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The “Right Not to Know” in the Genomic Era: Time to Break From Tradition?
American Journal of Bioethics 14 (3):28-31 (2014)
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The “Right Not to Know” in the Genomic Era: Time to Break From Tradition?Benjamin E. Berkman & Sara Chandros Hull - 2014 - American Journal of Bioethics 14 (3):28-31.
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Citations of this work
A Framework for Unrestricted Prenatal Whole-Genome Sequencing: Respecting and Enhancing the Autonomy of Prospective Parents.Stephanie C. Chen & David T. Wasserman - 2017 - American Journal of Bioethics 17 (1):3-18.
The Right to Know: A Revised Standard for Reporting Incidental Findings.G. Owen Schaefer & Julian Savulescu - 2018 - Hastings Center Report 48 (2):22-32.
Induced Pluripotent Stem Cell-Based Systems for Personalising Epilepsy Treatment: Research Ethics Challenges and New Insights for the Ethics of Personalised Medicine.Mary Jean Walker, Jane Nielsen, Eliza Goddard, Alex Harris & Katrina Hutchison - 2022 - American Journal of Bioethics Neuroscience 13 (2):120-131.
Incidental findings of uncertain significance: To know or not to know - that is not the question.Bjørn Hofmann - 2016 - BMC Medical Ethics 17 (1):1-9.
Fetal information as shared information: using NIPT to test for adult-onset conditions.Michelle Taylor-Sands & Hilary Bowman-Smart - 2021 - Monash Bioethics Review 39 (Suppl 1):82-102.
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