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Author Details

Luisa Mestroni
University of Colorado Anschutz Medical Campus
1983
215
52
PMIDPaper TitleJournal TitlePublished Year
37788487Genetics of Dilated Cardiomyopathy.Annu Rev Med2024
36281440Myocardial Injury and Altered Gene Expression Associated With SARS-CoV-2 Infection or mRNA Vaccination.JACC Basic Transl Sci2023
37593875Risks of Ventricular Arrhythmia and Heart Failure in Carriers of <i>RBM20</i> Variants.Circ Genom Precis Med2023
37800334Myocardial Recovery in Recent Onset Dilated Cardiomyopathy: Role of <i>CDCP1</i> and Cardiac Fibrosis.Circ Res2023
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
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
36515663Efficacy and Safety of ARRY-371797 in <i>LMNA</i>-Related Dilated Cardiomyopathy: A Phase 2 Study.Circ Genom Precis Med2023
36029423Neonatal rat ventricular myocytes interfacing conductive polymers and carbon nanotubes.Cell Biol Toxicol2023
34304293Microfabricated cantilevers for parallelized cell-cell adhesion measurements.Eur Biophys J2022
35409059Atomic Force Microscopy (AFM) Applications in Arrhythmogenic Cardiomyopathy.Int J Mol Sci2022
35569524Regulation of extracellular matrix composition by fibroblasts during perinatal cardiac maturation.J Mol Cell Cardiol2022
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
36109106Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy.J Am Coll Cardiol2022
36000547Sex differences in natural history of cardiovascular magnetic resonance- and biopsy-proven lymphocytic myocarditis.ESC Heart Fail2022
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
33551194Cardiac MR Imaging of Muscular Dystrophies.Curr Probl Diagn Radiol2022
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
34776072The Arrhythmic Phenotype in Cardiomyopathy.Heart Fail Clin2022
34652067An LMNA synonymous variant associated with severe dilated cardiomyopathy: Case report.Am J Med Genet A2022
33162390Precision medicine in laminopathies: insights from the REDLAMINA registry.Rev Esp Cardiol (Engl Ed)2021
33769382Genetics of dilated cardiomyopathy.Curr Opin Cardiol2021
33682427HDAC Inhibition Reverses Preexisting Diastolic Dysfunction and Blocks Covert Extracellular Matrix Remodeling.Circulation2021
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
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
34273475Prevalence and Evolution of Right Ventricular Dysfunction Among Different Genetic Backgrounds in Dilated Cardiomyopathy.Can J Cardiol2021
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
33961942Antiarrhythmic therapy and risk of cumulative ventricular arrhythmias in arrhythmogenic right ventricle cardiomyopathy.Int J Cardiol2021
34269900The Sarcomeric Spring Protein Titin: Biophysical Properties, Molecular Mechanisms, and Genetic Mutations Associated with Heart Failure and Cardiomyopathy.Curr Cardiol Rep2021
34120153The genetic architecture of Plakophilin 2 cardiomyopathy.Genet Med2021
32452075Contemporary survival trends and aetiological characterization in non-ischaemic dilated cardiomyopathy.Eur J Heart Fail2020
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
33171802Nanomaterials for Cardiac Tissue Engineering.Molecules2020
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Collaborators

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Co-authored papers 15
UCL Great Ormond Street Institute of Child Health
Co-authored papers 9
University of Tennessee Health Science Center
Co-authored papers 7
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Co-authored papers 7
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Co-authored papers 7
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University of Washington
Co-authored papers 5
Harvard Medical School and Cardiovascular Division, Brigham and Women's Hospital
Co-authored papers 5
Brigham and Women's Hospital (Y.K.
Co-authored papers 5
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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
Vanderbilt University Medical Center
Co-authored papers 3
Maastricht University Medical Centre
Co-authored papers 2
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Mayo Clinic, Windland Smith Rice Genetic Heart Rhythm Clinic)
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Center for Inherited Cardiovascular Disease, Stanford University School of Medicine
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University of Colorado
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Co-authored papers 1
Guys and St Thomas' NHS Trust
Co-authored papers 1
Earle A. Chiles Research Institute, Providence Cancer Institute
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University of Colorado
Co-authored papers 1