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Lisa S. Parker [25]Lisa Parker [3]
  1. Lisa S. Parker & Thomas G. Buller (forthcoming). Case Study: A Hard Policy to Swallow. Hastings Center Report.
     
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  2. Lisa Parker & Lisa Watts (2013). Ethics Ward Rounds: A Conduit to Finding Meaning and Value in Medical School. Journal of Evaluation in Clinical Practice 19 (6):1084-1084.
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  3. Valerie B. Satkoske & Lisa S. Parker (2013). Preserving Testicular Tissue and a Boy's Open Reproductive Future. TThe American Journal of Bioethics 13 (3):36 - 37.
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  4. Lisa S. Parker (2012). In Sport and Social Justice, Is Genetic Enhancement a Game Changer? Health Care Analysis 20 (4):328-346.
    The possibility of genetic enhancement to increase the likelihood of success in sport and life’s prospects raises questions for accounts of sport and theories of justice. These questions obviously include the fairness of such enhancement and its relationship to the goals of sport and demands of justice. Of equal interest, however, is the effect on our understanding of individual effort, merit, and desert of either discovering genetic contributions to components of such effort or recognizing the influence of social factors on (...)
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  5. Lisa S. Parker (2012). The Immortal Life of Henrietta Lacks, Feminist Themes, and Research Ethics. International Journal of Feminist Approaches to Bioethics 5 (1):159-165.
    In 1951 Henrietta Lacks felt a lump in her cervix, entered Johns Hopkins Hospital, and was examined in a colored-only exam room by a physician who biopsied the lump. Called back to Hopkins for treatment of diagnosed carcinoma of the cervix, Henrietta signed a one-line “Operation Permit,” and under general anesthesia received her first round of radium treatment. Before sewing a tube of radium into her cervix, the surgeon on duty took samples of tumor and healthy tissue, and as with (...)
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  6. Lisa S. Parker (2012). The Immortal Life of Henrietta LacksRebecca Skloot. International Journal of Feminist Approaches to Bioethics 5 (1):159-165.
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  7. Lisa S. Parker & Valerie B. Satkoske (2012). Ethical Dimensions of Disparities in Depression Research and Treatment in the Pharmacogenomic Era. Journal of Law, Medicine and Ethics 40 (4):886-903.
    Disparities in access to, and utilization of, treatment for depression among African-American and Caucasian elderly adults have been well-documented. Less fully explored are the multidimensional factors responsible for these disparities. The intersection of cultural constructs, socioeconomic factors, multiple levels of racism, and stigma attending both mental health issues and older age may help to explain disparities in the treatment of the depressed elderly. Personalized medicine with its promise of developing interventions tailored to an individual's health needs and genetically related response (...)
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  8. Valerie B. Satkoske & Lisa S. Parker (2010). Practicing Preventive Ethics, Protecting Patients: Challenges of the Electronic Health Record. Journal of Clinical Ethics 21 (1):36.
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  9. Lisa Parker (2008). Review of Neil C. Manson and Onora O'Neill, Rethinking Informed Consent in Bioethics. [REVIEW] American Journal of Bioethics 8 (8):68-69.
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  10. Lisa S. Parker (2008). The Future of Incidental Findings: Should They Be Viewed as Benefits? Journal of Law, Medicine and Ethics 36 (2):341-351.
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  11. Susan M. Wolf, Frances P. Lawrenz, Charles A. Nelson, Jeffrey P. Kahn, Mildred K. Cho, Ellen Wright Clayton, Joel G. Fletcher, Michael K. Georgieff, Dale Hammerschmidt, Kathy Hudson, Judy Illes, Vivek Kapur, Moira A. Keane, Barbara A. Koenig, Bonnie S. LeRoy, Elizabeth G. McFarland, Jordan Paradise, Lisa S. Parker, Sharon F. Terry, Brian van Ness & Benjamin S. Wilfond (2008). Managing Incidental Findings in Human Subjects Research: Analysis and Recommendations. Journal of Law, Medicine and Ethics 36 (2):219-248.
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  12. Lisa S. Parker (2007). Bioethics as Activism. In Lisa A. Eckenwiler & Felicia Cohn (eds.), The Ethics of Bioethics: Mapping the Moral Landscape. Johns Hopkins University Press. 144--157.
     
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  13. Lisa S. Parker (2006). Best Laid Plans for Offering Results Go Awry. American Journal of Bioethics 6 (6):22 – 23.
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  14. Lisa Parker & Lauren Matukaitis Broyles (2006). Ethical Issues in the Conduct of Genetic Research. In Ana Smith Iltis (ed.), Research Ethics. Routledge.
     
