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

Social aspects of genetic testing for factor V Leiden mutation in healthy individuals and their importance for daily practice.

Thrombosis research - 1 Jan 2004

Bank Ivan, Scavenius Michael P R B, Büller Harry R, Middeldorp Saskia

Abstract excerpt

To explore social aspects of asymptomatic carriership of factor V Leiden mutation (FVL) and how carriers have experienced procedure of screening for FVL, we have performed a qualitative study using semi-structured interviews. Seventeen carriers of FVL without history of venous thromboembolism (VTE) were interviewed. Carriership of FVL has the potential to influence daily life by inducing concerns, stigmatisation...

Read the complete abstract on PubMed

Topics

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

Share to Factor V
Share to Genetic Carrier Screening

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Health Knowledge, Attitudes, Practice

Share to Interviews as Topic

Share to Life Style

Share to Netherlands

Share to Social Support

Share to Venous Thrombosis

Source

Identifiers

PMID: 15081560
DOI: 10.1016/j.thromres.2004.02.002

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Social aspects of genetic testing for factor V Leiden mutation in healthy individuals and their importance for daily practice.PMID 15081560Read ↗

The emotional impact of genetic testing and aspects of counseling prior to prescription of oral contraceptives.Semantic proximity Read ↗

Are genetic tests exceptional? Lessons from a qualitative study on thrombophilia.Semantic proximity Read ↗

“It was a lot Tougher than I Thought It would be”. A Qualitative Study on the Changing Nature of Being a Hemophilia CarrierSemantic proximity Read ↗

The embodied experience of genetic inheritance in hereditary thrombophilia.Semantic proximity Read ↗

Implementing carrier screening for cystic fibrosis outside the clinic: ethical analysis in the light of the personalist view.Semantic proximity Read ↗

Using the experiences of people with familial hypercholesterolaemia to help reduce the risk of cardiovascular disease: a qualitative systematic review.Semantic proximity Read ↗

Supporting disclosure of genetic information to family members: professional practice and timelines in cancer genetics.Semantic proximity Read ↗

Clinical follow-up and breast and ovarian cancer screening of true BRCA1/2 noncarriers: a qualitative investigation.Semantic proximity Read ↗

Ethical Dilemmas Linked to Fragile X Testing of Minors-a Preliminary Survey Among Professionals.Semantic proximity Read ↗

Motivating factors for physician ordering of factor V Leiden genetic tests.Semantic proximity Read ↗

Attitudes towards and beliefs about genetic testing in the haemophilia community: a qualitative studySemantic proximity Read ↗

To be or not to be: the patient's view of thrombophilia testing.Semantic proximity Read ↗

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