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Author Details
Full Name
Johan M Bos
Affiliation
Mayo Clinic, Windland Smith Rice Genetic Heart Rhythm Clinic)
ORCID
Career Start Year
2005
Papers
152
H Index
39
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35772688
Precision therapy in congenital long QT syndrome.
Trends Cardiovasc Med
2024
36369981
Repeatability of ventricular arrhythmia characteristics on the exercise-stress test in RYR2-mediated catecholaminergic polymorphic ventricular tachycardia.
Europace
2023
37528649
Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.
Eur Heart J
2023
37558373
Fatal Cardiac Arrhythmias During Electronic Gaming in Patients With Genetically Mediated Heart Diseases.
J Am Coll Cardiol
2023
37658118
Proteomic and phosphoproteomic analyses of myectomy tissue reveals difference between sarcomeric and genotype-negative hypertrophic cardiomyopathy.
Sci Rep
2023
37587576
Return-to-Play for Elite Athletes With Genetic Heart Diseases Predisposing to Sudden Cardiac Death.
J Am Coll Cardiol
2023
37116851
Septal Myectomy Outcomes in Children and Adolescents With Obstructive Hypertrophic Cardiomyopathy.
Ann Thorac Surg
2023
36987533
Clinical course of patients with hypertrophic cardiomyopathy away from tertiary referral care.
ESC Heart Fail
2023
37436769
Association Between Syncope Trigger Type and Risk of Subsequent Life-Threatening Events in Patients With Long QT Syndrome.
JAMA Cardiol
2023
37195701
Vigorous Exercise in Patients With Hypertrophic Cardiomyopathy.
JAMA Cardiol
2023
36725176
Phenotypes of Overdiagnosed Long QT Syndrome.
J Am Coll Cardiol
2023
36508762
Cardiopulmonary Exercise Testing in Athletes With Hypertrophic Cardiomyopathy.
Am J Cardiol
2023
36934983
Bilateral cardiac sympathetic denervation in patients with congenital long QT syndrome.
Heart Rhythm
2023
36802768
Multi-Omic Architecture of Obstructive Hypertrophic Cardiomyopathy.
Circ Genom Precis Med
2023
34798354
A phenotype-enhanced variant classification framework to decrease the burden of missense variants of uncertain significance in type 1 long QT syndrome.
Heart Rhythm
2022
35710045
Spectrum and prevalence of side effects and complications with guideline-directed therapies for congenital long QT syndrome.
Heart Rhythm
2022
35621913
Deep Neural Network for Cardiac Magnetic Resonance Image Segmentation.
J Imaging
2022
35985858
Outcomes of Athletes With Genetic Heart Diseases and Implantable Cardioverter-Defibrillators Who Chose to Return to Play.
Mayo Clin Proc
2022
36258218
Natural language processing for identification of hypertrophic cardiomyopathy patients from cardiac magnetic resonance reports.
BMC Med Inform Decis Mak
2022
35144017
Diagnostic accuracy of the 12-lead electrocardiogram in the first 48 hours of life for newborns of a parent with congenital long QT syndrome.
Heart Rhythm
2022
34874747
An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia.
Circulation
2022
34537410
Role of chronic continuous intravenous lidocaine in the clinical management of patients with malignant type 3 long QT syndrome.
Heart Rhythm
2022
33325582
Conversion of left atrial volume to diameter for automated estimation of sudden cardiac death risk in hypertrophic cardiomyopathy.
Echocardiography
2021
33602408
Prevalence of Suicide Among Patients With Sudden Death-Predisposing Genetic Heart Diseases.
JACC Clin Electrophysiol
2021
33517677
Artificial Intelligence-Enabled Assessment of the Heart Rate Corrected QT Interval Using a Mobile Electrocardiogram Device.
Circulation
2021
33566059
Use of Artificial Intelligence and Deep Neural Networks in Evaluation of Patients With Electrocardiographically Concealed Long QT Syndrome From the Surface 12-Lead Electrocardiogram.
JAMA Cardiol
2021
33512040
Efficacy of intentional permanent atrial pacing in the long-term management of congenital long QT syndrome.
J Cardiovasc Electrophysiol
2021
33926651
Myocardial Histopathology in Patients With Obstructive Hypertrophic Cardiomyopathy.
