These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. A new scoring system in cancer genetics: application to criteria for BRCA1 and BRCA2 mutation screening. Bonaïti B; Alarcon F; Andrieu N; Bonadona V; Dondon MG; Pennec S; Stoppa-Lyonnet D; Bonaïti-Pellié C; Perdry H J Med Genet; 2014 Feb; 51(2):114-21. PubMed ID: 24343917 [TBL] [Abstract][Full Text] [Related]
6. Performance of BOADICEA and BRCAPRO genetic models and of empirical criteria based on cancer family history for predicting BRCA mutation carrier probabilities: a retrospective study in a sample of Italian cancer genetics clinics. Varesco L; Viassolo V; Viel A; Gismondi V; Radice P; Montagna M; Alducci E; Della Puppa L; Oliani C; Tommasi S; Caligo MA; Vivanet C; Zuradelli M; Mandich P; Tibiletti MG; Cavalli P; Lucci Cordisco E; Turchetti D; Boggiani D; Bracci R; Bruzzi P; Bonelli L Breast; 2013 Dec; 22(6):1130-5. PubMed ID: 24011770 [TBL] [Abstract][Full Text] [Related]
8. Prevalence of BRCA1/2 mutations in sporadic breast/ovarian cancer patients and identification of a novel de novo BRCA1 mutation in a patient diagnosed with late onset breast and ovarian cancer: implications for genetic testing. De Leeneer K; Coene I; Crombez B; Simkens J; Van den Broecke R; Bols A; Stragier B; Vanhoutte I; De Paepe A; Poppe B; Claes K Breast Cancer Res Treat; 2012 Feb; 132(1):87-95. PubMed ID: 21553119 [TBL] [Abstract][Full Text] [Related]
9. Selecting Patients with Ovarian Cancer for Germline BRCA Mutation Testing: Findings from Guidelines and a Systematic Literature Review. Eccles DM; Balmaña J; Clune J; Ehlken B; Gohlke A; Hirst C; Potter D; Schroeder C; Tyczynski JE; Gomez Garcia EB Adv Ther; 2016 Feb; 33(2):129-50. PubMed ID: 26809252 [TBL] [Abstract][Full Text] [Related]
10. Statewide Retrospective Review of Familial Pancreatic Cancer in Delaware, and Frequency of Genetic Mutations in Pancreatic Cancer Kindreds. Catts ZA; Baig MK; Milewski B; Keywan C; Guarino M; Petrelli N Ann Surg Oncol; 2016 May; 23(5):1729-35. PubMed ID: 26727920 [TBL] [Abstract][Full Text] [Related]
11. Risk of ovarian cancer in BRCA1 and BRCA2 mutation-negative hereditary breast cancer families. Kauff ND; Mitra N; Robson ME; Hurley KE; Chuai S; Goldfrank D; Wadsworth E; Lee J; Cigler T; Borgen PI; Norton L; Barakat RR; Offit K J Natl Cancer Inst; 2005 Sep; 97(18):1382-4. PubMed ID: 16174860 [TBL] [Abstract][Full Text] [Related]
12. Hereditary ovarian cancer: recent molecular insights and their impact on screening strategies. Long KC; Kauff ND Curr Opin Oncol; 2011 Sep; 23(5):526-30. PubMed ID: 21734577 [TBL] [Abstract][Full Text] [Related]
13. Eligibility Criteria and Genetic Testing Results from a High-Risk Cohort for Hereditary Breast and Ovarian Cancer Syndrome in Southeastern Ontario. Dos Santos Vidal R; Hawrysh A; Walia JS; Davey S; Feilotter H J Mol Diagn; 2016 May; 18(3):362-369. PubMed ID: 26941049 [TBL] [Abstract][Full Text] [Related]
14. Frequency of three BRCA1 gene founder mutations in breast/ovarian cancer families from the Pomerania-Kujawy region of Poland. Janiszewska H; Haus O; Lauda-Swieciak A; Pasińska M; Laskowski R; Szymański W; Górski B; Lubiński J Clin Genet; 2003 Dec; 64(6):502-8. PubMed ID: 14986830 [TBL] [Abstract][Full Text] [Related]
15. The clinical utility of genetic testing in breast cancer kindreds: a prospective study in families without a demonstrable BRCA mutation. Møller P; Stormorken A; Holmen MM; Hagen AI; Vabø A; Mæhle L Breast Cancer Res Treat; 2014 Apr; 144(3):607-14. PubMed ID: 24619173 [TBL] [Abstract][Full Text] [Related]
16. Limited family structure and BRCA gene mutation status in single cases of breast cancer. Weitzel JN; Lagos VI; Cullinane CA; Gambol PJ; Culver JO; Blazer KR; Palomares MR; Lowstuter KJ; MacDonald DJ JAMA; 2007 Jun; 297(23):2587-95. PubMed ID: 17579227 [TBL] [Abstract][Full Text] [Related]
17. Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: Recommendation Statement. Am Fam Physician; 2020 Feb; 101(4):233-238. PubMed ID: 32053325 [No Abstract] [Full Text] [Related]
18. Outcome of risk-reducing salpingo-oophorectomy in BRCA carriers and women of unknown mutation status. Manchanda R; Abdelraheim A; Johnson M; Rosenthal AN; Benjamin E; Brunell C; Burnell M; Side L; Gessler S; Saridogan E; Oram D; Jacobs I; Menon U BJOG; 2011 Jun; 118(7):814-24. PubMed ID: 21392246 [TBL] [Abstract][Full Text] [Related]
19. Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer. A Continuing Debate. Piver MS Oncologist; 1996; 1(5):326-330. PubMed ID: 10388011 [TBL] [Abstract][Full Text] [Related]
20. Prevalence of BRCA1 mutations among 403 women with triple-negative breast cancer: implications for genetic screening selection criteria: a Hellenic Cooperative Oncology Group Study. Fostira F; Tsitlaidou M; Papadimitriou C; Pertesi M; Timotheadou E; Stavropoulou AV; Glentis S; Bournakis E; Bobos M; Pectasides D; Papakostas P; Pentheroudakis G; Gogas H; Skarlos P; Samantas E; Bafaloukos D; Kosmidis PA; Koutras A; Yannoukakos D; Konstantopoulou I; Fountzilas G Breast Cancer Res Treat; 2012 Jul; 134(1):353-62. PubMed ID: 22434525 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]