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RNASEL 1623A> C variant is associated with the risk of prostate cancer in African descendants
Association of IRS1 genetic variants with glucose control and insulin resistance in type 2 diabetic patients from Bosnia and Herzegovina
Identification of novel susceptibility genes associated with seven autoimmune disorders using whole genome molecular interaction networks
Genetic polymorphisms in IL1B predict susceptibility to steroid-induced osteonecrosis of the femoral head in Chinese Han population
Mutations of ARX and non-syndromic intellectual disability in Chinese population
UNC13A variant rs12608932 is associated with increased risk of amyotrophic lateral sclerosis and reduced patient survival: a meta-analysis
Association of PTTG1 polymorphism rs1895320, rs2910200 and rs6882742 with non-functioning pituitary adenomas in Chinese Han population: a case-control study
Synergistic triad epistasis of epigenetic H3K27me modifier genes, EZH2, KDM6A, and KDM6B, in gastric cancer susceptibility
Interaction between interferon regulatory factor 6 and glycine receptor beta shows a protective effect on developing nonsyndromic cleft lip with or without cleft palate in the Han Chinese population
The association between bone mineral density gene variants and osteocalcin at baseline, and in response to exercise: The Gene SMART study