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French college of gynecologists and obstetricians (CNGOF) recommendations for clinical practice: Place of breast self-examination in screening strategies

Breast (Edinburgh), 2024-06, Vol.75, p.103619, Article 103619

2024

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Molecular description of a 3D in vitro model for the study of epithelial ovarian cancer (EOC)

Molecular carcinogenesis, 2007-10, Vol.46 (10), p.872-885

2007

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Germ-line exon 21 EGFR mutations, V843I and P848L, in nonsmall cell lung cancer patients

European respiratory review, 2014-09, Vol.23 (133), p.390-392

2014

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Discrimination between serous low malignant potential and invasive epithelial ovarian tumors using molecular profiling

Oncogene, 2005-07, Vol.24 (29), p.4672-4687

2005

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Gene‐ and pathway‐level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility

International journal of cancer, 2021-04, Vol.148 (8), p.1895-1909

2021

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Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation

Breast cancer research : BCR, 2021-08, Vol.23 (1), p.79-18, Article 79

2021

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First case report of an adrenocortical carcinoma caused by a BRCA2 mutation

Medicine (Baltimore), 2016-09, Vol.95 (36), p.e4756-e4756

2016

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A focus group study on breast cancer risk presentation: one format does not fit all

European journal of human genetics : EJHG, 2013-07, Vol.21 (7), p.719-724

2013

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Breast Cancer Risk Associated with Estrogen Exposure and Truncating Mutation Location in BRCA1/2 Carriers

Cancer epidemiology, biomarkers & prevention, 2015-04, Vol.24 (4), p.698-707

2015

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Place of breast self-examination in screening strategies. French College of Gynecologists and Obstetricians (CNGOF) recommendations for clinical practice

Gynécologie, obstétrique, fertilité & sénologie, 2023-10, Vol.51 (10), p.437-447

2023

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Medulloblastomas with ELP1 pathogenic variants: A weakly penetrant syndrome with a restricted spectrum in a limited age window

Neuro-oncology advances, 2024-01, Vol.6 (1), p.vdae075

2024

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Multidisciplinary team meetings settings on the management of women at high risk of inherited breast cancer. A French study

Bulletin du cancer, 2016-06, Vol.103 (6), p.571

2016

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Non-genetic indications for risk reducing mastectomies: Guidelines of the National College of French Gynecologists and Obstetricians (CNGOF)

Gynécologie, obstétrique, fertilité & sénologie, 2022-02, Vol.50 (2), p.107

2022

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Germline TP53 mutations in BRCA1 and BRCA2 mutation-negative French Canadian breast cancer families

Breast cancer research and treatment, 2008-04, Vol.108 (3), p.399-408

2008

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Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer

Familial cancer, 2010-12, Vol.9 (4), p.507-517

2010

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Higher Frequency of Familial Clustering of Prostate Cancer in French-Canadian Men

The Journal of urology, 2007-10, Vol.178 (4), p.1265-1270

2007

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Allelic transcripts dosage effect in morphologically normal ovarian cells from heterozygous carriers of a BRCA1/2 French Canadian founder mutation

Cancer prevention research (Philadelphia, Pa.), 2012-05, Vol.5 (5), p.765-777

2012

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A review of histopathological subtypes of ovarian cancer in BRCA-related French Canadian cancer families

Familial cancer, 2007-12, Vol.6 (4), p.491-497

2007

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Genetic polymorphism at the glutathione S‐tranferase (GST) P1 locus is a breast cancer risk modifier

International journal of cancer, 2001-02, Vol.91 (3), p.334-339

2001

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Signature of a silent killer: expression profiling in epithelial ovarian cancer

Expert review of molecular diagnostics, 2004-03, Vol.4 (2), p.157-167

2004

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Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing

International journal of cancer, 2019-04, Vol.144 (8), p.1962-1974

2019

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Allelic deletion at glutathione S-transferase M1 locus and its association with breast cancer susceptibility

Chemico-biological interactions, 1998-04, Vol.111, p.365-375

1998

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Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease

European journal of cancer (1990), 2023-01, Vol.179, p.76-86

2023

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TUMOSPEC: A Nation-Wide Study of Hereditary Breast and Ovarian Cancer Families with a Predicted Pathogenic Variant Identified through Multigene Panel Testing

Cancers, 2021-07, Vol.13 (15), p.3659

2021

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French college of gynecologists and obstetricians (CNGOF) recommendations for clinical practice: Place of breast self-examination in screening strategies

Molecular description of a 3D in vitro model for the study of epithelial ovarian cancer (EOC)

Germ-line exon 21 EGFR mutations, V843I and P848L, in nonsmall cell lung cancer patients

Germline BAP1 Mutations Predispose to Renal Cell Carcinomas

Discrimination between serous low malignant potential and invasive epithelial ovarian tumors using molecular profiling

Gene‐ and pathway‐level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility

Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation

First case report of an adrenocortical carcinoma caused by a BRCA2 mutation

A focus group study on breast cancer risk presentation: one format does not fit all

Breast Cancer Risk Associated with Estrogen Exposure and Truncating Mutation Location in BRCA1/2 Carriers

Place of breast self-examination in screening strategies. French College of Gynecologists and Obstetricians (CNGOF) recommendations for clinical practice

Medulloblastomas with ELP1 pathogenic variants: A weakly penetrant syndrome with a restricted spectrum in a limited age window

Multidisciplinary team meetings settings on the management of women at high risk of inherited breast cancer. A French study

Non-genetic indications for risk reducing mastectomies: Guidelines of the National College of French Gynecologists and Obstetricians (CNGOF)

Germline TP53 mutations in BRCA1 and BRCA2 mutation-negative French Canadian breast cancer families

Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer

Higher Frequency of Familial Clustering of Prostate Cancer in French-Canadian Men

Allelic transcripts dosage effect in morphologically normal ovarian cells from heterozygous carriers of a BRCA1/2 French Canadian founder mutation

A review of histopathological subtypes of ovarian cancer in BRCA-related French Canadian cancer families

Genetic polymorphism at the glutathione S‐tranferase (GST) P1 locus is a breast cancer risk modifier

Signature of a silent killer: expression profiling in epithelial ovarian cancer

Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing

Allelic deletion at glutathione S-transferase M1 locus and its association with breast cancer susceptibility

Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease

TUMOSPEC: A Nation-Wide Study of Hereditary Breast and Ovarian Cancer Families with a Predicted Pathogenic Variant Identified through Multigene Panel Testing

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