Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting

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dc.contributor.authorKalman, Lisa V.
dc.contributor.authorAgúndez, José A.G.
dc.contributor.authorAppell, Malin Lindqvist
dc.contributor.authorBell, Gillian C.
dc.contributor.authorBoukouvala, Sotiria
dc.contributor.authorBruckner, Carsten
dc.contributor.authorBruford, Elspeth
dc.contributor.authorBruckner, Carsten
dc.contributor.authorCaudle, Kelly
dc.contributor.authorCoulthard, Sally
dc.contributor.authorDaly, Ann K.
dc.contributor.authorDel Tredici, Johan T.
dc.contributor.authorDrozda, Katarzyna
dc.contributor.authorEverts, Robin
dc.contributor.authorFlockhart, David
dc.contributor.authorFreimuth, Robert
dc.contributor.authorGaedigk, Andrea
dc.contributor.authorHachad, Houda
dc.contributor.authorHartshorne, Toinette
dc.contributor.authorIngelman-Sundberg, Magnus
dc.contributor.authorKlein, Teri E.
dc.contributor.authorLauschke, Volker M.
dc.contributor.authorMaglott, Donna R.
dc.contributor.authorMcLeod, Howard L.
dc.contributor.authorMcMillin, Gwendolyn A.
dc.contributor.authorMeyer, Urs A.
dc.contributor.authorMüller, Daniel J.
dc.contributor.authorNickerson, Deborah A.
dc.contributor.authorOetting, William S.
dc.contributor.authorPacanowski, Michael
dc.contributor.authorPratt, Victoria M.
dc.contributor.authorRelling, Mary V.
dc.contributor.authorRoberts, Ali
dc.contributor.authorRubinstein, Wendy S.
dc.contributor.authorSangkuhl, Katrin
dc.contributor.authorSchwab, Matthias
dc.contributor.authorScott, Stuart A.
dc.contributor.authorSim, Sarah C.
dc.contributor.authorThirumaran, Ranjit K.
dc.contributor.authorToji, Lorraine H.
dc.contributor.authorTyndale, Rachel
dc.contributor.authorvan Schaik, Ron HN
dc.contributor.authorWhirl-Carrillo, Michelle
dc.contributor.authorYeo, Kiang-Teck J.
dc.contributor.authorZanger, Ulrich M.
dc.contributor.departmentDepartment of Medical & Molecular Genetics, IU School of Medicineen_US
dc.date.accessioned2017-06-19T19:01:13Z
dc.date.available2017-06-19T19:01:13Z
dc.date.issued2016-02
dc.description.abstractThis manuscript provides nomenclature recommendations developed by an international workgroup to increase transparency and standardization of pharmacogenetic (PGx) result reporting. Presently, sequence variants identified by PGx tests are described using different nomenclature systems. In addition, PGx analysis may detect different sets of variants for each gene, which can affect interpretation of results. This practice has caused confusion and may thereby impede the adoption of clinical PGx testing. Standardization is critical to move PGx forward.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationKalman, L. V., Agúndez, J. A. G., Appell, M. L., Black, J. L., Bell, G. C., Boukouvala, S., … Zanger, U. M. (2016). Pharmacogenetic Allele Nomenclature: International Workgroup Recommendations for Test Result Reporting. Clinical Pharmacology and Therapeutics, 99(2), 172–185. http://doi.org/10.1002/cpt.280en_US
dc.identifier.urihttps://hdl.handle.net/1805/13100
dc.language.isoen_USen_US
dc.publisherWileyen_US
dc.relation.isversionof10.1002/cpt.280en_US
dc.relation.journalClinical Pharmacology and Therapeuticsen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectPharmacogenetic PGx testingen_US
dc.subjectNomenclatureen_US
dc.subjectTest result reportingen_US
dc.subjectVariant descriptionen_US
dc.titlePharmacogenetic allele nomenclature: International workgroup recommendations for test result reportingen_US
dc.typeArticleen_US
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