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"Decoding hereditary breast cancer" benefits and questions from multigene panel testing

scientific article published on 08 January 2019

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

artículo científico publicado en 2015

Calibration of pathogenicity due to variant-induced leaky splicing defects by using BRCA2 exon 3 as a model system

artículo científico publicado en 2020

Cancer Risks Associated With and Pathogenic Variants

artículo científico publicado en 2022

Clinicopathologic Characteristics of Endometrial Cancer in Lynch Syndrome: A French Multicenter Study

artículo científico publicado en 2017

Co-occurrence of germline BRCA1 and CDH1 pathogenic variants

artículo científico publicado en 2020

Direct-to-consumer misleading information on cancer risks calls for an urgent clarification of health genetic testing performed by commercial companies

scientific article published on 23 April 2020

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

article

GENESIS: a French national resource to study the missing heritability of breast cancer

artículo científico publicado en 2016

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

artículo científico publicado en 2020

Prevalence of Pathogenic Variants of FAN1 in More Than 5000 Patients Assessed for Genetic Predisposition to Colorectal, Breast, Ovarian, or Other Cancers

scientific article published on 09 January 2019

Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO).

artículo científico publicado en 2012

[Constitutional MMR deficiency: Genetic bases and clinical implications]

scientific article published on 11 December 2018

[Familial disclosure by healthcare professionals in absence of genetic mutation]

artículo científico publicado en 2019

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