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1501 - 1510 of 7245 Topics

  • Publication

    Report on genetic data in private insurance

    National Bioethics Commission
    Vidalis, T., Hager-Theodorides, A.L., Maniatis, G.
    Digital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National…
  • Publication

    Free trade in human sequence data?

    Nature
    Staff, Editorial
    Digital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National…
  • Publication

    Is data-hoarding slowing the assault on pathogens?

    Science
    Marshall, Eliot
    Digital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National…
  • Publication

    Insurers agree moratorium on gene data

    Nature
    Staff, Editorial
    Digital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National…
  • Publication

    Sequencers split over data release

    Science
    Kahn, Patricia
    Digital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National…
  • Publication

    Genetic data ban for us insurers

    Nature
    Staff, Editorial
    Digital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National…
  • Publication

    Withholding of data among academic geneticists

    JAMA: The Journal of the American Medical Association
    Beaulieu, Anne, Campbell, Eric G.
    Digital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National…
  • Grant Abstract

    Unresolved Issues in Newborn Screening: Quantifying the Harms of a False Positive Result

    While newborn screening (NBS) programs have saved the lives of thousands of children with inherited disorders, the future success of this vital public health program depends on the ability to…
  • Publication

    Case for free access to fundamental data

    Lancet
    Staff, Editorial
    Digital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National…
  • Publication

    The societal impact of DNA fingerprint data

    Accountability in Research
    Roberts, Richard J.
    Digital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National…