Search Results - "Jorgensen, Andrea L."
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Biomarker-Guided Adaptive Trial Designs in Phase II and Phase III: A Methodological Review
Published in PloS one (24-02-2016)“…Personalized medicine is a growing area of research which aims to tailor the treatment given to a patient according to one or more personal characteristics…”
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Warfarin dosing algorithms: A systematic review
Published in British journal of clinical pharmacology (01-04-2021)“…Aims Numerous algorithms have been developed to guide warfarin dosing and improve clinical outcomes. We reviewed the algorithms available for various…”
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3
A Randomized Trial of Genotype-Guided Dosing of Warfarin
Published in The New England journal of medicine (12-12-2013)“…This trial compared genotype-guided dosing with standard dosing in patients with atrial fibrillation or venous thromboembolism initiating warfarin…”
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Influence of CYP2C9 and VKORC1 on patient response to warfarin: a systematic review and meta-analysis
Published in PloS one (29-08-2012)“…Warfarin is a highly effective anticoagulant however its effectiveness relies on maintaining INR in therapeutic range. Finding the correct dose is difficult…”
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STrengthening the Reporting Of Pharmacogenetic Studies: Development of the STROPS guideline
Published in PLoS medicine (01-09-2020)“…[...]large sample sizes are typically required to detect pharmacogenetic associations. Marty Chaplin (researcher into meta-analysis of pharmacogenetic…”
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Implementation of genotype-guided dosing of warfarin with point-of-care genetic testing in three UK clinics: a matched cohort study
Published in BMC medicine (08-04-2019)“…Warfarin is a widely used oral anticoagulant. Determining the correct dose required to maintain the international normalised ratio (INR) within a therapeutic…”
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Association of Human Leukocyte Antigen Alleles and Nevirapine Hypersensitivity in a Malawian HIV-Infected Population
Published in Clinical infectious diseases (01-05-2013)“…Background. The nonnucleoside reverse transcriptase inhibitor nevirapine is the cornerstone of treatment for human immunodeficiency virus (HIV) in many…”
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SurvivalGWAS_SV: software for the analysis of genome-wide association studies of imputed genotypes with "time-to-event" outcomes
Published in BMC bioinformatics (19-05-2017)“…Analysis of genome-wide association studies (GWAS) with "time to event" outcomes have become increasingly popular, predominantly in the context of…”
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A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients
Published in Frontiers in pharmacology (23-09-2022)“…Diversity in pharmacogenomic studies is poor, especially in relation to the inclusion of black African patients. Lack of funding and difficulties in…”
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10
Role of fatty liver index in risk-stratifying comorbid disease outcomes in non-alcoholic fatty liver disease
Published in JHEP reports (01-12-2023)“…Population screening for non-alcoholic fatty liver disease (NAFLD) and associated comorbidities remains an unaddressed clinical need. We aimed to assess the…”
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Methodological quality of pharmacogenetic studies: Issues of concern
Published in Statistics in medicine (30-12-2008)“…Pharmacogenetic studies investigate association between genetic variants‡ and drug efficacy and toxicity. Regardless of the extent of current knowledge…”
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Exploring the potential of BH3 mimetic therapy in squamous cell carcinoma of the head and neck
Published in Cell death & disease (04-12-2019)“…Squamous cell carcinoma of the head and neck (SCCHN) is the sixth most common cancer worldwide, with overall survival of less than 50%. Current therapeutic…”
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Stable warfarin dose prediction in sub‐Saharan African patients: A machine‐learning approach and external validation of a clinical dose–initiation algorithm
Published in CPT: pharmacometrics and systems pharmacology (01-01-2022)“…Warfarin remains the most widely prescribed oral anticoagulant in sub‐Saharan Africa. However, because of its narrow therapeutic index, dosing can be…”
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CYP genetic variants and toxicity related to anti-tubercular agents: a systematic review and meta-analysis
Published in Systematic reviews (20-11-2018)“…Treatment with anti-tuberculosis drugs may cause patients to experience serious adverse effects. Genetic factors, such as polymorphisms of CYP genes, may…”
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Effect of Genetic Variability in the CYP4F2 , CYP4F11 , and CYP4F12 Genes on Liver mRNA Levels and Warfarin Response
Published in Frontiers in pharmacology (31-05-2017)“…Genetic polymorphisms in the gene encoding cytochrome P450 (CYP) 4F2, a vitamin K oxidase, affect stable warfarin dose requirements and time to therapeutic…”
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Genome-Wide association between EYA1 and Aspirin-induced peptic ulceration
Published in EBioMedicine (01-12-2021)“…Low-dose aspirin can cause gastric and duodenal ulceration, hereafter called peptic ulcer disease (PUD). Predisposition is thought to be related to clinical…”
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A "Bundle of Care" to Improve Anticoagulation Control in Patients Receiving Warfarin in Uganda and South Africa: Protocol for an Implementation Study
Published in JMIR research protocols (19-07-2023)“…The quality of warfarin anticoagulation among Sub-Saharan African patients is suboptimal. This is due to several factors, including a lack of standardized…”
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Investigating the prevalence, predictors, and prognosis of suboptimal statin use early after a non-ST elevation acute coronary syndrome
Published in Journal of clinical lipidology (01-01-2017)“…Background High-potency statin therapy is recommended in the secondary prevention of cardiovascular disease but discontinuation, dose reduction, statin…”
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Effects of CYP4F2 genetic polymorphisms and haplotypes on clinical outcomes in patients initiated on warfarin therapy
Published in Pharmacogenetics and genomics (01-10-2009)“…BACKGROUNDA variant in the CYP4F2 gene, rs2108622, has been recently shown to determine stable warfarin dose requirements. CYP4F2 has also been shown recently…”
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Genetic and environmental factors determining clinical outcomes and cost of warfarin therapy: a prospective study
Published in Pharmacogenetics and genomics (01-10-2009)“…BACKGROUNDIn this prospective cohort study, we have undertaken a comprehensive evaluation of clinical parameters along with variation in 29 genes (including…”
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