| Ethics preparedness: facilitating ethics review during outbreaks - recommendations from an expert panel |
15 |
| Deconstructing the notion of global health research partnerships across Northern and African contexts |
13 |
| Impact of moral case deliberation in healthcare settings: a literature review |
11 |
| Relational autonomy: what does it mean and how is it used in end-of-life care? A systematic review of argument-based ethics literature |
11 |
| Standards of practice in empirical bioethics research: towards a consensus |
10 |
| Conscientious objection to participation in abortion by midwives and nurses: a systematic review of reasons |
10 |
| Medicine, market and communication: ethical considerations in regard to persuasive communication in direct-to-consumer genetic testing services |
9 |
| Leaving patients to their own devices? Smart technology, safety and therapeutic relationships |
9 |
| Conscientious objection to abortion, the law and its implementation in Victoria, Australia: perspectives of abortion service providers |
8 |
| Umbrella and basket trials in oncology: ethical challenges |
8 |
| Ethical considerations for HIV cure-related research at the end of life |
8 |
| Ethics of task shifting in the health workforce: exploring the role of community health workers in HIV service delivery in low- and middle-income countries |
7 |
| Women's perspectives on the ethical implications of non-invasive prenatal testing: a qualitative analysis to inform health policy decisions |
7 |
| Parental decision-making following a prenatal diagnosis that is lethal, life-limiting, or has long term implications for the future child and family: a meta-synthesis of qualitative literature |
7 |
| Analysis of official deceased organ donation data casts doubt on the credibility of China's organ transplant reform |
6 |
| Responsible data sharing in international health research: a systematic review of principles and norms |
6 |
| Rules of engagement: perspectives on stakeholder engagement for genomic biobanking research in South Africa |
6 |
| Autonomy and couples' joint decision-making in healthcare |
6 |
| Model consent clauses for rare disease research |
5 |
| Euthanasia requests in dementia cases; what are experiences and needs of Dutch physicians? A qualitative interview study |
5 |
| A framework for the ethical assessment of chimeric animal research involving human neural tissue |
5 |
| A review and analysis of new Italian law 219/2017: provisions for informed consent and advance directives treatment' |
5 |
| Experiences of pre-hospital emergency medical personnel in ethical decision-making: a qualitative study |
5 |
| Educational video-assisted versus conventional informed consent for trauma-related debridement surgery: a parallel group randomized controlled trial |
5 |
| What information and the extent of information research participants need in informed consent forms: a multi-country survey |
5 |
| Recent efforts to elucidate the scientific validity of animal-based drug tests by the pharmaceutical industry, pro-testing lobby groups, and animal welfare organisations |
5 |
| The involvement of family in the Dutch practice of euthanasia and physician assisted suicide: a systematic mixed studies review |
5 |
| Advance directives as a tool to respect patients' values and preferences: discussion on the case of Alzheimer's disease |
5 |
| Do we understand the intervention? What complex intervention research can teach us for the evaluation of clinical ethics support services (CESS) |
5 |
| Early-career researchers' views on ethical dimensions of patient engagement in research |
5 |
| Trust and the ethical challenges in the use of whole genome sequencing for tuberculosis surveillance: a qualitative study of stakeholder perspectives |
5 |
| The psychology of cure - unique challenges to consent processes in HIV cure research in South Africa |
5 |
| Conscientious objection to intentional killing: an argument for toleration |
5 |
| Exploring the ethics of global health research priority-setting |
5 |
| An update on the empirical turn in bioethics: analysis of empirical research in nine bioethics journals |
5 |
| Broad consent for biobanks is best - provided it is also deep |
4 |
| Who should decide about children's and adolescents' participation in health research? The views of childrenand adults in rural Kenya |
4 |
| Disparate compensation policies for research related injury in an era of multinational trials: a case study of Brazil, Russia, India, China and South Africa |
4 |
| Methodological challenges in European ethics approvals for a genetic epidemiology study in critically ill patients: the GenOSept experience |
4 |
| Ethical issues associated with HIV molecular epidemiology: a qualitative exploratory study using inductive analytic approaches |
4 |
| Frequency of use of the religious exemption in New Jersey cases of determination of brain death |
4 |
| Surgical informed consent in obstetric and gynecologic surgeries: experience from a comprehensive teaching hospital in Southern Ethiopia |
4 |
| Ethical implications of digital communication for the patient-clinician relationship: analysis of interviews with clinicians and young adults with long term conditions (the LYNC study) |
4 |
| Integrated primary health care in low- and middle-income countries: a double challenge |
4 |
| Using brain-computer interfaces: a scoping review of studies employing social research methods |
4 |
| Regulatory and policy tools to address unproven stem cell interventions in Canada: the need for action |
4 |
| The challenge of community engagement and informed consent in rural Zambia: an example from a pilot study |
4 |
| Management of financial conflicts of interests in clinical practice guidelines in Germany: results from the public database GuidelineWatch |
4 |
| Ethical issues in pragmatic randomized controlled trials: a review of the recent literature identifies gaps in ethical argumentation |
4 |
| The ethics of relationality in implementation and evaluation research in global health: reflections from the Dream-A-World program in Kingston, Jamaica |
4 |
