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Nature Communications|October 14, 2018
Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levelsAdrienne Tin, Yong Li, Jennifer A Brody, et al.JAMA Internal Medicine|January 28, 2022
APOL1 Risk Variants, Acute Kidney Injury, and Death in Participants With African Ancestry Hospitalized With COVID-19 From the Million Veteran ProgramAdriana M Hung, Shailja C Shah, Alexander G Bick, et al.Plos Genetics|April 28, 2022
A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran ProgramAnurag Verma, Noah L Tsao, Lauren O Thomann, et al.Nature Medicine|July 10, 2019
Genome-wide association study of peripheral artery disease in the Million Veteran ProgramDerek Klarin, Julie Lynch, Krishna Aragam, et al.Journal of the American Society of Nephrology : JASN|March 1, 2022
Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of UromodulinChristina B Joseph, Marta Mariniello, Ayumi Yoshifuji, et al.Human Molecular Genetics|May 13, 2022
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factorsNathan Pankratz, Peng Wei, Jennifer A Brody, et al.Circulation|July 25, 2019
Association of <i>APOL1</i> Risk Alleles With Cardiovascular Disease in Blacks in the Million Veteran ProgramAlexander G Bick, Elvis Akwo, Cassianne Robinson-Cohen, et al.Nature Communications|July 10, 2023
Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failureDanielle Rasooly, Gina M Peloso, Alexandre C Pereira, et al.Nature Genetics|November 3, 2019
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular diseaseDerek Klarin, Emma Busenkell, Renae Judy, et al.Diabetes|January 1, 2013
Mutations in HNF1A result in marked alterations of plasma glycan profileGaya Thanabalasingham, Jennifer E Huffman, Jayesh J Kattla, et al.Pageof 16