R. Meziani

Germline mutations of the INK4a-ARF gene in patients with suspected genetic predisposition to melanoma

H. Cavé, C. Lebbé, N. Basset-Seguin, 2004, British Journal of Cancer.

Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure

C. Lebbé, N. Basset-Seguin, P. Verpillat, 2004, Journal of Medical Genetics.

Association study of the g.8818A>G polymorphism of the human agouti gene with melanoma risk and pigmentary characteristics in a French population.

C. Lebbé, N. Basset-Seguin, B. Gérard, 2005, Journal of dermatological science.

Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma

F. Clerget-Darpoux, C. Lebbé, N. Basset-Seguin, 2005, European Journal of Human Genetics.

A trans-ethnic genetic study of rheumatoid arthritis identified FCGR2A as a candidate common risk factor in Japanese and European populations

S. Heath, M. Lathrop, T. Nomura, 2012, Modern rheumatology.

Association between endothelin receptor B nonsynonymous variants and melanoma risk.

C. Lebbé, N. Basset-Seguin, B. Gérard, 2005, Journal of the National Cancer Institute.

Association between endothelin receptor B nonsynonymous variants and melanoma risk.

C. Lebbé, N. Basset-Seguin, B. Gérard, 2005, Journal of the National Cancer Institute.