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  15. Charles W. Lidz & Lisa S. Parker (2003). Issues of Ethics and Identity in Diagnosis of Late Life Depression. Ethics and Behavior 13 (3):249 – 262.
    Depression is often diagnosed in patients nearing the end of their lives and medication or psychotherapy is prescribed. In many cases this is appropriate. However, it is widely agreed that a health care professional should treat sick persons so as to improve their condition as they define improvement. This raises questions about the contexts in which treatment of depression in late life is appropriate. This article reviews a problematic case concerning the appropriateness of treatment in light of the literature in (...)
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  16. Howard B. Degenholtz, Lisa S. Parker & I. I. I. Charles F. Reynolds (2002). Trial Design and Informed Consent for a Clinic-Based Study with a Treatment as Usual Control Arm. Ethics and Behavior 12 (1):43-62.
  17. Howard B. Degenholtz, Lisa S. Parker & Charles F. Reynolds (2002). Trial Design and Informed Consent for a Clinic-Based Study with a Treatment as Usual Control Arm. Ethics and Behavior 12 (1):43 – 62.
    Employing the National Institute of Mental Health-funded Prevention of Suicide in Primary Care Elderly Collaborative Trial as a case study, we discuss 2 sets of ethical issues: obtaining informed consent for a clinic-based intervention study and using treatment as usual (TAU) as the control condition. We then address these ethical issues in the context of the debate about the quality improvement efforts of health care organizations. Our analysis reveals the tension between ethics and scientific integrity involved with using TAU as (...)
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  18. Lisa S. Parker (2002). Information(Al) Matters: Bioethics and the Boundaries of the Public and the Private. Social Philosophy and Policy 19 (2):83-112.
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  19. Ryan Sauder & Lisa S. Parker (2001). Autonomy's Limits: Living Donation and Health-Related Harm. Cambridge Quarterly of Healthcare Ethics 10 (4):399-407.
    In late December 1998, Renada Daniel-Patterson's father offered to donate a kidney to his daughter and ignited a controversy in the bioethics community. Renada had been born with only one kidney, which began to fail early in her childhood. At age 6, Renada had to receive dialysis three times a week. She was unable to attend school or venture very far from home. This pattern continued until Renada was 13, when Mr. Patterson called from prison to offer her his kidney. (...)
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  20. Lisa S. Parker (1998). Susan M. Wolf (Ed.): Feminism and Bioethics: Beyond Reproduction. Theoretical Medicine and Bioethics 19 (4):411-418.
  21. Lisa S. Parker & Robert M. Arnold (1998). Confidentiality--Revealing Trends in Bioethics. Bioethics Forum 14 (3-4):32.
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  22. Lisa S. Parker (1995). Beauty and Breast Implantation: How Candidate Selection Affects Autonomy and Informed Consent. Hypatia 10 (1):183 - 201.
    Candidate evaluation for breast implantation presents a more important obstacle to the fulfillment of the normative requirements of informed consent than do the social roles of women or cultural norms governing female beauty. I argue that women's decisions to receive breast implants may indeed be informed, competently made, and substantially voluntary, but that the cultural construction of beauty may undermine women's autonomy by influencing the evaluation of surgical candidates and risk disclosure during informed consent.
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  23. Lisa S. Parker (1995). Breast Cancer Genetic Screening and Critical Bioethics' Gaze. Journal of Medicine and Philosophy 20 (3):313-337.
    This paper illustrates a role that bioethics should play in developing and criticizing protocols for breast cancer genetic screening. It demonstrates how a critical bioethics, using approaches and reflecting concerns of contemporary philosophy of science and science studies, may critically interrogate the normative and conceptual schemes within which ethical considerations about such screening protocols are framed. By exploring various factors that influence the development of such protocols, including politics, cultural norms, and conceptions of disease, this paper and the critical bioethics' (...)
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  24. Lisa S. Parker & Rachel Ankeny Majeske (1995). Incidental Findings: Patients' Knowledge, Rights, and Preferences. Journal of Clinical Ethics 6 (2):176.
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  25. Rosa Lynn Pinkus, Gretchen M. Aumann, Mark G. Kuczewski, Anne Medsger, Alan Meisel, Lisa S. Parker & Mark R. Wicclair (1995). The Consortium Ethics Program: An Approach to Establishing a Permanent Regional Ethics Network. [REVIEW] HEC Forum 7 (1):13-32.
    This paper describes the first three-year experience of the Consortium Ethics Program (CEP-1) of the University of Pittsburgh Center for Medical Ethics, and also outlines plans for the second three-year phase (CEP-2) of this experiment in continuing ethics education. In existence since 1990, the CEP has the primary goal of creating a cost-effective, permanent ethics resource network, by utilizing the educational resources of a university bioethics center and the practical expertise of a regional hospital council. The CEP's conception and specific (...)
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  26. Lachlan Forrow, Robert M. Arnold & Lisa S. Parker (1993). Preventive Ethics: Expanding the Horizons of Clinical Ethics. Journal of Clinical Ethics 4 (4):287.
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  27. Lisa S. Parker (1993). Social Justice, Federal Paternalism, and Feminism: Breast Implants in the Cultural Context of Female Beauty. Kennedy Institute of Ethics Journal 3 (1):57-76.
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