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Author Details
Full Name
Monica J Justice
Affiliation
The Hospital for Sick Children
ORCID
Career Start Year
1986
Papers
180
H Index
52
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37171606
A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects.
Hum Mol Genet
2023
35501690
Chromosomal localization of cohesin is differentially regulated by WIZ, WAPL, and G9a.
BMC Genomics
2022
34230964
Aberrant lung lipids cause respiratory impairment in a Mecp2-deficient mouse model of Rett syndrome.
Hum Mol Genet
2021
33760811
A cohesin cancer mutation reveals a role for the hinge domain in genome organization and gene expression.
PLoS Genet
2021
33735100
From its roots come branches and growth for Disease Models & Mechanisms.
Dis Model Mech
2021
33887117
CyTOF: An Emerging Technology for Single-Cell Proteomics in the Mouse.
Curr Protoc
2021
34464976
A new murine Rpl5 (uL18) mutation provides a unique model of variably penetrant Diamond-Blackfan anemia.
Blood Adv
2021
34515289
Developmental disorders Journal Meeting: a collaboration between Development and Disease Models & Mechanisms.
Dis Model Mech
2021
32317254
Suppressor mutations in <i>Mecp2</i>-null mice implicate the DNA damage response in Rett syndrome pathology.
Genome Res
2020
31836582
From blood development to disease: a paradigm for clinical translation.
Dis Model Mech
2020
32016392
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.
Hum Mol Genet
2020
32778134
Distinct and overlapping roles of STAG1 and STAG2 in cohesin localization and gene expression in embryonic stem cells.
Epigenetics Chromatin
2020
32541798
Rab11b-mediated integrin recycling promotes brain metastatic adaptation and outgrowth.
Nat Commun
2020
32294452
A WIZ/Cohesin/CTCF Complex Anchors DNA Loops to Define Gene Expression and Cell Identity.
Cell Rep
2020
30819728
From gene to treatment: supporting rare disease translational research through model systems.
Dis Model Mech
2019
33523198
Model systems inform rare disease diagnosis, therapeutic discovery and pre-clinical efficacy.
Emerg Top Life Sci
2019
31530540
Failure to identify modifiers of <i>NEBULIN</i>-related nemaline myopathy in two pre-clinical models of the disease.
Biol Open
2019
31130394
Off to a Bad Start: Cancer Initiation by Pluripotency Regulator PRDM14.
Trends Genet
2019
31015254
The Pluripotency Regulator PRDM14 Requires Hematopoietic Regulator CBFA2T3 to Initiate Leukemia in Mice.
Mol Cancer Res
2019
30923050
DMM Prize 2018 winner: Wenqing Zhou.
Dis Model Mech
2019
30854487
Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.
Commun Biol
2019
30820643
Treating Rett syndrome: from mouse models to human therapies.
Mamm Genome
2019
29445033
Rett syndrome: a neurological disorder with metabolic components.
Open Biol
2018
30157441
Rapid and Integrative Discovery of Retina Regulatory Molecules.
Cell Rep
2018
28774900
UBE2O remodels the proteome during terminal erythroid differentiation.
Science
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
28650483
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.
Nat Genet
2017
28670438
Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes.
Mol Autism
2017
26839397
Using the mouse to model human disease: increasing validity and reproducibility.
Dis Model Mech
2016
27638768
Lethal lung hypoplasia and vascular defects in mice with conditional Foxf1 overexpression.
Biol Open
2016
27626380
High-throughput discovery of novel developmental phenotypes.
Nature
2016
27288453
MeCP2 co-ordinates liver lipid metabolism with the NCoR1/HDAC3 corepressor complex.
Hum Mol Genet
2016
27106930
PRDM14 promotes RAG-dependent Notch1 driver mutations in mouse T-ALL.
Biol Open
2016
26069083
Tissue-Specific Regulation of Oncogene Expression Using Cre-Inducible ROSA26 Knock-In Transgenic Mice.
Curr Protoc Mouse Biol
2015
24203697
Novel mutations in Lrp6 orthologs in mouse and human neural tube defects affect a highly dosage-sensitive Wnt non-canonical planar cell polarity pathway.
Hum Mol Genet
2014
24722050
Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout mice.
PLoS One
2014
23300183
Identification and characterization of a novel murine allele of Tmprss6.
Haematologica
2013
26069093
Evaluation of Rett Syndrome Symptom Improvement by Metabolic Modulators in Mecp2-Mutant Mice.
Curr Protoc Mouse Biol
2013
25506514
A protocol for evaluation of Rett Syndrome symptom improvement by metabolic modulators in <i>Mecp2</i>-mutant mice.
Curr Protoc Mouse Biol
2013
25003017
A role for metabolism in Rett syndrome pathogenesis: New clinical findings and potential treatment targets.
Rare Dis
2013
24303013
A point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus).
PLoS One
2013
24046360
A mouse model for inducible overexpression of Prdm14 results in rapid-onset and highly penetrant T-cell acute lymphoblastic leukemia (T-ALL).
Dis Model Mech
2013
23828642
Of mice and men, and medicine: an interview with Monica Justice.
Dis Model Mech
2013
23892605
A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome.
Nat Genet
2013
23616075
Bridging the gap between basic and applied biology: towards preclinical translation.
Dis Model Mech
2013
23810381
TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.
Am J Hum Genet
2013
23451234
An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.
PLoS One
2013
23521771
Mouse Tenm4 is required for mesoderm induction.
BMC Dev Biol
2013
1 - 50 of 180
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