ArticleJAMA2010
Exclusion of genetic information from the medical record: ethical and medical dilemmas.
Article in JAMA, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 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
11 citing papers in PubMed.
- Ethical Considerations on Pediatric Genetic Testing Results in Electronic Health Records.Applied clinical informatics · 2020Article
- The Alzheimer's Prevention Clinic at Weill Cornell Medical College / New York - Presbyterian Hospital: Risk Stratification and Personalized Early Intervention.The journal of prevention of Alzheimer's disease · 2015Article
- Automatic Placement of Genomic Research Results in Medical Records: Do Researchers Have a Duty? Should Participants Have a Choice?The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics · 2015Article
- The fiduciary relationship model for managing clinical genomic "incidental" findings.The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics · 2014Article
- Ethical, legal, and social implications of incorporating genomic information into electronic health records.Genetics in medicine : official journal of the American College of Medical Genetics · 2013Review
- Consumer awareness and attitudes about insurance discrimination post enactment of the Genetic Information Nondiscrimination Act.Familial cancer · 2012Article
- Ethics and neuropsychiatric genetics: a review of major issues.The international journal of neuropsychopharmacology · 2012Review
- The Genetic Information Nondiscrimination Act (GINA): public policy and medical practice in the age of personalized medicine.Journal of general internal medicine · 2012Article
- Advising patients about obtaining genomic profiles.Neurology. Clinical practice · 2011Article
- Practical considerations to guide development of access controls and decision support for genetic information in electronic medical records.BMC health services research · 2011Article
- Genetic data and electronic health records: a discussion of ethical, logistical and technological considerations.Journal of the American Medical Informatics Association : JAMIAReview
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
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.