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A novel NR3C2 polymorphism and the increased thyroid-stimulating hormone concentration are associated with venlafaxine treatment outcome in Chinese Han MDD patients
S-Adenosylmethionine (SAMe) monotherapy for depression: an 8-week double-blind, randomised, controlled trial
Association of BDNF, HTR2A, TPH1, SLC6A4, and COMT polymorphisms with tDCS and escitalopram efficacy: ancillary analysis of a double-blind, placebo-controlled trial
Relationship between URAT1 Gene Polymorphism and Uric Acid-Lowering Effect of Losartan in Hypertensive Patients with Hyperuricemia
The presence of two reduced function variants in CYP2C9 influences the acute response to glipizide
Genetic Variants in DNA Mismatch Repair Pathway predict prognosis of Lung Cancer patients with receiving Platinum-Based Chemotherapy
Development and analytical validation of a 29 gene clinical pharmacogenetic genotyping panel: Multi‐ethnic allele and copy number variant detection
Genetic associations of docetaxel‐based chemotherapy‐induced myelosuppression in Chinese Han population
Genetic variation of pharmacogenomic VIP variants in Zhuang nationality of southern China
Kava for generalised anxiety disorder: A 16-week double-blind, randomised, placebo-controlled study
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