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BST1 rs4698412 allelic variant increases the risk of gait or balance deficits in patients with Parkinson’s disease
Childhood sleep duration modifies the polygenic risk for obesity in youth through leptin pathway: the Beijing Child and Adolescent Metabolic Syndrome cohort study
Comprehensive analysis of HPV infection, EGFR exon 20 mutations and LINE1 hypomethylation as risk factors for malignant transformation of sinonasal‐inverted papilloma to squamous cell carcinoma
Role of ectopically expressed mtDNA encoded cytochrome c oxidase subunit I (MT-COI) in tumorigenesis
Exhaled breath condensate biomarkers for lung cancer
The association between interleukin-1 polymorphisms and their protein expression in Chinese Han patients with breast cancer
Profiling of aberrant DNA methylation in acute myeloid leukemia reveals subclasses of CG-rich regions with epigenetic or genetic association
Relationship of common variants in CHRNA5 with early-onset schizophrenia and executive function
Single nucleotide polymorphism in the 3′ untranslated region of LPP is a risk factor for lung cancer: a case-control study
Development of nuclear and plastid SNP markers for genetic studies of Dipteryx tree species in Amazonia