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ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2021-08, Vol.23 (8), p.1381-1390

2021

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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2021-08, Vol.23 (8), p.1391-1398

2021

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ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2023-08, Vol.25 (8), p.100866-100866, Article 100866

2023

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Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death

European heart journal, 2022-04, Vol.43 (15), p.1500-1510

2022

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Importance of genetic testing in unexplained cardiac arrest

European heart journal, 2022-08, Vol.43 (32), p.3071-3081

2022

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Point-of-care genetic testing for personalisation of antiplatelet treatment (RAPID GENE): a prospective, randomised, proof-of-concept trial

The Lancet (British edition), 2012-05, Vol.379 (9827), p.1705-1711

2012

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Atrioventricular Block as the Initial Manifestation of Cardiac Sarcoidosis in Middle-Aged Adults

Journal of cardiovascular electrophysiology, 2014-08, Vol.25 (8), p.875-881

2014

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A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation

Nature communications, 2016-04, Vol.7 (1), p.11303-11303, Article 11303

2016

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Impact of Genetic Discoveries on the Classification of Lone Atrial Fibrillation

Journal of the American College of Cardiology, 2010-02, Vol.55 (8), p.705-712

2010

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Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardia

Heart rhythm, 2011-06, Vol.8 (6), p.864-871

2011

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Exercise Testing in Asymptomatic Gene Carriers Exposes a Latent Electrical Substrate of Arrhythmogenic Right Ventricular Cardiomyopathy

Journal of the American College of Cardiology, 2013-11, Vol.62 (19), p.1772-1779

2013

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Four TRPM4 Cation Channel Mutations Found in Cardiac Conduction Diseases Lead to Altered Protein Stability

Frontiers in physiology, 2018-03, Vol.9, p.177-177

2018

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Toward Translation of Genomic Discovery to Clinical Efficacy in Atrial Fibrillation

Journal of the American College of Cardiology, 2016-10, Vol.68 (17), p.1895-1897

Gollob, Michael H., MD

2016

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Assessment of Severity of Long QT Syndrome Phenotype and Risk of Fetal Death

Journal of the American Heart Association, 2023-12, Vol.12 (23), p.e029407-e029407

2023

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Derivation and Validation of a Simple Exercise-Based Algorithm for Prediction of Genetic Testing in Relatives of LQTS Probands

Circulation (New York, N.Y.), 2011-11, Vol.124 (20), p.2187-2194

2011

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Short QT syndrome: Advancing our understanding of genetics and cardiac physiology

Heart rhythm, 2023-08, Vol.20 (8), p.1144-1145

Gollob, Michael H.

2023

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COVID-19, Clinical Trials, and QT-Prolonging Prophylactic Therapy in Healthy Subjects: First, Do No Harm

Journal of the American College of Cardiology, 2020-06, Vol.75 (25), p.3184-3186

Gollob, Michael H

2020

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Somatic Mutations in the Connexin 40 Gene (GJA5) in Atrial Fibrillation

The New England journal of medicine, 2006-06, Vol.354 (25), p.2677-2688

2006

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Editorial commentary: Genetic testing in the absence of phenotype: When genetic testing may cause harm

Trends in cardiovascular medicine, 2017-04, Vol.27 (3), p.214-215

Gollob, Michael H., MD

2017

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Identification of a Gene Responsible for Familial Wolff–Parkinson–White Syndrome

The New England journal of medicine, 2001-06, Vol.344 (24), p.1823-1831

2001

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Long-Term Follow-Up of a Pediatric Cohort With Short QT Syndrome

Journal of the American College of Cardiology, 2013-03, Vol.61 (11), p.1183-1191

2013

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Safety of Outpatient Initiation of Disopyramide for Obstructive Hypertrophic Cardiomyopathy Patients

Journal of the American Heart Association, 2017-05, Vol.6 (6)

2017

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Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2021-08, Vol.23 (8), p.1582-1584

2021

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Primary prevention of idiopathic ventricular fibrillation: Not for the faint of heart

Heart rhythm, 2016-04, Vol.13 (4), p.913-914

2016

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Atrial arrhythmias in the young: early onset atrial arrhythmias preceding a diagnosis of a primary muscular dystrophy

Europace (London, England), 2014-12, Vol.16 (12), p.1814-1820

2014

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ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death

Importance of genetic testing in unexplained cardiac arrest

Point-of-care genetic testing for personalisation of antiplatelet treatment (RAPID GENE): a prospective, randomised, proof-of-concept trial

Atrioventricular Block as the Initial Manifestation of Cardiac Sarcoidosis in Middle-Aged Adults

A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation

Impact of Genetic Discoveries on the Classification of Lone Atrial Fibrillation

Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardia

Exercise Testing in Asymptomatic Gene Carriers Exposes a Latent Electrical Substrate of Arrhythmogenic Right Ventricular Cardiomyopathy

Four TRPM4 Cation Channel Mutations Found in Cardiac Conduction Diseases Lead to Altered Protein Stability

Toward Translation of Genomic Discovery to Clinical Efficacy in Atrial Fibrillation

Assessment of Severity of Long QT Syndrome Phenotype and Risk of Fetal Death

Derivation and Validation of a Simple Exercise-Based Algorithm for Prediction of Genetic Testing in Relatives of LQTS Probands

Short QT syndrome: Advancing our understanding of genetics and cardiac physiology

COVID-19, Clinical Trials, and QT-Prolonging Prophylactic Therapy in Healthy Subjects: First, Do No Harm

Somatic Mutations in the Connexin 40 Gene (GJA5) in Atrial Fibrillation

Editorial commentary: Genetic testing in the absence of phenotype: When genetic testing may cause harm

Identification of a Gene Responsible for Familial Wolff–Parkinson–White Syndrome

Long-Term Follow-Up of a Pediatric Cohort With Short QT Syndrome

Safety of Outpatient Initiation of Disopyramide for Obstructive Hypertrophic Cardiomyopathy Patients

Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Primary prevention of idiopathic ventricular fibrillation: Not for the faint of heart

Atrial arrhythmias in the young: early onset atrial arrhythmias preceding a diagnosis of a primary muscular dystrophy

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