Genetic information: Consumers' right to privacy versus insurance companies' right to know a public opinion survey [Book Review]
Journal of Business Ethics 19 (4):355 - 362 (1999)
Abstract
In this paper we present arguments for and against the disclosure of genetic information to the insurance companies. One of the main issues which emerges from these arguments is the question of who should be responsible for the health insurance costs of the individuals who are most likely to be affected by the disclosure of genetic information. The results of a resident opinion survey related to the above question are presented and public policy alternatives related to the survey findings are discussed at the end of this paper.Reprint years
2004
DOI
10.1023/a:1005716006206
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Citations of this work
The Use of Genetic Testing Information in the Insurance Industry: An Ethical and Societal Analysis of Public Policy Options.Paul Thistle, Gene Laczniak & Alexander Nill - 2019 - Journal of Business Ethics 156 (1):105-121.
Diminished or Just Different? A Factorial Vignette Study of Privacy as a Social Contract.Kirsten E. Martin - 2012 - Journal of Business Ethics 111 (4):519-539.
Protect My Privacy or Support the Common-Good? Ethical Questions About Electronic Health Information Exchanges.Corey M. Angst - 2009 - Journal of Business Ethics 90 (S2):169 - 178.
The Use of Data Mining by Private Health Insurance Companies and Customers’ Privacy.Yeslam Al-Saggaf - 2015 - Cambridge Quarterly of Healthcare Ethics 24 (3):281-292.
Considering Privacy as a Public Good and Its Policy Ramifications for Business Organizations.Shaheen Borna & Dheeraj Sharma - 2011 - Business and Society Review 116 (3):331-353.