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Author Details
Full Name
Luisa Mestroni
Affiliation
University of Colorado Anschutz Medical Campus
ORCID
Career Start Year
1983
Papers
215
H Index
52
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37788487
Genetics of Dilated Cardiomyopathy.
Annu Rev Med
2024
36281440
Myocardial Injury and Altered Gene Expression Associated With SARS-CoV-2 Infection or mRNA Vaccination.
JACC Basic Transl Sci
2023
37593875
Risks of Ventricular Arrhythmia and Heart Failure in Carriers of <i>RBM20</i> Variants.
Circ Genom Precis Med
2023
37800334
Myocardial Recovery in Recent Onset Dilated Cardiomyopathy: Role of <i>CDCP1</i> and Cardiac Fibrosis.
Circ Res
2023
37936669
Innate immune signaling in hearts and buccal mucosa cells of patients with arrhythmogenic cardiomyopathy.
Heart Rhythm O2
2023
37639473
Emery-Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure.
Eur Heart J
2023
37672268
Cardiac Remodeling in Subclinical Hypertrophic Cardiomyopathy: The VANISH Randomized Clinical Trial.
JAMA Cardiol
2023
37418234
A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients.
J Cardiovasc Transl Res
2023
36999957
Transforming Growth Factor-β Analysis of the VANISH Trial Cohort.
Circ Heart Fail
2023
37164047
Multicenter clinical and functional evidence reclassifies a recurrent noncanonical filamin C splice-altering variant.
Heart Rhythm
2023
36718638
Plain 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 Cardiol
2023
36515663
Efficacy and Safety of ARRY-371797 in <i>LMNA</i>-Related Dilated Cardiomyopathy: A Phase 2 Study.
Circ Genom Precis Med
2023
36029423
Neonatal rat ventricular myocytes interfacing conductive polymers and carbon nanotubes.
Cell Biol Toxicol
2023
34304293
Microfabricated cantilevers for parallelized cell-cell adhesion measurements.
Eur Biophys J
2022
35409059
Atomic Force Microscopy (AFM) Applications in Arrhythmogenic Cardiomyopathy.
Int J Mol Sci
2022
35569524
Regulation of extracellular matrix composition by fibroblasts during perinatal cardiac maturation.
J Mol Cell Cardiol
2022
36396199
Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies.
J Am Coll Cardiol
2022
36420863
Cellular Biomechanic Impairment in Cardiomyocytes Carrying the Progeria Mutation: An Atomic Force Microscopy Investigation.
Langmuir
2022
36109106
Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy.
J Am Coll Cardiol
2022
36000547
Sex differences in natural history of cardiovascular magnetic resonance- and biopsy-proven lymphocytic myocarditis.
ESC Heart Fail
2022
35980659
Hidden Risk: Arrhythmogenic Genes in the General Population.
Circ Genom Precis Med
2022
36114020
Long-Term Efficacy and Safety of ARRY-371797 (PF-07265803) in Patients With Lamin A/C-Related Dilated Cardiomyopathy.
Am J Cardiol
2022
33551194
Cardiac MR Imaging of Muscular Dystrophies.
Curr Probl Diagn Radiol
2022
35138330
Association of Titin Variations With Late-Onset Dilated Cardiomyopathy.
JAMA Cardiol
2022
35196083
Activation of PDGFRA signaling contributes to filamin C-related arrhythmogenic cardiomyopathy.
Sci Adv
2022
35229420
The response to cardiac resynchronization therapy in LMNA cardiomyopathy.
Eur J Heart Fail
2022
34776072
The Arrhythmic Phenotype in Cardiomyopathy.
Heart Fail Clin
2022
34652067
An LMNA synonymous variant associated with severe dilated cardiomyopathy: Case report.
Am J Med Genet A
2022
33162390
Precision medicine in laminopathies: insights from the REDLAMINA registry.
Rev Esp Cardiol (Engl Ed)
2021
33769382
Genetics of dilated cardiomyopathy.
Curr Opin Cardiol
2021
33682427
HDAC Inhibition Reverses Preexisting Diastolic Dysfunction and Blocks Covert Extracellular Matrix Remodeling.
