Zobrazeno 1 - 10
of 133
pro vyhledávání: '"Kristine Barlow-Stewart"'
Autor:
Yuyan Chen, Mark Pinese, Claire Wakefield, Frank Alvaro, Katherine Tucker, Tracey A O’Brien, Vanessa J Tyrrell, Judy Kirk, Kate Hetherington, Eliza Courtney, Kristine Barlow-Stewart, Noemi Auxiliadora Fuentes Bolanos, Bhavna Padhye, Macabe Daley, Jacqueline Hunter, Meera Warby, Sarah Josephi-Taylor, Marie Wong-Erasmus, Paulette Barahona, Pamela Ajuyah, Ann-Kristin Altekoester, Loretta M S Lau, Dianne Sylvester, Luciano Dalla Pozza
Publikováno v:
BMJ Open, Vol 13, Iss 5 (2023)
Introduction Identifying an underlying germline cancer predisposition (CP) in a child with cancer has potentially significant implications for both the child and biological relatives. Cohort studies indicate that 10%–15% of paediatric cancer patien
Externí odkaz:
https://doaj.org/article/da226946131d4fd0bb6f8385a8b6d90d
Autor:
Jane Tiller, Aideen McInerney-Leo, Andrea Belcher, Tiffany Boughtwood, Penny Gleeson, Martin Delatycki, Kristine Barlow-Stewart, Ingrid Winship, Margaret Otlowski, Louise Keogh, Paul Lacaze
Publikováno v:
BMC Medical Ethics, Vol 22, Iss 1, Pp 1-14 (2021)
Abstract Background The use of genetic test results in risk-rated insurance is a significant concern internationally, with many countries banning or restricting the use of genetic test results in underwriting. In Australia, life insurers’ use of ge
Externí odkaz:
https://doaj.org/article/6ad283767a6941b2b17b4811e5806dae
Publikováno v:
BMC Medical Ethics, Vol 21, Iss 1, Pp 1-10 (2020)
Abstract Background When a genetic mutation is identified in a family member (proband), internationally, it is usually the proband’s or another responsible family member’s role to disclose the information to at-risk relatives. However, both activ
Externí odkaz:
https://doaj.org/article/69fd698dbdf140c2b68926f665151398
Autor:
Alison D. Archibald, Belinda J. McClaren, Jade Caruana, Erin Tutty, Emily A. King, Jane L. Halliday, Stephanie Best, Anaita Kanga-Parabia, Bruce H. Bennetts, Corrina C. Cliffe, Evanthia O. Madelli, Gladys Ho, Jan Liebelt, Janet C. Long, Jeffrey Braithwaite, Jillian Kennedy, John Massie, Jon D. Emery, Julie McGaughran, Justine E. Marum, Kirsten Boggs, Kristine Barlow-Stewart, Leslie Burnett, Lisa Dive, Lucinda Freeman, Mark R. Davis, Martin J. Downes, Mathew Wallis, Monica M. Ferrie, Nicholas Pachter, Paul A. Scuffham, Rachael Casella, Richard J. N. Allcock, Royston Ong, Samantha Edwards, Sarah Righetti, Sebastian Lunke, Sharon Lewis, Susan P. Walker, Tiffany F. Boughtwood, Tristan Hardy, Ainsley J. Newson, Edwin P. Kirk, Nigel G. Laing, Martin B. Delatycki, The Mackenzie’s Mission Study Team
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 11, p 1781 (2022)
Reproductive genetic carrier screening (RGCS) provides people with information about their chance of having children with autosomal recessive or X-linked genetic conditions, enabling informed reproductive decision-making. RGCS is recommended to be of
Externí odkaz:
https://doaj.org/article/db45c3e4abc84d29b648a7552a4461f9
Autor:
Martin B Delatycki, Chris Jacobs, Bettina Meiser, Ian G Campbell, Lesley Andrews, Paul A James, Alison Trainer, AGNES BANKIER, Kristine Barlow-Stewart, Jane Tiller, Nicole E Cousens, Simone Rowley, Sakshi Mahale, Rajneesh Kaur, Leslie Burnett, Suzanne Neil
Publikováno v:
BMJ Open, Vol 11, Iss 6 (2021)
Introduction People of Ashkenazi Jewish (AJ) ancestry are more likely than unselected populations to have a BRCA1/2 pathogenic variant, which cause a significantly increased risk of breast, ovarian and prostate cancer. Three specific BRCA1/2 pathogen
Externí odkaz:
https://doaj.org/article/c13502b3150143889118fe9f14053fbc
Autor:
Jacqueline D. Hunter, Eden G. Robertson, Kate Hetherington, David S. Ziegler, Glenn M. Marshall, Judy Kirk, Jonathan M. Marron, Avram E. Denburg, Kristine Barlow-Stewart, Meera Warby, Katherine M. Tucker, Brittany M. Lee, Tracey A. O’Brien, Claire E. Wakefield
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 8, p 1327 (2022)
Current literature/guidelines regarding the most appropriate term to communicate a cancer-related disease-causing germline variant in childhood cancer lack consensus. Guidelines also rarely address preferences of patients/families. We aimed to assess
Externí odkaz:
https://doaj.org/article/4ab40699ed06468dabee240c8c8ed874
Autor:
Llewellyn Mills, Bettina Meiser, Raghib Ahmad, Peter R. Schofield, Michelle Peate, Charlene Levitan, Lyndal Trevena, Kristine Barlow-Stewart, Timothy Dobbins, Helen Christensen, Kerry A. Sherman, Kate Dunlop, Philip B. Mitchell
Publikováno v:
BMC Psychiatry, Vol 19, Iss 1, Pp 1-11 (2019)
Abstract Background People with a family history of major depressive disorder (MDD) or bipolar disorder (BD) report specific psychoeducational needs that are unmet by existing online interventions. This trial aimed to test whether an interactive webs
Externí odkaz:
https://doaj.org/article/11fa4b34758847909ecd9811297fd4a8
Autor:
Sian Karen Smith, Antonia Cai, Michelle Wong, Mariana S. Sousa, Michelle Peate, Alec Welsh, Bettina Meiser, Rajneesh Kaur, Jane Halliday, Sharon Lewis, Lyndal Trevena, Tatiane Yanes, Kristine Barlow-Stewart, Margot Barclay
Publikováno v:
BMC Pregnancy and Childbirth, Vol 18, Iss 1, Pp 1-14 (2018)
Abstract Background Access to information about prenatal screening is important particularly in light of new techniques such as non-invasive prenatal testing (NIPT). This study aimed to develop and examine the acceptability of a low literacy decision
Externí odkaz:
https://doaj.org/article/c5b8e40f369847d5b5742581d9bc7cc8
Autor:
Tatiane Yanes, Bettina Meiser, Mary-Anne Young, Rajneesh Kaur, Gillian Mitchell, Kristine Barlow-Stewart, Tony Roscioli, Jane Halliday, Paul James
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-11 (2017)
Abstract Background The ‘common variant, common disease’ model predicts that a significant component of hereditary breast cancer unexplained by pathogenic variants in moderate or high-penetrance genes is due to the cumulative effect of common ris
Externí odkaz:
https://doaj.org/article/6a5f88f754be48ca9cfc001fdac4d008
Publikováno v:
Human Reproduction. 37:2599-2610
STUDY QUESTION What are the roles of individual and interpersonal factors in couples’ decision-making regarding preimplantation genetic testing for monogenic disorders (PGT-M)? SUMMARY ANSWER Couples’ decision-making regarding PGT-M was associate