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Association of LAG3 genetic variation with an increased risk of PD in Chinese female population.
Association Study of Coronary Artery Disease-Associated Genome-Wide Significant SNPs with Coronary Stenosis in Pakistani Population
Combining newborn metabolic and genetic screening for neonatal intrahepatic cholestasis caused by citrin deficiency
PPARG Pro12Ala Polymorphism with CKD in Asians: A Meta-Analysis Combined with a Case-Control Study—A Key for Reaching Null Association
LRCH1 polymorphisms linked to delayed encephalopathy after acute carbon monoxide poisoning identified by GWAS analysis followed by Sequenom MassARRAY® validation
Lower S-adenosylmethionine Levels and DNA Hypomethylation of Placental Growth Factor (PlGF) in Placental Tissue of Early-Onset Preeclampsia-Complicated Pregnancies
UVB induces cutaneous squamous cell carcinoma progression by de novo ID4 methylation via methylation regulating enzymes
Characteristics of Head and Neck Squamous Cell Carcinoma Cell Lines Reflect Human Tumor Biology Independent of Primary Etiologies and HPV Status
Pri‐miR‐144 rs9279 is associated with type 2 diabetes and regulation of stress response
ATP-sensitive potassium channels gene polymorphism rs1799858 affects the risk of macro-/micro-vascular arteriosclerotic event in patients with increased low-density lipoprotein cholesterol levels.