Christine Grady
#12,389
Most Influential Person Now
Nurse-bioethicist and researcher
Christine Grady's AcademicInfluence.com Rankings
Christine Gradyphilosophy Degrees
Philosophy
#825
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#1595
Historical Rank
#363
USA Rank
Bioethics
#5
World Rank
#5
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#3
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Applied Ethics
#5
World Rank
#5
Historical Rank
#2
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Ethics
#78
World Rank
#100
Historical Rank
#38
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Nursing Philosophy
Christine Grady's Degrees
- Bachelors Nursing Georgetown University
- Masters Nursing Boston College
- PhD Philosophy Georgetown University
Why Is Christine Grady Influential?
(Suggest an Edit or Addition)According to Wikipedia, Christine Grady is an American nurse and bioethicist who serves as the head of the Department of Bioethics at the National Institutes of Health Clinical Center. Early life and education Grady was born and raised in Livingston, New Jersey. Her father, John H. Grady Jr., was a graduate of Yale University and a U.S. Navy veteran who served as the mayor of Livingston. Her mother, Barbara, was an assistant dean at Seton Hall University School of Law.
Christine Grady's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- What makes clinical research ethical? (2000) (2213)
- What makes clinical research in developing countries ethical? The benchmarks of ethical research. (2004) (868)
- Risks and benefits of phase 1 oncology trials, 1991 through 2002. (2005) (399)
- Clinical Trials and Medical Care: Defining the Therapeutic Misconception (2007) (394)
- What's the price of a research subject? Approaches to payment for research participation. (1999) (375)
- How much is life worth: cetuximab, non-small cell lung cancer, and the $440 billion question. (2009) (355)
- Ethical climate, ethics stress, and the job satisfaction of nurses and social workers in the United States. (2007) (352)
- Payment of clinical research subjects. (2005) (308)
- Misunderstanding in clinical research: distinguishing therapeutic misconception, therapeutic misestimation, and therapeutic optimism. (2003) (270)
- The Limitations of “Vulnerability” as a Protection for Human Research Participants (2004) (261)
- Money for Research Participation: Does It Jeopardize Informed Consent? (2001) (249)
- A Systematic Review of the Empirical Literature Evaluating IRBs: What We Know and What We Still Need to Learn (2011) (242)
- Everyday ethics: ethical issues and stress in nursing practice. (2010) (220)
- Does Ethics Education Influence the Moral Action of Practicing Nurses and Social Workers? (2008) (211)
- Broad Consent for Research With Biological Samples: Workshop Conclusions (2015) (207)
- Enrolling pregnant women: issues in clinical research. (2013) (202)
- Women’s autonomy in health care decision-making in developing countries: a synthesis of the literature (2016) (197)
- Oversight of Human Participants Research: Identifying Problems To Evaluate Reform Proposals (2004) (182)
- Enduring and emerging challenges of informed consent. (2015) (173)
- More than the money: a review of the literature examining healthy volunteer motivations. (2011) (165)
- Patients' decision-making process regarding participation in phase I oncology research. (2006) (161)
- Moral standards for research in developing countries: from "reasonable availability" to "fair benefits". (2004) (156)
- The quality of informed consent: mapping the landscape. A review of empirical data from developing and developed countries (2012) (153)
- Paying Research Subjects: An Analysis of Current Policies (2002) (147)
- A Broader Understanding of Moral Distress (2016) (146)
- Covid‐19: Ethical Challenges for Nurses (2020) (140)
- SHEA Guideline for Management of Healthcare Workers Who Are Infected with Hepatitis B Virus, Hepatitis C Virus, and/or Human Immunodeficiency Virus (2010) (131)
- Enduring and emerging challenges of informed consent. (2015) (128)
- The ethical challenge of infection-inducing challenge experiments. (2001) (122)
- Ethics: Fair benefits for research in developing countries: Participants in the 2001 conference on ethical aspects of research in developing countries (2002) (120)
- An ethical framework for biomedical research (2008) (118)
- The ethics of experimenting with human brain tissue (2018) (110)
- The ethics of paying for children's participation in research. (2002) (109)
