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Author Details

Johan M Bos
Mayo Clinic, Windland Smith Rice Genetic Heart Rhythm Clinic)
2005
152
39
PMIDPaper TitleJournal TitlePublished Year
35772688Precision therapy in congenital long QT syndrome.Trends Cardiovasc Med2024
36369981Repeatability of ventricular arrhythmia characteristics on the exercise-stress test in RYR2-mediated catecholaminergic polymorphic ventricular tachycardia.Europace2023
37528649Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.Eur Heart J2023
37558373Fatal Cardiac Arrhythmias During Electronic Gaming in Patients With Genetically Mediated Heart Diseases.J Am Coll Cardiol2023
37658118Proteomic and phosphoproteomic analyses of myectomy tissue reveals difference between sarcomeric and genotype-negative hypertrophic cardiomyopathy.Sci Rep2023
37587576Return-to-Play for Elite Athletes With Genetic Heart Diseases Predisposing to Sudden Cardiac Death.J Am Coll Cardiol2023
37116851Septal Myectomy Outcomes in Children and Adolescents With Obstructive Hypertrophic Cardiomyopathy.Ann Thorac Surg2023
36987533Clinical course of patients with hypertrophic cardiomyopathy away from tertiary referral care.ESC Heart Fail2023
37436769Association Between Syncope Trigger Type and Risk of Subsequent Life-Threatening Events in Patients With Long QT Syndrome.JAMA Cardiol2023
37195701Vigorous Exercise in Patients With Hypertrophic Cardiomyopathy.JAMA Cardiol2023
36725176Phenotypes of Overdiagnosed Long QT Syndrome.J Am Coll Cardiol2023
36508762Cardiopulmonary Exercise Testing in Athletes With Hypertrophic Cardiomyopathy.Am J Cardiol2023
36934983Bilateral cardiac sympathetic denervation in patients with congenital long QT syndrome.Heart Rhythm2023
36802768Multi-Omic Architecture of Obstructive Hypertrophic Cardiomyopathy.Circ Genom Precis Med2023
34798354A phenotype-enhanced variant classification framework to decrease the burden of missense variants of uncertain significance in type 1 long QT syndrome.Heart Rhythm2022
35710045Spectrum and prevalence of side effects and complications with guideline-directed therapies for congenital long QT syndrome.Heart Rhythm2022
35621913Deep Neural Network for Cardiac Magnetic Resonance Image Segmentation.J Imaging2022
35985858Outcomes of Athletes With Genetic Heart Diseases and Implantable Cardioverter-Defibrillators Who Chose to Return to Play.Mayo Clin Proc2022
36258218Natural language processing for identification of hypertrophic cardiomyopathy patients from cardiac magnetic resonance reports.BMC Med Inform Decis Mak2022
35144017Diagnostic accuracy of the 12-lead electrocardiogram in the first 48 hours of life for newborns of a parent with congenital long QT syndrome.Heart Rhythm2022
34874747An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia.Circulation2022
34537410Role of chronic continuous intravenous lidocaine in the clinical management of patients with malignant type 3 long QT syndrome.Heart Rhythm2022
33325582Conversion of left atrial volume to diameter for automated estimation of sudden cardiac death risk in hypertrophic cardiomyopathy.Echocardiography2021
33602408Prevalence of Suicide Among Patients With Sudden Death-Predisposing Genetic Heart Diseases.JACC Clin Electrophysiol2021
33517677Artificial Intelligence-Enabled Assessment of the Heart Rate Corrected QT Interval Using a Mobile Electrocardiogram Device.Circulation2021
33566059Use of Artificial Intelligence and Deep Neural Networks in Evaluation of Patients With Electrocardiographically Concealed Long QT Syndrome From the Surface 12-Lead Electrocardiogram.JAMA Cardiol2021
33512040Efficacy of intentional permanent atrial pacing in the long-term management of congenital long QT syndrome.J Cardiovasc Electrophysiol2021
33926651Myocardial Histopathology in Patients With Obstructive Hypertrophic Cardiomyopathy.J Am Coll Cardiol2021
33504163Suppression-Replacement <i>KCNQ1</i> Gene Therapy for Type 1 Long QT Syndrome.Circulation2021
34419527Detection of hypertrophic cardiomyopathy by an artificial intelligence electrocardiogram in children and adolescents.Int J Cardiol2021
34238014Risk Prediction in Women With Congenital Long QT Syndrome.J Am Heart Assoc2021
