Stoppa-Lyonnet D - Search Results

1

5' Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints.

Caputo SM, Telly D, Briaux A, Sesen J, Ceppi M, Bonnet F, Bourdon V, Coulet F, Castera L, Delnatte C, Hardouin A, Mazoyer S, Schultz I, Sevenet N, Uhrhammer N, Bonnet C, Tilkin-Mariamé AF, Houdayer C, Moncoutier V, Andrieu C, French Covar Group Collaborators, Bièche I, Stern MH, Stoppa-Lyonnet D, Lidereau R, Toulas C, Rouleau E. Caputo SM, et al. Cancers (Basel). 2021 Jun 25;13(13):3171. doi: 10.3390/cancers13133171. Cancers (Basel). 2021. PMID: 34202044 Free PMC article.

2

[Hereditary predisposition for cancer of the breast and the ovary].

Lalle P, Stoppa-Lyonnet D, Mazoyer S, Rio P, Girodet C, Hardouin A, Narod SA, Sobol H, Bignon YJ. Lalle P, et al. Bull Cancer. 1993 Oct;80(10):857-65. Bull Cancer. 1993. PMID: 8204923 French.

3

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. Cancer Res. 1999 Jan 15;59(2):455-61. Cancer Res. 1999. PMID: 9927062

4

[Role of the ATM gene in genetic predisposition to cancer].

Bay JO, Uhrhammer N, Stoppa-Lyonnet D, Hall J. Bay JO, et al. Bull Cancer. 2000 Jan;87(1):29-34. Bull Cancer. 2000. PMID: 10673629 Free article. French. No abstract available.

5

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. Genes Chromosomes Cancer. 2001 May;31(1):75-84. doi: 10.1002/gcc.1120. Genes Chromosomes Cancer. 2001. PMID: 11284038

6

Distinct BRCA1 rearrangements involving the BRCA1 pseudogene suggest the existence of a recombination hot spot.

Puget N, Gad S, Perrin-Vidoz L, Sinilnikova OM, Stoppa-Lyonnet D, Lenoir GM, Mazoyer S. Puget N, et al. Am J Hum Genet. 2002 Apr;70(4):858-65. doi: 10.1086/339434. Epub 2002 Mar 5. Am J Hum Genet. 2002. PMID: 11880951 Free PMC article.

7

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

8

The nonsense-mediated mRNA decay pathway triggers degradation of most BRCA1 mRNAs bearing premature termination codons.

Perrin-Vidoz L, Sinilnikova OM, Stoppa-Lyonnet D, Lenoir GM, Mazoyer S. Perrin-Vidoz L, et al. Hum Mol Genet. 2002 Nov 1;11(23):2805-14. doi: 10.1093/hmg/11.23.2805. Hum Mol Genet. 2002. PMID: 12393792

9

BRCA1 wild-type allele modifies risk of ovarian cancer in carriers of BRCA1 germ-line mutations.

Ginolhac SM, Gad S, Corbex M, Bressac-De-Paillerets B, Chompret A, Bignon YJ, Peyrat JP, Fournier J, Lasset C, Giraud S, Muller D, Fricker JP, Hardouin A, Berthet P, Maugard C, Nogues C, Lidereau R, Longy M, Olschwang S, Toulas C, Guimbaud R, Yannoukakos D, Szabo C, Durocher F, Moisan AM, Simard J, Mazoyer S, Lynch HT, Goldgar D, Stoppa-Lyonnet D, Lenoir GM, Sinilnikova OM. Ginolhac SM, et al. Cancer Epidemiol Biomarkers Prev. 2003 Feb;12(2):90-5. Cancer Epidemiol Biomarkers Prev. 2003. PMID: 12582017

10

Characterisation of a 161 kb deletion extending from the NBR1 to the BRCA1 genes in a French breast-ovarian cancer family.

Gad S, Bièche I, Barrois M, Casilli F, Pages-Berhouet S, Dehainault C, Gauthier-Villars M, Bensimon A, Aurias A, Lidereau R, Bressac-de Paillerets B, Tosi M, Mazoyer S, Stoppa-Lyonnet D. Gad S, et al. Hum Mutat. 2003 Jun;21(6):654. doi: 10.1002/humu.9148. Hum Mutat. 2003. PMID: 14961556

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