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745 results

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Page 1
A French CDK4-positive melanoma family with a co-inherited EDNRB mutation.
Soufir N, Ollivaud L, Bertrand G, Lacapère JJ, Descamps V, Vitoux D, Lebbe C, Wolkenstein P, Dupin N, Saiag P, Basset-Seguin N, Grandchamp B; MELAN-COHORT. Soufir N, et al. Among authors: bertrand g. J Dermatol Sci. 2007 Apr;46(1):61-4. doi: 10.1016/j.jdermsci.2006.11.016. Epub 2007 Jan 12. J Dermatol Sci. 2007. PMID: 17223014 No abstract available.
Association study of the g.8818A>G polymorphism of the human agouti gene with melanoma risk and pigmentary characteristics in a French population.
Meziani R, Descamps V, Gérard B, Matichard E, Bertrand G, Archimbaud A, Ollivaud L, Saiag P, Lebbé C, Basset-Seguin N, Alberti C, Crickx B, Grandchamp B, Soufir N. Meziani R, et al. Among authors: bertrand g. J Dermatol Sci. 2005 Nov;40(2):133-6. doi: 10.1016/j.jdermsci.2005.08.001. Epub 2005 Sep 23. J Dermatol Sci. 2005. PMID: 16183259 No abstract available.
Association between endothelin receptor B nonsynonymous variants and melanoma risk.
Soufir N, Meziani R, Lacapère JJ, Bertrand G, Fumeron F, Bourillon A, Gérard B, Descamps V, Crickx B, Ollivaud L, Archimbaud A, Lebbe C, Basset-Seguin N, Saiag P, Grandchamp B; Investigators of the Melan-Cohort. Soufir N, et al. Among authors: bertrand g. J Natl Cancer Inst. 2005 Sep 7;97(17):1297-301. doi: 10.1093/jnci/dji253. J Natl Cancer Inst. 2005. PMID: 16145050
EDNRB gene variants and melanoma risk in two southern European populations.
Spica T, Fargnoli MC, Hetet G, Bertrand G, Formicone F, Descamps V, Wolkenstein P, Dupin N, Lebbe C, Basset-Seguin N, Saiag P, Cambien F, Grandchamp B, Peris K, Soufir N. Spica T, et al. Among authors: bertrand g. Clin Exp Dermatol. 2011 Oct;36(7):782-7. doi: 10.1111/j.1365-2230.2011.04062.x. Epub 2011 Apr 20. Clin Exp Dermatol. 2011. PMID: 21507037
Germline mutations of the INK4a-ARF gene in patients with suspected genetic predisposition to melanoma.
Soufir N, Lacapere JJ, Bertrand G, Matichard E, Meziani R, Mirebeau D, Descamps V, Gérard B, Archimbaud A, Ollivaud L, Bouscarat F, Baccard M, Lanternier G, Saïag P, Lebbé C, Basset-Seguin N, Crickx B, Cave H, Grandchamp B. Soufir N, et al. Among authors: bertrand g. Br J Cancer. 2004 Jan 26;90(2):503-9. doi: 10.1038/sj.bjc.6601503. Br J Cancer. 2004. PMID: 14735200 Free PMC article.
Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma.
Jannot AS, Meziani R, Bertrand G, Gérard B, Descamps V, Archimbaud A, Picard C, Ollivaud L, Basset-Seguin N, Kerob D, Lanternier G, Lebbe C, Saiag P, Crickx B, Clerget-Darpoux F, Grandchamp B, Soufir N, Melan-Cohort. Jannot AS, et al. Among authors: bertrand g. Eur J Hum Genet. 2005 Aug;13(8):913-20. doi: 10.1038/sj.ejhg.5201415. Eur J Hum Genet. 2005. PMID: 15889046
Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure.
Matichard E, Verpillat P, Meziani R, Gérard B, Descamps V, Legroux E, Burnouf M, Bertrand G, Bouscarat F, Archimbaud A, Picard C, Ollivaud L, Basset-Seguin N, Kerob D, Lanternier G, Lebbe C, Crickx B, Grandchamp B, Soufir N. Matichard E, et al. Among authors: bertrand g. J Med Genet. 2004 Feb;41(2):e13. doi: 10.1136/jmg.2003.011536. J Med Genet. 2004. PMID: 14757863 Free PMC article. No abstract available.
745 results