Aleksi Tornio
aleksi.tornio@utu.fi +358 29 450 4608 +358 50 476 5715 Kiinamyllynkatu 10 Turku ORCID identifier: https://orcid.org/0000-0001-5713-5692 |
Areas of expertise
Clinical Pharmacology; Pharmacokinetics; Drug-drug interactions; Pharmacogenetics
Clinical Pharmacology; Pharmacokinetics; Drug-drug interactions; Pharmacogenetics
Publications
- CYP3A4*22 Impairs the Elimination of Ticagrelor, But Has No Significant Effect on the Bioactivation of Clopidogrel or Prasugrel (2019)
- Clinical Pharmacology and Therapeutics
(A1 Refereed original research article in a scientific journal) - Enantiospecific Pharmacogenomics of Fluvastatin (2019)
- Clinical Pharmacology and Therapeutics
(A1 Refereed original research article in a scientific journal) - Farmakogenetiikan merkitys lääkehoidolle (2019) Lääketieteellinen farmakologia ja toksikologia Mikko Niemi, Miia Turpeinen, Aleksi Tornio
(D2 Article in a professional compilation book) - Farmakokinetiikkaan vaikuttavat perintötekijät (2019) Lääketieteellinen farmakologia ja toksikologia Mikko Niemi, Miia Turpeinen, Aleksi Tornio
(D2 Article in a professional compilation book) - Itraconazole Increases Ibrutinib Exposure 10-Fold and Reduces Interindividual Variation-A Potentially Beneficial Drug-Drug Interaction (2019)
- Clinical and Translational Science
(A1 Refereed original research article in a scientific journal) - (2019) Lääketieteellinen farmakologia ja toksikologia Mikko Niemi, Miia Turpeinen, Aleksi Tornio
(D2 Article in a professional compilation book) - Response to "Interaction of Dasabuvir With Clopidogrel: Did Predictions by Physiologically Based Pharmacokinetics Modeling Pass the Test?" (2019) Itkonen MK, Tornio A, Lapatto-Reiniluoto O, Neuvonen M, Neuvonen PJ, Niemi M, Backman JT
(Other publication) - Clopidogrel but Not Prasugrel Significantly Inhibits the CYP2C8-Mediated Metabolism of Montelukast in Humans (2018)
- Clinical Pharmacology and Therapeutics
(A1 Refereed original research article in a scientific journal) - Clopidogrel Carboxylic Acid Glucuronidation is Mediated Mainly by UGT2B7, UGT2B4, and UGT2B17: Implications for Pharmacogenetics and Drug-Drug Interactions (2018)
- Drug Metabolism and DispositionClinical Pharmacology and Therapeutics
(A1 Refereed original research article in a scientific journal) - Comprehensive Pharmacogenomic Study Reveals an Important Role of UGT1A3 in Montelukast Pharmacokinetics (2018)
(A1 Refereed original research article in a scientific journal)



