[HTML][HTML] Recommendations for the management and treatment of dyslipidemia: Report of the Working Group on Hypercholesterolemia and Other Dyslipidemias

JG Fodor, JJ Frohlich, JJG Genest, PR McPherson - Cmaj, 2000 - Can Med Assoc
The following measures were recommended by the Working Group on Hypercholesterolemia
and Other Dyslipidemias in light of the new scientific evidence that became available since …

Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants

…, JF Meschia, S Kathiresan, MA Ikram, R McPherson… - Stroke, 2014 - Am Heart Assoc
Background and Purpose— Ischemic stroke (IS) and coronary artery disease (CAD) share
several risk factors and each has a substantial heritability. We conducted a genome-wide …

[PDF][PDF] Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

…, M Li, DJ Rader, MP Reilly, R McPherson… - The American Journal of …, 2014 - cell.com
Low-frequency coding DNA sequence variants in the proprotein convertase subtilisin/kexin
type 9 gene (PCSK9) lower plasma low-density lipoprotein cholesterol (LDL-C), protect …

[HTML][HTML] Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study

…, J Danesh, S Blankenberg, R Roberts, R McPherson… - The Lancet, 2012 - thelancet.com
Background High plasma HDL cholesterol is associated with reduced risk of myocardial
infarction, but whether this association is causal is unclear. Exploiting the fact that genotypes are …

[HTML][HTML] A Genome-Wide Association Study Reveals Variants in ARL15 that Influence Adiponectin Levels

…, T Pastinen, NJ Samani, R McPherson… - PLoS …, 2009 - journals.plos.org
The adipocyte-derived protein adiponectin is highly heritable and inversely associated with
risk of type 2 diabetes mellitus (T2D) and coronary heart disease (CHD). We meta-analyzed …

[HTML][HTML] A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

…, JG Wilson, H Schunkert, R McPherson… - PLoS …, 2020 - journals.plos.org
Analyzing 12,361 all-cause cirrhosis cases and 790,095 controls from eight cohorts, we
identify a common missense variant in the Mitochondrial Amidoxime Reducing Component 1 …

2021 Canadian Cardiovascular Society guidelines for the management of dyslipidemia for the prevention of cardiovascular disease in adults

…, E Lonn, GBJ Mancini, P Manjoo, R McPherson… - Canadian journal of …, 2021 - Elsevier
The 2021 guidelines primary panel selected clinically relevant questions and produced
updated recommendations, on the basis of important new findings that have emerged since the …

Low copy number of the salivary amylase gene predisposes to obesity

…, CJ Hammond, P Deloukas, PC Sham, R McPherson… - Nature …, 2014 - nature.com
Common multi-allelic copy number variants (CNVs) appear enriched for phenotypic associations
compared to their biallelic counterparts 1 , 2 , 3 , 4 . Here we investigated the influence …

[HTML][HTML] LDL-cholesterol concentrations: a genome-wide association study

…, P Barter, YA Kesäniemi, RW Mahley, R McPherson… - The Lancet, 2008 - thelancet.com
Background LDL cholesterol has a causal role in the development of cardiovascular disease.
Improved understanding of the biological mechanisms that underlie the metabolism and …

Gene dosage of the common variant 9p21 predicts severity of coronary artery disease

…, YQ Wang, M Labinaz, GA Wells, R McPherson… - Journal of the American …, 2010 - jacc.org
Objectives : The purpose of this study was to test the hypothesis that 9p21 gene dosage
determines the severity of coronary artery disease (CAD). Background : The 9p21 locus is the …