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

Evaluation of a decision aid for families considering p53 genetic counseling and testing.

Genetics in medicine : official journal of the American College of Medical Genetics - 1 Apr 2006

Peterson Susan K, Pentz Rebecca D, Blanco Amie M, Ward Patricia A, Watts Beatty G, Marani Salma K, James Leslie Colvin, Strong Louise C

Abstract excerpt

PURPOSE: Li-Fraumeni syndrome (LFS) is associated with p53 germline mutations, and carriers are at increased risk for multiple primary cancers. We evaluated outcomes following the administration of a video-based decision aid (DA) prior to clinical p53 genetic counseling and testing among persons...

Read the complete abstract on PubMed

Topics

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

Share to Decision Making
Share to Decision Support Techniques

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family

Share to Genetic Counseling

Share to Li-Fraumeni Syndrome

Share to Longitudinal Studies

Share to Outcome Assessment, Health Care

Share to Patient Participation

Source

Open in PubMed Open full text

Identifiers

PMID: 16617243
DOI: 10.1097/01.gim.0000214632.52958.01
PMCID: PMC4145599

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16617243-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evaluation of a decision aid for families considering p53 genetic counseling and testing.PMID 16617243Read ↗

Parent decision-making around the genetic testing of children for germline TP53 mutations.Semantic proximity Read ↗

Randomized trial of a decision aid for individuals considering genetic testing for hereditary nonpolyposis colorectal cancer risk.Semantic proximity Read ↗

Experiences and attitudes of hereditary cancer screening patients in a consumer directed testing model.Semantic proximity Read ↗

Psychological functioning in persons considering genetic counseling and testing for Li–Fraumeni syndromeSemantic proximity Read ↗

Interventions to support decision making in people considering germline genetic testing for BRCA 1/2 pathogenic and likely pathogenic variants: A scoping review.Semantic proximity Read ↗

Piloting a Spanish-Language Web-Based Tool for Hereditary Cancer Genetic Testing.Semantic proximity Read ↗

Using patient decision aids to inform decisions about cancer susceptibility genetic testing and risk management: A narrative review of impact and experienceSemantic proximity Read ↗

The development of an online decision aid to support persons having a genetic predisposition to cancer and their partners during reproductive decision-making: a usability and pilot study.Semantic proximity Read ↗

Patient and Clinician Decision Support to Increase Genetic Counseling for Hereditary Breast and Ovarian Cancer Syndrome in Primary CareSemantic proximity Read ↗

Cancer surveillance and distress among adult pathogenic TP53 germline variant carriers in Germany: A multicenter feasibility and acceptance survey.Semantic proximity Read ↗

Development and pilot testing of a decision aid for men considering genetic testing for breast and/or ovarian cancer-related mutations (BRCA1/2).Semantic proximity Read ↗

Psychosocial interventions and needs among individuals and families with Li-Fraumeni syndrome: A scoping review.Semantic proximity Read ↗

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