-
1
-
-
0018869385
-
Informed consent: How much does the patient understand?
-
Bergler, J. H., Pennington, A. C., Metcalfe, M., & Freis, E. D. (1980). Informed consent: How much does the patient understand? Clinical Pharmacology and Therapeutics, 27(4), 435-440.
-
(1980)
Clinical Pharmacology and Therapeutics
, vol.27
, Issue.4
, pp. 435-440
-
-
Bergler, J.H.1
Pennington, A.C.2
Metcalfe, M.3
Freis, E.D.4
-
2
-
-
77957228179
-
Simplifying informed consent for biorepositories: Stakeholder perspectives
-
Beskow, L. M., Friedman, J. Y., Hardy, N. C., Lin, L., & Weinfurt, K. P. (2010). Simplifying informed consent for biorepositories: Stakeholder perspectives. Genetics in Medicine, 12(9), 567-572.
-
(2010)
Genetics in Medicine
, vol.12
, Issue.9
, pp. 567-572
-
-
Beskow, L.M.1
Friedman, J.Y.2
Hardy, N.C.3
Lin, L.4
Weinfurt, K.P.5
-
3
-
-
84887501834
-
-
Code of Federal Regulations. Title 45, Part 46, Protection of human subjects
-
Code of Federal Regulations. Title 45, Part 46, Protection of human subjects. Retrieved from http://www.hhs.gov/ohrp/humansubjects/guidance/45cfr46. html.
-
-
-
-
4
-
-
80052857705
-
Human subjects research protections: Enhancing protections for research subjects and reducing burden, delay, and ambiguity for investigators. Advance notice of proposed rulemaking
-
Department of Health and Human Services
-
Department of Health and Human Services. 2011. Human subjects research protections: Enhancing protections for research subjects and reducing burden, delay, and ambiguity for investigators. Advance notice of proposed rulemaking. Federal Register, 76(143), 44512-44531. Retrieved from http://www.gpo.gov/fdsys/ pkg/FR-2011-07-26/html/2011-18792.htm.
-
(2011)
Federal Register
, vol.76
, Issue.143
, pp. 44512-44531
-
-
-
5
-
-
36048933619
-
Beyond misunderstanding: Written information and decisions about taking part in a genetic epidemiology study
-
Dixon-Woods, M., Ashcroft, R. E., Jackson, C. J., Tobin, M. D., Kivits, J., Burton, P. R., et al. (2007). Beyond misunderstanding: Written information and decisions about taking part in a genetic epidemiology study. Social Science and Medicine, 65(11), 2212-2222.
-
(2007)
Social Science and Medicine
, vol.65
, Issue.11
, pp. 2212-2222
-
-
Dixon-Woods, M.1
Ashcroft, R.E.2
Jackson, C.J.3
Tobin, M.D.4
Kivits, J.5
Burton, P.R.6
-
7
-
-
33748972418
-
Measuring trust in medical researchers
-
Hall, M. A., Camacho, F., Lawlor, J. S., Depuy, V., Sugarman, J., & Weinfurt, K. (2006). Measuring trust in medical researchers. Medical Care, 44(11), 1048-1053.
-
(2006)
Medical Care
, vol.44
, Issue.11
, pp. 1048-1053
-
-
Hall, M.A.1
Camacho, F.2
Lawlor, J.S.3
Depuy, V.4
Sugarman, J.5
Weinfurt, K.6
-
8
-
-
28244449608
-
How to handle informed consent in longitudinal studies when participants have a limited understanding of the study
-
Helgesson, G., Ludvigsson, J., & Gustafsson Stolt, U. (2005). How to handle informed consent in longitudinal studies when participants have a limited understanding of the study. Journal of Medical Ethics, 31(11), 670-673.
-
(2005)
Journal of Medical Ethics
, vol.31
, Issue.11
, pp. 670-673
-
-
Helgesson, G.1
Ludvigsson, J.2
Gustafsson Stolt, U.3
-
9
-
-
11844269810
-
The ethics of research using biobanks: Reason to question the importance attributed to informed consent
-
Hoeyer, K., Olofsson, B. O., Mjorndal, T., & Lynoe, N. (2005). The ethics of research using biobanks: Reason to question the importance attributed to informed consent. Archives of Internal Medicine, 165(1), 97-100.
-
(2005)
Archives of Internal Medicine
, vol.165
, Issue.1
, pp. 97-100
-
-
Hoeyer, K.1
Olofsson, B.O.2
Mjorndal, T.3
Lynoe, N.4
-
10
-
-
27844518793
-
Three approaches to qualitative content analysis
-
Hsieh, H. F., & Shannon, S. E. (2005). Three approaches to qualitative content analysis. Qualitative Health Research, 15(9), 1277-1288.
-
(2005)
Qualitative Health Research
, vol.15
, Issue.9
, pp. 1277-1288
-
-
Hsieh, H.F.1
Shannon, S.E.2
-
11
-
-
0035944839
-
Quality of informed consent in cancer clinical trials: A cross-sectional survey
-
Joffe, S., Cook, E. F., Cleary, P. D., Clark, J. W., & Weeks, J. C. (2001a). Quality of informed consent in cancer clinical trials: A cross-sectional survey. Lancet, 358(9295), 1772-1777.
-
(2001)
Lancet
, vol.358
, Issue.9295
, pp. 1772-1777
-
-
Joffe, S.1
Cook, E.F.2
Cleary, P.D.3
Clark, J.W.4
Weeks, J.C.5
-
12
-
-
0035900908
-
Quality of informed consent: A new measure of understanding among research subjects
-
Joffe, S., Cook, E. F., Cleary, P. D., Clark, J. W., & Weeks, J. C. (2001b). Quality of informed consent: A new measure of understanding among research subjects. Journal of National Cancer Institute, 93(2), 139-147.
