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Author Details

Monica J Justice
The Hospital for Sick Children
1986
180
52
PMIDPaper TitleJournal TitlePublished Year
37171606A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects.Hum Mol Genet2023
35501690Chromosomal localization of cohesin is differentially regulated by WIZ, WAPL, and G9a.BMC Genomics2022
34230964Aberrant lung lipids cause respiratory impairment in a Mecp2-deficient mouse model of Rett syndrome.Hum Mol Genet2021
33760811A cohesin cancer mutation reveals a role for the hinge domain in genome organization and gene expression.PLoS Genet2021
33735100From its roots come branches and growth for Disease Models & Mechanisms.Dis Model Mech2021
33887117CyTOF: An Emerging Technology for Single-Cell Proteomics in the Mouse.Curr Protoc2021
34464976A new murine Rpl5 (uL18) mutation provides a unique model of variably penetrant Diamond-Blackfan anemia.Blood Adv2021
34515289Developmental disorders Journal Meeting: a collaboration between Development and Disease Models & Mechanisms.Dis Model Mech2021
32317254Suppressor mutations in <i>Mecp2</i>-null mice implicate the DNA damage response in Rett syndrome pathology.Genome Res2020
31836582From blood development to disease: a paradigm for clinical translation.Dis Model Mech2020
32016392Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.Hum Mol Genet2020
32778134Distinct and overlapping roles of STAG1 and STAG2 in cohesin localization and gene expression in embryonic stem cells.Epigenetics Chromatin2020
32541798Rab11b-mediated integrin recycling promotes brain metastatic adaptation and outgrowth.Nat Commun2020
32294452A WIZ/Cohesin/CTCF Complex Anchors DNA Loops to Define Gene Expression and Cell Identity.Cell Rep2020
30819728From gene to treatment: supporting rare disease translational research through model systems.Dis Model Mech2019
33523198Model systems inform rare disease diagnosis, therapeutic discovery and pre-clinical efficacy.Emerg Top Life Sci2019
31530540Failure to identify modifiers of <i>NEBULIN</i>-related nemaline myopathy in two pre-clinical models of the disease.Biol Open2019
31130394Off to a Bad Start: Cancer Initiation by Pluripotency Regulator PRDM14.Trends Genet2019
31015254The Pluripotency Regulator PRDM14 Requires Hematopoietic Regulator CBFA2T3 to Initiate Leukemia in Mice.Mol Cancer Res2019
30923050DMM Prize 2018 winner: Wenqing Zhou.Dis Model Mech2019
30854487Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.Commun Biol2019
30820643Treating Rett syndrome: from mouse models to human therapies.Mamm Genome2019
29445033Rett syndrome: a neurological disorder with metabolic components.Open Biol2018
30157441Rapid and Integrative Discovery of Retina Regulatory Molecules.Cell Rep2018
28774900UBE2O remodels the proteome during terminal erythroid differentiation.Science2017
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
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
28670438Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes.Mol Autism2017
26839397Using the mouse to model human disease: increasing validity and reproducibility.Dis Model Mech2016
27638768Lethal lung hypoplasia and vascular defects in mice with conditional Foxf1 overexpression.Biol Open2016
27626380High-throughput discovery of novel developmental phenotypes.Nature2016
27288453MeCP2 co-ordinates liver lipid metabolism with the NCoR1/HDAC3 corepressor complex.Hum Mol Genet2016
27106930PRDM14 promotes RAG-dependent Notch1 driver mutations in mouse T-ALL.Biol Open2016
26069083Tissue-Specific Regulation of Oncogene Expression Using Cre-Inducible ROSA26 Knock-In Transgenic Mice.Curr Protoc Mouse Biol2015
24203697Novel 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 Genet2014
24722050Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout mice.PLoS One2014
23300183Identification and characterization of a novel murine allele of Tmprss6.Haematologica2013
26069093Evaluation of Rett Syndrome Symptom Improvement by Metabolic Modulators in Mecp2-Mutant Mice.Curr Protoc Mouse Biol2013
25506514A protocol for evaluation of Rett Syndrome symptom improvement by metabolic modulators in <i>Mecp2</i>-mutant mice.Curr Protoc Mouse Biol2013
25003017A role for metabolism in Rett syndrome pathogenesis: New clinical findings and potential treatment targets.Rare Dis2013
24303013A point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus).PLoS One2013
24046360A mouse model for inducible overexpression of Prdm14 results in rapid-onset and highly penetrant T-cell acute lymphoblastic leukemia (T-ALL).Dis Model Mech2013
23828642Of mice and men, and medicine: an interview with Monica Justice.Dis Model Mech2013
23892605A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome.Nat Genet2013
23616075Bridging the gap between basic and applied biology: towards preclinical translation.Dis Model Mech2013
23810381TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.Am J Hum Genet2013
23451234An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.PLoS One2013
23521771Mouse Tenm4 is required for mesoderm induction.BMC Dev Biol2013
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Collaborators

The Wellcome Trust Sanger Institute
Co-authored papers 12
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 11
Baylor College of Medicine
Co-authored papers 9
German Center for Diabetes Research (DZD e.V.)
Co-authored papers 8
Co-authored papers 7
Baylor College of Medicine
Co-authored papers 7
Baylor College of Medicine
Co-authored papers 7
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 7
Columbia University.
Co-authored papers 7
Wellcome Trust Sanger Institute
Co-authored papers 6
Nanjing Biomedical Research Institute, Nanjing University
Co-authored papers 6
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers 6
Wellcome Sanger Institute
Co-authored papers 6
Mary Lyon Centre at Medical Research Council
Co-authored papers 6
University of Maine
Co-authored papers 6
University of California davis
Co-authored papers 6
The Hospital for Sick Children
Co-authored papers 6
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers 6
European Bioinformatics Institute
Co-authored papers 6
Children's Hospital Oakland Research Institute
Co-authored papers 6
The Turing Institute
Co-authored papers 6
European Molecular Biology Laboratory - European Bioinformatics Institute
Co-authored papers 6
University of California davis
Co-authored papers 6
European Bioinformatics Institute
Co-authored papers 6
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 5
University of Virginia School of Medicine
Co-authored papers 5
Co-authored papers 5
European Bioinformatics Institute
Co-authored papers 5
Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
Co-authored papers 5
Wellcome Trust Sanger Institute
Co-authored papers 5