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Author Details
Full Name
Ann-Marie Mallon
Affiliation
The Turing Institute
ORCID
Career Start Year
1998
Papers
83
H Index
28
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36305825
The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease.
Nucleic Acids Res
2023
36305825
The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease.
Nucleic Acids Res
2023
37659414
Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background.
Am J Hum Genet
2023
37736706
Genic constraint against nonsynonymous variation across the mouse genome.
BMC Genomics
2023
37294348
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.
Mamm Genome
2023
37659414
Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background.
Am J Hum Genet
2023
37736706
Genic constraint against nonsynonymous variation across the mouse genome.
BMC Genomics
2023
37294348
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.
Mamm Genome
2023
34972825
Improving local prevalence estimates of SARS-CoV-2 infections using a causal debiasing framework.
Nat Microbiol
2022
35944064
Multivariate phenotype analysis enables genome-wide inference of mammalian gene function.
PLoS Biol
2022
35552317
Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.
Pain
2022
36327884
Application of a convolutional neural network to the quality control of MRI defacing.
Comput Biol Med
2022
35664221
Interoperability of statistical models in pandemic preparedness: principles and reality.
Stat Sci
2022
35317627
Modelling the genetic aetiology of complex disease: human-mouse conservation of noncoding features and disease-associated loci.
Biol Lett
2022
35044497
Introduction to Mammalian Genome Special Issue: Mammalian Genetic Resources.
Mamm Genome
2022
34972825
Improving local prevalence estimates of SARS-CoV-2 infections using a causal debiasing framework.
Nat Microbiol
2022
35187517
Time varying association between deprivation, ethnicity and SARS-CoV-2 infections in England: A population-based ecological study.
Lancet Reg Health Eur
2022
35090532
Making sense of the linear genome, gene function and TADs.
Epigenetics Chromatin
2022
35664221
Interoperability of statistical models in pandemic preparedness: principles and reality.
Stat Sci
2022
35552317
Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.
Pain
2022
36327884
Application of a convolutional neural network to the quality control of MRI defacing.
Comput Biol Med
2022
35944064
Multivariate phenotype analysis enables genome-wide inference of mammalian gene function.
PLoS Biol
2022
35044497
Introduction to Mammalian Genome Special Issue: Mammalian Genetic Resources.
Mamm Genome
2022
35317627
Modelling the genetic aetiology of complex disease: human-mouse conservation of noncoding features and disease-associated loci.
Biol Lett
2022
35187517
Time varying association between deprivation, ethnicity and SARS-CoV-2 infections in England: A population-based ecological study.
Lancet Reg Health Eur
2022
35090532
Making sense of the linear genome, gene function and TADs.
Epigenetics Chromatin
2022
34477842
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes.
Dis Model Mech
2021
33574040
LAMA: automated image analysis for the developmental phenotyping of mouse embryos.
Development
2021
34790983
Time varying association between deprivation, ethnicity and SARS-CoV-2 infections in England: a space-time study.
medRxiv
2021
34773974
Advancing data science in drug development through an innovative computational framework for data sharing and statistical analysis.
BMC Med Res Methodol
2021
34477842
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes.
Dis Model Mech
2021
33574040
LAMA: automated image analysis for the developmental phenotyping of mouse embryos.
Development
2021
34790983
Time varying association between deprivation, ethnicity and SARS-CoV-2 infections in England: a space-time study.
medRxiv
2021
34773974
Advancing data science in drug development through an innovative computational framework for data sharing and statistical analysis.
BMC Med Res Methodol
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
31836612
Protection Against XY Gonadal Sex Reversal by a Variant Region on Mouse Chromosome 13.
Genetics
2020
32348957
Genetic background influences tumour development in heterozygous Men1 knockout mice.
Endocr Connect
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
33138777
A holistic view of mouse enhancer architectures reveals analogous pleiotropic effects and correlation with human disease.
BMC Genomics
2020
31929527
High-throughput discovery of genetic determinants of circadian misalignment.
PLoS Genet
2020
31836612
Protection Against XY Gonadal Sex Reversal by a Variant Region on Mouse Chromosome 13.
Genetics
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
33138777
A holistic view of mouse enhancer architectures reveals analogous pleiotropic effects and correlation with human disease.
BMC Genomics
2020
32348957
Genetic background influences tumour development in heterozygous Men1 knockout mice.
Endocr Connect
2020
30395686
An 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 Res
2019
32257911
TarGo: network based target gene selection system for human disease related mouse models.
Lab Anim Res
2019
1 - 50 of 166
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