Titel	Veröffentlichungsdatum	Sprache	Zitate
Is the qualitative research interview an acceptable medium for research with palliative care patients and carers?	2008/04/24	English	75
Moral distress and ethical climate in intensive care medicine during COVID-19: a nationwide study	2021/06/17	English	74
The practice of defensive medicine among hospital doctors in the United Kingdom	2013/10/29	English	73
How do we know that research ethics committees are really working? The neglected role of outcomes assessment in research ethics review	2008/03/28	English	73
Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era	2016/07/12	English	73
Animal derived products may conflict with religious patients’ beliefs	2013/12/01	English	71
DNA databanks and consent: A suggested policy option involving an authorization model	2003/01/03	English	70
Responsible data sharing in international health research: a systematic review of principles and norms	2019/03/28	English	69
Impact of social stigma on the process of obtaining informed consent for genetic research on podoconiosis: a qualitative study	2009/08/22	English	68
Deconstructing the notion of “global health research partnerships” across Northern and African contexts	2018/06/01	English	66
Regulation of genomic and biobanking research in Africa: a content analysis of ethics guidelines, policies and procedures from 22 African countries	2017/02/02	English	66
Why is it hard to make progress in assessing children’s decision-making competence?	2015/01/10	English	64
Experiences with community engagement and informed consent in a genetic cohort study of severe childhood diseases in Kenya	2010/07/15	English	64
Risk communication and informed consent in the medical tourism industry: A thematic content analysis of canadian broker websites	2011/09/26	English	63
Decision making on organ donation: the dilemmas of relatives of potential brain dead donors	2015/09/17	English	62
How do parents experience being asked to enter a child in a randomised controlled trial?	2009/02/16	English	61
Paternalism and autonomy: views of patients and providers in a transitional (post-communist) country	2015/09/29	English	61
Benefits and payments for research participants: Experiences and views from a research centre on the Kenyan coast	2012/06/22	English	61
Consensus guidelines on analgesia and sedation in dying intensive care unit patients	2002/08/12	English	61
Ethical concerns with the use of intelligent assistive technology: findings from a qualitative study with professional stakeholders	2019/12/01	English	61
Bioethics education in clinical settings: theory and practice of the dilemma method of moral case deliberation	2016/07/22	English	59
Teaching seven principles for public health ethics: towards a curriculum for a short course on ethics in public health programmes	2014/10/07	English	59
Impact of moral case deliberation in healthcare settings: a literature review	2018/11/06	English	58
Underreporting of conflicts of interest in clinical practice guidelines: cross sectional study	2013/05/03	English	58
Clinical ethics revisited	2001/04/26	English	57
Standards of practice in empirical bioethics research: towards a consensus	2018/07/10	English	57
“It’s my blood”: ethical complexities in the use, storage and export of biological samples: perspectives from South African research participants	2014/01/22	English	56
Ethical issues in using Twitter for population-level depression monitoring: a qualitative study	2016/04/14	English	55
Ethical issues at the interface of clinical care and research practice in pediatric oncology: a narrative review of parents' and physicians' experiences	2011/09/27	English	54
Research participants’ perceptions and views on consent for biobank research: a review of empirical data and ethical analysis	2015/09/09	English	53