- Clinical ethics consultations: a scoping review of reported outcomes
- Parental waivers to enable adolescent participation in certain forms of health research: lessons from a South African case study
- How to deal with moral challenges around the decision-making competence in transgender adolescent care? Development of an ethics support tool
- Managing the moral expansion of medicine
- Exploring how biobanks communicate the possibility of commercial access and its associated benefits and risks in participant documents
- Moral values of Dutch physicians in relation to requests for euthanasia: a qualitative study
- Physicians’ legal knowledge of informed consent and confidentiality. A cross-sectional study
- Current status of umbilical cord blood storage and provision to private biobanks by institutions handling childbirth in Japan
- Decision-making ethics in regards to life-sustaining interventions: when physicians refer to what other patients decide
- Better governance starts with better words: why responsible human tissue research demands a change of language
- Performance of IRBs in China: a survey on IRB employees and researchers’ experiences and perceptions
- From a voluntary vaccination policy to mandatory vaccination against COVID-19 in cancer patients: an empirical and interdisciplinary study in bioethics
- A quantitative study of nurses perception to advance directive in selected private and public secondary healthcare facilities in Ibadan, Nigeria
- Perception and reaction of Nanyang Technological University (NTU) researchers to different forms of research integrity education modality
- How is physicians’ implicit prejudice against the obese and mentally ill moderated by specialty and experience?
- The concept of vulnerability in aged care: a systematic review of argument-based ethics literature
- Biobanks in the low- and middle-income countries of the Arab Middle East region: challenges, ethical issues, and governance arrangements—a qualitative study involving biobank managers
- Increasing physician participation as subjects in scientific and quality improvement research
- Current state of ethical challenges reported in Saudi Arabia: a systematic review & bibliometric analysis from 2010 to 2021
- Ethical challenges experienced by prehospital emergency personnel: a practice-based model of analysis
- Development of a core outcome set for informed consent for therapy: An international key stakeholder consensus study
- Do biomedical researchers differ in their perceptions of plagiarism across Europe? Findings from an online survey among leading universities
- Where the public health principles meet the individual: a framework for the ethics of compulsory outpatient treatment in psychiatry
- Ethics knowledge, attitudes, and experiences of tertiary care pediatricians in Ethiopia
- Junior Medical Officers’ knowledge of advance care directives and substitute decision making for people without decision making capacity: a cross sectional survey
- (Re)Conceptualising ‘good’ proxy decision-making for research: the implications for proxy consent decision quality
- Junior medical doctors’ decision making when using advance care directives to guide treatment for people with dementia: a cross-sectional vignette study
- Justification for requiring disclosure of diagnoses and prognoses to dying patients in saudi medical settings: a Maqasid Al-Shariah-based Islamic bioethics approach
- Ambivalence toward euthanasia and physician-assisted suicide has decreased among physicians in Finland
- Ethical values and principles to guide the fair allocation of resources in response to a pandemic: a rapid systematic review
- Consent in organ transplantation: putting legal obligations and guidelines into practice
- Practice of code of ethics and associated factors among health professionals in Central Gondar Zone public hospitals, Northwest Ethiopia, 2021: a mixed-method study design
- Ethical issues in oncology practice: a qualitative study of stakeholders’ experiences and expectations
- “Everything has been tried and his heart can’t recover…”: A Descriptive Review of “Do Everything!” in the Archive of Ontario Consent and Capacity Board
- On the person in personal health responsibility
- Data privacy protection in scientific publications: process implementation at a pharmaceutical company
- Withdrawing or withholding treatments in health care rationing: an interview study on ethical views and implications
- Patient participation in Dutch ethics support: practice, ideals, challenges and recommendations—a national survey
- Clinical ethical practice and associated factors in healthcare facilities in Ethiopia: a cross-sectional study
- Research based on existing clinical data and biospecimens: a systematic study of patients’ opinions
- Managing community engagement in research in Uganda: insights from practices in HIV/AIDS research
- Screening is not always healthy: an ethical analysis of health screening packages in Singapore
- Public attitudes towards sharing loyalty card data for academic health research: a qualitative study
- The challenges of keeping clinicians unaware of their participation in a national, cluster-randomised, implementation trial
- The red packet phenomenon from the perspective of young Chinese doctors: a questionnaire study
- The genetic technologies questionnaire: lay judgments about genetic technologies align with ethical theory, are coherent, and predict behaviour
- Patient consent preferences on sharing personal health information during the COVID-19 pandemic: “the more informed we are, the more likely we are to help”
