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Parathyroid Hormone Polymorphism RS6254 is Associated with the Development and Severity of Osteoporosis in Asymptomatic but not Normocalcemic Hyperthyroidism
TLR1 polymorphism rs4833095 as a risk factor for IgA nephropathy in a Chinese Han population: A case-control study
Impact of Genetic Loci Identified in Genome-Wide Association Studies on Diabetic Retinopathy in Chinese Patients With Type 2 Diabetes
Association of Neuropeptide Y Gene rs16147 Polymorphism with Cardiovascular Risk Factors, Adipokines, and Metabolic Syndrome in Patients with Obesity
Genetic variants of PPAR-gamma coactivator 1B augment NLRP3-mediated inflammation in gouty arthritis
IL6-174G>C genetic polymorphism influences antidepressant treatment outcome
Nitric oxide of genetic variants is associated with alcohol-induced osteonecrosis risk of the femoral head in a Han population
GENETIC VARIATION IN THE ALPHA1B – ADRENERGIC RECEPTOR AND VASCULAR RESPONSE
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration
Genetic analysis of innate immunity in Behcet’s disease identifies an association with IL-37 and IL-18RAP