受强制性开放获取政策约束的文章 - Vincent Plagnol了解详情
无法在其他位置公开访问的文章：3 篇
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Use of high-throughput targeted exome-sequencing to screen for copy number variation in hypertrophic cardiomyopathy
LR Lopes, C Murphy, P Syrris, C Dalageorgou, WJ McKenna, PM Elliott, ...
European journal of medical genetics 58 (11), 611-616, 2015
强制性开放获取政策： Fundação para a Ciência e a Tecnologia, Portugal, British Heart Foundation …
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The ophthalmic presentation of Hermansky–Pudlak syndrome 6
S Hull, G Arno, GE Holder, V Plagnol, K Gomez, R Liesner, AR Webster, ...
British Journal of Ophthalmology 100 (11), 1521-1524, 2016
强制性开放获取政策： National Institute for Health Research, UK
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Graphical modelling of molecular networks underlying sporadic inclusion body myositis
T Thorne, P Fratta, MG Hanna, A Cortese, V Plagnol, EM Fisher, ...
Molecular BioSystems 9 (7), 1736-1742, 2013
强制性开放获取政策： UK Biotechnology and Biological Sciences Research Council, UK Medical …
可在其他位置公开访问的文章：176 篇
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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
强制性开放获取政策： British Heart Foundation, UK Medical Research Council, National Institute …
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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
强制性开放获取政策： US National Institutes of Health
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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
强制性开放获取政策： British Heart Foundation
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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
强制性开放获取政策： US National Institutes of Health, Parkinson's UK
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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
强制性开放获取政策： US National Institutes of Health, Council of Scientific and Industrial …
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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
强制性开放获取政策： US National Institutes of Health, British Heart Foundation
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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
强制性开放获取政策： Versus Arthritis, UK, British Heart Foundation
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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
强制性开放获取政策： Parkinson's UK
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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
强制性开放获取政策： Swiss National Science Foundation, US National Institutes of Health …
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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
强制性开放获取政策： US National Institutes of Health
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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
强制性开放获取政策： German Research Foundation
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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
强制性开放获取政策： British Heart Foundation, UK Medical Research Council, National Institute …
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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
强制性开放获取政策： US National Institutes of Health, National Institute of Health and Medical …
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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
强制性开放获取政策： Canadian Institutes of Health Research, Fonds de recherche du Québec - Santé …
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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
强制性开放获取政策： European Molecular Biology Laboratory, UK Biotechnology and Biological …
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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
强制性开放获取政策： US Department of Defense, US National Institutes of Health, Helmholtz …
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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
强制性开放获取政策： US National Institutes of Health, Research Foundation (Flanders), Fondazione …
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