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Volumn 17, Issue 1, 2017, Pages 39-41

Providing Unrestricted Access to Prenatal Testing Does Not Translate to Enhanced Autonomy

Author keywords

[No Author keywords available]

Indexed keywords

FEMALE; GENETIC SCREENING; HUMAN; PERSONAL AUTONOMY; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 85008262663     PISSN: 15265161     EISSN: 15360075     Source Type: Journal    
DOI: 10.1080/15265161.2016.1251651     Document Type: Note
Times cited : (16)

References (13)
  • 1
    • 84966639523 scopus 로고    scopus 로고
    • Performance of ACMG-AMP variant-interpretation guidelines among nine laboratories in the clinical sequencing exploratory research consortium
    • Amendola, L. M., G. P., Jarvik, M. C., Leo, et al. 2016. Performance of ACMG-AMP variant-interpretation guidelines among nine laboratories in the clinical sequencing exploratory research consortium. American Journal of Human Genetics 98 (6):1067–76.
    • (2016) American Journal of Human Genetics , vol.98 , Issue.6 , pp. 1067-1076
    • Amendola, L.M.1    Jarvik, G.P.2    Leo, M.C.3
  • 2
    • 42049120470 scopus 로고    scopus 로고
    • Revisiting Wilson and Jungner in the genomic age: A review of screening criteria over the past 40 years
    • Anderman, A., I., Blancquaert, S., Beauchamp, and V., Déry. 2008. Revisiting Wilson and Jungner in the genomic age:A review of screening criteria over the past 40 years. Bulletin of the World Health Organization 86 (4):241–320.
    • (2008) Bulletin of the World Health Organization , vol.86 , Issue.4 , pp. 241-320
    • Anderman, A.1    Blancquaert, I.2    Beauchamp, S.3    Déry, V.4
  • 3
    • 85008264033 scopus 로고    scopus 로고
    • A framework for unrestricted prenatal whole-genome sequencing: Respecting and enhancing the autonomy of prospective parents
    • Chen, S. C., and D. T., Wasserman. 2017. A framework for unrestricted prenatal whole-genome sequencing:Respecting and enhancing the autonomy of prospective parents. American Journal of Bioethics 17(1):3–18.
    • (2017) American Journal of Bioethics , vol.17 , Issue.1 , pp. 3-18
    • Chen, S.C.1    Wasserman, D.T.2
  • 4
    • 84908296065 scopus 로고    scopus 로고
    • Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing
    • Dar, P., et al. 2014. Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing. American Journal of Obstetrics and Gynecology 211:527.
    • (2014) American Journal of Obstetrics and Gynecology , vol.211 , pp. 527
    • Dar, P.1
  • 6
    • 84895813688 scopus 로고    scopus 로고
    • The EGAPP initiative: Lessons learned
    • EGAPP:Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Working Group. 2014. The EGAPP initiative:Lessons learned. Genetics in Medicine 16 (3):217–24. http://www.nature.com/gim/journal/v16/n3/full/gim2013110a.html
    • (2014) Genetics in Medicine , vol.16 , Issue.3 , pp. 217-224
  • 7
    • 84958178191 scopus 로고    scopus 로고
    • Non-invasive prenatal testing for fetal chromosome abnormalities: Review of clinical and ethical issues
    • Gekas, J., L., Sylvie, R., Vardit, et al. 2016. Non-invasive prenatal testing for fetal chromosome abnormalities:Review of clinical and ethical issues. Application of Clinical Genetics 9:15–26.
    • (2016) Application of Clinical Genetics , vol.9 , pp. 15-26
    • Gekas, J.1    Sylvie, L.2    Vardit, R.3
  • 8
    • 84962662367 scopus 로고    scopus 로고
    • Relationships between health literacy and genomics-related knowledge, self-efficacy, perceived importance, and communication in a medically underserved population
    • Kaphingst, K. A., M., Blanchard, L., Milam, M., Pokharel, A., Elrick, and M. S., Goodman. 2016. Relationships between health literacy and genomics-related knowledge, self-efficacy, perceived importance, and communication in a medically underserved population. Journal of Health Communication 21 (Suppl. 1):58–68.
    • (2016) Journal of Health Communication , vol.21 , pp. 58-68
    • Kaphingst, K.A.1    Blanchard, M.2    Milam, L.3    Pokharel, M.4    Elrick, A.5    Goodman, M.S.6
  • 9
    • 69549126536 scopus 로고    scopus 로고
    • The scientific foundation for personal genomics: Recommendations from a National Institutes of Health–Centers for Disease Control and Prevention multidisciplinary workshop
    • Khoury, M. J., et al. 2009. The scientific foundation for personal genomics:Recommendations from a National Institutes of Health–Centers for Disease Control and Prevention multidisciplinary workshop. Genetics in Medicine 11(8):559–67.
    • (2009) Genetics in Medicine , vol.11 , Issue.8 , pp. 559-567
    • Khoury, M.J.1
  • 10
    • 84982187833 scopus 로고    scopus 로고
    • Genetic misdiagnoses and the potential for health disparities
    • Manrai, A. K., B. H., Funke, H. L., Rehm, et al. 2016. Genetic misdiagnoses and the potential for health disparities. New England Journal of Medicine 375 (7):655–65.
    • (2016) New England Journal of Medicine , vol.375 , Issue.7 , pp. 655-665
    • Manrai, A.K.1    Funke, B.H.2    Rehm, H.L.3
  • 11
    • 57449092873 scopus 로고    scopus 로고
    • An unwelcome side effect of direct-to-consumer personal genome testing: Raiding the medical commons
    • McGuire, A. L., and W., Burke. 2008. An unwelcome side effect of direct-to-consumer personal genome testing:Raiding the medical commons. Journal of the American Medical Association 300 (22):2669–71.
    • (2008) Journal of the American Medical Association , vol.300 , Issue.22 , pp. 2669-2671
    • McGuire, A.L.1    Burke, W.2
  • 12
    • 85008244797 scopus 로고    scopus 로고
    • Non-invasive prenatal testing (NIPT): Identifying key clinical, ethical, social, legal and policy issues
    • Report for the, at
    • Vardit, R., 2015. Non-invasive prenatal testing (NIPT):Identifying key clinical, ethical, social, legal and policy issues. Report for the Nuffield Council on Bioethics. Available at:http://nuffieldbioethics.org/wp-content/uploads/NIPT-background-paper-8-Nov-2015-FINAL.pdf
    • (2015) Nuffield Council on Bioethics
    • Vardit, R.1
  • 13
    • 84953297333 scopus 로고    scopus 로고
    • Association of arrhythmia-related genetic variants with phenotypes documented in electronic medical records
    • Van Driest, S. L., Q. S., Wells, S., Stallings, et al. 2016. Association of arrhythmia-related genetic variants with phenotypes documented in electronic medical records. Journal of the American Medical Association 315 (1):47–57.
    • (2016) Journal of the American Medical Association , vol.315 , Issue.1 , pp. 47-57
    • Van Driest, S.L.1    Wells, Q.S.2    Stallings, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.