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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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The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer

Clinical cancer research, 2006-02, Vol.12 (4), p.1157-1167

2006

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Diagnosis of PTEN mosaicism: the relevance of additional tumor DNA sequencing. A case report and review of the literature

BMC medical genomics, 2023-07, Vol.16 (1), p.166-166, Article 166

2023

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Detection Rate and Spectrum of Pathogenic Variations in a Cohort of 83 Patients with Suspected Hereditary Risk of Kidney Cancer

Genes, 2023-10, Vol.14 (11), p.1991

2023

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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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Involvement of IL17A, IL17F and IL23R Polymorphisms in Colorectal Cancer Therapy

PloS one, 2015-06, Vol.10 (6), p.e0128911-e0128911

2015

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Case Series of 11 CDH1 Families (47 Carriers) Including Incidental Findings, Signet Ring Cell Colon Cancer and Review of the Literature

Genes, 2023-08, Vol.14 (9), p.1677

2023

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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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Early Onset Multiple Primary Tumors in Atypical Presentation of Cowden Syndrome Identified by Whole-Exome-Sequencing

Frontiers in genetics, 2018-08, Vol.9, p.353-353

2018

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Rare duplication of the CDC73 gene and atypical hyperparathyroidism‐jaw tumor syndrome: A case report and review of the literature

Molecular genetics & genomic medicine, 2023-05, Vol.11 (5), p.e2133-n/a

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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Rad50 c.687delT Does Not Contribute Significantly to Familial Breast Cancer in a French Population

Cancer epidemiology, biomarkers & prevention, 2009-02, Vol.18 (2), p.684-685

2009

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Werner syndrome and mutations of the WRN and LMNA genes in France

Human mutation, 2006-07, Vol.27 (7), p.718-719

2006

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RNA Panel Sequencing Is an Effective Tool to Help Classify Splice Variants for Clinical Oncogenetic Diagnosis

Human mutation, 2024-04, Vol.2024, p.1-14

2024

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CHEK2 contribution to hereditary breast cancer in non-BRCA families

Breast cancer research : BCR, 2011-01, Vol.13 (6), p.R119-R119

2011

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Diet-induced hypoxia responsive element demethylation increases CEACAM6 expression, favouring Crohn's disease-associated Escherichia coli colonisation

Gut, 2015-03, Vol.64 (3), p.428-437

2015

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Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

Nature communications, 2016-09, Vol.7 (1), p.12675-22, Article 12675

2016

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

Nature communications, 2021-02, Vol.12 (1), p.1078-22, Article 1078

2021

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Case Series of 11 ICDH1/I Families Including Incidental Findings, Signet Ring Cell Colon Cancer and Review of the Literature

Genes, 2023-08, Vol.14 (9)

2023

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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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Mutation screening of the BRCA1 gene in early onset and familial breast/ovarian cancer in Moroccan population

International journal of medical sciences, 2013-01, Vol.10 (1), p.60-67

2013

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Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

Cancer research (Chicago, Ill.), 2010-12, Vol.70 (23), p.9742-9754

2010

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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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Germline mutations of the E‐cadherin gene in families with inherited invasive lobular breast carcinoma but no diffuse gastric cancer

Cancer, 2011-07, Vol.117 (14), p.3112-3117

2011

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

The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer

Diagnosis of PTEN mosaicism: the relevance of additional tumor DNA sequencing. A case report and review of the literature

Detection Rate and Spectrum of Pathogenic Variations in a Cohort of 83 Patients with Suspected Hereditary Risk of Kidney Cancer

Association between hereditary predisposition to common cancers and congenital multimalformations

Involvement of IL17A, IL17F and IL23R Polymorphisms in Colorectal Cancer Therapy

Case Series of 11 CDH1 Families (47 Carriers) Including Incidental Findings, Signet Ring Cell Colon Cancer and Review of the Literature

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

Early Onset Multiple Primary Tumors in Atypical Presentation of Cowden Syndrome Identified by Whole-Exome-Sequencing

Rare duplication of the CDC73 gene and atypical hyperparathyroidism‐jaw tumor syndrome: A case report and review of the literature

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

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

Rad50 c.687delT Does Not Contribute Significantly to Familial Breast Cancer in a French Population

Werner syndrome and mutations of the WRN and LMNA genes in France

RNA Panel Sequencing Is an Effective Tool to Help Classify Splice Variants for Clinical Oncogenetic Diagnosis

CHEK2 contribution to hereditary breast cancer in non-BRCA families

Diet-induced hypoxia responsive element demethylation increases CEACAM6 expression, favouring Crohn's disease-associated Escherichia coli colonisation

Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

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

Case Series of 11 ICDH1/I Families Including Incidental Findings, Signet Ring Cell Colon Cancer and Review of the Literature

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

Mutation screening of the BRCA1 gene in early onset and familial breast/ovarian cancer in Moroccan population

Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

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

Germline mutations of the E‐cadherin gene in families with inherited invasive lobular breast carcinoma but no diffuse gastric cancer

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