Circulation
2021
33526513
Induction of ADAM10 by Radiation Therapy Drives Fibrosis, Resistance, and Epithelial-to-Mesenchyal Transition in Pancreatic Cancer.
Cancer Res
2021
34970070
Clinical and genetic features of arrhythmogenic cardiomyopathy: diagnosis, management and the heart failure perspective.
Prog Pediatr Cardiol
2021
34502098
Compromised Biomechanical Properties, Cell-Cell Adhesion and Nanotubes Communication in Cardiac Fibroblasts Carrying the Lamin A/C D192G Mutation.
Int J Mol Sci
2021
34587765
Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.
Circulation
2021
34408292
Correction to: The genetic architecture of Plakophilin 2 cardiomyopathy.
Genet Med
2021
34572260
Mechanisms and Insights for the Development of Heart Failure Associated with Cancer Therapy.
Children (Basel)
2021
34845930
Myocardial Strain and Association With Clinical Outcomes in Danon Disease: A Model for Monitoring Progression of Genetic Cardiomyopathies.
J Am Heart Assoc
2021
34716744
Mortality risk in chronic Chagas cardiomyopathy: a systematic review and meta-analysis.
ESC Heart Fail
2021
34273475
Prevalence and Evolution of Right Ventricular Dysfunction Among Different Genetic Backgrounds in Dilated Cardiomyopathy.
Can J Cardiol
2021
34072787
Experiences 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 Dis
2021
33961942
Antiarrhythmic therapy and risk of cumulative ventricular arrhythmias in arrhythmogenic right ventricle cardiomyopathy.
Int J Cardiol
2021
34269900
The Sarcomeric Spring Protein Titin: Biophysical Properties, Molecular Mechanisms, and Genetic Mutations Associated with Heart Failure and Cardiomyopathy.
Curr Cardiol Rep
2021
34120153
The genetic architecture of Plakophilin 2 cardiomyopathy.
Genet Med
2021
32452075
Contemporary survival trends and aetiological characterization in non-ischaemic dilated cardiomyopathy.
Eur J Heart Fail
2020
32083564
Viscoelastic behavior of cardiomyocytes carrying LMNA mutations.
Biorheology
2020
32021920
Altered microtubule structure, hemichannel localization and beating activity in cardiomyocytes expressing pathologic nuclear lamin A/C.
Heliyon
2020
31958463
Transcriptome signature of ventricular arrhythmia in dilated cardiomyopathy reveals increased fibrosis and activated TP53.
J Mol Cell Cardiol
2020
31924696
<i>FLNC</i> truncations cause arrhythmogenic right ventricular cardiomyopathy.
J Med Genet
2020
33171802
Nanomaterials for Cardiac Tissue Engineering.
Molecules
2020
1 - 50 of 215
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row(s) 1 - 30 of 30
Collaborators
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Cardiovascular Institute, University of Colorado
Co-authored papers
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15
Francesco Muntoni
UCL Great Ormond Street Institute of Child Health
Co-authored papers
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University of Tennessee Health Science Center
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Johns Hopkins University
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7
Matthew T Wheeler
Stanford University School of Medicine
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7
Victoria N Parikh
Stanford University
Co-authored papers
7
Euan A Ashley
Stanford University
Co-authored papers
6
Charles E Canter
University of Washington
Co-authored papers
5
Calum A MacRae
Harvard Medical School and Cardiovascular Division, Brigham and Women's Hospital
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5
Christine E Seidman
Brigham and Women's Hospital (Y.K.
Co-authored papers
5
Endel J Orav
Brigham and Women's Hospital
Co-authored papers
5
Diane Fatkin
Co-authored papers
4
John L Jefferies
University of Tennessee Health Sciences Centre
Co-authored papers
4
Steven D Colan
Boston Children's Hospital, Harvard Medical School
Co-authored papers
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Birgit Funke
Partners Healthcare Center for Personalized Genetic Medicine
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3
Robert L Nussbaum
Invitae Corporation
Co-authored papers
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JoAnn Lindenfeld
Vanderbilt University Medical Center
Co-authored papers
3
Han G Brunner
Maastricht University Medical Centre
Co-authored papers
2
Stuart A Cook
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