- Moral Distress: A Growing Problem in the Health Professions? (2010) (106)
- An analysis of U.S. practices of paying research participants. (2005) (102)
- Descriptions of benefits and risks in consent forms for phase 1 oncology trials. (2002) (100)
- The 2000 revision of the Declaration of Helsinki: a step forward or more confusion? (2001) (98)
- The standard of care debate: the Declaration of Helsinki versus the international consensus opinion (2004) (93)
- Money, coercion, and undue inducement: attitudes about payments to research participants. (2012) (92)
- Reframing Consent for Clinical Research: A Function-Based Approach (2017) (89)
- Institutional Review Boards: Purpose and Challenges. (2015) (88)
- Clinical research with economically disadvantaged populations (2007) (87)
- Including persons with HIV infection in cancer clinical trials. (2008) (83)
- What Should Research Participants Understand to Understand They are Participants in Research? (2008) (83)
- A Response to Commentators on “The Limitations of ‘Vulnerability’ as a Protection for Human Research Participants” (2004) (81)
- The Invisible Hand in Clinical Research: The Study Coordinator's Critical Role in Human Subjects Protection (2002) (81)
- The ethics of placebo-controlled trials: methodological justifications. (2013) (80)
- Do IRBs protect human research participants? (2010) (80)
- Clinical vs. sonographic estimate of birth weight in term parturients. A randomized clinical trial. (2000) (72)
- Comprehension and informed consent: assessing the effect of a short consent form. (2010) (70)
- Respondent burden in clinical research: when are we asking too much of subjects? (2005) (69)
- Does It Pay to Pay?: A Randomized Trial of Prepaid Financial Incentives and Lottery Incentives in Surveys of Nonphysician Healthcare Professionals (2005) (69)
- Ethical considerations in HIV cure research: points to consider (2013) (65)
- Why patients continue to participate in clinical research. (2008) (64)
- The Ancillary-Care Obligations of Medical Researchers Working in Developing Countries (2008) (62)
- Predictors of Ethical Stress, Moral Action and Job Satisfaction in Health Care Social Workers (2008) (60)
- Neuroethics in the Age of Brain Projects (2016) (59)
- Moral Distress in the Health Professions (2018) (58)
- Four Paradigms of Clinical Research and Research Oversight (2006) (57)
- The quality of informed consent in a clinical research study in Thailand. (2005) (56)
- The challenge of assuring continued post-trial access to beneficial treatment. (2005) (56)
- Misconceptions About Coercion and Undue Influence: Reflections on the Views of IRB Members (2013) (56)
- Informed Consent. (2017) (55)
- Quality of parental consent in a Ugandan malaria study. (2005) (52)
- Commonly performed procedures in clinical research: a benchmark for payment. (2012) (51)
- Developing a Model of the Benefits and Burdens of Research Participation in Cancer Clinical Trials (2012) (48)
- Participants in phase 1 oncology research trials: are they vulnerable? (2008) (48)
- Clinical research enrolling pregnant women: a workshop summary. (2011) (46)
- Ethics of clinical research in the developing world (2002) (43)
- Randomization to standard and concise informed consent forms: development of evidence-based consent practices. (2012) (43)
- Neuroethics Guiding Principles for the NIH BRAIN Initiative (2018) (43)
- Motivations, enrollment decisions, and socio-demographic characteristics of healthy volunteers in phase 1 research (2017) (42)
- Fair Benefits for Research in Developing Countries (2002) (42)
- FACTORS ASSOCIATED WITH WOMEN'S HEALTH CARE DECISION-MAKING AUTONOMY: EMPIRICAL EVIDENCE FROM NIGERIA. (2018) (42)
- Science, technology, and innovation: nursing responsibilities in clinical research. (2009) (41)
- Ethical Challenges of Risk, Informed Consent, and Posttrial Responsibilities in Human Research With Neural Devices: A Review. (2019) (41)
- Bioethical considerations of monoclonal B‐cell lymphocytosis: donor transfer after haematopoietic stem cell transplantation (2007) (41)
- Views of Adolescents and Parents on Pediatric Research Without the Potential for Clinical Benefit (2012) (41)
- "Ethics and Clinical Research"--The 50th Anniversary of Beecher's Bombshell. (2016) (40)
- The Limits of Disclosure: What Research Subjects Want to Know about Investigator Financial Interests (2006) (40)
- Ethics in the time of COVID (2020) (39)
- Assent in research: the voices of adolescents. (2014) (39)
- Nurses confronting the coronavirus: Challenges met and lessons learned to date (2020) (39)
