Hutter P - Search Results

1

Disease severity and genetic pathways in attenuated familial adenomatous polyposis vary greatly but depend on the site of the germline mutation.

Sieber OM, Segditsas S, Knudsen AL, Zhang J, Luz J, Rowan AJ, Spain SL, Thirlwell C, Howarth KM, Jaeger EE, Robinson J, Volikos E, Silver A, Kelly G, Aretz S, Frayling I, Hutter P, Dunlop M, Guenther T, Neale K, Phillips R, Heinimann K, Tomlinson IP. Sieber OM, et al. Among authors: hutter p. Gut. 2006 Oct;55(10):1440-8. doi: 10.1136/gut.2005.087106. Epub 2006 Feb 4. Gut. 2006. PMID: 16461775 Free PMC article.

2

Prevalence of MYH germline mutations in Swiss APC mutation-negative polyposis patients.

Russell AM, Zhang J, Luz J, Hutter P, Chappuis PO, Berthod CR, Maillet P, Mueller H, Heinimann K. Russell AM, et al. Among authors: hutter p. Int J Cancer. 2006 Apr 15;118(8):1937-40. doi: 10.1002/ijc.21470. Int J Cancer. 2006. PMID: 16287072

3

Evidence for genetic anticipation in hereditary non-polyposis colorectal cancer.

Westphalen AA, Russell AM, Buser M, Berthod CR, Hutter P, Plasilova M, Mueller H, Heinimann K. Westphalen AA, et al. Among authors: hutter p. Hum Genet. 2005 May;116(6):461-5. doi: 10.1007/s00439-005-1272-5. Epub 2005 Mar 17. Hum Genet. 2005. PMID: 15772852

4

N-acetyltransferase 2 influences cancer prevalence in hMLH1/hMSH2 mutation carriers.

Heinimann K, Scott RJ, Chappuis P, Weber W, Müller H, Dobbie Z, Hutter P. Heinimann K, et al. Among authors: hutter p. Cancer Res. 1999 Jul 1;59(13):3038-40. Cancer Res. 1999. PMID: 10397239

5

An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1.

Hutter P, Wijnen J, Rey-Berthod C, Thiffault I, Verkuijlen P, Farber D, Hamel N, Bapat B, Thibodeau SN, Burn J, Wu J, MacNamara E, Heinimann K, Chong G, Foulkes WD. Hutter P, et al. J Med Genet. 2002 May;39(5):323-7. doi: 10.1136/jmg.39.5.323. J Med Genet. 2002. PMID: 12011148 Free PMC article.

6

High-resolution breakpoint analysis provides evidence for the sequence-directed nature of genome rearrangements in hereditary disorders.

Kovac MB, Kovacova M, Bachraty H, Bachrata K, Piscuoglio S, Hutter P, Ilencikova D, Bartosova Z, Tomlinson I, Roethlisberger B, Heinimann K. Kovac MB, et al. Among authors: hutter p. Hum Mutat. 2015 Feb;36(2):250-9. doi: 10.1002/humu.22734. Hum Mutat. 2015. PMID: 25418510

7

Molecular and clinical characteristics in 32 families affected with familial adenomatous polyposis.

Hutter P, Rey-Berthod C, Chappuis PO, Couturier A, Membrez V, Murphy A, Joris F, Schorderet DF, Delozier-Blanchet C, Soravia C. Hutter P, et al. Hum Mutat. 2001 Dec;18(6):550. doi: 10.1002/humu.1242. Hum Mutat. 2001. PMID: 11748858

8

An unexpected Cowden syndrome case found among members of a large familial adenomatous polyposis kindred.

Mehenni H, Friedl W, Nelen MR, Hutter P, Brundler MA. Mehenni H, et al. Among authors: hutter p. Eur J Gastroenterol Hepatol. 2005 Dec;17(12):1407-12. doi: 10.1097/01.meg.0000184983.38398.b6. Eur J Gastroenterol Hepatol. 2005. PMID: 16292097

9

Detection of protein truncating mutations in exons 1-14 of the APC gene using an in vivo fusion protein assay. Mutations in brief no. 214. Online.

Andreutti-Zaugg C, Couturier A, Chappuis P, Hutter P. Andreutti-Zaugg C, et al. Among authors: hutter p. Hum Mutat. 1999;13(2):170-1. doi: 10.1002/(SICI)1098-1004(1999)13:2<170::AID-HUMU12>3.0.CO;2-7. Hum Mutat. 1999. PMID: 10094557

10

Distinct patterns of germ-line deletions in MLH1 and MSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC).

Li L, McVety S, Younan R, Liang P, Du Sart D, Gordon PH, Hutter P, Hogervorst FB, Chong G, Foulkes WD. Li L, et al. Among authors: hutter p. Hum Mutat. 2006 Apr;27(4):388. doi: 10.1002/humu.9417. Hum Mutat. 2006. PMID: 16541406

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