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104: Analyse simultanée de multiples gènes impliqués dans le risque héréditaire de cancer du sein dans les familles sans mutation BRCA: séquençage à haut débit

Bulletin du cancer, 2010-03, Vol.97 (1), p.S83-S84

2010

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111: Analyse des gènes BRCA1 et BRCA2 par pyro-séquençage Roche-454: comparaison avec la technique de Sanger

Bulletin du cancer, 2010-03, Vol.97 (1), p.S87-S88

2010

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3020insC NOD2/CARD15 polymorphism associated with treatment of colorectal cancer

Medical oncology (Northwood, London, England), 2014-05, Vol.31 (5), p.954, Article 954

2014

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72: Germline mutation of the E-cadherin gene in a family with inherited invasive lobular breast carcinoma but no diffuse gastric cancer

Bulletin du cancer, 2010-03, Vol.97 (1), p.S62-S62

2010

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91: Analyse fonctionnelle des mutations faux-sens et non-sens du gène hCHEK2

Bulletin du cancer, 2010-03, Vol.97 (1), p.S74-S75

2010

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Abstract 1842: Familial demonstration of the involvement of E-cadherine germ-line mutation in inherited invasive lobular breast carcinomas

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8_Supplement), p.1842-1842

2010

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Abstract 2602: CHEK2 contribution to hereditary breast cancer in non-BRCA famillies

Cancer research (Chicago, Ill.), 2012-04, Vol.72 (8_Supplement), p.2602-2602

2012

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Abstract 3988: Mutation screening of the BRCA genes using Roche-454 pyrosequencing: comparison with fluorescent dideoxy sequencing

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8_Supplement), p.3988-3988

2010

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Abstract 4669: Response to the anti-EGFR antibody panitumumab combined with standard neoadjuvant chemotherapy in triple negative breast cancer (TNBC): the immune and IGFR pathways

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.4669-4669

2013

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Abstract 4854: Mutations activating proliferation pathways in ovarian cancer

Cancer research (Chicago, Ill.), 2011-04, Vol.71 (8_Supplement), p.4854-4854

2011

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Abstract 5224: Next-generation sequencing of a panel of genes contributing to breast cancer risk

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (14_Supplement), p.5224-5224

2016

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Abstract P1-03-06: BRCA1 and BRCA2 mutations in ethnic Lebanese Arab high risk women for hereditary breast cancer

Cancer research (Chicago, Ill.), 2015-05, Vol.75 (9_Supplement), p.P1-P1-03-06

2015

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Allelic imbalance at NBS1 is frequent in both proximal and distal colorectal carcinoma

Oncology reports, 2000-03, Vol.7 (2), p.427

2000

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Analysis of 11 candidate genes in 849 adult patients with suspected hereditary cancer predisposition

Genes chromosomes & cancer, 2021-02, Vol.60 (2), p.73-78

2021

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Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

PloS one, 2015-04, Vol.10 (4), p.e0120020

2015

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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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Association and Performance of Polygenic Risk Scores for Breast Cancer Among French Women Presenting or Not a Familial Predisposition to the Disease

SSRN Electronic Journal

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Association between hereditary predisposition to common cancers and congenital multimalformations

Congenital anomalies, 2020-01, Vol.60 (1), p.22-31

2020

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Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

Nature communications, 2021-05, Vol.12 (1), p.2986-2, Article 2986

2021

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Bell RFLP at the DXSl6 locus

Nucleic acids research, 1988-11, Vol.16 (22), p.10949-10949

1988

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BRCA Genetic Screening in Middle Eastern and North African: Mutational Spectrum and Founder BRCA1 Mutation (c.798_799delTT) in North African

Disease markers, 2015-01, Vol.2015 (2015), p.1-8

2015

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BRCA Mutations Increase Fertility in Families at Hereditary Breast/Ovarian Cancer Risk

PloS one, 2015-06, Vol.10 (6), p.e0127363-e0127363

2015

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BRCA Mutations Increase Fertility in Families at Hereditary Breast/Ovarian Cancer Risk: e0127363

PloS one, 2015-06, Vol.10 (6)

2015

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BRCA1 and BRCA2 Mutations in Ethnic Lebanese Arab Women With High Hereditary Risk Breast Cancer

The oncologist (Dayton, Ohio), 2015-04, Vol.20 (4), p.357-364

2015

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104: Analyse simultanée de multiples gènes impliqués dans le risque héréditaire de cancer du sein dans les familles sans mutation BRCA: séquençage à haut débit

111: Analyse des gènes BRCA1 et BRCA2 par pyro-séquençage Roche-454: comparaison avec la technique de Sanger

3020insC NOD2/CARD15 polymorphism associated with treatment of colorectal cancer

5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints

72: Germline mutation of the E-cadherin gene in a family with inherited invasive lobular breast carcinoma but no diffuse gastric cancer

91: Analyse fonctionnelle des mutations faux-sens et non-sens du gène hCHEK2

Abstract 1842: Familial demonstration of the involvement of E-cadherine germ-line mutation in inherited invasive lobular breast carcinomas

Abstract 2602: CHEK2 contribution to hereditary breast cancer in non-BRCA famillies

Abstract 3988: Mutation screening of the BRCA genes using Roche-454 pyrosequencing: comparison with fluorescent dideoxy sequencing

Abstract 4669: Response to the anti-EGFR antibody panitumumab combined with standard neoadjuvant chemotherapy in triple negative breast cancer (TNBC): the immune and IGFR pathways

Abstract 4854: Mutations activating proliferation pathways in ovarian cancer

Abstract 5224: Next-generation sequencing of a panel of genes contributing to breast cancer risk

Abstract P1-03-06: BRCA1 and BRCA2 mutations in ethnic Lebanese Arab high risk women for hereditary breast cancer

Allelic imbalance at NBS1 is frequent in both proximal and distal colorectal carcinoma

Analysis of 11 candidate genes in 849 adult patients with suspected hereditary cancer predisposition

Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

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

Association and Performance of Polygenic Risk Scores for Breast Cancer Among French Women Presenting or Not a Familial Predisposition to the Disease

Association between hereditary predisposition to common cancers and congenital multimalformations

Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

Bell RFLP at the DXSl6 locus

BRCA Genetic Screening in Middle Eastern and North African: Mutational Spectrum and Founder BRCA1 Mutation (c.798_799delTT) in North African

BRCA Mutations Increase Fertility in Families at Hereditary Breast/Ovarian Cancer Risk

BRCA Mutations Increase Fertility in Families at Hereditary Breast/Ovarian Cancer Risk: e0127363

BRCA1 and BRCA2 Mutations in Ethnic Lebanese Arab Women With High Hereditary Risk Breast Cancer

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