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Page 1
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.
[Patched/Sonic Hedgehog pathway and basal cell carcinoma].
Basset-Seguin N, Soufir N. Basset-Seguin N, et al. Among authors: soufir n. Med Sci (Paris). 2004 Oct;20(10):899-903. doi: 10.1051/medsci/20042010899. Med Sci (Paris). 2004. PMID: 15461968 Free article. Review. French.
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. 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.
Variants of the MATP/SLC45A2 gene are protective for melanoma in the French population.
Guedj M, Bourillon A, Combadières C, Rodero M, Dieudé P, Descamps V, Dupin N, Wolkenstein P, Aegerter P, Lebbe C, Basset-Seguin N, Prum B, Saiag P, Grandchamp B, Soufir N; MelanCohort Investigators. Guedj M, et al. Among authors: soufir n. Hum Mutat. 2008 Sep;29(9):1154-60. doi: 10.1002/humu.20823. Hum Mutat. 2008. PMID: 18683857
Variants of the xeroderma pigmentosum variant gene (POLH) are associated with melanoma risk.
Di Lucca J, Guedj M, Lacapère JJ, Fargnoli MC, Bourillon A, Dieudé P, Dupin N, Wolkenstein P, Aegerter P, Saiag P, Descamps V, Lebbe C, Basset-Seguin N, Peris K, Grandchamp B, Soufir N. Di Lucca J, et al. Among authors: soufir n. Eur J Cancer. 2009 Dec;45(18):3228-36. doi: 10.1016/j.ejca.2009.04.034. Epub 2009 May 26. Eur J Cancer. 2009. PMID: 19477635
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: soufir n. Genes Chromosomes Cancer. 2018 Jun;57(6):294-303. doi: 10.1002/gcc.22528. Epub 2018 Feb 21. Genes Chromosomes Cancer. 2018. PMID: 29359367
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 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
80 results