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368 results

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Page 1
Clinical management of TP53 mosaic variants found on germline genetic testing.
Ward A, Farengo-Clark D, McKenna DB, Safonov A, Good M, Le A, Kessler L, Shah PD, Bradbury AR, Domchek SM, Nathanson KL, Powers J, Maxwell KN. Ward A, et al. Among authors: nathanson kl. Cancer Genet. 2024 Jun;284-285:43-47. doi: 10.1016/j.cancergen.2024.04.002. Epub 2024 Apr 23. Cancer Genet. 2024. PMID: 38677009 Free article.
Risk of metachronous breast cancer after BRCA mutation-associated ovarian cancer.
Domchek SM, Jhaveri K, Patil S, Stopfer JE, Hudis C, Powers J, Stadler Z, Goldstein L, Kauff N, Khasraw M, Offit K, Nathanson KL, Robson M. Domchek SM, et al. Among authors: nathanson kl. Cancer. 2013 Apr 1;119(7):1344-8. doi: 10.1002/cncr.27842. Epub 2012 Nov 16. Cancer. 2013. PMID: 23165893 Free article.
Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility.
Bradbury AR, Patrick-Miller L, Long J, Powers J, Stopfer J, Forman A, Rybak C, Mattie K, Brandt A, Chambers R, Chung WK, Churpek J, Daly MB, Digiovanni L, Farengo-Clark D, Fetzer D, Ganschow P, Grana G, Gulden C, Hall M, Kohler L, Maxwell K, Merrill S, Montgomery S, Mueller R, Nielsen S, Olopade O, Rainey K, Seelaus C, Nathanson KL, Domchek SM. Bradbury AR, et al. Among authors: nathanson kl. Genet Med. 2015 Jun;17(6):485-92. doi: 10.1038/gim.2014.134. Epub 2014 Oct 9. Genet Med. 2015. PMID: 25297947 Free PMC article.
Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer.
Maxwell KN, Wubbenhorst B, D'Andrea K, Garman B, Long JM, Powers J, Rathbun K, Stopfer JE, Zhu J, Bradbury AR, Simon MS, DeMichele A, Domchek SM, Nathanson KL. Maxwell KN, et al. Among authors: nathanson kl. Genet Med. 2015 Aug;17(8):630-8. doi: 10.1038/gim.2014.176. Epub 2014 Dec 11. Genet Med. 2015. PMID: 25503501 Free PMC article.
Patient feedback and early outcome data with a novel tiered-binned model for multiplex breast cancer susceptibility testing.
Bradbury AR, Patrick-Miller LJ, Egleston BL, DiGiovanni L, Brower J, Harris D, Stevens EM, Maxwell KN, Kulkarni A, Chavez T, Brandt A, Long JM, Powers J, Stopfer JE, Nathanson KL, Domchek SM. Bradbury AR, et al. Among authors: nathanson kl. Genet Med. 2016 Jan;18(1):25-33. doi: 10.1038/gim.2015.19. Epub 2015 Apr 2. Genet Med. 2016. PMID: 25834950 Free article.
Population Frequency of Germline BRCA1/2 Mutations.
Maxwell KN, Domchek SM, Nathanson KL, Robson ME. Maxwell KN, et al. Among authors: nathanson kl. J Clin Oncol. 2016 Dec;34(34):4183-4185. doi: 10.1200/JCO.2016.67.0554. Epub 2016 Oct 31. J Clin Oncol. 2016. PMID: 27551127 No abstract available.
Application of Panel-Based Tests for Inherited Risk of Cancer.
Shah PD, Nathanson KL. Shah PD, et al. Among authors: nathanson kl. Annu Rev Genomics Hum Genet. 2017 Aug 31;18:201-227. doi: 10.1146/annurev-genom-091416-035305. Epub 2017 May 15. Annu Rev Genomics Hum Genet. 2017. PMID: 28504904 Review.
Research participants' experiences with return of genetic research results and preferences for web-based alternatives.
Gaieski JB, Patrick-Miller L, Egleston BL, Maxwell KN, Walser S, DiGiovanni L, Brower J, Fetzer D, Ganzak A, McKenna D, Long JM, Powers J, Stopfer JE, Nathanson KL, Domchek SM, Bradbury AR. Gaieski JB, et al. Among authors: nathanson kl. Mol Genet Genomic Med. 2019 Sep;7(9):e898. doi: 10.1002/mgg3.898. Epub 2019 Aug 3. Mol Genet Genomic Med. 2019. PMID: 31376244 Free PMC article. Clinical Trial.
368 results