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

Australian Adaptation of Resources to Communicate Hereditary Cancer Risk With Family Members.

Psycho-oncology - 1 Jun 2026

Rodriguez Grieve Luna, Galpin Kirsty, Thorne Heather, Powell Sarah, Bartley Nicci, Dhillon Haryana M, Shirts Brian, Shaw Joanne

Abstract excerpt

BACKGROUND: Communicating genetic test results within families can facilitate cascade testing that informs cancer prevention and surveillance. Researchers at the University of Washington, USA, developed a public website called ConnectMyVariant to support family communication of genetic test results. Australian families share similar challenges communicating genetic information. AIMS: To explore the acceptability...

Read the complete abstract on PubMed

Topics

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

Share to Australia
Share to Communication

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family

Share to Genetic Counseling

Share to Genetic Predisposition to Disease

Share to Genetic Testing

Share to Neoplasms

Share to Qualitative Research

Source

Identifiers

PMID: 42234591
DOI: 10.1002/pon.70513

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Australian Adaptation of Resources to Communicate Hereditary Cancer Risk With Family Members.PMID 42234591Read ↗

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

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

What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk?Semantic proximity Read ↗

Health professionals contacting patients' relatives directly about genetic risk (with patient consent): current clinical practice and perspectives.Semantic proximity Read ↗

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

Patients' perspectives regarding health professionals contacting their relatives about genetic risk directly (with patient consent).Semantic proximity Read ↗

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

Development of a Tool to Guide Parents Carrying a BRCA1/2 Mutation Share Genetic Results with Underage Children.Semantic proximity Read ↗

Digital genetic counselling services for cascade cardiogenetic testing: a focus group study on proband, relative, and provider perspectivesSemantic proximity Read ↗

Development and Evaluation of a Telephone Communication Protocol for the Delivery of Personalized Melanoma Genomic Risk to the General PopulationSemantic proximity Read ↗

GP attitudes to and expectations for providing personal genomic risk information to the public: a qualitative studySemantic proximity Read ↗

Digital innovation for cancer risk assessment allows large-scale service redevelopment of regional cancer genetics service delivery.Semantic proximity Read ↗

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