Pagès S - Search Results

1

Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions.

Puget N, Stoppa-Lyonnet D, Sinilnikova OM, Pagès S, Lynch HT, Lenoir GM, Mazoyer S. Puget N, et al. Among authors: pages s. Cancer Res. 1999 Jan 15;59(2):455-61. Cancer Res. 1999. PMID: 9927062

2

Color bar coding the BRCA1 gene on combed DNA: a useful strategy for detecting large gene rearrangements.

Gad S, Aurias A, Puget N, Mairal A, Schurra C, Montagna M, Pages S, Caux V, Mazoyer S, Bensimon A, Stoppa-Lyonnet D. Gad S, et al. Among authors: pages s. Genes Chromosomes Cancer. 2001 May;31(1):75-84. doi: 10.1002/gcc.1120. Genes Chromosomes Cancer. 2001. PMID: 11284038

3

An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation?

Puget N, Sinilnikova OM, Stoppa-Lyonnet D, Audoynaud C, Pagès S, Lynch HT, Goldgar D, Lenoir GM, Mazoyer S. Puget N, et al. Among authors: pages s. Am J Hum Genet. 1999 Jan;64(1):300-2. doi: 10.1086/302211. Am J Hum Genet. 1999. PMID: 9915971 Free PMC article. No abstract available.

4

Screening of male breast cancer and of breast-ovarian cancer families for BRCA2 mutations using large bifluorescent amplicons.

Pages S, Caux V, Stoppa-Lyonnet D, Tosi M. Pages S, et al. Br J Cancer. 2001 Feb;84(4):482-8. doi: 10.1054/bjoc.2000.1627. Br J Cancer. 2001. PMID: 11207042 Free PMC article.

5

Marker segregation information in breast/ovarian cancer genetic counseling: is it still useful? Groupe Génétique et Cancer de la Fédération Nationale des Centres de Lutte Contre le Cancer.

Essioux L, Girodet C, Sinilnikova O, Pagès S, Eisinger F, de Résende S, Maugard C, Lanoë D, Longy M, Bignon YJ, Sobol H, Bonaïti-Pellié C, Stoppa-Lyonnet D. Essioux L, et al. Among authors: pages s. Am J Med Genet. 1998 Sep 23;79(3):175-83. doi: 10.1002/(sici)1096-8628(19980923)79:3<175::aid-ajmg5>3.0.co;2-m. Am J Med Genet. 1998. PMID: 9788557

6

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. Among authors: pages s. Am J Hum Genet. 1997 May;60(5):1021-30. Am J Hum Genet. 1997. PMID: 9150149 Free PMC article.

7

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. Among authors: pages s. 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.

8

p53 mutations in BRCA1-associated familial breast cancer.

Schlichtholz B, Bouchind'homme B, Pagés S, Martin E, Liva S, Magdelenat H, Sastre-Garau X, Stoppa-Lyonnet D, Soussi T. Schlichtholz B, et al. Among authors: pages s. Lancet. 1998 Aug 22;352(9128):622. doi: 10.1016/S0140-6736(05)79576-3. Lancet. 1998. PMID: 9746028 No abstract available.

9

Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations.

Wagner T, Stoppa-Lyonnet D, Fleischmann E, Muhr D, Pagès S, Sandberg T, Caux V, Moeslinger R, Langbauer G, Borg A, Oefner P. Wagner T, et al. Among authors: pages s. Genomics. 1999 Dec 15;62(3):369-76. doi: 10.1006/geno.1999.6026. Genomics. 1999. PMID: 10644434 Free article.

10

Segregation of two BRCA1 mutations in a single family.

Stoppa-Lyonnet D, Fricker JP, Essioux L, Pages S, Limacher JM, Sobol H, Laurent-Puig P, Thomas G. Stoppa-Lyonnet D, et al. Among authors: pages s. Am J Hum Genet. 1996 Aug;59(2):479-81. Am J Hum Genet. 1996. PMID: 8755940 Free PMC article. No abstract available.

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