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COMT by DRD3 Epistatic Interaction in Modulating Behaviors in Children with ADHD: A Pharmaco-Dynamic Behavioral Approach
The Effect of Common Variants in SLC44A2 on the Contribution to the Risk of Deep Cein Thrombosis after Orthopedic Surgery
The genetic risk for hypertension is lower among the Hungarian Roma population compared to the general population
The association between Single Nucleotide Polymorphisms of Klotho Gene and Mortality in Elderly Men: The MrOS Sweden Study
Epigenetic silencing of AATK in acinar to ductal metaplasia in murine model of pancreatic cancer
Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome
Associations between IFI44L gene variants and rates of respiratory tract infections during early childhood
Genomic and signalling pathway characterisation of the NZM panel of melanoma cell lines: a valuable model for studying the impact of genetic diversity in melanoma
Assessing vitamin D related genetic variants, status, and influence factors in pregnant women in Eastern and Central China
Association of genetic variants in lncRNA GAS5/miR‐21/mTOR axis with risk and prognosis of coronary artery disease among a Chinese population