ... Nature 536 (7614), 41-47, 2016	1262	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	1141	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	983	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	940	2010

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