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Author Details
Full Name
Lauryl M J Nutter
Affiliation
The Hospital for Sick Children
ORCID
Career Start Year
2006
Papers
38
H Index
16
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36995664
Genetic and Molecular Quality Control of Genetically Engineered Mice.
Methods Mol Biol
2023
37628590
The <i>ATP6V1B2</i> DDOD/DOORS-Associated p.Arg506* Variant Causes Hyperactivity and Seizures in Mice.
Genes (Basel)
2023
37623890
Sexual Dimorphism of the Mouse Plasma Metabolome Is Associated with Phenotypes of 30 Gene Knockout Lines.
Metabolites
2023
37301944
Whole genome analysis for 163 gRNAs in Cas9-edited mice reveals minimal off-target activity.
Commun Biol
2023
37294348
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.
Mamm Genome
2023
34536110
Importing genetically altered animals: ensuring quality.
Mamm Genome
2022
35552317
Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.
Pain
2022
35445787
Genetic mouse models of autism spectrum disorder present subtle heterogenous cardiac abnormalities.
Autism Res
2022
35245675
Multiple-mouse magnetic resonance imaging with cryogenic radiofrequency probes for evaluation of brain development.
Neuroimage
2022
33151080
Process and Workflow for Preparation of Disparate Mouse Tissues for Proteomic Analysis.
J Proteome Res
2021
33757588
Neuroanatomy and behavior in mice with a haploinsufficiency of AT-rich interactive domain 1B (ARID1B) throughout development.
Mol Autism
2021
34050187
Proteotyping of knockout mouse strains reveals sex- and strain-specific signatures in blood plasma.
NPJ Syst Biol Appl
2021
31512207
Targeted Mutations in the Mouse via Embryonic Stem Cells.
Methods Mol Biol
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
32341096
Structural Variant in Mitochondrial-Associated Gene (MRPL3) Induces Adult-Onset Neurodegeneration with Memory Impairment in the Mouse.
J Neurosci
2020
32554600
Electrophysiological Alterations of Pyramidal Cells and Interneurons of the CA1 Region of the Hippocampus in a Novel Mouse Model of Dravet Syndrome.
Genetics
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
30737279
A novel isoform of myosin 18A (Myo18Aγ) is an essential sarcomeric protein in mouse heart.
J Biol Chem
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
30040228
Engineering Point Mutant and Epitope-Tagged Alleles in Mice Using Cas9 RNA-Guided Nuclease.
Curr Protoc Mouse Biol
2018
29600991
Response to "Unexpected mutations after CRISPR-Cas9 editing in vivo".
Nat Methods
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
27626380
High-throughput discovery of novel developmental phenotypes.
Nature
2016
26214591
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.
Nat Genet
2015
24888589
MuLV-related endogenous retroviral elements and Flt3 participate in aberrant end-joining events that promote B-cell leukemogenesis.
Genes Dev
2014
24828076
Therapeutic potential of spleen tyrosine kinase inhibition for treating high-risk precursor B cell acute lymphoblastic leukemia.
Sci Transl Med
2014
22968824
The mammalian gene function resource: the International Knockout Mouse Consortium.
Mamm Genome
2012
21527721
Engineering the embryo.
Proc Natl Acad Sci U S A
2011
20582321
Efficient generation of germ line transmitting chimeras from C57BL/6N ES cells by aggregation with outbred host embryos.
PLoS One
2010
19245749
Sperm freezing and in vitro fertilization in three substrains of C57BL/6 mice.
J Am Assoc Lab Anim Sci
2009
17077325
ATM deficiency disrupts Tcra locus integrity and the maturation of CD4+CD8+ thymocytes.
Blood
2007
17785508
Chromosomal reinsertion of broken RSS ends during T cell development.
J Exp Med
2007
16687486
p53-Independent apoptosis disrupts early organogenesis in embryos lacking both ataxia-telangiectasia mutated and Prkdc.
Mol Cancer Res
2006
1 - 38 of 38
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Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
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17
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Jacqueline K White
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Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
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10
Stephen A Murray
Columbia University.
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Anne M Dickinson
Translational and Clinical Research Institute, Newcastle University
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Helen Parkinson
European Bioinformatics Institute
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Terrence F Meehan
European Bioinformatics Institute
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Robert E Braun
University of Maine
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Jeremy Mason
European Molecular Biology Laboratory - European Bioinformatics Institute
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Wolfgang Wurst
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Luis Santos
The Turing Institute
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Mark Moore
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