Michael Gollob, University of Toronto

Research

Arrhythmia Mouse

Latest papers

RBM20 Truncating Variants and Human Cardiomyopathy
JAMA cardiology · 2026
Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions
Genome Medicine · 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions
bioRxiv (Cold Spring Harbor Laboratory) · 2023

All 9 publications

Latest funding

A Novel Genetic Subtype of Human Atrial Fibrillation: Physiologic Characterization and Therapeutic Drug Targeting
CIHR · 2018 · Nominated PI
$650,250

All 1 grants and awards

9 publications.

01

RBM20 Truncating Variants and Human Cardiomyopathy

Floyd BJ, Njoroge JN, Krysov VA, Gomes B, Murtha R, Aribeana C, Cannie D, Smith E, Paldino A, Brown EE

JAMA cardiology20264 citations

DOI: 10.1001/jamacardio.2026.0401

02

Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions

Josephs KS, Roberts AM, Theotokis P, Walsh R, Ostrowski PJ, Edwards M, Fleming A, Thaxton C, Roberts JD, Care M

Genome Medicine202337 citationsOpen Access

DOI: 10.1186/s13073-023-01246-8 PMID: W4387874656

03

Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions

Josephs KS, Roberts AM, Theotokis P, Walsh R, Ostrowski PJ, Edwards M, Fleming A, Thaxton C, Roberts JD, Care M

bioRxiv (Cold Spring Harbor Laboratory)20233 citationsOpen Access

DOI: 10.1101/2023.04.03.23287612 PMID: W4362600604

04

Use of Wearable Technology and Deep Learning to Improve the Diagnosis of Brugada Syndrome.

Liao S, Bokhari M, Chakraborty P, Suszko A, Jones G, Spears D, Gollob M, Zhang Z, Wang B, Chauhan VS

JACC. Clinical electrophysiology2022

DOI: 10.1016/j.jacep.2022.05.003 PMID: 35981788

05

The Role of Interventional Irisin on Heart Molecular Physiology.

Alzoughool F, Al-Zghoul MB, Ghanim BY, Gollob M, Idkaidek N, Qinna NA

Pharmaceuticals (Basel, Switzerland)2022

DOI: 10.3390/ph15070863 PMID: 35890161

06

Complex interactions in a novel SCN5A compound mutation associated with long QT and Brugada syndrome: Implications for Na+ channel blocking pharmacotherapy for de novo conduction disease.

Liu J, Bayer JD, Aschar-Sobbi R, Wauchop M, Spears D, Gollob M, Vigmond EJ, Tsushima R, Backx PH, Chauhan VS

PloS one2018

DOI: 10.1371/journal.pone.0197273 PMID: 29791480

07

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

Viswanathan K, Suszko AM, DAS M, Jackson N, Gollob M, Cameron D, Spears D, Woo A, Rakowski H, Khurana M, Chauhan VS

Pacing and clinical electrophysiology : PACE2016

DOI: 10.1111/pace.12861 PMID: 27027856

08

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

Roeske C, Martinuk A, Choudhry A, Hendy GN, Gollob M, Li Q, Georgalis T, de Bold AJ

Journal of molecular endocrinology2015

DOI: 10.1530/jme-15-0081 PMID: 25917834

09

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

Xi Y, Honeywell C, Zhang D, Schwartzentruber J, Beaulieu CL, Tetreault M, Hartley T, Marton J, Vidal SM, Majewski J, Aravind L, Care4Rare Canada Consortium, Gollob M, Boycott KM, Gow RM

International journal of cardiology2015

DOI: 10.1016/j.ijcard.2015.03.130 PMID: 25791106

A Novel Genetic Subtype of Human Atrial Fibrillation: Physiologic Characterization and Therapeutic Drug Targeting

Nominated PICIHR2018Project Grant

Principal investigators: Gollob, Michael H

Keywords: Arrhythmia; Mouse

$650,250

From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.

Frequent collaborators

Pathology and Laboratory Medicine
Medicine
Family Medicine
Human Genetics
Terrence Donnelly Centre for Cellular and Biomolecular Research
Other

Co-authors at University of Toronto, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.

Lucas Bronicki

Pathology and Laboratory Medicine

2 shared papers, latest 2023

Olga Jarinova

Pathology and Laboratory Medicine

2 shared papers, latest 2023

Christina Honeywell

Family Medicine

1 shared papers, latest 2015

Zhaolei Zhang

Terrence Donnelly Centre for Cellular and Biomolecular Research

1 shared papers, latest 2022

Jacek Majewski

Human Genetics

1 shared papers, latest 2015

Write to this professor

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Subject: Prospective PhD student: Arrhythmia Dear Professor Gollob, My name is [your name], and I am a [your current degree or role] at [your institution]. I am applying for a PhD position starting in [term and year]. I read your paper "RBM20 Truncating Variants and Human Cardiomyopathy" (2026), and it connects closely to my own work on [your research topic]. [One or two sentences on what you did and what you learned.] Are you accepting new PhD students for [term and year]? I have attached my CV and transcripts, and I would be glad to talk at a time that suits you. Thank you for your time. Kind regards, [your name]

Michael Gollob

Research

Latest papers

Latest funding

RBM20 Truncating Variants and Human Cardiomyopathy

Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions

Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions

Use of Wearable Technology and Deep Learning to Improve the Diagnosis of Brugada Syndrome.

The Role of Interventional Irisin on Heart Molecular Physiology.

Complex interactions in a novel SCN5A compound mutation associated with long QT and Brugada syndrome: Implications for Na+ channel blocking pharmacotherapy for de novo conduction disease.

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

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

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

A Novel Genetic Subtype of Human Atrial Fibrillation: Physiologic Characterization and Therapeutic Drug Targeting

Frequent collaborators

Jason Roberts

Lucas Bronicki

Olga Jarinova

Rafik Tadros

Julia Cadrin-Tourigny

Christina Honeywell

Zhaolei Zhang

BO WANG

Taila Hartley

Michael Gollob

Jacek Majewski

Michael Gollob

Research

Latest papers

Latest funding

RBM20 Truncating Variants and Human Cardiomyopathy

Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions

Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions

Use of Wearable Technology and Deep&#xa0;Learning to Improve the Diagnosis&#xa0;of&#xa0;Brugada Syndrome.

The Role of Interventional Irisin on Heart Molecular Physiology.

Complex interactions in a novel SCN5A compound mutation associated with long QT and Brugada syndrome: Implications for Na+ channel blocking pharmacotherapy for de novo conduction disease.

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

Go protein subunit Go&#x3b1; and the secretory process of the natriuretic peptide hormones ANF and BNP.

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

A Novel Genetic Subtype of Human Atrial Fibrillation: Physiologic Characterization and Therapeutic Drug Targeting

Frequent collaborators

Jason Roberts

Lucas Bronicki

Olga Jarinova

Rafik Tadros

Julia Cadrin-Tourigny

Christina Honeywell

Zhaolei Zhang

BO WANG

Taila Hartley

Michael Gollob

Jacek Majewski

Use of Wearable Technology and Deep Learning to Improve the Diagnosis of Brugada Syndrome.

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