Genetics of common, complex coronary artery disease

K Musunuru, S Kathiresan - Cell, 2019 - cell.com
Coronary artery disease represents the leading cause of death worldwide, sparing no
nation, ethnicity, or economic stratum. Coronary artery disease is partly heritable. While …

[HTML][HTML] Genomics of blood pressure and hypertension: extending the mosaic theory toward stratification

S Lip, S Padmanabhan - Canadian Journal of Cardiology, 2020 - Elsevier
The genetic architecture of blood pressure (BP) now includes more than 30 genes, with rare
mutations resulting in inherited forms of hypertension or hypotension, and 1477 common …

Chromosome 1q21. 2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction

J Saw, ML Yang, M Trinder, C Tcheandjieu… - Nature …, 2020 - nature.com
Spontaneous coronary artery dissection (SCAD) is a non-atherosclerotic cause of
myocardial infarction (MI), typically in young women. We undertook a genome-wide …

Insights from complex trait fine-mapping across diverse populations

M Kanai, JC Ulirsch, J Karjalainen, M Kurki… - medrxiv, 2021 - medrxiv.org
Despite the great success of genome-wide association studies (GWAS) in identifying genetic
loci significantly associated with diseases, the vast majority of causal variants underlying …

Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

A Georges, ML Yang, TE Berrandou, MK Bakker… - Nature …, 2021 - nature.com
Fibromuscular dysplasia (FMD) is an arteriopathy associated with hypertension, stroke and
myocardial infarction, affecting mostly women. We report results from the first genome-wide …

Identification of susceptibility loci for spontaneous coronary artery dissection

TN Turley, MM O'Byrne, ML Kosel… - JAMA …, 2020 - jamanetwork.com
Importance Spontaneous coronary artery dissection (SCAD), an idiopathic disorder that
predominantly affects young to middle-aged women, has emerged as an important cause of …

Migraine, stroke, and cervical arterial dissection: shared genetics for a triad of brain disorders with vascular involvement

I Daghlas, M Sargurupremraj, R Danning… - Neurology …, 2022 - AAN Enterprises
Background and Objectives Migraine, stroke, and cervical artery dissection (CeAD)
represent a triad of cerebrovascular disorders with pairwise comorbid relationships and …

Deficiency of macrophage PHACTR1 impairs efferocytosis and promotes atherosclerotic plaque necrosis

C Kasikara, M Schilperoort, B Gerlach… - The Journal of …, 2021 - Am Soc Clin Investig
Efferocytosis, the process through which apoptotic cells (ACs) are cleared through actin-
mediated engulfment by macrophages, prevents secondary necrosis, suppresses …

Genetic Association Analyses Highlight IL6, ALPL, and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis

S Thériault, C Dina, D Messika-Zeitoun… - Circulation: Genomic …, 2019 - Am Heart Assoc
Background: Calcific aortic valve stenosis (CAVS) is a frequent and life-threatening
cardiovascular disease for which there is currently no medical treatment available. To date …

FMD and SCAD: sex-biased arterial diseases with clinical and genetic pleiotropy

ESH Kim, J Saw, D Kadian-Dodov, M Wood… - Circulation …, 2021 - Am Heart Assoc
Multifocal fibromuscular dysplasia (FMD) and spontaneous coronary artery dissection are
both sex-biased diseases disproportionately affecting women over men in a 9: 1 ratio …