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The impact of genetic variations in the serotonergic system on symptom severity and clinical outcome in functional neurological disorders
Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
Association of MTHFR C677T, MTHFRA1298C and MTRRA66G gene polymorphisms with hyperhomocysteinemia and its modulation by the combined effect of vitamin B12 and folate in a hypertensive Chinese population
Effect and interaction of PINK1 genetic polymorphisms and environmental factors on blood pressure in COEs-exposed workers
CYP2C19 genotype and sodium channel blockers in lacosamide-treated children with epilepsy: two major determinants of trough lacosamide concentration or clinical response
Peripheral pathway gene variants in lifelong premature ejaculation: CYP19A1, CYP1A1, and CYP1A2 enzymes polymorphisms in Chinese Han men
Downregulated Expression and Hypermethylation of SIRT1 in Patients with Kashin-Beck Disease–Mediated Chondrocyte Apoptosis May Potentially Be Ameliorated by Selenium Supplement
Impact of Suppressor of Mothers Against Decapentaplegic (SMAD) 7 Gene Single Nucleotide Polymorphisms on Colorectal Cancer Risk and Prognosis
The Mediating Role of Abnormal ZEB1 Methylation in the Association between Nickel Exposure and Non-Syndromic Orofacial Cleft
Folate and cobalamin status, indicators, modulators, interactions and reference ranges from early pregnancy until birth: The Reus-Tarragona Birth Cohort Study