34288227Comparison of electrocardiograms (ECG) waveforms and centralized ECG measurements between a simple 6-lead mobile ECG device and a standard 12-lead ECG.Ann Noninvasive Electrocardiol2021
34330632Return-to-Play for Athletes With Long QT Syndrome or Genetic Heart Diseases Predisposing to Sudden Death.J Am Coll Cardiol2021
32533187An autoantibody profile detects Brugada syndrome and identifies abnormally expressed myocardial proteins.Eur Heart J2020
32088002Cardiac Magnetic Resonance Imaging Features in Hypertrophic Cardiomyopathy Diagnosed at &lt;21 Years of Age.Am J Cardiol2020
32105774Intentional nontherapy in long QT syndrome.Heart Rhythm2020
32063070Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia.Circ Arrhythm Electrophysiol2020
33198487Left Cardiac Sympathetic Denervation Monotherapy in Patients With Congenital Long QT Syndrome.Circ Arrhythm Electrophysiol2020
33164571<i>SCN5A</i> Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in <i>SCN5A</i> Families.Circ Genom Precis Med2020
33190526Patients With Hypertrophic Cardiomyopathy Deemed Genotype Negative Based on Research Grade Genetic Analysis: Time for Repeat Diagnostic Testing With Next-Generation Sequencing.Circ Genom Precis Med2020
33303072Echocardiography-Guided Risk Stratification for Long QT Syndrome.J Am Coll Cardiol2020
33213816Genotype Predicts Outcomes in Fetuses and Neonates With Severe Congenital Long QT Syndrome.JACC Clin Electrophysiol2020
32894683Clinical Utility of a Phenotype-Enhanced <i>MYH7</i>-Specific Variant Classification Framework in Hypertrophic Cardiomyopathy Genetic Testing.Circ Genom Precis Med2020
32469608Corrected QT Interval-Polygenic Risk Score and Its Contribution to Type 1, Type 2, and Type 3 Long-QT Syndrome in Probands and Genotype-Positive Family Members.Circ Genom Precis Med2020
32429735Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.Circulation2020
29513133QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy.Acta Cardiol2019
31638832<i>MRAS</i> Variants Cause Cardiomyocyte Hypertrophy in Patient-Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes: Additional Evidence for <i>MRAS</i> as a Definitive Noonan Syndrome-Susceptibility Gene.Circ Genom Precis Med2019
30219255Prevalence and clinical phenotype of concomitant long QT syndrome and arrhythmogenic bileaflet mitral valve prolapse.Int J Cardiol2019
30170228Linking the heart and the brain: Neurodevelopmental disorders in patients with catecholaminergic polymorphic ventricular tachycardia.Heart Rhythm2019
31430211Characterization of the CACNA1C-R518C Missense Mutation in the Pathobiology of Long-QT Syndrome Using Human Induced Pluripotent Stem Cell Cardiomyocytes Shows Action Potential Prolongation and L-Type Calcium Channel Perturbation.Circ Genom Precis Med2019
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Collaborators

Mayo Clinic, Windland Smith Rice Genetic Heart Rhythm Clinic)
Co-authored papers 147
Mayo Clinic
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Mayo Clinic
Co-authored papers 13
Mayo Clinic College of Medicine and Science
Co-authored papers 13
Mayo Clinic
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Mayo Clinic
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Mayo Clinic
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Mayo Clinic
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Mayo Clinic
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University of Tennessee Health Science Center
Co-authored papers 5
Mayo Clinic
Co-authored papers 4
Mayo Clinic
Co-authored papers 3
Mayo Clinic
Co-authored papers 3
Mayo Clinic
Co-authored papers 3
Vanderbilt University Medical Center
Co-authored papers 2
Mayo Clinic
Co-authored papers 2
Technical University of Munich, Institute of Human Genetics
Co-authored papers 2
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Stanford University
Co-authored papers 2
Victor Chang Cardiac Research Institute
Co-authored papers 2
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Brigham and Women's Hospital, Harvard Medical School
Co-authored papers 2
Center for Multimodal Imaging and Genetics, University of California San Diego
Co-authored papers 2
University of Toronto, The Hospital for Sick Children, University Avenue
Co-authored papers 2
Institute of Research, Tokyo Medical and Dental University
Co-authored papers 2
Stanford University
Co-authored papers 1