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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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Stimulant therapy in children with attention-deficit/hyperactivity disorder and concomitant long QT syndrome: A safe combination?

Heart rhythm, 2015-08, Vol.12 (8), p.1807-1812

2015

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Mexiletine Shortens the QT Interval in Patients With Potassium Channel–Mediated Type 2 Long QT Syndrome

Circulation. Arrhythmia and electrophysiology, 2019-05, Vol.12 (5), p.e007280-e007280

2019

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Contemporary Outcomes in Patients With Long QT Syndrome

Journal of the American College of Cardiology, 2017-07, Vol.70 (4), p.453-462

2017

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Targeted Neonatal Echocardiography in Patients With Hemodynamic Instability

Pediatrics (Evanston), 2022-11, Vol.150 (Supplement 2), p.1

2022

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Variant Frequency and Clinical Phenotype Call Into Question the Nature of Minor, Nonsyndromic Long-QT Syndrome–Susceptibility Gene-Disease Associations

Circulation (New York, N.Y.), 2020-02, Vol.141 (6), p.495-497

2020

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Limited Utility of Surveillance Echocardiograms in Pediatric Patients with Isolated Secundum Atrial Septal Defects

Journal of the American Society of Echocardiography, 2021-02, Vol.34 (2), p.197-199

2021

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Utilizing median and maximum QTc values improves prediction of breakthrough cardiac events in pediatric long QT syndrome

Journal of cardiovascular electrophysiology, 2024-07, Vol.35 (7), p.1370-1381

2024

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Intentional nontherapy in long QT syndrome

Heart rhythm, 2020-07, Vol.17 (7), p.1147-1150

2020

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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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Beyond the length and look of repolarization: Defining the non-QTc electrocardiographic profiles of patients with congenital long QT syndrome

Heart rhythm, 2018-09, Vol.15 (9), p.1413-1419

2018

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Long QT syndrome type 5-Lite: Defining the clinical phenotype associated with the potentially proarrhythmic p.Asp85Asn-KCNE1 common genetic variant

Heart rhythm, 2018-08, Vol.15 (8), p.1223-1230

2018

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Prevalence and clinical phenotype of concomitant long QT syndrome and arrhythmogenic bileaflet mitral valve prolapse

International journal of cardiology, 2019-01, Vol.274, p.175-178

2019

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Assessment and Validation of a Phenotype-Enhanced Variant Classification Framework to Promote or Demote RYR2 Missense Variants of Uncertain Significance

Circulation. Genomic and precision medicine, 2019-05, Vol.12 (5), p.e002510-e002510

2019

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The Effect of Left Cardiac Sympathetic Denervation on Exercise in Patients With Long QT Syndrome

JACC. Clinical electrophysiology, 2019-09, Vol.5 (9), p.1084-1090

2019

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Architectural T-Wave Analysis and Identification of On-Therapy Breakthrough Arrhythmic Risk in Type 1 and Type 2 Long-QT Syndrome

Circulation. Arrhythmia and electrophysiology, 2017-11, Vol.10 (11)

2017

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Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?

Circulation. Arrhythmia and electrophysiology, 2017-08, Vol.10 (8), p.e005282-e005282

2017

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Identification of Concealed and Manifest Long QT Syndrome Using a Novel T Wave Analysis Program

Circulation. Arrhythmia and electrophysiology, 2016-07, Vol.9 (7), p.e003830-e003830

2016

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Automated T‐wave analysis can differentiate acquired QT prolongation from congenital long QT syndrome

Annals of noninvasive electrocardiology, 2017-11, Vol.22 (6), p.n/a

2017

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Clinical Significance of Early Repolarization in Long QT Syndrome

JACC. Clinical electrophysiology, 2018-09, Vol.4 (9), p.1238-1244

2018

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Surveillance Echocardiograms Have Minimal Clinical Utility in Pediatric Patients with Isolated Secundum Atrial Septal Defects

Pediatrics (Evanston), 2020-07, Vol.146 (1_MeetingAbstract), p.616-616

2020

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International Triadin Knockout Syndrome Registry

Circulation. Genomic and precision medicine, 2019-02, Vol.12 (2), p.e002419-e002419

2019

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Impact of Right-sided Obstructive Lesions in Children & Adolescents having Cone Repair for Ebstein Anomaly

Pediatrics (Evanston), 2020-07, Vol.146 (1_MeetingAbstract), p.615-616

2020

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Evaluation of AI-Assisted Stethoscope for Cardiac Time Intervals in Pediatric Patients: A Viable Echocardiographic Alternative

JACC. Advances (Online), 2024-09, Vol.3 (9), p.101078

2024

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Evaluation of AI-Assisted Stethoscope for Cardiac Time Intervals in Pediatric Patients

JACC. Advances (Online), 2024-09, Vol.3 (9), p.101078, Article 101078

2024

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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

Stimulant therapy in children with attention-deficit/hyperactivity disorder and concomitant long QT syndrome: A safe combination?

Mexiletine Shortens the QT Interval in Patients With Potassium Channel–Mediated Type 2 Long QT Syndrome

Contemporary Outcomes in Patients With Long QT Syndrome

Targeted Neonatal Echocardiography in Patients With Hemodynamic Instability

Variant Frequency and Clinical Phenotype Call Into Question the Nature of Minor, Nonsyndromic Long-QT Syndrome–Susceptibility Gene-Disease Associations

Limited Utility of Surveillance Echocardiograms in Pediatric Patients with Isolated Secundum Atrial Septal Defects

Utilizing median and maximum QTc values improves prediction of breakthrough cardiac events in pediatric long QT syndrome

Intentional nontherapy in long QT syndrome

Return-to-Play for Athletes With Genetic Heart Diseases

Beyond the length and look of repolarization: Defining the non-QTc electrocardiographic profiles of patients with congenital long QT syndrome

Long QT syndrome type 5-Lite: Defining the clinical phenotype associated with the potentially proarrhythmic p.Asp85Asn-KCNE1 common genetic variant

Prevalence and clinical phenotype of concomitant long QT syndrome and arrhythmogenic bileaflet mitral valve prolapse

Assessment and Validation of a Phenotype-Enhanced Variant Classification Framework to Promote or Demote RYR2 Missense Variants of Uncertain Significance

The Effect of Left Cardiac Sympathetic Denervation on Exercise in Patients With Long QT Syndrome

Architectural T-Wave Analysis and Identification of On-Therapy Breakthrough Arrhythmic Risk in Type 1 and Type 2 Long-QT Syndrome

Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?

Identification of Concealed and Manifest Long QT Syndrome Using a Novel T Wave Analysis Program

Automated T‐wave analysis can differentiate acquired QT prolongation from congenital long QT syndrome

Clinical Significance of Early Repolarization in Long QT Syndrome

Surveillance Echocardiograms Have Minimal Clinical Utility in Pediatric Patients with Isolated Secundum Atrial Septal Defects

International Triadin Knockout Syndrome Registry

Impact of Right-sided Obstructive Lesions in Children & Adolescents having Cone Repair for Ebstein Anomaly

Evaluation of AI-Assisted Stethoscope for Cardiac Time Intervals in Pediatric Patients: A Viable Echocardiographic Alternative

Evaluation of AI-Assisted Stethoscope for Cardiac Time Intervals in Pediatric Patients

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