Interventions to support patients with sharing genetic test results with at-risk relatives: a synthesis without meta-analysis (SWiM)

LM Ballard, R Band, AM Lucassen - European Journal of Human …, 2023 - nature.com
Whilst the finding of heritable susceptibility to disease was once relatively rare,
mainstreaming of genetic testing has resulted in a steady increase. Patients are often …

The communication chain of genetic risk: analyses of narrative data exploring proband–provider and proband–family communication in hereditary breast and ovarian …

C Pedrazzani, M Aceti, R Schweighoffer… - Journal of personalized …, 2022 - mdpi.com
Low uptake of genetic services among members of families with hereditary breast and
ovarian cancer (HBOC) suggests limitations of proband-mediated communication of genetic …

Psychosocial barriers and facilitators for cascade genetic testing in hereditary breast and ovarian cancer: a sco** review

A Afaya, SW Kim, HS Park, MC Lim, MS Jung, EJ Nam… - Familial Cancer, 2024 - Springer
Despite increased awareness and availability of genetic testing for hereditary breast and
ovarian cancer (HBOC) syndrome for over 20 years, there is still significant underuse of …

Cascade testing in Italian Hereditary Breast Ovarian Cancer families: a missed opportunity for cancer prevention?

L Trevisan, L Godino, L Battistuzzi, G Innella, E Luppi… - Familial Cancer, 2024 - Springer
Healthy carriers of BRCA1/2 pathogenic variants (PVs) may benefit from risk-reducing
measures of proven efficacy. The main approach to identify these individuals is cascade …

Survey on determinants of intention to reduce nasopharyngeal cancer risk: an application of the theory of planned behavior

SH Ting, RK Brahmana, C Jerome, Y Podin - BMC Public Health, 2022 - Springer
Background To have better prognostic outcomes and minimize deaths due to
nasopharyngeal cancer, it is vital to understand factors that motivate the public to undertake …

Co** response and family communication of cancer risk in men harboring a BRCA mutation: A mixed methods study

AA Dwyer, S Hesse‐Biber, H Shea, Z Zeng… - Psycho …, 2022 - Wiley Online Library
Objective Providing genetic counseling and genetic testing to at‐risk blood relatives
(cascade screening) is important for improving BRCA cancer outcomes. Intra‐familial …

Exploring rare disease patient attitudes and beliefs regarding genetic testing: implications for person-centered care

AA Dwyer, MK Uveges, S Dockray, N Smith - Journal of Personalized …, 2022 - mdpi.com
Most rare diseases are genetic in etiology and characterized by a 'diagnostic odyssey'.
Genomic advances have helped speed up the diagnosis for many rare disorders, opening …

[HTML][HTML] Predicting Openness of Communication in Families With Hereditary Breast and Ovarian Cancer Syndrome: Natural Language Processing Analysis

V Baroutsou, R Cerqueira Gonzalez Pena… - JMIR Formative …, 2023 - formative.jmir.org
Background In health care research, patient-reported opinions are a critical element of
personalized medicine and contribute to optimal health care delivery. The importance of …

Framing effects on decision-making for diagnostic genetic testing: Results from a randomized trial

AA Dwyer, H Shen, Z Zeng, M Gregas, M Zhao - Genes, 2021 - mdpi.com
Genetic testing is increasingly part of routine clinical care. However, testing decisions may
be characterized by regret as findings also implicate blood relatives. It is not known if genetic …

Impact of BRCA Status on Reproductive Decision-Making and Self-Concept: A Mixed-Methods Study Informing the Development of Tailored Interventions

S Hesse-Biber, M Seven, J Jiang, S Van Schaik… - Cancers, 2022 - mdpi.com
Simple Summary Reproductive decision-making is a complex process and is influenced by
personal, medical, and sociocultural factors. Relatively little is known about reproductive …