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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.Circulation|August 16, 2014
Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillationMoritz F Sinner, Nathan R Tucker, Kathryn L Lunetta, et al.Nature Genetics|March 8, 2022
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence dataPierrick Wainschtein, Deepti Jain, Zhili Zheng, 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.HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.Nature Genetics|February 23, 2010
Common variants in KCNN3 are associated with lone atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Nicole L Glazer, 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 Communications|March 15, 2023
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular diseaseWilliam J Young, Jeffrey Haessler, Jan-Walter Benjamins, et al.Diabetes|June 11, 2026
Colocalization of eQTLs With Type 2 Diabetes and Glycemic Traits Using Whole-Genome Sequences in Diverse Populations From the NHLBI Trans-Omics in Precision Medicine (TOPMed) ProgramNingyuan Wang, Daniel A DiCorpo, Yixin Zhang, et al.Pageof 18