Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Victoria N Parikh

Showing results (51-60 of 69) with videos related to

Pageof 7
Sort By:
Circulation|April 17, 2026
The Natural History of Massive Left Ventricular Hypertrophy in Pediatric Hypertrophic Cardiomyopathy: A Multiregistry AnalysisRobert Przybylski, Gabrielle Norrish, Brian Claggett, et al.
Circulation|September 30, 2021
Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating VariantsMarta Gigli, Davide Stolfo, Sharon L Graw, et al.
Science (New York, N.Y.)|October 30, 2025
The functional landscape of coding variation in the familial hypercholesterolemia gene <i>LDLR</i>Daniel R Tabet, Atina G Coté, Megan C Lancaster, et al.
JACC. Heart Failure|July 18, 2025
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric StudyMaria Perotto, Alessia Paldino, Francesco Mazzarotto, et al.
Journal of the American College of Cardiology|May 20, 2026
Sex and Age Specific Genetic Risk Across the Dilated and Arrhythmogenic Cardiomyopathy Spectrum: Insights From the SHaRe RegistrySophie L V M Stroeks, Nicole K Bart, Joseph Rossano, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
The contribution of <i>RBM20</i> truncating variants to human cardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
Medrxiv : the Preprint Server for Health Sciences|August 9, 2020
High-throughput SARS-CoV-2 and host genome sequencing from single nasopharyngeal swabsJohn E Gorzynski, Hannah N De Jong, David Amar, et al.
JAMA Cardiology|April 8, 2026
RBM20 Truncating Variants and Human CardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
Circulation. Genomic and Precision Medicine|July 8, 2026
Variant Site-Specific Natural History of Titin-Induced Cardiomyopathy: An International Multicenter RegistryMaria Perotto, Cinzia Radesich, Alessia Paldino, et al.
Science Translational Medicine|January 10, 2024
Allele-specific control of rodent and human lncRNA KMT2E-AS1 promotes hypoxic endothelial pathology in pulmonary hypertensionYi-Yin Tai, Qiujun Yu, Ying Tang, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
Circulation|April 17, 2026
The Natural History of Massive Left Ventricular Hypertrophy in Pediatric Hypertrophic Cardiomyopathy: A Multiregistry AnalysisRobert Przybylski, Gabrielle Norrish, Brian Claggett, et al.
Circulation|September 30, 2021
Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating VariantsMarta Gigli, Davide Stolfo, Sharon L Graw, et al.
Science (New York, N.Y.)|October 30, 2025
The functional landscape of coding variation in the familial hypercholesterolemia gene <i>LDLR</i>Daniel R Tabet, Atina G Coté, Megan C Lancaster, et al.
JACC. Heart Failure|July 18, 2025
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric StudyMaria Perotto, Alessia Paldino, Francesco Mazzarotto, et al.
Journal of the American College of Cardiology|May 20, 2026
Sex and Age Specific Genetic Risk Across the Dilated and Arrhythmogenic Cardiomyopathy Spectrum: Insights From the SHaRe RegistrySophie L V M Stroeks, Nicole K Bart, Joseph Rossano, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
The contribution of <i>RBM20</i> truncating variants to human cardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
Medrxiv : the Preprint Server for Health Sciences|August 9, 2020
High-throughput SARS-CoV-2 and host genome sequencing from single nasopharyngeal swabsJohn E Gorzynski, Hannah N De Jong, David Amar, et al.
JAMA Cardiology|April 8, 2026
RBM20 Truncating Variants and Human CardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
Circulation. Genomic and Precision Medicine|July 8, 2026
Variant Site-Specific Natural History of Titin-Induced Cardiomyopathy: An International Multicenter RegistryMaria Perotto, Cinzia Radesich, Alessia Paldino, et al.
Science Translational Medicine|January 10, 2024
Allele-specific control of rodent and human lncRNA KMT2E-AS1 promotes hypoxic endothelial pathology in pulmonary hypertensionYi-Yin Tai, Qiujun Yu, Ying Tang, et al.
Pageof 7