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Swen, Jesse J, van der Wouden, Cathelijne H, Manson, Lisanne En, Abdullah-Koolmees, Heshu, Blagec, Kathrin, Blagus, Tanja, Böhringer, Stefan, Cambon-Thomsen, Anne, Cecchin, Erika, Cheung, Ka-Chun et al (show 32 more authors)
(2023)
A 12-gene pharmacogenetic panel to prevent adverse drug reactions: an open-label, multicentre, controlled, cluster-randomised crossover implementation study.
Lancet (London, England), 401 (10374).
pp. 347-356.
Dickens, David ORCID: 0000-0001-8295-0752, Rädisch, Steffen, Chiduza, George N ORCID: 0000-0003-1037-5749, Giannoudis, Athina ORCID: 0000-0002-7200-1497, Cross, Michael J ORCID: 0000-0002-5533-1232, Malik, Hassan, Schaeffeler, Elke, Sison-Young, Rowena L, Wilkinson, Emma L, Goldring, Christopher E et al (show 3 more authors)
(2018)
Cellular Uptake of the Atypical Antipsychotic Clozapine Is a Carrier-Mediated Process.
Molecular Pharmaceutics, 15 (8).
pp. 3557-3572.
van der Wouden, Cathelijne H, Bohringer, Stefan, Cecchin, Erika, Cheung, Ka-Chun, Lucia Davila-Fajardo, Cristina, Deneer, Vera HM, Dolzan, Vita, Ingelman-Sundberg, Magnus, Jonsson, Siv, Karlsson, Mats O et al (show 17 more authors)
(2020)
Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study.
Pharmacogenetics and Genomics, 30 (6).
pp. 131-144.
Chenoweth, Meghan J, Giacomini, Kathleen M, Pirmohamed, Munir ORCID: 0000-0002-7534-7266, Hill, Susan L, van Schaik, Ron HN, Schwab, Matthias, Shuldiner, Alan R, Relling, Mary V and Tyndale, Rachel F
(2020)
Global Pharmacogenomics Within Precision Medicine: Challenges and Opportunities.
CLINICAL PHARMACOLOGY & THERAPEUTICS, 107 (1).
pp. 57-61.
Neumann, Eva, Schreeck, Filippa, Herberg, Jethro, Aigrain, Evelyne Jacqz, Maitland-van der Zee, Anke H, Perez-Martinez, Antonio, Hawcutt, Daniel B ORCID: 0000-0002-8120-6507, Schaeffeler, Elke, Rane, Anders, de Wildt, Saskia N et al (show 1 more authors)
(2022)
How paediatric drug development and use could benefit from OMICs: A c4c expert group white paper.
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 88 (12).
pp. 5017-5033.
Wolking, Stefan, Moreau, Claudia, Nies, Anne T, Schaeffeler, Elke, McCormack, Mark, Auce, Pauls, Avbersek, Andreja, Becker, Felicitas, Krenn, Martin, Moller, Rikke S et al (show 21 more authors)
(2020)
Testing association of rare genetic variants with resistance to three common antiseizure medications.
EPILEPSIA, 61 (4).
pp. 657-666.