Fornasarig M - Search Results

1

Somatic mosaicism in a patient with Lynch syndrome.

Pastrello C, Fornasarig M, Pin E, Berto E, Pivetta B, Viel A. Pastrello C, et al. Among authors: fornasarig m. Am J Med Genet A. 2009 Feb;149A(2):212-5. doi: 10.1002/ajmg.a.32620. Am J Med Genet A. 2009. PMID: 19133695

2

Integrated analysis of unclassified variants in mismatch repair genes.

Pastrello C, Pin E, Marroni F, Bedin C, Fornasarig M, Tibiletti MG, Oliani C, Ponz de Leon M, Urso ED, Della Puppa L, Agostini M, Viel A. Pastrello C, et al. Among authors: fornasarig m. Genet Med. 2011 Feb;13(2):115-24. doi: 10.1097/GIM.0b013e3182011489. Genet Med. 2011. PMID: 21239990 Free article.

3

Different molecular mechanisms underlie genomic deletions in the MLH1 Gene.

Viel A, Petronzelli F, Della Puppa L, Lucci-Cordisco E, Fornasarig M, Pucciarelli S, Rovella V, Quaia M, Ponz de Leon M, Boiocchi M, Genuardi M. Viel A, et al. Among authors: fornasarig m. Hum Mutat. 2002 Nov;20(5):368-74. doi: 10.1002/humu.10138. Hum Mutat. 2002. PMID: 12402334

4

Stability of BAT26 in tumours of hereditary nonpolyposis colorectal cancer patients with MSH2 intragenic deletion.

Pastrello C, Baglioni S, Tibiletti MG, Papi L, Fornasarig M, Morabito A, Agostini M, Genuardi M, Viel A. Pastrello C, et al. Among authors: fornasarig m. Eur J Hum Genet. 2006 Jan;14(1):63-8. doi: 10.1038/sj.ejhg.5201517. Eur J Hum Genet. 2006. PMID: 16251890

5

Molecular and Pathological Features of Gastric Cancer in Lynch Syndrome and Familial Adenomatous Polyposis.

Fornasarig M, Magris R, De Re V, Bidoli E, Canzonieri V, Maiero S, Viel A, Cannizzaro R. Fornasarig M, et al. Int J Mol Sci. 2018 Jun 6;19(6):1682. doi: 10.3390/ijms19061682. Int J Mol Sci. 2018. PMID: 29882764 Free PMC article.

6

Toward a better definition of EPCAM deletions in Lynch Syndrome: Report of new variants in Italy and the associated molecular phenotype.

Cini G, Quaia M, Canzonieri V, Fornasarig M, Maestro R, Morabito A, D'Elia AV, Urso ED, Mammi I, Viel A. Cini G, et al. Among authors: fornasarig m. Mol Genet Genomic Med. 2019 May;7(5):e587. doi: 10.1002/mgg3.587. Epub 2019 Mar 27. Mol Genet Genomic Med. 2019. PMID: 30916491 Free PMC article.

7

Amsterdam criteria II and endometrial cancer index cases for an accurate selection of HNPCC families.

Fornasarig M, Viel A, Bidoli E, Campagnutta E, Minisini AM, Cannizzaro R, Della Puppa L, Boiocchi M. Fornasarig M, et al. Tumori. 2002 Jan-Feb;88(1):18-20. Tumori. 2002. PMID: 12004844

8

MUTYH c.933+3A>C, associated with a severely impaired gene expression, is the first Italian founder mutation in MUTYH-Associated Polyposis.

Pin E, Pastrello C, Tricarico R, Papi L, Quaia M, Fornasarig M, Carnevali I, Oliani C, Fornasin A, Agostini M, Maestro R, Barana D, Aretz S, Genuardi M, Viel A. Pin E, et al. Among authors: fornasarig m. Int J Cancer. 2013 Mar 1;132(5):1060-9. doi: 10.1002/ijc.27761. Epub 2012 Aug 28. Int J Cancer. 2013. PMID: 22865608 Free article.

9

Evaluation of the replication error phenotype in relation to molecular and clinicopathological features in hereditary and early onset colorectal cancer.

Capozzi E, Della Puppa L, Fornasarig M, Pedroni M, Boiocchi M, Viel A. Capozzi E, et al. Among authors: fornasarig m. Eur J Cancer. 1999 Feb;35(2):289-95. doi: 10.1016/s0959-8049(98)00317-7. Eur J Cancer. 1999. PMID: 10448273

10

Microsatellite instability and MLH1 and MSH2 germline defects are related to clinicopathological features in sporadic colorectal cancer.

Fornasarig M, Viel A, Valentini M, Capozzi E, Sigon R, De Paoli A, Della Puppa L, Boiocchi M. Fornasarig M, et al. Oncol Rep. 2000 Jan-Feb;7(1):39-43. doi: 10.3892/or.7.1.39. Oncol Rep. 2000. PMID: 10601588

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