Lay understanding of genetic disease: a British study of families attending a genetic counseling service.

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. Navigating the Genetic Frontier for the Integration of Genetic Services into African Healthcare Systems: A scoping review.Research square · 2024
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2. Identifying and Addressing Genetic Counseling Challenges among Indigenous People of Oaxaca-One Center's Experience with Two Immigrant Farmworker Families in the Central Valley of California.Journal of genetic counseling · 2018
   Article
3. "It was a lot Tougher than I Thought It would be". A Qualitative Study on the Changing Nature of Being a Hemophilia Carrier.Journal of genetic counseling · 2017
   Article
4. A Qualitative Study to Explore the Views and Attitudes towards Prenatal Testing in Adults Who Have Muenke Syndrome and their Partners.Journal of genetic counseling · 2017
   Article
5. Dual Perspectives On Stigma: Reports of Experienced and Enacted Stigma by Those Affected and Unaffected by Podoconiosis.Journal of public health research · 2016
   Article
6. Perception of Lay People Regarding Determinants of Health and Factors Affecting It: An Aggregated Analysis from 29 Countries.Iranian journal of public health · 2015
   Article
7. UK Pakistani views on the adverse health risks associated with consanguineous marriages.Journal of community genetics · 2015
   Article
8. Personalized genomic results: analysis of informational needs.Journal of genetic counseling · 2014
   Article
9. What's at stake? Genetic information from the perspective of people with epilepsy and their family members.Social science & medicine (1982) · 2011
   Article
10. Explaining Mendelian inheritance in genetic consultations: an IPR study of counselor and counselee experiences.Journal of genetic counseling · 2010
    Article
11. Decisions to seek healthcare based on family health history among urban Appalachian women.Journal of genetic counseling · 2009
    Article
12. How parents search, interpret, and evaluate genetic information obtained from the internet.Journal of genetic counseling · 2009
    Article
13. "What is this genetics, anyway?" Understandings of genetics, illness causality and inheritance among British Pakistani users of genetic services.Journal of genetic counseling · 2008
    Article
14. Coming full circle: a reciprocal-engagement model of genetic counseling practice.Journal of genetic counseling · 2007
    Article
15. Improving service evaluation in clinical genetics: identifying effects of genetic diseases on individuals and families.Journal of genetic counseling · 2007
    Article
16. Exploring the public understanding of basic genetic concepts.Journal of genetic counseling · 2004
    Article
17. Parental attitudes toward genetic testing for pediatric deafness.American journal of human genetics · 2000
    Article

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

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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