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309 results

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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: crickx b. 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. Among authors: crickx b. 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: crickx b. 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: crickx b. 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.
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: crickx b. 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. Among authors: crickx b. 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.
PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French study.
Soufir N, Gerard B, Portela M, Brice A, Liboutet M, Saiag P, Descamps V, Kerob D, Wolkenstein P, Gorin I, Lebbe C, Dupin N, Crickx B, Basset-Seguin N, Grandchamp B. Soufir N, et al. Among authors: crickx b. Br J Cancer. 2006 Aug 21;95(4):548-53. doi: 10.1038/sj.bjc.6603303. Br J Cancer. 2006. PMID: 16909134 Free PMC article.
[Kaposi disease].
Belaïch S, Crickx B, Picard C, Bouscarat F, Descamps V. Belaïch S, et al. Among authors: crickx b. Presse Med. 1998 Jan 31;27(4):189. Presse Med. 1998. PMID: 9768036 French. No abstract available.
309 results