B. Bressac- de Paillerets

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

F. Révillion, R. Lidereau, N. Sevenet, 2021, American journal of human genetics.

Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3

Jeffrey E. Lee, S. Puig, K. Brown, 2011, Nature Genetics.

Novel FH mutation in a patient with cutaneous leiomyomatosis associated with cutis verticis gyrata, eruptive collagenoma and Charcot‐Marie‐Tooth disease

P. Rustin, B. Guillot, B. Bressac de Paillerets, 2010, The British journal of dermatology.

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

Mads Thomassen, Nina Ditsch, Vijai Joseph, 2012, Breast Cancer Research.

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers

V. Pankratz, F. Couch, B. Bonanni, 2012, Breast Cancer Research.

Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers.

F. Couch, T. Rebbeck, J. Benítez, 2011, Human molecular genetics.

[MITF: a genetic key to melanoma and renal cell carcinoma?].

C. Bertolotto, F. Lesueur, B. Bressac- de Paillerets, 2012, Medecine sciences : M/S.

Subungual squamous cell carcinoma in a BAP1 germline pathogenic variant carrier

B. Balme, L. Golmard, L. Thomas, 2021, Journal of the European Academy of Dermatology and Venereology : JEADV.