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

Family Communication in Inherited Cardiovascular Conditions in Ireland.

Journal of genetic counseling - 1 Dec 2016

Whyte Sinead, Green Andrew, McAllister Marion, Shipman Hannah

Abstract excerpt

Over 100,000 individuals living in Ireland carry a mutated gene for an inherited cardiac condition (ICC), most of which demonstrate an autosomal dominant pattern of inheritance. First-degree relatives of individuals with these mutations are at a 50 % risk of being a carrier: disclosing genetic information to family members can be complex. This study explored how families living in Ireland communicate genetic...

Read the complete abstract on PubMed

Topics

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

Share to Cardiovascular Diseases
Share to Communication
Share to Disclosure

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

Share to Family

Share to Family Relations

Share to Genetic Predisposition to Disease

Share to Genetic Testing

Share to Ireland

Source

Identifiers

PMID: 27271705
DOI: 10.1007/s10897-016-9974-5

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Family Communication in Inherited Cardiovascular Conditions in Ireland.PMID 27271705Read ↗

Family Communication About Genetic Risk of Hereditary Cardiomyopathies and Arrhythmias: an Integrative Review.Semantic proximity Read ↗

Public perspectives on healthcare professional-directed communication of hereditary genetic risks: a mixed-method systematic review.Semantic proximity Read ↗

Communicating genetic risk information within families: a review.Semantic proximity Read ↗

Challenges and strategies proposed by genetic health professionals to assist with family communicationSemantic proximity Read ↗

Communicating inherited genetic risk between parent and child: a meta-thematic synthesis.Semantic proximity Read ↗

What facilitates or impedes family communication following genetic testing for cancer risk? A systematic review and meta-synthesis of primary qualitative research.Semantic proximity Read ↗

Communicating genetic information in families – a review of guidelines and position papersSemantic proximity Read ↗

Process and outcome in communication of genetic information within families: a systematic review.Semantic proximity Read ↗

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

A Family Experience of Personal GenomicsSemantic proximity Read ↗

Communication of genetic information to families with inherited rhythm disorders.Semantic proximity Read ↗

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

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