Baert-Desurmont S - Search Results

1

MUTYH-associated polyposis: Review and update of the French recommendations established in 2012 under the auspices of the National Cancer institute (INCa).

Colas C, Bonadona V, Baert-Desurmont S, Bonnet D, Coulet F, Dhooge M, Saurin JC, Remenieras A, Bignon YJ, Caron O, De Pauw A, Buisine MP, Buecher B. Colas C, et al. Eur J Med Genet. 2020 Dec;63(12):104078. doi: 10.1016/j.ejmg.2020.104078. Epub 2020 Oct 12. Eur J Med Genet. 2020. PMID: 33059073 Review.

2

The 5' region of the MSH2 gene involved in hereditary non-polyposis colorectal cancer contains a high density of recombinogenic sequences.

Charbonnier F, Baert-Desurmont S, Liang P, Di Fiore F, Martin C, Frerot S, Olschwang S, Wang Q, Buisine MP, Gilbert B, Nilbert M, Lindblom A, Frebourg T. Charbonnier F, et al. Hum Mutat. 2005 Sep;26(3):255-61. doi: 10.1002/humu.20216. Hum Mutat. 2005. PMID: 16086322

3

Partial duplications of the MSH2 and MLH1 genes in hereditary nonpolyposis colorectal cancer.

Baert-Desurmont S, Buisine MP, Bessenay E, Frerot S, Lovecchio T, Martin C, Olschwang S, Wang Q, Frebourg T. Baert-Desurmont S, et al. Eur J Hum Genet. 2007 Mar;15(3):383-6. doi: 10.1038/sj.ejhg.5201765. Epub 2007 Jan 17. Eur J Hum Genet. 2007. PMID: 17228328

4

Duodenal adenocarcinoma and Mut Y human homologue-associated polyposis.

Buecher B, Baert-Desurmont S, Leborgne J, Humeau B, Olschwang S, Frébourg T. Buecher B, et al. Eur J Gastroenterol Hepatol. 2008 Oct;20(10):1024-7. doi: 10.1097/MEG.0b013e3282f5f749. Eur J Gastroenterol Hepatol. 2008. PMID: 18787472

5

Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers.

Olschwang S, Yu K, Lasset C, Baert-Desurmont S, Buisine MP, Wang Q, Hutter P, Rouleau E, Caron O, Bourdon V, Thomas G. Olschwang S, et al. J Cancer Epidemiol. 2009;2009:791754. doi: 10.1155/2009/791754. Epub 2009 Mar 8. J Cancer Epidemiol. 2009. PMID: 20445804 Free PMC article.

6

Evaluation of Lynch syndrome modifier genes in 748 MMR mutation carriers.

Houlle S, Charbonnier F, Houivet E, Tinat J, Buisine MP, Caron O, Benichou J, Baert-Desurmont S, Frebourg T. Houlle S, et al. Eur J Hum Genet. 2011 Aug;19(8):887-92. doi: 10.1038/ejhg.2011.44. Epub 2011 Mar 16. Eur J Hum Genet. 2011. PMID: 21407259 Free PMC article.

7

Frequent mutation in North African patients with MUTYH-associated polyposis.

Lefevre JH, Colas C, Coulet F, Baert-Desurmont S, Mongin C, Tiret E, Frebourg T, Soubrier F, Parc Y. Lefevre JH, et al. Clin Genet. 2011 Oct;80(4):389-93. doi: 10.1111/j.1399-0004.2010.01528.x. Epub 2010 Sep 8. Clin Genet. 2011. PMID: 21443744

8

A remarkable APC mosaicism with two mutant alleles in a family with familial adenomatous polyposis.

Baert-Desurmont S, Piton N, Bou J, Tinat J, Guimbaud R, Selves J, Frébourg T. Baert-Desurmont S, et al. Am J Med Genet A. 2011 Jun;155A(6):1500-2. doi: 10.1002/ajmg.a.34017. Epub 2011 May 12. Am J Med Genet A. 2011. PMID: 21567933 No abstract available.

9

Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.

Bonadona V, Bonaïti B, Olschwang S, Grandjouan S, Huiart L, Longy M, Guimbaud R, Buecher B, Bignon YJ, Caron O, Colas C, Noguès C, Lejeune-Dumoulin S, Olivier-Faivre L, Polycarpe-Osaer F, Nguyen TD, Desseigne F, Saurin JC, Berthet P, Leroux D, Duffour J, Manouvrier S, Frébourg T, Sobol H, Lasset C, Bonaïti-Pellié C; French Cancer Genetics Network. Bonadona V, et al. JAMA. 2011 Jun 8;305(22):2304-10. doi: 10.1001/jama.2011.743. JAMA. 2011. PMID: 21642682

10

UMD-MLH1/MSH2/MSH6 databases: description and analysis of genetic variations in French Lynch syndrome families.

Grandval P, Fabre AJ, Gaildrat P, Baert-Desurmont S, Buisine MP, Ferrari A, Wang Q, Béroud C, Olschwang S. Grandval P, et al. Database (Oxford). 2013 May 31;2013:bat036. doi: 10.1093/database/bat036. Print 2013. Database (Oxford). 2013. PMID: 23729658 Free PMC article.

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