메뉴 건너뛰기




Volumn 149, Issue 1, 2015, Pages 223-227

Erratum to: Incidence of BRCA1 and BRCA2 non-founder mutations in patients of Ashkenazi Jewish ancestry [Breast Cancer Research and Treatment, 149, 1, (2015) 223-227, DOI 10.1007/s10549-014-3218-x];Incidence of BRCA1 and BRCA2 non-founder mutations in patients of Ashkenazi Jewish ancestry

Author keywords

Ashkenazi Jewish; BRCA1; BRCA2; Founder mutations; Hereditary Breast and Ovarian Cancer

Indexed keywords

BRCA1 PROTEIN; BRCA2 PROTEIN;

EID: 84925543786     PISSN: 01676806     EISSN: 15737217     Source Type: Journal    
DOI: 10.1007/s10549-015-3361-z     Document Type: Erratum
Times cited : (43)

References (13)
  • 1
    • 33845654907 scopus 로고    scopus 로고
    • Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada
    • COI: 1:CAS:528:DC%2BD28XhtlCru7nJ, PID: 17148771
    • Risch HA, McLaughlin JR, Cole DE, Rosen B, Bradley L, Fan I, Tang J, Li S, Zhang S, Shaw PA, Narod SA (2006) Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada. J Natl Cancer Inst 98(23):1694–1706. doi:10.1093/jnci/djj465
    • (2006) J Natl Cancer Inst , vol.98 , Issue.23 , pp. 1694-1706
    • Risch, H.A.1    McLaughlin, J.R.2    Cole, D.E.3    Rosen, B.4    Bradley, L.5    Fan, I.6    Tang, J.7    Li, S.8    Zhang, S.9    Shaw, P.A.10    Narod, S.A.11
  • 2
    • 0033740880 scopus 로고    scopus 로고
    • Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases
    • Anglian Breast Cancer Study Group (2000) Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Br J Cancer 83(10):1301–1308. doi:10.1054/bjoc.2000.1407
    • (2000) Br J Cancer , vol.83 , Issue.10 , pp. 1301-1308
    • Anglian Breast Cancer Study Group1
  • 3
    • 0033955496 scopus 로고    scopus 로고
    • Risk models for familial ovarian and breast cancer
    • COI: 1:STN:280:DC%2BD3c7gvVyksQ%3D%3D, PID: 10642429
    • Antoniou AC, Gayther SA, Stratton JF, Ponder BA, Easton DF (2000) Risk models for familial ovarian and breast cancer. Genet Epidemiol 18(2):173–190. doi:10.1002/(SICI)1098-2272(200002)18:2<173:AID-GEPI6>3.0.CO;2-R
    • (2000) Genet Epidemiol , vol.18 , Issue.2 , pp. 173-190
    • Antoniou, A.C.1    Gayther, S.A.2    Stratton, J.F.3    Ponder, B.A.4    Easton, D.F.5
  • 4
    • 0029794992 scopus 로고    scopus 로고
    • Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2
    • COI: 1:CAS:528:DyaK28XmtVKntLs%3D, PID: 8841191
    • Roa BB, Boyd AA, Volcik K, Richards CS (1996) Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2. Nat Genet 14(2):185–187. doi:10.1038/ng1096-185
    • (1996) Nat Genet , vol.14 , Issue.2 , pp. 185-187
    • Roa, B.B.1    Boyd, A.A.2    Volcik, K.3    Richards, C.S.4
  • 5
    • 0033237314 scopus 로고    scopus 로고
    • The prevalence of common BRCA1 and BRCA2 mutations among Ashkenazi Jews
    • COI: 1:STN:280:DyaK1M7pt1ensA%3D%3D, PID: 10090881
    • Hartge P, Struewing JP, Wacholder S, Brody LC, Tucker MA (1999) The prevalence of common BRCA1 and BRCA2 mutations among Ashkenazi Jews. Am J Hum Genet 64(4):963–970
    • (1999) Am J Hum Genet , vol.64 , Issue.4 , pp. 963-970
    • Hartge, P.1    Struewing, J.P.2    Wacholder, S.3    Brody, L.C.4    Tucker, M.A.5
  • 6
    • 0142178215 scopus 로고    scopus 로고
    • Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2
    • COI: 1:CAS:528:DC%2BD3sXotlWqt7Y%3D, PID: 14576434
    • King MC, Marks JH, Mandell JB, New York Breast Cancer Study Group (2003) Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2. Science 302(5645):643–646. doi:10.1126/science.1088759
    • (2003) Science , vol.302 , Issue.5645 , pp. 643-646
    • King, M.C.1    Marks, J.H.2    Mandell, J.B.3    New York Breast Cancer Study Group4
  • 8
    • 84977819490 scopus 로고    scopus 로고
    • Genetic/familial high-risk assessment: breast and ovarian
    • National Comprehensive Cancer Network (2014) Genetic/familial high-risk assessment: breast and ovarian. NCCN Clinical Practice Guidelines in Oncology (1.2014)
    • (2014) NCCN Clinical Practice Guidelines in Oncology (1 , pp. 2014
  • 12
    • 77956191564 scopus 로고    scopus 로고
    • Absence of genomic BRCA1 and BRCA2 rearrangements in Ashkenazi breast and ovarian cancer families
    • COI: 1:CAS:528:DC%2BC3cXpvFegtbg%3D, PID: 20221693
    • Stadler ZK, Saloustros E, Hansen NA, Schluger AE, Kauff ND, Offit K, Robson ME (2010) Absence of genomic BRCA1 and BRCA2 rearrangements in Ashkenazi breast and ovarian cancer families. Breast Cancer Res Treat 123(2):581–585. doi:10.1007/s10549-010-0818-y
    • (2010) Breast Cancer Res Treat , vol.123 , Issue.2 , pp. 581-585
    • Stadler, Z.K.1    Saloustros, E.2    Hansen, N.A.3    Schluger, A.E.4    Kauff, N.D.5    Offit, K.6    Robson, M.E.7
  • 13
    • 0027295745 scopus 로고
    • A suggested nomenclature for designating mutations
    • COI: 1:CAS:528:DyaK2cXht1Kqsbs%3D, PID: 8401532
    • Beaudet AL, Tsui LC (1993) A suggested nomenclature for designating mutations. Hum Mutat 2(4):245–248. doi:10.1002/humu.1380020402
    • (1993) Hum Mutat , vol.2 , Issue.4 , pp. 245-248
    • Beaudet, A.L.1    Tsui, L.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.