Linked bibliography for the SEP article "Privacy and Medicine" by Anita Allen
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- Allen, Anita, 1997, “Genetic Privacy: Emerging Concepts and
Values”, in Genetic Secrets: Protecting Privacy and
Confidentiality in the Genetic Era, M. Rothstein (ed.), New
Haven: Yale University Press, pp. 31–59. (Scholar)
- –––, 2000, “Gender and Privacy in
Cyberspace”, Stanford Law Review, 52(5):
1175–1200. (Scholar)
- –––, 2003, Privacy Isn’t Everything:
Feminist Reflections on Personal Accountability, Lanham: Roman
and Littlefield. (Scholar)
- –––, 2007, “Face to Face With
‘It’: And Other Neglected Contexts of Health
Privacy”, American Philosophical Society, 151(3):
300–308. (Scholar)
- –––, 2014, “Privacy in Health Care”, in Encyclopedia of Bioethics, 4rd edition, Bruce Jennings (ed.), New York: MacMillan Reference Books, pp. 2064–2073. (Scholar)
- –––, 2015, “Compliance Limited Health
Privacy Laws”, in Social Dimensions of Privacy, Beate
Roessler and Dorota Mokrosinska (eds.), Cambridge: Cambridge
University Press, pp. 261– 277. (Scholar)
- –––, 2016, “Protecting One’s Own Privacy
in a Big Data Economy” Harvard Law Review Forum, 130:
71–80. (Scholar)
- Allen, Anita and Marc Rotenberg (with contributions by Rok Lampe),
2016, Privacy Law and Society, 3rd edition, Minneapolis: West
Academic Publishing. (Scholar)
- American Association of Marriage and Family Therapists [AAMFT],
2015, AAMFT Code of Ethics, Alexandria, VA: American
Association of Marriage and Family Therapists.
[AAMFT 2015 available online] (Scholar)
- American Pharmacists Association, [APhA], 1994, Code of Ethics
for Pharmacists, Washington, D.C.: American Pharmaceutical
Association
[AphA 1994 available online]. (Scholar)
- American Psychological Association [APA], 2017, Ethical
Principles of Psychologists and Code of Conduct, Washington,
D.C.: American Psychological Association
[APA 2017 available online]. (Scholar)
- Annas, J., 1989, “Self-Love in Aristotle”, The Southern Journal of Philosophy, 27 (Supplement): 1–18. (Scholar)
- Annas, G.J., S.S. Crosby, & L.H. Glantz, 2013,
“Guantanamo Bay: A Medical Ethics-free Zone?” New
England Journal of Medicine, 369: 101–103. (Scholar)
- Baer, Atar, Stefan Saroiu, and Laura A. Koutsky, 2002,
“Obtaining Sensitive Data through the Web: An Example of Design
and Methods”, Epidemiology, 13 (6): 640–645. (Scholar)
- Barbour, John D., 2004, The Value of Solitude: the Ethics and Spirituality of Aloneness in Autobiography, Charlottesville: University of Virginia Press. (Scholar)
- Beauchamp, T., 2000, “The Right to Privacy and the Right to Die”, Social Policy and Practice, 1(2): 276–292. (Scholar)
- Beauchamp, T. and J. Childress, 2008, Principles of Biomedical Ethics, 6th edition, New York: Oxford. (Scholar)
- Benn, S., 1988, A Theory of Freedom, Cambridge: Cambridge University Press. (Scholar)
- Bible, Jon D., and Darien A McWhirter, 1990, Privacy in the
Workplace: A Guide for Human Resource Managers, New York: Quorum
Books. (Scholar)
- Biegelman, Martin T., 2009, Identity Theft Handbook:
Detection, Prevention, and Security, New York: John Wiley and
Sons. (Scholar)
- Birenbaum-Carmeli, Daphna, Yoram Carmeli, and Sergei Gornostayev,
2008, “Researching Sensitive Fields: Some lessons from a study
of sperm donors”, Israel International Journal of Sociology
and Social Policy, 28 (11/12): 425–439. (Scholar)
- Blaauw, C.B., J.J. van den Dobbelsteen, F.W. Jansen, & J.H.
