메뉴 건너뛰기




Volumn 24, Issue 10, 2016, Pages 1496-1500

Unsolicited findings of next-generation sequencing for tumor analysis within a Dutch consortium: Clinical daily practice reconsidered

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

EID: 84963541069     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2016.27     Document Type: Article
Times cited : (19)

References (26)
  • 1
    • 84868674671 scopus 로고    scopus 로고
    • Diagnostic exome sequencing: Are we there yet?
    • Melford HC: Diagnostic exome sequencing: are we there yet? N Engl J Med 2012; 367: 1951-1953.
    • (2012) N Engl J Med , vol.367 , pp. 1951-1953
    • Melford, H.C.1
  • 2
    • 79960834031 scopus 로고    scopus 로고
    • Feedback of individual genetic results to research participants: In favor of a qualified disclosure policy
    • Bredenoord AL, Onland-Moret NC, van Delden JJM: Feedback of individual genetic results to research participants: in favor of a qualified disclosure policy. Hum Mutat 2011; 32: 861-867.
    • (2011) Hum Mutat , vol.32 , pp. 861-867
    • Bredenoord, A.L.1    Onland-Moret, N.C.2    Van Delden, J.J.M.3
  • 3
    • 84920528362 scopus 로고    scopus 로고
    • ACMG policy statement: Updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing
    • ACMG Board of Directors
    • ACMG Board of Directors: ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. Genet Med 2015; 17: 68-69.
    • (2015) Genet Med , vol.17 , pp. 68-69
  • 4
    • 38549085235 scopus 로고    scopus 로고
    • Research ethics and the challenge of whole-genome sequencing
    • McGuire AL, Caulfield T, Cho MK: Research ethics and the challenge of whole-genome sequencing. Nat Rev Genet 2008; 9: 152-156.
    • (2008) Nat Rev Genet , vol.9 , pp. 152-156
    • McGuire, A.L.1    Caulfield, T.2    Cho, M.K.3
  • 5
    • 77949653046 scopus 로고    scopus 로고
    • Ethical implications of the use of whole genome methods in medical research
    • Kaye J, Boddington P, De Vries J, Hawkins N, Melham K: Ethical implications of the use of whole genome methods in medical research. Eur J Hum Genet 2009; 18: 398-403.
    • (2009) Eur J Hum Genet , vol.18 , pp. 398-403
    • Kaye, J.1    Boddington, P.2    De Vries, J.3    Hawkins, N.4    Melham, K.5
  • 6
    • 84881420673 scopus 로고    scopus 로고
    • Whole-genome sequencing in health care
    • Recommendations of the European Society of Human Genetics
    • El CG, Cornel MC, Borry P et al: Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. Eur J Hum Genet 2013; 21: 580-584.
    • (2013) Eur J Hum Genet , vol.21 , pp. 580-584
    • El, C.G.1    Cornel, M.C.2    Borry, P.3
  • 7
    • 12844261878 scopus 로고    scopus 로고
    • The therapeutic misconception: Problems and solutions
    • Lidz CW, Appelbaum PS: The therapeutic misconception: problems and solutions. Med Care 2002; 40: V55-V63.
    • (2002) Med Care , vol.40 , pp. V55-V63
    • Lidz, C.W.1    Appelbaum, P.S.2
  • 9
    • 79151476271 scopus 로고    scopus 로고
    • Disclosure of individual genetic data to research participants: The debate reconsidered
    • Bredenoord AL, Kroes HY, Cuppen E, Parker M, van Delden JJM: Disclosure of individual genetic data to research participants: the debate reconsidered. Trends Genet 2011; 27: 41-47.
    • (2011) Trends Genet , vol.27 , pp. 41-47
    • Bredenoord, A.L.1    Kroes, H.Y.2    Cuppen, E.3    Parker, M.4    Van Delden, J.J.M.5
  • 10
    • 84973387103 scopus 로고    scopus 로고
    • Dynamic consent: A possible solution to improve patient confidence and trust in how electronic patient records are used in medical research
    • Williams H, Spencer K, Snaders C et al: Dynamic consent: a possible solution to improve patient confidence and trust in how electronic patient records are used in medical research. JMIR Med Inform 2015; 3: e3.
    • (2015) JMIR Med Inform , vol.3 , pp. e3
    • Williams, H.1    Spencer, K.2    Snaders, C.3
  • 11
    • 84904255226 scopus 로고    scopus 로고
    • Genetic counselors' views and experiences with the clinical integration of genome sequencing
    • Machini K, Douglas J, Braxton A, Tsipis J, Kramer K: Genetic counselors' views and experiences with the clinical integration of genome sequencing. J Genet Counsel 2014; 23: 496-505.
    • (2014) J Genet Counsel , vol.23 , pp. 496-505
    • Machini, K.1    Douglas, J.2    Braxton, A.3    Tsipis, J.4    Kramer, K.5
  • 14
    • 84904264208 scopus 로고    scopus 로고
    • Points to consider in the clinical use of NGS panels for mitochondrial disease: An analysis of gene inclusion and consent forms
