ReviewThe American journal of nursing2009
Disclosure of genetic information within families.
Review in The American journal of nursing, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 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
29 citing papers in PubMed.
- Perception of young adults with sickle cell disease or sickle cell trait about participation in the CHOICES randomized controlled trial.Journal of advanced nursing · 2016Trial
- Young people's experience of predictive genetic testing for inherited cardiac conditions: a qualitative study.European journal of human genetics : EJHG · 2026Article
- Interests and Experiences of Young Adults with Muscular Dystrophy in Receiving Genetic Information.Journal of child neurology · 2025Article
- Nigerian parents' perspectives on genetic testing in their children with genetic eye diseases.Journal of community genetics · 2023Article
- Family Communication about Diagnostic Genetic Testing for Younger-Onset Dementia.Journal of personalized medicine · 2023Article
- A qualitative study utilizing Interpretative phenomenological analysis to explore disclosure in adolescents with turner syndrome.British journal of health psychology · 2022Article
- Comparing the attitudes of physicians and non-physicians toward communicating a patient's BRCA1 mutation to a first-degree relative against a patient's wishes.Journal of community genetics · 2022Article
- Germline testing and genetic counselling in prostate cancer.Nature reviews. Urology · 2022Review
- Not just carriers: experiences of X-linked female heterozygotes.Journal of assisted reproduction and genetics · 2021Article
- Tracing the Use of the Family Management Framework and Measure: A Scoping Review.Journal of family nursing · 2021Article
- Stakeholder Perspectives on Overcoming Barriers to Cascade Testing in Lynch Syndrome: A Qualitative Study.Cancer prevention research (Philadelphia, Pa.) · 2020Article
- Reasonable expectations of privacy in non-disclosure of familial genetic risk: What is it reasonable to expect?European journal of medical genetics · 2019Article
- Disclosure of diagnosis to at-risk relatives by individuals diagnosed with hypertrophic cardiomyopathy (HCM).Journal of community genetics · 2019Article
- Family health history and genetic services-the East Baltimore community stakeholder interview project.Journal of community genetics · 2019Article
- Communication about genetic testing with breast and ovarian cancer patients: a scoping review.European journal of human genetics : EJHG · 2019Article
- Genetic Privacy, Disease Prevention, and the Principle of Rescue.The Hastings Center report · 2018Article
- Development of a Web-based Family Intervention for BRCA Carriers and Their Biological Relatives: Acceptability, Feasibility, and Usability Study.JMIR cancer · 2018Article
- Effect of Disclosing Genetic Risk for Coronary Heart Disease on Information Seeking and Sharing: The MI-GENES Study (Myocardial Infarction Genes).Circulation. Cardiovascular genetics · 2017Article
- Cancer Risk Information Sharing: The Experience of Individuals Receiving Genetic Counseling for BRCA1/2 Mutations.Journal of health communication · 2017Article
- Children with sex chromosome trisomies: parental disclosure of genetic status.European journal of human genetics : EJHG · 2016Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 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.