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Diagnostic, Prognostic, and Therapeutic Implications of Genetic Testing for Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, 2009-07, Vol.54 (3), p.201-211

2009

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Artificial Intelligence-Enabled Assessment of the Heart Rate Corrected QT Interval Using a Mobile Electrocardiogram Device

Circulation (New York, N.Y.), 2021-03, Vol.143 (13), p.1274-1286

2021

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Prevalence, Clinical Significance, and Natural History of Left Ventricular Apical Aneurysms in Hypertrophic Cardiomyopathy

Circulation (New York, N.Y.), 2008-10, Vol.118 (15), p.1541-1549

2008

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MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathy

PloS one, 2017-06, Vol.12 (6), p.e0180064-e0180064

2017

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Myofilament Protein Gene Mutation Screening and Outcome of Patients With Hypertrophic Cardiomyopathy

Mayo Clinic proceedings, 2008-06, Vol.83 (6), p.630-638

2008

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Microvascular Function Is Selectively Impaired in Patients With Hypertrophic Cardiomyopathy and Sarcomere Myofilament Gene Mutations

Journal of the American College of Cardiology, 2011-08, Vol.58 (8), p.839-848

2011

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Characterization of a Phenotype-Based Genetic Test Prediction Score for Unrelated Patients With Hypertrophic Cardiomyopathy

Mayo Clinic proceedings, 2014-06, Vol.89 (6), p.727-737

2014

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Institution-Wide QT Alert System Identifies Patients With a High Risk of Mortality

Mayo Clinic proceedings, 2013-04, Vol.88 (4), p.315-325

2013

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Cardiac Ankyrin Repeat Protein Gene ( ANKRD1 ) Mutations in Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, 2009-07, Vol.54 (4), p.334-342

2009

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Implantable cardioverter-defibrillator use in catecholaminergic polymorphic ventricular tachycardia: A systematic review

Heart rhythm, 2018-12, Vol.15 (12), p.1791-1799

2018

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Detection of hypertrophic cardiomyopathy by an artificial intelligence electrocardiogram in children and adolescents

International journal of cardiology, 2021-10, Vol.340, p.42-47

2021

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Return-to-Play for Athletes With Genetic Heart Diseases

Circulation (New York, N.Y.), 2018-03, Vol.137 (10), p.1086-1088

2018

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Role of Family History of Sudden Death in Risk Stratification and Prevention of Sudden Death With Implantable Defibrillators in Hypertrophic Cardiomyopathy

The American journal of cardiology, 2010-11, Vol.106 (10), p.1481-1486

2010

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A modifier screen identifies DNAJB6 as a cardiomyopathy susceptibility gene

JCI insight, 2016-09, Vol.1 (14)

2016

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A phenotype-enhanced variant classification framework to decrease the burden of missense variants of uncertain significance in type 1 long QT syndrome

Heart rhythm, 2022-03, Vol.19 (3), p.435-442

2022

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Electromechanical window negativity in genotyped long-QT syndrome patients: relation to arrhythmia risk

European heart journal, 2015-01, Vol.36 (3), p.179-186

2015

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PLN -encoded phospholamban mutation in a large cohort of hypertrophic cardiomyopathy cases: Summary of the literature and implications for genetic testing

The American heart journal, 2011, Vol.161 (1), p.165-171

2011

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Implantable cardioverter-defibrillator explantation for overdiagnosed or overtreated congenital long QT syndrome

Heart rhythm, 2016-04, Vol.13 (4), p.879-885

2016

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The Natural History of Nonobstructive Hypertrophic Cardiomyopathy

Mayo Clinic proceedings, 2016-03, Vol.91 (3), p.279-287

2016

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Mutations in JPH2 -encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humans

Journal of molecular and cellular cardiology, 2007-06, Vol.42 (6), p.1026-1035

2007

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Myofilament Protein Gene Mutation Screening and Outcome of Patients With Hypertrophic Cardiomyopathy

Mayo Clinic proceedings, 2008-06, Vol.83 (6), p.630-638

2008

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Prevalence and spectrum of electroencephalogram-identified epileptiform activity among patients with long QT syndrome

Heart rhythm, 2014, Vol.11 (1), p.53-57

2014

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Unraveling the Puzzle of the Role of Heritability in the Variability of the QT Interval Using Exome Array Analysis

Circulation. Genomic and precision medicine, 2018-01, Vol.11 (1), p.e002007-e002007

2018

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Providers’ Response to Clinical Decision Support for QT Prolonging Drugs

Journal of medical systems, 2017-10, Vol.41 (10), p.161-161, Article 161

2017

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Quality of life after videoscopic left cardiac sympathetic denervation in patients with potentially life-threatening cardiac channelopathies/cardiomyopathies

Heart rhythm, 2016, Vol.13 (1), p.62-69

2016

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Diagnostic, Prognostic, and Therapeutic Implications of Genetic Testing for Hypertrophic Cardiomyopathy

Artificial Intelligence-Enabled Assessment of the Heart Rate Corrected QT Interval Using a Mobile Electrocardiogram Device

Prevalence, Clinical Significance, and Natural History of Left Ventricular Apical Aneurysms in Hypertrophic Cardiomyopathy

MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathy

Myofilament Protein Gene Mutation Screening and Outcome of Patients With Hypertrophic Cardiomyopathy

Microvascular Function Is Selectively Impaired in Patients With Hypertrophic Cardiomyopathy and Sarcomere Myofilament Gene Mutations

Characterization of a Phenotype-Based Genetic Test Prediction Score for Unrelated Patients With Hypertrophic Cardiomyopathy

Institution-Wide QT Alert System Identifies Patients With a High Risk of Mortality

Cardiac Ankyrin Repeat Protein Gene ( ANKRD1 ) Mutations in Hypertrophic Cardiomyopathy

Implantable cardioverter-defibrillator use in catecholaminergic polymorphic ventricular tachycardia: A systematic review

Detection of hypertrophic cardiomyopathy by an artificial intelligence electrocardiogram in children and adolescents

Return-to-Play for Athletes With Genetic Heart Diseases

Role of Family History of Sudden Death in Risk Stratification and Prevention of Sudden Death With Implantable Defibrillators in Hypertrophic Cardiomyopathy

A modifier screen identifies DNAJB6 as a cardiomyopathy susceptibility gene

A phenotype-enhanced variant classification framework to decrease the burden of missense variants of uncertain significance in type 1 long QT syndrome

Electromechanical window negativity in genotyped long-QT syndrome patients: relation to arrhythmia risk

PLN -encoded phospholamban mutation in a large cohort of hypertrophic cardiomyopathy cases: Summary of the literature and implications for genetic testing

Implantable cardioverter-defibrillator explantation for overdiagnosed or overtreated congenital long QT syndrome

The Natural History of Nonobstructive Hypertrophic Cardiomyopathy

Mutations in JPH2 -encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humans

Myofilament Protein Gene Mutation Screening and Outcome of Patients With Hypertrophic Cardiomyopathy

Prevalence and spectrum of electroencephalogram-identified epileptiform activity among patients with long QT syndrome

Unraveling the Puzzle of the Role of Heritability in the Variability of the QT Interval Using Exome Array Analysis

Providers’ Response to Clinical Decision Support for QT Prolonging Drugs

Quality of life after videoscopic left cardiac sympathetic denervation in patients with potentially life-threatening cardiac channelopathies/cardiomyopathies

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