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Author Details

Salvador Capella-Gutierrez
Spanish National Bioinformatics Institute (INB/ELIXIR-ES)
2009
50
25
Mohammad Sadnan Al Manir (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37971353RegulonDB v12.0: a comprehensive resource of transcriptional regulation in E. coli K-12.Nucleic Acids Res2024
38038272WOMBAT-P: Benchmarking Label-Free Proteomics Data Analysis Workflows.J Proteome Res2024
37971353RegulonDB v12.0: a comprehensive resource of transcriptional regulation in E. coli K-12.Nucleic Acids Res2024
38038272WOMBAT-P: Benchmarking Label-Free Proteomics Data Analysis Workflows.J Proteome Res2024
37208467The FAIR Cookbook - the essential resource for and by FAIR doers.Sci Data2023
37563883DEBBIE: The Open Access Database of Experimental Scaffolds and Biomaterials Built Using an Automated Text Mining Pipeline.Adv Healthc Mater2023
37208467The FAIR Cookbook - the essential resource for and by FAIR doers.Sci Data2023
37316648eTRANSAFE: data science to empower translational safety assessment.Nat Rev Drug Discov2023
37563883DEBBIE: The Open Access Database of Experimental Scaffolds and Biomaterials Built Using an Automated Text Mining Pipeline.Adv Healthc Mater2023
37316648eTRANSAFE: data science to empower translational safety assessment.Nat Rev Drug Discov2023
34718760PhylomeDB V5: an expanding repository for genome-wide catalogues of annotated gene phylogenies.Nucleic Acids Res2022
35953718Detection of early seeding of Richter transformation in chronic lymphocytic leukemia.Nat Med2022
35552456The Quest for Orthologs orthology benchmark service in 2022.Nucleic Acids Res2022
36124809ECCB2022: the 21st European Conference on Computational Biology.Bioinformatics2022
36777183The landscape of expression and alternative splicing variation across human traits.Cell Genom2022
34718760PhylomeDB V5: an expanding repository for genome-wide catalogues of annotated gene phylogenies.Nucleic Acids Res2022
35552456The Quest for Orthologs orthology benchmark service in 2022.Nucleic Acids Res2022
36777183The landscape of expression and alternative splicing variation across human traits.Cell Genom2022
35953718Detection of early seeding of Richter transformation in chronic lymphocytic leukemia.Nat Med2022
36124809ECCB2022: the 21st European Conference on Computational Biology.Bioinformatics2022
33262138FGFR Inhibition Overcomes Resistance to EGFR-targeted Therapy in Epithelial-like Cutaneous Carcinoma.Clin Cancer Res2021
33800393The eTRANSAFE Project on Translational Safety Assessment through Integrative Knowledge Management: Achievements and Perspectives.Pharmaceuticals (Basel)2021
33452270A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration.Sci Data2021
34249331Recommendations for the FAIRification of genomic track metadata.F1000Res2021
33262138FGFR Inhibition Overcomes Resistance to EGFR-targeted Therapy in Epithelial-like Cutaneous Carcinoma.Clin Cancer Res2021
34848723COVID-19 Flow-Maps an open geographic information system on COVID-19 and human mobility for Spain.Sci Data2021
34804501Perspectives on automated composition of workflows in the life sciences.F1000Res2021
33800393The eTRANSAFE Project on Translational Safety Assessment through Integrative Knowledge Management: Achievements and Perspectives.Pharmaceuticals (Basel)2021
34804501Perspectives on automated composition of workflows in the life sciences.F1000Res2021
34848723COVID-19 Flow-Maps an open geographic information system on COVID-19 and human mobility for Spain.Sci Data2021
34249331Recommendations for the FAIRification of genomic track metadata.F1000Res2021
33452270A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration.Sci Data2021
32374845The Quest for Orthologs benchmark service and consensus calls in 2020.Nucleic Acids Res2020
32374845The Quest for Orthologs benchmark service and consensus calls in 2020.Nucleic Acids Res2020
33381810ECCB2020: the 19th European Conference on Computational Biology.Bioinformatics2020
32504002Interpreting molecular similarity between patients as a determinant of disease comorbidity relationships.Nat Commun2020
34367618The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research.F1000Res2020
34367618The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research.F1000Res2020
33381810ECCB2020: the 19th European Conference on Computational Biology.Bioinformatics2020
32504002Interpreting molecular similarity between patients as a determinant of disease comorbidity relationships.Nat Commun2020
31455890Leveraging European infrastructures to access 1 million human genomes by 2022.Nat Rev Genet2019
31824649An intrinsically disordered proteins community for ELIXIR.F1000Res2019
31520075Author Correction: Leveraging European infrastructures to access 1 million human genomes by 2022.Nat Rev Genet2019
31455890Leveraging European infrastructures to access 1 million human genomes by 2022.Nat Rev Genet2019
31824649An intrinsically disordered proteins community for ELIXIR.F1000Res2019
31520075Author Correction: Leveraging European infrastructures to access 1 million human genomes by 2022.Nat Rev Genet2019
28968857Gearing up to handle the mosaic nature of life in the quest for orthologs.Bioinformatics2018
28968857Gearing up to handle the mosaic nature of life in the quest for orthologs.Bioinformatics2018
29568489Ten steps to get started in Genome Assembly and Annotation.F1000Res2018
29568489Ten steps to get started in Genome Assembly and Annotation.F1000Res2018
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Collaborators

Catalan Institution for Research and Advanced Studies
Co-authored papers 26
Josep Carreras Leukaemia Research Institute (IJC)
Co-authored papers 11
Hospital Universitario y Politecnico la Fe
Co-authored papers 7
Institute for Research in Biomedicine (IRB)
Co-authored papers 6
Barcelona Institute of Science and Technology
Co-authored papers 5
University of Lausanne
Co-authored papers 4
Spain Universitat de Barcelona (UB)
Co-authored papers 4
ETH Zurich, Universitatstr. 6
Co-authored papers 4
Stockholm University
Co-authored papers 4
Hospital del Mar Medical Research Institute (IMIM), Pompeu Fabra University
Co-authored papers 4
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers 4
Universitat Tubingen, Institut fur Arbeitsmedizin
Co-authored papers 4
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers 3
University of Zurich
Co-authored papers 3
Co-authored papers 3
University of Groningen, University Medical Center Groningen
Co-authored papers 3
Institute of Computer Science, Masaryk University
Co-authored papers 3
University of California san francisco
Co-authored papers 3
Universitat de Barcelona (UB)
Co-authored papers 3
University of Cambridge
Co-authored papers 3
University of Southern California
Co-authored papers 3
Barcelonabeta Brain Research Center (BBRC), Pasqual Maragall Foundation
Co-authored papers 3
Hospital Universitari Vall d'Hebron
Co-authored papers 3
University of Manchester
Co-authored papers 3
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers 3
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Pfizer Ltd
Co-authored papers 3
European Bioinformatics Institute
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Novo Nordisk Foundation Center for Protein Research, University of Copenhagen
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European Bioinformatics Institute
Co-authored papers 2