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Biorxiv : the Preprint Server for Biology|June 3, 2024
Accelerating Genome- and Phenome-Wide Association Studies using GPUs - A case study using data from the Million Veteran ProgramAlex Rodriguez, Youngdae Kim, Tarak Nath Nandi, et al.Cell Metabolism|November 19, 2024
Human genetics identify convergent signals in mitochondrial LACTB-mediated lipid metabolism in cardiovascular-kidney-metabolic syndromeShen Li, Hongbo Liu, Hailong Hu, et al.Circulation. Genomic and Precision Medicine|February 10, 2022
Coronary Artery Disease Risk of Familial Hypercholesterolemia Genetic Variants Independent of Clinically Observed Longitudinal Cholesterol ExposureShoa L Clarke, Catherine Tcheandjieu, Austin T Hilliard, et al.Implementation Science Communications|December 2, 2024
A qualitative study of perceptions of the care pathway for familial hypercholesterolemia: screening, diagnosis, treatment, and family cascade screeningAmy R Pettit, Tamar Klaiman, Rebecca Connelly Kersting, et al.Cell Reports. Medicine|December 13, 2022
Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobankJoseph Park, Matthew T MacLean, Anastasia M Lucas, et al.Science Advances|November 7, 2019
Myeloid Tribbles 1 induces early atherosclerosis via enhanced foam cell expansionJessica M Johnston, Adrienn Angyal, Robert C Bauer, et al.Med (New York, N.Y.)|May 22, 2024
The common p.Ile291Val variant of ERLIN1 enhances TM6SF2 function and is associated with protection against MASLDMiriam Daphne Rendel, Cecilia Vitali, Kate Townsend Creasy, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|August 26, 2017
Lipoprotein(a) and Risk of Myocardial Infarction and Death in Chronic Kidney Disease: Findings From the CRIC Study (Chronic Renal Insufficiency Cohort)Archna Bajaj, Scott M Damrauer, Amanda H Anderson, et al.Plos Genetics|February 4, 2015
Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarctionAenne S Thormaehlen, Christian Schuberth, Hong-Hee Won, et al.Circulation. Genomic and Precision Medicine|April 1, 2026
Friend of GATA2 Variant Ser657Gly Is Associated With Coronary Microvascular DiseaseMarie A Guerraty, S Shefali Verma, Yi-An Ko, et al.Pageof 89