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Showing results (701-710 of 721) with videos related to

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Circulation. Genomic and Precision Medicine|December 29, 2022
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (<i>DSP</i>) Truncating VariantEdgar T Hoorntje, Charlotte Burns, Luisa Marsili, et al.
European Heart Journal|September 17, 2024
Clinical features and outcomes in carriers of pathogenic desmoplakin variantsAlessio Gasperetti, Richard T Carrick, Alexandros Protonotarios, et al.
European Heart Journal|July 16, 2024
A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriersRichard T Carrick, Alessio Gasperetti, Alexandros Protonotarios, et al.
Circulation|August 20, 2025
Prognostic Role of Myocarditis-Like Episodes and Their Treatment in Patients With Pathogenic Desmoplakin VariantsAlessio Gasperetti, Steven A Muller, Giovanni Peretto, et al.
Medrxiv : the Preprint Server for Health Sciences|January 10, 2024
Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project dataValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.
Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathyRafik Tadros, Sean L Zheng, Christopher Grace, et al.
Nature Genetics|November 21, 2024
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilienceSean J Jurgens, Joel T Rämö, Daria R Kramarenko, et al.
Nature|May 29, 2020
The mutational constraint spectrum quantified from variation in 141,456 humansKonrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
Nature|February 4, 2021
Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humansKonrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
Nature|February 26, 2025
Rare disease gene association discovery in the 100,000 Genomes ProjectValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.
Pageof 73

Showing results (701-710 of 721) with videos related to

Sort By:
Pageof 73
Circulation. Genomic and Precision Medicine|December 29, 2022
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (<i>DSP</i>) Truncating VariantEdgar T Hoorntje, Charlotte Burns, Luisa Marsili, et al.
European Heart Journal|September 17, 2024
Clinical features and outcomes in carriers of pathogenic desmoplakin variantsAlessio Gasperetti, Richard T Carrick, Alexandros Protonotarios, et al.
European Heart Journal|July 16, 2024
A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriersRichard T Carrick, Alessio Gasperetti, Alexandros Protonotarios, et al.
Circulation|August 20, 2025
Prognostic Role of Myocarditis-Like Episodes and Their Treatment in Patients With Pathogenic Desmoplakin VariantsAlessio Gasperetti, Steven A Muller, Giovanni Peretto, et al.
Medrxiv : the Preprint Server for Health Sciences|January 10, 2024
Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project dataValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.
Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathyRafik Tadros, Sean L Zheng, Christopher Grace, et al.
Nature Genetics|November 21, 2024
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilienceSean J Jurgens, Joel T Rämö, Daria R Kramarenko, et al.
Nature|May 29, 2020
The mutational constraint spectrum quantified from variation in 141,456 humansKonrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
Nature|February 4, 2021
Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humansKonrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
Nature|February 26, 2025
Rare disease gene association discovery in the 100,000 Genomes ProjectValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.
Pageof 73