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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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Fear of cancer recurrence in breast cancer survivors carrying a BRCA1/2 mutation: A qualitative study

Cancer medicine (Malden, MA), 2024-01, Vol.13 (1), p.e6889-n/a

2024

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Whether, when, how, and how much? General public's and cancer patients' views about the disclosure of genomic secondary findings

BMC medical genomics, 2021-06, Vol.14 (1), p.167-13, Article 167

2021

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Addressing cancer family history at the end of life: How frequent, relevant, and feasible is it? A survey of palliative care providers

Palliative medicine, 2019-07, Vol.33 (7), p.856-858

2019

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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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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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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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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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Usefulness of Canadian Public Health Insurance Administrative Databases to Assess Breast and Ovarian Cancer Screening Imaging Technologies for BRCA1/2 Mutation Carriers

Canadian Association of Radiologists journal, 2016-11, Vol.67 (4), p.308-312

2016

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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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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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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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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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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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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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Systematic review of educational tools used during the

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

2014

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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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Protocole de prise en charge multidisciplinaire : expérience de femmes québécoises ayant subi une mastectomie prophylactique

Bulletin du cancer, 2013-03, Vol.100 (3), p.201-211

2013

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

Fear of cancer recurrence in breast cancer survivors carrying a BRCA1/2 mutation: A qualitative study

Whether, when, how, and how much? General public's and cancer patients' views about the disclosure of genomic secondary findings

Addressing cancer family history at the end of life: How frequent, relevant, and feasible is it? A survey of palliative care providers

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

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

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

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

Usefulness of Canadian Public Health Insurance Administrative Databases to Assess Breast and Ovarian Cancer Screening Imaging Technologies for BRCA1/2 Mutation Carriers

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

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”

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

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

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

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

Systematic review of educational tools used during the

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

Protocole de prise en charge multidisciplinaire : expérience de femmes québécoises ayant subi une mastectomie prophylactique

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