Hubben, 2014, “Privacy Aspects of Video Recording in the
Operating Room”, in J. van den Hoven, N. Doorn, T. Swierstra,
B.-J. Koops, and H. Romijn (eds.), Responsible Innovation 1,
Dordrecht: Springer, pp. 293–300. (Scholar)
- Bok, S., 1982, Secrets: On the Ethics of Concealment and Revelation, New York: Pantheon Books. (Scholar)
- Boling, Patricia, 1996, Privacy and the Politics of Intimate
Life, Ithaca, NY: Cornell University Press. (Scholar)
- Boone, C., 1983, “Privacy and Community”, Social Theory and Practice, 9(1): 1–30. (Scholar)
- Bridges, Khiara, 2017, The Poverty of Privacy Rights,
Stanford: Stanford University Press. (Scholar)
- Brody, H., 1993, “Causing, Intending, and Assisting Death”, Journal of Clinical Ethics, 4: 112–117. (Scholar)
- Burr, Chandler, 1999, “The AIDS Exception: Privacy vs.
Public Health”, in Dan E. Beauchamp and Bonnie Steinbock (eds.),
New Ethics for Public Health, New York: Oxford University
Press, pp. 212–224. (Scholar)
- Burton, Lynda C., Gerard F. Anderson, Irvin W. Kues, 2004,
“Using Electronic Health Records to Help Coordinate Care”,
Milbank Quarterly, 82(3): 457–481. (Scholar)
- Buss, A., 1980, Self-Consciousness and Social Anxiety,
San Francisco: W.H. Freeman. (Scholar)
- Callahan, D., 1992, “When Self Determination Runs Amok”, Hastings Center Report, 22 (March-April): 52–55. (Scholar)
- Cato, Kenrick D. et al., 2016, “Did I Tell You That? Ethical
Issues Related to Using Computational Methods to Discover
Non-Disclosed Patient Characteristics,” Journal of Empirical
Research on Human Research Ethics, 11(3): 214-219. (Scholar)
- Chadwick, R., M. Levitt, & D. Shickle (eds.), 2014, The Right to Know and the Right Not to Know: Genetic Privacy and Responsibility, Cambridge: Cambridge University Press. (Scholar)
- Chepesiuk, Ron, 1999, “Making House Calls: Using
Telecommunications to Bring Health Care into the Home”,
Environmental Health Perspectives, 107 (11):
A556–A560. (Scholar)
- Chretien, K.C., J. Azar, & T. Kind, 2011, “Physicians on
twitter”, Journal of the American Medical Association,
305(6): 566–568. (Scholar)
- Currie, Peter M., 2005, “Balancing Privacy Protections with Efficient Research: Institutional Review Boards and the Use of Certificates of Confidentiality”, IRB: Ethics and Human Research, 27(5): 7–12 (Scholar)
- Dankar, F and Khaled Emam, 2013, “Practicing Differential
privacy in Health Care”, Transactions in Data Privacy,
6(1): 35–65. (Scholar)
- DeCew, J., 1997, In Pursuit of Privacy: Law, Ethics, and the Rise of Technology, Ithaca, NY: Cornell University Press. (Scholar)
- –––, 2000, “The Priority of Privacy for Medical Information”, Social Policy and Practice, 1(2): 213–234. (Scholar)
- Department of Health and Human Services [DHHS], 2015, Health
Information Privacy,
[DHHS 2015 available online]. (Scholar)
- Dickson, Donald T., 1998, Confidentiality and Privacy in
Social Work: a Guide to the Law for Practitioners and Students,
New York: Simon and Schuster. (Scholar)
- Dresser, Rebecca, 2005, “At Law: Professionals, Conformity, and Conscience”, The Hastings Center Report, 35(6): 9–10. (Scholar)
- Dwork, Cynthia, 2006, “Differential Privacy,”
ICALP 2006: Automata, Languages and Programming, pp.
1–12. (Scholar)
- Dworkin, R., T. Nagel, R. Nozick, . Rawls, T. Scanlon, and J. J.
