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Author Details

Matthew R G Taylor
Cardiovascular Institute, University of Colorado
2001
158
46
PMIDPaper TitleJournal TitlePublished Year
37788487Genetics of Dilated Cardiomyopathy.Annu Rev Med2024
36515663Efficacy and Safety of ARRY-371797 in <i>LMNA</i>-Related Dilated Cardiomyopathy: A Phase 2 Study.Circ Genom Precis Med2023
37593875Risks of Ventricular Arrhythmia and Heart Failure in Carriers of <i>RBM20</i> Variants.Circ Genom Precis Med2023
37936669Innate immune signaling in hearts and buccal mucosa cells of patients with arrhythmogenic cardiomyopathy.Heart Rhythm O22023
37639473Emery-Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure.Eur Heart J2023
37672268Cardiac Remodeling in Subclinical Hypertrophic Cardiomyopathy: The VANISH Randomized Clinical Trial.JAMA Cardiol2023
37418234A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients.J Cardiovasc Transl Res2023
37010012Long-term effectiveness of ARRY-371797 in people with dilated cardiomyopathy and a faulty LMNA gene: a plain language summary.Future Cardiol2023
36999957Transforming Growth Factor-β Analysis of the VANISH Trial Cohort.Circ Heart Fail2023
37164047Multicenter clinical and functional evidence reclassifies a recurrent noncanonical filamin C splice-altering variant.Heart Rhythm2023
36718638Plain Language Summary of Publication of the safety and efficacy of ARRY-371797 in people with dilated cardiomyopathy and a faulty <i>LMNA</i> gene.Future Cardiol2023
34304293Microfabricated cantilevers for parallelized cell-cell adhesion measurements.Eur Biophys J2022
36396199Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies.J Am Coll Cardiol2022
36420863Cellular Biomechanic Impairment in Cardiomyocytes Carrying the Progeria Mutation: An Atomic Force Microscopy Investigation.Langmuir2022
35980659Hidden Risk: Arrhythmogenic Genes in the General Population.Circ Genom Precis Med2022
36114020Long-Term Efficacy and Safety of ARRY-371797 (PF-07265803) in Patients With Lamin A/C-Related Dilated Cardiomyopathy.Am J Cardiol2022
35073209Nrf2 signaling in heart failure: expression of Nrf2, Keap1, antioxidant, and detoxification genes in dilated or ischemic cardiomyopathy.Physiol Genomics2022
35138330Association of Titin Variations With Late-Onset Dilated Cardiomyopathy.JAMA Cardiol2022
35196083Activation of PDGFRA signaling contributes to filamin C-related arrhythmogenic cardiomyopathy.Sci Adv2022
35229420The response to cardiac resynchronization therapy in LMNA cardiomyopathy.Eur J Heart Fail2022
34775111Cardiac Transplantation in Danon Disease.J Card Fail2022
34652067An LMNA synonymous variant associated with severe dilated cardiomyopathy: Case report.Am J Med Genet A2022
32951257Research participant understanding and engagement in an institutional, self-consent biobank model.J Genet Couns2021
33769382Genetics of dilated cardiomyopathy.Curr Opin Cardiol2021
33816656Parkinsonism and Positive Dopamine Transporter Imaging in a Patient with a Novel KMT2B Variant.Mov Disord Clin Pract2021
33636116Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy.Stem Cell Reports2021
33526513Induction of ADAM10 by Radiation Therapy Drives Fibrosis, Resistance, and Epithelial-to-Mesenchyal Transition in Pancreatic Cancer.Cancer Res2021
34970070Clinical and genetic features of arrhythmogenic cardiomyopathy: diagnosis, management and the heart failure perspective.Prog Pediatr Cardiol2021
34502098Compromised Biomechanical Properties, Cell-Cell Adhesion and Nanotubes Communication in Cardiac Fibroblasts Carrying the Lamin A/C D192G Mutation.Int J Mol Sci2021
34383712Serum circulating proteins from pediatric patients with dilated cardiomyopathy cause pathologic remodeling and cardiomyocyte stiffness.JCI Insight2021
34587765Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.Circulation2021
34408292Correction to: The genetic architecture of Plakophilin 2 cardiomyopathy.Genet Med2021
34572260Mechanisms and Insights for the Development of Heart Failure Associated with Cancer Therapy.Children (Basel)2021
