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Testing for the mediating role of endophenotypes using molecular genetic data in a twin study of ADHD traits
Analysis of receptor tyrosine kinase genetics identifies two novel risk loci in GAS6 and PROS1 in Behçet’s disease
Clinical Significance of Long Non-Coding RNA CASC8 rs10505477 Polymorphism in Lung Cancer Susceptibility, Platinum-Based Chemotherapy Response, and Toxicity
The Sp1-mediaded allelic regulation of MMP13 expression by an ESCC susceptibility SNP rs2252070
Association of single nucleotide polymorphism rs2076185 in chromosome 6P24.1 with premature coronary artery diseases in Chinese Han population
Genetic Variants of CD40 Gene Are Associated with Coronary Artery Disease and Blood Lipid Levels
Multicentric Genome-Wide Association Study for Primary Spontaneous Pneumothorax
Polymorphisms in the vascular endothelial growth factor (VEGF) gene associated with asthma
Genetic variation in WDR1 is associated with gout risk and gout-related metabolic indices in the Han Chinese population
NEDD4 single nucleotide polymorphism rs2271289 is associated with keloids in Chinese Han population