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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 2, 2023
Benefits, harms, and costs of newborn genetic screening for hypertrophic cardiomyopathy: Estimates from the PreEMPT model
Kurt D Christensen, Pamela M McMahon, Lauren N Galbraith, et al.
Circulation. Genomic and Precision Medicine
|
March 29, 2019
Phenotypic Characterization of Individuals With Variants in Cardiovascular Genes in the Absence of a Primary Cardiovascular Indication for Testing
Robyn J Hylind, Stephanie F Chandler, Virginie Beausejour Ladouceur, et al.
Circulation
|
June 4, 2019
Gene Therapy for Catecholaminergic Polymorphic Ventricular Tachycardia by Inhibition of Ca<sup>2+</sup>/Calmodulin-Dependent Kinase II
Vassilios J Bezzerides, Ana Caballero, Suya Wang, et al.
Circulation. Genomic and Precision Medicine
|
May 10, 2022
Population Prevalence of Premature Truncating Variants in Plakophilin-2 and Association With Arrhythmogenic Right Ventricular Cardiomyopathy: A UK Biobank Analysis
Robyn J Hylind, Alexandre C Pereira, Daniel Quiat, et al.
Journal of the American Heart Association
|
May 12, 2020
Clinical and Genetic Findings in Children Presenting With Ventricular Fibrillation as the First Manifestation of Cardiovascular Disease
Robyn J Hylind, Stephanie F Chandler, Virginie Beausejour Ladouceur, et al.
Journal of the American College of Cardiology
|
July 20, 2019
Phenotypic Manifestations of Arrhythmogenic Cardiomyopathy in Children and Adolescents
Elizabeth S DeWitt, Stephanie F Chandler, Robyn J Hylind, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 19, 2025
Cardiovascular genetic counseling is associated with improved patient-reported outcomes across clinical indications and settings
Brittney Murray, Catherine Gordon, Susan Christian, et al.
European Heart Journal
|
July 16, 2024
A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriers
Richard T Carrick, Alessio Gasperetti, Alexandros Protonotarios, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 2, 2023
Benefits, harms, and costs of newborn genetic screening for hypertrophic cardiomyopathy: Estimates from the PreEMPT model
Kurt D Christensen, Pamela M McMahon, Lauren N Galbraith, et al.
Circulation. Genomic and Precision Medicine
|
March 29, 2019
Phenotypic Characterization of Individuals With Variants in Cardiovascular Genes in the Absence of a Primary Cardiovascular Indication for Testing
Robyn J Hylind, Stephanie F Chandler, Virginie Beausejour Ladouceur, et al.
Circulation
|
June 4, 2019
Gene Therapy for Catecholaminergic Polymorphic Ventricular Tachycardia by Inhibition of Ca<sup>2+</sup>/Calmodulin-Dependent Kinase II
Vassilios J Bezzerides, Ana Caballero, Suya Wang, et al.
Circulation. Genomic and Precision Medicine
|
May 10, 2022
Population Prevalence of Premature Truncating Variants in Plakophilin-2 and Association With Arrhythmogenic Right Ventricular Cardiomyopathy: A UK Biobank Analysis
Robyn J Hylind, Alexandre C Pereira, Daniel Quiat, et al.
Journal of the American Heart Association
|
May 12, 2020
Clinical and Genetic Findings in Children Presenting With Ventricular Fibrillation as the First Manifestation of Cardiovascular Disease
Robyn J Hylind, Stephanie F Chandler, Virginie Beausejour Ladouceur, et al.
Journal of the American College of Cardiology
|
July 20, 2019
Phenotypic Manifestations of Arrhythmogenic Cardiomyopathy in Children and Adolescents
Elizabeth S DeWitt, Stephanie F Chandler, Robyn J Hylind, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 19, 2025
Cardiovascular genetic counseling is associated with improved patient-reported outcomes across clinical indications and settings
Brittney Murray, Catherine Gordon, Susan Christian, et al.
European Heart Journal
|
July 16, 2024
A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriers
Richard T Carrick, Alessio Gasperetti, Alexandros Protonotarios, et al.
Page
of 2