Stoppa-Lyonnet D - Search Results

1

Genotype-phenotype correlations in hereditary familial retinoblastoma.

Taylor M, Dehainault C, Desjardins L, Doz F, Levy C, Sastre X, Couturier J, Stoppa-Lyonnet D, Houdayer C, Gauthier-Villars M. Taylor M, et al. Hum Mutat. 2007 Mar;28(3):284-93. doi: 10.1002/humu.20443. Hum Mutat. 2007. PMID: 17096365

2

BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group.

Stoppa-Lyonnet D, Laurent-Puig P, Essioux L, Pagès S, Ithier G, Ligot L, Fourquet A, Salmon RJ, Clough KB, Pouillart P, Bonaïti-Pellié C, Thomas G. Stoppa-Lyonnet D, et al. Am J Hum Genet. 1997 May;60(5):1021-30. Am J Hum Genet. 1997. PMID: 9150149 Free PMC article.

3

Germline brca2 sequence variants in patients with ocular melanoma.

Sinilnikova OM, Egan KM, Quinn JL, Boutrand L, Lenoir GM, Stoppa-Lyonnet D, Desjardins L, Levy C, Goldgar D, Gragoudas ES. Sinilnikova OM, et al. Int J Cancer. 1999 Jul 30;82(3):325-8. doi: 10.1002/(sici)1097-0215(19990730)82:3<325::aid-ijc3>3.0.co;2-g. Int J Cancer. 1999. PMID: 10399947 Free article. Clinical Trial.

4

Genetic testing for breast cancer predisposition.

Gauthier-Villars M, Gad S, Caux V, Pagès S, Blandy C, Stoppa-Lyonnet D. Gauthier-Villars M, et al. Surg Clin North Am. 1999 Oct;79(5):1171-87, xxi. doi: 10.1016/s0039-6109(05)70067-0. Surg Clin North Am. 1999. PMID: 10572557 Review.

5

[Under what conditions should we propose a prophylactic mastectomy for a woman at risk?].

Gauthier-Villars M, Blandy C, Stoppa-Lyonnet D. Gauthier-Villars M, et al. Bull Cancer. 1999 Sep;86(9):754-9. Bull Cancer. 1999. PMID: 10576812 Free article. French. No abstract available.

6

Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16INK4A, P14ARF or cdk4 genes.

Soufir N, Bressac-de Paillerets B, Desjardins L, Lévy C, Bombled J, Gorin I, Schlienger P, Stoppa-Lyonnet D. Soufir N, et al. Br J Cancer. 2000 Feb;82(4):818-22. doi: 10.1054/bjoc.1999.1005. Br J Cancer. 2000. PMID: 10732752 Free PMC article.

7

Familial invasive breast cancers: worse outcome related to BRCA1 mutations.

Stoppa-Lyonnet D, Ansquer Y, Dreyfus H, Gautier C, Gauthier-Villars M, Bourstyn E, Clough KB, Magdelénat H, Pouillart P, Vincent-Salomon A, Fourquet A, Asselain B. Stoppa-Lyonnet D, et al. J Clin Oncol. 2000 Dec 15;18(24):4053-9. doi: 10.1200/JCO.2000.18.24.4053. J Clin Oncol. 2000. PMID: 11118466

8

Genome instability in secondary solid tumors developing after radiotherapy of bilateral retinoblastoma.

Lefèvre SH, Vogt N, Dutrillaux AM, Chauveinc L, Stoppa-Lyonnet D, Doz F, Desjardins L, Dutrillaux B, Chevillard S, Malfoy B. Lefèvre SH, et al. Oncogene. 2001 Dec 6;20(56):8092-9. doi: 10.1038/sj.onc.1205009. Oncogene. 2001. PMID: 11781822

9

Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families.

Gad S, Caux-Moncoutier V, Pagès-Berhouet S, Gauthier-Villars M, Coupier I, Pujol P, Frénay M, Gilbert B, Maugard C, Bignon YJ, Chevrier A, Rossi A, Fricker JP, Nguyen TD, Demange L, Aurias A, Bensimon A, Stoppa-Lyonnet D. Gad S, et al. Oncogene. 2002 Oct 3;21(44):6841-7. doi: 10.1038/sj.onc.1205685. Oncogene. 2002. PMID: 12360411

10

Phenotypic cellular characterization of an ataxia telangiectasia patient carrying a causal homozygous missense mutation.

Angèle S, Laugé A, Fernet M, Moullan N, Beauvais P, Couturier J, Stoppa-Lyonnet D, Hall J. Angèle S, et al. Hum Mutat. 2003 Feb;21(2):169-70. doi: 10.1002/humu.9107. Hum Mutat. 2003. PMID: 12552566

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