Copy number variation and warfarin dosing: evaluation of CYP2C9, VKORC1, CYP4F2, GGCX and CALU (Q35795982)

10 August 2017

title

Copy number variation and warfarin dosing: evaluation of CYP2C9, VKORC1, CYP4F2, GGCX and CALU (English)

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10 August 2017

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8

Jonathan L Halperin

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10 August 2017

4

Steven A Lubitz

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10 August 2017

9

Robert J Desnick

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10 August 2017

Stuart A Scott

1

1 reference

10 August 2017

Manishkumar Patel

2

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10 August 2017

Suparna Martis

3

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10 August 2017

Sarina van der Zee

5

1 reference

10 August 2017

Chang Yoo

6

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10 August 2017

Lisa Edelmann

7

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10 August 2017

publication date

21 December 2011

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10 August 2017

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10 August 2017

volume

13

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10 August 2017

issue

3

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10 August 2017

page(s)

297-307

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Natural genetic variation caused by small insertions and deletions in the human genome

10 August 2017

cites work

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A polymorphism in the VKORC1 regulator calumenin predicts higher warfarin dose requirements in African Americans

27 July 2018

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Comparative performance of gene-based warfarin dosing algorithms in a multiethnic population.

27 July 2018

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Pharmacogenetics: technologies to detect copy number variations.

27 July 2018

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Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans

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CYP2C9*8 is prevalent among African-Americans: implications for pharmacogenetic dosing

27 July 2018

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A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose

27 July 2018

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Sulfotransferase gene copy number variation: pharmacogenetics and function

27 July 2018

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27 July 2018

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Estimation of the warfarin dose with clinical and pharmacogenetic data

27 July 2018

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Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis

27 July 2018

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Ethnic differences in warfarin maintenance dose requirement and its relationship with genetics

27 July 2018

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27 July 2018

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CYP4F2 genetic variant alters required warfarin dose

27 July 2018

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27 July 2018

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27 July 2018

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Copy number variants and pharmacogenomics

27 July 2018

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Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose

27 July 2018

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Segmental duplications and copy-number variation in the human genome

27 July 2018

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Common VKORC1 and GGCX polymorphisms associated with warfarin dose

27 July 2018

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Detection of large-scale variation in the human genome

27 July 2018

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Oral anticoagulants: mechanism of action, clinical effectiveness, and optimal therapeutic range

27 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3292047

27 July 2018

Oral anticoagulant drugs

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Deletion of the entire cytochrome P450 CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism

27 July 2018

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Pharmacogenetics of warfarin: current status and future challenges

27 July 2018

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https://api.crossref.org/works/10.2217%2FPGS.11.156

The impact of CYP2C9 and VKORC1 genetic polymorphism and patient characteristics upon warfarin dose requirements: proposal for a new dosing regimen

21 January 2018

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https://api.crossref.org/works/10.2217%2FPGS.11.156

Pharmacogenetics of warfarin: development of a dosing algorithm for brazilian patients

21 January 2018

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https://api.crossref.org/works/10.2217%2FPGS.11.156

Dosing algorithm for warfarin using CYP2C9 and VKORC1 genotyping from a multi-ethnic population: comparison with other equations

21 January 2018

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https://api.crossref.org/works/10.2217%2FPGS.11.156

Comparison of warfarin pharmacogenetic dosing algorithms in a racially diverse large cohort

21 January 2018

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https://api.crossref.org/works/10.2217%2FPGS.11.156

Genetic and clinical predictors of warfarin dose requirements in African Americans

21 January 2018

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https://api.crossref.org/works/10.2217%2FPGS.11.156

Gamma-glutamyl carboxylase and its influence on warfarin dose

21 January 2018

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https://api.crossref.org/works/10.2217%2FPGS.11.156

Origins and functional impact of copy number variation in the human genome

21 January 2018

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Copy-number variation genotyping of GSTT1 and GSTM1 gene deletions by real-time PCR.

21 January 2018

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Population-specific GSTM1 copy number variation

21 January 2018

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https://api.crossref.org/works/10.2217%2FPGS.11.156

Human SULT1A1 gene: copy number differences and functional implications

21 January 2018

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Warfarin pharmacogenetics: CYP2C9 and VKORC1 genotypes predict different sensitivity and resistance frequencies in the Ashkenazi and Sephardi Jewish populations.

21 January 2018

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https://api.crossref.org/works/10.2217%2FPGS.11.156

Association between CYP2C9 genetic variants and anticoagulation-related outcomes during warfarin therapy

21 January 2018

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https://api.crossref.org/works/10.2217%2FPGS.11.156

High-resolution SNP and haplotype maps of the human gamma-glutamyl carboxylase gene (GGCX) and association study between polymorphisms in GGCX and the warfarin maintenance dose requirement of the Japanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.156

Genetic factors (VKORC1, CYP2C9, EPHX1, and CYP4F2) are predictor variables for warfarin response in very elderly, frail inpatients

21 January 2018

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https://api.crossref.org/works/10.2217%2FPGS.11.156

Warfarin pharmacogenomics.

21 January 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3292047

EPHX1 Polymorphisms Are Not Associated With Warfarin Response in an Italian Population

25 September 2018

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https://api.crossref.org/works/10.2217%2FPGS.11.156

Association of polymorphisms in the cytochrome P450 CYP2C9 with warfarin dose requirement and risk of bleeding complications

21 January 2018

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12 December 2020

A high-resolution survey of deletion polymorphism in the human genome

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12 December 2020

Gamma-glutamyl carboxylase (GGCX) tagSNPs have limited utility for predicting warfarin maintenance dose

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12 December 2020

Warfarin pharmacogenetics

1 reference

12 December 2020

Identifiers

DOI

10.2217/PGS.11.156

1 reference

10 August 2017

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10 August 2017

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