(Q36240653)

English

CYP2D6 Haplotype Determination Using Long Range Allele-Specific Amplification: Resolution of a Complex Genotype and a Discordant Genotype Involving the CYP2D6*59 Allele

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

CYP2D6 Haplotype Determination Using Long Range Allele-Specific Amplification: Resolution of a Complex Genotype and a Discordant Genotype Involving the CYP2D6*59 Allele (English)

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

author name string

Andrea Gaedigk

1

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Amanda K Riffel

2

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

J Steven Leeder

3

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

publication date

31 August 2015

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

The Journal of Molecular Diagnostics

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

17

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

740-748

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2D6 and CYP2C19 Genotypes and Dosing of Selective Serotonin Reuptake Inhibitors

1 reference

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1 October 2017

SNP genotyping using TaqMan technology: the CYP2D6*17 assay conundrum.

1 reference

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1 October 2017

The potential utility of pharmacogenetic testing in psychiatry

1 reference

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1 October 2017

Challenges in CYP2D6 phenotype assignment from genotype data: a critical assessment and call for standardization

1 reference

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1 October 2017

Clinical Pharmacogenetics Implementation Consortium guidelines for cytochrome P450 2D6 genotype and codeine therapy: 2014 update.

1 reference

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1 October 2017

Towards the implementation of CYP2D6 and CYP2C19 genotypes in clinical practice: update and report from a pharmacogenetic service clinic

1 reference

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1 October 2017

Complexities of CYP2D6 gene analysis and interpretation

1 reference

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1 October 2017

Clinical Pharmacogenetics Implementation Consortium guideline for CYP2D6 and CYP2C19 genotypes and dosing of tricyclic antidepressants

1 reference

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1 October 2017

Cytochrome P450 enzymes in drug metabolism: regulation of gene expression, enzyme activities, and impact of genetic variation

1 reference

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1 October 2017

Pharmacogenomics of CYP2D6: molecular genetics, interethnic differences and clinical importance

1 reference

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1 October 2017

Polymorphism of human cytochrome P450 2D6 and its clinical significance: Part I.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

1 October 2017

Functional pharmacogenetics/genomics of human cytochromes P450 involved in drug biotransformation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

1 October 2017

A silent mutation (2939G>A, exon 6; CYP2D6*59) leading to impaired expression and function of CYP2D6.

1 reference

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1 October 2017

Identification and characterization of novel sequence variations in the cytochrome P4502D6 (CYP2D6) gene in African Americans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

1 October 2017

Cytochrome P450 2D6: overview and update on pharmacology, genetics, biochemistry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

1 October 2017

Identification of Novel CYP2D7-2D6 Hybrids: Non-Functional and Functional Variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

29 June 2018

An allele-specific PCR system for rapid detection and discrimination of the CYP2C19∗4A, ∗4B, and ∗17 alleles: implications for clopidogrel response testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

22 September 2018

Update on allele nomenclature for human cytochromes P450 and the Human Cytochrome P450 Allele (CYP-allele) Nomenclature Database

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

22 September 2018

CYP2D6, SULT1A1 and UGT2B17 copy number variation: quantitative detection by multiplex PCR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

22 September 2018

Discovery of the nonfunctional CYP2D6 31 allele in Spanish, Puerto Rican, and US Hispanic populations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

22 September 2018

CYP2D7-2D6 hybrid tandems: identification of novel CYP2D6 duplication arrangements and implications for phenotype prediction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

22 September 2018

The effect of primer-template mismatches on the detection and quantification of nucleic acids using the 5' nuclease assay

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

22 September 2018

Polymorphism of human cytochrome P450 2D6 and its clinical significance: part II.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

22 September 2018

Identification of a novel non-functional CYP2D6 allele, CYP2D6*69, in a Caucasian poor metabolizer individual

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

22 September 2018

The CYP2D6 activity score: translating genotype information into a qualitative measure of phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

22 September 2018

Identification and characterization of CYP2D6*56B, an allele associated with the poor metabolizer phenotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

22 September 2018

Cytochrome P4502D6 (CYP2D6) gene locus heterogeneity: characterization of gene duplication events.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

22 September 2018

CYP2D6*36 gene arrangements within the cyp2d6 locus: association of CYP2D6*36 with poor metabolizer status

1 reference

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22 September 2018

Discovery of a novel nonfunctional cytochrome P450 2D6 allele, CYP2D642, in African American subjects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4630174

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Resolution of a clinical AmpliChip CYP450 Test™ no call: discovery and characterization of novelCYP2D6*1haplotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/26335396

12 December 2020

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Identifiers

10.1016/J.JMOLDX.2015.06.007

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

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