Showing results (311-320 of 417) with videos related to

Sort By:
Pageof 42
Nature Genetics|July 27, 2010
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 21, 2011
An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
Frontiers in Genetics|February 21, 2022
Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic LociTiffany R Bellomo, William P Bone, Brian Y Chen, et al.
Bioorganic & Medicinal Chemistry|November 20, 2019
Synthesis and evaluation of 2'-dihalo ribonucleotide prodrugs with activity against hepatitis C virusA Chris Krueger, Hui-Ju Chen, John T Randolph, et al.
Plos Genetics|August 20, 2011
Pervasive sharing of genetic effects in autoimmune diseaseChris Cotsapas, Benjamin F Voight, Elizabeth Rossin, et al.
Diabetologia|May 12, 2023
Genetically proxied glucose-lowering drug target perturbation and risk of cancer: a Mendelian randomisation analysisJames Yarmolinsky, Emmanouil Bouras, Andrei Constantinescu, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Unravelling the molecular mechanisms causal to type 2 diabetes across global populations and disease-relevant tissuesOzvan Bocher, Ana Luiza Arruda, Satoshi Yoshiji, et al.
Journal of the American College of Cardiology|July 16, 2011
Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarctionDiego Ardissino, Carlo Berzuini, Piera Angelica Merlini, et al.
Atherosclerosis|June 16, 2015
Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease riskHenning Jansen, Christina Loley, Wolfgang Lieb, et al.
Pageof 42