Interventions facilitating family communication of genetic testing results and cascade screening in hereditary breast/ovarian cancer or lynch syndrome: a systematic …
V Baroutsou, ML Underhill-Blazey… - Cancers, 2021 - mdpi.com
Simple Summary In general, 5–20% of all cancers are due to pathogenic variants in cancer
genes that are passed down in the family. It is recommended that blood relatives of …
genes that are passed down in the family. It is recommended that blood relatives of …
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 …
ovarian cancer (HBOC) suggests limitations of proband-mediated communication of genetic …
Breast cancer genetic mutation: Synthesis of women's experience
N McNamara, M Feeney, M Giltenane… - Journal of Clinical …, 2023 - Wiley Online Library
Abstract Aims and Objectives To systematically identify and synthesise the experiences
reported by women with a breast cancer mutation who do not have cancer as reported in …
reported by women with a breast cancer mutation who do not have cancer as reported in …
[HTML][HTML] Using a tailored digital health intervention for family communication and cascade genetic testing in Swiss and Korean families with hereditary breast and …
S Kim, M Aceti, V Baroutsou, N Bürki… - JMIR research …, 2021 - researchprotocols.org
Background: In hereditary breast and ovarian cancer (HBOC), family communication of
genetic test results is essential for cascade genetic screening, that is, identifying and testing …
genetic test results is essential for cascade genetic screening, that is, identifying and testing …
[HTML][HTML] Modes of responsibility in disclosing cancer genetic test results to relatives: An analysis of Swiss and Korean narrative data
M Aceti, M Caiata-Zufferey, C Pedrazzani… - Patient Education and …, 2024 - Elsevier
Objective We examined how responsibility (the “duty to inform relatives about genetic testing
results”) is understood and enacted among Swiss and Korean women carrying BRCA1 or …
results”) is understood and enacted among Swiss and Korean women carrying BRCA1 or …
Providing evidence-based health information in easy and plain language
K Leyerer, A Tüchler, R Schmutzler… - … Approaches to an …, 2022 - books.google.com
The Cancer Information Service (CIS) of the German Cancer Research Center is a publicly
funded institution dedicated to providing evidence-based information on cancer to the …
funded institution dedicated to providing evidence-based information on cancer to the …
[HTML][HTML] Shared decision-making in genetic counseling: a scoping review
P Chenyang, N Ning, L Yiyu, T Xiangmin… - Acta …, 2022 - pesquisa.bvsalud.org
Background: It is challenging to make informed decision in genetic counseling. Shared
decision-making provides a chance in balancing the information and preferences between …
decision-making provides a chance in balancing the information and preferences between …
[HTML][HTML] La toma de decisiones compartida en el asesoramiento genético: una revisión del ámbito de aplicación
P Chenyang, L Yiyu, T Xiangmin, T Chaofeng, S Mei - Acta bioethica, 2022 - SciELO Chile
CHENYANG, Peng et al. Shared decision-making in genetic counseling: A scoping review.
Acta bioeth.[online]. 2022, vol. 28, n. 2, pp. 227-237. ISSN 1726-569X. http://dx. doi …
Acta bioeth.[online]. 2022, vol. 28, n. 2, pp. 227-237. ISSN 1726-569X. http://dx. doi …
[PDF][PDF] AUTÓNOMA DE MÉXICO
MYNS ZUBIRÁN - 2023 - ru.dgb.unam.mx
Antecedentes: las malformaciones congénitas (MC) son un desafío para la salud pública
por su elevada prevalencia y consecuencias a lo largo de la vida. Se han identificado …
por su elevada prevalencia y consecuencias a lo largo de la vida. Se han identificado …
Analyse critique de la méthode des forums citoyens à propos des craintes et espoirs associés aux progrès de la génomique en oncologie
M Aceti, P Tsantoulis, PO Chappuis… - Recherches …, 2022 - erudit.org
La méthode des forums citoyens a été utilisée dans le cadre d'une étude réalisée en Suisse
romande afin de recueillir les opinions–quant aux espoirs et aux craintes–à propos des …
romande afin de recueillir les opinions–quant aux espoirs et aux craintes–à propos des …