V. Vidal

New nonsense mutation in the breast cancer‐1 gene in a French site‐specific breast cancer family

Y. Bignon, N. Presneau, C. Vaurs, 1997 .

Comparative clinical and transcriptomal profiles of breast cancer between French and South Mediterranean patients show minor but significative biological differences.

F. de Longueville, V. Bertholet, J. Remacle, 2008, Cancer genomics & proteomics.

DNA Methylation and Intra-Clonal Heterogeneity: The Chronic Myeloid Leukemia Model

M. Berger, C. Bourgne, V. Vidal, 2021, Cancers.

Use of Gene Expression Profiles of Peripheral Blood Lymphocytes to Distinguish BRCA1 Mutation Carriers in High Risk Breast Cancer Families

V. Chabaud, Y. Bignon, F. Kwiatkowski, 2009, Cancer informatics.

The 1396del a mutation and a missense mutation or a rare polymorphism of the WRN gene detected in a French Werner family with a severe phenotype and a case of an unusual vulvar cancer

Y. Bignon, J. Bay, M. Ferrara, 1998, Human mutation.

Pathology of sporadic breast tumors with LOH at the BRCA1 locus: correlation with histopathological features specific to familial BRCA1 tumors and absence of microsatellite instability.

F. Penault-Llorca, Y. Bignon, F. Kwiatkowski, 1998, International journal of oncology.

Rare germline large rearrangements in the BRCA1/2 genes and eight candidate genes in 472 patients with breast cancer predisposition

I. Bièche, V. Chabaud, J. Peyrat, 2012, Breast Cancer Research and Treatment.

Prenatal diagnosis of X-linked hydrocephalus in a family with a novel mutation in L1CAM gene

M. Acién, J. Gascon, I. Ochando, 2016, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.