- Vulnerability in Research: Individuals with Limited Financial and/or Social Resources (2009) (38)
- COVID-19 vaccine trial ethics once we have efficacious vaccines (2020) (38)
- Ethics Education in Nursing: Instruction for Future Generations of Nurses (2018) (36)
- Nurse Practitioners' attitudes about cancer clinical trials and willingness to recommend research participation. (2012) (36)
- Points to consider: The research ethics consultation service and the IRB. (2009) (36)
- The misguided ethics of crossover trials. (2014) (35)
- Points to consider (2009) (33)
- Regional ethics organizations for protection of human research participants (2004) (33)
- Fatigue in HIV-infected men receiving investigational interleukin-2. (1998) (33)
- Detection and Management of Geographic Disparities in the TOPCAT Trial (2016) (32)
- Reciprocity and post-trial access for participants in antiretroviral therapy trials (2006) (31)
- Autonomy and couples’ joint decision-making in healthcare (2018) (31)
- Research vulnerability and patient advocacy: balance-seeking perspectives for the clinical nurse scientist? (2002) (30)
- Research on stored biological samples: the views of Ugandans. (2005) (30)
- Philosophical justifications of informed consent in research (2008) (29)
- Science in the service of healing. (1998) (29)
- Quality Improvement and Ethical Oversight (2007) (29)
- Exploring the ethics of clinical research in an urban community. (2006) (28)
- Undue worry about paying research participants (2012) (28)
- Ethics of vaccine research (2004) (28)
- The NIH BRAIN Initiative: Integrating Neuroethics and Neuroscience (2019) (27)
- Special Scrutiny: A Targeted Form of Research Protocol Review (2004) (27)
- Clinical research: Should patients pay to play? (2015) (27)
- A randomized trial comparing concise and standard consent forms in the START trial (2017) (26)
- To friend or not to friend: the use of social media in clinical oncology. (2012) (25)
- A Clinical Service to Support the Return of Secondary Genomic Findings in Human Research. (2016) (25)
- The Search for an AIDS Vaccine: Ethical Issues in the Development and Testing of a Preventive HIV Vaccine (1995) (25)
- An update on biostatistics requirements in U.S. medical schools (1998) (25)
- Palliative Care: A Supportive Adjunct to Pediatric Phase I Clinical Trials for Anticancer Agents? (2004) (25)
- Circumcision and HIV prevention research: an ethical analysis (2006) (25)
- Planning for posttrial access to antiretroviral treatment for research participants in developing countries. (2009) (25)
- Exploring Decision‐Making of HIV‐Infected Hispanics and African Americans Participating in Clinical Trials (2011) (24)
- Post-trial access to tested interventions: the views of IRB/REC chair, investigators, and research participants in a multinational HIV/AIDS study. (2006) (24)
- Phase 1 healthy volunteer willingness to participate and enrollment preferences (2017) (24)
- Ethics and genetic testing. (1999) (23)
- Cancer clinical trial participants' assessment of risk and benefit (2016) (23)
- Is It Ethical to Use Genealogy Data to Solve Crimes? (2018) (23)
- Dealing With the Long-Term Social Implications of Research (2011) (23)
- Ethical issues in cancer chemoprevention trials: considerations for IRBs and investigators. (2007) (22)
- Research into a functional cure for HIV in neonates: the need for ethical foresight. (2014) (22)
- Introduction: The Fogarty International Research Ethics Education and Curriculum Development Program in Historical Context (2013) (22)
- Responsiveness to Host Community Health Needs (2007) (21)
- Research Ethics Consultation: A Casebook (2012) (20)
- Personal and community benefits and harms of research: views from Rakai, Uganda (2007) (19)
- Ethical issues in clinical trials. (1991) (19)
- Ethical Conflict in Nurse Practitioners and Physician Assistants in Managed Care (2006) (18)
- So much at stake: Ethical tradeoffs in accelerating SARSCoV-2 vaccine development (2020) (18)
- Research benefits for hypothetical HIV vaccine trials: The views of Ugandans in the Rakai District. (2008) (18)
- Patient and Family Descriptions of Ethical Concerns (2020) (18)
- Ethical Principles in Clinical Research (2007) (17)
- Conducting HIV Research in Racial and Ethnic Minority Communities: Building a Successful Interdisciplinary Research Team (2011) (17)
- The impact of ethics and work-related factors on nurse practitioners' and physician assistants' views on quality of primary healthcare in the United States. (2014) (17)
