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Author Details

Kent C Lloyd
University of California davis
1985
165
43
PMIDPaper TitleJournal TitlePublished Year
37294348Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.Mamm Genome2023
37623890Sexual Dimorphism of the Mouse Plasma Metabolome Is Associated with Phenotypes of 30 Gene Knockout Lines.Metabolites2023
37301944Whole genome analysis for 163 gRNAs in Cas9-edited mice reveals minimal off-target activity.Commun Biol2023
37294348Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.Mamm Genome2023
37081156Topologically associating domain boundaries are required for normal genome function.Commun Biol2023
37623890Sexual Dimorphism of the Mouse Plasma Metabolome Is Associated with Phenotypes of 30 Gene Knockout Lines.Metabolites2023
37081156Topologically associating domain boundaries are required for normal genome function.Commun Biol2023
37301944Whole genome analysis for 163 gRNAs in Cas9-edited mice reveals minimal off-target activity.Commun Biol2023
34313795The Mutant Mouse Resource and Research Center (MMRRC): the NIH-supported National Public Repository and Distribution Archive of Mutant Mouse Models in the USA.Mamm Genome2022
36125045Promoting validation and cross-phylogenetic integration in model organism research.Dis Model Mech2022
36044375Animal models for studies of HIV-1 brain reservoirs.J Leukoc Biol2022
35758026Arap1 loss causes retinal pigment epithelium phagocytic dysfunction and subsequent photoreceptor death.Dis Model Mech2022
35705716The GA4GH Phenopacket schema defines a computable representation of clinical data.Nat Biotechnol2022
35552317Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.Pain2022
35482014A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder.Genet Med2022
34313795The Mutant Mouse Resource and Research Center (MMRRC): the NIH-supported National Public Repository and Distribution Archive of Mutant Mouse Models in the USA.Mamm Genome2022
35482014A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder.Genet Med2022
35705716The GA4GH Phenopacket schema defines a computable representation of clinical data.Nat Biotechnol2022
35758026Arap1 loss causes retinal pigment epithelium phagocytic dysfunction and subsequent photoreceptor death.Dis Model Mech2022
35552317Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.Pain2022
36044375Animal models for studies of HIV-1 brain reservoirs.J Leukoc Biol2022
36125045Promoting validation and cross-phylogenetic integration in model organism research.Dis Model Mech2022
33420346Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay.Genet Med2021
33420346Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay.Genet Med2021
33402233Injection Reactions after Administration of Sustained-release Meloxicam to BALB/cJ, C57BL/6J, and Crl:CD1(ICR) Mice.J Am Assoc Lab Anim Sci2021
34654818A metabolome atlas of the aging mouse brain.Nat Commun2021
34532411Retinal degeneration in mice and humans with neuronal ceroid lipofuscinosis type 8.Ann Transl Med2021
34112927Supplier-origin mouse microbiomes significantly influence locomotor and anxiety-related behavior, body morphology, and metabolism.Commun Biol2021
34050187Proteotyping of knockout mouse strains reveals sex- and strain-specific signatures in blood plasma.NPJ Syst Biol Appl2021
33969705On the potential role of globins in brown adipose tissue: a novel conceptual model and studies in myoglobin knockout mice.Am J Physiol Endocrinol Metab2021
33969704Metabolic physiology and skeletal muscle phenotypes in male and female myoglobin knockout mice.Am J Physiol Endocrinol Metab2021
33827648Response to correspondence on "Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation".Genome Biol2021
33827648Response to correspondence on "Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation".Genome Biol2021
34654818A metabolome atlas of the aging mouse brain.Nat Commun2021
34532411Retinal degeneration in mice and humans with neuronal ceroid lipofuscinosis type 8.Ann Transl Med2021
33969705On the potential role of globins in brown adipose tissue: a novel conceptual model and studies in myoglobin knockout mice.Am J Physiol Endocrinol Metab2021
33969704Metabolic physiology and skeletal muscle phenotypes in male and female myoglobin knockout mice.Am J Physiol Endocrinol Metab2021
34112927Supplier-origin mouse microbiomes significantly influence locomotor and anxiety-related behavior, body morphology, and metabolism.Commun Biol2021
34050187Proteotyping of knockout mouse strains reveals sex- and strain-specific signatures in blood plasma.NPJ Syst Biol Appl2021
33402233Injection Reactions after Administration of Sustained-release Meloxicam to BALB/cJ, C57BL/6J, and Crl:CD1(ICR) Mice.J Am Assoc Lab Anim Sci2021
31591642Soft windowing application to improve analysis of high-throughput phenotyping data.Bioinformatics2020
33370286Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.PLoS Genet2020
32928340Injection-site Reactions to Sustained-release Meloxicam in Sprague-Dawley Rats.J Am Assoc Lab Anim Sci2020
32893996Generation of desminopathy in rats using CRISPR-Cas9.J Cachexia Sarcopenia Muscle2020
32123279DNA fragmentation index (DFI) as a measure of sperm quality and fertility in mice.Sci Rep2020
32014086Hypoglycemia after Bariatric Surgery in Mice and Optimal Dosage and Efficacy of Glucose Supplementation.Comp Med2020
31929527High-throughput discovery of genetic determinants of circadian misalignment.PLoS Genet2020
31634437Cytoglobin deficiency potentiates Crb1-mediated retinal degeneration in rd8 mice.Dev Biol2020
31591642Soft windowing application to improve analysis of high-throughput phenotyping data.Bioinformatics2020
31929527High-throughput discovery of genetic determinants of circadian misalignment.PLoS Genet2020
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Collaborators

Colin McKerlie
The Hospital for Sick Children
Co-authored papers 20
Ann M Flenniken
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers 17
Lauryl M J Nutter
The Hospital for Sick Children
Co-authored papers 16
Ann-Marie Mallon
The Turing Institute
Co-authored papers 15
Martin Hrab?? de Angelis
German Center for Diabetes Research (DZD e.V.)
Co-authored papers 15
Helen Parkinson
European Bioinformatics Institute
Co-authored papers 15
Terrence F Meehan
European Bioinformatics Institute
Co-authored papers 14
Yann Herault
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers 14
Lynette Bower
University of California davis
Co-authored papers 14
Steve D M Brown
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 14
Jeremy Mason
European Molecular Biology Laboratory - European Bioinformatics Institute
Co-authored papers 13
Jacqueline K White
Wellcome Trust Sanger Institute
Co-authored papers 12
John R Seavitt
Baylor College of Medicine
Co-authored papers 12
Anne M Dickinson
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 12
Stephen A Murray
Columbia University.
Co-authored papers 12
David B West
Children's Hospital Oakland Research Institute
Co-authored papers 12
Sara Wells
Mary Lyon Centre at Medical Research Council
Co-authored papers 11
Wolfgang Wurst
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 10
Mark Moore
Co-authored papers 10
Robert E Braun
University of Maine
Co-authored papers 10
Karen L Svenson
Co-authored papers 10
Damian Smedley
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 10
Glauco P Tocchini-Valentini
Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
Co-authored papers 9
Ala Moshiri
Co-authored papers 9
Paul Flicek
European Bioinformatics Institute
Co-authored papers 9
Je Kyung Seong
Seoul National University
Co-authored papers 9
William C Skarnes
Wellcome Trust Sanger Institute
Co-authored papers 8
Allan Bradley
The Wellcome Trust Sanger Institute
Co-authored papers 8
Arthur L Beaudet
Baylor College of Medicine
Co-authored papers 8
Tania Sorg
Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
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Release 1.2