1
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The limitations of "vulnerability" as a protection for human research participants.
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Am J Bioeth
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2004
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14.06
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2
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Patients' views on identifiability of samples and informed consent for genetic research.
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Am J Bioeth
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2008
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5.73
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3
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Dealing with the long-term social implications of research.
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Am J Bioeth
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2011
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5.41
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4
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5.24
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5
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Ethics and best practice guidelines for training experiences in global health.
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5.05
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6
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4.94
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7
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A national survey of provisions in clinical-trial agreements between medical schools and industry sponsors.
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N Engl J Med
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4.42
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8
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3.58
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9
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Ethical goals of community consultation in research.
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Am J Public Health
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3.46
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10
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The cost of institutional review boards in academic medical centers.
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N Engl J Med
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3.06
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11
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Bioethics consultation in the private sector.
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Hastings Cent Rep
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3.01
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12
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The inescapable relevance of bioethics for the practicing clinician.
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2006
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2.70
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13
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New ISSCR guidelines underscore major principles for responsible translational stem cell research.
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Cell Stem Cell
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2008
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2.61
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14
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Protecting research subjects under the waiver of informed consent for emergency research: experiences with efforts to inform the community.
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15
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Ethical considerations for short-term experiences by trainees in global health.
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JAMA
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2.48
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16
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The Presidential Bioethics Commission's database of human subjects research.
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IRB
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2013
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1.98
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17
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Universal antiretroviral therapy for HIV infection: should US treatment guidelines be applied to resource-limited settings?
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Clin Infect Dis
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2013
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1.92
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18
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Informed consent in a clinical trial of a novel treatment for rheumatoid arthritis.
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1.86
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Measuring trust in medical researchers.
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Study of the media's potential influence on prospective research participants' understanding of and motivations for participation in a high-profile phase I trial.
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Do patients treated with dignity report higher satisfaction, adherence, and receipt of preventive care?
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Ann Fam Med
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1.62
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26
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Back to the rough ground: working in international HIV prevention as ethical debates continue.
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IRB
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1.62
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27
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Permission and assent for clinical research in pediatric anesthesia.
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Anesth Analg
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2002
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1.56
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28
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Ethical and practical issues associated with aggregating databases.
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PLoS Med
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2008
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1.53
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29
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Community hospital oversight of clinical investigators' financial relationships.
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IRB
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1.51
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30
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Patient reactions to confidentiality, liability, and financial aspects of informed consent in cardiology research.
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Circ Cardiovasc Qual Outcomes
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1.50
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31
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Applying justice in clinical trials for diverse populations.
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Clin Trials
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1.46
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32
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Policies of academic medical centers for disclosing financial conflicts of interest to potential research participants.
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Acad Med
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1.43
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33
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Untying the Gordian knot: policies, practices, and ethical issues related to banking of umbilical cord blood.
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J Clin Invest
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34
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Implications of universal screening for HIV infection.
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The Bio-PIN: a concept to improve biobanking.
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Nat Rev Cancer
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36
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Beyond "compliance": the role of institutional culture in promoting research integrity.
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1.30
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Preventive misconception: its nature, presence, and ethical implications for research.
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Am J Prev Med
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38
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Fertility patients' views about frozen embryo disposition: results of a multi-institutional U.S. survey.
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1.30
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39
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Regulatory challenges for the resuscitation outcomes consortium.
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Circulation
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1.26
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40
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Variability in the costs of institutional review board oversight.
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Acad Med
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1.25
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41
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Toward protecting the safety of participants in clinical trials.
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Control Clin Trials
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42
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Effects of disclosing financial interests on attitudes toward clinical research.
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1.23
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Improving informed consent: the medium is not the message.
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Controversy and quality improvement: lingering questions about ethics, oversight, and patient safety research.
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Ethical issues in identifying and recruiting participants for familial genetic research.
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Disclosing conflicts of interest in clinical research: views of institutional review boards, conflict of interest committees, and investigators.
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An intervention to improve cancer patients' understanding of early-phase clinical trials.
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Disclosure of cancer diagnosis and prognosis in Northern Tanzania.
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Developing ethics guidance for HIV prevention research: the HIV Prevention Trials Network approach.
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Establishing HIV treatment as prevention in the HIV Prevention Trials Network 052 randomized trial: an ethical odyssey.
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Reflecting on short-term international service-learning trips.
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Purpose and benefits of early phase cancer trials: what do oncologists say? What do patients hear?
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