J Am Coll Cardiol
2021
33504163
Suppression-Replacement <i>KCNQ1</i> Gene Therapy for Type 1 Long QT Syndrome.
Circulation
2021
34419527
Detection of hypertrophic cardiomyopathy by an artificial intelligence electrocardiogram in children and adolescents.
Int J Cardiol
2021
34238014
Risk Prediction in Women With Congenital Long QT Syndrome.
J Am Heart Assoc
2021
34288227
Comparison of electrocardiograms (ECG) waveforms and centralized ECG measurements between a simple 6-lead mobile ECG device and a standard 12-lead ECG.
Ann Noninvasive Electrocardiol
2021
34330632
Return-to-Play for Athletes With Long QT Syndrome or Genetic Heart Diseases Predisposing to Sudden Death.
J Am Coll Cardiol
2021
32533187
An autoantibody profile detects Brugada syndrome and identifies abnormally expressed myocardial proteins.
Eur Heart J
2020
32088002
Cardiac Magnetic Resonance Imaging Features in Hypertrophic Cardiomyopathy Diagnosed at <21 Years of Age.
Am J Cardiol
2020
32105774
Intentional nontherapy in long QT syndrome.
Heart Rhythm
2020
32063070
Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia.
Circ Arrhythm Electrophysiol
2020
33198487
Left Cardiac Sympathetic Denervation Monotherapy in Patients With Congenital Long QT Syndrome.
Circ Arrhythm Electrophysiol
2020
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 Med
2020
33190526
Patients With Hypertrophic Cardiomyopathy Deemed Genotype Negative Based on Research Grade Genetic Analysis: Time for Repeat Diagnostic Testing With Next-Generation Sequencing.
Circ Genom Precis Med
2020
33303072
Echocardiography-Guided Risk Stratification for Long QT Syndrome.
J Am Coll Cardiol
2020
33213816
Genotype Predicts Outcomes in Fetuses and Neonates With Severe Congenital Long QT Syndrome.
JACC Clin Electrophysiol
2020
32894683
Clinical Utility of a Phenotype-Enhanced <i>MYH7</i>-Specific Variant Classification Framework in Hypertrophic Cardiomyopathy Genetic Testing.
Circ Genom Precis Med
2020
32469608
Corrected 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 Med
2020
32429735
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
Circulation
2020
29513133
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy.
Acta Cardiol
2019
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 Med
2019
30219255
Prevalence and clinical phenotype of concomitant long QT syndrome and arrhythmogenic bileaflet mitral valve prolapse.
Int J Cardiol
2019
30170228
Linking the heart and the brain: Neurodevelopmental disorders in patients with catecholaminergic polymorphic ventricular tachycardia.
Heart Rhythm
2019
31430211
Characterization 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 Med
2019
1 - 50 of 152
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row(s) 1 - 30 of 30
Collaborators
Michael J Ackerman
Mayo Clinic, Windland Smith Rice Genetic Heart Rhythm Clinic)
Co-authored papers
147
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Mayo Clinic
Co-authored papers
37
Jeffrey B Geske
Mayo Clinic
Co-authored papers
13
Bernard J Gersh
Mayo Clinic College of Medicine and Science
Co-authored papers
13
Peter A Noseworthy
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Co-authored papers
9
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Mayo Clinic
Co-authored papers
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7
Paul A Friedman
Mayo Clinic
Co-authored papers
7
Alan Sugrue
Mayo Clinic
Co-authored papers
7
Jonathan N Johnson
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7
Zachi I Attia
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6
Rick A Nishimura
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Joseph A Dearani
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Co-authored papers
6
Jeffrey A Towbin
University of Tennessee Health Science Center
Co-authored papers
5
Adelaide M Arruda-Olson
Mayo Clinic
Co-authored papers
4
Conor M Lane
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Co-authored papers
3
Christopher G Scott
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Co-authored papers
3
Peter A Brady
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Co-authored papers
3
Dan M Roden
Vanderbilt University Medical Center
Co-authored papers
2
David O Hodge
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Co-authored papers
2
Thomas Meitinger
Technical University of Munich, Institute of Human Genetics
Co-authored papers
2
Stephen C Ekker
Co-authored papers
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Anne M Dubin
Stanford University
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