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Crossing Borders: A Systematic Review with Quantitative Analysis of Genetic Mutations of Carcinomas of the Biliary Tract
HFE H63D Polymorphism and the Risk for Systemic Hypertension, Myocardial Remodeling, and Adverse Cardiovascular Events in the ARIC Study
Diabetes mellitus, genetic variants in the insulin‐like growth factor pathway and colorectal cancer risk
IRAK2 and TLR10 confer risk of Hashimoto’s disease: a genetic association study based on the Han Chinese population
Different Methylation of CpG-SNPs in Behcet’s Disease
Correlation of MCT1 and ABCC2 gene polymorphisms with valproic acid resistance in patients with epilepsy on valproic acid monotherapy
Association between DIO2 polymorphism and the risk of Kashin-beck disease in Tibetan
Silencing of tumor-suppressive NR_023387 in renal cell carcinoma via promoter hypermethylation and HNF4A deficiency
LPP and RYR2 Gene Polymorphisms Correlate with the Risk and the Prognosis of Astrocytoma
Development of a general logistic model for disease risk prediction using multiple SNPs