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Profile: John Fletcher
  1.  23
    John C. Fletcher, F. William Dommel & Daniel D. Cowell (forthcoming). A Trial Policy for the Intramural Programs of the National Institutes of Health: Consent to Research with Impaired Human Subjects. IRB: Ethics & Human Research.
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  2.  7
    John C. Fletcher & Mark Siegler (1996). What Are the Goals of Ethics Consultation? A Consensus Statement. Journal of Clinical Ethics 7 (2):122.
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  3.  9
    Giles R. Scofield, John C. Fletcher, Albert R. Jonsen, Christian Lilje, Donnie J. Self & Judith Wilson Ross (1993). Ethics Consultation: The Least Dangerous Profession? Cambridge Quarterly of Healthcare Ethics 2 (4):417.
    Whether ethics is too important to be left to the experts or so important that it must be is an age-old question. The emergence of clinical ethicists raises it again, as a question about professionalism. What role clinical ethicists should play in healthcare decision making – teacher, mediator, or consultant – is a question that has generated considerable debate but no consensus.
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  4.  12
    Dorothy C. Wertz & John C. Fletcher (1991). Privacy and Disclosure in Medical Genetics Examined in an Ethics of Care. Bioethics 5 (3):212–232.
  5. John C. Fletcher, Norman Quist & Albert R. Jonsen (eds.) (1989). Ethics Consultation in Health Care. Health Administration Press.
     
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  6.  4
    John C. Fletcher (1995). Clinical Bioethics at NIH: History and A New Vision. Kennedy Institute of Ethics Journal 5 (4):355-364.
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  7.  6
    John C. Fletcher (1990). The Patient Self‐Determination Act: Yes. Hastings Center Report 20 (5):33-35.
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  8.  11
    Robin Fretwell Wilson, Martha Neff-Smith, Donald Phillips & John C. Fletcher (1993). HECs: Are They Evaluating Their Performance? [REVIEW] HEC Forum 5 (1):1-34.
    Although the incidence and composition of HECs has been well characterized, little is known about how HECs assess their performance. In order to describe the incidence of HEC self-evaluation, the methods HECs use to evaluate their performance, and the characteristics of HECs that influence self-evaluation, we surveyed the readers ofHospital Ethics. 290 HECs in 45 U.S. states, the District of Columbia, Puerto Rico and three Canadian provinces, completed questionnaires. Of the 241 HECs included in the data analysis, 97.9% had performed (...)
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  9.  4
    Franklin G. Miller & John C. Fletcher (1995). Criticism or Caricature? Hastings Center Report 25 (2):3-3.
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  10.  3
    Dorothy C. Wertz & John C. Fletcher (1989). Fatal Knowledge? Prenatal Diagnosis and Sex Selection. Hastings Center Report 19 (3):21-27.
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  11.  1
    John C. Fletcher & Joseph D. Schulman (1985). Fetal Research: The State of the Question. Hastings Center Report 15 (2):6-12.
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  12.  14
    Robert D. Truog & John C. Fletcher (1990). Brain Death and the Anencephalic Newborn. Bioethics 4 (3):199–215.
  13.  4
    Cavin P. Leeman, John C. Fletcher, Edward M. Spencer & Sigrid Fry-Revere (1997). Quality Control for Hospitals' Clinical Ethics Services: Proposed Standards. Cambridge Quarterly of Healthcare Ethics 6 (3):257-.
    Hospital ethics committees have become widespread over the last 25 years, stimulated by the Quinlan decision of the New Jersey Supreme Court, the report of a President's Commission, and most recently by the Joint Commission on Accreditation of Health Care Organizations , which now man dates that each hospital seeking accreditation have a functioning process for the consideration of ethical issues in patient care. Laws and regulations in several states require that hospitals establish ethics committees, and some states stipulate that (...)
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  14.  3
    John C. Fletcher (1973). Who Should Teach Medical Ethics? Hastings Center Report 3 (6):4-6.
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  15.  29
    John C. Fletcher, Margo L. White & Philip J. Foubert (1990). Biomedical Ethics and an Ethics Consultation Service at the University of Virginia. HEC Forum 2 (2):89-99.
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  16.  17
    John C. Fletcher (1985). Ethical Issues in and Beyond Prospective Clinical Trials of Human Gene Therapy. Journal of Medicine and Philosophy 10 (3):293-310.
    As the potential for the first human trials of somatic cell gene therapy nears, two ethical issues are examined: (1) problems of moral choice for members of institutional review boards who consider the first protocols, for parents, and for the clinical researchers, and the special protections that may be required for the infants and children to be involved, and (2) ethical objections to somatic cell therapy made by those concerned about a putative inevitable progression of genetic knowledge from therapy to (...)
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  17.  2
    John C. Fletcher & Dorothy C. Wertz (1988). Medical Genetics. Hastings Center Report 18 (6):48-48.
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  18.  3
    John C. Fletcher (1980). Ethics and Amniocentesis for Fetal Sex Identification. Hastings Center Report 10 (1):15-17.
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  19. Mortimer B. Lipsett & John C. Fletcher (1983). Do Vitamins Prevent Neural Tube Defects (and Can We Find Out Ethically)? Hastings Center Report 13 (4):5-8.
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  20.  11
    Martha Neff-Smith, Scott Giles, Edward M. Spencer & John C. Fletcher (1997). Ethics Program Evaluation: The Virginia Hospital Ethics Fellows Example. [REVIEW] HEC Forum 9 (4):375-388.
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  21.  3
    James F. Childress & John C. Fletcher (1994). Respect for Autonomy. Hastings Center Report 24 (3):34-35.
  22.  6
    John C. Fletcher & W. French Anderson (1992). Germ-Line Gene Therapy: A New Stage of Debate. Journal of Law, Medicine & Ethics 20 (1-2):26-39.
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  23.  9
    Dorothy C. Wertz & John C. Fletcher (1989). Moral Reasoning Among Medical Geneticists in Eighteen Nations. Theoretical Medicine and Bioethics 10 (2).
    We surveyed the approaches of 661 geneticists in 18 nations to 14 clinical cases and asked them to give their ethical reasons for choosing these approaches. Patient autonomy was the dominant value in clinical decision-making, with 59% of responses, followed by non-maleficence (20%), beneficence (11%) and justice (5%). In all, 39% described the consequences of their actions, 26% mentioned conflicts of interest between different parties and 72% placed patient welfare above the welfare of others. The U.S., Canada, Sweden, and U.K. (...)
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  24.  2
    Franklin G. Miller & John C. Fletcher (1992). The Case for Legalized Euthanasia. Perspectives in Biology and Medicine 36 (2):159-176.
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  25.  2
    Dorothy C. Wertz, John C. Fletcher, Irmgard Nippert, Gerhard Wolff & Segolene Ayme (2001). In Focus. Has Patient Autonomy Gone to Far? Geneticists' Views in 36 Nations. American Journal of Bioethics: Ajob 2 (4):W21 - W21.
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  26.  2
    Abbyann Lynch, John C. Fletcher, Dorothy Wertz, Andrew Czeizel, Francisco M. Salzano & Kåre Berg (forthcoming). Case Studies: The Price of Silence. Hastings Center Report.
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  27.  2
    John C. Fletcher (1997). Ethics Consultants and Surrogates: Can We Do Better? Journal of Clinical Ethics 8 (1):50.
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  28.  5
    John C. Fletcher (2003). Sham Neurosurgery in Parkinson's Disease: Ethical at the Time. American Journal of Bioethics 3 (4):54-56.
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  29.  4
    John C. Fletcher (1988). What Are Society's Interests in Human Genetics and Reproductive Technologies? Journal of Law, Medicine & Ethics 16 (1-2):131-137.
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  30.  3
    John C. Fletcher & Kenneth J. Ryan (1987). Federal Regulations for Fetal Research: A Case for Reform. Journal of Law, Medicine & Ethics 15 (3):126-138.
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  31.  4
    John C. Fletcher (2001). A Good Idea Whose Time Will Come. American Journal of Bioethics 1 (3):11 – 13.
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  32.  1
    Dorothy C. Wertz & John C. Fletcher (1989). Ethics and Genetics: An International Survey. Hastings Center Report 19 (4):20-24.
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  33.  1
    John C. Fletcher (1992). Ethics Committees and Due Process. Journal of Law, Medicine & Ethics 20 (4):291-293.
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  34. Alastair V. Campbell, John C. Fletcher, Andrew Jameton & William F. May (1985). Professional Care: Its Meaning and Practice. Journal of Religious Ethics 13 (2):360-363.
     
