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Predictive clinical‐genetic model of long‐term non‐response to tumor necrosis factor‐alpha inhibitor therapy in spondyloarthritis
Effects of TCF7L2 rs7903146 variant on metformin response in patients with type 2 diabetes
The A/A Genotype of XPO1 rs4430924 Is Associated With Higher Risk of Antituberculosis Drug‐Induced Hepatotoxicity in Chinese Patients
Possible association of HMOX1 and NQO1 polymorphisms with anti‐tuberculosis drug‐induced liver injury: A matched case‐control study
Precision therapy of 6‐mercaptopurine in Chinese children with acute lymphoblastic leukemia
Association of SCN1A, SCN2A, and UGT2B7 Polymorphisms with Responsiveness to Valproic Acid in the Treatment of Epilepsy
CYP3A4 and CYP11A1 variants are risk factors for ischemic stroke: a case control study.
A missense variant in complement factor B (CFB) is a potential predictor of 24‐week off‐treatment response to PegIFNα therapy in Chinese HBeAg‐positive chronic hepatitis B patients
Genetic influence of ABCG2, UGT1A1 and NR1I2 on dolutegravir plasma pharmacokinetics
Model‐based assessment of variability in isoniazid pharmacokinetics and metabolism in patients co‐infected with tuberculosis and HIV: implications for a novel dosing strategy