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Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting
Centre Disease Control and Prevent, GA USA.
University of Extremadura, Spain.
Linköpings universitet, Institutionen för medicin och hälsa, Avdelningen för läkemedelsforskning. Linköpings universitet, Medicinska fakulteten.ORCID-id: 0000-0002-2809-7591
Mayo Clin, MN USA.
Vise andre og tillknytning
2016 (engelsk)Inngår i: Clinical Pharmacology and Therapeutics, ISSN 0009-9236, E-ISSN 1532-6535, Vol. 99, nr 2, s. 172-185Artikkel i tidsskrift (Fagfellevurdert) Published
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Abstract [en]

This article 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.

sted, utgiver, år, opplag, sider
WILEY-BLACKWELL , 2016. Vol. 99, nr 2, s. 172-185
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URN: urn:nbn:se:liu:diva-125677DOI: 10.1002/cpt.280ISI: 000369533100020PubMedID: 26479518OAI: oai:DiVA.org:liu-125677DiVA, id: diva2:908356
Tilgjengelig fra: 2016-03-02 Laget: 2016-02-29 Sist oppdatert: 2017-11-30

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