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

Lack of association between variations of PDE4D and ischemic 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

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

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

Functional SNP of ARHGEF10 confers risk of atherothrombotic stroke

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

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

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

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

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

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese

Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population

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