Informed consent for biobanking: consensus-based guidelines for adequate comprehension
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Kevin P. Weinfurt | Laura M. Beskow | K. Weinfurt | L. Beskow | C. Dombeck | C. Thompson | J. K. Watson-Ormond | Carrie B. Dombeck | Cole P. Thompson | J. Kemp Watson-Ormond | Carrie Dombeck | Laura M Beskow | Carrie B Dombeck | Ma | Cole P Thompson | J. Kemp Watson-Ormond | Kevin P Ba | Weinfurt
[1] Alanna Kulchak Rahm,et al. Biobanking for research: a survey of patient population attitudes and understanding , 2013, Journal of Community Genetics.
[2] K. Weinfurt,et al. Simplifying informed consent for biorepositories: Stakeholder perspectives , 2010, Genetics in Medicine.
[3] D. Wendler. Can we ensure that all research subjects give valid consent? , 2004, Archives of internal medicine.
[4] Monya Baker,et al. Biorepositories: Building better biobanks , 2012, Nature.
[5] Kari Sand,et al. The Understanding of Informed Consent Information—Definitions and Measurements in Empirical Studies , 2010 .
[6] L. Damschroder,et al. Assessing the quality of democratic deliberation: a case study of public deliberation on the ethics of surrogate consent for research. , 2010, Social science & medicine.
[7] David Wendler,et al. What Should Research Participants Understand to Understand They are Participants in Research? , 2008, Bioethics.
[8] S Holm,et al. Principles of Biomedical Ethics, 5th edn. , 2002 .
[9] F. Collins,et al. Keeping pace with the times--the Genetic Information Nondiscrimination Act of 2008. , 2008, The New England journal of medicine.
[10] F. Hasson,et al. Research guidelines for the Delphi survey technique. , 2000, Journal of advanced nursing.
[11] R. D. de Vries,et al. Assessing the Public's Views in Research Ethics Controversies: Deliberative Democracy and Bioethics as Natural Allies , 2009, Journal of empirical research on human research ethics : JERHRE.
[12] J. Couzin-Frankel. Ethics. DNA returned to tribe, raising questions about consent. , 2010, Science.
[13] James Flory,et al. Interventions to improve research participants' understanding in informed consent for research: a systematic review. , 2004, JAMA.
[14] N. Black,et al. Consensus Development Methods: A Review of Best Practice in Creating Clinical Guidelines , 1999, Journal of health services research & policy.
[15] Laura Lyman Rodriguez,et al. Responsible Research: A Systems Approach to Protecting Research Participants , 2003 .
[16] G. Henderson,et al. Characterizing biobank organizations in the U.S.: results from a national survey , 2013, Genome Medicine.
[17] D. Check,et al. Research Participants’ Understanding of and Reactions to Certificates of Confidentiality , 2014, AJOB primary research.
[18] Michelle M Mello,et al. The Havasupai Indian tribe case--lessons for research involving stored biologic samples. , 2010, The New England journal of medicine.
[19] E. Callaway. HeLa publication brews bioethical storm , 2013, Nature.
[20] R. Brook,et al. Consensus methods: characteristics and guidelines for use. , 1984, American journal of public health.
[21] Catherine A. McCarty,et al. Informed Consent and Subject Motivation to Participate in a Large, Population-Based Genomics Study: The Marshfield Clinic Personalized Medicine Research Project , 2006, Public Health Genomics.
[22] J. Sheikh,et al. Effective use of consent forms and interactive questions in the consent process. , 2008, IRB.
[23] K. Weinfurt,et al. Developing a Simplified Consent Form for Biobanking , 2010, PloS one.
[24] Rosalind Raine,et al. A comparison of formal consensus methods used for developing clinical guidelines , 2006, Journal of health services research & policy.
[25] Jim Vaught,et al. The evolution of biobanking best practices. , 2012, Clinica chimica acta; international journal of clinical chemistry.
[26] Wendy A. Wolf,et al. Assessing the understanding of biobank participants , 2009, American journal of medical genetics. Part A.
[27] S. Niemeyer,et al. Informed consent in biobank research: a deliberative approach to the debate. , 2009, Social science & medicine.
[28] P. Appelbaum. Understanding “Understanding”: An Important Step Toward Improving Informed Consent to Research , 2010 .
[29] Glenn Regehr,et al. Delphi as a method to establish consensus for diagnostic criteria. , 2003, Journal of clinical epidemiology.
[30] F. Hasson,et al. The Delphi Technique in Nursing and Health Research , 2011 .
[31] A. McGuire,et al. Informed consent in genomics and genetic research. , 2010, Annual review of genomics and human genetics.
[32] Marianne K Henderson,et al. Biospecimens and Biorepositories: From Afterthought to Science , 2012, Cancer Epidemiology, Biomarkers & Prevention.
[33] J. Brady,et al. The Belmont Report. Ethical principles and guidelines for the protection of human subjects of research. , 2014, The Journal of the American College of Dentists.
[34] S. Athar. Principles of Biomedical Ethics , 2011, The Journal of IMA.
[35] Ezekiel J Emanuel,et al. Reforming the regulations governing research with human subjects. , 2011, The New England journal of medicine.
[36] S. Levitus,et al. US Government Printing Office , 1998 .