Hampel H - Search Results

1

Hereditary colorectal cancer: risk assessment and management.

Hampel H, Peltomaki P. Hampel H, et al. Clin Genet. 2000 Aug;58(2):89-97. doi: 10.1034/j.1399-0004.2000.580201.x. Clin Genet. 2000. PMID: 11005140 Review.

2

Efficacy of a touchscreen computer based family cancer history questionnaire and subsequent cancer risk assessment.

Westman J, Hampel H, Bradley T. Westman J, et al. Among authors: hampel h. J Med Genet. 2000 May;37(5):354-60. doi: 10.1136/jmg.37.5.354. J Med Genet. 2000. PMID: 10807694 Free PMC article.

3

Genetic testing for cancer predisposition.

Eng C, Hampel H, de la Chapelle A. Eng C, et al. Among authors: hampel h. Annu Rev Med. 2001;52:371-400. doi: 10.1146/annurev.med.52.1.371. Annu Rev Med. 2001. PMID: 11160785 Review.

4

Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2.

Pyatt RE, Nakagawa H, Hampel H, Sedra M, Fuchik MB, Comeras I, de la Chapelle A, Prior TW. Pyatt RE, et al. Among authors: hampel h. Clin Genet. 2003 Mar;63(3):215-8. doi: 10.1034/j.1399-0004.2003.00040.x. Clin Genet. 2003. PMID: 12694232

5

Referral for cancer genetics consultation: a review and compilation of risk assessment criteria.

Hampel H, Sweet K, Westman JA, Offit K, Eng C. Hampel H, et al. J Med Genet. 2004 Feb;41(2):81-91. doi: 10.1136/jmg.2003.010918. J Med Genet. 2004. PMID: 14757853 Free PMC article. Review.

6

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Nakagawa H, Sotamaa K, Prior TW, Westman J, Panescu J, Fix D, Lockman J, Comeras I, de la Chapelle A. Hampel H, et al. N Engl J Med. 2005 May 5;352(18):1851-60. doi: 10.1056/NEJMoa043146. N Engl J Med. 2005. PMID: 15872200 Free article.

7

Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset.

Hampel H, Stephens JA, Pukkala E, Sankila R, Aaltonen LA, Mecklin JP, de la Chapelle A. Hampel H, et al. Gastroenterology. 2005 Aug;129(2):415-21. doi: 10.1016/j.gastro.2005.05.011. Gastroenterology. 2005. PMID: 16083698

8

Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1.

Raevaara TE, Korhonen MK, Lohi H, Hampel H, Lynch E, Lönnqvist KE, Holinski-Feder E, Sutter C, McKinnon W, Duraisamy S, Gerdes AM, Peltomäki P, Kohonen-Ccorish M, Mangold E, Macrae F, Greenblatt M, de la Chapelle A, Nyström M. Raevaara TE, et al. Among authors: hampel h. Gastroenterology. 2005 Aug;129(2):537-49. doi: 10.1016/j.gastro.2005.06.005. Gastroenterology. 2005. PMID: 16083711

9

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.

Hampel H, Frankel W, Panescu J, Lockman J, Sotamaa K, Fix D, Comeras I, La Jeunesse J, Nakagawa H, Westman JA, Prior TW, Clendenning M, Penzone P, Lombardi J, Dunn P, Cohn DE, Copeland L, Eaton L, Fowler J, Lewandowski G, Vaccarello L, Bell J, Reid G, de la Chapelle A. Hampel H, et al. Cancer Res. 2006 Aug 1;66(15):7810-7. doi: 10.1158/0008-5472.CAN-06-1114. Cancer Res. 2006. PMID: 16885385

10

Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein.

Ollila S, Sarantaus L, Kariola R, Chan P, Hampel H, Holinski-Feder E, Macrae F, Kohonen-Corish M, Gerdes AM, Peltomäki P, Mangold E, de la Chapelle A, Greenblatt M, Nyström M. Ollila S, et al. Among authors: hampel h. Gastroenterology. 2006 Nov;131(5):1408-17. doi: 10.1053/j.gastro.2006.08.044. Epub 2006 Aug 22. Gastroenterology. 2006. PMID: 17101317

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