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Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility
RNASEL 1623A> C variant is associated with the risk of prostate cancer in African descendants
Gemcitabine induces Epithelial-to-Mesenchymal Transition in patient-derived pancreatic ductal adenocarcinoma xenografts
Association of IRS1 genetic variants with glucose control and insulin resistance in type 2 diabetic patients from Bosnia and Herzegovina
Mutations of ARX and non-syndromic intellectual disability in Chinese population
Identification of novel susceptibility genes associated with seven autoimmune disorders using whole genome molecular interaction networks
Whole-blood DNA Methylation Markers for Risk Stratification in Colorectal Cancer Screening: A Systematic Review
Genetic polymorphisms in IL1B predict susceptibility to steroid-induced osteonecrosis of the femoral head in Chinese Han population
UNC13A variant rs12608932 is associated with increased risk of amyotrophic lateral sclerosis and reduced patient survival: a meta-analysis
Development of SNP for the deep-sea fish blue ling, Molva dypterygia (Pennant, 1784) from ddRAD sequencing data