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Gil McVean
Gil McVean
Professor of Statistical Genetics, University of Oxford
Dirección de correo verificada de bdi.ox.ac.uk
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The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
125202011
A map of human genome variation from population-scale sequencing
The 1000 Genomes Project Consortium
Nature 467 (7319), 1061-1073, 2010
87412010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82512012
A haplotype map of the human genome
International HapMap Consortium Altshuler David altshuler@ molbio. mgh ...
Nature 437 (7063), 1299-1320, 2005
6120*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
57562018
A second generation human haplotype map of over 3.1 million SNPs
International HapMap Consortium
Nature 449 (7164), 851, 2007
53592007
Integrating common and rare genetic variation in diverse human populations
International HapMap 3 Consortium
Nature 467 (7311), 52, 2010
31432010
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
30672007
Detecting novel associations in large data sets
DN Reshef, YA Reshef, HK Finucane, SR Grossman, G McVean, ...
science 334 (6062), 1518-1524, 2011
30572011
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
29542011
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
21962007
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
1459*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
13232013
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
12722011
The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 2016
12362016
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
11222004
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
10872014
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
10752013
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
9552011
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
9312010
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
Artículos 1–20