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Genetic variants in GHR and PLCE1 genes are associated with susceptibility to esophageal cancer
Association Between Genetic Polymorphisms In TYMS And Glioma Risk In Chinese Patients: A Case-Control Study
A genetic association study of heart failure: more evidence for the role of BAG3 in idiopathic dilated cardiomyopathy
Association of apoptosis genes in PDCD1 but not PDCD1LG2, FAS, and FASLG with pediatric idiopathic uveitis in Han Chinese
A genetic variant in the promoter of CD46 is associated with the risk and prognosis of hepatocellular carcinoma
Intra-Patient Heterogeneity of Circulating Tumor Cells and Circulating Tumor DNA in Blood of Melanoma Patients
Polymorphisms of NF-κB pathway genes influence adverse drug reactions of gefitinib in NSCLC patients
Association of polymorphisms in LOC105377871 and CASC16 with Breast Cancer in the Northwest Chinese Han Population
DNA methylation of antisense noncoding RNA in the INK locus (ANRIL) is associated with coronary artery disease in a Chinese population
Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing.