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Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome

Journal of the American College of Cardiology, 2015-11, Vol.66 (18), p.1976-1986

2015

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Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

American journal of human genetics, 2012-10, Vol.91 (4), p.703-712

2012

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Clinical Differentiation Between Physiological Remodeling and Arrhythmogenic Right Ventricular Cardiomyopathy in Athletes With Marked Electrocardiographic Repolarization Anomalies

Journal of the American College of Cardiology, 2015-06, Vol.65 (25), p.2702-2711

2015

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Explaining the unexplained: applying genetic testing after cardiac arrest and sudden death

European heart journal, 2022-08, Vol.43 (32), p.3082-3084

Behr, Elijah R

2022

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J-Wave Syndromes, SCN5A, and Cardiac Conduction Reserve: Two Sides of the Same Coin?

Journal of the American College of Cardiology, 2021-10, Vol.78 (16), p.1618-1620

Behr, Elijah R.

2021

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Sudden death and cardiac arrest without phenotype: the utility of genetic testing

Trends in cardiovascular medicine, 2017-04, Vol.27 (3), p.207-213

2017

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The genomic architecture of the Brugada syndrome

Heart rhythm, 2021-10, Vol.18 (10), p.1707-1708

Behr, Elijah R.

2021

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Genetic testing in Idiopathic Ventricular Fibrillation: Searching for a needle in a haystack?

Heart rhythm, 2017-07, Vol.14 (7), p.1041-1042

2017

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Late gadolinium enhancement in Brugada syndrome: A marker for subtle underlying cardiomyopathy?

Heart rhythm, 2017-04, Vol.14 (4), p.583-589

2017

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Common Variation in the NOS1AP Gene Is Associated With Drug-Induced QT Prolongation and Ventricular Arrhythmia

Journal of the American College of Cardiology, 2012-08, Vol.60 (9), p.841-850

2012

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Genetic susceptibility and the Brugada syndrome

European heart journal, 2019-10, Vol.40 (37), p.3094-3096

Behr, Elijah R

2019

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Application of artificial intelligence to the electrocardiogram

European heart journal, 2021-12, Vol.42 (46), p.4717-4730

2021

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Fever vs. Drug: Battling with the Brugada syndrome substrate

Heart rhythm, 2017-04, Vol.14 (4), p.518-519

2017

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Is right ventricular outflow tract epicardial substrate ablation the standard of care in high-risk Brugada syndrome?

Europace (London, England), 2023-12, Vol.26 (1)

2023

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Implantable loop recorders in Brugada syndrome

Europace (London, England), 2023-02, Vol.25 (2), p.775-775

2023

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Genetics of sudden cardiac death

Current opinion in cardiology, 2022-05, Vol.37 (3), p.212

2022

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Confirmation of Cause of Death Via Comprehensive Autopsy and Whole Exome Molecular Sequencing in People With Epilepsy and Sudden Unexpected Death

Journal of the American Heart Association, 2021-12, Vol.10 (23), p.e021170-e021170

2021

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Cardiogenetics: the role of genetic testing for inherited arrhythmia syndromes and sudden death

Heart (British Cardiac Society), 2023-03, Vol.109 (6), p.434

2023

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SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes

Heart rhythm, 2020-09, Vol.17 (9), p.1456-1462

2020

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Pharmacological treatment of acquired QT prolongation and torsades de pointes

British journal of clinical pharmacology, 2016-03, Vol.81 (3), p.420-427

2016

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Mapping and Ablation of Ventricular Fibrillation Associated With Early Repolarization Syndrome

Circulation (New York, N.Y.), 2019-10, Vol.140 (18), p.1477-1490

2019

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Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome

Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

Clinical Differentiation Between Physiological Remodeling and Arrhythmogenic Right Ventricular Cardiomyopathy in Athletes With Marked Electrocardiographic Repolarization Anomalies

Explaining the unexplained: applying genetic testing after cardiac arrest and sudden death

J-Wave Syndromes, SCN5A, and Cardiac Conduction Reserve: Two Sides of the Same Coin?

HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes

Executive Summary: HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes

Sudden death and cardiac arrest without phenotype: the utility of genetic testing

The genomic architecture of the Brugada syndrome

Genetic testing in Idiopathic Ventricular Fibrillation: Searching for a needle in a haystack?

Late gadolinium enhancement in Brugada syndrome: A marker for subtle underlying cardiomyopathy?

Common Variation in the NOS1AP Gene Is Associated With Drug-Induced QT Prolongation and Ventricular Arrhythmia

Genetic susceptibility and the Brugada syndrome

Application of artificial intelligence to the electrocardiogram

Fever vs. Drug: Battling with the Brugada syndrome substrate

Is right ventricular outflow tract epicardial substrate ablation the standard of care in high-risk Brugada syndrome?

Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice

Implantable loop recorders in Brugada syndrome

Genetics of sudden cardiac death

Confirmation of Cause of Death Via Comprehensive Autopsy and Whole Exome Molecular Sequencing in People With Epilepsy and Sudden Unexpected Death

Cardiogenetics: the role of genetic testing for inherited arrhythmia syndromes and sudden death

SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes

Pharmacological treatment of acquired QT prolongation and torsades de pointes

HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013

Mapping and Ablation of Ventricular Fibrillation Associated With Early Repolarization Syndrome

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