Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Laura E Forrest"'
Autor:
Laura E. Forrest, Erin Tutty, Anurika P. De Silva, Lara Petelin, Amy Ruscigno, Rebecca Purvis, Katrina Monohan, Maira Kentwell, Adrienne Sexton, Lesley Stafford, Paul A. James
Publikováno v:
Trials, Vol 24, Iss 1, Pp 1-11 (2023)
Abstract Background Genetic counselling aims to identify, and address, patient needs while facilitating informed decision-making about genetic testing and promoting empowerment and adaptation to genetic information. Increasing demand for cancer genet
Externí odkaz:
https://doaj.org/article/e5874e1e0bdc4279bbdf44d233160c6f
Autor:
Alison Luk Young, Aalya Imran, Michael J. Spoelma, Rachel Williams, Katherine M. Tucker, Jane Halliday, Laura E. Forrest, Claire E. Wakefield, Phyllis N. Butow
Publikováno v:
European Journal of Human Genetics. 31:18-34
Interventions to assist family communication about inherited cancer risk have the potential to improve family cancer outcomes. This review aimed to evaluate the efficacy of proband-mediated interventions employed within genetics clinics to increase d
Autor:
Erin Tutty, Rowan Forbes Shepherd, Cass Hoskins, Rebecca Purvis, Mary Shanahan, Alex Boussioutas, Laura E. Forrest
Publikováno v:
Journal of Psychosocial Oncology. 41:286-302
Autor:
Kirsten Allan, Linda Cicciarelli, Catherine Beard, Geoffrey J. Lindeman, G Bruce Mann, Paul James, Laura E. Forrest
Germline genetic testing is an increasingly important component of treatment decision-making for clinicians and patients with breast cancer. To address increased demand and expedite access to genetic testing for these patients, the Parkville Familial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8ef508846e14fef7b941004053795c8
https://doi.org/10.21203/rs.3.rs-2483180/v1
https://doi.org/10.21203/rs.3.rs-2483180/v1
Autor:
Joanne Isbister, Adrienne Sexton, Laura E. Forrest, Paul James, James Dowty, Jessica Taylor, Jehannine Austin, Ingrid Winship
Publikováno v:
Journal of genetic counselingREFERENCES.
Genetic counseling plays a critical role in supporting individuals and their families' adaption to psychiatric conditions, addressing the multifactorial nature of these conditions in a personally meaningful and empowering way. Yet data related to the
Autor:
Rowan Forbes Shepherd, Allison Werner-Lin, Louise Keogh, Martin B. Delatycki, Laura E Forrest
Publikováno v:
Australian Journal of General Practice. 50:538-544
BACKGROUND AND OBJECTIVES: Discussing population-based cancer risk and screening is common in general practice. Patients with an inherited cancer syndrome, however, may need more nuanced discussions. Li-Fraumeni syndrome (LFS) is a rare, inherited ca
Publikováno v:
Journal of Genetic Counseling. 31:242-251
The most effective option for gastric cancer risk management in individuals with a CDH1 germline pathogenic or likely pathogenic variant (PV) in Australia is prophylactic total gastrectomy (PTG). There is, however, increasing confidence in endoscopic
Autor:
Laura E. Forrest, Rowan Forbes Shepherd, Erin Tutty, Angela Pearce, Ian Campbell, Lisa Devereux, Alison H. Trainer, Paul A. James, Mary-Anne Young
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 7; Pages: 1112
Background Research identifying and returning clinically actionable germline variants offer a new avenue of access to genetic information. The psychosocial and clinical outcomes for women who have received this ‘genome-first care’ delivering here
Autor:
Rowan Forbes Shepherd, Louise Keogh, Laura E Forrest, Martin B. Delatycki, Allison Werner-Lin
Publikováno v:
Journal of Psychosocial Oncology. 39:54-73
This study explored the genetic testing experiences of adolescents and young adults (AYAs; aged 15-39 years) with, or at 50% risk of, an early onset cancer predisposition syndrome: Li-Fraumeni syndrome (LFS).We used interpretive description and condu
Autor:
Rowan Forbes Shepherd, Laura E. Forrest, Erin Tutty, Angela Pearce, Lisa Devereux, Paul A. James, Ian G. Campbell, Alison Trainer, Mary-Anne Young
Publikováno v:
Genetic testing and molecular biomarkers. 25(12)