Stoffel E - Search Results

1

Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer.

Roberts NJ, Norris AL, Petersen GM, Bondy ML, Brand R, Gallinger S, Kurtz RC, Olson SH, Rustgi AK, Schwartz AG, Stoffel E, Syngal S, Zogopoulos G, Ali SZ, Axilbund J, Chaffee KG, Chen YC, Cote ML, Childs EJ, Douville C, Goes FS, Herman JM, Iacobuzio-Donahue C, Kramer M, Makohon-Moore A, McCombie RW, McMahon KW, Niknafs N, Parla J, Pirooznia M, Potash JB, Rhim AD, Smith AL, Wang Y, Wolfgang CL, Wood LD, Zandi PP, Goggins M, Karchin R, Eshleman JR, Papadopoulos N, Kinzler KW, Vogelstein B, Hruban RH, Klein AP. Roberts NJ, et al. Among authors: stoffel e. Cancer Discov. 2016 Feb;6(2):166-75. doi: 10.1158/2159-8290.CD-15-0402. Epub 2015 Dec 9. Cancer Discov. 2016. PMID: 26658419 Free PMC article.

2

Physician assessment of family cancer history and referral for genetic evaluation in colorectal cancer patients.

Grover S, Stoffel EM, Bussone L, Tschoegl E, Syngal S. Grover S, et al. Among authors: stoffel em. Clin Gastroenterol Hepatol. 2004 Sep;2(9):813-9. doi: 10.1016/s1542-3565(04)00352-0. Clin Gastroenterol Hepatol. 2004. PMID: 15354282

3

Adenomas in young patients: what is the optimal evaluation?

Stoffel EM, Syngal S. Stoffel EM, et al. Am J Gastroenterol. 2005 May;100(5):1150-3. doi: 10.1111/j.1572-0241.2005.41967.x. Am J Gastroenterol. 2005. PMID: 15842592

4

Detection of stool DNA mutations before and after treatment of colorectal neoplasia.

Syngal S, Stoffel E, Chung D, Willett C, Schoetz D, Schroy P, Jagadeesh D, Morel K, Ross M. Syngal S, et al. Among authors: stoffel e. Cancer. 2006 Jan 15;106(2):277-83. doi: 10.1002/cncr.21558. Cancer. 2006. PMID: 16342248 Free article.

5

Factors associated with enrollment in cancer genetics research.

Ford BM, Evans JS, Stoffel EM, Balmaña J, Regan MM, Syngal S. Ford BM, et al. Cancer Epidemiol Biomarkers Prev. 2006 Jul;15(7):1355-9. doi: 10.1158/1055-9965.EPI-05-0816. Cancer Epidemiol Biomarkers Prev. 2006. PMID: 16835336

6

Prediction of MLH1 and MSH2 mutations in Lynch syndrome.

Balmaña J, Stockwell DH, Steyerberg EW, Stoffel EM, Deffenbaugh AM, Reid JE, Ward B, Scholl T, Hendrickson B, Tazelaar J, Burbidge LA, Syngal S. Balmaña J, et al. Among authors: stoffel em. JAMA. 2006 Sep 27;296(12):1469-78. doi: 10.1001/jama.296.12.1469. JAMA. 2006. PMID: 17003395

7

Colon cancer screening strategies.

Stoffel EM, Syngal S. Stoffel EM, et al. Curr Opin Gastroenterol. 2002 Sep;18(5):595-601. doi: 10.1097/00001574-200209000-00012. Curr Opin Gastroenterol. 2002. PMID: 17033339

8

Attitudes toward prenatal genetic testing in patients with familial adenomatous polyposis.

Kastrinos F, Stoffel EM, Balmaña J, Syngal S. Kastrinos F, et al. Am J Gastroenterol. 2007 Jun;102(6):1284-90. doi: 10.1111/j.1572-0241.2007.01168.x. Epub 2007 Mar 13. Am J Gastroenterol. 2007. PMID: 17355417

9

Sharing genetic test results in Lynch syndrome: communication with close and distant relatives.

Stoffel EM, Ford B, Mercado RC, Punglia D, Kohlmann W, Conrad P, Blanco A, Shannon KM, Powell M, Gruber SB, Terdiman J, Chung DC, Syngal S. Stoffel EM, et al. Clin Gastroenterol Hepatol. 2008 Mar;6(3):333-8. doi: 10.1016/j.cgh.2007.12.014. Epub 2008 Feb 7. Clin Gastroenterol Hepatol. 2008. PMID: 18258490 Free PMC article.

10

Phenotype comparison of MLH1 and MSH2 mutation carriers in a cohort of 1,914 individuals undergoing clinical genetic testing in the United States.

Kastrinos F, Stoffel EM, Balmaña J, Steyerberg EW, Mercado R, Syngal S. Kastrinos F, et al. Cancer Epidemiol Biomarkers Prev. 2008 Aug;17(8):2044-51. doi: 10.1158/1055-9965.EPI-08-0301. Cancer Epidemiol Biomarkers Prev. 2008. PMID: 18708397

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