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Showing results (721-730 of 750) with videos related to

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Nature Aging|June 4, 2024
Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rateTaralynn M Mack, Michael A Raddatz, Yash Pershad, et al.
Circulation|December 21, 2021
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing StudyAndrew M Glazer, Giovanni Davogustto, Christian M Shaffer, et al.
JAMA|December 12, 2018
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial FibrillationSeung Hoan Choi, Lu-Chen Weng, Carolina Roselli, et al.
JAMA Cardiology|February 12, 2025
Arrhythmic Risk Stratification of Carriers of Filamin C Truncating Variants, Marta Gigli, Davide Stolfo, et al.
Circulation|January 17, 2020
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic ConditionJason D Roberts, S Yukiko Asaki, Andrea Mazzanti, et al.
Circulation. Genomic and Precision Medicine|May 28, 2024
Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular ArrhythmiasLu-Chen Weng, Shaan Khurshid, Amelia Weber Hall, et al.
Nature Communications|October 3, 2024
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with heightGareth Hawkes, Robin N Beaumont, Zilin Li, et al.
Scientific Reports|September 14, 2017
Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen ConsortiumLu-Chen Weng, Kathryn L Lunetta, Martina Müller-Nurasyid, et al.
Nature Genetics|January 2, 2025
The impact of common and rare genetic variants on bradyarrhythmia developmentLu-Chen Weng, Joel T Rämö, Sean J Jurgens, et al.
Research Square|May 18, 2026
Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillationSean Jurgens, Nobuyuki Enzan, Ian Dinsmore, et al.
Pageof 75

Showing results (721-730 of 750) with videos related to

Sort By:
Pageof 75
Nature Aging|June 4, 2024
Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rateTaralynn M Mack, Michael A Raddatz, Yash Pershad, et al.
Circulation|December 21, 2021
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing StudyAndrew M Glazer, Giovanni Davogustto, Christian M Shaffer, et al.
JAMA|December 12, 2018
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial FibrillationSeung Hoan Choi, Lu-Chen Weng, Carolina Roselli, et al.
JAMA Cardiology|February 12, 2025
Arrhythmic Risk Stratification of Carriers of Filamin C Truncating Variants, Marta Gigli, Davide Stolfo, et al.
Circulation|January 17, 2020
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic ConditionJason D Roberts, S Yukiko Asaki, Andrea Mazzanti, et al.
Circulation. Genomic and Precision Medicine|May 28, 2024
Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular ArrhythmiasLu-Chen Weng, Shaan Khurshid, Amelia Weber Hall, et al.
Nature Communications|October 3, 2024
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with heightGareth Hawkes, Robin N Beaumont, Zilin Li, et al.
Scientific Reports|September 14, 2017
Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen ConsortiumLu-Chen Weng, Kathryn L Lunetta, Martina Müller-Nurasyid, et al.
Nature Genetics|January 2, 2025
The impact of common and rare genetic variants on bradyarrhythmia developmentLu-Chen Weng, Joel T Rämö, Sean J Jurgens, et al.
Research Square|May 18, 2026
Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillationSean Jurgens, Nobuyuki Enzan, Ian Dinsmore, et al.
Pageof 75