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  1. (26 other versions)CQ Sources/Bibliography.Bette Anton - 1999 - Cambridge Quarterly of Healthcare Ethics 8 (4):348-350.
    These CQ Sources were compiled by Bette Anton.
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  • Genethics 2.0: Phenotypes, Genotypes, and the Challenge of Databases Generated by Personal Genome Testing.Karin Esposito & Kenneth Goodman - 2009 - American Journal of Bioethics 9 (6-7):19-21.
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  • The Symbolic Relevance of Feedback: Return and Disclosure of Genomic Research Results of Breast Cancer Patients in Belgium, Germany and the UK.Imme Petersen Regine Kollek - 2015 - Journal of Clinical Research and Bioethics 6 (4).
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  • Explanation and trust: what to tell the user in security and AI? [REVIEW]Wolter Pieters - 2011 - Ethics and Information Technology 13 (1):53-64.
    There is a common problem in artificial intelligence (AI) and information security. In AI, an expert system needs to be able to justify and explain a decision to the user. In information security, experts need to be able to explain to the public why a system is secure. In both cases, an important goal of explanation is to acquire or maintain the users’ trust. In this paper, I investigate the relation between explanation and trust in the context of computing science. (...)
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  • (26 other versions)CQ Sources/Bibliography.Bette Anton - 2008 - Cambridge Quarterly of Healthcare Ethics 17 (4):465-467.
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  • Are Social Networkers and Genome Testers One in the Same? The Limitations of Public Opinion Research for Guiding Clinical Practice.Michelle L. McGowan & Marcie A. Lambrix - 2009 - American Journal of Bioethics 9 (6-7):21-23.
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  • The consent process in medical research involving DNA databanks: some ethical implications and challenges.Herman T. Tavani & Maria Bottis - 2010 - Acm Sigcas Computers and Society 40 (2):11-21.
    Organized into three main parts, this paper examines some challenges for the informed-consent process in medical research where DNA databanks are employed. In Part 1, we briefly describe the principle of informed consent and show why it is ethically important. Part 2 focuses on some specific challenges that that arise for the traditional informed-consent process in population-wide genetics/genomics research, especially where data-mining techniques are used. In the third and final section, we defend a model of consent based on the notion (...)
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  • (26 other versions)CQ Sources/Bibliography.Bette Anton - 2008 - Cambridge Quarterly of Healthcare Ethics 17 (2).
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