Julie A. Hathaway

1033 Davie St, Rm 211
Vancouver, BC, Canada

Last Updated: 09/26/2026

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Found 12 publications

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

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

Journal: Frontiers in cardiovascular medicine
Published: July 06, 2023

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

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

Journal: Frontiers in genetics
Published: September 30, 2021

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.

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.

Journal: Circulation. Genomic and precision medicine
Published: May 07, 2021

Exploring Patients' Values and Preferences for Initial Atrial Fibrillation Education.

Exploring Patients' Values and Preferences for Initial Atrial Fibrillation Education.

Journal: The Journal of cardiovascular nursing
Published: July 11, 2020

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

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

Journal: PloS one
Published: June 18, 2020

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

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

Journal: BMC cardiovascular disorders
Published: May 24, 2020

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

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

Journal: 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
Published: March 12, 2019

Perceptions of genetic variant reclassification in patients with inherited cardiac disease.

Perceptions of genetic variant reclassification in patients with inherited cardiac disease.

Journal: European journal of human genetics : EJHG
Published: November 10, 2018

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

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

Journal: Journal of community genetics
Published: April 18, 2017

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

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

Journal: 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
Published: August 17, 2016

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

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

Journal: Journal of genetic counseling
Published: January 05, 2016

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

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

Journal: JAMA ophthalmology
Published: August 16, 2014
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Last Updated: 09/26/2026