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Genetic Variants of TPCN2 Associated with Type 2 Diabetes Risk in the Chinese Population
CFI-rs7356506 polymorphisms associated with Vogt-Koyanagi-Harada syndrome
Associations of Plasma FGF2 Levels and Polymorphisms in the FGF2 Gene with Obesity Phenotypes in Han Chinese Population
Association of single nucleotide polymorphisms in UBR2 gene with idiopathic aspermia or oligospermia in Sichuan, China
Muscle strength is associated with vitamin D receptor gene variants
Associations of polymorphisms in circadian genes with abdominal obesity in Chinese adult population
PON1 as a model for integration of genetic, epigenetic, and expression data on candidate susceptibility genes
Attention Deficit/Hyperactivity Disorder and Urinary Nonylphenol Levels: A Case-Control Study in Taiwanese Children
Pigmentary Markers in Danes – Associations with Quantitative Skin Colour, Nevi Count, Familial Atypical Multiple-Mole, and Melanoma Syndrome
A genetic variation in microRNA target site of ETS2 is associated with clinical outcomes of paclitaxel-cisplatin chemotherapy in non-small cell lung cancer