Francoise Bonnet

Bordeaux, France

Last Updated: 09/26/2026

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Found 14 publications

MLH1 Constitutional Epimutation Screening Requires Highly Sensitive Assays to Identify Lynch Syndrome Patients With Very Low Mosaic Methylation Level.

MLH1 Constitutional Epimutation Screening Requires Highly Sensitive Assays to Identify Lynch Syndrome Patients With Very Low Mosaic Methylation Level.

Journal: Human mutation

Published: November 29, 2024

Classification of PTEN germline non-truncating variants: a new approach to interpretation.

Classification of PTEN germline non-truncating variants: a new approach to interpretation.

Journal: Journal of medical genetics

Published: March 11, 2024

PTEN alterations in sporadic and BRCA1-associated triple negative breast carcinomas.

PTEN alterations in sporadic and BRCA1-associated triple negative breast carcinomas.

Journal: Cancer genetics

Published: October 19, 2021

Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.

Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.

Journal: American journal of human genetics

Published: June 15, 2021

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.

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.

Journal: Cancers

Published: April 30, 2021

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

Combined tumor genomic profiling and exome sequencing in a breast cancer family implicates ATM in tumorigenesis: A proof of principle study.

Combined tumor genomic profiling and exome sequencing in a breast cancer family implicates ATM in tumorigenesis: A proof of principle study.

Journal: Genes, chromosomes & cancer

Published: October 14, 2016

Insertion of Alu elements at a PTEN hotspot in Cowden syndrome.

Insertion of Alu elements at a PTEN hotspot in Cowden syndrome.

Journal: European journal of human genetics : EJHG

Published: June 14, 2016

High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome.

High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome.

Journal: Journal of medical genetics

Published: January 22, 2013

Deletion of chromosomes 13q and 14q is a common feature of tumors with BRCA2 mutations.

Deletion of chromosomes 13q and 14q is a common feature of tumors with BRCA2 mutations.

Journal: PloS one

Published: August 22, 2012

Comprehensive analysis of PTEN status in breast carcinomas.

Comprehensive analysis of PTEN status in breast carcinomas.

Journal: International journal of cancer

Published: July 10, 2012

A homozygous balanced reciprocal translocation suggests LINC00237 as a candidate gene for MOMO (macrosomia, obesity, macrocephaly, and ocular abnormalities) syndrome.

A homozygous balanced reciprocal translocation suggests LINC00237 as a candidate gene for MOMO (macrosomia, obesity, macrocephaly, and ocular abnormalities) syndrome.

Journal: American journal of medical genetics. Part A

Published: April 07, 2012

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Last Updated: 09/26/2026