372 related articles for article (PubMed ID: 15986039)
1. Potential harms, anonymization, and the right to withdraw consent to biobank research.
Eriksson S; Helgesson G
Eur J Hum Genet; 2005 Sep; 13(9):1071-6. PubMed ID: 15986039
[TBL] [Abstract][Full Text] [Related]
2. The right to withdraw consent to research on biobank samples.
Helgesson G; Johnsson L
Med Health Care Philos; 2005; 8(3):315-21. PubMed ID: 16283494
[TBL] [Abstract][Full Text] [Related]
3. Building on relationships of trust in biobank research.
Hansson MG
J Med Ethics; 2005 Jul; 31(7):415-8. PubMed ID: 15994363
[TBL] [Abstract][Full Text] [Related]
4. Biobank research and the right to privacy.
Ursin LO
Theor Med Bioeth; 2008; 29(4):267-85. PubMed ID: 18855123
[TBL] [Abstract][Full Text] [Related]
5. Broadening consent--and diluting ethics?
Hofmann B
J Med Ethics; 2009 Feb; 35(2):125-9. PubMed ID: 19181887
[TBL] [Abstract][Full Text] [Related]
6. Withdrawing from research: a rethink in the context of research biobanks.
Holm S
Health Care Anal; 2011 Sep; 19(3):269-81. PubMed ID: 21918887
[TBL] [Abstract][Full Text] [Related]
7. A proposal for a model of informed consent for the collection, storage and use of biological materials for research purposes.
Porteri C; Borry P
Patient Educ Couns; 2008 Apr; 71(1):136-42. PubMed ID: 18243633
[TBL] [Abstract][Full Text] [Related]
8. Ethical genetic research on human subjects.
Harris J
Jurimetrics; 1999; 40():77-91. PubMed ID: 16285118
[TBL] [Abstract][Full Text] [Related]
9. Examining the public refusal to consent to DNA biobanking: empirical data from a Swedish population-based study.
Melas PA; Sjöholm LK; Forsner T; Edhborg M; Juth N; Forsell Y; Lavebratt C
J Med Ethics; 2010 Feb; 36(2):93-8. PubMed ID: 20133403
[TBL] [Abstract][Full Text] [Related]
10. The need to downregulate: a minimal ethical framework for biobank research.
Hansson MG
Methods Mol Biol; 2011; 675():39-59. PubMed ID: 20949383
[TBL] [Abstract][Full Text] [Related]
11. Rethinking research ethics.
Rhodes R
Am J Bioeth; 2005; 5(1):7-28. PubMed ID: 16036651
[TBL] [Abstract][Full Text] [Related]
12. Reconsidering the value of consent in biobank research.
Allen J; McNamara B
Bioethics; 2011 Mar; 25(3):155-66. PubMed ID: 19659851
[TBL] [Abstract][Full Text] [Related]
13. How not to rethink research ethics.
Beauchamp TL
Am J Bioeth; 2005; 5(1):31-3; author reply W15-8. PubMed ID: 16036653
[No Abstract] [Full Text] [Related]
14. [The origin of informed consent].
Mallardi V
Acta Otorhinolaryngol Ital; 2005 Oct; 25(5):312-27. PubMed ID: 16602332
[TBL] [Abstract][Full Text] [Related]
15. Confidentiality and autonomy: the challenge(s) of offering research participants a choice of disclosing their identity.
Giordano J; O'Reilly M; Taylor H; Dogra N
Qual Health Res; 2007 Feb; 17(2):264-75. PubMed ID: 17220396
[TBL] [Abstract][Full Text] [Related]
16. Biobank research, informed consent and society. Towards a new alliance?
D'Abramo F
J Epidemiol Community Health; 2015 Nov; 69(11):1125-8. PubMed ID: 25669218
[TBL] [Abstract][Full Text] [Related]
17. Ethical framework for previously collected biobank samples.
Helgesson G; Dillner J; Carlson J; Bartram CR; Hansson MG
Nat Biotechnol; 2007 Sep; 25(9):973-6. PubMed ID: 17846619
[No Abstract] [Full Text] [Related]
18. Informed consent in human subject research: a comparison of current international and Nigerian guidelines.
Fadare JO; Porteri C
J Empir Res Hum Res Ethics; 2010 Mar; 5(1):67-73. PubMed ID: 20235864
[TBL] [Abstract][Full Text] [Related]
19. The use of personal data from medical records and biological materials: ethical perspectives and the basis for legal restrictions in health research.
Regidor E
Soc Sci Med; 2004 Nov; 59(9):1975-84. PubMed ID: 15312931
[TBL] [Abstract][Full Text] [Related]
20. The right to withdraw from research.
Schaefer GO; Wertheimer A
Kennedy Inst Ethics J; 2010 Dec; 20(4):329-52. PubMed ID: 21338028
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