- The ethics of uninsured participants accessing healthcare in biomedical research: A literature review (2018) (16)
- Ethics of international research: what does responsiveness mean? (2006) (16)
- Enrolling Minors in COVID-19 Vaccine Trials (2020) (16)
- Financial incentives and response rates in nursing research. (2004) (16)
- Ethical considerations of COVID-19-related adjustments to clinical research (2021) (15)
- The Ethics of Empowering Patients as Partners in Healthcare-Associated Infection Prevention (2014) (15)
- Making the transition to a learning health care system. Commentary. (2013) (15)
- Data and Safety Monitoring Board evaluation and management of a renal adverse event signal in TOPCAT (2017) (15)
- Cardiopulmonary Resuscitation for Ebola patients: Ethical considerations (2015) (15)
- Informing egg donors of the potential for embryonic research: a survey of consent forms from U.S. in vitro fertilization clinics. (2012) (14)
- Post-trial responsibilities beyond post-trial access (2018) (14)
- Deciphering assumptions about stepped wedge designs: the case of Ebola vaccine research (2016) (14)
- Does fear of retaliation deter requests for ethics consultation? (2008) (14)
- Confidentiality: A Survey in a Research Hospital (1991) (14)
- A consent form template for phase I oncology trials. (2009) (14)
- Investigating chronic symptoms in HIV: an opportunity for collaborative nursing research. (1995) (13)
- Development and Preliminary Testing of the Perceived Benefit and Burden Scales for Cancer Clinical Trial Participation (2018) (13)
- Zika Virus: Promoting Male Involvement in the Health of Women and Families (2016) (13)
- Benefits and Burdens of Participation in a Longitudinal Clinical Trial (2009) (13)
- The Continued Complexities of Paying Research Participants (2019) (13)
- Informed consent: practices and views of investigators in a multinational clinical trial. (2005) (12)
- Genethics (1995) (12)
- Incentives for Research Participants (2008) (12)
- A New Ethical Framework for Assessing the Unique Challenges of Fetal Therapy Trials (2021) (12)
- Empirical evaluation of the need for ‘on-going consent’ in clinical research (2011) (12)
- The Role of the Virtuous Investigator in Protecting Human Research Subjects (2016) (11)
- Contrasting Views of Risk Perception and Influence of Financial Compensation Between Adolescent Research Participants and Their Parents (2015) (11)
- The nursing shortage and the quality of care. (2002) (11)
- Cancer Clinical Trial Patient-Participants’ Perceptions about Provider Communication and Dropout Intentions (2019) (9)
- Healthcare professional narratives on moral distress: Disciplinary perspectives (2018) (9)
- Body composition in clinically stable men with HIV infection. (1996) (9)
- Acquired immunodeficiency syndrome: The impact on professional nursing practice (1989) (9)
- Innovative approaches to track lymph node germinal center responses to evaluate development of broadly neutralizing antibodies in human HIV vaccine trials. (2018) (9)
- Is Longer Always Better (2008) (8)
- NeuroEthics and the BRAIN Initiative: Where Are We? Where Are We Going? (2020) (8)
- Oncology clinical trials (2013) (7)
- Response: Re: How Much Is Life Worth: Cetuximab, Non–Small Cell Lung Cancer, and the $440 Billion Question (2010) (7)
- Children as hematopoietic cell donors in research: when is it approvable? (2015) (7)
- The Contribution of Ethics Review to Protection of Human Participants: Comment on “Measuring the Quality and Performance of Institutional Review Boards” (2019) (7)
- Informed consent and patient registry for the rare disease community: Editorial. (2012) (7)
- A Proposed Process for Reliably Updating the Common Rule (2017) (7)
- HIV preventive vaccine research: selected ethical issues. (1994) (7)
- The Standard of Care in Multinational Research (2008) (7)
- Comprar The Oxford Textbook of Clinical Research Ethics | David D. Wendler | 9780199768639 | Oxford University Press (2011) (6)
- Reflections on Two Decades of Bioethics: Where We Have Been and Where We Are Going (2013) (6)
- Research on very early ART in neonates at risk of HIV infection. (2014) (6)
- Reported consent processes and demographics: a substudy of the INSIGHT Strategic Timing of AntiRetroviral Treatment (START) trial (2015) (6)
- Motivations and decision-making of adult sickle cell patients in high-risk clinical research. (2020) (6)
- Ethical challenges for a new generation of early-phase pediatric gene therapy trials (2021) (6)