    • Platt J, Cox R, Enns GM: Points to consider in the clinical use of NGS panels for mitochondrial disease: an analysis of gene inclusion and consent forms. J Genet Counsel 2014; 23: 594-603.
    • (2014) J Genet Counsel , vol.23 , pp. 594-603
    • Platt, J.1    Cox, R.2    Enns, G.M.3
  • 16
    • 79959276553 scopus 로고    scopus 로고
    • Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time
    • Berg JS, Khoury MJ, Evans JP: Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time. Genet Med 2011; 13: 499-504.
    • (2011) Genet Med , vol.13 , pp. 499-504
    • Berg, J.S.1    Khoury, M.J.2    Evans, J.P.3
  • 17
    • 84924557599 scopus 로고    scopus 로고
    • Postmortem disclosure of genetic information to family members: Active or passive?
    • Boers SN, van Delden JJ, Knoers NV, Bredenoord AL: Postmortem disclosure of genetic information to family members: active or passive?Trends Mol Med 2015; 21: 148-153.
    • (2015) Trends Mol Med , vol.21 , pp. 148-153
    • Boers, S.N.1    Van Delden, J.J.2    Knoers, N.V.3    Bredenoord, A.L.4
  • 18
    • 82655184653 scopus 로고    scopus 로고
    • Personalized oncology through integrative high-throughput sequencing: A pilot study
    • Roychowdhury S, Iyer MK, Robinson DR et al: Personalized oncology through integrative high-throughput sequencing: a pilot study. Sci Transl Med 2011; 3: 111ra121.
    • (2011) Sci Transl Med , vol.3 , pp. 111ra121
    • Roychowdhury, S.1    Iyer, M.K.2    Robinson, D.R.3
  • 19
    • 84880535720 scopus 로고    scopus 로고
    • American College of Medical Genetics and Genomics (ACMG) recommendations for reporting of incidental findings in clinical exome and genome sequencing
    • Green RC, Berg JS, Grody WW et al: American College of Medical Genetics and Genomics (ACMG) recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet Med 2013; 15: 565-574.
    • (2013) Genet Med , vol.15 , pp. 565-574
    • Green, R.C.1    Berg, J.S.2    Grody, W.W.3
  • 20
    • 84904266922 scopus 로고    scopus 로고
    • Lynch syndrome patients' views of and preferences for return of results following whole exome sequencing
    • Hitch K, Joseph G, Guiltinan J, Kianmahd J, Youngblom J, Blanco A: Lynch syndrome patients' views of and preferences for return of results following whole exome sequencing. J Genet Couns 2014; 23: 539-551.
    • (2014) J Genet Couns , vol.23 , pp. 539-551
    • Hitch, K.1    Joseph, G.2    Guiltinan, J.3    Kianmahd, J.4    Youngblom, J.5    Blanco, A.6
  • 21
    • 84902271056 scopus 로고    scopus 로고
    • Return of genomic results to research participants: The floor, the ceiling, and the choices in between
    • Jarvik GP, Amendola LM, Berg JS et al: Return of genomic results to research participants: the floor, the ceiling, and the choices in between. Am J Hum Gen 2014; 94: 818-882.
    • (2014) Am J Hum Gen , vol.94 , pp. 818-882
    • Jarvik, G.P.1    Amendola, L.M.2    Berg, J.S.3
  • 22
    • 34548164155 scopus 로고    scopus 로고
    • Disclosure of genetics research results after the death of the patient participant: A qualitative study of the impact on relatives
    • Ormondroyd E, Moynihan C, Watson M et al: Disclosure of genetics research results after the death of the patient participant: a qualitative study of the impact on relatives. J Genet Couns 2007; 16: 527-538.
    • (2007) J Genet Couns , vol.16 , pp. 527-538
    • Ormondroyd, E.1    Moynihan, C.2    Watson, M.3
  • 23
    • 84859583108 scopus 로고    scopus 로고
    • Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: Lessons from the ClinSeq project
    • Biesecker LG: Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project. Genet Med 2012; 14: 393-398.
    • (2012) Genet Med , vol.14 , pp. 393-398
    • Biesecker, L.G.1
  • 25
    • 84899979578 scopus 로고    scopus 로고
    • Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencing
    • Shahmirzadi L, Chao EC, Palmaer E et al: Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencing. Genet Med 2014; 16: 395-399.
    • (2014) Genet Med , vol.16 , pp. 395-399
    • Shahmirzadi, L.1    Chao, E.C.2    Palmaer, E.3
  • 26
    • 84894358831 scopus 로고    scopus 로고
    • Testing personalized medicine: Patient and physician expectations of next-generation genomic sequencing in late-stage cancer care
    • Miller FA, Hayeems RZ, Bytautas JP et al: Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care. Eur J Hum Genet 2014; 22: 391-395.
    • (2014) Eur J Hum Genet , vol.22 , pp. 391-395
    • Miller, F.A.1    Hayeems, R.Z.2    Bytautas, J.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.