Vincent Plagnol
Vincent Plagnol
Reader in Statistical Genetics, University College London
Verified email at ucl.ac.uk - Homepage
TitleCited byYear
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
15552009
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
13722007
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
10602003
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
9442005
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
7742010
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
7332008
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
7322011
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
6312011
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
4722008
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, 2007
4552007
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
4292007
Bayesian test for colocalisation between pairs of genetic association studies using summary statistics
C Giambartolomei, D Vukcevic, EE Schadt, L Franke, AD Hingorani, ...
PLoS genetics 10 (5), e1004383, 2014
3972014
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
3552013
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
2912012
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, 2014
2832014
Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource
CA Dendrou, V Plagnol, E Fung, JHM Yang, K Downes, JD Cooper, ...
Nature genetics 41 (9), 1011-1015, 2009
2652009
Possible ancestral structure in human populations
V Plagnol, JD Wall
PLoS Genetics 2 (7), e105, 2006
2522006
Inflammatory Skin and Bowel Disease Linked to ADAM17 Deletion
DC Blaydon, P Biancheri, WL Di, V Plagnol, RM Cabral, MA Brooke, ...
New England Journal of Medicine 365 (16), 1502-1508, 2011
2302011
Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake
LC Willcocks, PA Lyons, MR Clatworthy, JI Robinson, W Yang, ...
Journal of Experimental Medicine 205 (7), 1573-1582, 2008
2222008
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
2132014
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