Author

Julie Hathaway

Observed names: Hathaway, Julie, J. Hathaway, Julie A Hathaway

Observed institutions: Providence Health Care, Vancouver Coastal Health, University of British Columbia, Marlboro College, Children's Hospital of Eastern Ontario, St. Paul's Hospital, Newborn Screening Ontario, Seattle Foundation, Blueprint Genetics (Finland), Quest Diagnostics (United States)

ORCID: 0000-0002-0144-4653

Observed ORCID: 0000-0002-0144-4653

OpenAlex ID: A5035489215

Phenotypic Overlap Between Familial Exudative Vitreoretinopathy and Microcephaly, Lymphedema, and Chorioretinal Dysplasia Caused by KIF11 Mutations

2014 · Johane M. Robitaille, Roxanne M. Gillett, et al. · JAMA Ophthalmology · 144

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

2016 · Thomas M Roston, Zhiguang Yuchi, et al. · EP Europace · 122

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

2021 · Julie Hathaway, Krista Heliö, et al. · BMC Cardiovascular Disorders · 53

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Perceptions of genetic variant reclassification in patients with inherited cardiac disease

2019 · Eugene K. Wong, Kirsten Bartels, et al. · European Journal of Human Genetics · 44

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

2021 · Juha W. Koskenvuo, Inka Saarinen, et al. · PLoS ONE · 26

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

2023 · Krista Heliö, Marcos Cicerchia, et al. · Frontiers in Cardiovascular Medicine · 25

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

2019 · Greg J Mellor, Pankaj Panwar, et al. · EP Europace · 20

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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

2021 · Brianna Davies, Kirsten Bartels, et al. · Circulation Genomic and Precision Medicine · 19

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

2016 · Sarah Predham, Julie Hathaway, et al. · Journal of Genetic Counseling · 17

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

2021 · Krista Heliö, Mikko I. Mäyränpää, et al. · Frontiers in Genetics · 15

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

2017 · Thomas M. Roston, Laura Dewar, et al. · Journal of Community Genetics · 8

Lexigene®: An online medical genetics translation tool to facilitate communication

2019 · Mireille Cloutier, Julie Hathaway, et al. · Journal of Genetic Counseling · 4

Catecholaminergic Polymorphic Ventricular Tachycardia in the Young: an Analysis of Genetic Data From an International, Multicentre Registry

2014 · T.M. Roston, J. Hathaway, et al. · Canadian Journal of Cardiology · 2

The Bc Inherited Arrhythmia Program: a Multidisciplinary Approach to Families at Risk for Sudden Death

2014 · J. Hathaway, K. Gibbs, et al. · Canadian Journal of Cardiology · 1

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

2014 · Mikyla Janzen, Shubhayan Sanatani, et al. · Journal of Nursing Education and Practice · 1

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260 A novel missense SCN5A gene mutation causing LQT3 in a large first nations family

2011 · M.J. Gardner, J. Marcadier, et al. · Canadian Journal of Cardiology · 1

PO12 Genetic Findings in a Cohort of Over 2,300 Individuals with Clinically Suspected Heritable Thoracic Aortic Disease

2026 · Mia Toivonen, Rosa Woldegebriel, et al. · European Journal of Preventive Cardiology

P669: Empowering clinicians to resolve VUS: Presenting VUS clarification outcomes

2025 · Laura Fuqua, Eija Seppälä, et al. · Genetics in Medicine Open

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Postmortem Genetic Testing Following Sudden Cardiac Death Using a Cardiomyopathy and Arrhythmia Next-Generation Sequencing Panel

2024 · E. Zilliacus, J. Hathaway, et al. · Heart Lung and Circulation

P577: Genetic findings in afor cohort of over 1,800 patients tested with a combined cardiomyopathy and arrhythmia panel*

2024 · Julie Hathaway, Johanna Huusko, et al. · Genetics in Medicine Open

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P622: Genetic results in a cohort of 489 patients with inherited myopathies

2024 · Kim Gall, Julie Hathaway, et al. · Genetics in Medicine Open

Po-01-015 Yield of Genetic Testing and Result Utility in a Cohort of 2100 Dcm Patients

2023 · Krista Heliö, Julie Hathaway, et al. · Heart Rhythm

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eP399: Characterizing molecular diagnostic findings from next-generation sequencing panel testing for individuals with suspected congenital hypothyroidism or resistance to thyroid hormone

2022 · Alicia Scocchia, Kimberly Gall, et al. · Genetics in Medicine

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eP358: Genetic findings in a cohort of patients with pulmonary arterial hypertension referred for NGS panel testing

2022 · Julie Hathaway, Marcos Cicerchia, et al. · Genetics in Medicine

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eP359: Diagnostic yield of genetic testing in an unselected cohort of patients with congenital heart disease

2022 · Julie Hathaway, Marcos Cicerchia, et al. · Genetics in Medicine

Works count: 35

Citation count: 502

H-index: 10

I10-index: 10