Published Erratum
doi: 10.1038/npjgenmed.2016.39.
eCollection 2017.
Erratum: Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences
- PMID: 29266105
- PMCID: PMC5685321
- DOI: 10.1038/npjgenmed.2016.39
Item in Clipboard
Published Erratum
Erratum: Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences
NPJ Genom Med.
.
Abstract
[This corrects the article DOI: 10.1038/npjgenmed.2015.7.].
Erratum for
-
Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences.NPJ Genom Med. 2016 Jan 13;1:15007. doi: 10.1038/npjgenmed.2015.7. eCollection 2016. NPJ Genom Med. 2016. PMID: 29263805 Free PMC article.
Similar articles
-
Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences.NPJ Genom Med. 2016 Jan 13;1:15007. doi: 10.1038/npjgenmed.2015.7. eCollection 2016. NPJ Genom Med. 2016. PMID: 29263805 Free PMC article.
-
Erratum: A de novo 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotype.NPJ Genom Med. 2017 Aug 25;2:17001. doi: 10.1038/npjgenmed.2017.1. eCollection 2017. NPJ Genom Med. 2017. PMID: 29263847 Free PMC article.
-
Challenges in CYP2D6 phenotype assignment from genotype data: a critical assessment and call for standardization.Curr Drug Metab. 2014 Feb;15(2):218-32. doi: 10.2174/1389200215666140202215316. Curr Drug Metab. 2014. PMID: 24524666 Review.
-
Erratum.Sci Technol Adv Mater. 2016 Apr 19;17(1):188. doi: 10.1080/14686996.2016.1176342. eCollection 2016. Sci Technol Adv Mater. 2016. PMID: 27889790 Free PMC article.
-
Cytochrome P450 2D6 and Parkinson's Disease: Polymorphism, Metabolic Role, Risk and Protection.Neurochem Res. 2017 Dec;42(12):3353-3361. doi: 10.1007/s11064-017-2384-8. Epub 2017 Sep 4. Neurochem Res. 2017. PMID: 28871472 Review.
Cited by
-
The Identification of Novel CYP2D6 Variants in US Hmong: Results From Genome Sequencing and Clinical Genotyping.Front Pharmacol. 2022 Mar 21;13:867331. doi: 10.3389/fphar.2022.867331. eCollection 2022. Front Pharmacol. 2022. PMID: 35387332 Free PMC article.
-
Applying Next-Generation Sequencing Platforms for Pharmacogenomic Testing in Clinical Practice.Front Pharmacol. 2021 Aug 25;12:693453. doi: 10.3389/fphar.2021.693453. eCollection 2021. Front Pharmacol. 2021. PMID: 34512329 Free PMC article. Review.
-
Determination of the Duplicated CYP2D6 Allele Using Real-Time PCR Signal: An Alternative Approach.J Pers Med. 2023 May 24;13(6):883. doi: 10.3390/jpm13060883. J Pers Med. 2023. PMID: 37373874 Free PMC article.
-
Pediatric CYP2D6 metabolizer status and post-tonsillectomy nausea and vomiting after ondansetron.Clin Transl Sci. 2023 Feb;16(2):269-278. doi: 10.1111/cts.13447. Epub 2022 Nov 25. Clin Transl Sci. 2023. PMID: 36350309 Free PMC article.
-
Impact of SLCO1B1 Genetic Variation on Rosuvastatin Systemic Exposure in Pediatric Hypercholesterolemia.Clin Transl Sci. 2020 May;13(3):628-637. doi: 10.1111/cts.12749. Epub 2020 Mar 9. Clin Transl Sci. 2020. PMID: 31981411 Free PMC article.
Publication types
LinkOut - more resources
Full Text Sources
Other Literature Sources
