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Author Details
Full Name
Terrence F Meehan
Affiliation
European Bioinformatics Institute
ORCID
Career Start Year
1999
Papers
43
H Index
27
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34021280
REMBI: Recommended Metadata for Biological Images-enabling reuse of microscopy data in biology.
Nat Methods
2021
34021280
REMBI: Recommended Metadata for Biological Images-enabling reuse of microscopy data in biology.
Nat Methods
2021
31591642
Soft windowing application to improve analysis of high-throughput phenotyping data.
Bioinformatics
2020
31591642
Soft windowing application to improve analysis of high-throughput phenotyping data.
Bioinformatics
2020
31844327
High-throughput phenotyping reveals expansive genetic and structural underpinnings of immune variation.
Nat Immunol
2020
31929527
High-throughput discovery of genetic determinants of circadian misalignment.
PLoS Genet
2020
33378393
OpenStats: A robust and scalable software package for reproducible analysis of high-throughput phenotypic data.
PLoS One
2020
33370286
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.
PLoS Genet
2020
33017400
Ten simple rules for annotating sequencing experiments.
PLoS Comput Biol
2020
31844327
High-throughput phenotyping reveals expansive genetic and structural underpinnings of immune variation.
Nat Immunol
2020
31929527
High-throughput discovery of genetic determinants of circadian misalignment.
PLoS Genet
2020
33378393
OpenStats: A robust and scalable software package for reproducible analysis of high-throughput phenotypic data.
PLoS One
2020
33370286
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.
PLoS Genet
2020
33017400
Ten simple rules for annotating sequencing experiments.
PLoS Comput Biol
2020
30535239
PDX Finder: A portal for patient-derived tumor xenograft model discovery.
Nucleic Acids Res
2019
30535239
PDX Finder: A portal for patient-derived tumor xenograft model discovery.
Nucleic Acids Res
2019
30854487
Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.
Commun Biol
2019
31481418
Know Thy PDX Model.
Cancer Res
2019
31481418
Know Thy PDX Model.
Cancer Res
2019
30854487
Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.
Commun Biol
2019
29348434
Identification of genetic elements in metabolism by high-throughput mouse phenotyping.
Nat Commun
2018
30100824
The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation.
Conserv Genet
2018
29626206
High-throughput mouse phenomics for characterizing mammalian gene function.
Nat Rev Genet
2018
29567993
Unexplored therapeutic opportunities in the human genome.
Nat Rev Drug Discov
2018
29348434
Identification of genetic elements in metabolism by high-throughput mouse phenotyping.
Nat Commun
2018
29472638
Unexplored therapeutic opportunities in the human genome.
Nat Rev Drug Discov
2018
30100824
The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation.
Conserv Genet
2018
29472638
Unexplored therapeutic opportunities in the human genome.
Nat Rev Drug Discov
2018
29567993
Unexplored therapeutic opportunities in the human genome.
Nat Rev Drug Discov
2018
29626206
High-throughput mouse phenomics for characterizing mammalian gene function.
Nat Rev Genet
2018
28650483
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.
Nat Genet
2017
28650954
Prevalence of sexual dimorphism in mammalian phenotypic traits.
Nat Commun
2017
29026089
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.
Nat Commun
2017
28650483
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.
Nat Genet
2017
29092942
PDX-MI: Minimal Information for Patient-Derived Tumor Xenograft Models.
Cancer Res
2017
29144450
Corrigendum: High-throughput discovery of novel developmental phenotypes.
Nature
2017
29026089
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.
Nat Commun
2017
29144450
Corrigendum: High-throughput discovery of novel developmental phenotypes.
Nature
2017
29092942
PDX-MI: Minimal Information for Patient-Derived Tumor Xenograft Models.
Cancer Res
2017
28650954
Prevalence of sexual dimorphism in mammalian phenotypic traits.
Nat Commun
2017
26865945
Reporting phenotypes in mouse models when considering body size as a potential confounder.
J Biomed Semantics
2016
27377652
The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability.
J Biomed Semantics
2016
26865945
Reporting phenotypes in mouse models when considering body size as a potential confounder.
J Biomed Semantics
2016
27626380
High-throughput discovery of novel developmental phenotypes.
Nature
2016
27626380
High-throughput discovery of novel developmental phenotypes.
Nature
2016
27377652
The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability.
J Biomed Semantics
2016
25723102
Gateways to the FANTOM5 promoter level mammalian expression atlas.
Genome Biol
2015
25678556
Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells.
Science
2015
25723102
Gateways to the FANTOM5 promoter level mammalian expression atlas.
Genome Biol
2015
26314589
A mouse informatics platform for phenotypic and translational discovery.
Mamm Genome
2015
1 - 50 of 86
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Sean Davis
Johns Hopkins School of Medicine, National Cancer Institute, Princeton University, University of Colorado Anschutz Medical Campus, University of Pittsburgh, University of Washington
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The Turing Institute
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Co-authored papers
17
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Co-authored papers
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Steve D M Brown
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Co-authored papers
13
Jacqueline K White
Wellcome Trust Sanger Institute
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12
Martin Hrab?? de Angelis
German Center for Diabetes Research (DZD e.V.)
Co-authored papers
12
Colin McKerlie
The Hospital for Sick Children
Co-authored papers
12
Ann M Flenniken
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
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12
Damian Smedley
William Harvey Research Institute, Queen Mary University of London
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Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
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11
Karen L Svenson
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10
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Mary Lyon Centre at Medical Research Council
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10
Paul Flicek
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10
Christopher J Mungall
International Society for Biocuration, Lawrence Berkeley National Laboratory, University of Edinburgh, University of Edinburgh School of Biological Sciences
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10
Natasha A Karp
Wellcome Sanger Institute
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10
Stephen A Murray
Columbia University.
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9
John R Seavitt
Baylor College of Medicine
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David B West
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Robert E Braun
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