- Self-assessed learning needs of oncology nurses caring for individuals with HIV-related disorders: A national survey (1990) (6)
- Ethical issues in providing nursing care to human immunodeficiency virus-infected populations. (1989) (6)
- Grappling with global concerns in the search for an HIV vaccine. (1999) (6)
- Chapter 2 – Ethical Principles in Clinical Research (2002) (6)
- Perceptions of appropriateness of care in the intensive care unit. (2012) (5)
- Communicating With Pediatric Families at End-of-Life Is Not a Fantasy (2018) (5)
- State of the science. HIV vaccine development. (1996) (5)
- A Hybrid Approach to Obtaining Research Consent (2019) (5)
- Experiences of Patients After Withdrawal From Cancer Clinical Trials (2021) (5)
- Management of healthcare personnel living with hepatitis B, hepatitis C, or human immunodeficiency virus in US healthcare institutions (2020) (5)
- Adolescent research participants' descriptions of medical research (2016) (4)
- HIV: epidemiology, immunopathogenesis, and clinical consequences. (1988) (4)
- Cultivating Synergy in Nursing, Bioethics, and Policy. (2016) (4)
- Recommending Research Participation to Patients: An Ethical Imperative? (2009) (4)
- Comparative effectiveness research: what to do when experts disagree about risks (2017) (4)
- “It’s Just Another Added Benefit”: Women’s Experiences with Employment-Based Egg Freezing Programs (2020) (4)
- Ethical issues related to clinical research and rare diseases (2017) (4)
- Informed consent template for patient participation in rare disease registries linked to biorepositories (2014) (4)
- Exploring the Concept of Vulnerability in the Work of the US Presidential Commission for the Study of Bioethical Issues (2015) (3)
- SHAH AND GRADY RESPOND (2010) (3)
- Research mentors: an understated value? (2003) (3)
- Beyond Open Communication: A Call for Partnership Between Clinical Ethics and Research Ethics Committees (2018) (3)
- Thinking further about value: commentary on "A taxonomy of value in clinical research". (2002) (3)
- Reflections on Moral Distress and Moral Success (2018) (3)
- A comparison of calculated energy requirements to measured resting energy expenditure in HIV-1-infected subjects. (1994) (3)
- Laboratory methods for diagnosing and monitoring HIV infection. (1993) (3)
- Avoiding exploitation in multinational covid-19 vaccine trials (2021) (3)
- Moral Distress and Moral Strength Among Clinicians in Health Care Systems: A Call for Research. (2019) (3)
- Response to Open Peer Commentaries on “A Broader Understanding of Moral Distress” (2016) (2)
- Correction in response to the review of ethical issues in international biomedical research. (2009) (2)
- Doing “Good” With Limited Resources: Is It Good Enough in the Provision of Quality Clinical Care? (2009) (2)
- Bioethics in the Oversight of Clinical Research: Institutional Review Boards and Data and Safety Monitoring Boards (2019) (2)
- Institutional Review Board review and consent for research: what's behind the statistics? (1998) (2)
- Response to Peer Commentary on “Does Ethics Education Influence the Moral Action of Practicing Nurses and Social Workers?” (2008) (2)
- Emergency Nursing, Ebola, and Public Policy: The Contributions of Nursing to the Public Policy Conversation. (2016) (2)
- Ethics and Genetics: What Should Every Advanced Practice Nurse Know? (2008) (2)
- Attrition in NRG Oncology's Radiation-Based Clinical Trials. (2018) (2)
- Response to "Nurses at the Table: Nursing, Ethics, and Health Policy". (2017) (2)
- Clinical research: the power of the nurse. (2001) (2)
- Surgical Medicine: Imperfect and Extraordinary (2015) (2)
- Writing a Consent Form (2018) (2)
- Another Cautionary Lesson from COVID Research (2021) (1)
- Time for Advance Care Planning Discussions During Transitions in Care in Cancer Clinical Trials. (2019) (1)
- The Competing Demands of Patient Privacy and Clinical Research. (2021) (1)
- Case: responding to a request for genetic testing that is still in the lab. (1995) (1)
- Design of placebo-controlled randomized trials of anticancer agents: Ethical considerations based on a review of published trials (2021) (1)
- Navigating Pandemic Moral Distress at Home and at Work: Frontline Workers’ Experiences (2022) (1)
- Addressing Patient Bias Against Health Care Workers: Time for Meaningful Change (2020) (1)
- Assessment tool for nurses' learning needs and priorities relative to caring for patients with AIDS and Kaposi's sarcoma. (1989) (1)
- STATE OF THE SCIENCE (1996) (1)
- When to start ART in Africa. (2013) (1)
- Phase I participants as a vulnerable population (2004) (1)
