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Vincent Plagnol
Vincent Plagnol
Chief Scientific Officer, Genomics plc
Verified email at genomicsplc.com
Title
Cited by
Cited by
Year
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
23212014
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
21522009
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
16552007
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
15662003
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
11002005
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
10112011
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
9522011
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
9352010
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
9302008
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
6942012
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
6362013
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
6172008
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
6012007
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
5752015
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
5362007
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
4262017
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
4182016
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
4082015
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
4002016
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ...
Brain 140 (12), 3191-3203, 2017
3852017
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