J. Hathaway

Type 8 long QT syndrome: pathogenic variants in CACNA1C-encoded Cav1.2 cluster in STAC protein binding site.

E. Kaufman, C. January, E. Behr, 2019, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients

M. Gentile, T. Heliö, S. Tuupanen, 2021, BMC Cardiovascular Disorders.

Exploring Patients' Values and Preferences for Initial Atrial Fibrillation Education

Pamela J. McCabe, A. Kumbamu, J. Hathaway, 2020, The Journal of cardiovascular nursing.

Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations.

Marissa A. LeBlanc, C. McMaster, J. Majewski, 2014, JAMA ophthalmology.

Inherited heart rhythm disorders: Diagnostic dilemmas after the sudden death of a young family member

A. Krahn, L. Arbour, S. Sanatani, 2014 .

Variant Reinterpretation in Survivors of Cardiac Arrest With Preserved Ejection Fraction (the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry) by Clinicians and Clinical Commercial Laboratories

J. Healey, A. Krahn, M. Gardner, 2021, Circulation. Genomic and precision medicine.

Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy.

T. Ojala, M. Gentile, S. Ahonen, 2021, PloS one.

The accessibility and utilization of genetic testing for inherited heart rhythm disorders: a Canadian cross-sectional survey study

S. Sheps, A. Krahn, S. Franciosi, 2018, Journal of Community Genetics.

GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy

K. Nikus, M. Gentile, S. Ahonen, 2021, Frontiers in Genetics.

The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry

Jeffrey M. Vinocur, P. Kannankeril, K. Collins, 2017, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Perceptions of genetic variant reclassification in patients with inherited cardiac disease

E. Wong, A. Krahn, L. Yeates, 2019, European Journal of Human Genetics.

Patient Recall, Interpretation, and Perspective of an Inconclusive Long QT Syndrome Genetic Test Result

A. Lehman, L. Arbour, J. Hathaway, 2017, Journal of Genetic Counseling.

Diagnostic yield of genetic testing in a multinational heterogeneous cohort of 2088 DCM patients

T. Heliö, S. Myllykangas, J. Koskenvuo, 2023, Frontiers in cardiovascular medicine.

The accessibility and utilization of genetic testing for inherited heart rhythm disorders: a Canadian cross-sectional survey study

S. Sheps, A. Krahn, S. Franciosi, 2017, Journal of Community Genetics.

Perceptions of genetic variant reclassification in patients with inherited cardiac disease

E. Wong, A. Krahn, L. Yeates, 2019, European Journal of Human Genetics.