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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.
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.
Circulation
|
October 11, 2024
A Rare Noncoding Enhancer Variant in <i>SCN5A</i> Contributes to the High Prevalence of Brugada Syndrome in Thailand
Roddy Walsh, John Mauleekoonphairoj, Isabella Mengarelli, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 15, 2021
Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
Doris Škorić-Milosavljević, Najim Lahrouchi, Fernanda M Bosada, et al.
Science Translational Medicine
|
January 16, 2015
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease
Angharad M Roberts, James S Ware, Daniel S Herman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 11, 2021
Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
Doris Škorić-Milosavljević, Najim Lahrouchi, Fernanda M Bosada, et al.
Circulation. Genomic and Precision Medicine
|
August 21, 2020
Genetic Studies of Hypertrophic Cardiomyopathy in Singaporeans Identify Variants in <i>TNNI3</i> and <i>TNNT2</i> That Are Common in Chinese Patients
Chee Jian Pua, Nevin Tham, Calvin W L Chin, et al.
Circulation
|
April 17, 2019
Genetic Variants Associated With Cancer Therapy-Induced Cardiomyopathy
Pablo Garcia-Pavia, Yuri Kim, Maria Alejandra Restrepo-Cordoba, et al.
Research Square
|
February 6, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies
Daria Kramarenko, Poeya Haydarlou, George Powell, et al.
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Search research articles
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Showing results (71-80 of 89) with videos related to
Sort By:
Page
of 9
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.
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.
Circulation
|
October 11, 2024
A Rare Noncoding Enhancer Variant in <i>SCN5A</i> Contributes to the High Prevalence of Brugada Syndrome in Thailand
Roddy Walsh, John Mauleekoonphairoj, Isabella Mengarelli, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 15, 2021
Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
Doris Škorić-Milosavljević, Najim Lahrouchi, Fernanda M Bosada, et al.
Science Translational Medicine
|
January 16, 2015
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease
Angharad M Roberts, James S Ware, Daniel S Herman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 11, 2021
Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
Doris Škorić-Milosavljević, Najim Lahrouchi, Fernanda M Bosada, et al.
Circulation. Genomic and Precision Medicine
|
August 21, 2020
Genetic Studies of Hypertrophic Cardiomyopathy in Singaporeans Identify Variants in <i>TNNI3</i> and <i>TNNT2</i> That Are Common in Chinese Patients
Chee Jian Pua, Nevin Tham, Calvin W L Chin, et al.
Circulation
|
April 17, 2019
Genetic Variants Associated With Cancer Therapy-Induced Cardiomyopathy
Pablo Garcia-Pavia, Yuri Kim, Maria Alejandra Restrepo-Cordoba, et al.
Research Square
|
February 6, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies
Daria Kramarenko, Poeya Haydarlou, George Powell, et al.
Page
of 9