Thomson, 1997 [2007], “Amicus Curare Brief,” submitted in
the cases of State of Washington et al. v. Glucksberg et al. and Vacco
et al. v. Quill et al., argued January 8, 1997 before the U.S. Supreme
Court; reprinted as “The Philosophers’ Brief”, in
Bioethics: Introduction to History, Method, and practice,
2nd edition, N. Jecker et al. (eds.), Sudbury, MA: Jones
& Bartlett Publishers, 2007, pp. 490–502. (Scholar)
- Easter, Michele M., Arlene M. Davis, and Gail E. Henderson, 2004, “Confidentiality: More than a Linkage File and a Locked Drawer”, IRB: Ethics and Human Research, 26(2): 13–17. (Scholar)
- Electronic Privacy Information Center [EPIC], 2006, Privacy
& Human Rights: An International Survey of Privacy Laws and
Developments, Washington, D.C.: Electronic Privacy Information
Center. (Scholar)
- El Emam, K. & E. Moher, 2013, “Privacy and anonymity
challenges when collecting data for public health purposes”,
The Journal of Law, Medicine & Ethics, 41:
37–41. (Scholar)
- Ely, J., 1974, “The Wages of Crying Wolf: A Comment on Roe
v. Wade”, Yale Law Journal, 82(5): 920–949. (Scholar)
- Englehardt, H. Tristram, 2000a, “Privacy and Limited
Democracy, the Moral Centrality of Persons”, Social Policy
and Practice, 1(2): 120–140. (Scholar)
- –––, 2000b, The Philosophy of Medicine:
Framing the Field, Dordrecht: Kluwer Academic Publishers. (Scholar)
- Etzioni, Amitai, 2000, The Limits of Privacy, New York: Basic Books. (Scholar)
- Faden, R., T. Beauchamp, and N. King, 1986, A History of Informed Consent, New York: Oxford University Press. (Scholar)
- Faden, R.R., N.E. Kass, S.N. Goodman, P. Pronovost, S. Tunis,
& T.L. Beauchamp, 2013, “An ethics framework for a learning
health care system: a departure from traditional research ethics and
clinical ethics”, Hastings Center Report, 43:
S16–S27. (Scholar)
- Fairchild, Amy L., Lance Gable, Lawrence O. Gostin, Ronald Bayer,
Patricia Sweeney, Robert S. Janssen, 2007a, “Public Goods,
Private Data: HIV and the History, Ethics, and Uses of Identifiable
Public Health Information”, Public Health Reports, 122:
7–15. (Scholar)
- Fairchild, Amy L., Ronald Bayer, James Keith Colgrove, and Daniel
Wolfe, 2007b, Searching eyes: privacy, the state, and disease
surveillance in America. Berkeley: University of California
Press. (Scholar)
- Farahany, N.A., 2012, “Incriminating thoughts”,
Stanford Law Review, 64: 351–408. (Scholar)
- Fefferman N.H., E.A. O’Neil, and E.N. Naumova, 2005, “
Confidentiality and Confidence: Is data aggregation a means to achieve
both?”, Public Health Policy, 26(4):
430–449. (Scholar)
- Feinberg, J., 1983, “Autonomy, Sovereignty, and Privacy:
Moral Ideals and the Constitution”, Notre Dame Law
Review, 58(3): 445–492. (Scholar)
- Finnis, John, 1998, Thomas Aquinas, Moral, Political, and Legal Theory, Oxford: Oxford University Press. (Scholar)
- Fisher, Celia B., 2006, “Privacy and Ethics in Pediatric
Environmental Health Research: Part II: Protecting Families and
Communities”, Environmental Health Perspectives,
114(3): 1622–1625. (Scholar)
- Foucault, Michel, 1977, Discipline and Punish: The Birth of the Prison, Alan Sheridan (trans.), New York: Pantheon. (Scholar)
- Francis, Leslie P. and John G. Francis, 2017, “Privacy and
Health Information”, in Privacy: What Everyone Needs to
Know, New York: Oxford University Press, pp. 62–101. (Scholar)
- Freedman, Benjamin, 1978, “A Meta-Ethics for Professional Morality”, Ethics, 89(1): 1–19 (Scholar)
- Frey, R.G., 2000, “Privacy Control and Talk of Rights”, Social Policy and Practice, 1(2): 45–67. (Scholar)
- Gallagher, Kathleen M., Patrick S. Sullivan, Amy Lansky, Ida M.
