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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. Among authors: euhus d. JAMA. 2006 Sep 27;296(12):1479-87. doi: 10.1001/jama.296.12.1479. JAMA. 2006. PMID: 17003396 Free PMC article.
Characterization of BRCA1 and BRCA2 mutations in a large United States sample.
Chen S, Iversen ES, Friebel T, Finkelstein D, Weber BL, Eisen A, Peterson LE, Schildkraut JM, Isaacs C, Peshkin BN, Corio C, Leondaridis L, Tomlinson G, Dutson D, Kerber R, Amos CI, Strong LC, Berry DA, Euhus DM, Parmigiani G. Chen S, et al. Among authors: euhus dm. J Clin Oncol. 2006 Feb 20;24(6):863-71. doi: 10.1200/JCO.2005.03.6772. J Clin Oncol. 2006. PMID: 16484695 Free PMC article.
Validity of models for predicting BRCA1 and BRCA2 mutations.
Parmigiani G, Chen S, Iversen ES Jr, Friebel TM, Finkelstein DM, Anton-Culver H, Ziogas A, Weber BL, Eisen A, Malone KE, Daling JR, Hsu L, Ostrander EA, Peterson LE, Schildkraut JM, Isaacs C, Corio C, Leondaridis L, Tomlinson G, Amos CI, Strong LC, Berry DA, Weitzel JN, Sand S, Dutson D, Kerber R, Peshkin BN, Euhus DM. Parmigiani G, et al. Among authors: euhus dm. Ann Intern Med. 2007 Oct 2;147(7):441-50. doi: 10.7326/0003-4819-147-7-200710020-00002. Ann Intern Med. 2007. PMID: 17909205 Free PMC article.
Breast cancer phenotype in women with TP53 germline mutations: a Li-Fraumeni syndrome consortium effort.
Masciari S, Dillon DA, Rath M, Robson M, Weitzel JN, Balmana J, Gruber SB, Ford JM, Euhus D, Lebensohn A, Telli M, Pochebit SM, Lypas G, Garber JE. Masciari S, et al. Among authors: euhus d. Breast Cancer Res Treat. 2012 Jun;133(3):1125-30. doi: 10.1007/s10549-012-1993-9. Epub 2012 Mar 4. Breast Cancer Res Treat. 2012. PMID: 22392042 Free PMC article.
Legacy Genetic Testing Results for Cancer Susceptibility: How Common are Conflicting Classifications in a Large Variant Dataset from Multiple Practices?
Yin K, Liu Y, Lamichhane B, Sandbach JF, Patel G, Compagnoni G, Kanak RH, Rosen B, Ondrula DP, Smith L, Brown E, Gold L, Whitworth P, App C, Euhus D, Semine A, Dwight Lyons S, Lazarte MAC, Parmigiani G, Braun D, Hughes KS. Yin K, et al. Among authors: euhus d. Ann Surg Oncol. 2020 Jul;27(7):2212-2220. doi: 10.1245/s10434-020-08492-9. Epub 2020 Apr 27. Ann Surg Oncol. 2020. PMID: 32342295
Comparison between CaGene 5.1 and 6.0 for BRCA1/2 mutation prediction: a retrospective study of 150 BRCA1/2 genetic tests in 517 families with breast/ovarian cancer.
Antonucci I, Provenzano M, Sorino L, Balsamo M, Aceto GM, Battista P, Euhus D, Cianchetti E, Ballerini P, Natoli C, Palka G, Stuppia L. Antonucci I, et al. Among authors: euhus d. J Hum Genet. 2017 Mar;62(3):379-387. doi: 10.1038/jhg.2016.138. Epub 2016 Dec 8. J Hum Genet. 2017. PMID: 27928164
A model for individualized risk prediction of contralateral breast cancer.
Chowdhury M, Euhus D, Onega T, Biswas S, Choudhary PK. Chowdhury M, et al. Among authors: euhus d. Breast Cancer Res Treat. 2017 Jan;161(1):153-160. doi: 10.1007/s10549-016-4039-x. Epub 2016 Nov 4. Breast Cancer Res Treat. 2017. PMID: 27815748 Free PMC article.
Genetic testing today.
Euhus D. Euhus D. Ann Surg Oncol. 2014 Oct;21(10):3209-15. doi: 10.1245/s10434-014-3906-0. Epub 2014 Jul 17. Ann Surg Oncol. 2014. PMID: 25029991
149 results