R03 CA103500-02/CA/NCI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2004	2
2005	4
2006	3
2007	1
2024	0

1

TGFBR1*6A may contribute to hereditary colorectal cancer.

Bian Y, Caldes T, Wijnen J, Franken P, Vasen H, Kaklamani V, Nafa K, Peterlongo P, Ellis N, Baron JA, Burn J, Moeslein G, Morrison PJ, Chen Y, Ahsan H, Watson P, Lynch HT, de la Chapelle A, Fodde R, Pasche B. Bian Y, et al. J Clin Oncol. 2005 May 1;23(13):3074-8. doi: 10.1200/JCO.2005.00.281. J Clin Oncol. 2005. PMID: 15860866

2

Prediction of germline mutations and cancer risk in the Lynch syndrome.

Chen S, Wang W, Lee S, Nafa K, Lee J, Romans K, Watson P, Gruber SB, Euhus D, Kinzler KW, Jass J, Gallinger S, Lindor NM, Casey G, Ellis N, Giardiello FM, Offit K, Parmigiani G; Colon Cancer Family Registry. Chen S, et al. JAMA. 2006 Sep 27;296(12):1479-87. doi: 10.1001/jama.296.12.1479. JAMA. 2006. PMID: 17003396 Free PMC article.

3

The utility of immunohistochemical detection of DNA mismatch repair gene proteins.

Shia J, Ellis NA, Klimstra DS. Shia J, et al. Virchows Arch. 2004 Nov;445(5):431-41. doi: 10.1007/s00428-004-1090-5. Epub 2004 Sep 29. Virchows Arch. 2004. PMID: 15455227 Review.

4

Localization of cancer susceptibility genes by genome-wide single-nucleotide polymorphism linkage-disequilibrium mapping.

Mitra N, Ye TZ, Smith A, Chuai S, Kirchhoff T, Peterlongo P, Nafa K, Phillips MS, Offit K, Ellis NA. Mitra N, et al. Cancer Res. 2004 Nov 1;64(21):8116-25. doi: 10.1158/0008-5472.CAN-04-1411. Cancer Res. 2004. PMID: 15520224

5

Value of immunohistochemical detection of DNA mismatch repair proteins in predicting germline mutation in hereditary colorectal neoplasms.

Shia J, Klimstra DS, Nafa K, Offit K, Guillem JG, Markowitz AJ, Gerald WL, Ellis NA. Shia J, et al. Am J Surg Pathol. 2005 Jan;29(1):96-104. doi: 10.1097/01.pas.0000146009.85309.3b. Am J Surg Pathol. 2005. PMID: 15613860

6

Single-amplicon MSH2 A636P mutation testing in Ashkenazi Jewish patients with colorectal cancer: role in presurgical management.

Guillem JG, Glogowski E, Moore HG, Nafa K, Markowitz AJ, Shia J, Offit K, Ellis NA. Guillem JG, et al. Ann Surg. 2007 Apr;245(4):560-5. doi: 10.1097/01.sla.0000252589.26244.d4. Ann Surg. 2007. PMID: 17414604 Free PMC article.

7

Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping.

Ellis NA, Kirchhoff T, Mitra N, Ye TZ, Chuai S, Huang H, Nafa K, Norton L, Neuhausen S, Gordon D, Struewing JP, Narod S, Offit K. Ellis NA, et al. Genet Epidemiol. 2006 Jan;30(1):48-61. doi: 10.1002/gepi.20101. Genet Epidemiol. 2006. PMID: 16206141

8

Germline mutations of AXIN2 are not associated with nonsyndromic colorectal cancer.

Peterlongo P, Howe LR, Radice P, Sala P, Hong YJ, Hong SI, Mitra N, Offit K, Ellis NA. Peterlongo P, et al. Hum Mutat. 2005 May;25(5):498-500. doi: 10.1002/humu.20189. Hum Mutat. 2005. PMID: 15841489 No abstract available.

9

Increased frequency of disease-causing MYH mutations in colon cancer families.

Peterlongo P, Mitra N, Sanchez de Abajo A, de la Hoya M, Bassi C, Bertario L, Radice P, Glogowski E, Nafa K, Caldes T, Offit K, Ellis NA. Peterlongo P, et al. Carcinogenesis. 2006 Nov;27(11):2243-9. doi: 10.1093/carcin/bgl093. Epub 2006 Jun 14. Carcinogenesis. 2006. PMID: 16774938

10

Colorectal cancer risk in individuals with biallelic or monoallelic mutations of MYH.

Peterlongo P, Mitra N, Chuai S, Kirchhoff T, Palmer C, Huang H, Nafa K, Offit K, Ellis NA. Peterlongo P, et al. Int J Cancer. 2005 Apr 10;114(3):505-7. doi: 10.1002/ijc.20767. Int J Cancer. 2005. PMID: 15578699 No abstract available.

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