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List of works by Michael H. Gollob

A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation

scientific article published on 25 January 2013

A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation

scientific article published in March 2014

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

scientific article

A novel mutation in the RYR2 gene leading to catecholaminergic polymorphic ventricular tachycardia and paroxysmal atrial fibrillation: dose-dependent arrhythmia-event suppression by β-blocker therapy

scientific article published on 08 June 2011

A practical guide to early repolarization.

scientific article

A prospective randomized evaluation of a pharmacogenomic approach to antiplatelet therapy among patients with ST-elevation myocardial infarction: the RAPID STEMI study.

scientific article published on 7 April 2015

AMP-activated protein kinase and familial Wolff-Parkinson-White syndrome: new perspectives on heart development and arrhythmogenesis

scientific article published on 01 May 2002

Accelerating risk of Fidelis lead fracture.

scientific article

An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition

scientific article published on 16 January 2020

An unusual accessory pathway: anteroseptal to ventricular outflow region connection

scientific article published on 01 May 2005

Appropriate result from an inappropriate ICD shock.

scientific article published in October 2006

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

scientific article published on 17 June 2014

Atrial fibrillation as an autoimmune disease?

scientific article published on 17 January 2013

Atrioventricular block as the initial manifestation of cardiac sarcoidosis in middle-aged adults.

scientific article

Begetting atrial fibrillation: Connexins and arrhythmogenesis.

scientific article published on 04 December 2007

Bundle Branch Re-Entrant Ventricular Tachycardia: Novel Genetic Mechanisms in a Life-Threatening Arrhythmia

scientific article published on 21 December 2016

Cardiac connexins as candidate genes for idiopathic atrial fibrillation.

scientific article

Characterization of a novel mutation in the cardiac ryanodine receptor that results in catecholaminergic polymorphic ventricular tachycardia ⬇️

scientific article published on July 14, 2010

Chronic AMPK activity dysregulation produces myocardial insulin resistance in the human Arg302Gln-PRKAG2 glycogen storage disease mouse model.

scientific article published on 05 July 2013

Clinical trials, the renin angiotensin system and atrial fibrillation.

scientific article

Comment on "Familial pseudo-Wolff-Parkinson-White syndrome".

scientific article published on 10 November 2006

Corrigendum to: 'HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies' [Europace 2011;13:1077-109, doi: 10.1093/europace/eur245]

scientific article published on 20 January 2012

Degenerating regenerating torsades de pointes.

scientific article published in April 2012

Derivation and validation of a simple exercise-based algorithm for prediction of genetic testing in relatives of LQTS probands

scientific article published on 31 October 2011

Discrepant DNA analysis in three patients with inherited arrhythmia: molecular genetic test results deserve a second glance

scientific article published on 01 June 2008

Distinct early signaling events resulting from the expression of the PRKAG2 R302Q mutant of AMPK contribute to increased myocardial glycogen.

scientific article published on 15 July 2009

Distinguishing pathogenic mutations from innocuous rare variants in gene discovery for Brugada syndrome

scientific article published on 14 February 2012

Early repolarization: a rare primary arrhythmic syndrome and common modifier of arrhythmic risk

scientific article published on 30 April 2013

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

scientific article

Epinephrine infusion in the evaluation of unexplained cardiac arrest and familial sudden death: from the cardiac arrest survivors with preserved Ejection Fraction Registry

scientific article published on 03 September 2012

Epsilon wave uncovered by exercise test in a patient with desmoplakin-positive arrhythmogenic right ventricular cardiomyopathy

scientific article published on 29 January 2015

Evaluation of Prolonged QT Interval: Structural Heart Disease Mimicking Long QT Syndrome

scientific article published on 3 February 2017

Evaluation of genes encoding for the transient outward current (Ito) identifies the KCND2 gene as a cause of J-wave syndrome associated with sudden cardiac death

scientific article published on 11 September 2014

Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation

scientific article

Evolution of a genetic diagnosis

scientific article published on 20 December 2013

Evolution of clinical diagnosis in patients presenting with unexplained cardiac arrest or syncope due to polymorphic ventricular tachycardia

scientific article published on 14 November 2013

Exercise testing in asymptomatic gene carriers exposes a latent electrical substrate of arrhythmogenic right ventricular cardiomyopathy.

scientific article published on 27 June 2013

Feasibility study of endocardial mapping of ganglionated plexuses during catheter ablation of atrial fibrillation.

scientific article published on 28 February 2006

First report of a large duplication of the KCNQ1 gene in a patient with long QT syndrome.

scientific article

Frequency of peripartum cardiomyopathy.

scientific article

Gain-of-function mutation of Nav1.5 in atrial fibrillation enhances cellular excitability and lowers the threshold for action potential firing

scientific article

Genetic determinants of atrial fibrillation: SNPs are riding the wave(lets)

scientific article published on 22 April 2006

Genetics of cardiac electrical disease

scientific article published on 11 October 2012

Genetics of inherited primary arrhythmia disorders

scientific article

Go protein subunit Goα and the secretory process of the natriuretic peptide hormones ANF and BNP.

scientific article published on 27 April 2015

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

scientific article published on August 2011

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

scientific article published on August 2011

In vivo assessment of myocardial glucose uptake by positron emission tomography in adults with the PRKAG2 cardiac syndrome.

