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Author Details
Full Name
Gillian Mitchell
Affiliation
Familial Cancer Centre Peter MacCallum Cancer Centre Parkville Victoria 0 Australia.
ORCID
Career Start Year
1998
Papers
121
H Index
40
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36618023
The Risk-Reducing Effect of Aspirin in Lynch Syndrome Carriers: Development and Evaluation of an Educational Leaflet.
Adv Genet (Hoboken)
2022
36618023
The Risk-Reducing Effect of Aspirin in Lynch Syndrome Carriers: Development and Evaluation of an Educational Leaflet.
Adv Genet (Hoboken)
2022
33168572
Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility.
J Med Genet
2021
33836815
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.
Hered Cancer Clin Pract
2021
33168572
Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility.
J Med Genet
2021
33836815
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.
Hered Cancer Clin Pract
2021
31595523
The predicted impact and cost-effectiveness of systematic testing of people with incident colorectal cancer for Lynch syndrome.
Med J Aust
2020
31595523
The predicted impact and cost-effectiveness of systematic testing of people with incident colorectal cancer for Lynch syndrome.
Med J Aust
2020
31996782
Cost-effectiveness of long-term clinical management of BRCA pathogenic variant carriers.
Genet Med
2020
32565470
Pathways to a cancer-free future: a protocol for modelled evaluations to minimise the future burden of colorectal cancer in Australia.
BMJ Open
2020
31996782
Cost-effectiveness of long-term clinical management of BRCA pathogenic variant carriers.
Genet Med
2020
32565470
Pathways to a cancer-free future: a protocol for modelled evaluations to minimise the future burden of colorectal cancer in Australia.
BMJ Open
2020
30525267
Assessing the medical workforces perceived barriers to the prescription of risk-reducing medication for women at high-risk of breast cancer.
Breast J
2019
30525267
Assessing the medical workforces perceived barriers to the prescription of risk-reducing medication for women at high-risk of breast cancer.
Breast J
2019
31221211
Comparing theory and non-theory based implementation approaches to improving referral practices in cancer genetics: a cluster randomised trial protocol.
Trials
2019
31426925
A Microsimulation Model for Evaluating the Effectiveness of Cancer Risk Management for BRCA Pathogenic Variant Carriers: miBRovaCAre.
Value Health
2019
31384883
Cancer screening in Australia: future directions in melanoma, Lynch syndrome, and liver, lung and prostate cancers.
Public Health Res Pract
2019
31384883
Cancer screening in Australia: future directions in melanoma, Lynch syndrome, and liver, lung and prostate cancers.
Public Health Res Pract
2019
31426925
A Microsimulation Model for Evaluating the Effectiveness of Cancer Risk Management for BRCA Pathogenic Variant Carriers: miBRovaCAre.
Value Health
2019
31221211
Comparing theory and non-theory based implementation approaches to improving referral practices in cancer genetics: a cluster randomised trial protocol.
Trials
2019
28822109
Consumer attitudes towards the establishment of a national Australian familial cancer research database by the Inherited Cancer Connect (ICCon) Partnership.
J Community Genet
2018
28822109
Consumer attitudes towards the establishment of a national Australian familial cancer research database by the Inherited Cancer Connect (ICCon) Partnership.
J Community Genet
2018
30294856
Current mismatch repair deficiency tumor testing practices and capabilities: A survey of Australian pathology providers.
Asia Pac J Clin Oncol
2018
30005762
Heterogeneity and Uncertainties Specific to Genome-Based Health Technological Assessments.
Value Health
2018
29168041
Making Sense of SNPs: Women's Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks.
J Genet Couns
2018
29599518
Psychological outcomes and surgical decisions after genetic testing in women newly diagnosed with breast cancer with and without a family history.
Eur J Hum Genet
2018
29506471
A population-based analysis of germline BRCA1 and BRCA2 testing among ovarian cancer patients in an era of histotype-specific approaches to ovarian cancer prevention.
BMC Cancer
2018
29323669
Cost-effectiveness and comparative effectiveness of cancer risk management strategies in BRCA1/2 mutation carriers: a systematic review.
Genet Med
2018
30005762
Heterogeneity and Uncertainties Specific to Genome-Based Health Technological Assessments.
Value Health
2018
30294856
Current mismatch repair deficiency tumor testing practices and capabilities: A survey of Australian pathology providers.
Asia Pac J Clin Oncol
2018
29599518
Psychological outcomes and surgical decisions after genetic testing in women newly diagnosed with breast cancer with and without a family history.
Eur J Hum Genet
2018
29506471
A population-based analysis of germline BRCA1 and BRCA2 testing among ovarian cancer patients in an era of histotype-specific approaches to ovarian cancer prevention.
BMC Cancer
2018
29323669
Cost-effectiveness and comparative effectiveness of cancer risk management strategies in BRCA1/2 mutation carriers: a systematic review.
Genet Med
2018
29168041
Making Sense of SNPs: Women's Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks.
J Genet Couns
2018
27171545
Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab.
Genet Med
2017
28772290
Surveillance in Germline TP53 Mutation Carriers Utilizing Whole-Body Magnetic Resonance Imaging.
JAMA Oncol
2017
28346442
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Nat Genet
2017
28943990
Motivators and barriers of tamoxifen use as risk-reducing medication amongst women at increased breast cancer risk: a systematic literature review.
Hered Cancer Clin Pract
2017
28720130
Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study.
BMC Cancer
2017
28448241
Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores.
J Clin Oncol
2017
29058716
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
Nat Genet
2017
29224207
Acute kidney injury is under-recognised and under-reported in hospitalised patients in Australia.
Intern Med J
2017
27171545
Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab.
Genet Med
2017
27684037
Streamlined genetic education is effective in preparing women newly diagnosed with breast cancer for decision making about treatment-focused genetic testing: a randomized controlled noninferiority trial.
Genet Med
2017
27677266
Exploring clinicians' attitudes about using aspirin for risk reduction in people with Lynch Syndrome with no personal diagnosis of colorectal cancer.
Fam Cancer
2017
28124295
Psychosocial morbidity in TP53 mutation carriers: is whole-body cancer screening beneficial?
Fam Cancer
2017
28124295
Psychosocial morbidity in TP53 mutation carriers: is whole-body cancer screening beneficial?
Fam Cancer
2017
28448241
Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores.
J Clin Oncol
2017
28346442
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Nat Genet
2017
29058716
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
Nat Genet
2017
1 - 50 of 242
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Co-authored papers
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Siranoush Manoukian
Fondazione IRCCS Istituto Nazionale dei Tumori
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Esther M John
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Judy E Garber
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9
Paolo Radice
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Beth Y Karlan
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Katherine L Nathanson
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