Select Publications
Journal articles
2024, '“Out of the blue”: A qualitative study exploring the experiences of women and next of kin receiving unexpected results from BRA-STRAP research gene panel testing', Journal of Genetic Counseling, 33, pp. 973 - 984, http://dx.doi.org/10.1002/jgc4.1803
,2023, 'In person and virtual process mapping experiences to capture and explore variability in clinical practice: application to genetic referral pathways across seven Australian hospital networks', Translational Behavioral Medicine, 13, pp. 561 - 570, http://dx.doi.org/10.1093/tbm/ibad009
,2023, 'Examining the effectiveness and implementation of patient treatment decision-aid tools for men with localised prostate cancer: A systematic review', Psycho-Oncology, 32, pp. 469 - 491, http://dx.doi.org/10.1002/pon.6094
,2022, 'Lynch syndrome testing of colorectal cancer patients in a high-income country with universal healthcare: a retrospective study of current practice and gaps in seven australian hospitals', Hereditary Cancer in Clinical Practice, 20, http://dx.doi.org/10.1186/s13053-022-00225-1
,2022, 'What would I do? Perspectives on the factors underlying Lynch syndrome genetic testing and results sharing decisions for high-risk colorectal cancer patients', Psycho-Oncology, 31, pp. 587 - 596, http://dx.doi.org/10.1002/pon.5840
,2022, 'Building capacity from within: Qualitative evaluation of a training program aimed at upskilling healthcare workers in delivering an evidence-based implementation approach', Translational Behavioral Medicine, 12, pp. 39 - 62, http://dx.doi.org/10.1093/tbm/ibab094
,2021, 'Impact of national guidelines on use of BRCA1/2 germline testing, risk management advice given to women with pathogenic BRCA1/2 variants and uptake of advice', Hereditary Cancer in Clinical Practice, 19, http://dx.doi.org/10.1186/s13053-021-00180-3
,2021, 'Population-based estimates of breast cancer risk for carriers of pathogenic variants identified by gene-panel testing', npj Breast Cancer, 7, http://dx.doi.org/10.1038/s41523-021-00360-3
,2021, 'The design, implementation, and effectiveness of intervention strategies aimed at improving genetic referral practices: a systematic review of the literature', Genetics in Medicine, 23, pp. 2239 - 2249, http://dx.doi.org/10.1038/s41436-021-01272-0
,2021, 'Cancer care disruption and reorganisation during the COVID-19 pandemic in Australia: A patient, carer and healthcare worker perspective', PLoS ONE, 16, pp. e0257420, http://dx.doi.org/10.1371/journal.pone.0257420
,2020, 'Aligning intuition and theory: enhancing the replicability of behaviour change interventions in cancer genetics', Implementation Science Communications, 1, pp. 90, http://dx.doi.org/10.1186/s43058-020-00054-0
,2020, 'The health and economic impact of implementation strategies for improving detection of hereditary cancer patients—protocol for an in-depth cost-effectiveness evaluation with microsimulation modelling', Implementation Science Communications, 1, http://dx.doi.org/10.1186/s43058-020-00058-w
,2020, 'Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinics', Familial Cancer, 19, pp. 337 - 346, http://dx.doi.org/10.1007/s10689-020-00183-4
,2020, 'Understanding implementation success: Protocol for an in-depth, mixed-methods process evaluation of a cluster randomised controlled trial testing methods to improve detection of Lynch syndrome in Australian hospitals', BMJ Open, 10, http://dx.doi.org/10.1136/bmjopen-2019-033552
,2019, 'Comparing theory and non-theory based implementation approaches to improving referral practices in cancer genetics: A cluster randomised trial protocol', Trials, 20, http://dx.doi.org/10.1186/s13063-019-3457-6
,2018, 'Genetics in palliative oncology: a missing agenda? A review of the literature and future directions', Supportive Care in Cancer, 26, pp. 721 - 730, http://dx.doi.org/10.1007/s00520-017-4017-9
,2016, 'Referral of patients for pre-implantation genetic diagnosis: A survey of obstetricians', Australian and New Zealand Journal of Obstetrics and Gynaecology, 56, pp. 585 - 590, http://dx.doi.org/10.1111/ajo.12522
,Conference Papers
2020, 'Population-based estimates of breast cancer risk for germline pathogenic variants identified by gene-panel testing: An Australian perspective', in ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, WILEY, pp. 85 - 85, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000790145400063&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2014, 'THE INHERITED CANCER CONNECT (ICCON) MUTATION-CARRIER DATABASE', in ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, WILEY-BLACKWELL, pp. 167 - 168, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000345350900279&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,Conference Abstracts
2021, 'Population-based estimates of breast cancer risk for germline pathogenic variants identified by gene-panel testing: An Australian perspective', in CANCER RESEARCH, AMER ASSOC CANCER RESEARCH, Vol. 81, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000618737701097&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
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