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Laura Arbour

Showing results (61-70 of 118) with videos related to

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Molecular Genetics & Genomic Medicine|January 30, 2020
Cardiac arrest in a mother and daughter and the identification of a novel RYR2 variant, predisposing to low penetrant catecholaminergic polymorphic ventricular tachycardia in a four-generation Canadian familyMatthew Tung, Filip Van Petegem, Samantha Lauson, et al.
American Journal of Human Genetics|June 6, 2022
Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?Paul S Appelbaum, Wylie Burke, Erik Parens, et al.
Annual Review of Genomics and Human Genetics|March 21, 2019
Genomic Research Through an Indigenous Lens: Understanding the ExpectationsNanibaa' A Garrison, Māui Hudson, Leah L Ballantyne, et al.
The Canadian Journal of Cardiology|October 18, 2023
The Impact of Chronic Disease on the Corrected QT (QTc) Value in Women in a British Columbia First Nations PopulationMiles Marchand, Anders C Erickson, Lawrence Gillman, et al.
International Journal of Occupational and Environmental Health|September 13, 2011
Congenital anomalies in the offspring of nurses: association with area of employment during pregnancyHelen Dimich-Ward, D Le Nhu, Kris Beking, et al.
The Canadian Journal of Cardiology|June 20, 2021
Development and Evaluation of Decision Aids to Guide Families' Predictive Testing Choices for Children at Risk for Arrhythmia or CardiomyopathySusan Christian, Alicia Welsh, Jeremy Yetman, et al.
European Journal of Medical Genetics|June 17, 2018
Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplicationYing Qiao, Hani Bagheri, Flamingo Tang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2008
A KCNQ1 V205M missense mutation causes a high rate of long QT syndrome in a First Nations community of northern British Columbia: a community-based approach to understanding the impactLaura Arbour, Saman Rezazadeh, Jodene Eldstrom, et al.
The Canadian Journal of Cardiology|June 19, 2022
A Call to Action: Optimizing Indigenous Cardiovascular Health in CanadaHaya Aziz, Miles Marchand, Cristina Pop, et al.
The Canadian Journal of Cardiology|December 18, 2025
Canadian Cardiovascular Society Clinical Practice Update on Cardiogenetic TestingMelanie Care, Laura Arbour, Liam R Brunham, et al.
Pageof 12

Showing results (61-70 of 118) with videos related to

Sort By:
Pageof 12
Molecular Genetics & Genomic Medicine|January 30, 2020
Cardiac arrest in a mother and daughter and the identification of a novel RYR2 variant, predisposing to low penetrant catecholaminergic polymorphic ventricular tachycardia in a four-generation Canadian familyMatthew Tung, Filip Van Petegem, Samantha Lauson, et al.
American Journal of Human Genetics|June 6, 2022
Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?Paul S Appelbaum, Wylie Burke, Erik Parens, et al.
Annual Review of Genomics and Human Genetics|March 21, 2019
Genomic Research Through an Indigenous Lens: Understanding the ExpectationsNanibaa' A Garrison, Māui Hudson, Leah L Ballantyne, et al.
The Canadian Journal of Cardiology|October 18, 2023
The Impact of Chronic Disease on the Corrected QT (QTc) Value in Women in a British Columbia First Nations PopulationMiles Marchand, Anders C Erickson, Lawrence Gillman, et al.
International Journal of Occupational and Environmental Health|September 13, 2011
Congenital anomalies in the offspring of nurses: association with area of employment during pregnancyHelen Dimich-Ward, D Le Nhu, Kris Beking, et al.
The Canadian Journal of Cardiology|June 20, 2021
Development and Evaluation of Decision Aids to Guide Families' Predictive Testing Choices for Children at Risk for Arrhythmia or CardiomyopathySusan Christian, Alicia Welsh, Jeremy Yetman, et al.
European Journal of Medical Genetics|June 17, 2018
Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplicationYing Qiao, Hani Bagheri, Flamingo Tang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2008
A KCNQ1 V205M missense mutation causes a high rate of long QT syndrome in a First Nations community of northern British Columbia: a community-based approach to understanding the impactLaura Arbour, Saman Rezazadeh, Jodene Eldstrom, et al.
The Canadian Journal of Cardiology|June 19, 2022
A Call to Action: Optimizing Indigenous Cardiovascular Health in CanadaHaya Aziz, Miles Marchand, Cristina Pop, et al.
The Canadian Journal of Cardiology|December 18, 2025
Canadian Cardiovascular Society Clinical Practice Update on Cardiogenetic TestingMelanie Care, Laura Arbour, Liam R Brunham, et al.
Pageof 12