메뉴 건너뛰기




Volumn 139, Issue 2, 2015, Pages 211-215

Rescreening for genetic mutations using multi-gene panel testing in patients who previously underwent non-informative genetic screening

Author keywords

Multi gene panel testing; Ovarian cancer; Single gene testing

Indexed keywords

BONE MORPHOGENETIC PROTEIN RECEPTOR 1A; BRCA1 ASSOCIATED RING DOMAIN PROTEIN 1; BRCA1 PROTEIN; BRCA2 PROTEIN; CHECKPOINT KINASE 2; CYCLIN DEPENDENT KINASE INHIBITOR 2A; EPITHELIAL CELL ADHESION MOLECULE; PROTEIN MLH1; PROTEIN MSH2; PROTEIN MSH6; PROTEIN P53; RAD50 PROTEIN; RAD51 PROTEIN; SMAD4 PROTEIN; ADENOSINE TRIPHOSPHATASE; CADHERIN; CDH1 PROTEIN, HUMAN; DNA BINDING PROTEIN; DNA LIGASE; MLH1 PROTEIN, HUMAN; NUCLEAR PROTEIN; PMS2 PROTEIN, HUMAN; RAD51D PROTEIN, HUMAN; SIGNAL TRANSDUCING ADAPTOR PROTEIN;

EID: 84952630873     PISSN: 00908258     EISSN: 10956859     Source Type: Journal    
DOI: 10.1016/j.ygyno.2015.08.006     Document Type: Article
Times cited : (42)

