Γενετική Μηχανική

• Chen, Stephanie C. and Wasserman, David T.: A Framework for Unrestricted Prenatal Whole-Genome Sequencing: Respecting and Enhancing the Autonomy of Prospective Parents, The American Journal of Bioethics 17 (1): 3-18, January 2017.
• May, Thomas; Strong, Kimberly, A.; Zusevics, Kaija L.; Jeruzal, Jessica; Farrell, Michael H.; Kirschner, Alison LaPean; Derse, Arthur R.; Evans, James P. and Grotevant, Harold D.: Does Lack of “Genetic-Relative Family Health History” Represent a Potentially Avoidable health Disparity for Adoptees?, The American Journal of Bioethics 16 (12): 33-38, December 2016.
• Juengst, Eric; McGowan, Michelle L.; Fishman, Jennifer R. and Settersten Richard A, Jr.: From “Personalized” to “Precision” Medicine: The Ethical and Social Implications of Rhetorical Reform in Genomic Medicine, Hastings Center Report 46 (5): 21-33, September-October 2016.
• Sankar, Pamela L. and Cho, Mildred K.: Engineering Values into Genetic Engineering: A Proposed Analytic Framework for Scientific Social Responsibility, The American Journal of Bioethics 15 (12): 18-24, December 2015.
• Panofsky, Aaron: What Does Behavioral Genetics Offer for Improving Education?, The Hastings Center Report/Special Report 45 (5): 43-49, September-October 2015.
• Lázaro-Munoz, Gabriel: Conley, John M.; Davis, Arlene M.; Van Riper, Marcia; Walker, Rebecca L. and Juengst, Eric T.: Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice, The American Journal of Bioethics 15 (7): 3-14, July 2015.
• Sparrow, Robert: Imposing Genetic Diversity, The American Journal of Bioethics 15 (6): 2-10, June 2015.
• Hallowell, N.; Hall, A.; Alberg, C. and Zimmern, R.: Revealing the Results of Whole-Genome Sequencing and Whole-Exome Sequencing in Research and Clinical Investigations: Some Ethical Issues, Journal of Medical Ethics 41 (4): 317-321, April 2015.
• Malmqvist, E.: Reprogenetics and the “Parents Have Always Done It Argument”, Hastings Center Report 41 (1): 43-49, January-February 2011.
• Sparrow, R.: A-Not-So-Eugenics, Hastings Center Report 41 (1): 32-42, January-February 2011.
• Coggon, J.: Confrontation in “Genethics”: Rationalities, Challenges and Methodological responses, Cambridge Quarterly of Healthcare Ethics 20 (1): 46-55, January 2011.
• Douglas, T.; Savulescu, J.: Synthetic biology and the ethics of knowledge, Journal of Medical Ethics 36 (11): 687-693, November 2010.
• de Melo-Martin, I.: Defending human enhancement technologies: unveiling normativity, Journal of Medical Ethics 36 (8): 483-487, August 2010.
• Jordan, B. R.; Tsai, D. F. C.: Whole-genome association studies for multigenic diseases: ethical dilemmas arising from commercialization-the case of genetic testing for autism, Journal of Medical Ethics 36 (7): 440-444, July 2010.
• Jotterand, F.: Human Dignity and Transhumanism: Do Anthro-Technological Devices Have Moral Status?, The American Journal of Bioethics, 10 (7): 45-52, July 2010.
• Melas, P.A.; Sjoholm, L.K.; Forsner, T.; Edhborg, M.; Juth, N.; Forsell, Y. and Lavenbratt, C.: Examining the Public Refusal to Consent to DNA Biobanking: Empirical Data from a Swedish Population-based Study, Journal of Medical Ethics 36 (2): 93-98, February 2010.
• Wilkinson, Ruth: When Is My Genetic Information Your Business? Biological, Emotional and Financial Claims to Knowledge, Cambridge Quarterly of Healthcare Ethics 19 (1): 110-117, January 2010.
• Chan, S.: Should We Enhance Animals?, Journal of Medical Ethics 35 (11): 678-683, November 2009.
• Appel, J. M.: Is all Fair in Biological Warfare? The Controversy over Genetically Engineered Biological Weapons, Journal of Medical Ethics 35 (7): 429-432, July 2009.
• Sorensen, K.: Genetic Enhancements and Expectations, Journal of Medical Ethics 35 (7): 433-435, July 2009.
• Capron, Alexander Morgan; Mauron, Alexandre; Elger, Bernice Simone; Boggio, Andrea; Ganguli-Mitra, Agomoni and Biller-Andorno, Nikola: Ethical Norms and the International Governance of Genetic Databases and Biobanks: Findings from an International Study, Kennedy Institute of Ethics Journal 19 (2): 101-124, June 2009.
• Ruiz-Canela, M.; Valle-Mansilla, J. I. and Sulmasy, D. P.: Researchers’ Preferences and Attitudes on Ethical Aspects of Genomics Research: a Comparative Study between the USA and Spain, Journal of Medical Ethics 35 (4): 251-257, April 2009.
• Hansson, M. G.: Ethics and Biobanks, British Journal of Cancer, 100 (1): 8-12, January 2009.
• Garfinkel, Michele S.; Endy, Drew; Epstein, Gerald L. and Friedman, Robert M.: Synthetic Biology, From Birth to Death and Bench to Clinic: The Hastings Center Bioethics Briefing Book, p. 163-168, 2008.
• Laberge, Anne-Marie and Burke, Wylie: Personalized Medicine and Genomics, From Birth to Death and Bench to Clinic: The Hastings Center Bioethics Briefing Book, p. 133-136, 2008.
