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| Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes JC Barrett, DG Clayton, P Concannon, B Akolkar, JD Cooper, HA Erlich, ... Nature genetics 41 (6), 703-707, 2009 | 2131 | 2009 |
| Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes JA Todd, NM Walker, JD Cooper, DJ Smyth, K Downes, V Plagnol, ... Nature genetics 39 (7), 857-864, 2007 | 1646 | 2007 |
| Markov chain Monte Carlo without likelihoods P Marjoram, J Molitor, V Plagnol, S Tavaré Proceedings of the National Academy of Sciences of the United States of …, 2003 | 1542 | 2003 |
| The pattern of polymorphism in Arabidopsis thaliana M Nordborg, TT Hu, Y Ishino, J Jhaveri, C Toomajian, H Zheng, E Bakker, ... PLoS Biology 3 (7), e196, 2005 | 1095 | 2005 |
| Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. MA Nalls, V Plagnol, DG Hernandez, M Sharma, UM Sheerin, M Saad, ... Lancet 377 (9766), 641, 2011 | 1004 | 2011 |
| 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), 713-720, 2010 | 930 | 2010 |
| Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease G Trynka, KA Hunt, NA Bockett, J Romanos, V Mistry, A Szperl, SF Bakker, ... Nature Genetics, 2011 | 927 | 2011 |
| Shared and distinct genetic variants in type 1 diabetes and celiac disease DJ Smyth, V Plagnol, NM Walker, JD Cooper, K Downes, JHM Yang, ... New England Journal of Medicine 359 (26), 2767-2777, 2008 | 926 | 2008 |
| A robust model for read count data in exome sequencing experiments and implications for copy number variant calling V Plagnol, J Curtis, M Epstein, KY Mok, E Stebbings, S Grigoriadou, ... Bioinformatics 28 (21), 2747-2754, 2012 | 682 | 2012 |
| Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damage I Angulo, O Vadas, F Garçon, E Banham-Hall, V Plagnol, TR Leahy, ... Science 342 (6160), 866-871, 2013 | 625 | 2013 |
| Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci JD Cooper, DJ Smyth, AM Smiles, V Plagnol, NM Walker, JE Allen, ... Nature genetics 40 (12), 1399-1401, 2008 | 613 | 2008 |
| Recombination and linkage disequilibrium in Arabidopsis thaliana S Kim, V Plagnol, TT Hu, C Toomajian, RM Clark, S Ossowski, JR Ecker, ... Nature genetics 39 (9), 1151-1155, 2007 | 598 | 2007 |
| Atlas of the clinical genetics of human dilated cardiomyopathy J Haas, KS Frese, B Peil, W Kloos, A Keller, R Nietsch, Z Feng, S Müller, ... European heart journal 36 (18), 1123-1135, 2015 | 565 | 2015 |
| Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes CE Lowe, JD Cooper, T Brusko, NM Walker, DJ Smyth, R Bailey, ... Nature genetics 39 (9), 1074-1082, 2007 | 534 | 2007 |
| Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... The American Journal of Human Genetics 98 (3), 500-513, 2016 | 410 | 2016 |
| Comprehensive rare variant analysis via whole-genome sequencing to determine the molecular pathology of inherited retinal disease KJ Carss, G Arno, M Erwood, J Stephens, A Sanchis-Juan, S Hull, K Megy, ... The American Journal of Human Genetics 100 (1), 75-90, 2017 | 408 | 2017 |
| Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel J Huang, B Howie, S McCarthy, Y Memari, K Walter, JL Min, P Danecek, ... Nature communications 6 (1), 8111, 2015 | 399 | 2015 |
| CHiCAGO: robust detection of DNA looping interactions in Capture Hi-C data J Cairns, P Freire-Pritchett, SW Wingett, C Várnai, A Dimond, V Plagnol, ... Genome biology 17, 1-17, 2016 | 391 | 2016 |
| Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ... Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014 | 380 | 2014 |
Prof David KelsellBlizard Institute, Faculty of Medicine and Dentistry, QMULAdresse e-mail validée de qmul.ac.uk
