Literature DB >> 8230598

Privacy rules for DNA databanks. Protecting coded 'future diaries'.

G J Annas1.   

Abstract

In privacy terms, genetic information is like medical information. But the information contained in the DNA molecule itself is more sensitive because it contains an individual's probabilistic "future diary," is written in a code that has only partially been broken, and contains information about an individual's parents, siblings, and children. Current rules for protecting the privacy of medical information cannot protect either genetic information or identifiable DNA samples stored in DNA databanks. A review of the legal and public policy rationales for protecting genetic privacy suggests that specific enforceable privacy rules for DNA databanks are needed. Four preliminary rules are proposed to govern the creation of DNA databanks, the collection of DNA samples for storage, limits on the use of information derived from the samples, and continuing obligations to those whose DNA samples are in the databanks.

Entities:  

Keywords:  Genetics and Reproduction; Legal Approach

Mesh:

Substances:

Year:  1993        PMID: 8230598

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


  21 in total

Review 1.  Ethical reflections on pharmacogenetics and DNA banking in a cohort of HIV-infected patients.

Authors:  Sandrine de Montgolfier; Grégoire Moutel; Nathalie Duchange; Ioannis Theodorou; Christian Hervé; Catherine Leport
Journal:  Pharmacogenetics       Date:  2002-12

Review 2.  The nature and significance of behavioural genetic information.

Authors:  Ainsley Newson
Journal:  Theor Med Bioeth       Date:  2004

Review 3.  The routinisation of genomics and genetics: implications for ethical practices.

Authors:  M W Foster; C D M Royal; R R Sharp
Journal:  J Med Ethics       Date:  2006-11       Impact factor: 2.903

4.  Biological sample collections from minors for genetic research: a systematic review of guidelines and position papers.

Authors:  Kristien Hens; Herman Nys; Jean-Jacques Cassiman; Kris Dierickx
Journal:  Eur J Hum Genet       Date:  2009-08       Impact factor: 4.246

5.  Barbarians at the Gate: Consumer-Driven Health Data Commons and the Transformation of Citizen Science.

Authors:  Barbara J Evans
Journal:  Am J Law Med       Date:  2016-11

Review 6.  Can you keep a (genetic) secret? The genetic privacy movement.

Authors:  Margaret Everett
Journal:  J Genet Couns       Date:  2004-08       Impact factor: 2.537

Review 7.  Genetic research, adolescents, and informed consent.

Authors:  R F Weir; J R Horton
Journal:  Theor Med       Date:  1995-12

Review 8.  Advances in information technology. Implications for medical education.

Authors:  D R Masys
Journal:  West J Med       Date:  1998-05

Review 9.  Molecular genetic testing for adult-onset disorders: the evolving laboratory, physician, patient interface.

Authors:  R T Acton
Journal:  J Clin Lab Anal       Date:  1997       Impact factor: 2.352

Review 10.  Evolving approaches to the ethical management of genomic data.

Authors:  Jean E McEwen; Joy T Boyer; Kathie Y Sun
Journal:  Trends Genet       Date:  2013-02-28       Impact factor: 11.639

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