Lista de obras -

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

artículo científico publicado en 2011

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

artículo científico publicado en 2015

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

BRCA1 wild-type allele modifies risk of ovarian cancer in carriers of BRCA1 germ-line mutations

artículo científico publicado en 2003

BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

artículo científico publicado en 2015

Common BRCA2 variants and modification of breast and ovarian cancer risk in BRCA1 mutation carriers

scientific article published on 01 January 2005

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2014

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

Morphology and genomic hallmarks of breast tumours developed by ATM deleterious variant carriers

artículo científico publicado en 2018

Mutation analysis of PALB2 gene in French breast cancer families

article

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

artículo científico publicado en 2015

Rapid progression of prostate cancer in men with a BRCA2 mutation

artículo científico publicado en 2008

Significant contribution of germline BRCA2 rearrangements in male breast cancer families

artículo científico publicado en 2004

Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families

scientific article published on 01 October 2002

Lista de obras de

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

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

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

BRCA1 wild-type allele modifies risk of ovarian cancer in carriers of BRCA1 germ-line mutations

BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

Common BRCA2 variants and modification of breast and ovarian cancer risk in BRCA1 mutation carriers

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

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

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

Morphology and genomic hallmarks of breast tumours developed by ATM deleterious variant carriers

Mutation analysis of PALB2 gene in French breast cancer families

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

Rapid progression of prostate cancer in men with a BRCA2 mutation

Significant contribution of germline BRCA2 rearrangements in male breast cancer families

Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families