219 related articles for article (PubMed ID: 16459412)
21. Tissue issues: the ethical dilemma of collecting human tissues for research.
Veatch RM
Taiwan Yi Xue Ren Wen Xue Kan; 2005 Sep; 6(1-2):3-13. PubMed ID: 16538762
[No Abstract] [Full Text] [Related]
22. The Babel of genetic data terminology.
Knoppers BM; Saginur M
Nat Biotechnol; 2005 Aug; 23(8):925-7. PubMed ID: 16082354
[No Abstract] [Full Text] [Related]
23. Can informed consent go too far? Balancing consent and public benefit in research.
Milner LC; Magnus D
Am J Bioeth; 2013; 13(4):1-2. PubMed ID: 23514383
[No Abstract] [Full Text] [Related]
24. Database research: public and private interests.
Arnason V
Camb Q Healthc Ethics; 2011 Oct; 20(4):563-71. PubMed ID: 21843387
[No Abstract] [Full Text] [Related]
25. Data citizenship and informed consent.
Francis LP; Francis JG
Am J Bioeth; 2013; 13(4):38-9. PubMed ID: 23514394
[No Abstract] [Full Text] [Related]
26. European biobanks forge cross-border ties.
Keogh B
J Natl Cancer Inst; 2011 Oct; 103(19):1429-31. PubMed ID: 21934073
[No Abstract] [Full Text] [Related]
27. Informed consent, big data, and the oxymoron of research that is not research.
Ioannidis JP
Am J Bioeth; 2013; 13(4):40-2. PubMed ID: 23514395
[No Abstract] [Full Text] [Related]
28. How and when does consent bias research?
Groenwold RH; van der Graaf R; van Delden JJ
Am J Bioeth; 2013; 13(4):46-8. PubMed ID: 23514398
[No Abstract] [Full Text] [Related]
29. Legal aspects of biobanks.
Macilotti M; Izzo U; Pascuzzi G; Barbareschi M
Pathologica; 2008 Apr; 100(2):86-115. PubMed ID: 18792524
[No Abstract] [Full Text] [Related]
30. [Ethical problems presented by collections of biological material and associated data: "biobanks", "bioethics"].
France. Comite consultatif national d'ethique pour les sciences de la vie et de la sante
J Int Bioethique; 2005; 16(3-4):141-51. PubMed ID: 17058808
[No Abstract] [Full Text] [Related]
31. The interaction between research consent and random error.
Trafimow D
Am J Bioeth; 2013; 13(4):49-50. PubMed ID: 23514399
[No Abstract] [Full Text] [Related]
32. A review of evidence on consent bias in research.
El Emam K; Jonker E; Moher E; Arbuckle L
Am J Bioeth; 2013; 13(4):42-4. PubMed ID: 23514396
[No Abstract] [Full Text] [Related]
33. Human gene banks.
Williams G
Med Ethics (Burlingt Mass); 2005; 12(1):1-2. PubMed ID: 15856601
[No Abstract] [Full Text] [Related]
34. Biobanking in the subcontinent: exploring concerns.
Jafarey AM; Shekhani SS; Shirazi B
Indian J Med Ethics; 2017; 2(4):248-254. PubMed ID: 28803222
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Patient consent in the era of de-identified research databases.
Anderson JR; Schonfeld TL
J Clin Oncol; 2006 Feb; 24(4):720-1. PubMed ID: 16446347
[No Abstract] [Full Text] [Related]
37. An unbiased response to the open peer commentaries on "does consent bias research?".
Rothstein MA; Shoben AB
Am J Bioeth; 2013; 13(4):W1-4. PubMed ID: 23514403
[No Abstract] [Full Text] [Related]
38. Is emergency research without initial consent justified? The consent substitute model.
Kierzek G; Rac V; Pourriat JL
Arch Intern Med; 2010 Sep; 170(16):1508-9; author reply 1509. PubMed ID: 20837844
[No Abstract] [Full Text] [Related]
39. Rules tightened for aboriginal studies.
Hoag H
Nature; 2007 May; 447(7142):241. PubMed ID: 17507944
[No Abstract] [Full Text] [Related]
40. Clarity and appeal of a multimedia informed consent tool for biobanking.
McGraw SA; Wood-Nutter CA; Solomon MZ; Maschke KJ; Bensen JT; Irwin DE
IRB; 2012; 34(1):9-19. PubMed ID: 22338402
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
