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Atherosclerosis|October 18, 2017
Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisationRona J Strawbridge, Angela Silveira, Marcel den Hoed, et al.
Circulation. Genomic and Precision Medicine|December 15, 2020
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes MellitusNatalie R van Zuydam, Claes Ladenvall, Benjamin F Voight, et al.
Circulation. Cardiovascular Genetics|November 16, 2012
Identification of the BCAR1-CFDP1-TMEM170A locus as a determinant of carotid intima-media thickness and coronary artery disease riskKarl Gertow, Bengt Sennblad, Rona J Strawbridge, et al.
Obesity Reviews : an Official Journal of the International Association for the Study of Obesity|March 11, 2015
Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adultsE Zimmermann, L H Ängquist, S S Mirza, et al.
Human Molecular Genetics|July 29, 2016
Analysis with the exome array identifies multiple new independent variants in lipid lociStavroula Kanoni, Nicholas G D Masca, Kathleen E Stirrups, et al.
Medrxiv : the Preprint Server for Health Sciences|April 14, 2021
Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19Lucija Klaric, Jack S Gisby, Artemis Papadaki, et al.
American Journal of Human Genetics|January 24, 2023
Loci for insulin processing and secretion provide insight into type 2 diabetes riskK Alaine Broadaway, Xianyong Yin, Alice Williamson, et al.
Circulation|May 3, 2017
Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking InteractionsDanish Saleheen, Wei Zhao, Robin Young, et al.
Blood|June 25, 2015
Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFJennifer E Huffman, Paul S de Vries, Alanna C Morrison, et al.
Journal of the American College of Cardiology|August 18, 2012
Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolismAnna Helgadottir, Solveig Gretarsdottir, Gudmar Thorleifsson, et al.
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