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

An exploration of the communication preferences regarding genetic testing in individuals from families with identified breast/ovarian cancer mutations.

Familial cancer - 1 Mar 2011

Ratnayake Paboda, Wakefield Claire E, Meiser Bettina, Suthers Graeme, Price Melanie A, Duffy Jessica, Tucker Kathy

Abstract excerpt

The responsibility for informing at-risk relatives of the availability of genetic testing for breast/ovarian cancer gene (BRCA1 or BRCA2) mutations currently falls on the probands. This study explored the support needs of individuals from families with identified BRCA1 or BRCA2 mutations when communicating about genetic risk and genetic testing with at-risk family members. Thirty-nine semi-structured telephone...

Read the complete abstract on PubMed

Topics

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

Share to BRCA1 Protein
Share to BRCA2 Protein

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Breast Neoplasms

Share to Communication

Share to DNA, Neoplasm

Share to Genetic Counseling

Share to Interviews as Topic

Share to Ovarian Neoplasms

Source

Identifiers

PMID: 20878485
DOI: 10.1007/s10689-010-9383-0

Genes

BRCA1
BRCA2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

An exploration of the communication preferences regarding genetic testing in individuals from families with identified breast/ovarian cancer mutations.PMID 20878485Read ↗

Perceptions and care Recommendations from Previvors: Qualitative analysis of female BRCA1/2 mutation Carriers’ experience with genetic testing and counselingSemantic proximity Read ↗

Exploring family communication preferences in hereditary breast and ovarian cancer and Lynch syndrome: A national Canadian surveySemantic proximity Read ↗

Key messages for communicating information about BRCA1 and BRCA2 to women with breast or ovarian cancer: Consensus across health professionals and service users.Semantic proximity Read ↗

Communicating BRCA1/2 genetic test results within the family: a qualitative analysis.Semantic proximity Read ↗

Understanding the Information Needs of Patients With Ovarian Cancer Regarding Genetic Testing to Inform Intervention Design: Interview StudySemantic proximity Read ↗

Experiences of BRCA1/2 Gene Mutation-Positive Women With Cancer in Communicating Genetic Risk to Their Relatives.Semantic proximity Read ↗

Informational needs of individuals from families harboring BRCA pathogenic variants: A systematic review and content analysis.Semantic proximity Read ↗

The effect of BRCA gene testing on family relationships: A thematic analysis of qualitative interviews.Semantic proximity Read ↗

Experiences of Family Communication and Cascade Genetic Testing for Hereditary Cancer in Medically Underserved Populations-A Qualitative Study.Semantic proximity Read ↗

Identifying Needs: a Qualitative Study of women's Experiences Regarding Rapid Genetic Testing for Hereditary Breast and Ovarian Cancer in the DNA BONus Study.Semantic proximity Read ↗

Genetic testing for hereditary cancer syndromes: patient recommendations for improved risk communication.Semantic proximity Read ↗

Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population.Semantic proximity Read ↗

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