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Circulation. Genomic and Precision Medicine
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April 21, 2025
Clinical Validity of Autosomal Dominant <i>ALPK3</i> Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy
Sophie Hespe, Emma S Singer, Chloe Reuter, et al.
Circulation
|
June 22, 2026
Correction to: The Natural History of Massive Left Ventricular Hypertrophy in Pediatric Hypertrophic Cardiomyopathy: A Multiregistry Analysis
Robert Przybylski, Gabrielle Norrish, Brian Claggett, et al.
Circulation
|
September 26, 2022
Genetic Architecture of Acute Myocarditis and the Overlap With Inherited Cardiomyopathy
Amrit S Lota, Mark R Hazebroek, Pantazis Theotokis, et al.
Nature Medicine
|
May 29, 2020
The effect of LRRK2 loss-of-function variants in humans
Nicola Whiffin, Irina M Armean, Aaron Kleinman, et al.
Science (New York, N.Y.)
|
January 20, 2016
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies
Jason Homsy, Samir Zaidi, Yufeng Shen, et al.
Nature Genetics
|
November 22, 2016
Titin-truncating variants affect heart function in disease cohorts and the general population
Sebastian Schafer, Antonio de Marvao, Eleonora Adami, et al.
Journal of the American College of Cardiology
|
July 30, 2025
Sex Differences in the Genetic Causes of Dilated Cardiomyopathy
Massimo Mangino, Kathryn A McGurk, Pantazis Theotokis, et al.
JACC. Advances
|
June 28, 2024
Long-Term Arrhythmic Follow-Up and Risk Stratification of Patients With Desmoplakin-Associated Arrhythmogenic Right Ventricular Cardiomyopathy
Alessio Gasperetti, Richard Carrick, Alexandros Protonotarios, 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 Registry
Sophie L V M Stroeks, Nicole K Bart, Joseph Rossano, et al.
Nature Genetics
|
February 18, 2025
Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings
Sean L Zheng, Sean J Jurgens, Kathryn A McGurk, et al.
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of 73
Search research articles
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Showing results (681-690 of 721) with videos related to
Sort By:
Page
of 73
Circulation. Genomic and Precision Medicine
|
April 21, 2025
Clinical Validity of Autosomal Dominant <i>ALPK3</i> Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy
Sophie Hespe, Emma S Singer, Chloe Reuter, et al.
Circulation
|
June 22, 2026
Correction to: The Natural History of Massive Left Ventricular Hypertrophy in Pediatric Hypertrophic Cardiomyopathy: A Multiregistry Analysis
Robert Przybylski, Gabrielle Norrish, Brian Claggett, et al.
Circulation
|
September 26, 2022
Genetic Architecture of Acute Myocarditis and the Overlap With Inherited Cardiomyopathy
Amrit S Lota, Mark R Hazebroek, Pantazis Theotokis, et al.
Nature Medicine
|
May 29, 2020
The effect of LRRK2 loss-of-function variants in humans
Nicola Whiffin, Irina M Armean, Aaron Kleinman, et al.
Science (New York, N.Y.)
|
January 20, 2016
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies
Jason Homsy, Samir Zaidi, Yufeng Shen, et al.
Nature Genetics
|
November 22, 2016
Titin-truncating variants affect heart function in disease cohorts and the general population
Sebastian Schafer, Antonio de Marvao, Eleonora Adami, et al.
Journal of the American College of Cardiology
|
July 30, 2025
Sex Differences in the Genetic Causes of Dilated Cardiomyopathy
Massimo Mangino, Kathryn A McGurk, Pantazis Theotokis, et al.
JACC. Advances
|
June 28, 2024
Long-Term Arrhythmic Follow-Up and Risk Stratification of Patients With Desmoplakin-Associated Arrhythmogenic Right Ventricular Cardiomyopathy
Alessio Gasperetti, Richard Carrick, Alexandros Protonotarios, 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 Registry
Sophie L V M Stroeks, Nicole K Bart, Joseph Rossano, et al.
Nature Genetics
|
February 18, 2025
Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings
Sean L Zheng, Sean J Jurgens, Kathryn A McGurk, et al.
Page
of 73