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Author Details
Full Name
Gemma F Codner
Affiliation
Medical Research Council Harwell Institute
ORCID
Career Start Year
2008
Papers
26
H Index
14
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37996040
Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6.
Neurobiol Dis
2024
36995665
Genotyping Genome-Edited Founders and Subsequent Generation.
Methods Mol Biol
2023
34192966
Screening and validation of genome-edited animals.
Lab Anim
2022
35416977
An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1Y446C/Y446C mutation.
Hum Mol Genet
2022
35100259
Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing.
PLoS Genet
2022
35296030
Erratum: Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models.
iScience
2022
32599056
Universal Southern blot protocol with cold or radioactive probes for the validation of alleles obtained by homologous recombination.
Methods
2021
33729479
Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2.
Hum Mol Genet
2021
31020388
The guanine nucleotide exchange factor, Spata13, influences social behaviour and nocturnal activity.
Mamm Genome
2019
31748609
Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight.
Sci Rep
2019
31448880
Clarin-2 is essential for hearing by maintaining stereocilia integrity and function.
EMBO Mol Med
2019
31127293
Microhomologies are prevalent at Cas9-induced larger deletions.
Nucleic Acids Res
2019
29764981
Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis.
EMBO J
2018
29925374
Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants.
BMC Biol
2018
30464345
Helios is a key transcriptional regulator of outer hair cell maturation.
Nature
2018
28650483
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.
Nat Genet
2017
28363792
Analysing the outcome of CRISPR-aided genome editing in embryos: Screening, genotyping and quality control.
Methods
2017
26876963
Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair.
Genome Med
2016
26604141
Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration.
Hum Mol Genet
2016
27496052
Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction.
BMC Cell Biol
2016
26214591
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.
Nat Genet
2015
23690615
Analysis of core circadian feedback loop in suprachiasmatic nucleus of mCry1-luc transgenic reporter mouse.
Proc Natl Acad Sci U S A
2013
21466899
The impact of MHC diversity on cattle T cell responses.
Vet Immunol Immunopathol
2012
22454046
Constraints on haplotype structure and variable gene frequencies suggest a functional hierarchy within cattle MHC class I.
Immunogenetics
2012
22486494
Selective forces shaping diversity in the class I region of the major histocompatibility complex in dairy cattle.
Anim Genet
2012
18431566
Genomic location and characterisation of nonclassical MHC class I genes in cattle.
Immunogenetics
2008
1 - 26 of 26
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