Cited by 2

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Beyond babies: Implications of human genome editing for women, children, and families

M. Farrell, Ruth, Malek, Janet, Thomas Scott, Christopher·2022·Accountability in Research

Abstract

Scholarship on human germline editing has centered on the risks to the genetically-modified child. However, far less emphasis is focused on women who will become pregnant with a genetically modified embryo as part of human subject research or the families that raise children whose genomes were modified as an embryo. The lack of attention on women and families places these key stakeholders in genomic technologies at significant medical, ethical, and personal harm as research rapidly moves forward to advance the science of genomic modification. Now is the time to address how the interests of women and families should be represented in the ethical and scientific frameworks of human genomic modification, with specific considerations for Institutional Review Boards who review protocols for rigorous human subject protections and scientists who develop scientific methodologies that dictate the potential risks conferred to research participants. In this paper, we examine the implications of genomic modification of human embryo for women, children, and families to explore how to review a first-in-human clinical protocol of human genomic officiation responsibly.

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Crossref · 10.1080/08989621.2021.1899824

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Citations

Cites

  • Adopt a moratorium on heritable genome editing

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    “These risks, along with the He Jiankui affair, have divided ethicists, policymakers, and scientists on whether and how we can responsibly proceed with the National Academies of Science, Engineering, and Medicine (NASEM) recommendations that germline editing should be used only in narrow therapeutic case (NASEM 2017; L…”
    Background

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Metadata

Authors
M. Farrell, R., Malek, J., & Thomas Scott, C.
Venue
Accountability in Research
Published
2021-04-01
Volume
29
Issue
2
Pages
67-76
ISSN
  • 0898-9621
  • 1545-5815
Cited by
2
References
1
Language
en
Funders
NIH (1RO1HG010332-01)

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