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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
Complement factor H and LOC387715/ARMS2/HTRA1 variant’s frequencies and phenotypic associations in neovascular age-related macular degeneration, a pilot study
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
SLC1A2 rs3794087 are associated with susceptibility to Parkinson’s disease, but not essential tremor, amyotrophic lateral sclerosis or multiple system atrophy in a Chinese population