A warfarin‐dosing model in Asians that uses single‐nucleotide polymorphisms in vitamin K epoxide reductase complex and cytochrome P450 2C9
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Ling-Zhi Wang | Richie Soong | B. Goh | R. Soong | L. Tham | A. Nafziger | Soo-Chin Lee | Soo-Chin Lee | Boon-Cher Goh | Lingzhi Wang | Jiayi Guo | Lai-San Tham | Anne Nafziger | Jia-Yi Guo
[1] Howard L McLeod,et al. Use of pharmacogenetics and clinical factors to predict the maintenance dose of warfarin , 2003, Thrombosis and Haemostasis.
[2] Peter Wood,et al. The impact of CYP2C9 and VKORC1 genetic polymorphism and patient characteristics upon warfarin dose requirements: proposal for a new dosing regimen. , 2005, Blood.
[3] J. Jespersen,et al. Multicentre randomised study of computerised anticoagulant dosage , 1998, The Lancet.
[4] M. Rieder,et al. Association of Vitamin K epoxide reductase complex 1 (VKORC1) variants with warfarin dose in a Hong Kong Chinese patient population , 2005, Pharmacogenetics and genomics.
[5] J Jespersen,et al. Multicentre randomised study of computerised anticoagulant dosage. European Concerted Action on Anticoagulation. , 1998, Lancet.
[6] M. Caldwell,et al. A prospective, randomized pilot trial of model-based warfarin dose initiation using CYP2C9 genotype and clinical data. , 2005, Clinical medicine & research.
[7] T. Baglin,et al. Influence of cytochrome P-450 CYP2C9 polymorphisms on warfarin sensitivity and risk of over-anticoagulation in patients on long-term treatment. , 2000 .
[8] Howard L McLeod,et al. The pharmacogenetics of coumarin therapy. , 2005, Pharmacogenomics.
[9] T. Baglin,et al. Influence of cytochrome P-450 CYP2C9 polymorphisms on warfarin sensitivity and risk of over-anticoagulation in patients on long-term treatment. , 2000, Blood.
[10] Howard L McLeod,et al. Prospective dosing of warfarin based on cytochrome P-450 2C9 genotype , 2005, Thrombosis and Haemostasis.
[11] S. McGrath,et al. The frequency and effects of cytochrome P450 (CYP) 2C9 polymorphisms in patients receiving warfarin. , 2002, Journal of the American College of Surgeons.
[12] Yusuke Nakamura,et al. Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients , 2006, Journal of Human Genetics.
[13] H. Echizen,et al. Population differences in S‐warfarin metabolism between CYP2C9 genotype‐matched Caucasian and Japanese patients , 2003, Clinical pharmacology and therapeutics.
[14] H Furuya,et al. Genetic polymorphism of CYP2C9 and its effect on warfarin maintenance dose requirement in patients undergoing anticoagulation therapy. , 1995, Pharmacogenetics.
[15] J. Hirsh,et al. A randomized trial comparing 5-mg and 10-mg warfarin loading doses. , 1999, Archives of internal medicine.
[16] K. Hampton,et al. A comparison of a low-dose warfarin induction regimen with the modified Fennerty regimen in elderly inpatients. , 2000, Age and ageing.
[17] J. Hirsh,et al. Oral anticoagulants: mechanism of action, clinical effectiveness, and optimal therapeutic range. , 2001, Chest.
[18] E. Nanba,et al. Polymorphism of the cytochrome P450 (CYP) 2C9 gene in Japanese epileptic patients: genetic analysis of the CYP2C9 locus. , 2000, Pharmacogenetics.
[19] Deborah A Nickerson,et al. Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose. , 2005, The New England journal of medicine.
[20] H. Halkin,et al. Combined genetic profiles of components and regulators of the vitamin K-dependent γ-carboxylation system affect individual sensitivity to warfarin , 2006, Thrombosis and Haemostasis.
