Search Results - "Kentwell, Maira"

Stakeholders' views of integrating universal tumour screening and genetic testing for colorectal and endometrial cancer into routine oncology by O'Shea, Rosie, Rankin, Nicole M, Kentwell, Maira, Gleeson, Margaret, Tucker, Katherine M, Hampel, Heather, Taylor, Natalie, Lewis, Sarah

“…Mainstream genetic testing in routine oncology care requires implementation research to inform intervention design. In Australia, funding is available for…”
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How can Australia integrate routine genetic sequencing in oncology: a qualitative study through an implementation science lens by O’Shea, Rosie, Rankin, Nicole M., Kentwell, Maira, Gleeson, Margaret, Salmon, Lucinda, Tucker, Katherine M., Lewis, Sarah, Taylor, Natalie

“…Purpose This study sought to determine genetics and oncology specialists’ views of integrating BRCA1 and BRCA2 testing in epithelial ovarian and breast cancer…”
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Pilot study of an online training program to increase genetic literacy and communication skills in oncology healthcare professionals discussing BRCA1/2 genetic testing with breast and ovarian cancer patients by Meiser, Bettina, Woodward, Paula, Gleeson, Margaret, Kentwell, Maira, Fan, Helen Mar, Antill, Yoland, Butow, Phyllis N., Boyle, Frances, Best, Megan, Taylor, Natalie, Bell, Katy, Tucker, Kathy

“…The increasing use of genetic testing for BRCA1/2 and other pathogenic variants in the management of women with breast and ovarian cancer necessitates…”
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Personalising genetic counselling (POETIC) trial: Protocol for a hybrid type II effectiveness-implementation randomised clinical trial of a patient screening tool to improve patient empowerment after cancer genetic counselling by Forrest, Laura E, Tutty, Erin, De Silva, Anurika P, Petelin, Lara, Ruscigno, Amy, Purvis, Rebecca, Monohan, Katrina, Kentwell, Maira, Sexton, Adrienne, Stafford, Lesley, James, Paul A

“…Abstract Background Genetic counselling aims to identify, and address, patient needs while facilitating informed decision-making about genetic testing and…”
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A mainstreaming oncogenomics model: improving the identification of Lynch syndrome by O'Shea, Rosie, Crook, Ashley, Jacobs, Chris, Kentwell, Maira, Gleeson, Margaret, Tucker, Katherine M, Hampel, Heather, Rahm, Alanna Kulchak, Taylor, Natalie, Lewis, Sarah, Rankin, Nicole M

“…"Mainstreaming" is a proposed strategy to integrate genomic testing into oncology. The aim of this paper is to develop a mainstreaming oncogenomics model by…”
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Mainstreaming cancer genetics: A model integrating germline BRCA testing into routine ovarian cancer clinics by Kentwell, Maira, Dow, Eryn, Antill, Yoland, Wrede, C. David, McNally, Orla, Higgs, Emily, Hamilton, Anne, Ananda, Sumitra, Lindeman, Geoffrey J, Scott, Clare L

“…Abstract Objective Owing to the rapid increase in clinical need, we aimed to implement and review the performance of a mainstreaming model of germline BRCA1/2…”
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Assessing the acceptability, feasibility, and usefulness of a psychosocial screening tool to patients and clinicians in a clinical genetics service in Australia by Monohan, Katrina, Purvis, Rebecca, Sexton, Adrienne, Kentwell, Maira, Thet, Monica, Stafford, Lesley, Forrest, Laura

“…Increasing demand for clinical genetic services may impact the resources and quality of genetic counseling, potentially impacting patient outcomes. Using a…”
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Abstract P3-09-02: Mutational assessment of newly diagnosed breast cancer using Germline and tumor genomICs by De Silva, Dilanka L, Skandarajah, Anita R, Sinclair, Michelle, Kentwell, Maira, Devereux, Lisa, Zeethoven, Magnus, Hogg, Kirsten, Lal, Luxi, Stafford, Lesley, James, Paul A, Lindeman, Geoffrey J, Mann, Gregory B, Campbell, Ian G

“…Abstract Background :For patients with newly diagnosed breast cancer, real-time identification of pathogenic germline mutations in hereditary breast cancer…”
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Universal genetic testing for women with newly diagnosed breast cancer in the context of multidisciplinary team care by De Silva, Dilanka L, Stafford, Lesley, Skandarajah, Anita R, Sinclair, Michelle, Devereux, Lisa, Hogg, Kirsten, Kentwell, Maira, Park, Allan, Lal, Luxi, Zethoven, Magnus, Jayawardana, Madawa W, Chan, Fiona, Butow, Phyllis N, James, Paul A, Mann, G Bruce, Campbell, Ian G, Lindeman, Geoffrey J

“…Objective To determine the feasibility of universal genetic testing of women with newly diagnosed breast cancer, to estimate the incidence of pathogenic gene…”
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Abstract PO1-09-02: Universal genetic testing for women with newly diagnosed breast cancer identified many mutations, impacted clinical management and caused no psychological distress to patients by De Silva, Dilanka, Stafford, Lesley, Skandarajah, Anita, Sinclair, Michelle, Devereux, Lisa, Hogg, Kirsten, Kentwell, Maira, Park, Allan, Lal, luxi, Zethoven, Magnus, Jayawardena, Madawa, Chan, Fiona, James, Paul, Lindeman, Geoffrey, Campbell, Ian, Mann, Bruce

“…Abstract Background: For newly diagnosed breast cancer (BC) patients, identification of pathogenic germline mutations in hereditary breast cancer (HBC) genes…”
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Experiences and interpretations of BRCA1/2 testing among women affected by breast or ovarian cancer who received a negative result by Stafford, Lesley, Flehr, Alison, Judd, Fiona, Lindeman, Geoffrey J., Gibson, Penny, Komiti, Angela, Mann, G. Bruce, Kentwell, Maira

“…The aim of this study was to retrospectively describe the genetic testing motives and experiences of women with a previous breast and/or ovarian cancer…”
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Vestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review by Huq, Aamira, Kentwell, Maira, Tirimacco, Amanda, Rossini, Jacqueline, Rawlings, Lesley, Winship, Ingrid

“…We describe a young patient with typical neurofibromatosis type 1 on the basis of a mutation in the NF1 gene, who was diagnosed with a unilateral vestibular…”
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