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  1. The silent world of doctor and patient.Jay Katz - 1984 - Baltimore: Johns Hopkins University Press.
    In this eye-opening look at the doctor-patient decision-making process, physician and law professor Jay Katz examines the time-honored belief in the virtue of silent care and patient compliance. Historically, the doctor-patient relationship has been based on a one-way trust -- despite recent judicial attempts to give patients a greater voice through the doctrine of informed consent. Katz criticizes doctors for encouraging patients to relinquish their autonomy, and demonstrates the detrimental effect their silence has on good patient care. Seeing a growing (...)
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  2.  31
    The Silent World of Doctor and Patient.Daniel Callahan & Jay Katz - 1984 - Hastings Center Report 14 (6):47.
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  3.  34
    Why Doctors Don't Disclose Uncertainty.Jay Katz - 1984 - Hastings Center Report 14 (1):35-44.
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  4.  25
    “Ethics and Clinical Research” Revisited: A Tribute to Henry K. Beecher.Jay Katz - 1993 - Hastings Center Report 23 (5):31-39.
    The doctrine of informed consent, borrowed from the law of torts, cannot be readily transplanted into therapeutic settings. The broader, as yet unrealized, idea of informed consent, which suggests that parties must make decisions jointly, should guide interactions between physicians and patients or investigators and subjects.
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  5.  41
    The Regulation of Human Experimentation in the United States: A Personal Odyssey.Jay Katz - 1987 - IRB: Ethics & Human Research 9 (1):1.
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  6.  14
    Catastrophic Diseases: Who Decides What?Jay Katz & Alexander Morgan Capron - 1975 - Russell Sage Foundation.
    People do not choose to suffer from catastrophic illnesses, but considerable human choice is involved in the ways in which the participants in the process treat and conduct research on these diseases. Catastrophic Diseases draws a powerful and humane portrait of the patients who suffer from these illnesses as well as of the physician-investigators who treat them, and describes the major pressures, conflicts, and decisions which confront all of them. By integrating a discussion of "facts" and "values," the authors highlight (...)
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  7.  25
    Do We Need Another Advisory Commission on Human Experimentation?Jay Katz - 1995 - Hastings Center Report 25 (1):29-31.
    Instead of another federal advisory panel to identify ethical principles governing human subjects research, it is time we had a national board with authority to regulate and review such research.
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  8.  25
    Blurring the Lines: Research, Therapy, and IRBs.Jay Katz - 1997 - Hastings Center Report 27 (1):9-11.
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  9.  10
    On Touching "The Happy Isles": Reflections about Past, Future, and Present.Jay Katz - 1989 - Journal of Law, Medicine and Ethics 17 (2):110-113.
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  10.  49
    Reflections on Unethical Experiments and the Beginnings of Bioethics in the United States.Jay Katz - 1994 - Kennedy Institute of Ethics Journal 4 (2):85-92.
    The author offers personal reflections on the development of research ethics in the United States, primarily during the 1960s. He explores the efforts of the pioneers in the field of human experimentation ethics to raise and discuss issues such as the value conflict between the acquisition of knowledge and respect for the autonomy of research subjects and the crucial importance of disclosure in the informed consent process.
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  11.  25
    Some Basic Questions About Human Research.Jay Katz, Alexander M. Capron & Eleanor Swift Glass - 1972 - Hastings Center Report 2 (6):1-3.
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  12.  10
    The Senate's Definition of Voluntary and Informed Consent: Another View.Jay Katz - 1980 - IRB: Ethics & Human Research 2 (6):5.
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    Talking with Patients. [REVIEW]Jay Katz & Eric J. Cassell - 1986 - Hastings Center Report 16 (3):41.
    Book reviewed in this article: Talking with Patients. By Eric J. Cassell.
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