Steffany Grondin
Montreal, QC, Canada
Last Updated: 09/26/2026
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Found 8 publications
Polygenic and Monogenic Contributions to Tachycardia-Associated Cardiomyopathy.
Journal: Circulation
Published: February 23, 2026
Congenital Long QT Syndrome: A Focus on Risk Stratification and Management.
Journal: Reviews in cardiovascular medicine
Published: January 04, 2025
Clinical Effect of Genetic Testing in Inherited Cardiovascular Diseases: A 14-Year Retrospective Study.
Journal: Journal of the American College of Cardiology
Published: June 11, 2024
Importance of genetic testing in unexplained cardiac arrest.
Journal: European heart journal
Published: October 08, 2021
Novel Gain-of-Function Variant in CACNA1C Associated With Timothy Syndrome, Multiple Accessory Pathways, and Noncompaction Cardiomyopathy.
Journal: Circulation. Genomic and precision medicine
Published: November 16, 2020
Missense variants in the spectrin repeat domain of DSP are associated with arrhythmogenic cardiomyopathy: A family report and systematic review.
Journal: American journal of medical genetics. Part A
Published: May 06, 2020
Diagnostic and Therapeutic Misconception: Parental Expectations and Perspectives Regarding Genetic Testing for Developmental Disorders.
Journal: Journal of autism and developmental disorders
Published: October 05, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026