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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.
BMC Genomics|February 20, 2022
Rare coding variants in RCN3 are associated with blood pressureKaren Y He, Tanika N Kelly, Heming Wang, et al.
American Journal of Human Genetics|October 6, 2023
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing studyYuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, et al.
Diabetes|August 26, 2017
A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 DiabetesJosep M Mercader, Rachel G Liao, Avery D Bell, et al.
American Journal of Human Genetics|April 22, 2021
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed programYao Hu, Adrienne M Stilp, Caitlin P McHugh, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing StudyYuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, 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.
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