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Author Details

Ian Dunham
European Bioinformatics Institute (EMBL-EBI)
1987
175
64
Trey Ideker (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36399499The next-generation Open Targets Platform: reimagined, redesigned, rebuilt.Nucleic Acids Res2023
36399499The next-generation Open Targets Platform: reimagined, redesigned, rebuilt.Nucleic Acids Res2023
37749083Integrative GWAS and co-localisation analysis suggests novel genes associated with age-related multimorbidity.Sci Data2023
37609366Sex difference contributes to phenotypic diversity in individuals with neurodevelopmental disorders.Front Pediatr2023
37337100Democratizing knowledge representation with BioCypher.Nat Biotechnol2023
36963162Future prospects for human genetics and genomics in drug discovery.Curr Opin Struct Biol2023
37749083Integrative GWAS and co-localisation analysis suggests novel genes associated with age-related multimorbidity.Sci Data2023
37609366Sex difference contributes to phenotypic diversity in individuals with neurodevelopmental disorders.Front Pediatr2023
37337100Democratizing knowledge representation with BioCypher.Nat Biotechnol2023
36963162Future prospects for human genetics and genomics in drug discovery.Curr Opin Struct Biol2023
34996498Integrative analysis of 3604 GWAS reveals multiple novel cell type-specific regulatory associations.Genome Biol2022
35772218Multi-ancestry Mendelian randomization of omics traits revealing drug targets of COVID-19 severity.EBioMedicine2022
35568032Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites.Am J Hum Genet2022
35804044Human genetics evidence supports two-thirds of the 2021 FDA-approved drugs.Nat Rev Drug Discov2022
34996498Integrative analysis of 3604 GWAS reveals multiple novel cell type-specific regulatory associations.Genome Biol2022
35804044Human genetics evidence supports two-thirds of the 2021 FDA-approved drugs.Nat Rev Drug Discov2022
35772218Multi-ancestry Mendelian randomization of omics traits revealing drug targets of COVID-19 severity.EBioMedicine2022
35568032Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites.Am J Hum Genet2022
33045747Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics.Nucleic Acids Res2021
34285415The PROTACtable genome.Nat Rev Drug Discov2021
33045747Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics.Nucleic Acids Res2021
33196847Open Targets Platform: supporting systematic drug-target identification and prioritisation.Nucleic Acids Res2021
34402426A proteome-wide genetic investigation identifies several SARS-CoV-2-exploited host targets of clinical relevance.Elife2021
34711957An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci.Nat Genet2021
34402426A proteome-wide genetic investigation identifies several SARS-CoV-2-exploited host targets of clinical relevance.Elife2021
34711957An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci.Nat Genet2021
34285415The PROTACtable genome.Nat Rev Drug Discov2021
33196847Open Targets Platform: supporting systematic drug-target identification and prioritisation.Nucleic Acids Res2021
33289971Mining a GWAS of Severe Covid-19.N Engl J Med2020
31930349The open targets post-GWAS analysis pipeline.Bioinformatics2020
33289972Mining a GWAS of Severe Covid-19.N Engl J Med2020
33289971Mining a GWAS of Severe Covid-19.N Engl J Med2020
33060197Comparative host-coronavirus protein interaction networks reveal pan-viral disease mechanisms.Science2020
31930349The open targets post-GWAS analysis pipeline.Bioinformatics2020
33060197Comparative host-coronavirus protein interaction networks reveal pan-viral disease mechanisms.Science2020
33289972Mining a GWAS of Severe Covid-19.N Engl J Med2020
30692680GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals.Nat Genet2019
30462303Open Targets Platform: new developments and updates two years on.Nucleic Acids Res2019
30976107Applications of machine learning in drug discovery and development.Nat Rev Drug Discov2019
30692680GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals.Nat Genet2019
31161210eFORGE v2.0: updated analysis of cell type-specific signal in epigenomic data.Bioinformatics2019
30976107Applications of machine learning in drug discovery and development.Nat Rev Drug Discov2019
31161210eFORGE v2.0: updated analysis of cell type-specific signal in epigenomic data.Bioinformatics2019
30462303Open Targets Platform: new developments and updates two years on.Nucleic Acids Res2019
29229604Transcription Factor Activities Enhance Markers of Drug Sensitivity in Cancer.Cancer Res2018
30256779Human genes: Time to follow the roads less traveled?PLoS Biol2018
30439935Ten simple rules for delivering live distance training in bioinformatics across the globe using webinars.PLoS Comput Biol2018
30293088The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers.Nat Rev Cancer2018
30285606Uncovering new disease indications for G-protein coupled receptors and their endogenous ligands.BMC Bioinformatics2018
29229604Transcription Factor Activities Enhance Markers of Drug Sensitivity in Cancer.Cancer Res2018
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Co-authored papers 22
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4Wellcome Trust Sanger Institute
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The Wellcome Trust Sanger Institute
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UCL Cancer Institute, University College London
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William Harvey Research Institute, Queen Mary University of London
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Wellcome Sanger Institute
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University of Cambridge
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European Bioinformatics Institute
Co-authored papers 10
Illumina Ltd.
Co-authored papers 10
Illumina Cambridge Ltd.
Co-authored papers 8
University of Oxford
Co-authored papers 8
Wellcome Trust Sanger Institute
Co-authored papers 8
Altius Institute for Biomedical Sciences
Co-authored papers 7
Co-authored papers 7
Institute of Biotechnology, University of Cambridge
Co-authored papers 6
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 6
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HudsonAlpha Institute for Biotechnology
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The University of Chicago
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