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Author Details

Michael Baudis
University of Zurich
1995
78
28
PMIDPaper TitleJournal TitlePublished Year
36726722Candidate targets of copy number deletion events across 17 cancer types.Front Genet2023
37196000Phenopacket-tools: Building and validating GA4GH Phenopackets.PLoS One2023
36726722Candidate targets of copy number deletion events across 17 cancer types.Front Genet2023
37196000Phenopacket-tools: Building and validating GA4GH Phenopackets.PLoS One2023
35297548Beacon v2 and Beacon networks: A "lingua franca" for federated data discovery in biomedical genomics, and beyond.Hum Mutat2022
35705716The GA4GH Phenopacket schema defines a computable representation of clinical data.Nat Biotechnol2022
36910590GA4GH Phenopackets: A Practical Introduction.Adv Genet (Hoboken)2022
35297548Beacon v2 and Beacon networks: A "lingua franca" for federated data discovery in biomedical genomics, and beyond.Hum Mutat2022
35705716The GA4GH Phenopacket schema defines a computable representation of clinical data.Nat Biotechnol2022
36910590GA4GH Phenopackets: A Practical Introduction.Adv Genet (Hoboken)2022
34054918Signatures of Discriminative Copy Number Aberrations in 31 Cancer Subtypes.Front Genet2021
34054918Signatures of Discriminative Copy Number Aberrations in 31 Cancer Subtypes.Front Genet2021
34272855The Progenetix oncogenomic resource in 2021.Database (Oxford)2021
35311178The GA4GH Variation Representation Specification: A computational framework for variation representation and federated identification.Cell Genom2021
35128509International federation of genomic medicine databases using GA4GH standards.Cell Genom2021
35072136GA4GH: International policies and standards for data sharing across genomic research and healthcare.Cell Genom2021
35128509International federation of genomic medicine databases using GA4GH standards.Cell Genom2021
35072136GA4GH: International policies and standards for data sharing across genomic research and healthcare.Cell Genom2021
35311178The GA4GH Variation Representation Specification: A computational framework for variation representation and federated identification.Cell Genom2021
34272855The Progenetix oncogenomic resource in 2021.Database (Oxford)2021
30368507Mountains and Chasms: Surveying the Oncogenomic Publication Landscape.Oncology2020
32413400Minimum error calibration and normalization for genomic copy number analysis.Genomics2020
32246132A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer.Nat Genet2020
32179800Enabling population assignment from cancer genomes with SNP2pop.Sci Rep2020
32408309Oncology Informatics: Status Quo and Outlook.Oncology2020
32755579The Ubiquitin Ligase TRIP12 Limits PARP1 Trapping and Constrains PARP Inhibitor Efficiency.Cell Rep2020
33344238DNA Copy Number Changes in Diffuse Large B Cell Lymphomas.Front Oncol2020
34367618The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research.F1000Res2020
30368507Mountains and Chasms: Surveying the Oncogenomic Publication Landscape.Oncology2020
34367618The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research.F1000Res2020
33344238DNA Copy Number Changes in Diffuse Large B Cell Lymphomas.Front Oncol2020
32755579The Ubiquitin Ligase TRIP12 Limits PARP1 Trapping and Constrains PARP Inhibitor Efficiency.Cell Rep2020
32246132A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer.Nat Genet2020
32179800Enabling population assignment from cancer genomes with SNP2pop.Sci Rep2020
32413400Minimum error calibration and normalization for genomic copy number analysis.Genomics2020
32408309Oncology Informatics: Status Quo and Outlook.Oncology2020
30894680Publisher Correction: Federated discovery and sharing of genomic data using Beacons.Nat Biotechnol2019
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
30894680Publisher Correction: Federated discovery and sharing of genomic data using Beacons.Nat Biotechnol2019
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
29930344Krüppel-Like Factor 10 participates in cervical cancer immunoediting through transcriptional regulation of Pregnancy-Specific Beta-1 Glycoproteins.Sci Rep2018
30069064Registered access: authorizing data access.Eur J Hum Genet2018
29930344Krüppel-Like Factor 10 participates in cervical cancer immunoediting through transcriptional regulation of Pregnancy-Specific Beta-1 Glycoproteins.Sci Rep2018
30069064Registered access: authorizing data access.Eur J Hum Genet2018
28966033Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma.Cancer Cell2017
28966033Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma.Cancer Cell2017
27198223PKCα and HMGB1 antagonistically control hydrogen peroxide-induced poly-ADP-ribose formation.Nucleic Acids Res2016
27198223PKCα and HMGB1 antagonistically control hydrogen peroxide-induced poly-ADP-ribose formation.Nucleic Acids Res2016
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Collaborators

Universitat Pompeu Fabra
Co-authored papers 8
German Cancer Research Center (DKFZ)
Co-authored papers 8
Co-authored papers 7
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers 6
Iowa State University, Mayo Clinic, Nationwide Children's Hospital, The Ohio State University College of Medicine, University of Iowa, Washington University in Saint Louis
Co-authored papers 6
American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
Co-authored papers 5
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 5
European Bioinformatics Institute
Co-authored papers 5
Barcelonabeta Brain Research Center (BBRC), Pasqual Maragall Foundation
Co-authored papers 5
Co-authored papers 5
Ontario Institute for Cancer Research
Co-authored papers 5
Pfizer Ltd
Co-authored papers 5
Broad Institute
Co-authored papers 5
European Bioinformatics Institute
Co-authored papers 4
ELIXIR Finland CSC - IT Center for Science Ltd
Co-authored papers 4
CSC - IT Center for Science Ltd
Co-authored papers 4
European Bioinformatics Institute
Co-authored papers 4
The Broad Institute of MIT and Harvard
Co-authored papers 4
Center for Individualized Medicine, Mayo Clinic
Co-authored papers 4
Perth Children's Hospital
Co-authored papers 4
Josep Carreras Leukaemia Research Institute (IJC)
Co-authored papers 4
Ontario Institute for Cancer Research
Co-authored papers 4
University of Leicester
Co-authored papers 4
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers 4
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 4
CSC - IT Center for Science Ltd
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European Bioinformatics Institute
Co-authored papers 4
European Bioinformatics Institute
Co-authored papers 4
University of Colorado Anschutz Medical Campus
Co-authored papers 4
Oregon Health & Science University
Co-authored papers 4