[21] H. Halkin,et al. Interindividual variability in sensitivity to warfarin‐Nature or nurture? , 2001, Clinical pharmacology and therapeutics.
[22] H. Chow,et al. Genetic polymorphism in exon 4 of cytochrome P450 CYP2C9 may be associated with warfarin sensitivity in Chinese patients. , 2001, Blood.
[23] H. Echizen,et al. CYP2C9 and Oral Anticoagulation Therapy with Acenocoumarol and Warfarin: Similarities yet Differences , 2004, Clinical pharmacology and therapeutics.
[24] B. Goh,et al. Interethnic variability of warfarin maintenance requirement is explained by VKORC1 genotype in an Asian population , 2006, Clinical pharmacology and therapeutics.
[25] D. Anderson,et al. Comparison of 10-mg and 5-mg Warfarin Initiation Nomograms Together with Low-Molecular-Weight Heparin for Outpatient Treatment of Acute Venous Thromboembolism , 2003, Annals of Internal Medicine.
[26] W. Hayes. Control of Norway rats with residual rodenticide warfarin. , 1950, Public health reports.
[27] P. Watkins,et al. Heterogeneity of CYP3A isoforms metabolizing erythromycin and cortisol , 1992, Clinical pharmacology and therapeutics.
[28] F. Kamali,et al. Contribution of age, body size, and CYP2C9 genotype to anticoagulant response to warfarin , 2004, Clinical pharmacology and therapeutics.
[29] L. Teh,et al. Malaysian Indians are genetically similar to Caucasians: CYP2C9 polymorphism , 2006, Journal of clinical pharmacy and therapeutics.
[30] C. Jang,et al. Allele and genotype frequencies of CYP2C9 in a Korean population. , 2005, British journal of clinical pharmacology.
[31] Julie A. Johnson,et al. Influence of coagulation factor, vitamin K epoxide reductase complex subunit 1, and cytochrome P450 2C9 gene polymorphisms on warfarin dose requirements , 2006, Clinical pharmacology and therapeutics.
[32] M. Rieder,et al. CYP2C9 Haplotype Structure in European American Warfarin Patients and Association with Clinical Outcomes , 2005, Clinical pharmacology and therapeutics.
[33] Yi-ping Fu,et al. CYP2C9 polymorphism and warfarin sensitivity in Taiwan Chinese. , 2006, Clinica chimica acta; international journal of clinical chemistry.
[34] C. Hunt,et al. Effect of age and gender on the activity of human hepatic CYP3A. , 1992, Biochemical pharmacology.
[35] D. P. Bentley,et al. Flexible induction dose regimen for warfarin and prediction of maintenance dose. , 1984, British medical journal.
[36] E. Spina,et al. Influence of CYP2C9 and CYP2C19 genetic polymorphisms on warfarin maintenance dose and metabolic clearance , 2002, Clinical pharmacology and therapeutics.
[37] J. Goldstein,et al. Identification of a null allele of CYP2C9 in an African-American exhibiting toxicity to phenytoin. , 2001, Pharmacogenetics.
[38] M. Ritchie,et al. Different contributions of polymorphisms in VKORC1 and CYP2C9 to intra- and inter-population differences in maintenance dose of warfarin in Japanese, Caucasians and African-Americans , 2006, Pharmacogenetics and genomics.
[39] Y. Lim,et al. Novel CYP2C9 genetic variants in asian subjects and their influence on maintenance warfarin dose , 2004, Clinical pharmacology and therapy.
[40] S. Hunt,et al. Common VKORC1 and GGCX polymorphisms associated with warfarin dose , 2005, The Pharmacogenomics Journal.
[41] A. Rettie,et al. A common genetic basis for idiosyncratic toxicity of warfarin and phenytoin , 1999, Epilepsy Research.
[42] David L Veenstra,et al. Association between CYP2C9 genetic variants and anticoagulation-related outcomes during warfarin therapy. , 2002, JAMA.