- Decision-making approaches for children with life-limiting conditions: results from a qualitative phenomenological study
- A chronological discourse analysis of ancillary care provision in guidance documents for research conduct in the global south
- “Many roads lead to Rome and the Artificial Intelligence only shows me one road”: an interview study on physician attitudes regarding the implementation of computerised clinical decision support systems
- Combining rules and dialogue: exploring stakeholder perspectives on preventing sexual boundary violations in mental health and disability care organizations
- Travelling to die: views, attitudes and end-of-life preferences of Israeli considering receiving aid-in-dying in Switzerland
- Asking the right questions: towards a person-centered conception of shared decision-making regarding treatment of advanced chronic kidney disease in older patients
- Ethical considerations around volunteer payments in a malaria human infection study in Kenya: an embedded empirical ethics study
- Gender differences in response to medical red packets (Hongbao, monetary gifts): a questionnaire study on young doctors in China
- Ethical decision-making climate, moral distress, and intention to leave among ICU professionals in a tertiary academic hospital center
- Participant recall and understandings of information on biobanking and future genomic research: experiences from a multi-disease community-based health screening and biobank platform in rural South Africa
- Situational judgment using ethical reasoning in Saudi undergraduate pharmacy students
- What ethical approaches are used by scientists when sharing health data? An interview study
- Ethical and practical considerations for cell and gene therapy toward an HIV cure: findings from a qualitative in-depth interview study in the United States
- Dealing with sexual boundary violation in mental healthcare institutions by government policies: the case of Flanders, Belgium
- Patient-centred care and patient autonomy: doctors’ views in Chinese hospitals
- Pursuing impact in research: towards an ethical approach
- ‘I feel that injustice is being done to me’: a qualitative study of women’s viewpoints on the (lack of) reimbursement for social egg freezing
- Collection and use of human materials during TB clinical research; a review of practices
- Experimenting with modifications to consent forms in comparative effectiveness research: understanding the impact of language about financial implications and key information
- Which features of patients are morally relevant in ventilator triage? A survey of the UK public
- Ethical and regulatory implications of the COVID-19 pandemic for the medical devices industry and its representatives
- Participatory development of CURA, a clinical ethics support instrument for palliative care
- Indicators and criteria of consciousness: ethical implications for the care of behaviourally unresponsive patients
- The effect of deliberative process on the self-sacrificial decisions of utilitarian healthcare students
- Ethics education to support ethical competence learning in healthcare: an integrative systematic review
- Perspectives on returning individual and aggregate genomic research results to study participants and communities in Kenya: a qualitative study
- Health professionals’ knowledge and attitude towards patient confidentiality and associated factors in a resource-limited setting: a cross-sectional study
- Ethics framework for citizen science and public and patient participation in research
- What if some patients are more “important” than others? A possible framework for Covid-19 and other emergency care situations
- The public impact of academic and print media portrayals of TMS: shining a spotlight on discrepancies in the literature
- Social network-based ethical analysis of COVID-19 vaccine supply policy in three Central Asian countries
- Qualitative inquiry into adolescents’ experience of ethical challenges during enrollment and adherence to antiretroviral therapy (ART) in Temeke Regional Referral Hospital, Tanzania
- Consent to organ offers from public health service “Increased Risk” donors decreases time to transplant and waitlist mortality
- Perceptions on using surplus embryos for the treatment of Parkinson’s disease among the Swedish population: a qualitative study
- A qualitative interview study of Australian physicians on defensive practice and low value care: “it’s easier to talk about our fear of lawyers than to talk about our fear of looking bad in front of each other”
- Shifting to a model of donor conception that entails a communication agreement among the parents, donor, and offspring
- Chinese physicians’ perceptions of palliative care integration for advanced cancer patients: a qualitative analysis at a tertiary hospital in Changsha, China
- Trust and digital privacy in healthcare: a cross-sectional descriptive study of trust and attitudes towards uses of electronic health data among the general public in Sweden
- Development and validation of an instrument to measure pediatric nurses’ adherence to ethical codes
- Attitudes about withholding or withdrawing life-prolonging treatment, euthanasia, assisted suicide, and physician assisted suicide: a cross-sectional survey among the general public in Croatia
- Experiences and attitudes of medical professionals on treatment of end-of-life patients in intensive care units in the Republic of Croatia: a cross-sectional study
- An ethical analysis of clinical triage protocols and decision-making frameworks: what do the principles of justice, freedom, and a disability rights approach demand of us?
