Hampel H - Search Results

1

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

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

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

5

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.

6

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

7

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

8

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.

9

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

10

MSH6 missense mutations are often associated with no or low cancer susceptibility.

Kariola R, Hampel H, Frankel WL, Raevaara TE, de la Chapelle A, Nyström-Lahti M. Kariola R, et al. Among authors: hampel h. Br J Cancer. 2004 Oct 4;91(7):1287-92. doi: 10.1038/sj.bjc.6602129. Br J Cancer. 2004. PMID: 15354210 Free PMC article.

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