ArticleLancet (London, England)2010
The personal genome--the future of personalised medicine?
Article in Lancet (London, England), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.
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
17 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Use of Genomic Information in Health Impact Assessment is Yet to Come: A Systematic Review.International journal of environmental research and public health · 2020Pooled it
- A typology of useful evidence: approaches to increase the practical value of intervention research.BMC medical research methodology · 2020Article
- Clinically relevant pharmacogenetic markers in Tatars and Balkars.Molecular biology reports · 2020Article
- Information Needs and Information-Seeking Behavior of Italian Neurologists: Exploratory Mixed Methods Study.Journal of medical Internet research · 2020Article
- Conceptual and terminological confusion around personalised medicine: a coping strategy.BMC medical ethics · 2016Article
- Using complex networks for refining survival prognosis in prostate cancer patient.F1000Research · 2016Article
- Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects.European journal of human genetics : EJHG · 2015Article
- Pre-graduate and post-graduate education in personalized medicine in the Czech Republic: statistics, analysis and recommendations.The EPMA journal · 2014Review
- Genetics patients' perspectives on clinical genomic testing.Personalized medicine · 2013Article
- The 'thousand-dollar genome': an ethical exploration.European journal of human genetics : EJHG · 2013Article
- Molecular diversity and population structure at the Cytochrome P450 3A5 gene in Africa.BMC genetics · 2013Article
- The coming age of data-driven medicine: translational bioinformatics' next frontier.Journal of the American Medical Informatics Association : JAMIA · 2012Article
- Quality standards and samples in genetic testing.Journal of clinical pathology · 2012Article
- Translational bioinformatics embraces big data.Yearbook of medical informatics · 2012Review
- Phased whole-genome genetic risk in a family quartet using a major allele reference sequence.PLoS genetics · 2011Article
- A 'biomarker signature' for tolerance in transplantation.Nature reviews. Nephrology · 2010Review
- Individualized medicine 2010.Journal of cellular and molecular medicine · 2010Article
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
20435212What 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.