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Prolactin gene polymorphism (?1149 G/T) is associated with hyperprolactinemia in patients with schizophrenia treated with antipsychotics
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration
Exome-chip association analysis reveals an Asian-specific missense variant in PAX4 associated with type 2 diabetes in Chinese individuals
Association of rs11643718 SLC12A3 and rs741301 ELMO1Variants with Diabetic Nephropathy in South Indian Population
Association of FKBP5 polymorphisms and resting-state activity in a frontotemporal–parietal network
Evaluation of the Obesity Genes FTO and MC4R for Contribution to the Risk of Large Artery Atherosclerotic Stroke in a Chinese Population
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