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Novel blood-based hypomethylation of SH3BP5 is associated with very early-stage lung adenocarcinoma
Whole-exome sequencing reveals novel candidate single nucleotide variations for preventing adverse effects of levonorgestrel implantation
Association of Melanoma-Risk Variants with Primary Melanoma Tumor Prognostic Characteristics and Melanoma-Specific Survival in the GEM Study
Genetic polymorphisms in the PCNXL2 gene are risk factors for thyroid cancer in the Chinese population
GABAA subunit single nucleotide polymorphisms show sex-specific association to alcohol consumption and mental distress in a Norwegian population-based sample
MTHFR polymorphism in patients with epilepsy in eastern Turkey
Prenatal exposure to polycyclic aromatic hydrocarbons could increase the risk of low birth weight by affecting the DNA methylation states in a Chinese cohort
NLRP3-Inflammasome Gene Variations in the Risk of Type 2 Diabetes
The genetic susceptibility profile of type 2 diabetes and reflection of its possible role related to reproductive dysfunctions in the southern Indian population of Hyderabad
Inadequate design of mutation detection panels prevents interpretation of variants of concern: results of an external quality assessment for SARS-CoV-2 variant detection