Virginie Moncoutier-Caux

Paris, 75005, France

Last Updated: 09/26/2026

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Found 32 publications

Corrigendum: Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort.

Corrigendum: Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort.

Journal: Nucleic acids research

Published: October 16, 2018

Full in-frame exon 3 skipping of BRCA2 confers high risk of breast and/or ovarian cancer.

Full in-frame exon 3 skipping of BRCA2 confers high risk of breast and/or ovarian cancer.

Journal: Oncotarget

Published: September 07, 2017

Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic MSH2 somatic mutations.

Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic MSH2 somatic mutations.

Journal: Familial cancer

Published: August 19, 2017

Contribution of germline deleterious variants in the RAD51 paralogs to breast and ovarian cancers.

Contribution of germline deleterious variants in the RAD51 paralogs to breast and ovarian cancers.

Journal: European journal of human genetics : EJHG

Published: June 05, 2017

Detecting splicing patterns in genes involved in hereditary breast and ovarian cancer.

Detecting splicing patterns in genes involved in hereditary breast and ovarian cancer.

Journal: European journal of human genetics : EJHG

Published: November 30, 2016

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.

Journal: Nature genetics

Published: May 30, 2016

Genomic hallmarks of homologous recombination deficiency in invasive breast carcinomas.

Genomic hallmarks of homologous recombination deficiency in invasive breast carcinomas.

Journal: International journal of cancer

Published: January 14, 2015

Breast and ovarian cancer predisposition due to de novo BRCA1 and BRCA2 mutations.

Breast and ovarian cancer predisposition due to de novo BRCA1 and BRCA2 mutations.

Journal: Oncogene

Published: January 08, 2015

Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers.

Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers.

Journal: Breast cancer research : BCR

Published: January 01, 2014

Germline mutation in the RAD51B gene confers predisposition to breast cancer.

Germline mutation in the RAD51B gene confers predisposition to breast cancer.

Journal: BMC cancer

Published: August 03, 2013

Streamlined ion torrent PGM-based diagnostics: BRCA1 and BRCA2 genes as a model.

Streamlined ion torrent PGM-based diagnostics: BRCA1 and BRCA2 genes as a model.

Journal: European journal of human genetics : EJHG

Published: January 25, 2013

Loss of heterozygosity at 13q13 and 14q32 predicts BRCA2 inactivation in luminal breast carcinomas.

Loss of heterozygosity at 13q13 and 14q32 predicts BRCA2 inactivation in luminal breast carcinomas.

Journal: International journal of cancer

Published: January 24, 2013

Showing 1-12 of 32

Last Updated: 09/26/2026