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321 results

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Page 1
Truncating mutations of TP53AIP1 gene predispose to cutaneous melanoma.
Benfodda M, Gazal S, Descamps V, Basset-Seguin N, Deschamps L, Thomas L, Lebbe C, Saiag P, Zanetti R, Sacchetto L, Chiorino G, Scatolini M, Grandchamp B, Bensussan A, Soufir N. Benfodda M, et al. Among authors: saiag p. Genes Chromosomes Cancer. 2018 Jun;57(6):294-303. doi: 10.1002/gcc.22528. Epub 2018 Feb 21. Genes Chromosomes Cancer. 2018. PMID: 29359367
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: saiag p. 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: saiag p. Eur J Hum Genet. 2005 Aug;13(8):913-20. doi: 10.1038/sj.ejhg.5201415. Eur J Hum Genet. 2005. PMID: 15889046
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: saiag p. J Natl Cancer Inst. 2005 Sep 7;97(17):1297-301. doi: 10.1093/jnci/dji253. J Natl Cancer Inst. 2005. PMID: 16145050
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: saiag p. 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: saiag p. 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.
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: saiag p. 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.
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: saiag p. 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.
Melanoma susceptibility and progression: Association study between polymorphisms of the chemokine (CCL2) and chemokine receptors (CX3CR1, CCR5).
Rodero M, Rodero P, Descamps V, Lebbe C, Wolkenstein P, Aegerter P, Vitoux D, Basset-Seguin N, Dupin N, Grandchamp B, Soufir N, Combadière C, Saiag P; Melan-cohort investigators. Rodero M, et al. Among authors: saiag p. J Dermatol Sci. 2007 Apr;46(1):72-6. doi: 10.1016/j.jdermsci.2006.11.007. Epub 2006 Dec 13. J Dermatol Sci. 2007. PMID: 17169533 No abstract available.
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: saiag p. 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.
321 results