scientific article published on 17 September 2009

In-hospital mortality in 13,263 survivors of out-of-hospital cardiac arrest in Canada

scientific article published in April 2010

Influence of gender on ICD implantation for primary and secondary prevention of sudden cardiac death.

scientific article published on 13 November 2006

Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy.

scientific article

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

scientific article published on 14 August 2014

Isorhythmic interaction between a dual-chamber pacemaker and an intrinsic rhythm: pacemaker malfunctioning or not?

scientific article published in December 2004

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

scientific article published on August 2017

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

scientific article published on 29 April 2012

Modulating phenotypic expression of the PRKAG2 cardiac syndrome.

scientific article

Myocardial infarction in a teenager

scientific article published on 03 February 2014

No long-term psychological morbidity living with an implantable cardioverter defibrillator under advisory: the Medtronic Marquis experience.

scientific article published on 13 November 2008

Normal atrial activation and voltage during sinus rhythm in the human heart: an endocardial and epicardial mapping study in patients with a history of atrial fibrillation.

scientific article published in April 2007

Outcome of Apparently Unexplained Cardiac Arrest: Results From Investigation and Follow-Up of the Prospective Cardiac Arrest Survivors With Preserved Ejection Fraction Registry

scientific article published on January 2016

PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy

scientific article (publication date: May 2002)

Patient Outcomes From a Specialized Inherited Arrhythmia Clinic.

scientific article published on January 2016

Predictors of fracture risk of a small caliber implantable cardioverter defibrillator lead.

scientific article

Prevalence and Characteristics of Early Repolarization in the CASPER Registry

scientific article published on 01 August 2011

Prevalence and Clinical Implication of Double Mutations in Hypertrophic Cardiomyopathy: Revisiting the Gene-Dose Effect.

scientific article published on April 2017

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

scientific article published on 29 December 2015

Procainamide infusion in the evaluation of unexplained cardiac arrest: from the Cardiac Arrest Survivors with Preserved Ejection Fraction Registry (CASPER).

scientific article published on 18 March 2014

Psychological adjustment in ICD patients living with advisory fidelis leads.

scientific article published on 19 August 2010

Rapid Device-Detected Nonsustained Ventricular Tachycardia in the Risk Stratification of Hypertrophic Cardiomyopathy.

scientific article

Reasons for escalating pacemaker implants

scientific article published on 6 May 2006

Recommendations for the use of genetic testing in the clinical evaluation of inherited cardiac arrhythmias associated with sudden cardiac death: Canadian Cardiovascular Society/Canadian Heart Rhythm Society joint position paper

scientific article

Reduced septal glucose metabolism predicts response to cardiac resynchronization therapy

scientific article published on 10 December 2011

Repeatable noninvasive measurement of mouse myocardial glucose uptake with 18F-FDG: evaluation of tracer kinetics in a type 1 diabetes model.

scientific article

Reply: Noninvasive measurement of mouse myocardial glucose uptake with 18F-FDG

scientific article published on 20 March 2014

Response to Letter Regarding Article, "Outcome of Apparently Unexplained Cardiac Arrest: Results From Investigation and Follow-Up of the Prospective Cardiac Arrest Survivors With Preserved Ejection Fraction Registry".

scientific article published in April 2016

Safety of Outpatient Initiation of Disopyramide for Obstructive Hypertrophic Cardiomyopathy Patients.

scientific article published on 26 May 2017

Sentinel symptoms in patients with unexplained cardiac arrest: from the cardiac arrest survivors with preserved ejection fraction registry (CASPER).

scientific article published on 28 September 2011

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

scientific article

Successful ablation of a concealed parahisian accessory pathway using a remote magnetic navigation system following failure by conventional methods.

scientific article published in September 2006

Systematic Assessment of Patients With Unexplained Cardiac Arrest

scientific article published on 13 July 2009

Targeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation.

scientific article

Ten-year follow-up of cardiac sympathectomy in a young woman with catecholaminergic polymorphic ventricular tachycardia and an implantable cardioverter defibrillator

scientific article published on 26 February 2009

The Phenotypic Spectrum of a Mutation Hotspot Responsible for the Short QT Syndrome

scientific article published on 01 February 2017

The evolution of gene discovery and the revelation of truth

scientific article published on 11 January 2011

The genetic and clinical features of cardiac channelopathies.

scientific article published on July 2010

The genetics of cardiac disease associated with sudden cardiac death: a paper from the 2011 William Beaumont Hospital Symposium on molecular pathology.

scientific article published on 27 June 2012

The role of atrial natriuretic peptide in modulating cardiac electrophysiology.

scientific article

The short QT syndrome: proposed diagnostic criteria.

scientific article published in February 2011

Toward Translation of Genomic Discovery to Clinical Efficacy in Atrial Fibrillation

scientific article published on 01 October 2016

Transgenic mouse model of ventricular preexcitation and atrioventricular reentrant tachycardia induced by an AMP-activated protein kinase loss-of-function mutation responsible for Wolff-Parkinson-White syndrome.

scientific article

Use of implantable cardioverter defibrillators in Canadian and US survivors of out-of-hospital cardiac arrest

scientific article

Usefulness of 14-Day Holter for Detection of Nonsustained Ventricular Tachycardia in Patients With Hypertrophic Cardiomyopathy.

scientific article published on 29 July 2016

Voltage-gated sodium channels: biophysics, pharmacology, and related channelopathies.

scientific article published on 11 July 2012

Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia.

scientific article

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