We aimed to evaluate the association of rs964184 of BUD13-ZNF259 gene with the risk of
hemorrhagic stroke (HS). A total of 138 HS cases and 587 controls were recruited for the …

Background Ischemic stroke is one of the most common diseases with a high burden of
neurological deficits, disability and death. Zinc finger protein 208 (ZNF208) was found to be …

Background and Purpose—Genome-wide association studies found that the common allele
T of single nucleotide polymorphism rs11206510 on chromosome 1p32 was associated with …

Objectives-Stroke evolves depending on the accumulation of risk factors within the vessel
wall, which leads to atherosclerotic lesions. Vascular endothelial growth factor (VEGF) plays …

Background: Two single-nucleotide polymorphisms rs11833579 and rs12425791 located on
chromosome 12p13 were reported to be associated with ischemic stroke in Caucasians. In …

Background and Purpose—The first genomewide association study of ischemic stroke in
whites has identified multiple susceptibility loci. We confirmed this study by examining …

BACKGROUND: In 2009, a GWAS has confirmed that rs11833579 and rs12425791 near the
NINJ2 gene could increase the stroke and ischemic stroke (IS) risk. Recently, several …

Although genetic epidemiological studies have implicated several genetic variants as risk
factors for hemorrhagic stroke, the genetic determinants of this condition remain largely …

Background Large artery disease (LAD), cardioembolism (CE), and small vessel disease
(SVD) are well-established causes of ischemic stroke. Although a founder variant of RNF213 …

Genome-wide association studies (GWAS) have revealed two single-nucleotide
polymorphisms (SNPs) on chromosome 4q25, rs2200733, and rs6843082, associated with …