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Arthur L. Caplan
Researcher at New York University
Publications - 700
Citations - 15574
Arthur L. Caplan is an academic researcher from New York University. The author has contributed to research in topics: Transplantation & Bioethics. The author has an hindex of 57, co-authored 664 publications receiving 13978 citations. Previous affiliations of Arthur L. Caplan include University of Strasbourg & University of Pittsburgh.
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The OHRP and SUPPORT
Benjamin S. Wilfond,Benjamin S. Wilfond,David Magnus,Armand H. Matheny Antommaria,Armand H. Matheny Antommaria,Paul S. Appelbaum,Judy L. Aschner,Keith J. Barrington,Tom L. Beauchamp,Renee D. Boss,Wylie Burke,Arthur L. Caplan,Alexander Morgan Capron,Mildred K. Cho,Ellen Wright Clayton,F. Sessions Cole,Brian A Darlow,Douglas S. Diekema,Douglas S. Diekema,Ruth R. Faden,Chris Feudtner,Joseph J. Fins,Norman Fost,Joel Frader,D. Micah Hester,Annie Janvier,Steven Joffe,Jeffrey P. Kahn,Nancy E. Kass,Eric Kodish,John D. Lantos,Laurence B. McCullough,Ross E. McKinney,William Meadow,P. Pearl O'Rourke,Kathleen E. Powderly,DeWayne M. Pursley,Lainie Friedman Ross,Sadath Sayeed,Richard R. Sharp,Jeremy Sugarman,William Tarnow-Mordi,Holly A. Taylor,Tom Tomlinson,Robert D. Truog,Yoram Unguru,Kathryn L. Weise,David E Woodrum,David E Woodrum,Stuart J. Youngner +49 more
TL;DR: A group of medical ethicists and pediatricians asks for reconsideration of the recent Office for Human Research Protections decision about informed consent in SUPPORT.
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The politics of human-embryo research--avoiding ethical gridlock.
TL;DR: In late January 1996, President Bill Clinton signed a continuing resolution to keep the government open that prohibits the use of federal funds for research on human rights abuses.
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Clarifying the Language of Clinician Distress.
Journal ArticleDOI
Organ Transplants: The Costs of Success
TL;DR: David Caplan advocates a public policy of "presumed consent" whereby hospitals may harvest all suitable cadaver organs unless objection is indicated by family members or by the individual beforehand.
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Protecting Subjects’ Interests in Genetics Research
TL;DR: All participants should be given a voice in decisions affecting ownership, access to, and use of commercialized products and services, and that researchers and institutions should negotiate issues relating to control of research results and the sharing of benefits before the research is performed.