Hampel H - Search Results

1

Genotyping panel for assessing response to cancer chemotherapy.

Dai Z, Papp AC, Wang D, Hampel H, Sadee W. Dai Z, et al. Among authors: hampel h. BMC Med Genomics. 2008 Jun 11;1:24. doi: 10.1186/1755-8794-1-24. BMC Med Genomics. 2008. PMID: 18547414 Free PMC article.

2

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.

3

A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome.

Clendenning M, Senter L, Hampel H, Robinson KL, Sun S, Buchanan D, Walsh MD, Nilbert M, Green J, Potter J, Lindblom A, de la Chapelle A. Clendenning M, et al. Among authors: hampel h. J Med Genet. 2008 Jun;45(6):340-5. doi: 10.1136/jmg.2007.056150. Epub 2008 Jan 4. J Med Genet. 2008. PMID: 18178629 Free PMC article.

4

Allele-specific imbalance mapping at human orthologs of mouse susceptibility to colon cancer (Scc) loci.

Gerber MM, Hampel H, Zhou XP, Schulz NP, Suhy A, Deveci M, Çatalyürek ÜV, Ewart Toland A. Gerber MM, et al. Among authors: hampel h. Int J Cancer. 2015 Nov 15;137(10):2323-31. doi: 10.1002/ijc.29599. Epub 2015 May 29. Int J Cancer. 2015. PMID: 25973956 Free PMC article.

5

Implementing universal upfront multi-gene panel testing in endometrial cancer: From cost to practical considerations.

Levine MD, Barrington DA, Hampel H, Goodfellow PJ, Cohn DE. Levine MD, et al. Among authors: hampel h. Gynecol Oncol. 2022 Sep;166(3):538-542. doi: 10.1016/j.ygyno.2022.07.016. Epub 2022 Jul 21. Gynecol Oncol. 2022. PMID: 35871048 Free article.

6

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.

7

Histologic features distinguish microsatellite-high from microsatellite-low and microsatellite-stable colorectal carcinomas, but do not differentiate germline mutations from methylation of the MLH1 promoter.

Yearsley M, Hampel H, Lehman A, Nakagawa H, de la Chapelle A, Frankel WL. Yearsley M, et al. Among authors: hampel h. Hum Pathol. 2006 Jul;37(7):831-8. doi: 10.1016/j.humpath.2006.02.009. Epub 2006 May 19. Hum Pathol. 2006. PMID: 16784982

8

Immunohistochemistry staining for the mismatch repair proteins in the clinical care of patients with colorectal cancer.

South CD, Yearsley M, Martin E, Arnold M, Frankel W, Hampel H. South CD, et al. Among authors: hampel h. Genet Med. 2009 Nov;11(11):812-7. doi: 10.1097/GIM.0b013e3181b99b75. Genet Med. 2009. PMID: 19752738 Free article.

9

Genetic testing for hereditary colorectal cancer.

Hampel H. Hampel H. Surg Oncol Clin N Am. 2009 Oct;18(4):687-703. doi: 10.1016/j.soc.2009.08.001. Surg Oncol Clin N Am. 2009. PMID: 19793575 Free PMC article. Review.

10

Allele-specific expression of TGFBR1 in colon cancer patients.

Tomsic J, Guda K, Liyanarachchi S, Hampel H, Natale L, Markowitz SD, Tanner SM, de la Chapelle A. Tomsic J, et al. Among authors: hampel h. Carcinogenesis. 2010 Oct;31(10):1800-4. doi: 10.1093/carcin/bgq165. Epub 2010 Aug 12. Carcinogenesis. 2010. PMID: 20705955 Free PMC article.

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