Hampel H - Search Results

1

How do we approach the goal of identifying everybody with Lynch syndrome?

Hampel H, de la Chapelle A. Hampel H, et al. Fam Cancer. 2013 Jun;12(2):313-7. doi: 10.1007/s10689-013-9611-5. Fam Cancer. 2013. PMID: 23568035 Free PMC article. Review. No abstract available.

2

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.

3

Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinoma.

Chadwick RB, Pyatt RE, Niemann TH, Richards SK, Johnson CK, Stevens MW, Meek JE, Hampel H, Prior TW, de la Chapelle A. Chadwick RB, et al. Among authors: hampel h. J Med Genet. 2001 Jul;38(7):461-6. doi: 10.1136/jmg.38.7.461. J Med Genet. 2001. PMID: 11474654 Free PMC article. No abstract available.

4

Gene expression in papillary thyroid carcinoma reveals highly consistent profiles.

Huang Y, Prasad M, Lemon WJ, Hampel H, Wright FA, Kornacker K, LiVolsi V, Frankel W, Kloos RT, Eng C, Pellegata NS, de la Chapelle A. Huang Y, et al. Among authors: hampel h. Proc Natl Acad Sci U S A. 2001 Dec 18;98(26):15044-9. doi: 10.1073/pnas.251547398. Proc Natl Acad Sci U S A. 2001. PMID: 11752453 Free PMC article.

5

Allele separation facilitates interpretation of potential splicing alterations and genomic rearrangements.

Nakagawa H, Yan H, Lockman J, Hampel H, Kinzler KW, Vogelstein B, De La Chapelle A. Nakagawa H, et al. Among authors: hampel h. Cancer Res. 2002 Aug 15;62(16):4579-82. Cancer Res. 2002. PMID: 12183410

6

The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.

Foulkes WD, Thiffault I, Gruber SB, Horwitz M, Hamel N, Lee C, Shia J, Markowitz A, Figer A, Friedman E, Farber D, Greenwood CM, Bonner JD, Nafa K, Walsh T, Marcus V, Tomsho L, Gebert J, Macrae FA, Gaff CL, Paillerets BB, Gregersen PK, Weitzel JN, Gordon PH, MacNamara E, King MC, Hampel H, De La Chapelle A, Boyd J, Offit K, Rennert G, Chong G, Ellis NA. Foulkes WD, et al. Among authors: hampel h. Am J Hum Genet. 2002 Dec;71(6):1395-412. doi: 10.1086/345075. Epub 2002 Nov 26. Am J Hum Genet. 2002. PMID: 12454801 Free PMC article.

7

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

8

Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques.

Nakagawa H, Hampel H, de la Chapelle A. Nakagawa H, et al. Among authors: hampel h. Hum Mutat. 2003 Sep;22(3):258. doi: 10.1002/humu.9171. Hum Mutat. 2003. PMID: 12938096

9

A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States.

Lynch HT, Coronel SM, Okimoto R, Hampel H, Sweet K, Lynch JF, Barrows A, Wijnen J, van der Klift H, Franken P, Wagner A, Fodde R, de la Chapelle A. Lynch HT, et al. Among authors: hampel h. JAMA. 2004 Feb 11;291(6):718-24. doi: 10.1001/jama.291.6.718. JAMA. 2004. PMID: 14871915

10

Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation.

Nakagawa H, Lockman JC, Frankel WL, Hampel H, Steenblock K, Burgart LJ, Thibodeau SN, de la Chapelle A. Nakagawa H, et al. Among authors: hampel h. Cancer Res. 2004 Jul 15;64(14):4721-7. doi: 10.1158/0008-5472.CAN-03-2879. Cancer Res. 2004. PMID: 15256438

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