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American Journal of Human Genetics|November 1, 2019
Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation LevelJingjing Liang, Brian E Cade, Karen Y He, et al.
Circulation. Genomic and Precision Medicine|June 9, 2020
Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid LevelsZhe Wang, Han Chen, Traci M Bartz, et al.
Nature Genetics|February 27, 2019
Biological and clinical insights from genetics of insomnia symptomsJacqueline M Lane, Samuel E Jones, Hassan S Dashti, et al.
Human Molecular Genetics|November 8, 2018
Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino AmericansHeming Wang, Brian E Cade, Tamar Sofer, et al.
Nature Communications|August 15, 2019
Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypesHeming Wang, Jacqueline M Lane, Samuel E Jones, et al.
American Journal of Respiratory Cell and Molecular Biology|October 28, 2017
Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in MenHan Chen, Brian E Cade, Kevin J Gleason, 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.
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