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Page 1
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: soufir n. 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.
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. J Natl Cancer Inst. 2005 Sep 7;97(17):1297-301. doi: 10.1093/jnci/dji253. J Natl Cancer Inst. 2005. PMID: 16145050
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: soufir n. Eur J Hum Genet. 2005 Aug;13(8):913-20. doi: 10.1038/sj.ejhg.5201415. Eur J Hum Genet. 2005. PMID: 15889046
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: soufir n. 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.
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: soufir n. 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
New trends in the susceptibility to melanoma.
Soufir N, Grandchamp B, Basset-Seguin N. Soufir N, et al. Cancer Treat Res. 2009;146:213-23. doi: 10.1007/978-0-387-78574-5_19. Cancer Treat Res. 2009. PMID: 19415206 Review. No abstract available.
The A148T variant of the CDKN2A gene is not associated with melanoma risk in the French and Italian populations.
Spica T, Portela M, Gérard B, Formicone F, Descamps V, Crickx B, Ollivaud L, Archimbaud A, Dupin N, Wolkenstein P, Vitoux D, Lebbe C, Saiag P, Basset-Seguin N, Fargnoli MC, Grandchamp B, Peris K, Soufir N; MELAN-COHORT. Spica T, et al. Among authors: soufir n. J Invest Dermatol. 2006 Jul;126(7):1657-60. doi: 10.1038/sj.jid.5700293. Epub 2006 Apr 13. J Invest Dermatol. 2006. PMID: 16614725 Free article. No abstract available.
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. 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.
MC1R and PTCH gene polymorphism in French patients with basal cell carcinomas.
Liboutet M, Portela M, Delestaing G, Vilmer C, Dupin N, Gorin I, Saiag P, Lebbé C, Kerob D, Dubertret L, Grandchamp B, Basset-Seguin N, Soufir N. Liboutet M, et al. Among authors: soufir n. J Invest Dermatol. 2006 Jul;126(7):1510-7. doi: 10.1038/sj.jid.5700263. Epub 2006 Apr 27. J Invest Dermatol. 2006. PMID: 16645598 Free article.
80 results