ArticleGenetics in medicine : official journal of the American College of Medical Genetics2009
Personal utility and genomic information: look before you leap.
Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 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
41 citing papers in PubMed.
- Patient preferences for massively parallel sequencing genetic testing of colorectal cancer risk: a discrete choice experiment.European journal of human genetics : EJHG · 2018Trial
- Participant Satisfaction With a Preference-Setting Tool for the Return of Individual Research Results in Pediatric Genomic Research.Journal of empirical research on human research ethics : JERHRE · 2015Trial
- Patients offered genomic testing for rare disease and cancer: a real-world evaluation of impact and processes of care.European journal of human genetics : EJHG · 2026Article
- Review
- Determining the utility of diagnostic genomics: a conceptual framework.Human genomics · 2023Review
- Perceived utility and disutility of genomic sequencing for pediatric patients: Perspectives from parents with diverse sociodemographic characteristics.American journal of medical genetics. Part A · 2022Article
- Conceptualising 'Benefits Beyond Health' in the Context of the Quality-Adjusted Life-Year: A Critical Interpretive Synthesis.PharmacoEconomics · 2021Review
- Conceptualization of utility in translational clinical genomics research.American journal of human genetics · 2021Review
- Qualitative study of system-level factors related to genomic implementation.Genetics in medicine : official journal of the American College of Medical Genetics · 2019Article
- "Well, good luck with that": reactions to learning of increased genetic risk for Alzheimer disease.Genetics in medicine : official journal of the American College of Medical Genetics · 2018Article
- Public Understanding and Opinions regarding Genetic Research on Alzheimer's Disease.Public health genomics · 2018Article
- Diagnosis of rare diseases under focus: impacts for Canadian patients.Journal of community genetics · 2018Article
- Article
- Attitudes to incorporating genomic risk assessments into population screening programs: the importance of purpose, context and deliberation.BMC medical genomics · 2016Article
- Was it worth it? Patients' perspectives on the perceived value of genomic-based individualized medicine.Journal of community genetics · 2016Article
- Ethical signposts for clinical geneticists in secondary variant and incidental finding disclosure discussions.Medicine, health care, and philosophy · 2015Article
- Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2015Article
- Valuations of genetic test information for treatable conditions: the case of colorectal cancer screening.Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research · 2014Article
- Public preferences for the return of research results in genetic research: a conjoint analysis.Genetics in medicine : official journal of the American College of Medical Genetics · 2014Article
- Incidental findings from clinical genome-wide sequencing: a review.Journal of genetic counseling · 2014Review
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
What 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.