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Author Details

Ann-Marie Mallon
The Turing Institute
1998
83
28
PMIDPaper TitleJournal TitlePublished Year
36305825The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease.Nucleic Acids Res2023
36305825The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease.Nucleic Acids Res2023
37659414Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background.Am J Hum Genet2023
37736706Genic constraint against nonsynonymous variation across the mouse genome.BMC Genomics2023
37294348Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.Mamm Genome2023
37659414Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background.Am J Hum Genet2023
37736706Genic constraint against nonsynonymous variation across the mouse genome.BMC Genomics2023
37294348Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.Mamm Genome2023
34972825Improving local prevalence estimates of SARS-CoV-2 infections using a causal debiasing framework.Nat Microbiol2022
35944064Multivariate phenotype analysis enables genome-wide inference of mammalian gene function.PLoS Biol2022
35552317Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.Pain2022
36327884Application of a convolutional neural network to the quality control of MRI defacing.Comput Biol Med2022
35664221Interoperability of statistical models in pandemic preparedness: principles and reality.Stat Sci2022
35317627Modelling the genetic aetiology of complex disease: human-mouse conservation of noncoding features and disease-associated loci.Biol Lett2022
35044497Introduction to Mammalian Genome Special Issue: Mammalian Genetic Resources.Mamm Genome2022
34972825Improving local prevalence estimates of SARS-CoV-2 infections using a causal debiasing framework.Nat Microbiol2022
35187517Time varying association between deprivation, ethnicity and SARS-CoV-2 infections in England: A population-based ecological study.Lancet Reg Health Eur2022
35090532Making sense of the linear genome, gene function and TADs.Epigenetics Chromatin2022
35664221Interoperability of statistical models in pandemic preparedness: principles and reality.Stat Sci2022
35552317Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.Pain2022
36327884Application of a convolutional neural network to the quality control of MRI defacing.Comput Biol Med2022
35944064Multivariate phenotype analysis enables genome-wide inference of mammalian gene function.PLoS Biol2022
35044497Introduction to Mammalian Genome Special Issue: Mammalian Genetic Resources.Mamm Genome2022
35317627Modelling the genetic aetiology of complex disease: human-mouse conservation of noncoding features and disease-associated loci.Biol Lett2022
35187517Time varying association between deprivation, ethnicity and SARS-CoV-2 infections in England: A population-based ecological study.Lancet Reg Health Eur2022
35090532Making sense of the linear genome, gene function and TADs.Epigenetics Chromatin2022
34477842Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes.Dis Model Mech2021
33574040LAMA: automated image analysis for the developmental phenotyping of mouse embryos.Development2021
34790983Time varying association between deprivation, ethnicity and SARS-CoV-2 infections in England: a space-time study.medRxiv2021
34773974Advancing data science in drug development through an innovative computational framework for data sharing and statistical analysis.BMC Med Res Methodol2021
34477842Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes.Dis Model Mech2021
33574040LAMA: automated image analysis for the developmental phenotyping of mouse embryos.Development2021
34790983Time varying association between deprivation, ethnicity and SARS-CoV-2 infections in England: a space-time study.medRxiv2021
34773974Advancing data science in drug development through an innovative computational framework for data sharing and statistical analysis.BMC Med Res Methodol2021
31591642Soft windowing application to improve analysis of high-throughput phenotyping data.Bioinformatics2020
31591642Soft windowing application to improve analysis of high-throughput phenotyping data.Bioinformatics2020
31836612Protection Against XY Gonadal Sex Reversal by a Variant Region on Mouse Chromosome 13.Genetics2020
32348957Genetic background influences tumour development in heterozygous Men1 knockout mice.Endocr Connect2020
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
33138777A holistic view of mouse enhancer architectures reveals analogous pleiotropic effects and correlation with human disease.BMC Genomics2020
31929527High-throughput discovery of genetic determinants of circadian misalignment.PLoS Genet2020
31836612Protection Against XY Gonadal Sex Reversal by a Variant Region on Mouse Chromosome 13.Genetics2020
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
33138777A holistic view of mouse enhancer architectures reveals analogous pleiotropic effects and correlation with human disease.BMC Genomics2020
32348957Genetic background influences tumour development in heterozygous Men1 knockout mice.Endocr Connect2020
30395686An N-Ethyl-N-Nitrosourea (ENU)-Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice.J Bone Miner Res2019
32257911TarGo: network based target gene selection system for human disease related mouse models.Lab Anim Res2019
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Collaborators

Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 36
Mary Lyon Centre at Medical Research Council
Co-authored papers 28
European Bioinformatics Institute
Co-authored papers 21
German Center for Diabetes Research (DZD e.V.)
Co-authored papers 19
the University of Texas Health Science Center at Houston
Co-authored papers 18
European Bioinformatics Institute
Co-authored papers 17
Harwell Institute
Co-authored papers 16
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers 16
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 16
Wellcome Trust Sanger Institute
Co-authored papers 16
University of California davis
Co-authored papers 15
The Turing Institute
Co-authored papers 15
MRC Harwell Institute
Co-authored papers 15
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers 15
The Hospital for Sick Children
Co-authored papers 15
European Molecular Biology Laboratory - European Bioinformatics Institute
Co-authored papers 14
MRC Harwell Institute
Co-authored papers 12
European Bioinformatics Institute
Co-authored papers 12
Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
Co-authored papers 11
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers 11
Columbia University.
Co-authored papers 11
Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
Co-authored papers 11
The Hospital for Sick Children
Co-authored papers 11
Co-authored papers 10
Baylor College of Medicine
Co-authored papers 10
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 10
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 9
Institute of Cancer and Genomic Sciences, University of Birmingham
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University of California davis
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Wellcome Sanger Institute
Co-authored papers 9