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Volumn 47, Issue 4, 2008, Pages 772-777

BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer

Author keywords

[No Author keywords available]

Indexed keywords

BRCA1 PROTEIN; BRCA2 PROTEIN;

EID: 45149114013     PISSN: 0284186X     EISSN: 1651226X     Source Type: Journal    
DOI: 10.1080/02841860802004974     Document Type: Article
Times cited : (44)

References (13)
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    • Evaluation of two different models to predict BRCA1 and BRCA2 mutations in a cohort of Danish hereditary breast and/or ovarian cancer families
    • Gerdes AM, Crüger DG, Thomassen M, Kruse TA. Evaluation of two different models to predict BRCA1 and BRCA2 mutations in a cohort of Danish hereditary breast and/or ovarian cancer families. Clin Genet 2006;69:171-8.
    • (2006) Clin Genet , vol.69 , pp. 171-178
    • Gerdes, A.M.1    Crüger, D.G.2    Thomassen, M.3    Kruse, T.A.4
  • 2
    • 33745617425 scopus 로고    scopus 로고
    • A missense mutation in exon 13 in BRCA2, c.7235G>A, results in skipping of exon 13
    • Thomassen M, Kruse TA, Jensen PK, Gerdes AM. A missense mutation in exon 13 in BRCA2, c.7235G>A, results in skipping of exon 13. Genet Test 2006;10:116-20.
    • (2006) Genet Test , vol.10 , pp. 116-120
    • Thomassen, M.1    Kruse, T.A.2    Jensen, P.K.3    Gerdes, A.M.4
  • 4
    • 33847314487 scopus 로고    scopus 로고
    • Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis
    • Carvalho MA, Marsillac SM, Karchin R, Manoukian S, Grist S, Swaby RF, et al. Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis. Cancer Res 2007;67:1494-501.
    • (2007) Cancer Res , vol.67 , pp. 1494-1501
    • Carvalho, M.A.1    Marsillac, S.M.2    Karchin, R.3    Manoukian, S.4    Grist, S.5    Swaby, R.F.6
  • 5
    • 13444292150 scopus 로고    scopus 로고
    • Classification of BRCA1 missense variants of unknown clinical significance
    • Phelan CM, Dapic V, Tice B, Favis R, Kwan E, Barany F, et al. Classification of BRCA1 missense variants of unknown clinical significance. J Med Genet 2005;42:138-46.
    • (2005) J Med Genet , vol.42 , pp. 138-146
    • Phelan, C.M.1    Dapic, V.2    Tice, B.3    Favis, R.4    Kwan, E.5    Barany, F.6
  • 6
    • 33847259648 scopus 로고    scopus 로고
    • Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer
    • Simard J, Dumont M, Moisan AM, Gaborieau V, Malouin H, Durocher F, et al. Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer. J Med Genet 2007;44:107-21.
    • (2007) J Med Genet , vol.44 , pp. 107-121
    • Simard, J.1    Dumont, M.2    Moisan, A.M.3    Gaborieau, V.4    Malouin, H.5    Durocher, F.6
  • 7
    • 0032736585 scopus 로고    scopus 로고
    • BRCA1 1675delA and 1135insA account for one third of Norwegian familial breast-ovarian cancer and are associated with later disease onset than less frequent mutations
    • Borg A, Dorum A, Heimdal K, Maehle L, Hovig E, Moller P. BRCA1 1675delA and 1135insA account for one third of Norwegian familial breast-ovarian cancer and are associated with later disease onset than less frequent mutations. Dis Markers 1999;15:79-84.
    • (1999) Dis Markers , vol.15 , pp. 79-84
    • Borg, A.1    Dorum, A.2    Heimdal, K.3    Maehle, L.4    Hovig, E.5    Moller, P.6
  • 8
    • 0033591850 scopus 로고    scopus 로고
    • Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer
    • Warner E, Foulkes W, Goodwin P, Meschino W, Blondal J, Paterson C, et al. Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer. J Natl Cancer Inst 1999;91:1241-7.
    • (1999) J Natl Cancer Inst , vol.91 , pp. 1241-1247
    • Warner, E.1    Foulkes, W.2    Goodwin, P.3    Meschino, W.4    Blondal, J.5    Paterson, C.6
  • 10
    • 16944367027 scopus 로고    scopus 로고
    • Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer
    • Hakansson S, Johannsson O, Johansson U, Sellberg G, Loman N, Gerdes AM, et al. Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer. Am J Hum Genet 1997;60:1068-78.
    • (1997) Am J Hum Genet , vol.60 , pp. 1068-1078
    • Hakansson, S.1    Johannsson, O.2    Johansson, U.3    Sellberg, G.4    Loman, N.5    Gerdes, A.M.6
  • 12
    • 33745726046 scopus 로고    scopus 로고
    • Low frequency of large genomic rearrangements of BRCA1 and BRCA2 in Western Denmark
    • Thomassen M, Gerdes AM, Crüger D, Kruse TA. Low frequency of large genomic rearrangements of BRCA1 and BRCA2 in Western Denmark. Cancer Genet Cytogenet 2006;168:168-71.
    • (2006) Cancer Genet Cytogenet , vol.168 , pp. 168-171
    • Thomassen, M.1    Gerdes, A.M.2    Crüger, D.3    Kruse, T.A.4
  • 13
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    • BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age
    • Bergthorsson J, Ejlertsen B, Olsen JH, Borg A, Nielsen KV, Barkardottir RB, et al. BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age. J Med Genet 2001;38:361-8.
    • (2001) J Med Genet , vol.38 , pp. 361-368
    • Bergthorsson, J.1    Ejlertsen, B.2    Olsen, J.H.3    Borg, A.4    Nielsen, K.V.5    Barkardottir, R.B.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.