Onorato, 2007, “Behavioral Surveillance among People at Risk for
HIV Infection in the U.S.: The National HIV Behavioral Surveillance
System”, Public Health Reports, 22: 32–38. (Scholar)
- Gandy, O., 1993, The Panoptic Sort: A Political Economy of
Personal Information, Boulder, San Francisco, Oxford: Westview
Press. (Scholar)
- General Accounting Office [GAO], 2001, Medical Privacy
Regulation: Questions Remain about Implementing the New Consent
Requirement, (Report to the Chairman, Committee on Health,
Education, Labor, and Pensions), U.S. Senate, Washington, D.C.: U.S.
General Accounting Office.
[GAO 2001 available online] (Scholar)
- Genetic Information Non-Discrimination Act [GINA], 2008,
[GINA 2008 available online].
- Goffman, E., 1959, The Presentation of Self in Everyday
Life, Garden City, NY: Doubleday. (Scholar)
- –––, 1963, Behavior in Public Places,
New York: Free Press. (Scholar)
- Green, R., 2008, Babies by Design: The Ethics of Genetic
Choice, New Haven: Yale University Press. (Scholar)
- Green, R.C., D. Lautenbach, & A.L. McGuire, 2015, “GINA,
Genetic Discrimination, and Genomic Medicine”, New England
Journal of Medicine, 372: 397–399. (Scholar)
- Gates John J. and Bernard S. Arons, 1999, Privacy and
Confidentiality in Mental Health Care, Baltimore: Paul H. Brookes
Pub. Co. (Scholar)
- Hall, Joseph and Deven McGraw, 2014, “For Telehealth to
Succeed, Privacy and Security Risks Must be Identified and
Addressed”, Health Affairs , 33(2): 216–221. (Scholar)
- Hare, R.M., 1993, Essays on Bioethics, Oxford: Clarendon Press. (Scholar)
- Harris, J., 2007, Enhancing Evolution: The Ethical Case for Making Better People, Princeton, NJ: Princeton University Press. (Scholar)
- Harsanyi, D., 2007, Nanny State: How Food Fascists,
Teetotaling Do-Gooders, Priggish Moralists, and other Boneheaded
Bureaucrats are Turning America into a Nation of Children, New
York: Broadway Books. (Scholar)
- Health Insurance Portability and Accountability Act of 1996
[HIPAA] Privacy Rule,
[HIPAA 1996 available online]. (Scholar)
- Hiatt, Robert A., 2003, “HIPAA: The End of Epidemiology, or
a New Social Contract?” Epidemiology, 14(6):
637–639. (Scholar)
- Hixson, R., 1987, Privacy in Public Society: Human Rights in
Conflict, New York: Oxford University Press. (Scholar)
- Honore, A., 1961, “Ownership”, in A.G. Guest (ed.),
Oxford Essays in Jurisprudence, Oxford: Oxford University
Press, pp. 107–47. (Scholar)
- Humber, James M. and Robert F. Almeder, 2001, Privacy and
Health Care, New York: Humana Press. (Scholar)
- Hursthouse, Rosalind., 1991, “Virtue Theory and Abortion”, Philosophy and Public Affairs, 20(3): 223–246. (Scholar)
- Institute of Medicine [IOM], 1994, Health Data in the
Information Age: Use, Disclosure, and Privacy, Washington, D.C.:
National Academy Press. (Scholar)
- –––, 2000, “Committee on the Role of
Institutional Review Boards in Health Services Research Data Privacy
Protection, Division of Health Care Services”, Protecting
Data Privacy in Health Services Research, Washington, D.C.:
National Academies Press
[IOM 2000 available online]. (Scholar)
- Jasti, D., K.V.N.R. Pratap, V.S. Kalyan, M.P. Sandhya, &
A.S.K. Bhargava, 2015, “Health Care Apps-will they be a Facelift
for Today’s Medical/Dental Practice?”, Journal of
Mobile Technology in Medicine, 4: 8–14. (Scholar)
- Jonsen, A., 1998, The Birth of Bioethics, New York: Oxford. (Scholar)
- Juengst, Eric, et al., 2016, “Ethical and Social
Implications of Rhetorical Reform in Genomic Medicine”,
Hastings Center Report 46(5): 21–33. (Scholar)
- Kamoie, Brian and James G. Hodge Jr., 2004, “HIPAA’S
Implications for Public Health Policy and Practice: Guidance from the
CDC”, Public Health Reports, 119(2):
216–219.