-
(2001)
Journal of National Cancer Institute
, vol.93
, Issue.2
, pp. 139-147
-
-
Joffe, S.1
Cook, E.F.2
Cleary, P.D.3
Clark, J.W.4
Weeks, J.C.5
-
13
-
-
84859922074
-
The tension between data sharing and the protection of privacy in genomics research
-
Kaye, J. (2012). The tension between data sharing and the protection of privacy in genomics research. Annual Review of Genomics and Human Genetics, 13, 415-431.
-
(2012)
Annual Review of Genomics and Human Genetics
, vol.13
, pp. 415-431
-
-
Kaye, J.1
-
14
-
-
79960145563
-
Communicating genetic and genomic information: Health literacy and numeracy considerations
-
Lea, D. H., Kaphingst, K. A., Bowen, D., Lipkus, I., & Hadley, D. W. (2011). Communicating genetic and genomic information: Health literacy and numeracy considerations. Public Health Genomics, 14(4-5), 279-289.
-
(2011)
Public Health Genomics
, vol.14
, Issue.4-5
, pp. 279-289
-
-
Lea, D.H.1
Kaphingst, K.A.2
Bowen, D.3
Lipkus, I.4
Hadley, D.W.5
-
15
-
-
84867149839
-
A randomized controlled trial of short and standard-length consent forms for a genetic cohort study: Is longer better?
-
Matsui, K., Lie, R. K., Turin, T. C., & Kita, Y. (2012). A randomized controlled trial of short and standard-length consent forms for a genetic cohort study: Is longer better? Journal of Epidemiology, 22(4), 308-316.
-
(2012)
Journal of Epidemiology
, vol.22
, Issue.4
, pp. 308-316
-
-
Matsui, K.1
Lie, R.K.2
Turin, T.C.3
Kita, Y.4
-
17
-
-
38149081397
-
DNA data sharing: Research participants' perspectives
-
McGuire, A. L., Hamilton, J. A., Lunstroth, R., McCullough, L. B., & Goldman, A. (2008). DNA data sharing: Research participants' perspectives. Genetics in Medicine, 10(1), 46-53.
-
(2008)
Genetics in Medicine
, vol.10
, Issue.1
, pp. 46-53
-
-
McGuire, A.L.1
Hamilton, J.A.2
Lunstroth, R.3
McCullough, L.B.4
Goldman, A.5
-
18
-
-
80755139422
-
To share or not to share: A randomized trial of consent for data sharing in genome research
-
McGuire, A. L., Oliver, J. M., Slashinski, M. J., Graves, J. L., Wang, T., Kelly, P. A., et al. (2011). To share or not to share: A randomized trial of consent for data sharing in genome research. Genetics in Medicine, 13(10).
-
(2011)
Genetics in Medicine
, vol.13
, Issue.10
-
-
McGuire, A.L.1
Oliver, J.M.2
Slashinski, M.J.3
Graves, J.L.4
Wang, T.5
Kelly, P.A.6
-
20
-
-
0028795768
-
Validation of a decisional conflict scale
-
O'Connor, A. M. (1995). Validation of a decisional conflict scale. Medical Decision Making, 15(1), 25-30.
-
(1995)
Medical Decision Making
, vol.15
, Issue.1
, pp. 25-30
-
-
O'Connor, A.M.1
-
21
-
-
84857038889
-
Balancing the risks and benefits of genomic data sharing: Genome research participants' perspectives
-
Oliver, J. M., Slashinski, M. J., Wang, T., Kelly, P. A., Hilsenbeck, S. G., & McGuire, A. L. (2012). Balancing the risks and benefits of genomic data sharing: Genome research participants' perspectives. Public Health Genomics, 15(2), 106-114.
-
(2012)
Public Health Genomics
, vol.15
, Issue.2
, pp. 106-114
-
-
Oliver, J.M.1
Slashinski, M.J.2
Wang, T.3
Kelly, P.A.4
Hilsenbeck, S.G.5
McGuire, A.L.6
-
22
-
-
77957602401
-
How does feeling informed relate to being informed? The DECISIONS survey
-
Sepucha, K. R., Fagerlin, A., Couper, M. P., Levin, C. A., Singer, E., & Zikmund-Fisher, B. J. (2010). How does feeling informed relate to being informed? The DECISIONS survey. Medical Decision Making, 30(5 Suppl), 77S-84S.
-
(2010)
Medical Decision Making
, vol.30
, Issue.5 SUPPL.
-
-
Sepucha, K.R.1
Fagerlin, A.2
Couper, M.P.3
Levin, C.A.4
Singer, E.5
Zikmund-Fisher, B.J.6
-
23
-
-
14944357163
-
Information and informed consent in a longitudinal screening involving children: A questionnaire survey
-
Stolt, U. G., Helgesson, G., Liss, P. E., Svensson, T., & Ludvigsson, J. (2005). Information and informed consent in a longitudinal screening involving children: A questionnaire survey. European Journal of Human Genetics, 13(3), 376-383.
-
(2005)
European Journal of Human Genetics
, vol.13
, Issue.3
, pp. 376-383
-
-
Stolt, U.G.1
Helgesson, G.2
Liss, P.E.3
Svensson, T.4
Ludvigsson, J.5
-
26
-
-
42149126151
-
What should research participants understand to understand they are participants in research?
-
Wendler, D., & Grady, C. (2008). What should research participants understand to understand they are participants in research? Bioethics, 22(4), 203-208.
-
(2008)
Bioethics
, vol.22
, Issue.4
, pp. 203-208
-
-
Wendler, D.1
Grady, C.2
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