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Nature Communications|October 11, 2022
Whole genome sequence analysis of blood lipid levels in >66,000 individualsMargaret Sunitha Selvaraj, Xihao Li, Zilin Li, et al.Circulation. Genomic and Precision Medicine|June 7, 2018
ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT IntervalsNathan A Bihlmeyer, Jennifer A Brody, Albert Vernon Smith, 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.Circulation. Genomic and Precision Medicine|May 12, 2018
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR IntervalHonghuang Lin, Jessica van Setten, Albert V Smith, et al.Circulation|May 21, 2020
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT SyndromeNajim Lahrouchi, Rafik Tadros, Lia Crotti, et al.Nature Communications|December 19, 2020
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular diseaseJonas B Nielsen, Oren Rom, Ida Surakka, 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|April 29, 2021
COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targetsToni M Delorey, Carly G K Ziegler, Graham Heimberg, et al.Nature Communications|April 13, 2021
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indicesPradeep Natarajan, Akhil Pampana, Sarah E Graham, 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.Pageof 52