Hampel H - Search Results

1

Double somatic mismatch repair gene pathogenic variants as common as Lynch syndrome among endometrial cancer patients.

Hampel H, Pearlman R, de la Chapelle A, Pritchard CC, Zhao W, Jones D, Yilmaz A, Chen W, Frankel WL, Suarez AA, Cosgrove C, Backes F, Copeland L, Fowler J, O'Malley D, Salani R, McElroy JP, Stanich PP, Goodfellow P, Cohn DE. Hampel H, et al. Gynecol Oncol. 2021 Jan;160(1):161-168. doi: 10.1016/j.ygyno.2020.10.012. Epub 2020 Oct 21. Gynecol Oncol. 2021. PMID: 33393477 Free PMC article.

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

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

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

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

867 results

Search Page