- Clinical Research: The Power of the Nurse: Every nurse working in clinical research has a responsibility to promote ethical conduct (2001) (1)
- The ethics of encouraging employees to get the COVID-19 vaccination (2022) (1)
- The evolution of research participant as partner: the seminal contributions of Bob Veatch (2022) (1)
- Ethical Challenges Experienced by Clinical Ethicists during COVID-19 (2022) (1)
- Genethics -- Responding to a Request for Genetic Testing That Is Still in the Lab (1995) (1)
- Patients' decision-making process of participating in phase I oncology studies (2005) (1)
- Broadening the Scope of Health Care Ethics Consultation: A Response to Open Peer Commentaries on Patient and Family Description of Ethical Concerns (2020) (1)
- Beneficent Deception: Whose Best Interests Are We Serving? (2004) (1)
- The Ethics of Studying Financial Incentives in Public Health Implementation: Study Design Challenges (2016) (1)
- An Alternative Account of Clinical Ethics: Leveraging the Strength of the Health Care Team (2018) (1)
- Informing egg donors of the potential for embryonic research: A survey of consent forms from US IVF clinics (2013) (1)
- Research involving pediatric stem cell donors: A way forward (2016) (1)
- Perceived Benefit and Burden Scales for Cancer (2020) (0)
- A New Ethical Framework for Assessing the Unique Challenges of Fetal Therapy Trials: Response to Commentaries (2022) (0)
- Moral Distress: A Lens to Focus on Moral Strength and Clinician Well-Being (2019) (0)
- The ethics of experimenting with human brain tissue (2018) (0)
- Moral Distress and Moral Strength among Clinicians in Health Care Systems: A Call for Research. (2019) (0)
- Participants in Phase 1 Oncology Research Trials Are Vulnerable--Reply (2008) (0)
- 67 Responsiveness to Host Community Health Needs (2007) (0)
- Measuring Moral Distress and its Various Sources (2023) (0)
- Association of Perceived Benefit or Burden of Research Participation With Participants’ Withdrawal From Cancer Clinical Trials (2022) (0)
- Autonomy and couples’ joint decision-making in healthcare (2018) (0)
- Ugandans in the Rakai District (2016) (0)
- Preface (1988) (0)
- Nurses and Industry: Conflict or Collaboration? (2016) (0)
- Commentary Surgical Medicine: Imperfect and Extraordinary (2015) (0)
- Body Composition HIV Infection in Clinically Stable Men With (1996) (0)
- A Tribute to Dr. Fauci. (2022) (0)
- developing and developed countries landscape . A review of empirical data from The quality of informed consent : mapping the and (0)
- Ethical trade-offs in vaccine development and distribution—Response to Gurwitz (2021) (0)
- Informed Consent. (2017) (0)
- Phase I participants as a vulnerable population. (2004) (0)
- COVID-19 Resource: What Are Our Professional and Ethical Obligations to Patients and Ourselves? (2020) (0)
- Deciding with Others: Interdependent Decision-Making. (2022) (0)
- NIH Clinical Center Names Chief of Department of Bioethics (2012) (0)
- Making the Choices Necessary to Make a Difference: The Responsibility of National Bioethics Commissions. (2017) (0)
- IRB Decision-Making about Minimal Risk Research with Pregnant Participants. (2021) (0)
- Institutional Review Boards and Protecting Human Research Participants—Reply (2010) (0)
- In memoriam: Alan Wertheimer. (2015) (0)
- A Reference in Research Ethics (2004) (0)
- Factors Associated with Attrition in RTOG Clinical Trials (2009) (0)
- Institutional Review Boards and Protecting Human Research Participants. Author's reply (2010) (0)
- State of the science : HIV vaccine development : HIV infection (1996) (0)
- “Ethics and Clinical Research”: (2019) (0)
- Ethical Considerations in the Second Decade of Pediatric Phase I CAR T-Cell Trials (2023) (0)
- Ethics and Genetic Research in Africa (2004) (0)
- Survey of Investigators About Sharing Human Research Data in the Neurosciences (2022) (0)
- Ethical and legal issues in infectious disease research and control. (2001) (0)
- Comparative effectiveness research: what to do when experts disagree about risks (2017) (0)
- A new ethical framework to determine acceptable risks in fetal therapy trials (2022) (0)
- A Modified Simulation Program Addressing a Staff Nurse Educational Need Identified by a Student Clinical Nurse Specialist Across Three Shifts in a Cardiac Step-Down Unit (2006) (0)
- Conducting ethical post-event medical countermeasure trials with children (2013) (0)
- Case study. Is longer always better? Commentary. (2008) (0)
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