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Nature Genetics|April 8, 2025
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.Circulation|July 25, 2019
Association of APOL1 Risk Alleles With Cardiovascular Disease in Blacks in the Million Veteran ProgramAlexander G Bick, Elvis Akwo, Cassianne Robinson-Cohen, et al.Cardiovascular Diabetology|January 28, 2014
Residual macrovascular risk in 2013: what have we learned?Jean-Charles Fruchart, Jean Davignon, Michel P Hermans, et al.Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.Biorxiv : the Preprint Server for Biology|February 17, 2023
Prior vaccination enhances immune responses during SARS-CoV-2 breakthrough infection with early activation of memory T cells followed by production of potent neutralizing antibodiesMark M Painter, Timothy S Johnston, Kendall A Lundgreen, et al.Journal of the American Heart Association|April 29, 2023
Contemporary Homozygous Familial Hypercholesterolemia in the United States: Insights From the CASCADE FH RegistryMarina Cuchel, Paul C Lee, Lisa C Hudgins, 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.Circulation. Cardiovascular Genetics|October 7, 2010
Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controlsMichael Preuss, Inke R König, John R Thompson, et al.Journal of the American College of Cardiology|December 24, 2016
Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) LevelsConnor A Emdin, Amit V Khera, Pradeep Natarajan, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|September 28, 2013
Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemiaNathan O Stitziel, Sigrid W Fouchier, Barbara Sjouke, et al.Pageof 75