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Author Details

Jacqueline K White
Wellcome Trust Sanger Institute
1994
92
39
PMIDPaper TitleJournal TitlePublished Year
36703722Leveraging genetic diversity in mice to inform individual differences in brain microstructure and memory.Front Behav Neurosci2023
37301944Whole genome analysis for 163 gRNAs in Cas9-edited mice reveals minimal off-target activity.Commun Biol2023
34435363The venous system of E14.5 mouse embryos-reference data and examples for diagnosing malformations in embryos with gene deletions.J Anat2022
35552317Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.Pain2022
35296311Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.BMC Biol2022
33473114Accelerating functional gene discovery in osteoarthritis.Nat Commun2021
33584208Hypoglossal Nerve Abnormalities as Biomarkers for Central Nervous System Defects in Mouse Lines Producing Embryonically Lethal Offspring.Front Neuroanat2021
34050183Publisher Correction: Accelerating functional gene discovery in osteoarthritis.Nat Commun2021
31591642Soft windowing application to improve analysis of high-throughput phenotyping data.Bioinformatics2020
31844327High-throughput phenotyping reveals expansive genetic and structural underpinnings of immune variation.Nat Immunol2020
33370286Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.PLoS Genet2020
32938729T Cells from NOD-<i>PerIg</i> Mice Target Both Pancreatic and Neuronal Tissue.J Immunol2020
32955381Machine learning-based automated phenotyping of inflammatory nocifensive behavior in mice.Mol Pain2020
32542000The occurrence of tarsal injuries in male mice of C57BL/6N substrains in multiple international mouse facilities.PLoS One2020
30659012Large-scale discovery of mouse transgenic integration sites reveals frequent structural variation and insertional mutagenesis.Genome Res2019
31243271Common and distinct transcriptional signatures of mammalian embryonic lethality.Nat Commun2019
31371714Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis.Nat Commun2019
31331924The <i>Col4a2<sup>em1(IMPC)Wtsi</sup></i> mouse line: lessons from the Deciphering the Mechanisms of Developmental Disorders program.Biol Open2019
30840666FBXO7 sensitivity of phenotypic traits elucidated by a hypomorphic allele.PLoS One2019
30973865Mouse screen reveals multiple new genes underlying mouse and human hearing loss.PLoS Biol2019
30854487Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.Commun Biol2019
30937403Robust mouse tracking in complex environments using neural networks.Commun Biol2019
29348434Identification of genetic elements in metabolism by high-throughput mouse phenotyping.Nat Commun2018
30558275Visualising the Cardiovascular System of Embryos of Biomedical Model Organisms with High Resolution Episcopic Microscopy (HREM).J Cardiovasc Dev Dis2018
30275110A synthesis approach of mouse studies to identify genes and proteins in arterial thrombosis and bleeding.Blood2018
29539633Placentation defects are highly prevalent in embryonic lethal mouse mutants.Nature2018
29703891Targeting of NAT10 enhances healthspan in a mouse model of human accelerated aging syndrome.Nat Commun2018
27666489The AMP-activated protein kinase beta 1 subunit modulates erythrocyte integrity.Exp Hematol2017
29026089A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.Nat Commun2017
29144450Corrigendum: High-throughput discovery of novel developmental phenotypes.Nature2017
29019987Establishment of mouse expanded potential stem cells.Nature2017
28650954Prevalence of sexual dimorphism in mammalian phenotypic traits.Nat Commun2017
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
28869591Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.Nat Genet2017
27932544Improving the Identification of Phenotypic Abnormalities and Sexual Dimorphism in Mice When Studying Rare Event Categorical Characteristics.Genetics2017
26865945Reporting phenotypes in mouse models when considering body size as a potential confounder.J Biomed Semantics2016
26604141Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration.Hum Mol Genet2016
27626380High-throughput discovery of novel developmental phenotypes.Nature2016
27383011S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse.Sci Rep2016
26881968Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing.EMBO Mol Med2016
25281652Right Ventricular Epicardial Fibrosis in Mice With Sternal Segment Dislocation.Vet Pathol2015
28843321Corrigendum to "Disruption of the potassium channel regulatory subunit KCNE2 causes iron-deficient anemia" [Experimental Hematology, Vol. 42, Issue 12, p1053-1058.e1].Exp Hematol2015
26398943A gene expression resource generated by genome-wide lacZ profiling in the mouse.Dis Model Mech2015
26214591Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.Nat Genet2015
25992600Applying the ARRIVE Guidelines to an In Vivo Database.PLoS Biol2015
25736793Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunction.Invest Ophthalmol Vis Sci2015
25526730MacroH2A1 isoforms are associated with epigenetic markers for activation of lipogenic genes in fat-induced steatosis.FASEB J2015
24652767Histopathology reveals correlative and unique phenotypes in a high-throughput mouse phenotyping screen.Dis Model Mech2014
25343444Impact of temporal variation on design and analysis of mouse knockout phenotyping studies.PLoS One2014
25340873Identification of genes important for cutaneous function revealed by a large scale reverse genetic screen in the mouse.PLoS Genet2014
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Collaborators

David J Adams
Wellcome Sanger Institute
Co-authored papers 34
Natasha A Karp
Wellcome Sanger Institute
Co-authored papers 23
Martin Hrab?? de Angelis
German Center for Diabetes Research (DZD e.V.)
Co-authored papers 17
Ann-Marie Mallon
The Turing Institute
Co-authored papers 16
Steve D M Brown
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 16
Sara Wells
Mary Lyon Centre at Medical Research Council
Co-authored papers 15
Colin McKerlie
The Hospital for Sick Children
Co-authored papers 14
Yann Herault
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers 14
Helen Parkinson
European Bioinformatics Institute
Co-authored papers 13
Jenefer M Blackwell
Co-authored papers 13
Ann M Flenniken
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers 13
Terrence F Meehan
European Bioinformatics Institute
Co-authored papers 12
Robert E Braun
University of Maine
Co-authored papers 12
Jeremy Mason
European Molecular Biology Laboratory - European Bioinformatics Institute
Co-authored papers 12
Kent C Lloyd
University of California davis
Co-authored papers 12
Anne M Dickinson
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 11
John R Seavitt
Baylor College of Medicine
Co-authored papers 11
Lauryl M J Nutter
The Hospital for Sick Children
Co-authored papers 10
Valerie Gailus-Durner
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers 10
Stephen A Murray
Columbia University.
Co-authored papers 10
Glauco P Tocchini-Valentini
Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
Co-authored papers 10
Karen L Svenson
Co-authored papers 10
Wolfgang Wurst
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 9
Damian Smedley
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 9
Tania Sorg
Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
Co-authored papers 9
Lynette Bower
University of California davis
Co-authored papers 8
Luis Santos
The Turing Institute
Co-authored papers 8
Paul Flicek
European Bioinformatics Institute
Co-authored papers 8
Helmut Fuchs
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers 8
Simon Greenaway
Harwell Institute
Co-authored papers 7
Release 1.2