ArticleJournal of genetic counseling2009
Professional ambivalence: accounts of ethical practice in childhood genetic testing.
Article in Journal of genetic counseling, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
What it found
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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.
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Who cites it
10 citing papers in PubMed, 31 citations in OpenAlex.
- Professionals' views on providing personalized recurrence risks for de novo mutations: Implications for genetic counseling.Journal of genetic counseling · 2025Article
- Dealing with ambivalence in the practice of advanced genetic healthcare: towards an ethical choreography.European journal of human genetics : EJHG · 2023Article
- Professionals' accounts of genetic testing in adoption: a qualitative study.Archives of disease in childhood · 2020Article
- Ethics in genetic counselling.Journal of community genetics · 2019Review
- Failed surrogate conceptions: social and ethical aspects of preconception disruptions during commercial surrogacy in India.Philosophy, ethics, and humanities in medicine : PEHM · 2016Article
- A qualitative study to explore how professionals in the United Kingdom make decisions to test children for a sickle cell carrier status.European journal of human genetics : EJHG · 2016Article
- Support Seeking or Familial Obligation: An Investigation of Motives for Disclosing Genetic Test Results.Health communication · 2016Article
- Disparities in current and future childhood and newborn carrier identification.Journal of genetic counseling · 2014Article
- Challenges of genetic testing in adolescents with cardiac arrhythmia syndromes.Journal of medical ethics · 2012Article
- DSD and Professionalism from a Multilateral View: Supplementing the Consensus Statement on the Basis of a Qualitative Survey.Advances in urology · 2012Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Childhood genetic testing raises complex ethical and moral dilemmas for both families and professionals. In the family sphere, the role of communication is a key aspect in the transmission of 'genetic responsibility' between adults and children. In the professional sphere, genetic responsibility is an interactional accomplishment emerging from the sometimes competing views over what constitutes the 'best interests' of the child in relation to parental preferences on the one hand, and professional judgements on the other. In the present paper we extend our previous research into parental accounts of childhood genetic testing and explore the ethical accounts of professionals in research interviews. Interviews (n = 20) were conducted with professional practitioners involved in the genetic diagnosis and management of children and their families. We first identify four inter-related themes-juxtaposition of parental rights vis-à-vis child's autonomy, elicitation of the child's autonomy, avoidance of parental responsibility and recognition of professional uncertainty. Then, using Rhetorical Discourse Analysis, we examine the range of discourse devices through which ethical accounts are situationally illustrated: contrast, reported speech, constructed dialogue, character and event work. An overarching device in these ethical accounts is the use of extreme case scenarios, which reconstruct dilemmas as justifications of professional conduct. While acknowledging ambivalence, our analysis suggests that professional judgement is not a simple matter of implementing ethical principles but rather of managing the practical conditions and consequences of interactions with parents and children. We conclude that more attention is needed to understand the way professional practitioners formulate judgements about ethical practice.
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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.