- Kasperbauer, T., 2020, “Protecting Health Privacy Even When Health Privacy is Lost”, Journal of Medical Ethics, 46(11): 768–772. (Scholar)
- Kato, Pamela M. and Traci Mann, 1996, Handbook of Diversity
Issues in Health, Berlin: Springer Verlag. (Scholar)
- Kenny, D., 1982, “Confidentiality: The Confusion Continues”, Journal of Medical Ethics, 8(1): 5–8. (Scholar)
- Koelewijn, Wouter, 2018, “Privacy from a Medical Perspective
”, in Bart van der Sloot and Aviva de Groot, The Handbook of
Privacy Studies: An Interdisciplinary Introduction, Amsterdam:
University of Amsterdam Press, pp. 333–349. (Scholar)
- Lakoff, G. and Mark Johnson, 1999, Philosophy in the Flesh: The Embodied Mind and its Challenge to Western Thought, New York: Basic Books. (Scholar)
- Laurie, Graeme T., 2002, Genetic Privacy: a Challenge to Medico-Legal Norms, Cambridge: Cambridge University Press. (Scholar)
- Little, Margaret, 1999, “Abortion, Intimacy and the Duty to Gestate”, Ethical Theory and Moral Practice, 2(3): 295–312. (Scholar)
- Louch, A., 1982, “Is Privacy Immoral?”, Human
Rights, 10(3): 22–54. (Scholar)
- MacKinnon, C., 1984, “Roe v. Wade: A Study in Male
Ideology”, in Abortion: Moral and Legal Perspectives,
J. Garfield and P. Hennessy (eds.), Amherst, MA: University of
Massachusetts Press, pp. 45–54. (Scholar)
- Makary, M.A., 2013, “The Power of Video Recording: Taking
Quality to the Next Level”, Journal of the American Medical
Association, 309: 1591–1592. (Scholar)
- Marx, Gary T., 2007, “Privacy and Social Stratification”, Knowledge, Technology & Policy, 20(2): 91–95. (Scholar)
- Martin, Mike W., 1981, “Rights and the Meta-Ethics of Professional Morality”, Ethics, 91(4): 619–625. (Scholar)
- May, L., 1988, “Privacy and Property”, Philosophy
in Context, 10(40): 40–53. (Scholar)
- McCloskey, H., 1971, “The Political Ideal of Privacy”, The Philosophical Quarterly, 21(85): 303–314. (Scholar)
- McDonagh, Eileen L., 1996, Breaking the abortion deadlock: from choice to consent. New York: Oxford University Press. (Scholar)
- McGee, Glenn, 1999, Pragmatic Bioethics, Nashville: Vanderbilt University Press. (Scholar)
- Mill, J., 1869, On Liberty, D. Bromwich and G. Kateb (eds.), New Haven: Yale University Press (2003). (Scholar)
- Minichiello Victor, Rodrigo Mariño, Jan Browne, Maggie
Jamieson, Kirk Peterson, Brad Reuter, and Kenn Robinson, 2000,
“Commercial Sex between Men: A Prospective Diary-Based
Study”, The Journal of Sex Research, 37(2):
151–160. (Scholar)
- Mohapatra, Seema and Lindsay F. Wiley, 2020, “Feminist Perspectives in Health Law,” Journal of Law, Medicine and Ethics, 47(4_suppl): 103–115. (Scholar)
- Moore, A. (ed.), 2005, Information Ethics: Privacy, Property,
and Power, Seattle: University of Washington Press. (Scholar)
- National Research Council, 1991, The Computerized Patient
Record: An Essential Technology for Health Care, Washington,
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- Negley, G., 1966, “Philosophical Views on the Value of
Privacy”, Law and Contemporary Problems, 31(1):
319–325. (Scholar)
- Newcombe, Howard B., 1994, “Cohorts and Privacy”,
Cancer Causes and Control, 5(3): 287–291. (Scholar)
- Newell, B.C., A.D. Moore, & C. Metoyer, 2015, “Privacy in the Family”, in Beate Rössler and Dorota Mokrosinska (eds.), The Social Dimensions of Privacy, Cambridge: Cambridge University Press, pp. 104–121. (Scholar)
- Nissenbaum, H., 2009, Privacy in Context: Technology, Policy
and the Integrity of Social Life, Stanford: Stanford University