• Baily, Mary Ann: Newborn Screening, From Birth to Death and Bench to Clinic: The Hastings Center Bioethics Briefing Book, p. 125-128, 2008.
• Kaebnick, Gregory E.: Nature, Human Nature, and Biotechnology, From Birth to Death and Bench to Clinic: The Hastings Center Bioethics Briefing Book, p. 117-120, 2008.
• Johnston, Josephine: Intellectual Property and Biomedicine, From Birth to Death and Bench to Clinic: The Hastings Center Bioethics Briefing Book, p. 93-96, 2008.
• Press, Nancy: Genetic Testing and Screening, From Birth to Death and Bench to Clinic: The Hastings Center Bioethics Briefing Book, p. 73-78, 2008.
• Cook-Deegan, Robert: Gene Patents, From Birth to Death and Bench to Clinic: The Hastings Center Bioethics Briefing Book, p. 69-72, 2008.
• Maschke, Karen J.: Biobanks: DNA and Research, From Birth to Death and Bench to Clinic: The Hastings Center Bioethics Briefing Book, p. 11-14, 2008.
• Malpas, P. J.: Is Genetic Information Relevantly Different from Other Kinds of Non-Genetic Information In the Life Insurance Context?, Journal of Medical Ethics 34 (7): 548-551, July 2008.
• Wilkinson, S.: “Eugenics Talk” and the Language of Bioethics, Journal of Medical Ethics 34 (6): 467-471, June 2008.
• Peterson-Iyer, Karen: Pharmacogenomics, Ethics and Public Policy, Kennedy Institute of Ethics Journal 18 (1): 35-56, March 2008.
• Hausman, Daniel M.: Group Risks, Risks to Groups, and Group Engagement in Genetics Research, Kennedy Institute of Ethics Journal 17 (4): 351-370, December 2007.
• Gilbar, R.: Communicating Genetic Information in the Family: the Familial Relationship as the Forgotten Factor, Journal of Medical Ethics 33 (7): 390-393, July 2007.
• Brody, Baruch: Intellectual Property and Biotechnology: The European Debate, Kennedy Institute of Ethics Journal 17 (2): 69-110, June 2007.
• O’Malley, Maureen A.; Calvert, Jane and Dupré, John: The Study of Socioethical Issues in System Biology, The American Journal of Bioethics 7 (4): 67-78, April 2007.
• Mameli, M.: Reproductive Cloning, Genetic Engineering and the Autonomy of the Child: The Moral Agent and the Open Future, Journal of Medical Ethics 33 (2): 87-93, February 2007.
• Lucassen, A. and Kaye, J.: Genetic Testing without Consent: the Implications of the New Human Tissue Act 2004, Journal of Medical Ethics 32 (12): 690-692, December 2006.
• Fenton, Elizabeth: Liberal Eugenics and Human Nature: Against Habermas, Hastings Center Report 36 (6): 35-42, November-December 2006.
• Foster, M.W.; Royal, C.D.M. and Sharp, R.R.: The Routinisation of Genomics and Genetics: Implications for Ethical Practices, Journal of Medical Ethics 32 (11): 635-638, November 2006.
• Kerruish, N.J. & Robertson, S.P.: Newborn Screening: New Developments, New Dilemmas, Journal of Medical Ethics 31 (7): 393-398, July 2005.
• Cameron, C. & Wiliamson, R.: In the World of Dolly, When Does a Human Embryo Acquire Respect?, Journal of Medical Ethics 31 (4): 215-220, April 2005.
• Stanton, C. & Harris, J.: The Moral Status of the Embryo Post-Dolly, Journal of Medical Ethics 31 (4): 221-225, April 2005.
• Davis, Dena S.: Genetic Research and Communal Narratives, Hastings Center Report 34 (4): 40-49, July-August 2004.
• Farrelly, Colin: The Genetic Difference Principle, The American Journal of Bioethics 4 (2): W21-W28, Spring 2004. 
• Parens, Erik: Genetic Differences and Human Identities, A Special Supplement to the Hastings Center Report 34 (1), January-February 2004.
• Kriari-Catranis, Ismini: Genetic Data and Confidentiality, the Estonian Experiment, Law Hum Genome Rev. (19): 147-57, Jul-Dec 2003.
• Wolf, Susan M.; P. Kahn, Jeffrey and E. Wagner, John: Using Preimplantation Genetic Diagnosis to Create a Stem Cell Donor: Issues, Guidelines & Limits, Journal of Law, Medicine and Ethics 31: 3, Fall 2003.
• Commoner, Barry: Unraveling the secret of life, Bulletin of Medical Ethics 189: 20-24, June/July 2003.
• Scott Robert, Jason and Baylis, Francoise: Crossing Species Boundaries, The American Journal of Bioethics 3 (3): 1-13, Summer 2003.
• Zandonella, Catherine: Tissue engineering: The beat goes on, Nature 421: 884 – 886, February 2003.
• Robertson, J. A.: Extending Preimplantation Genetic Diagnosis: Medical and Non-medical Uses, Journal of Medical Ethics 29: 213-216, 2003.
• Boyd, Ann Lewis: Genetics and Social Justice, Eubios Journal of Asian and International Bioethics 12 (5): 167-171, September 2002.
• World Health Organization: Genomics and World Health, Bulletin of Medical Ethics 179: 21-24, June/July 2002.
• Caplan, Arthur L.: If Gene Therapy Is the Cure, What Is the Disease?, Bioethics.net, 2002.
• Mahowald, Mary B.: Reproductive Genetics and Gender Justice, Bioethics.net, 2002.
• McGee, Glenn: Ethical Issues in Genetics in the Next 100 Years, Bioethics.net, 2002.