| A map of human genome variation from population-scale sequencing The 1000 Genomes Project Consortium Nature 467 (7319), 1061-1073, 2010 | 6651 | 2010 |
| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 6018 | 2012 |
| A haplotype map of the human genome International HapMap Consortium Nature 437 (7063), 1299, 2005 | 5153* | 2005 |
| A second generation human haplotype map of over 3.1 million SNPs International HapMap Consortium Nature 449 (7164), 851, 2007 | 4436 | 2007 |
| The variant call format and VCFtools P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ... Bioinformatics 27 (15), 2156-2158, 2011 | 4154 | 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, 2007 | 2390 | 2007 |
| Integrating common and rare genetic variation in diverse human populations International HapMap 3 Consortium Nature 467 (7311), 52, 2010 | 2223 | 2010 |
| Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis S Sawcer, G Hellenthal, M Pirinen, CCA Spencer, NA Patsopoulos, ... Nature 476 (7359), 214, 2011 | 1889 | 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, 2007 | 1447 | 2007 |
| Detecting novel associations in large data sets DN Reshef, YA Reshef, HK Finucane, SR Grossman, G McVean, ... science 334 (6062), 1518-1524, 2011 | 1373 | 2011 |
| 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 | 1188* | 2005 |
| 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, 2011 | 960 | 2011 |
| 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 | 940 | 2004 |
| Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls N Craddock, ME Hurles, N Cardin, RD Pearson, V Plagnol, S Robson, ... Nature 464 (7289), 713, 2010 | 775 | 2010 |
| A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 A Strange, F Capon, CCA Spencer, J Knight, ME Weale, MH Allen, ... Nature genetics 42 (11), 985, 2010 | 753 | 2010 |
| A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC PIW De Bakker, G McVean, PC Sabeti, MM Miretti, T Green, J Marchini, ... Nature genetics 38 (10), 1166, 2006 | 747 | 2006 |
| Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis AH Beecham, NA Patsopoulos, DK Xifara, MF Davis, A Kemppinen, ... Nature genetics 45 (11), 1353, 2013 | 724 | 2013 |
| A coalescent-based method for detecting and estimating recombination from gene sequences G McVean, P Awadalla, P Fearnhead Genetics 160 (3), 1231-1241, 2002 | 694 | 2002 |
| 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, 2013 | 654 | 2013 |
| Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility DM Evans, CCA Spencer, JJ Pointon, Z Su, D Harvey, G Kochan, ... Nature genetics 43 (8), 761, 2011 | 635 | 2011 |
Simon MyersLecturer in Bioinformatics, Oxford UniversityVerified email at stats.ox.ac.uk
