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Fear of cancer recurrence in breast cancer survivors carrying a BRCA1 or 2 genetic mutation : a cross-sectional study

Hereditary cancer in clinical practice, 2024-08, Vol.22 (1), p.16-13

2024

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A Randomized Double-Blind Placebo-Controlled Trial of the Effect of Vitamin D3 Supplementation on Breast Density in Premenopausal Women

Cancer epidemiology, biomarkers & prevention, 2017-08, Vol.26 (8), p.1233-1241

2017

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Cross-Cultural Adaptation and Validation of a French Version of the Genetic Counseling Satisfaction Scale (GCSS) as an Outcome Measure of Genetic Counseling for Hereditary Breast and Ovarian Cancer

Healthcare (Basel), 2021-09, Vol.9 (9), p.1145

2021

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QIM19-119: Validity of the French-Language Mammography Satisfaction Instrument Evaluating Women’s Satisfaction With an Organized Breast Cancer Screening Program: A Confirmatory Study

Journal of the National Comprehensive Cancer Network, 2019-03, Vol.17 (3.5), p.QIM19-119

2019

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Increased Use of BRCA Mutation Test in Unaffected Women Over the Period 2004–2014 in the U.S.: Further Evidence of the “Angelina Jolie Effect”?

American journal of preventive medicine, 2017-11, Vol.53 (5), p.e195-e196

2017

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Mapping inter-professional collaboration in oncogenetics: Results from a scoping review

Critical reviews in oncology/hematology, 2024-07, Vol.199, p.104364, Article 104364

2024

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Polygenic risk scores and risk-stratified breast cancer screening: Familiarity and perspectives of health care professionals

Genetics in medicine, 2022-11, Vol.24 (11), p.2380-2388

2022

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Cross-cultural adaptation and validation of a French version of the perceived personal control questionnaire as an outcome measure instrument for genetic counseling

Journal of genetic counseling, 2024-10

2024

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General Medical Practitioners Acting as Geneticists, a Risky Business?

Lex Electronica, 2023, Vol.28 (1), p.152-171

2023

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Personalized Risk Assessment for Prevention and Early Detection of Breast Cancer: Integration and Implementation (PERSPECTIVE I&I)

Journal of personalized medicine, 2021-06, Vol.11 (6), p.511

2021

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Polymorphic variations in the FANCA gene in high-risk non-BRCA1/2 breast cancer individuals from the French Canadian population

Molecular oncology, 2013-02, Vol.7 (1), p.85-100

2013

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Women's Views on Multifactorial Breast Cancer Risk Assessment and Risk-Stratified Screening: A Population-Based Survey from Four Provinces in Canada

Journal of personalized medicine, 2021-02, Vol.11 (2), p.95

2021

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Survey of palliative care providers’ needs, perceived roles, and ethical concerns about addressing cancer family history at the end of life

Palliative & supportive care, 2021-04, Vol.19 (2), p.217-222

2021

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P336 Issues Related to Family History of Cancer at the End of Life: A Palliative Care Providers’ Survey

Journal of pain and symptom management, 2016-12, Vol.52 (6), p.e153-e153

2016

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Systematic review of educational tools used during the BRCA1/2 genetic testing process

Personalized medicine, 2014-01, Vol.11 (1), p.113-124

2014

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Should Age-Dependent Absolute Risk Thresholds Be Used for Risk Stratification in Risk-Stratified Breast Cancer Screening?

