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European Urology|October 29, 2021
Association of Inherited Mutations in DNA Repair Genes with Localized Prostate CancerDaniel J Lee, Ryan Hausler, Anh N Le, et al.
The Journal of Clinical Investigation|July 4, 2012
Hepatic sortilin regulates both apolipoprotein B secretion and LDL catabolismAlanna Strong, Qiurong Ding, Andrew C Edmondson, et al.
JCI Insight|July 8, 2021
Health care worker seromonitoring reveals complex relationships between common coronavirus antibodies and COVID-19 symptom durationSigrid Gouma, Madison E Weirick, Marcus J Bolton, et al.
Plos Genetics|January 10, 2020
Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseasesSylvia T Nurnberg, Marie A Guerraty, Robert C Wirka, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|August 8, 2016
Cholesterol efflux capacity of high-density lipoprotein correlates with survival and allograft vasculopathy in cardiac transplant recipientsAli Javaheri, Maria Molina, Payman Zamani, et al.
Medrxiv : the Preprint Server for Health Sciences|April 1, 2025
Trans-ancestry genome-wide association meta-analysis of gallstone diseaseJunghyun Lim, Marijana Vujkovic, Michael G Levin, et al.
The Journal of Clinical Investigation|March 17, 2009
Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humansAndrew C Edmondson, Robert J Brown, Sekar Kathiresan, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Mapping rare protein-coding variants on multi-organ imaging traitsYijun Fan, Jie Chen, Zirui Fan, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 15, 2021
Association Between Genetic Variation in Blood Pressure and Increased Lifetime Risk of Peripheral Artery DiseaseMichael G Levin, Derek Klarin, Venexia M Walker, et al.
Nature Communications|December 23, 2025
Mapping rare protein-coding variants on multi-organ imaging traitsYijun Fan, Jie Chen, Zirui Fan, et al.
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