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CFI-rs7356506 polymorphisms associated with Vogt-Koyanagi-Harada syndrome
Forensic and population genetic characteristics of 62 X chromosome SNPs revealed by multiplex PCR and MALDI-TOF mass spectrometry genotyping in 4 North Eurasian populations
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
DNA methylation in PRDM8 is indicative for dyskeratosis congenita
PON1 as a model for integration of genetic, epigenetic, and expression data on candidate susceptibility genes
A genetic variation in microRNA target site of ETS2 is associated with clinical outcomes of paclitaxel-cisplatin chemotherapy in non-small cell lung cancer
Attention Deficit/Hyperactivity Disorder and Urinary Nonylphenol Levels: A Case-Control Study in Taiwanese Children