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Author Details

Sara Wells
Mary Lyon Centre at Medical Research Council
2004
119
42
PMIDPaper TitleJournal TitlePublished Year
36305825The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease.Nucleic Acids Res2023
37283649A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (<i>NFIX</i>) Gene Has Phenotypic Features of Marshall-Smith Syndrome.JBMR Plus2023
37035623Longitudinal home-cage automated assessment of climbing behavior shows sexual dimorphism and aging-related decrease in C57BL/6J healthy mice and allows early detection of motor impairment in the N171-82Q mouse model of Huntington's disease.Front Behav Neurosci2023
37294348Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.Mamm Genome2023
36148902Improving biomedical research by automated behaviour monitoring in the animal home cage - action needed for networking.Lab Anim2023
34328547INFRAFRONTIER quality principles in systemic phenotyping.Mamm Genome2022
35510549Perspectives on Cognitive Phenotypes and Models of Vascular Disease.Arterioscler Thromb Vasc Biol2022
35552317Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.Pain2022
36280881Early embryonic lethality in complex I associated p.L104P Nubpl mutant mice.Orphanet J Rare Dis2022
35949916Investigating audible and ultrasonic noise in modern animal facilities.F1000Res2022
35044497Introduction to Mammalian Genome Special Issue: Mammalian Genetic Resources.Mamm Genome2022
35100259Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing.PLoS Genet2022
35315790Gadd45g is required for timely Sry expression independently of RSPO1 activity.Reproduction2022
34536110Importing genetically altered animals: ensuring quality.Mamm Genome2022
32599056Universal Southern blot protocol with cold or radioactive probes for the validation of alleles obtained by homologous recombination.Methods2021
33574040LAMA: automated image analysis for the developmental phenotyping of mouse embryos.Development2021
33713180A novel knockout mouse for the small EDRK-rich factor 2 (Serf2) showing developmental and other deficits.Mamm Genome2021
33729479Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2.Hum Mol Genet2021
34477842Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes.Dis Model Mech2021
33446734Maternal and offspring high-fat diet leads to platelet hyperactivation in male mice offspring.Sci Rep2021
32542000The occurrence of tarsal injuries in male mice of C57BL/6N substrains in multiple international mouse facilities.PLoS One2020
31836612Protection Against XY Gonadal Sex Reversal by a Variant Region on Mouse Chromosome 13.Genetics2020
31949211Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function.Sci Rep2020
33370286Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.PLoS Genet2020
33103030Calcilytic NPSP795 Increases Plasma Calcium and PTH in an Autosomal Dominant Hypocalcemia Type 1 Mouse Model.JBMR Plus2020
32608086Age-related changes in the biophysical and morphological characteristics of mouse cochlear outer hair cells.J Physiol2020
32851175Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficits.Sci Adv2020
32813317Phenotyping in Mice Using Continuous Home Cage Monitoring and Ultrasonic Vocalization Recordings.Curr Protoc Mouse Biol2020
32243835Variability in Genome Editing Outcomes: Challenges for Research Reproducibility and Clinical Safety.Mol Ther2020
30692144Loss of <i>Frrs1l</i> disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities.Dis Model Mech2019
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
31593567Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons.PLoS Biol2019
31479441Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons.PLoS Biol2019
31477900When all is not lost: considering genetic compensation in laboratory animals.Lab Anim (NY)2019
30830987Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.J Bone Miner Res2019
30854487Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.Commun Biol2019
31085319Drug safety Africa: An overview of safety pharmacology &amp; toxicology in South Africa.J Pharmacol Toxicol Methods2019
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
29348434Identification of genetic elements in metabolism by high-throughput mouse phenotyping.Nat Commun2018
30068994Leukemia Inhibitory Factor-Receptor is Dispensable for Prenatal Testis Development but is Required in Sertoli cells for Normal Spermatogenesis in Mice.Sci Rep2018
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
30470800Characterisation and use of a functional Gadd45g bacterial artificial chromosome.Sci Rep2018
28456660Assessing mouse behaviour throughout the light/dark cycle using automated in-cage analysis tools.J Neurosci Methods2018
29746474Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration.PLoS Genet2018
29626206High-throughput mouse phenomics for characterizing mammalian gene function.Nat Rev Genet2018
29735715ZNRF3 functions in mammalian sex determination by inhibiting canonical WNT signaling.Proc Natl Acad Sci U S A2018
29145650Loss of p300 and CBP disrupts histone acetylation at the mouse Sry promoter and causes XY gonadal sex reversal.Hum Mol Genet2018
28575322Mutant Mice With Calcium-Sensing Receptor Activation Have Hyperglycemia That Is Rectified by Calcilytic Therapy.Endocrinology2017
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Collaborators

Steve D M Brown
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 37
Ann-Marie Mallon
The Turing Institute
Co-authored papers 28
Michelle Stewart
Mary Lyon Centre at Medical Research Council
Co-authored papers 28
Martin Hrab?? de Angelis
German Center for Diabetes Research (DZD e.V.)
Co-authored papers 16
Andy Greenfield
MRC Harwell Institute
Co-authored papers 16
Jacqueline K White
Wellcome Trust Sanger Institute
Co-authored papers 15
Yann Herault
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers 15
Ann M Flenniken
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers 14
Colin McKerlie
The Hospital for Sick Children
Co-authored papers 13
Kent C Lloyd
University of California davis
Co-authored papers 11
Gemma F Codner
Medical Research Council Harwell Institute
Co-authored papers 11
Helen Parkinson
European Bioinformatics Institute
Co-authored papers 11
Anne M Dickinson
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 11
Lauryl M J Nutter
The Hospital for Sick Children
Co-authored papers 11
Terrence F Meehan
European Bioinformatics Institute
Co-authored papers 10
Luis Santos
The Turing Institute
Co-authored papers 10
John R Seavitt
Baylor College of Medicine
Co-authored papers 10
Karen L Svenson
Co-authored papers 10
Glauco P Tocchini-Valentini
Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
Co-authored papers 10
Jeremy Mason
European Molecular Biology Laboratory - European Bioinformatics Institute
Co-authored papers 10
Tania Sorg
Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
Co-authored papers 10
Simon Greenaway
Harwell Institute
Co-authored papers 9
Robert E Braun
University of Maine
Co-authored papers 9
Lynette Bower
University of California davis
Co-authored papers 9
Valerie Gailus-Durner
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers 9
Stephen A Murray
Columbia University.
Co-authored papers 9
Wolfgang Wurst
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 8
David J Adams
Wellcome Sanger Institute
Co-authored papers 8
Helmut Fuchs
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers 8
Damian Smedley
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 8
Release 1.2