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Plos Genetics|June 2, 2022
A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran ProgramSridharan Raghavan, Jie Huang, Catherine Tcheandjieu, et al.
Lancet (London, England)|November 6, 2012
Efficacy and safety of a microsomal triglyceride transfer protein inhibitor in patients with homozygous familial hypercholesterolaemia: a single-arm, open-label, phase 3 studyMarina Cuchel, Emma A Meagher, Hendrik du Toit Theron, et al.
Kidney International|April 6, 2020
Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathwaysArchna Bajaj, Andrea Ihegword, Chengxiang Qiu, et al.
American Heart Journal|March 1, 2014
Rationale and design of the familial hypercholesterolemia foundation CAscade SCreening for Awareness and DEtection of Familial Hypercholesterolemia registryEmily C O'Brien, Matthew T Roe, Elizabeth S Fraulo, et al.
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.
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.
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