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Stacey Knight

Showing results (101-110 of 113) with videos related to

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JHEP Reports : Innovation in Hepatology|August 18, 2025
Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma developmentJonas Ghouse, Helene Gellert-Kristensen, Colm J O'Rourke, et al.
Journal of Personalized Medicine|December 29, 2022
The Development of an Infrastructure to Facilitate the Use of Whole Genome Sequencing for Population HealthNephi A Walton, Brent Hafen, Sara Graceffo, et al.
Medrxiv : the Preprint Server for Health Sciences|September 26, 2025
The genetic architecture of fibromyalgia across 2.5 million individualsIsabel Kerrebijn, Gyda Bjornsdottir, Keon Arbabi, et al.
Annals of Internal Medicine|July 28, 2025
Social Determinants of Health and Risk for Long COVID in the U.S. RECOVER-Adult CohortCandace H Feldman, Leah Santacroce, Ingrid V Bassett, 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|March 26, 2025
Missense variants in FRS3 affect body mass index in populations of diverse ancestriesAndrea B Jonsdottir, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, 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.
Nature Genetics|December 19, 2025
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease predictionAeron M Small, Ta-Yu Yang, Shinsuke Itoh, 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.
Pageof 12

Showing results (101-110 of 113) with videos related to

Sort By:
Pageof 12
JHEP Reports : Innovation in Hepatology|August 18, 2025
Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma developmentJonas Ghouse, Helene Gellert-Kristensen, Colm J O'Rourke, et al.
Journal of Personalized Medicine|December 29, 2022
The Development of an Infrastructure to Facilitate the Use of Whole Genome Sequencing for Population HealthNephi A Walton, Brent Hafen, Sara Graceffo, et al.
Medrxiv : the Preprint Server for Health Sciences|September 26, 2025
The genetic architecture of fibromyalgia across 2.5 million individualsIsabel Kerrebijn, Gyda Bjornsdottir, Keon Arbabi, et al.
Annals of Internal Medicine|July 28, 2025
Social Determinants of Health and Risk for Long COVID in the U.S. RECOVER-Adult CohortCandace H Feldman, Leah Santacroce, Ingrid V Bassett, 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|March 26, 2025
Missense variants in FRS3 affect body mass index in populations of diverse ancestriesAndrea B Jonsdottir, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, 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.
Nature Genetics|December 19, 2025
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease predictionAeron M Small, Ta-Yu Yang, Shinsuke Itoh, 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.
Pageof 12