Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic research on rare familial disorders: consent and the blurred boundaries between clinical service and research.

Journal of medical ethics - 1 Sept 2008

Ponder M, Statham H, Hallowell N, Moon J A, Richards M, Raymond F L

Abstract excerpt

OBJECTIVES: To study the consent process experienced by participants who are enrolled in a molecular genetic research study that aims to find new genetic mutations responsible for an apparently inherited disorder. DESIGN: Semi-structured interviews and analysis/description of main themes. PARTICI...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Clinical Trials as Topic
Share to Family
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Research

Share to Informed Consent

Share to Patient Selection

Share to Rare Diseases

Share to United Kingdom

Source

Open in PubMed Open full text

Identifiers

PMID: 18757643
DOI: 10.1136/jme.2006.018564
PMCID: PMC2771893

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18757643-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic research on rare familial disorders: consent and the blurred boundaries between clinical service and research.PMID 18757643Read ↗

Informed consent for exome sequencing research in families with genetic disease: The emerging issue of incidental findingsSemantic proximity Read ↗

Old Challenges or New Issues? Genetic Health Professionals' Experiences Obtaining Informed Consent in Diagnostic Genomic Sequencing.Semantic proximity Read ↗

Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research settingSemantic proximity Read ↗

A genetic researcher's devil's dilemma: Warn relatives about their genetic risk or respect confidentiality agreements with research participants?Semantic proximity Read ↗

What does a consent conversation for whole genome sequencing look like in the NHS Genomic Medicine Service? An observational studySemantic proximity Read ↗

Informed Consent in Genomics and Genetic ResearchSemantic proximity Read ↗

Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patientsSemantic proximity Read ↗

Implementing Electronic Informed Consent in Rare Disease GenomicsSemantic proximity Read ↗

Consent and Autonomy in the Genomics EraSemantic proximity Read ↗

Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research ResultsSemantic proximity Read ↗

To disclose, or not to disclose? Perspectives of clinical genomics professionals toward returning incidental findings from genomic researchSemantic proximity Read ↗

Family consent and the pursuit of better medicines through genetic research.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.