Susan S. Conacher
London, ON, Canada
Last Updated: 09/26/2026
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Found 9 publications
ALU transposition induces familial hypertrophic cardiomyopathy.
Journal: Molecular genetics & genomic medicine
Published: April 03, 2019
A large familial pathogenic Plakophilin-2 gene (PKP2) deletion manifesting with sudden cardiac death and lone atrial fibrillation: Evidence for alternating atrial and ventricular phenotypes.
Journal: HeartRhythm case reports
Published: October 27, 2018
Pregnancy in Catecholaminergic Polymorphic Ventricular Tachycardia.
Journal: JACC. Clinical electrophysiology
Published: September 10, 2018
Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?
Journal: Circulation. Arrhythmia and electrophysiology
Published: January 09, 2017
A detailed description and assessment of outcomes of patients with hospital recorded QTc prolongation.
Journal: The American journal of cardiology
Published: October 17, 2014
Arrhythmogenic right ventricular cardiomyopathy with recessive inheritance related to a new homozygous desmocollin-2 mutation.
Journal: The Canadian journal of cardiology
Published: November 15, 2013
Reduced Uptake of Family Screening in Genotype-Negative Versus Genotype-Positive Long QT Syndrome.
Journal: Journal of genetic counseling
Published: October 31, 2013
End-recovery QTc: a useful metric for assessing genetic variants of unknown significance in long-QT syndrome.
Journal: Journal of cardiovascular electrophysiology
Published: March 21, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026