References (23)
  • 1
    • 84920784458 scopus 로고    scopus 로고
    • Panel testing for inherited susceptibility to breast, ovarian, and colorectal cancer
    • S.M. Domchek, and K.L. Nathanson Panel testing for inherited susceptibility to breast, ovarian, and colorectal cancer Genet. Med. 16 11 2014 827 829
    • (2014) Genet. Med. , vol.16 , Issue.11 , pp. 827-829
    • Domchek, S.M.1    Nathanson, K.L.2
  • 2
    • 84933279541 scopus 로고    scopus 로고
    • Two decades beyond BRCA1/2: Homologous recombination, hereditary cancer risk and a target for ovarian cancer therapy
    • C.S. Walsh Two decades beyond BRCA1/2: homologous recombination, hereditary cancer risk and a target for ovarian cancer therapy Gynecol. Oncol. 137 2 2015 343 350
    • (2015) Gynecol. Oncol. , vol.137 , Issue.2 , pp. 343-350
    • Walsh, C.S.1
  • 4
    • 81055126264 scopus 로고    scopus 로고
    • Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing
    • T. Walsh, S. Casadei, M.K. Lee, C.C. Pennil, A.S. Nord, A.M. Thornton, and et al. Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing Proc. Natl. Acad. Sci. U. S. A. 108 2011 18032 18037
    • (2011) Proc. Natl. Acad. Sci. U. S. A. , vol.108 , pp. 18032-18037
    • Walsh, T.1    Casadei, S.2    Lee, M.K.3    Pennil, C.C.4    Nord, A.S.5    Thornton, A.M.6
  • 5
    • 84856015503 scopus 로고    scopus 로고
    • Hereditary ovarian cancer: Beyond the usual suspects
    • K.P. Pennington, and E.M. Swisher Hereditary ovarian cancer: beyond the usual suspects Gynecol. Oncol. 124 2012 347 353
    • (2012) Gynecol. Oncol. , vol.124 , pp. 347-353
    • Pennington, K.P.1    Swisher, E.M.2
  • 6
    • 84928209346 scopus 로고    scopus 로고
    • Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
    • S. Richards, N. Aziz, S. Bale, D. Bick, S. Das, J. Gastier-Foster, and et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Genet. Med. 17 2015 405 423
    • (2015) Genet. Med. , vol.17 , pp. 405-423
    • Richards, S.1    Aziz, N.2    Bale, S.3    Bick, D.4    Das, S.5    Gastier-Foster, J.6
  • 8
  • 9
    • 0038744296 scopus 로고    scopus 로고
    • Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: A combined analysis of 22 studies
    • A. Antoniou, P.D. Pharoah, S. Narod, H.A. Risch, J.E. Eyfjord, J.L. Hopper, and et al. Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies Am. J. Hum. Genet. 72 2003 1117 1130
    • (2003) Am. J. Hum. Genet. , vol.72 , pp. 1117-1130
    • Antoniou, A.1    Pharoah, P.D.2    Narod, S.3    Risch, H.A.4    Eyfjord, J.E.5    Hopper, J.L.6
  • 10
    • 84864026311 scopus 로고    scopus 로고
    • BRCA mutation frequency and patterns of treatment response in BRCA mutation-positive women with ovarian cancer: A report from the Australian Ovarian Cancer Study Group
    • K. Alsop, S. Fereday, C. Meldrum, A. deFazio, C. Emmanuel, J. George, and et al. BRCA mutation frequency and patterns of treatment response in BRCA mutation-positive women with ovarian cancer: a report from the Australian Ovarian Cancer Study Group J. Clin. Oncol. 30 2012 2654 2663
    • (2012) J. Clin. Oncol. , vol.30 , pp. 2654-2663
    • Alsop, K.1    Fereday, S.2    Meldrum, C.3    DeFazio, A.4    Emmanuel, C.5    George, J.6
  • 11
    • 84921898753 scopus 로고    scopus 로고
    • Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer
    • F.J. Couch, S.N. Hart, P. Sharma, A.E. Toland, X. Wang, P. Miron, and et al. Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer J. Clin. Oncol. 33 2015 304 311
    • (2015) J. Clin. Oncol. , vol.33 , pp. 304-311
    • Couch, F.J.1    Hart, S.N.2    Sharma, P.3    Toland, A.E.4    Wang, X.5    Miron, P.6
  • 15
    • 0028575693 scopus 로고
    • Cancer risks in A-T heterozygotes
    • D.F. Easton Cancer risks in A-T heterozygotes Int. J. Radiat. Biol. 66 1994 S177 S182
    • (1994) Int. J. Radiat. Biol. , vol.66 , pp. S177-S182
    • Easton, D.F.1
  • 17
    • 84899413123 scopus 로고    scopus 로고
    • Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer
    • (e1-5)
    • A.K. Win, J.G. Dowty, S.P. Cleary, H. Kim, D.D. Buchanan, J.P. Young, and et al. Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer Gastroenterology 146 2014 1208 1211 (e1-5)
    • (2014) Gastroenterology , vol.146 , pp. 1208-1211
    • Win, A.K.1    Dowty, J.G.2    Cleary, S.P.3    Kim, H.4    Buchanan, D.D.5    Young, J.P.6
  • 19
    • 0031440709 scopus 로고    scopus 로고
    • The I1307K APC mutation does not predispose to colorectal cancer in Jewish Ashkenazi breast and breast-ovarian cancer kindreds
    • L. Petrukhin, J. Dangel, L. Vanderveer, J. Costalas, A. Bellacosa, G. Grana, and et al. The I1307K APC mutation does not predispose to colorectal cancer in Jewish Ashkenazi breast and breast-ovarian cancer kindreds Cancer Res. 57 1997 5480 5484
    • (1997) Cancer Res. , vol.57 , pp. 5480-5484
    • Petrukhin, L.1    Dangel, J.2    Vanderveer, L.3    Costalas, J.4    Bellacosa, A.5    Grana, G.6
  • 20
    • 79951581268 scopus 로고    scopus 로고
    • Genetic testing and cancer risk management recommendations by physicians for at-risk relatives
    • S.E. Plon, H.P. Cooper, B. Parks, S.U. Dhar, P.A. Kelly, A.D. Weinberg, and et al. Genetic testing and cancer risk management recommendations by physicians for at-risk relatives Genet. Med. 13 2011 148 154
    • (2011) Genet. Med. , vol.13 , pp. 148-154
    • Plon, S.E.1    Cooper, H.P.2    Parks, B.3    Dhar, S.U.4    Kelly, P.A.5    Weinberg, A.D.6
  • 22
    • 34249949487 scopus 로고    scopus 로고
    • Risk assessment and genetic counseling for hereditary breast and ovarian cancer: Recommendations of the National Society of Genetic Counselors
    • J.L. Berliner, A.M. Fay Practice Issues Subcommittee of the National Society of Genetic Counselors' Familial Cancer Risk Counseling Special Interest G Risk assessment and genetic counseling for hereditary breast and ovarian cancer: recommendations of the National Society of Genetic Counselors J. Genet. Couns. 16 2007 241 260
    • (2007) J. Genet. Couns. , vol.16 , pp. 241-260
    • Berliner, J.L.1    Fay, A.M.2
  • 23
    • 84907597238 scopus 로고    scopus 로고
    • A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genes
    • J.M. Eggington, K.R. Bowles, K. Moyes, S. Manley, L. Esterling, S. Sizemore, and et al. A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genes Clin. Genet. 86 2014 229 237
    • (2014) Clin. Genet. , vol.86 , pp. 229-237
    • Eggington, J.M.1    Bowles, K.R.2    Moyes, K.3    Manley, S.4    Esterling, L.5    Sizemore, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.