Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction

Predictive Utility of a Coronary Artery Disease Polygenic Risk Score in Primary Prevention

Genome-Wide Association Study of Intracranial Artery Stenosis Followed by Phenome-Wide Association Study

Genome-wide Association Studies Categorized by Class of Antihypertensive Drugs Reveal Complex Pathogenesis of Hypertension with Drug Resistance

Genetic Risk Score of Cerebral Infarction in Atrial Fibrillation Genome-Wide Association Study

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

Stroke genetics informs drug discovery and risk prediction across ancestries

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

Genetic analysis of right heart structure and function in 40,000 people

A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study

Genome-wide risk prediction of common diseases across ancestries in one million people

A genome-wide association study identifies a novel candidate locus at the DLGAP1 gene with susceptibility to resistant hypertension in the Japanese population

Genome-wide analysis identifies novel susceptibility loci for myocardial infarction

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease

Transethnic Meta-Analysis of Genome-Wide Association Studies Identifies Three New Loci and Characterizes Population-Specific Differences for Coronary Artery Disease

Genetically Determined Levels of Circulating Cytokines and Risk of Stroke

A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation

Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study

Moyamoya Disease Susceptibility Variant RNF213 p.R4810K Increases the Risk of Ischemic Stroke Attributable to Large-Artery Atherosclerosis

Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke

Identification of LEF1 as a Susceptibility Locus for Kawasaki Disease in Patients Younger than 6 Months of Age

Multi-ethnic genome-wide association study for atrial fibrillation

Blood lipid-related low-frequency variants in LDLR and PCSK9 are associated with onset age and risk of myocardial infarction in Japanese

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Genetic Variants of RAMP2 and CLR are Associated with Stroke

A genome-wide association analysis identifies NMNAT2 and HCP5 as susceptibility loci for Kawasaki disease

Genetic Variants Associated With Uncontrolled Blood Pressure on Thiazide Diuretic/β-Blocker Combination Therapy in the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) and INVEST (International Verapamil-SR Trandolapril Study) Trials

Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease

Identification of six new genetic loci associated with atrial fibrillation in the Japanese population

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

A functional SNP in FLT1 increases risk of coronary artery disease in a Japanese population

Meta-analysis identifies six new susceptibility loci for atrial fibrillation.

Machine learning reveals heterogeneous associations between environmental factors and cardiometabolic diseases across polygenic risk scores

Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA

SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population

Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese population

Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk

Functional SNP of ARHGEF10 confers risk of atherothrombotic stroke

Genome-wide association study of intracranial aneurysm identifies three new risk loci

Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population

Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population

Lack of association between variations of PDE4D and ischemic stroke in the Japanese population

A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction

RNF213 Variants, Vasospastic Angina, and Risk of Fatal Myocardial Infarction

A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese

Risk prediction models for mortality in patients with cardiovascular disease: The BioBank Japan project