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Nature Communications|October 15, 2020
Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participantsXutong Zhao, Dandi Qiao, Chaojie Yang, et al.Human Molecular Genetics|September 23, 2021
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiativeAmarise Little, Yao Hu, Quan Sun, 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.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.Medrxiv : the Preprint Server for Health Sciences|March 24, 2021
Collaborative Cohort of Cohorts for COVID-19 Research (C4R) Study: Study DesignElizabeth C Oelsner, Norrina Bai Allen, Tauqeer Ali, et al.Plos Genetics|December 24, 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populationsMadeline H Kowalski, Huijun Qian, Ziyi Hou, et al.American Journal of Epidemiology|March 13, 2022
Collaborative Cohort of Cohorts for COVID-19 Research (C4R) Study: Study DesignElizabeth C Oelsner, Akshaya Krishnaswamy, Pallavi P Balte, et al.Blood|September 20, 2012
Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulationJie Huang, Maria Sabater-Lleal, Folkert W Asselbergs, et al.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.Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.Pageof 51