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M Benjamin Shoemaker

Showing results (91-100 of 116) with videos related to

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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.
Science Advances|May 1, 2023
The genetic determinants of recurrent somatic mutations in 43,693 blood genomesJoshua S Weinstock, Cecelia A Laurie, Jai G Broome, et al.
Nature Genetics|March 6, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation riskSeung Hoan Choi, Sean J Jurgens, Ling Xiao, et al.
Nature Communications|May 24, 2024
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genesRebecca Keener, Surya B Chhetri, Carla J Connelly, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controlsRoddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
Pageof 12

Showing results (91-100 of 116) with videos related to

Sort By:
Pageof 12
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.
Science Advances|May 1, 2023
The genetic determinants of recurrent somatic mutations in 43,693 blood genomesJoshua S Weinstock, Cecelia A Laurie, Jai G Broome, et al.
Nature Genetics|March 6, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation riskSeung Hoan Choi, Sean J Jurgens, Ling Xiao, et al.
Nature Communications|May 24, 2024
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genesRebecca Keener, Surya B Chhetri, Carla J Connelly, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controlsRoddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
Pageof 12