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David Salgado

Université Claude Bernard Lyon 1
H指数:30
被引数:4,628

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The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases
2022-02-1732
OAAI
Standardisation of pathogenicity classification for somatic alterations in solid tumours and haematologic malignancies
2021-12-019
OAAI
The lncRNA 44s2 Study Applicability to the Design of 45-55 Exon Skipping Therapeutic Strategy for DMD
2021-02-206
OAAI
Leveraging European infrastructures to access 1 million human genomes by 2022 (vol 20, pg 693, 2019)
2019-09-132
OAAI
Leveraging European infrastructures to access 1 million human genomes by 2022
2019-08-2757
OAAI
Whole Exome Sequencing Reveals a Large Genetic Heterogeneity and Revisits the Causes of Hypertrophic Cardiomyopathy Experience of a Multicentric Study of 200 French Patients
2019-05-0111
OAAI
Human pre-valvular endocardial cells derived from pluripotent stem cells recapitulate cardiac pathophysiological valvulogenesis
2019-04-2667
OAAI
Exome sequencing identifies recurrent BCOR alterations and the absence of KLF2, TNFAIP3 and MYD88 mutations in splenic diffuse red pulp small B-cell lymphoma
2017-07-2759
OAAI
Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis

类风湿关节炎-间质性肺疾病和家族性肺纤维化的共同遗传易感性

2017-05-11146
OAAI
BRCA Share: A Collection of Clinical BRCA Gene Variants
2016-09-2849
OAAI
Actionable Genes, Core Databases, and Locus-Specific Databases

可操作基因、核心数据库和基因座特异性数据库

2016-09-266
OAAI
Overview of the interactive task in BioCreative V
2016-09-0124
OAAI