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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
Association of common variants in MTAP with susceptibility and overall survival of osteosarcoma: a two-stage population-based study in Han Chinese
The obesity associated FTO gene variant and the risk of adverse pregnancy outcomes: Evidence from the SCOPE study
MMP-2 gene polymorphisms are associated with type A aortic dissection and aortic diameters in patients
Methylome analysis for spina bifida shows SOX18 hypomethylation as a risk factor with evidence for a complex (epi)genetic interplay to affect neural tube development