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Association of α-, β-, and γ–synuclein with diffuse Lewy body disease
Association of IL1A, IL1B, and TNF gene polymorphisms with chronic rhinosinusitis with and without nasal polyposis
Association of genetic variants in the neurotrophic receptor-encoding gene NTRK2 and a lifetime history of suicide attempts in depressed patients
Increased BDNF promoter methylation in the Wernicke area of suicide subjects
Association of STAT3 and TNFRSF1A with ankylosing spondylitis in Han Chinese
Variants in linkage disequilibrium with the gene cluster deletion are associated with susceptibility to psoriatic arthritis
rs5888 variant of SCARB1 gene is a possible susceptibility factor for age-related macular degeneration
Phosphatidylinositol-3-kinase and AKT1 mutations occur early in breast carcinoma.
PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with Type 2 Diabetes in a Chinese Population
A genetic variant of G6PC2 is associated with type 2 diabetes and fasting plasma glucose level in the Chinese population