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Author Details

Gemma F Codner
Medical Research Council Harwell Institute
2008
26
14
PMIDPaper TitleJournal TitlePublished Year
37996040Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6.Neurobiol Dis2024
36995665Genotyping Genome-Edited Founders and Subsequent Generation.Methods Mol Biol2023
34192966Screening and validation of genome-edited animals.Lab Anim2022
35416977An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1Y446C/Y446C mutation.Hum Mol Genet2022
35100259Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing.PLoS Genet2022
35296030Erratum: Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models.iScience2022
32599056Universal Southern blot protocol with cold or radioactive probes for the validation of alleles obtained by homologous recombination.Methods2021
33729479Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2.Hum Mol Genet2021
31020388The guanine nucleotide exchange factor, Spata13, influences social behaviour and nocturnal activity.Mamm Genome2019
31748609Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight.Sci Rep2019
31448880Clarin-2 is essential for hearing by maintaining stereocilia integrity and function.EMBO Mol Med2019
31127293Microhomologies are prevalent at Cas9-induced larger deletions.Nucleic Acids Res2019
29764981Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis.EMBO J2018
29925374Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants.BMC Biol2018
30464345Helios is a key transcriptional regulator of outer hair cell maturation.Nature2018
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
28363792Analysing the outcome of CRISPR-aided genome editing in embryos: Screening, genotyping and quality control.Methods2017
26876963Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair.Genome Med2016
26604141Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration.Hum Mol Genet2016
27496052Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction.BMC Cell Biol2016
26214591Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.Nat Genet2015
23690615Analysis of core circadian feedback loop in suprachiasmatic nucleus of mCry1-luc transgenic reporter mouse.Proc Natl Acad Sci U S A2013
21466899The impact of MHC diversity on cattle T cell responses.Vet Immunol Immunopathol2012
22454046Constraints on haplotype structure and variable gene frequencies suggest a functional hierarchy within cattle MHC class I.Immunogenetics2012
22486494Selective forces shaping diversity in the class I region of the major histocompatibility complex in dairy cattle.Anim Genet2012
18431566Genomic location and characterisation of nonclassical MHC class I genes in cattle.Immunogenetics2008
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Collaborators

Mary Lyon Centre at Medical Research Council
Co-authored papers 11
Mary Lyon Centre at Medical Research Council
Co-authored papers 8
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 6
Wellcome Trust Sanger Institute
Co-authored papers 3
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers 3
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Co-authored papers 3
The Turing Institute
Co-authored papers 3
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 2
The Turing Institute
Co-authored papers 2
Wellcome Sanger Institute
Co-authored papers 2
MRC Harwell Institute
Co-authored papers 2
German Center for Diabetes Research (DZD e.V.)
Co-authored papers 2
MRC Harwell Institute
Co-authored papers 2
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers 2
Wellcome Sanger Institute
Co-authored papers 2
UCL Queen Square Institute of Neurology
Co-authored papers 2
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
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The Hospital for Sick Children
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Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
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University of Maryland School of Medicine
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The Hospital for Sick Children
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Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
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Harwell Institute
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Columbia University.
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William Harvey Research Institute, Queen Mary University of London
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