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Polymorphisms of microRNAs are associated with salt sensitivity in a Han Chinese population: the EpiSS study
Thyrotroph embryonic factor polymorphism predicts faster progression of Parkinson’s disease in a longitudinal study
Household mold exposure interacts with inflammation-related genetic variants on childhood asthma: a case-control study
Improving the Identification of Patients with a Genetic Diagnosis of Familial Hypercholesterolaemia in Primary Care; A Strategy to achieve the NHS Long Term Plan
Genetics of Iron Metabolism and Premenstrual Symptoms: A Mendelian Randomization Study
Association of the host genetic factors, hypercholesterolemia and diabetes with mild influenza in an Iranian population
Common variants in KCNK5 and FHL5 genes contributed to the susceptibility of migraine without aura in Han Chinese population
Downregulation of STAT3 enhanced chemokine expression and neutrophil recruitment in biliary atresia
Interaction between the STAT4 rs11889341(T) risk allele and smoking confers increased risk of myocardial infarction and nephritis in patients with systemic lupus erythematosus
A 3′ Untranslated Region Polymorphism of CTNNB1 (Rs2953) Alters MiR-3161 Binding and Affects the Risk of Ischemic Stroke and Coronary Artery Disease in Chinese Han Population