Pharmacogenomics in Clinical Care and Drug Discovery

Author:

Mendrinou E.,Katsila T.,Innocenti F.,Squassina A.,Patrinos G.P.

Publisher

Elsevier

Reference184 articles.

1. Merging pharmacometabolomics with pharmacogenomics using ‘1000 Genomes’ single-nucleotide polymorphism imputation: selective serotonin reuptake inhibitor response pharmacogenomics;Abo;Pharmacogenet. Genomics,2012

2. Frequency of common CYP3A5 gene variants in healthy Polish newborn infants;Adler;Pharmacol. Rep.,2009

3. Pre-authorisation Evaluation of Medicines for Human Use. 2008;Agency,2007

4. Association of polymorphisms in the cytochrome P450 CYP2C9 with warfarin dose requirement and risk of bleeding complications;Aithal;Lancet,1999

5. Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese;Akaba;Biochem. Mol. Biol. Int.,1998

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