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- Obasagie, Osagie and M. Darnovsky (eds.), 2018, Beyond Bioethics: Toward a New Biopolitics, Berkeley: University of California Press. (Scholar)
- Olanrewaju, R.F., N.A. Ali, O. Khalifa, & A.A. Manaf, 2013,
“ICT in Telemedicine: Conquering Privacy and Security Issues In
Health Care Services”, Electronic Journal of Computer
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- Parens, Erik and Lori P. Knowles, 2003, “Reprogenetics and
Public Policy: Reflections and Recommendations”, The
Hastings Center Report (Special Supplement), 33(4):
S1–S24. (Scholar)
- Parens, Erik and Josephine Johnston, 2014, “Neuroimaging: Beginning to Appreciate Its Complexities”, in Interpreting Neuroimages: An Introduction to the Technology and Its Limits, The Hastings Center Report, 44(s2): 52–57. (Scholar)
- Parent, W., 1983, “Recent Work on the Concept of Privacy”, American Philosophical Quarterly, 20(3): 341–355. (Scholar)
- Paul VI, 1968, “Encyclical Letter, Humanae Vitae of the
Supreme Pontiff Paul VI to his venerable brothers the patriarchs,
archbishops, bishops and other local ordinaries in peace and communion
with the apostolic see, to the clergy and faithful of the whole
catholic world, and to all men of good will, on the regulation of
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- Pennock, J. and J. Chapman (eds.), 1971, Privacy: Nomos
XIII, New York: Atherton Press. (Scholar)
- Pierce, Robin, 2018, “Medical Privacy: Where Deontology and
Consequentialism Meet”, in Bart van der Sloot and Aviva de Groot
(eds.), The Handbook of Privacy Studies: An Interdisciplinary
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- Post, R., 1989, “The Social Foundations of Privacy:
Community and Self in the Common Law Tort”, California Law
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- Powers, Madison and Ruth Faden, 2008, Social Justice: The Moral Foundations of Public Health and Health Policy, New York: Oxford University Press. (Scholar)
- Presidential Commission for the Study of Bioethical Issues:
- 2012, Privacy and Progress in Whole Genome
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- 2014, Grey Matters, Vol. 1: Integrative Approaches to
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- 2015a, Ethics and Ebola: Public Health Planning and
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- 2015b, Grey Matters, Vol. 2: Topics at the Intersection of
Neuroscience, Ethics, and Society.
- Prosser, W., 1960, “Privacy”, California Law
Review, 48(3): 383–423. (Scholar)
- Rachels, J., 1975, “Why Privacy is Important”, Philosophy and Public Affairs, 4(3): 323–333. (Scholar)
- Radden, Jennifer (ed.), 2004, The Philosophy of Psychiatry, A Companion, Oxford: Oxford University Press. (Scholar)
- Radin, M., 1987, “Market-Inalienability”, Harvard
Law Review, 100(8): 1849–1937. (Scholar)
- Richards, D., 1986, Toleration and the Constitution, New
York: Oxford University Press. (Scholar)
- Robins, Robert S. and Henry Rothschild, 1988, “Ethical
Dilemmas of the President’s Physician”, Politics and
the Life Sciences, 7(1): 3–11. (Scholar)
- Rössler, B. (ed.), 2004, Privacies: Philosophical Evaluations, Stanford: Stanford University Press. (Scholar)
- Rosenberg, Alexander, 2000, “Privacy as a Matter of Taste and Right”, Social Policy and Practice, 1(2): 68–90. (Scholar)
- Rotenberg, M. (ed.), 2004, The Privacy Law Sourcebook: United
States Law, International Law, and Recent Developments,
Washington, D.C.: Electronic Privacy Information Center. (Scholar)
- Rothstein, M. (ed.), 1997, Genetic Secrets: Protecting Privacy
