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Circulation Research|May 17, 2017
Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart DiseaseAkihiro Nomura, Hong-Hee Won, Amit V Khera, et al.Nature Genetics|October 31, 2017
Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery diseaseXiangfeng Lu, Gina M Peloso, Dajiang J Liu, et al.Annals of Neurology|October 8, 2016
Genetic variants in CETP increase risk of intracerebral hemorrhageChristopher D Anderson, Guido J Falcone, Chia-Ling Phuah, et al.Nature Genetics|December 23, 2022
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studiesXihao Li, Corbin Quick, Hufeng Zhou, et al.Nature Genetics|October 31, 2017
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biologyManuel A Ferreira, Judith M Vonk, Hansjörg Baurecht, et al.Nature Genetics|August 26, 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scaleXihao Li, Zilin Li, Hufeng Zhou, et al.Nature Methods|October 27, 2022
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studiesZilin Li, Xihao Li, Hufeng Zhou, et al.Nature Genetics|November 17, 2020
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factorsMark K Bakker, Rick A A van der Spek, Wouter van Rheenen, et al.The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, 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.Pageof 20