The Icelandic Healthcare Database and Informed Consent
- 15 June 2000
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 342 (24), 1827-1830
- https://doi.org/10.1056/nejm200006153422411
Abstract
Modern information technology is rapidly changing how new knowledge is discovered in most fields of science, including medicine. This technology offers interesting possibilities in the development of methods to understand diseases better, but it also presents new ethical challenges. The new technology offers the possibility of mining large data sets for knowledge, without a priori hypotheses, by systematically juxtaposing various data in the search for the best fit. This kind of pure combinatorial analysis may be particularly powerful in the case of the common diseases, most of which are complex and have remained beyond the reach of the classic hypothesis-driven . . .Keywords
This publication has 6 references indexed in Scilit:
- Gene Therapy on TrialScience, 2000
- A Model Agreement for Genetic Research in Socially Identifiable PopulationsAmerican Journal of Human Genetics, 1998
- Population Genomics: Laying the Groundwork for Genetic Disease Modeling and Targetingcclm, 1998
- Informed consent for genetic research on stored tissue samplesPublished by American Medical Association (AMA) ,1995
- Genetic prophecy and genetic privacy--can we prevent the dream from becoming a nightmare?American Journal of Public Health, 1995
- Generic Consent for Genetic ScreeningNew England Journal of Medicine, 1994