Citations (51)
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Read on this site (19)
Chris Kaposy. (2023) Prospects for limiting access to prenatal genetic information about Down syndrome in light of the expansion of prenatal genomics. The New Bioethics 29:3, pages 226-246.
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Rosamond Rhodes & Matthew J. Drago. (2023) Prenatal Testing: Responsibility and Reality. The American Journal of Bioethics 23:5, pages 128-131.
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Kelsey Mumford, Nina Roesner & Benjamin E. Berkman. (2023) The Potential Role of Nudging in Expanded Noninvasive Prenatal Testing. The American Journal of Bioethics 23:3, pages 61-63.
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David Wasserman. (2023) Noninvasive Testing for “Non-Medical” Traits: A Misplaced Expressive Concern, Tough Policy Choices. The American Journal of Bioethics 23:3, pages 59-61.
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Angus Clarke. (2023) Terminology and Consistency. The American Journal of Bioethics 23:3, pages 53-55.
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Hilary Bowman-Smart, Christopher Gyngell, Cara Mand, David J. Amor, Martin B. Delatycki & Julian Savulescu. (2023) Non-Invasive Prenatal Testing for “Non-Medical” Traits: Ensuring Consistency in Ethical Decision-Making. The American Journal of Bioethics 23:3, pages 3-20.
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Katharine Press Callahan & Chris Feudtner. (2022) Genetic Testing Is Messier in Practice than in Theory: Lessons from Neonatology. The American Journal of Bioethics 22:2, pages 37-39.
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Michelle J. Bayefsky & Benjamin E. Berkman. (2022) Implementing Expanded Prenatal Genetic Testing: Should Parents Have Access to Any and All Fetal Genetic Information?. The American Journal of Bioethics 22:2, pages 4-22.
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Stephanie C. Chen & David T. Wasserman. (2017) Response to Open Peer Commentaries on “A Framework for Unrestricted Prenatal Whole-Genome Sequencing: Respecting and Enhancing the Autonomy of Prospective Parents”. The American Journal of Bioethics 17:1, pages W1-W3.
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Benjamin S. Wilfond. (2017) Breaking the Sounds of Silence: Respecting People With Disabilities and Reproductive Decision Making. The American Journal of Bioethics 17:1, pages 37-39.
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Rosamond Rhodes. (2017) Resisting Paternalism in Prenatal Whole-Genome Sequencing. The American Journal of Bioethics 17:1, pages 35-37.
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Jeffrey R. Botkin, Leslie P. Francis & Nancy C. Rose. (2017) Concerns About Justification for Fetal Genome Sequencing. The American Journal of Bioethics 17:1, pages 23-25.
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Megan Allyse, James P. Evans & Marsha Michie. (2017) Dr. Pangloss's Clinic: Prenatal Whole Genome Sequencing and a Return to Reality. The American Journal of Bioethics 17:1, pages 21-23.
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Christian Munthe. (2017) Permissibility or Priority? Testing or Screening? Essential Distinctions in the Ethics of Prenatal Testing. The American Journal of Bioethics 17:1, pages 30-32.
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W. Kevin Conley II, Douglas C. McAdams, G. Kevin Donovan & Kevin T. FitzGerald. (2017) Beneficence In Utero: A Framework for Restricted Prenatal Whole-Genome Sequencing to Respect and Enhance the Well-Being of Children. The American Journal of Bioethics 17:1, pages 28-29.
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Jessica Mozersky & Pamela Sankar. (2017) Mandating Moral Reflection?. The American Journal of Bioethics 17:1, pages 32-34.
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Benjamin E. Berkman & Michelle Bayefsky. (2017) Prenatal Whole Genome Sequencing: An Argument for Professional Self-Regulation. The American Journal of Bioethics 17:1, pages 26-28.
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Vardit Ravitsky, Francois Rousseau & Anne-Marie Laberge. (2017) Providing Unrestricted Access to Prenatal Testing Does Not Translate to Enhanced Autonomy. The American Journal of Bioethics 17:1, pages 39-41.
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Chris Kaposy. (2017) Noninvasive Prenatal Whole-Genome Sequencing: A Solution in Search of a Problem. The American Journal of Bioethics 17:1, pages 42-44.
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Articles from other publishers (32)
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Margot Kelly-Hedrick, Gail Geller, Angie C. Jelin & Marielle S. Gross. (2022) Perceived Value of Prenatal Ultrasound Screening: A Survey of Pregnant Women. Maternal and Child Health Journal 27:1, pages 101-110.
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Hazar Haidar, Stanislav Birko, Anne-Marie Laberge, Jessica Le Clerc-Blain & Vardit Ravitsky. (2022) Views of Canadian healthcare professionals on the future uses of non-invasive prenatal testing: a mixed method study. European Journal of Human Genetics 30:11, pages 1269-1275.
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Todd Lencz, Maya Sabatello, Anna Docherty, Roseann E Peterson, Takahiro Soda, Jehannine Austin, Laura Bierut, David Crepaz-Keay, David Curtis, Franziska Degenhardt, Laura Huckins, Gabriel Lazaro-Munoz, Manuel Mattheisen, Bettina Meiser, Holly Peay, Marcella Rietschel, Consuelo Walss-Bass & Lea K Davis. (2022) Concerns about the use of polygenic embryo screening for psychiatric and cognitive traits. The Lancet Psychiatry 9:10, pages 838-844.
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Esther Braun. (2022) An autonomy-based approach to assisted suicide: a way to avoid the expressivist objection against assisted dying laws. Journal of Medical Ethics, pages medethics-2022-108375.
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Tamar Nov-Klaiman, Marina Frisman, Aviad E. Raz & Christoph Rehmann-Sutter. (2022) Views on disability and prenatal testing among families with Down syndrome and disability activists: A comparative analysis of interviews from Germany and Israel. Social Science & Medicine 303, pages 115021.
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Hazar Haidar & Renata Iskander. (2022) Non-invasive Prenatal Testing for Fetal Whole Genome Sequencing: An Interpretive Critical Review of the Ethical, Legal, Social, and Policy Implications. Canadian Journal of Bioethics 5:1, pages 1.
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Alberto Asquer & Inna Krachkovskaya. (2021) A Bibliometric Analysis of Research on CRISPR in Social Sciences and Humanities. Re:GEN Open 1:1, pages 14-23.
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Greg Stapleton, Wybo Dondorp, Peter Schröder-Bäck & Guido de Wert. (2019) Just choice: a Danielsian analysis of the aims and scope of prenatal screening for fetal abnormalities. Medicine, Health Care and Philosophy 22:4, pages 545-555.
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Johannes Reinders, Tim Stainton & Trevor R. Parmenter. (2019) The Quiet Progress of the New Eugenics. Ending the Lives of Persons With Intellectual and Developmental Disabilities for Reasons of Presumed Poor Quality of Life. Journal of Policy and Practice in Intellectual Disabilities 16:2, pages 99-112.
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Carlo V Bellieni. (2018) Consumerism: a threat to health?. Journal of the Royal Society of Medicine 111:4, pages 112-112.
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