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Medrxiv : the Preprint Server for Health Sciences|August 30, 2023
Rare damaging CCR2 variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Medrxiv : the Preprint Server for Health Sciences|May 5, 2025
Genome-wide association study and multi-ancestry meta-analysis identify common variants associated with carotid artery intima-media thicknessDevendra Meena, Jian Huang, Marjan Zare, et al.
Nature Communications|June 15, 2018
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetesViktoria Gusarova, Colm O'Dushlaine, Tanya M Teslovich, et al.
Nature Medicine|August 1, 2022
Large-scale genome-wide association study of coronary artery disease in genetically diverse populationsCatherine Tcheandjieu, Xiang Zhu, Austin T Hilliard, et al.
Genome Biology|September 9, 2025
Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individualsMargaret Sunitha Selvaraj, Xihao Li, Zilin Li, 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|October 16, 2023
Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic targetTanmoy Roychowdhury, Derek Klarin, Michael G Levin, et al.
Circulation|September 26, 2022
Cross-Ancestry Investigation of Venous Thromboembolism Genomic PredictorsFlorian Thibord, Derek Klarin, Jennifer A Brody, et al.
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