Suivre
Arthur Gilly
Arthur Gilly
Head of Analytics, Institute of Translational Genomics, Helmholtz Munich
Adresse e-mail validée de helmholtz-muenchen.de
Titre
Citée par
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Année
A reference panel of 64,976 haplotypes for genotype imputation
Nature genetics 48 (10), 1279-1283, 2016
28222016
Mapping the epigenetic basis of complex traits
S Cortijo, R Wardenaar, M Colomé-Tatché, A Gilly, M Etcheverry, ...
Science 343 (6175), 1145-1148, 2014
4612014
Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis
E Zengini, K Hatzikotoulas, I Tachmazidou, J Steinberg, FP Hartwig, ...
Nature genetics 50 (4), 549-558, 2018
2812018
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
CG Boer, K Hatzikotoulas, L Southam, L Stefánsdóttir, Y Zhang, ...
Cell 184 (18), 4784-4818. e17, 2021
2752021
Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes
N Grarup, I Moltke, MK Andersen, M Dalby, K Vitting-Seerup, T Kern, ...
Nature genetics 50 (2), 172-174, 2018
1582018
Transposition favors the generation of large effect mutations that may facilitate rapid adaption
L Quadrana, M Etcheverry, A Gilly, E Caillieux, MA Madoui, J Guy, ...
Nature Communications 10 (1), 3421, 2019
1382019
Using population isolates in genetic association studies
K Hatzikotoulas, A Gilly, E Zeggini
Briefings in functional genomics 13 (5), 371-377, 2014
1182014
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits
L Southam, A Gilly, D Süveges, AE Farmaki, J Schwartzentruber, ...
Nature communications 8 (1), 15606, 2017
922017
The transferability of lipid loci across African, Asian and European cohorts
K Kuchenbaecker, N Telkar, T Reiker, RG Walters, K Lin, A Eriksson, ...
Nature communications 10 (1), 4330, 2019
762019
Very low-depth whole-genome sequencing in complex trait association studies
A Gilly, L Southam, D Suveges, K Kuchenbaecker, R Moore, GEM Melloni, ...
Bioinformatics 35 (15), 2555-2561, 2019
752019
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations
Y Xue, M Mezzavilla, M Haber, S McCarthy, Y Chen, V Narasimhan, ...
Nature communications 8 (1), 15927, 2017
712017
Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus
S Hackinger, K Trajanoska, U Styrkarsdottir, E Zengini, J Steinberg, ...
Human molecular genetics 26 (19), 3850-3858, 2017
582017
Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants
K Panoutsopoulou, K Hatzikotoulas, DK Xifara, V Colonna, AE Farmaki, ...
Nature communications 5 (1), 5345, 2014
542014
Whole-genome sequencing analysis of the cardiometabolic proteome
A Gilly, YC Park, G Png, A Barysenka, I Fischer, T Bjørnland, L Southam, ...
Nature communications 11 (1), 6336, 2020
462020
Hospital, F., Aury, J
S Cortijo, R Wardenaar, M Colomé-Tatché, A Gilly, M Etcheverry, ...
M., Wincker, P., Roudier, F., Jansen, RC, Colot, V., & Johannes, F, 1145-1148, 2014
442014
Mapping the serum proteome to neurological diseases using whole genome sequencing
G Png, A Barysenka, L Repetto, P Navarro, X Shen, M Pietzner, ...
Nature communications 12 (1), 7042, 2021
352021
Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits
A Gilly, D Suveges, K Kuchenbaecker, M Pollard, L Southam, ...
Nature communications 9 (1), 4674, 2018
322018
Genetic landscape of the ACE2 coronavirus receptor
Z Yang, E Macdonald-Dunlop, J Chen, R Zhai, T Li, A Richmond, L Klarić, ...
Circulation 145 (18), 1398-1411, 2022
262022
Mendelian randomization analysis reveals a causal influence of circulating sclerostin levels on bone mineral density and fractures
J Zheng, W Maerz, I Gergei, M Kleber, C Drechsler, C Wanner, ...
Journal of Bone and Mineral Research 34 (10), 1824-1836, 2019
262019
TE-Tracker: systematic identification of transposition events through whole-genome resequencing
A Gilly, M Etcheverry, MA Madoui, J Guy, L Quadrana, A Alberti, A Martin, ...
BMC bioinformatics 15, 1-16, 2014
262014
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