-
1
-
-
68449097072
-
Public health genomics (PHG) and public participation: Points to consider
-
Avard, D. 2009. Public health genomics (PHG) and public participation: points to consider. Journal of Public Deliberation 5(1), Article 7. http://services.bepress.com/jpd/vol5/iss1/art7.
-
(2009)
Journal of Public Deliberation
, vol.5
, Issue.1
-
-
Avard, D.1
-
2
-
-
34247635153
-
Legal pathways for cross-border research: Building a legal platform for biomedical academia
-
Bovenberg, J. 2007. Legal pathways for cross-border research: building a legal platform for biomedical academia. European Journal of Human Genetics 15: 522–524. doi:10.1038/sj.ejhg.5 201792;publishedonline28.
-
(2007)
European Journal of Human Genetics
, vol.15
, pp. 522-524
-
-
Bovenberg, J.1
-
5
-
-
0032982890
-
From cultural diversity to universal ethics: Three models
-
Fleischacker, S. 1999. From cultural diversity to universal ethics: three models. Cultural Dynamics 11: 105–128.
-
(1999)
Cultural Dynamics
, vol.11
, pp. 105-128
-
-
Fleischacker, S.1
-
7
-
-
77949693630
-
Biobank governance in the post-genomic age
-
Gottweis, H., and G. Lauss. 2010. Biobank governance in the post-genomic age. Personalized Medicine 7(2): 187–195.
-
(2010)
Personalized Medicine
, vol.7
, Issue.2
, pp. 187-195
-
-
Gottweis, H.1
Lauss, G.2
-
9
-
-
3543141747
-
Informed consent and biobanks: A population-based study of attitudes towards tissue donation for genetic research
-
Hoeyer, K., et al. 2004. Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research. Scand Journal Public Health 32(3): 224–229.
-
(2004)
Scand Journal Public Health
, vol.32
, Issue.3
, pp. 224-229
-
-
Hoeyer, K.1
-
10
-
-
44249083211
-
Tracing biological collections: Between books and clinicaltrials
-
Kauffmann, F., and A. Cambon-Thomsen. 2008. Tracing biological collections: between books and clinicaltrials. JAMA 299(19): 2316–2318.
-
(2008)
JAMA
, vol.299
, Issue.19
, pp. 2316-2318
-
-
Kauffmann, F.1
Cambon-Thomsen, A.2
-
11
-
-
33748207767
-
Genetic research and donation of tissue samples to biobanks. What do potential sample donors in the Swedish general public think? The European Journals of
-
Kettis-Lindblad, A., et al. 2007a. Genetic research and donation of tissue samples to biobanks. What do potential sample donors in the Swedish general public think? The European Journals of Public Health 16(4): 433–440.
-
(2007)
Public Health
, vol.16
, Issue.4
, pp. 433-440
-
-
Kettis-Lindblad, A.1
-
12
-
-
34147147584
-
Perceptions of potential donors in the Swedish public towards information and consent procedures in relation to use of human tissue samples in biobanks: A population-based study
-
Kettis-Lindblad, A., et al. 2007b. Perceptions of potential donors in the Swedish public towards information and consent procedures in relation to use of human tissue samples in biobanks: a population-based study. Scand Journal Public Health 35(2): 148–156.
-
(2007)
Scand Journal Public Health
, vol.35
, Issue.2
, pp. 148-156
-
-
Kettis-Lindblad, A.1
-
13
-
-
0037063480
-
Attitudes toward biotechnology in the European Union
-
Pardo, R., et al. 2002. Attitudes toward biotechnology in the European Union. Journal of Biotechnology 98(1): 9–24.
-
(2002)
Journal of Biotechnology
, vol.98
, Issue.1
, pp. 9-24
-
-
Pardo, R.1
-
14
-
-
85098055754
-
The human sample exchange regulation navigator (HSERN): A tool to help researchers with the legal requirements for the exchange of biological material
-
eds. Jane Kaye, and Mark Stranger, Farnham: Ashgate
-
Rial-Sebbag, E., et al. 2009a. The human sample exchange regulation navigator (hSERN): a tool to help researchers with the legal requirements for the exchange of biological material. In Principles and practice in biobank governance, eds. Jane Kaye, and Mark Stranger, 191– 200. Farnham: Ashgate.
-
(2009)
Principles and Practice in Biobank Governance
, pp. 191-200
-
-
Rial-Sebbag, E.1
-
15
-
-
84953323979
-
From medical biobanks to research tools: Re-use of samples, governance and human rights
-
eds. Kris Dierickx, and Pascal Borry, Cambridge: Intersentia
-
Rial-Sebbag, E., et al. 2009b. From medical biobanks to research tools: re-use of samples, governance and human rights. In New challenges for biobanks: ethics, law and governance, eds. Kris Dierickx, and Pascal Borry, 87–94. Cambridge: Intersentia.
-
(2009)
New Challenges for Biobanks: Ethics, Law and Governance
, pp. 87-94
-
-
Rial-Sebbag, E.1
-
16
-
-
76249122986
-
Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns
-
Tupasela, A., et al. 2010. Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns. Scandinavian Journal of Public Health 38(1): 46–52.
-
(2010)
Scandinavian Journal of Public Health
, vol.38
, Issue.1
, pp. 46-52
-
-
Tupasela, A.1
-
18
-
-
85098080268
-
-
Wallace, S., et al. 2008. Ethics and policymaking core, Centre de recherche en droit public (CRDP), Université de Montréal. Available on line at
-
Wallace, S., et al. 2008. Ethics and policymaking core, Centre de recherche en droit public (CRDP), Université de Montréal. Available on line at http://www.p3gobservatory.org/repository/ethics.htm.
-
-
-
-
19
-
-
38049144317
-
Biobanking for Europe
-
Yuille, M., et al. 2008. Biobanking for Europe. Brief Bioinform 9(1): 14–24.
-
(2008)
Brief Bioinform
, vol.9
, Issue.1
, pp. 14-24
-
-
Yuille, M.1
|