Pages-Berhouet S - Search Results

1

A high-throughput mutation detection method based on heteroduplex analysis using graft copolymer matrixes: application to Brca1 and Brca2 analysis.

Weber J, Barbier V, Pages-Berhouet S, Caux-Moncoutier V, Stoppa-Lyonnet D, Viovy JL. Weber J, et al. Among authors: pages berhouet s. Anal Chem. 2004 Aug 15;76(16):4839-48. doi: 10.1021/ac049878p. Anal Chem. 2004. PMID: 15307796

2

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. Among authors: pages berhouet s. Oncogene. 2002 Oct 3;21(44):6841-7. doi: 10.1038/sj.onc.1205685. Oncogene. 2002. PMID: 12360411

3

Fidelity of DNA double-strand break repair in heterozygous cell lines harbouring BRCA1 missense mutations.

Coupier I, Baldeyron C, Rousseau A, Mosseri V, Pages-Berhouet S, Caux-Moncoutier V, Papadopoulo D, Stoppa-Lyonnet D. Coupier I, et al. Among authors: pages berhouet s. Oncogene. 2004 Jan 29;23(4):914-9. doi: 10.1038/sj.onc.1207191. Oncogene. 2004. PMID: 14647443

4

Impact of BRCA1 and BRCA2 variants on splicing: clues from an allelic imbalance study.

Caux-Moncoutier V, Pagès-Berhouet S, Michaux D, Asselain B, Castéra L, De Pauw A, Buecher B, Gauthier-Villars M, Stoppa-Lyonnet D, Houdayer C. Caux-Moncoutier V, et al. Among authors: pages berhouet s. Eur J Hum Genet. 2009 Nov;17(11):1471-80. doi: 10.1038/ejhg.2009.89. Epub 2009 May 27. Eur J Hum Genet. 2009. PMID: 19471317 Free PMC article.

5

Multiplex PCR/liquid chromatography assay for detection of gene rearrangements: application to RB1 gene.

Dehainault C, Laugé A, Caux-Moncoutier V, Pagès-Berhouet S, Doz F, Desjardins L, Couturier J, Gauthier-Villars M, Stoppa-Lyonnet D, Houdayer C. Dehainault C, et al. Among authors: pages berhouet s. Nucleic Acids Res. 2004 Oct 11;32(18):e139. doi: 10.1093/nar/gnh137. Nucleic Acids Res. 2004. PMID: 15477586 Free PMC article.

6

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. Among authors: pages berhouet s. Hum Mutat. 2003 Jun;21(6):654. doi: 10.1002/humu.9148. Hum Mutat. 2003. PMID: 14961556

7

A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation.

Dehainault C, Michaux D, Pagès-Berhouet S, Caux-Moncoutier V, Doz F, Desjardins L, Couturier J, Parent P, Stoppa-Lyonnet D, Gauthier-Villars M, Houdayer C. Dehainault C, et al. Among authors: pages berhouet s. Eur J Hum Genet. 2007 Apr;15(4):473-7. doi: 10.1038/sj.ejhg.5201787. Epub 2007 Feb 14. Eur J Hum Genet. 2007. PMID: 17299438

8

Comprehensive screening for constitutional RB1 mutations by DHPLC and QMPSF.

Houdayer C, Gauthier-Villars M, Laugé A, Pagès-Berhouet S, Dehainault C, Caux-Moncoutier V, Karczynski P, Tosi M, Doz F, Desjardins L, Couturier J, Stoppa-Lyonnet D. Houdayer C, et al. Among authors: pages berhouet s. Hum Mutat. 2004 Feb;23(2):193-202. doi: 10.1002/humu.10303. Hum Mutat. 2004. PMID: 14722923

9

Evaluation of in silico splice tools for decision-making in molecular diagnosis.

Houdayer C, Dehainault C, Mattler C, Michaux D, Caux-Moncoutier V, Pagès-Berhouet S, d'Enghien CD, Laugé A, Castera L, Gauthier-Villars M, Stoppa-Lyonnet D. Houdayer C, et al. Among authors: pages berhouet s. Hum Mutat. 2008 Jul;29(7):975-82. doi: 10.1002/humu.20765. Hum Mutat. 2008. PMID: 18449911

10

Identification of a large rearrangement of the BRCA1 gene using colour bar code on combed DNA in an American breast/ovarian cancer family previously studied by direct sequencing.

Gad S, Scheuner MT, Pages-Berhouet S, Caux-Moncoutier V, Bensimon A, Aurias A, Pinto M, Stoppa-Lyonnet D. Gad S, et al. J Med Genet. 2001 Jun;38(6):388-92. doi: 10.1136/jmg.38.6.388. J Med Genet. 2001. PMID: 11424920 Free PMC article. No abstract available.

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