ArticleClinical pharmacology and therapeutics2014
Patients benefit from genetics-guided coumarin anticoagulant therapy.
Article in Clinical pharmacology and therapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
6 citing papers in PubMed.
- A systematic analysis and comparison of warfarin initiation strategies.Pharmacogenetics and genomics · 2016Article
- Contrasting Medical and Legal Standards of Evidence: A Precision Medicine Case Study.The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics · 2016Article
- A multi-factorial analysis of response to warfarin in a UK prospective cohort.Genome medicine · 2016Article
- Clinical Perspectives on Targeting Therapies for Personalized Medicine.Advances in protein chemistry and structural biology · 2016Review
- Genes affecting warfarin response-interactive or additive?Journal of clinical pharmacology · 2015Article
- Poor warfarin dose prediction with pharmacogenetic algorithms that exclude genotypes important for African Americans.Pharmacogenetics and genomics · 2015Article
Corrections and comments
- Comment on
- Comment on
- Comment on
- Erratum issuedManolopoulos, V G [corrected to Manolopoulous, V G]
Authors and funding
10 authors.
Funding
Abstract
Observational studies have overwhelmingly shown that variants in the genes CYP2C9 and VKORC1 are significant determinants of individual dose of coumarin anticoagulants needed to maintain a therapeutic international normalized ratio (INR).(1) Until recently, however, few randomized clinical trials had been performed relating to the use of genetic data to predict dosing. Three sucsh clinical trials have now reported their findings.
Indexed as
Identifiers
24942396What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.