Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Woodward, Beverly
1997.
Medical Record Confidentiality and Data Collection: Current Dilemmas.
Journal of Law, Medicine & Ethics,
Vol. 25,
Issue. 2-3,
p.
88.
1997.
Recent Developments in Health Law.
Journal of Law, Medicine & Ethics,
Vol. 25,
Issue. 4,
p.
314.
Bates, David W.
1997.
Commentary: Quality, Costs, Privacy and Electronic Medical Data.
Journal of Law, Medicine & Ethics,
Vol. 25,
Issue. 2-3,
p.
111.
1998.
Privacy and Medical-Records Research.
New England Journal of Medicine,
Vol. 338,
Issue. 15,
p.
1076.
Appelbaum, Paul S.
2000.
Protecting Privacy While Facilitating Research.
American Journal of Psychiatry,
Vol. 157,
Issue. 11,
p.
1725.
Sim, Ida
Owens, Douglas K.
Lavori, Philip W.
and
Rennels, Glenn D.
2000.
Electronic Trial Banks: A Complementary Method for Reporting Randomized Trials.
Medical Decision Making,
Vol. 20,
Issue. 4,
p.
440.
Wynia, Matthew K.
Coughlin, Steven S.
Alpert, Sheri
Cummins, Deborah S.
and
Emanuel, Linda L.
2001.
Shared expectations for protection of identifiable health care information.
Journal of General Internal Medicine,
Vol. 16,
Issue. 2,
p.
100.
Samarati, P.
2001.
Protecting respondents identities in microdata release.
IEEE Transactions on Knowledge and Data Engineering,
Vol. 13,
Issue. 6,
p.
1010.
Mandl, Kenneth D.
Feit, Shlomit
Larson, Cecilia
and
Kohane, Isaac S.
2002.
Newborn Screening Program Practices in the United States: Notification, Research, and Consent.
Pediatrics,
Vol. 109,
Issue. 2,
p.
269.
Blanchette, Jean-François
and
Johnson, Deborah G.
2002.
Data Retention and the Panoptic Society: The Social Benefits of Forgetfulness.
The Information Society,
Vol. 18,
Issue. 1,
p.
33.
Wactlar, H.D.
Christel, M.
Hauptmann, A.
Stevens, S.
and
Bbarucha, A.
2003.
A system of video information capture, indexing and retrieval for interpreting human activity.
Vol. 1,
Issue. ,
p.
278.
Waiden, Ian
2003.
Digital Anonymity and the Law.
Vol. 2,
Issue. ,
p.
147.
Wylie, Jean E
and
Mineau, Geraldine P
2003.
Biomedical databases: protecting privacy and promoting research.
Trends in Biotechnology,
Vol. 21,
Issue. 3,
p.
113.
Malin, Bradley
and
Sweeney, Latanya
2004.
How (not) to protect genomic data privacy in a distributed network: using trail re-identification to evaluate and design anonymity protection systems.
Journal of Biomedical Informatics,
Vol. 37,
Issue. 3,
p.
179.
Merz, Jon F.
McGee, Glenn E.
and
Sankar, Pamela
2004.
“Iceland Inc.”?: On the ethics of commercial population genomics.
Social Science & Medicine,
Vol. 58,
Issue. 6,
p.
1201.
Phillips, David J.
2004.
Privacy policy and PETs.
New Media & Society,
Vol. 6,
Issue. 6,
p.
691.
Ohno-Machado, Lucila
Silveira, Paulo Sérgio Panse
and
Vinterbo, Staal
2004.
Protecting patient privacy by quantifiable control of disclosures in disseminated databases.
International Journal of Medical Informatics,
Vol. 73,
Issue. 7-8,
p.
599.
Nicholson, Scott
and
Smith, Catherine Arnott
2005.
Using lessons from health care to protect the privacy of library users: Guidelines for the de‐identification of library data based on HIPAA.
Proceedings of the American Society for Information Science and Technology,
Vol. 42,
Issue. 1,
Friedman, Carol
2005.
Medical Informatics.
Vol. 8,
Issue. ,
p.
423.
Cooper, Ted
and
Collman, Jeff
2005.
Medical Informatics.
Vol. 8,
Issue. ,
p.
95.