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Stroke genetics informs drug discovery and risk prediction across ancestries
Association of common genetic variants with brain microbleeds
Heritable and non-heritable uncommon causes of stroke (vol 15, pg 961, 2020)
Heritable and non-heritable uncommon causes of stroke
Monogenic cerebral small-vessel diseases
The effect of NOTCH3 pathogenic variant position on CADASIL disease severity: NOTCH3 EGFr 1-6 pathogenic variants are associated with a more severe phenotype and lower survival compared with EGFr 7-34 pathogenic variants
Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting
Vascular dysfunction
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
APOE 2 is associated with white matter hyperintensity volume in CADASIL
Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants
Polygenic Overlap Between Kidney Function and Large Artery Atherosclerotic Stroke
Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12
Genome-Wide Genotyping Demonstrates a Polygenic Risk Score Associated With White Matter Hyperintensity Volume in CADASIL
Multiethnic Meta-Analysis of Genome-Wide Association Studies in > 100 000 Subjects Identifies 23 FibrinogenAssociated Loci but No Strong Evidence of a Causal Association Between Circulating Fibrinogen and Cardiovascular Disease
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies