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Bronchopulmonary dysplasia and wnt pathway-associated single nucleotide polymorphisms
Cell competition is driven by Xrp1-mediated phosphorylation of eukaryotic initiation factor 2α
Pharmacogenomic Single Nucleotide Polymorphism (SNP) Variants As Predictors of Toxicity Phenotypes in the Treatment of Acute Childhood Leukemia
Associations of MCM8 rs3761873 and rs16991617 variants with abnormal uterine bleeding induced by copper intrauterine device
Association of Renalase Genetic Variants With Longitudinal Blood Pressure Changes and Incidence of Hypertension
Assessment of the effectiveness of the EUROFORGEN NAME and Precision ID Ancestry panel markers for ancestry investigations
UMOD Polymorphisms Associated with Kidney Function, Serum Uromodulin and Risk of Mortality among Patients with Chronic Kidney Disease, Results from the C-STRIDE Study
Salicylic Acid and Risk of Colorectal Cancer: A Two-Sample Mendelian Randomization Study
Exploring the relation between high-activity COMT Val158Met genotype and psychopathy in male offenders
Evaluation of an ancestry prediction strategy for historical military remains using a World War II-era sample and pedigrees with family-level admixture
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