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JAMA|January 10, 2016
Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical RecordsSara L Van Driest, Quinn S Wells, Sarah Stallings, et al.European Heart Journal|October 30, 2025
Genetic evaluation of early-onset atrial fibrillation: impact on patient managementJ Lukas Laws, Mahsima Shabani, Hollie L Williams, et al.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.Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Systematic common and rare variant association testing in 392,030 whole genomes in All of UsWenhan Lu, Robert J Carroll, Matthew Solomonson, 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.Gastroenterology|April 21, 2016
Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association StudiesAmit D Joshi, Charlotte Andersson, Stephan Buch, et al.Nature Communications|September 27, 2023
Proteomic and genetic analyses of influenza A viruses identify pan-viral host targetsKelsey M Haas, Michael J McGregor, Mehdi Bouhaddou, et al.Medrxiv : the Preprint Server for Health Sciences|July 17, 2026
Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndromeAlex Lipov, Manon Baudic, Pierre Lindenbaum, et al.Pageof 54