34845930Myocardial Strain and Association With Clinical Outcomes in Danon Disease: A Model for Monitoring Progression of Genetic Cardiomyopathies.J Am Heart Assoc2021
34716744Mortality risk in chronic Chagas cardiomyopathy: a systematic review and meta-analysis.ESC Heart Fail2021
33941882The 2019 US medical genetics workforce: a focus on clinical genetics.Genet Med2021
34216016ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder.Clin Genet2021
34072787Experiences with Diagnosis and Treatment of Chagas Disease at a United States Teaching Hospital-Clinical Features of Patients with Positive Screening Serologic Testing.Trop Med Infect Dis2021
34269900The Sarcomeric Spring Protein Titin: Biophysical Properties, Molecular Mechanisms, and Genetic Mutations Associated with Heart Failure and Cardiomyopathy.Curr Cardiol Rep2021
34208743Whole Exome Sequencing of 23 Multigeneration Idiopathic Scoliosis Families Reveals Enrichments in Cytoskeletal Variants, Suggests Highly Polygenic Disease.Genes (Basel)2021
34120153The genetic architecture of Plakophilin 2 cardiomyopathy.Genet Med2021
33162390Precision medicine in laminopathies: insights from the REDLAMINA registry.Rev Esp Cardiol (Engl Ed)2021
33382518Mutations in KIF7 implicated in idiopathic scoliosis in humans and axial curvatures in zebrafish.Hum Mutat2021
31488898Regional models of genetic services in the United States.Genet Med2020
32083564Viscoelastic behavior of cardiomyocytes carrying LMNA mutations.Biorheology2020
32021920Altered microtubule structure, hemichannel localization and beating activity in cardiomyocytes expressing pathologic nuclear lamin A/C.Heliyon2020
31958463Transcriptome signature of ventricular arrhythmia in dilated cardiomyopathy reveals increased fibrosis and activated TP53.J Mol Cell Cardiol2020
31924696<i>FLNC</i> truncations cause arrhythmogenic right ventricular cardiomyopathy.J Med Genet2020
32634495Understanding the role of titin in dilated cardiomyopathy.Int J Cardiol2020
32859027Modifications of Titin Contribute to the Progression of Cardiomyopathy and Represent a Therapeutic Target for Treatment of Heart Failure.J Clin Med2020
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Collaborators

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Cardiovascular Institute, University of Colorado Denver Anschutz Medical Campus
Co-authored papers 10
Stanford University
Co-authored papers 7
Stanford University School of Medicine
Co-authored papers 7
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Co-authored papers 6
Johns Hopkins University
Co-authored papers 6
Harvard Medical School and Cardiovascular Division, Brigham and Women's Hospital
Co-authored papers 6
University of Washington
Co-authored papers 5
Brigham and Women's Hospital (Y.K.
Co-authored papers 5
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Co-authored papers 5
University of Tennessee Health Science Center
Co-authored papers 5
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University of Tennessee Health Sciences Centre
Co-authored papers 4
Boston Children's Hospital, Harvard Medical School
Co-authored papers 4
Partners Healthcare Center for Personalized Genetic Medicine
Co-authored papers 3
Invitae Corporation
Co-authored papers 3
UCL Great Ormond Street Institute of Child Health
Co-authored papers 2
Co-authored papers 2
Mayo Clinic, Windland Smith Rice Genetic Heart Rhythm Clinic)
Co-authored papers 2
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Center for Inherited Cardiovascular Disease, Stanford University School of Medicine
Co-authored papers 2
University of Colorado
Co-authored papers 2
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Johns Hopkins McKusick-Nathans Department of Genetic Medicine
Co-authored papers 2
University of Colorado
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University of Colorado Denver at Anschutz Medical Campus
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University of Colorado
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Guys and St Thomas' NHS Trust
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