Journal of personalized medicine, 2021-09, Vol.11 (9), p.916

2021

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Development of a Tool to Guide Parents Carrying a BRCA1/2 Mutation Share Genetic Results with Underage Children

Journal of cancer education, 2018-06, Vol.33 (3), p.569-575

2018

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Canadian Healthcare Professionals' Views and Attitudes toward Risk-Stratified Breast Cancer Screening

Journal of personalized medicine, 2023-06, Vol.13 (7), p.1027

2023

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Variations in the NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2 French Canadian families with high risk of breast cancer

BMC cancer, 2009-06, Vol.9 (181), p.181-181

2009

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Systematic review of educational tools used during the

Personalized medicine, 2014-01, Vol.11 (1), p.113-124

2014

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A Collaborative Model to Implement Flexible, Accessible and Efficient Oncogenetic Services for Hereditary Breast and Ovarian Cancer: The C-MOnGene Study

Cancers, 2021-05, Vol.13 (11), p.2729

2021

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Genetic sequence variations of BRCA1-interacting genes AURKA, BAP1, BARD1 and DHX9 in French Canadian families with high risk of breast cancer

Journal of human genetics, 2009-03, Vol.54 (3), p.152-161

2009

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Identification of twelve new susceptibility loci for different histotypes of epithelial ovarian cancer

Nature genetics, 2017-03, Vol.49 (5), p.680-691

2017

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Fear of cancer recurrence in breast cancer survivors carrying a BRCA1 or 2 genetic mutation : a cross-sectional study

A Randomized Double-Blind Placebo-Controlled Trial of the Effect of Vitamin D3 Supplementation on Breast Density in Premenopausal Women

Cross-Cultural Adaptation and Validation of a French Version of the Genetic Counseling Satisfaction Scale (GCSS) as an Outcome Measure of Genetic Counseling for Hereditary Breast and Ovarian Cancer

QIM19-119: Validity of the French-Language Mammography Satisfaction Instrument Evaluating Women’s Satisfaction With an Organized Breast Cancer Screening Program: A Confirmatory Study

Increased Use of BRCA Mutation Test in Unaffected Women Over the Period 2004–2014 in the U.S.: Further Evidence of the “Angelina Jolie Effect”?

Mapping inter-professional collaboration in oncogenetics: Results from a scoping review

Polygenic risk scores and risk-stratified breast cancer screening: Familiarity and perspectives of health care professionals

Cross-cultural adaptation and validation of a French version of the perceived personal control questionnaire as an outcome measure instrument for genetic counseling

General Medical Practitioners Acting as Geneticists, a Risky Business?

Personalized Risk Assessment for Prevention and Early Detection of Breast Cancer: Integration and Implementation (PERSPECTIVE I&I)

Polymorphic variations in the FANCA gene in high-risk non-BRCA1/2 breast cancer individuals from the French Canadian population

A response to “Personalised medicine and population health: breast and ovarian cancer”

Women's Views on Multifactorial Breast Cancer Risk Assessment and Risk-Stratified Screening: A Population-Based Survey from Four Provinces in Canada

Survey of palliative care providers’ needs, perceived roles, and ethical concerns about addressing cancer family history at the end of life

Implementing Multifactorial Risk Assessment with Polygenic Risk Scores for Personalized Breast Cancer Screening in the Population Setting: Challenges and Opportunities

P336 Issues Related to Family History of Cancer at the End of Life: A Palliative Care Providers’ Survey

Systematic review of educational tools used during the BRCA1/2 genetic testing process

Should Age-Dependent Absolute Risk Thresholds Be Used for Risk Stratification in Risk-Stratified Breast Cancer Screening?

Development of a Tool to Guide Parents Carrying a BRCA1/2 Mutation Share Genetic Results with Underage Children

Canadian Healthcare Professionals' Views and Attitudes toward Risk-Stratified Breast Cancer Screening

Variations in the NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2 French Canadian families with high risk of breast cancer

Systematic review of educational tools used during the

A Collaborative Model to Implement Flexible, Accessible and Efficient Oncogenetic Services for Hereditary Breast and Ovarian Cancer: The C-MOnGene Study

Genetic sequence variations of BRCA1-interacting genes AURKA, BAP1, BARD1 and DHX9 in French Canadian families with high risk of breast cancer

Identification of twelve new susceptibility loci for different histotypes of epithelial ovarian cancer

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