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Author Details
Full Name
Colin McKerlie
Affiliation
The Hospital for Sick Children
ORCID
Career Start Year
1996
Papers
95
H Index
39
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37294348
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.
Mamm Genome
2023
37623890
Sexual Dimorphism of the Mouse Plasma Metabolome Is Associated with Phenotypes of 30 Gene Knockout Lines.
Metabolites
2023
37421464
Bridging mouse and human anatomies; a knowledge-based approach to comparative anatomy for disease model phenotyping.
Mamm Genome
2023
34328547
INFRAFRONTIER quality principles in systemic phenotyping.
Mamm Genome
2022
35552317
Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.
Pain
2022
36211391
(NZW ÿ BXSB) F1 male mice: An unusual, severe and fatal mouse model of lupus erythematosus.
Front Immunol
2022
33151080
Process and Workflow for Preparation of Disparate Mouse Tissues for Proteomic Analysis.
J Proteome Res
2021
34050187
Proteotyping of knockout mouse strains reveals sex- and strain-specific signatures in blood plasma.
NPJ Syst Biol Appl
2021
31591642
Soft windowing application to improve analysis of high-throughput phenotyping data.
Bioinformatics
2020
32088735
PATHBIO: an international training program for precision mouse phenotyping.
Mamm Genome
2020
31929527
High-throughput discovery of genetic determinants of circadian misalignment.
PLoS Genet
2020
33370286
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.
PLoS Genet
2020
33297935
Variant in NHLRC2 leads to increased hnRNP C2 in developing neurons and the hippocampus of a mouse model of FINCAÂ disease.
Mol Med
2020
32542000
The occurrence of tarsal injuries in male mice of C57BL/6N substrains in multiple international mouse facilities.
PLoS One
2020
30854487
Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.
Commun Biol
2019
31121816
A Comprehensive Plasma Metabolomics Dataset for a Cohort of Mouse Knockouts within the International Mouse Phenotyping Consortium.
Metabolites
2019
29348434
Identification of genetic elements in metabolism by high-throughput mouse phenotyping.
Nat Commun
2018
30100824
The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation.
Conserv Genet
2018
30195700
Comparison of cryosurvival and spermatogenesis efficiency of cryopreserved neonatal mouse testicular tissue between three vitrification protocols and controlled-rate freezing.
Cryobiology
2018
30476141
A Review of Current Standards and the Evolution of Histopathology Nomenclature for Laboratory Animals.
ILAR J
2018
28650483
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.
Nat Genet
2017
29026089
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.
Nat Commun
2017
29144450
Corrigendum: High-throughput discovery of novel developmental phenotypes.
Nature
2017
28650954
Prevalence of sexual dimorphism in mammalian phenotypic traits.
Nat Commun
2017
27626380
High-throughput discovery of novel developmental phenotypes.
Nature
2016
25281652
Right Ventricular Epicardial Fibrosis in Mice With Sternal Segment Dislocation.
Vet Pathol
2015
26659567
Comment on "One health, one literature: Weaving together veterinary and medical research".
Sci Transl Med
2015
26332574
Timp3 loss accelerates tumour invasion and increases prostate inflammation in a mouse model of prostate cancer.
Prostate
2015
26569406
The Bulk of Autotaxin Activity Is Dispensable for Adult Mouse Life.
PLoS One
2015
26206923
Precision medicine: Look to the mice.
Science
2015
26214591
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.
Nat Genet
2015
25656291
Human Fetal Testicular Tissue Xenotransplantation: A Platform to Study the Effect of Gonadotropins on Human Germ Cell Development In Utero.
J Urol
2015
24449892
TAp73 is required for spermatogenesis and the maintenance of male fertility.
Proc Natl Acad Sci U S A
2014
24652767
Histopathology reveals correlative and unique phenotypes in a high-throughput mouse phenotyping screen.
Dis Model Mech
2014
23721968
Effect of different cryoprotectant agents on spermatogenesis efficiency in cryopreserved and grafted neonatal mouse testicular tissue.
Cryobiology
2013
23874215
ENU-induced mutation in the DNA-binding domain of KLF3 reveals important roles for KLF3 in cardiovascular development and function in mice.
PLoS Genet
2013
24033988
The mouse pathology ontology, MPATH; structure and applications.
J Biomed Semantics
2013
23676500
Endothelin-2 deficiency causes growth retardation, hypothermia, and emphysema in mice.
J Clin Invest
2013
23043807
Structural and functional concepts in current mouse phenotyping and archiving facilities.
J Am Assoc Lab Anim Sci
2012
22968824
The mammalian gene function resource: the International Knockout Mouse Consortium.
Mamm Genome
2012
22945696
Centralized mouse repositories.
Mamm Genome
2012
21155978
Arrhythmia and sudden death associated with elevated cardiac chloride channel activity.
J Cell Mol Med
2011
21444746
Pathology of the laboratory mouse: an International Workshop on Challenges for High Throughput Phenotyping.
Toxicol Pathol
2011
20728931
Comparison of sperm quality and DNA integrity in mouse sperm exposed to various cooling velocities and osmotic stress.
Theriogenology
2010
19243221
Neto1 is a novel CUB-domain NMDA receptor-interacting protein required for synaptic plasticity and learning.
PLoS Biol
2009
19131991
PRIME importance of pathology expertise.
Nat Biotechnol
2009
19245749
Sperm freezing and in vitro fertilization in three substrains of C57BL/6 mice.
J Am Assoc Lab Anim Sci
2009
18079496
Negative-pressure ventilation: better oxygenation and less lung injury.
Am J Respir Crit Care Med
2008
18524829
In vivo potential effects of adenovirus type 5 E1A and E1B on lung carcinogenesis and lymphoproliferative inflammation.
J Virol
2008
18509356
Oncolytic virotherapy for multiple myeloma using a tumour-specific double-deleted vaccinia virus.
Leukemia
2008
1 - 50 of 95
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Collaborators
Ann M Flenniken
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers
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University of California davis
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20
Martin Hrab?? de Angelis
German Center for Diabetes Research (DZD e.V.)
Co-authored papers
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Lauryl M J Nutter
The Hospital for Sick Children
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The Turing Institute
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15
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Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers
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Steve D M Brown
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers
15
Jacqueline K White
Wellcome Trust Sanger Institute
Co-authored papers
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European Bioinformatics Institute
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Sara Wells
Mary Lyon Centre at Medical Research Council
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Terrence F Meehan
European Bioinformatics Institute
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12
Jeremy Mason
European Molecular Biology Laboratory - European Bioinformatics Institute
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11
John R Seavitt
Baylor College of Medicine
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Anne M Dickinson
Translational and Clinical Research Institute, Newcastle University
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11
Stephen A Murray
Columbia University.
Co-authored papers
11
Wolfgang Wurst
Institute of Developmental Genetics, German Research Center for Environmental Health
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10
Tania Sorg
Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
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9
Mark Moore
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University of Maine
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Glauco P Tocchini-Valentini
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