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Author Details

Terrence F Meehan
European Bioinformatics Institute
1999
43
27
PMIDPaper TitleJournal TitlePublished Year
34021280REMBI: Recommended Metadata for Biological Images-enabling reuse of microscopy data in biology.Nat Methods2021
34021280REMBI: Recommended Metadata for Biological Images-enabling reuse of microscopy data in biology.Nat Methods2021
31591642Soft windowing application to improve analysis of high-throughput phenotyping data.Bioinformatics2020
31591642Soft windowing application to improve analysis of high-throughput phenotyping data.Bioinformatics2020
31844327High-throughput phenotyping reveals expansive genetic and structural underpinnings of immune variation.Nat Immunol2020
31929527High-throughput discovery of genetic determinants of circadian misalignment.PLoS Genet2020
33378393OpenStats: A robust and scalable software package for reproducible analysis of high-throughput phenotypic data.PLoS One2020
33370286Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.PLoS Genet2020
33017400Ten simple rules for annotating sequencing experiments.PLoS Comput Biol2020
31844327High-throughput phenotyping reveals expansive genetic and structural underpinnings of immune variation.Nat Immunol2020
31929527High-throughput discovery of genetic determinants of circadian misalignment.PLoS Genet2020
33378393OpenStats: A robust and scalable software package for reproducible analysis of high-throughput phenotypic data.PLoS One2020
33370286Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.PLoS Genet2020
33017400Ten simple rules for annotating sequencing experiments.PLoS Comput Biol2020
30535239PDX Finder: A portal for patient-derived tumor xenograft model discovery.Nucleic Acids Res2019
30535239PDX Finder: A portal for patient-derived tumor xenograft model discovery.Nucleic Acids Res2019
30854487Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.Commun Biol2019
31481418Know Thy PDX Model.Cancer Res2019
31481418Know Thy PDX Model.Cancer Res2019
30854487Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.Commun Biol2019
29348434Identification of genetic elements in metabolism by high-throughput mouse phenotyping.Nat Commun2018
30100824The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation.Conserv Genet2018
29626206High-throughput mouse phenomics for characterizing mammalian gene function.Nat Rev Genet2018
29567993Unexplored therapeutic opportunities in the human genome.Nat Rev Drug Discov2018
29348434Identification of genetic elements in metabolism by high-throughput mouse phenotyping.Nat Commun2018
29472638Unexplored therapeutic opportunities in the human genome.Nat Rev Drug Discov2018
30100824The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation.Conserv Genet2018
29472638Unexplored therapeutic opportunities in the human genome.Nat Rev Drug Discov2018
29567993Unexplored therapeutic opportunities in the human genome.Nat Rev Drug Discov2018
29626206High-throughput mouse phenomics for characterizing mammalian gene function.Nat Rev Genet2018
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
28650954Prevalence of sexual dimorphism in mammalian phenotypic traits.Nat Commun2017
29026089A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.Nat Commun2017
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
29092942PDX-MI: Minimal Information for Patient-Derived Tumor Xenograft Models.Cancer Res2017
29144450Corrigendum: High-throughput discovery of novel developmental phenotypes.Nature2017
29026089A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.Nat Commun2017
29144450Corrigendum: High-throughput discovery of novel developmental phenotypes.Nature2017
29092942PDX-MI: Minimal Information for Patient-Derived Tumor Xenograft Models.Cancer Res2017
28650954Prevalence of sexual dimorphism in mammalian phenotypic traits.Nat Commun2017
26865945Reporting phenotypes in mouse models when considering body size as a potential confounder.J Biomed Semantics2016
27377652The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability.J Biomed Semantics2016
26865945Reporting phenotypes in mouse models when considering body size as a potential confounder.J Biomed Semantics2016
27626380High-throughput discovery of novel developmental phenotypes.Nature2016
27626380High-throughput discovery of novel developmental phenotypes.Nature2016
27377652The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability.J Biomed Semantics2016
25723102Gateways to the FANTOM5 promoter level mammalian expression atlas.Genome Biol2015
25678556Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells.Science2015
25723102Gateways to the FANTOM5 promoter level mammalian expression atlas.Genome Biol2015
26314589A mouse informatics platform for phenotypic and translational discovery.Mamm Genome2015
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Collaborators

European Bioinformatics Institute
Co-authored papers 21
The Turing Institute
Co-authored papers 17
European Molecular Biology Laboratory - European Bioinformatics Institute
Co-authored papers 17
University of California davis
Co-authored papers 14
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 13
Wellcome Trust Sanger Institute
Co-authored papers 12
German Center for Diabetes Research (DZD e.V.)
Co-authored papers 12
The Hospital for Sick Children
Co-authored papers 12
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers 12
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 12
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers 11
Co-authored papers 10
Mary Lyon Centre at Medical Research Council
Co-authored papers 10
European Bioinformatics Institute
Co-authored papers 10
International Society for Biocuration, Lawrence Berkeley National Laboratory, University of Edinburgh, University of Edinburgh School of Biological Sciences
Co-authored papers 10
Wellcome Sanger Institute
Co-authored papers 10
Columbia University.
Co-authored papers 9
Baylor College of Medicine
Co-authored papers 9
Children's Hospital Oakland Research Institute
Co-authored papers 8
Nanjing Biomedical Research Institute, Nanjing University
Co-authored papers 8
University of Maine
Co-authored papers 8
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 8
Baylor College of Medicine
Co-authored papers 8
Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
Co-authored papers 8
Jacobs School of Medicine and Biomedical Sciences, University at Buffalo
Co-authored papers 8
The Hospital for Sick Children
Co-authored papers 8
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 7
University of California davis
Co-authored papers 7
Seoul National University
Co-authored papers 7
Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
Co-authored papers 7