and Confidentiality in the Genetic Era, New Haven: Yale
University Press. (Scholar)
- Sandel, M., 2007, The Case Against Perfection: Ethics in the Age of Genetic Engineering, Cambridge, MA: Belknap Press of Harvard University Press. (Scholar)
- Schoeman, F. (ed.), 1984, Philosophical Dimensions of Privacy: An Anthology, Cambridge: Cambridge University Press. (Scholar)
- Schueler, G.F., 1999, “Why IS Modesty a Virtue?”, Ethics, 109: 835–841. (Scholar)
- Schwartz, Paul, 1995, “The Protection of Privacy in Health
Care Reform”, Vanderbilt Law Review, 48: 295. (Scholar)
- Seh, Adil Hussain et al. 2020, “Health Care Data Breaches:
Insights and Implications,” Healthcare, 8(2): 133 (Scholar)
- Sharpe, Virginia A., 2005, “Perspective: Privacy and Security for Electronic Health Records”, The Hastings Center Report, 35(6): 18. (Scholar)
- Sheperd, Lois and Robin F. Wilson, 2018, “Introduction: The Medicalization of Poverty”, Journal of Law, Medicine and Ethics, 46: 563–566. (Scholar)
- Sher, G., 1981, “Subsidized Abortions: Moral Rights and Moral Compromise”, Philosophy and Public Affairs, 10(3): 361–372. (Scholar)
- Sinner-Thomson, Scott, 2020, Privacy at the Margins,
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- Solove, Daniel, 2004, The Digital Person: Technology and
Privacy in the Information Age, New York: NYU Press. (Scholar)
- –––, 2008, Understanding Privacy,
Cambridge, MA: Harvard University Press. (Scholar)
- Solove, Daniel and Richards, N., 2007, “Privacy’s
Other Path: Recovering the Law of Confidentiality”,
Georgetown Law Journal, 96(1): 123–182. (Scholar)
- Storr, Anthony, 2005, Solitude: A Return to the Self, New
York: Simon & Schuster. (Scholar)
- Thompson, Dennis, 1987, Poetical Ethics and Public Office. Cambridge, MA: Harvard University Press. (Scholar)
- Thomson, J., 1971, “A Defense of Abortion”, Philosophy and Public Affairs, 1: 47–67. (Scholar)
- –––, 1975, “The Right to Privacy”, Philosophy and Public Affairs, 4(3): 295–314. (Scholar)
- van der Sloot, Bart, 2018, Privacy as Virtue: Moving Beyond
the Individual in the Age of Big Data, Amsterdam: University of
Amsterdam Press. (Scholar)
- Veliz, Carissa, 2020, Privacy is Power: How and Why You Should Take Back Control of Your Data, London: Penguin Random House. (Scholar)
- Waldman, Ari E., 2018, Privacy as Trust: Information Privacy
for an Information Age, Cambridge: Cambridge University
Press. (Scholar)
- Weiss, R., 1991, Maimonides’ Ethics: The Encounter of
Philosophic and Religious Morality, Chicago: University of
Chicago Press. (Scholar)
- Wells, D.M., K. Lehavot, & M.L. Isaac, 2015, “Sounding
Off on Social Media: The Ethics of Patient Storytelling in the Modern
Era”, Academic Medicine: Journal of the Association of
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- Westin, A., 1967, Privacy and Freedom, New York: Atheneum. (Scholar)
- White Katherine A., 1999, “Crisis of Conscience: Reconciling
Religious Health Care Providers’ Beliefs and Patients’
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- Winslade, William J., 2014, “Confidentiality”, in
Encyclopedia of Bioethics, 4rd edition, Bruce
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494–503. (Scholar)
- Wolf, Leslie E. and Jolanta Zandecki, 2006, “Sleeping Better
at Night: Investigators’ Experiences with Certificates of
Confidentiality”, IRB: Ethics and Human Research,
28(6): 1–7. (Scholar)
- Wolf, Leslie E., Jolanta Zandecki, and Bernard Lo, 2004,
“The Certificate of Confidentiality Application: A View from the
NIH Institutes”, IRB: Ethics and Human Research, 26(1):
14–18. (Scholar)