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Circulation|September 26, 2022
Cross-Ancestry Investigation of Venous Thromboembolism Genomic PredictorsFlorian Thibord, Derek Klarin, Jennifer A Brody, et al.
NPJ Aging and Mechanisms of Disease|July 20, 2017
Fine mapping the <i>CETP</i> region reveals a common intronic insertion associated to HDL-CElisabeth M van Leeuwen, Jennifer E Huffman, Joshua C Bis, et al.
The Lancet. Diabetes & Endocrinology|June 30, 2014
Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation studyKarani S Vimaleswaran, Alana Cavadino, Diane J Berry, et al.
Nature Genetics|May 30, 2018
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive errorMilly S Tedja, Robert Wojciechowski, Pirro G Hysi, 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.
American Journal of Human Genetics|February 11, 2014
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacksGina M Peloso, Paul L Auer, Joshua C Bis, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 1, 2014
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2Jie Huang, Jennifer E Huffman, Munekazu Yamakuchi, et al.
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