Area of research
Pathology and Forensic Medicine · Surgery
Research interest
Research interests include Genetic factors in colorectal cancer, BRCA gene mutations in cancer, Colorectal and Anal Carcinomas, and Cancer Genomics and Diagnostics.
Results of a multigene panel testing approach targeting patients with suspected genetic predisposition to pancreatic ductal adenocarcinoma.
Follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: Data from the PRED-IdF network.
Serious immune‐related upper gastrointestinal toxicity of immune checkpoint inhibitors: a multicenter case series
First estimates of diffuse gastric cancer risks for carriers of <i>CTNNA1</i> germline pathogenic variants
Atezolizumab plus modified DCF (docetaxel, cisplatin, and 5-fluorouracil) as first-line treatment for metastatic or locally advanced squamous cell anal carcinoma: A SCARCE-PRODIGE 60 randomized phase II study.
Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Association of Genomic Domains in <i>BRCA1</i> and <i>BRCA2</i> with Prostate Cancer Risk and Aggressiveness
Mutational spectrum in a worldwide study of 29,700 families with<i>BRCA1</i>or<i>BRCA2</i>mutations
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing
The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations
GENESIS: a French national resource to study the missing heritability of breast cancer
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3
Breast Cancer Risk Associated with Estrogen Exposure and Truncating Mutation Location in <i>BRCA1/2</i> Carriers
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers
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)