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Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Genome sequencing of 35,024 predominantly African ancestry persons addresses gaps in genomics and healthcareCecile Avery, Mojgan Babanejad, James Baker, et al.Nature Communications|April 22, 2024
Clinical associations with a polygenic predisposition to benign lower white blood cell countsJonathan D Mosley, John P Shelley, Alyson L Dickson, et al.Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count geneticsJonathan D Mosley, John P Shelley, Alyson L Dickson, et al.Thrombosis and Haemostasis|December 22, 2011
Pharmacogenetic warfarin dose refinements remain significantly influenced by genetic factors after one week of therapyBenjamin D Horne, Petra A Lenzini, Mia Wadelius, et al.Circulation|April 29, 2018
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving StatinsWei-Qi Wei, Xiaohui Li, Qiping Feng, et al.NPJ Genomic Medicine|February 19, 2019
A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLRMaya S Safarova, Benjamin A Satterfield, Xiao Fan, et al.Nature Communications|September 1, 2018
A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkersJonathan D Mosley, QiPing Feng, Quinn S Wells, et al.Medrxiv : the Preprint Server for Health Sciences|July 17, 2026
Mapping Genetic Susceptibility to Urinary Tract Infection from Kidney Papilla to BladderKatherine Xu, Atlas Khan, Ning Shang, et al.Pageof 28