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A circadian rhythm-related MTNR1B genetic variant (rs10830963) modulate body weight change and insulin resistance after 9 months of a high protein/low carbohydrate vs a standard hypocaloric diet
HLA-G+ 3196 polymorphism as a risk factor for cell mediated rejection following heart transplant
The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1,-2 and-3 and Is Associated with Risk for Multiple Sclerosis
Genetic Variations of CYP19A1 Gene and Stroke Susceptibility: A Case-control Study in the Chinese Han Population
A functional variant in CHK1 contributes to increased risk of nasopharyngeal carcinoma in a Han Chinese population
Structural and functional alterations of Nitric Oxide Synthase 3 due to missense variants associate with High-Altitude Pulmonary Edema through Dynamic study
Effects of the dopamine transporter gene on striatal functional connectivity in youths with attention-deficit/hyperactivity disorder
Genotyping of T2D Susceptible Genes in a High Risk North-East Indian Population
Interactions among variants in P53 apoptotic pathway genes are associated with neurologic deterioration and functional outcome after acute ischemic stroke
Associations between period 3 gene polymorphisms and sleep-/chronotype-related variables in patients with late-life insomnia