Literature DB >> 15204918

Genetic Privacy: A Challenge to Medico-Legal Norms.

Stephanie L. Anderson1.   

Abstract

Year:  2004        PMID： 15204918     DOI： 10.1080/01947640490401975

Source DB:  PubMed          Journal:  J Leg Med        ISSN： 0194-7648


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  19 in total

1.  Genetic testing legislation in Western Europe-a fluctuating regulatory target.

Authors:  Sirpa Soini
Journal:  J Community Genet       Date:  2012-01-28

2.  Democracy and genetic privacy: the value of bodily integrity.

Authors:  Ludvig Beckman
Journal:  Med Health Care Philos       Date:  2005

3.  The complexities of ethical evaluation of genomics research.

Authors:  R Hoedemaekers; B Gordijn; Y Hekster; F van Agt
Journal:  HEC Forum       Date:  2006-03

4.  Questioning the consensus: managing carrier status results generated by newborn screening.

Authors:  Fiona Alice Miller; Jason Scott Robert; Robin Z Hayeems
Journal:  Am J Public Health       Date:  2008-12-04       Impact factor: 9.308

5.  Children, longitudinal studies, and informed consent.

Authors:  Gert Helgesson
Journal:  Med Health Care Philos       Date:  2005

6.  Support Seeking or Familial Obligation: An Investigation of Motives for Disclosing Genetic Test Results.

Authors:  Marisa Greenberg; Rachel A Smith
Journal:  Health Commun       Date:  2015-10-27

Review 7.  Communicating genetic information in the family: the familial relationship as the forgotten factor.

Authors:  Roy Gilbar
Journal:  J Med Ethics       Date:  2007-07       Impact factor: 2.903

8.  Inclusiveness, effectiveness and intrusiveness: issues in the developing uses of DNA profiling in support of criminal investigations.

Authors:  Robin Williams; Paul Johnson
Journal:  J Law Med Ethics       Date:  2005       Impact factor: 1.718

9.  Intrafamilial disclosure of risk for hereditary breast and ovarian cancer: points to consider.

Authors:  Lee Black; Kelly A McClellan; Denise Avard; Bartha Maria Knoppers
Journal:  J Community Genet       Date:  2012-12-29

10.  Caught you: threats to confidentiality due to the public release of large-scale genetic data sets.

Authors:  Matthias Wjst
Journal:  BMC Med Ethics       Date:  2010-12-29       Impact factor: 2.652
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