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Author Details
Full Name
Salvador Capella-Gutierrez
Affiliation
Spanish National Bioinformatics Institute (INB/ELIXIR-ES)
ORCID
Career Start Year
2009
Papers
50
H Index
25
Expertise
CM4AI Collaborator
Mohammad Sadnan Al Manir (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37971353
RegulonDB v12.0: a comprehensive resource of transcriptional regulation in E. coli K-12.
Nucleic Acids Res
2024
38038272
WOMBAT-P: Benchmarking Label-Free Proteomics Data Analysis Workflows.
J Proteome Res
2024
37971353
RegulonDB v12.0: a comprehensive resource of transcriptional regulation in E. coli K-12.
Nucleic Acids Res
2024
38038272
WOMBAT-P: Benchmarking Label-Free Proteomics Data Analysis Workflows.
J Proteome Res
2024
37208467
The FAIR Cookbook - the essential resource for and by FAIR doers.
Sci Data
2023
37563883
DEBBIE: The Open Access Database of Experimental Scaffolds and Biomaterials Built Using an Automated Text Mining Pipeline.
Adv Healthc Mater
2023
37208467
The FAIR Cookbook - the essential resource for and by FAIR doers.
Sci Data
2023
37316648
eTRANSAFE: data science to empower translational safety assessment.
Nat Rev Drug Discov
2023
37563883
DEBBIE: The Open Access Database of Experimental Scaffolds and Biomaterials Built Using an Automated Text Mining Pipeline.
Adv Healthc Mater
2023
37316648
eTRANSAFE: data science to empower translational safety assessment.
Nat Rev Drug Discov
2023
34718760
PhylomeDB V5: an expanding repository for genome-wide catalogues of annotated gene phylogenies.
Nucleic Acids Res
2022
35953718
Detection of early seeding of Richter transformation in chronic lymphocytic leukemia.
Nat Med
2022
35552456
The Quest for Orthologs orthology benchmark service in 2022.
Nucleic Acids Res
2022
36124809
ECCB2022: the 21st European Conference on Computational Biology.
Bioinformatics
2022
36777183
The landscape of expression and alternative splicing variation across human traits.
Cell Genom
2022
34718760
PhylomeDB V5: an expanding repository for genome-wide catalogues of annotated gene phylogenies.
Nucleic Acids Res
2022
35552456
The Quest for Orthologs orthology benchmark service in 2022.
Nucleic Acids Res
2022
36777183
The landscape of expression and alternative splicing variation across human traits.
Cell Genom
2022
35953718
Detection of early seeding of Richter transformation in chronic lymphocytic leukemia.
Nat Med
2022
36124809
ECCB2022: the 21st European Conference on Computational Biology.
Bioinformatics
2022
33262138
FGFR Inhibition Overcomes Resistance to EGFR-targeted Therapy in Epithelial-like Cutaneous Carcinoma.
Clin Cancer Res
2021
33800393
The eTRANSAFE Project on Translational Safety Assessment through Integrative Knowledge Management: Achievements and Perspectives.
Pharmaceuticals (Basel)
2021
33452270
A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration.
Sci Data
2021
34249331
Recommendations for the FAIRification of genomic track metadata.
F1000Res
2021
33262138
FGFR Inhibition Overcomes Resistance to EGFR-targeted Therapy in Epithelial-like Cutaneous Carcinoma.
Clin Cancer Res
2021
34848723
COVID-19 Flow-Maps an open geographic information system on COVID-19 and human mobility for Spain.
Sci Data
2021
34804501
Perspectives on automated composition of workflows in the life sciences.
F1000Res
2021
33800393
The eTRANSAFE Project on Translational Safety Assessment through Integrative Knowledge Management: Achievements and Perspectives.
Pharmaceuticals (Basel)
2021
34804501
Perspectives on automated composition of workflows in the life sciences.
F1000Res
2021
34848723
COVID-19 Flow-Maps an open geographic information system on COVID-19 and human mobility for Spain.
Sci Data
2021
34249331
Recommendations for the FAIRification of genomic track metadata.
F1000Res
2021
33452270
A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration.
Sci Data
2021
32374845
The Quest for Orthologs benchmark service and consensus calls in 2020.
Nucleic Acids Res
2020
32374845
The Quest for Orthologs benchmark service and consensus calls in 2020.
Nucleic Acids Res
2020
33381810
ECCB2020: the 19th European Conference on Computational Biology.
Bioinformatics
2020
32504002
Interpreting molecular similarity between patients as a determinant of disease comorbidity relationships.
Nat Commun
2020
34367618
The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research.
F1000Res
2020
34367618
The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research.
F1000Res
2020
33381810
ECCB2020: the 19th European Conference on Computational Biology.
Bioinformatics
2020
32504002
Interpreting molecular similarity between patients as a determinant of disease comorbidity relationships.
Nat Commun
2020
31455890
Leveraging European infrastructures to access 1 million human genomes by 2022.
Nat Rev Genet
2019
31824649
An intrinsically disordered proteins community for ELIXIR.
F1000Res
2019
31520075
Author Correction: Leveraging European infrastructures to access 1 million human genomes by 2022.
Nat Rev Genet
2019
31455890
Leveraging European infrastructures to access 1 million human genomes by 2022.
Nat Rev Genet
2019
31824649
An intrinsically disordered proteins community for ELIXIR.
F1000Res
2019
31520075
Author Correction: Leveraging European infrastructures to access 1 million human genomes by 2022.
Nat Rev Genet
2019
28968857
Gearing up to handle the mosaic nature of life in the quest for orthologs.
Bioinformatics
2018
28968857
Gearing up to handle the mosaic nature of life in the quest for orthologs.
Bioinformatics
2018
29568489
Ten steps to get started in Genome Assembly and Annotation.
F1000Res
2018
29568489
Ten steps to get started in Genome Assembly and Annotation.
F1000Res
2018
1 - 50 of 100
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