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Parathyroid Hormone Polymorphism RS6254 is Associated with the Development and Severity of Osteoporosis in Asymptomatic but not Normocalcemic Hyperthyroidism
Systemic klotho is associated with KLOTHOvariation and predicts intrinsic cortical connectivity in healthy human aging
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
New evidence for involvement of ESR1 gene in susceptibility to Chinese migraine
Variants in the CNR1 gene predispose to headache with nausea in the presence of life stress
Genetic analysis of innate immunity in Behcet’s disease identifies an association with IL-37 and IL-18RAP
Determinants of Neonatal Vitamin D Levels as Measured on Neonatal Dried Blood Spot Samples