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rs217727 of lncRNA H19 is Associated with Cervical Cancer Risk in the Chinese Han Population
Polymorphisms of IFN signaling genes and FOXP4 influence the severity of COVID-19
Fine mapping of qBK1.2, a major QTL governing resistance to bakanae disease in rice
Gene mutations and clinical manifestations of alpha-1 antitrypsin deficiency in Czech patients – a pilot study
Effects of dietary PUFA patterns and FADS genotype on breast milk PUFAs in Chinese lactating mothers
Genetic polymorphisms of GGT1 gene (rs8135987, rs5751901 and rs2017869) are associated with neoadjuvant chemotherapy efficacy and toxicities in breast cancer patients
Loss of fragile WWOX gene leads to senescence escape and genome instability
Hyper-Methylation of CpG Island in 5′ UTR of the HLA-G Gene Reduces Its Expression in Individuals with Immune Thrombocytopenia
Contrast Enhanced CT Radiogenomics in a Retrospective NSCLC Cohort: Models, Attempted Validation of a Published Model and the Relevance of the Clinical Context
Impact of Cytochrome P450 Genetic Variation on Patient-Reported Symptom Improvement and Side Effects Among Children and Adolescents Treated with Fluoxetine