Impact of genetic risk assessment on nutrition-related lifestyle behaviours

JA Vernarelli - Proceedings of the Nutrition Society, 2013 - cambridge.org
Genetic susceptibility testing for common complex disease is a practice that is currently in
clinical use. There are two types of gene mutations, and therefore, two varieties of genotype …

Unselected Women's Experiences of Receiving Genetic Research Results for Hereditary Breast and Ovarian Cancer: A Qualitative Study

R Forbes Shepherd, LE Forrest, E Tutty… - Genetic Testing and …, 2021 - liebertpub.com
Background: Although there is growing consensus that clinically actionable genetic research
results should be returned to participants, research on recipients' experiences and best …

Patient responses to genetic information: studies of patients with hereditary cancer syndromes identify issues for use of genetic testing in nephrology practice

KA Kaphingst, CM McBride - Seminars in nephrology, 2010 - Elsevier
Advances in the genetic basis of kidney disease may mean that genetic testing is
increasingly important in reducing disease morbidity and mortality among patients …

Cancer genetics: estimation of the needs of the population in France for the next ten years

C Bonaïti-Pellié, N Andrieu, P Arveux… - Bulletin du …, 2009 - inserm.hal.science
Résumé Organised since 1990 in France, cancer genetics has been strengthened since
2003 by the programme" Plan Cancer" which resulted in an improvement of the organisation …

Cancer risks for Australian women with a BRCA1 or a BRCA2 mutation

GK Suthers - ANZ Journal of Surgery, 2007 - Wiley Online Library
One of the primary purposes of genetic testing for mutations in the BRCA1 and BRCA2
genes in patients with familial breast/ovarian cancer has been to provide accurate advice to …

Cancer Risk Management Practices of Noncarriers Within BRCA1/2 Mutation–Positive Families in the Kathleen Cuningham Foundation Consortium for Research Into …

SJ Dawson, MA Price, MA Jenkins… - Journal of clinical …, 2008 - ascopubs.org
Purpose Women from BRCA mutation–positive families who do not carry the family-specific
mutation are generally at average cancer risk and therefore do not require intensive risk …

Adapting the coping in deliberation (CODE) framework: A multi-method approach in the context of familial ovarian cancer risk management

J Witt, G Elwyn, F Wood, MT Rogers, U Menon… - Patient education and …, 2014 - Elsevier
Objective To test whether the coping in deliberation (CODE) framework can be adapted to a
specific preference-sensitive medical decision: risk-reducing bilateral salpingo …

The frequency and outcome of breast cancer risk-reducing surgery in finnish BRCA1 and BRCA2 mutation carriers

L Koskenvuo, C Svarvar, S Suominen… - … Journal of Surgery, 2014 - journals.sagepub.com
Background and Aims: Risk-reducing mastectomy of BRCA1 and BRCA2 gene mutation
carriers is known to significantly reduce lifetime risk of breast cancer. Our aim was to study …

Cancer risk management in Tasmanian women with BRCA1 and BRCA2 mutations

S Kearton, K Wills, M Bunting, P Blomfield, PA James… - Familial cancer, 2018 - Springer
Women carrying germline mutations in BRCA1 or BRCA2 have significantly increased
lifetime risks of breast and tubo-ovarian cancer. To manage the breast cancer risk women …

Four actionable bottlenecks and potential solutions to translating psychiatric genetics research: An expert review

JL Bourdon, RA Davies, EC Long - Public health genomics, 2021 - karger.com
Background: Psychiatric genetics has had limited success in translational efforts. A thorough
understanding of the present state of translation in this field will be useful in the facilitation …