Suivre
Gil McVean
Gil McVean
Professor of Statistical Genetics, University of Oxford
Adresse e-mail validée de bdi.ox.ac.uk
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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
126932011
A map of human genome variation from population-scale sequencing
The 1000 Genomes Project Consortium
Nature 467 (7319), 1061-1073, 2010
87692010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82792012
A haplotype map of the human genome
International HapMap Consortium Altshuler David altshuler@ molbio. mgh ...
Nature 437 (7063), 1299-1320, 2005
6133*2005
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
59002018
A second generation human haplotype map of over 3.1 million SNPs
International HapMap Consortium
Nature 449 (7164), 851, 2007
53742007
Integrating common and rare genetic variation in diverse human populations
International HapMap 3 Consortium
Nature 467 (7311), 52, 2010
31532010
Detecting novel associations in large data sets
DN Reshef, YA Reshef, HK Finucane, SR Grossman, G McVean, ...
science 334 (6062), 1518-1524, 2011
30972011
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
30772007
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
29712011
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
22102007
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
1461*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
13352013
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
12742011
The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 2016
12432016
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
11242004
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
11002014
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
10792013
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
9612011
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
9352010
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