Objective: Coronary heart disease (CHD) is the most common cause of death worldwide.
This study aimed to validate the association of the rs964184 polymorphism with the CHD …

Although genetic variants that affect susceptibility to coronary artery disease (CAD) have
been greatly known, a number of these single nucleotide polymorphisms (SNPs) remain to …

The single nucleotide polymorphisms (SNP s) in the BUD 13 homolog (BUD 13) and zinc
finger protein 259 (ZNF 259) genes have been associated with one or more serum lipid traits …

A single nucleotide polymorphism (rs4804611) in zinc finger protein 627 (ZNF627) gene has
been demonstrated to be associated with the susceptibility to myocardial infarction (MI), but …

Aim: Our aim was to investigate the association between single nucleotide polymorphisms
(SNPs) of vascular endothelial growth factor (VEGF) and coronary heart disease (CHD) …

Background: Hyperlipidemia is a major risk factor for coronary artery disease (CAD). As F-
box and WD repeat domain-containing 7 (FBXW7) gene is an important regulating factor for …

Coronary artery disease (CAD), a leading cause of death worldwide, has a complex etiology
comprising both traditional risk factors (type 2 diabetes, dyslipidemia, arterial hypertension …

This study was purposed to investigate the vWF gene A1381T polymorphism in patients with
coronary heart disease (CHD). A case-control study was designed, including 104 …

Objective To assess the association of rs216293 T/G and rs1063857 T/C polymorphisms of
von Willebrand factor (vWF) gene with the morbidity of coronary artery disease (CAD) and …

We performed this study to better elucidate the relationship between vascular endothelial
growth factor (VEGF) polymorphisms and coronary heart disease (CHD). Eligible articles …