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  35. John C. Fletcher (1975). A Physician on Ethics. Hastings Center Report 5 (1):4-4.
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  36. John C. Fletcher (1992). Ethics Committees and Due Process. Journal of Law, Medicine and Ethics 20 (4):291-293.
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  37. John C. Fletcher & Kenneth J. Ryan (1987). Federal Regulations for Fetal Research: A Case for Reform. Journal of Law, Medicine and Ethics 15 (3):126-138.
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  38. John C. Fletcher & W. French Anderson (1992). Germ-Line Gene Therapy: A New Stage of Debate. Journal of Law, Medicine and Ethics 20 (1-2):26-39.
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  39. John C. Fletcher (forthcoming). Participation in Biomedical Research: The Consent Process as Viewed by Children, Adolescents, Young Adults, and Physicians. Research Ethics.
     
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  40. John C. Fletcher (1996). Responding to JCAHO Standards: Everybody's Business. Journal of Clinical Ethics 7 (2):182.
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  41. John C. Fletcher (1989). Standards for Evaluation of Ethics Consultation. In John C. Fletcher, Norman Quist & Albert R. Jonsen (eds.), Ethics Consultation in Health Care. Health Administration Press 171--184.
     
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  42. John C. Fletcher (1995). The Consultant's Credentials. Hastings Center Report 25 (4):39-40.
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  43. John C. Fletcher & D. Wertz (1990). The Price of Silence. Hastings Center Report 20 (3):31-35.
     
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  44. John C. Fletcher (1988). What Are Society's Interests in Human Genetics and Reproductive Technologies? Journal of Law, Medicine and Ethics 16 (1-2):131-137.
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  45. Mortimer B. Lipsett, John C. Fletcher & Marian Secundy (1979). Research Review at NIH. Hastings Center Report 9 (1):18-21.
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