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David Salgado
David Salgado
Collecteur Analyseur de Données - Plan France Médecine Génomique
Bestätigte E-Mail-Adresse bei inserm.fr
Titel
Zitiert von
Zitiert von
Jahr
The TREAT‐NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations
CL Bladen, D Salgado, S Monges, ME Foncuberta, K Kekou, K Kosma, ...
Human mutation 36 (4), 395-402, 2015
6942015
The king cobra genome reveals dynamic gene evolution and adaptation in the snake venom system
FJ Vonk, NR Casewell, CV Henkel, AM Heimberg, HJ Jansen, ...
Proceedings of the National Academy of Sciences 110 (51), 20651-20656, 2013
4932013
The CHEMDNER corpus of chemicals and drugs and its annotation principles
M Krallinger, O Rabal, F Leitner, M Vazquez, D Salgado, Z Lu, R Leaman, ...
Journal of cheminformatics 7, 1-17, 2015
3282015
The Protein-Protein Interaction tasks of BioCreative III: classification/ranking of articles and linking bio-ontology concepts to full text
M Krallinger, M Vazquez, F Leitner, D Salgado, A Chatr-Aryamontri, ...
BMC bioinformatics 12, 1-31, 2011
1932011
Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis
PA Juge, R Borie, C Kannengiesser, S Gazal, P Revy, ...
European Respiratory Journal 49 (5), 2017
1902017
Neural crest regulates myogenesis through the transient activation of NOTCH
AC Rios, O Serralbo, D Salgado, C Marcelle
Nature 473 (7348), 532-535, 2011
1772011
VarAFT: a variant annotation and filtration system for human next generation sequencing data
JP Desvignes, M Bartoli, V Delague, M Krahn, M Miltgen, C Béroud, ...
Nucleic acids research 46 (W1), W545-W553, 2018
1702018
Clinical outcomes in Duchenne muscular dystrophy: a study of 5345 patients from the TREAT-NMD DMD global database
Z Koeks, CL Bladen, D Salgado, E Van Zwet, O Pogoryelova, ...
Journal of neuromuscular diseases 4 (4), 293-306, 2017
1562017
UMD‐predictor: a high‐throughput sequencing compliant system for pathogenicity prediction of any human cDNA substitution
D Salgado, JP Desvignes, G Rai, A Blanchard, M Miltgen, A Pinard, ...
Human mutation 37 (5), 439-446, 2016
1322016
Minimum information specification for in situ hybridization and immunohistochemistry experiments (MISFISHIE)
EW Deutsch, CA Ball, JJ Berman, GS Bova, A Brazma, RE Bumgarner, ...
Nature biotechnology 26 (3), 305-312, 2008
1302008
The ANISEED database: digital representation, formalization, and elucidation of a chordate developmental program
O Tassy, D Dauga, F Daian, D Sobral, F Robin, P Khoueiry, D Salgado, ...
Genome research 20 (10), 1459-1468, 2010
1272010
A mutation in the Gardos channel is associated with hereditary xerocytosis
R Rapetti-Mauss, C Lacoste, V Picard, C Guitton, E Lombard, M Loosveld, ...
Blood, The Journal of the American Society of Hematology 126 (11), 1273-1280, 2015
1152015
The TREAT‐NMD D uchenne Muscular Dystrophy Registries: Conception, Design, and Utilization by Industry and Academia
CL Bladen, K Rafferty, V Straub, S Monges, A Moresco, H Dawkins, A Roy, ...
Human mutation 34 (11), 1449-1457, 2013
1092013
Mapping the differences in care for 5,000 spinal muscular atrophy patients, a survey of 24 national registries in North America, Australasia and Europe
CL Bladen, R Thompson, JM Jackson, C Garland, C Wegel, A Ambrosini, ...
Journal of neurology 261, 152-163, 2014
1082014
New advances in DPYD genotype and risk of severe toxicity under capecitabine
MC Etienne-Grimaldi, JC Boyer, C Beroud, L Mbatchi, A van Kuilenburg, ...
PLoS One 12 (5), e0175998, 2017
1072017
BioCreative III interactive task: an overview
CN Arighi, PM Roberts, S Agarwal, S Bhattacharya, G Cesareni, ...
BMC bioinformatics 12, 1-21, 2011
1022011
Leveraging European infrastructures to access 1 million human genomes by 2022
G Saunders, M Baudis, R Becker, S Beltran, C Béroud, E Birney, ...
Nature Reviews Genetics 20 (11), 693-701, 2019
852019
Human pre-valvular endocardial cells derived from pluripotent stem cells recapitulate cardiac pathophysiological valvulogenesis
T Neri, E Hiriart, PP Van Vliet, E Faure, RA Norris, B Farhat, B Jagla, ...
Nature Communications 10 (1), 1929, 2019
742019
BRCA share: a collection of clinical BRCA gene variants
C Béroud, SI Letovsky, CD Braastad, SM Caputo, O Beaudoux, YJ Bignon, ...
Human Mutation 37 (12), 1318-1328, 2016
662016
Exome sequencing identifies recurrent BCOR alterations and the absence of KLF2, TNFAIP3 and MYD88 mutations in splenic diffuse red pulp small B-cell lymphoma
L Jallades, L Baseggio, P Sujobert, S Huet, K Chabane, E Callet-Bauchu, ...
haematologica 102 (10), 1758, 2017
652017
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