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Author Details

Jeremy Mason
European Molecular Biology Laboratory - European Bioinformatics Institute
2011
28
19
PMIDPaper TitleJournal TitlePublished Year
36399494PDCM Finder: an open global research platform for patient-derived cancer models.Nucleic Acids Res2023
34524473Pleiotropy data resource as a primer for investigating co-morbidities/multi-morbidities and their role in disease.Mamm Genome2022
35552317Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.Pain2022
36509767Sex differences in allometry for phenotypic traits in mice indicate that females are not scaled males.Nat Commun2022
31591642Soft windowing application to improve analysis of high-throughput phenotyping data.Bioinformatics2020
32060626A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes.Mamm Genome2020
31844327High-throughput phenotyping reveals expansive genetic and structural underpinnings of immune variation.Nat Immunol2020
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
33247289Author Correction: A dynamic COVID-19 immune signature includes associations with poor prognosis.Nat Med2020
32807934A dynamic COVID-19 immune signature includes associations with poor prognosis.Nat Med2020
32908251Author Correction: A dynamic COVID-19 immune signature includes associations with poor prognosis.Nat Med2020
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
29348434Identification of genetic elements in metabolism by high-throughput mouse phenotyping.Nat Commun2018
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
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
27626380High-throughput discovery of novel developmental phenotypes.Nature2016
25992600Applying the ARRIVE Guidelines to an In Vivo Database.PLoS Biol2015
26314589A mouse informatics platform for phenotypic and translational discovery.Mamm Genome2015
26147094PhenStat: A Tool Kit for Standardized Analysis of High Throughput Phenotypic Data.PLoS One2015
24194600The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data.Nucleic Acids Res2014
22968824The mammalian gene function resource: the International Knockout Mouse Consortium.Mamm Genome2012
20929875The IKMC web portal: a central point of entry to data and resources from the International Knockout Mouse Consortium.Nucleic Acids Res2011
21930507BioMart Central Portal: an open database network for the biological community.Database (Oxford)2011
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Collaborators

Helen Parkinson
European Bioinformatics Institute
Co-authored papers 18
Terrence F Meehan
European Bioinformatics Institute
Co-authored papers 17
Ann-Marie Mallon
The Turing Institute
Co-authored papers 14
Kent C Lloyd
University of California davis
Co-authored papers 13
Steve D M Brown
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 13
Damian Smedley
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 13
Jacqueline K White
Wellcome Trust Sanger Institute
Co-authored papers 12
Martin Hrab?? de Angelis
German Center for Diabetes Research (DZD e.V.)
Co-authored papers 12
Ann M Flenniken
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers 11
Yann Herault
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers 11
Colin McKerlie
The Hospital for Sick Children
Co-authored papers 11
Sara Wells
Mary Lyon Centre at Medical Research Council
Co-authored papers 10
Wolfgang Wurst
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 9
John R Seavitt
Baylor College of Medicine
Co-authored papers 9
Luis Santos
The Turing Institute
Co-authored papers 9
Paul Flicek
European Bioinformatics Institute
Co-authored papers 9
Anne M Dickinson
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 9
Natasha A Karp
Wellcome Sanger Institute
Co-authored papers 9
Glauco P Tocchini-Valentini
Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
Co-authored papers 9
Karen L Svenson
Co-authored papers 9
William C Skarnes
Wellcome Trust Sanger Institute
Co-authored papers 8
Robert E Braun
University of Maine
Co-authored papers 8
Lynette Bower
University of California davis
Co-authored papers 8
Stephen A Murray
Columbia University.
Co-authored papers 8
Lauryl M J Nutter
The Hospital for Sick Children
Co-authored papers 8
David B West
Children's Hospital Oakland Research Institute
Co-authored papers 7
Mark Moore
Co-authored papers 7
Henrik Westerberg
MRC Harwell Institute
Co-authored papers 7
Valerie Gailus-Durner
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers 7
Arthur L Beaudet
Baylor College of Medicine
Co-authored papers 7
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