David Salgado
David Salgado
Aix-Marseille Université, INSERM U1251 - ARMI, EMBL Australia, Monash University
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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
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
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), 1-17, 2015
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
Neural crest regulates myogenesis through the transient activation of NOTCH
AC Rios, O Serralbo, D Salgado, C Marcelle
Nature 473 (7348), 532-535, 2011
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
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
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
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
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
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
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
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
BioCreative III interactive task: an overview
CN Arighi, PM Roberts, S Agarwal, S Bhattacharya, G Cesareni, ...
BMC bioinformatics 12 (8), 1-21, 2011
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
New advances in DPYD genotype and risk of severe toxicity under capecitabine
MC Etienne-Grimaldi, JC Boyer, C Béroud, L Mbatchi, A van Kuilenburg, ...
PLoS One 12 (5), e0175998, 2017
Effects of processing and storage on the measurement of nitrogenous compounds in ovine blood
CJ Laborde, AM Chapa, DW Burleigh, DJ Salgado, JM Fernandez
Small Ruminant Research 17 (2), 159-166, 1995
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
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
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
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