- What does coercion in intensive care mean for patients and their relatives? A thematic qualitative study
- Conceptualizing the impact of moral case deliberation: a multiple-case study in a health care institution for people with intellectual disabilities
- Health care providers’ ethical perspectives on waiver of final consent for Medical Assistance in Dying (MAiD): a qualitative study
- It is not a big deal: a qualitative study of clinical biobank donation experience and motives
- Who’s afraid of genetic tests?: An assessment of Singapore’s public attitudes and changes in attitudes after taking a genetic test
- Embedded ethics: a proposal for integrating ethics into the development of medical AI
- Future healthcare providers and professionalism on social media: a cross-sectional study
- Ethical and practical considerations for HIV cure-related research at the end-of-life: a qualitative interview and focus group study in the United States
- Operationalising a real-time research ethics approach: supporting ethical mindfulness in agriculture-nutrition-health research in Malawi
- The role of community advisory boards in community-based HIV clinical trials: a qualitative study from Tanzania
- Ethical considerations for HIV remission clinical research involving participants diagnosed during acute HIV infection
- How to reveal disguised paternalism: version 2.0
- A systematic approach to the disclosure of genomic findings in clinical practice and research: a proposed framework with colored matrix and decision-making pathways
- Navigating abortion law dilemmas: experiences and attitudes among Ethiopian health care professionals
- A scoping review of the perceptions of death in the context of organ donation and transplantation
- Secondary research use of personal medical data: patient attitudes towards data donation
- Capacity of community advisory boards for effective engagement in clinical research: a mixed methods study
- What drives public attitudes towards moral bioenhancement and why it matters: an exploratory study
- Attitudes on euthanasia among medical students and doctors in Sri Lanka: a cross sectional study
- Examining study participants’ decision-making and ethics-related experiences in a dietary community randomized controlled trial in Malawi
- Ethics experts and fetal patients: a proposal for modesty
- Making complex decisions in uncertain times: experiences of Dutch GPs as gatekeepers regarding hospital referrals during COVID-19—a qualitative study
- Being torn by inevitable moral dilemma: experiences of ICU nurses
- Beyond biopolitics: the importance of the later work of Foucault to understand care practices of healthcare workers caring for undocumented migrants
- A genetic researcher’s devil’s dilemma: Warn relatives about their genetic risk or respect confidentiality agreements with research participants?
- Genetic/genomic testing: defining the parameters for ethical, legal and social implications (ELSI)
- Ethical challenges faced by French military doctors deployed in the Sahel (Operation Barkhane): a qualitative study
- Perspectives and ethical considerations for return of genetics and genomics research results: a qualitative study of genomics researchers in Uganda
- Views of university students in Jordan towards Biobanking
- Informed consent in psychotherapy: a survey on attitudes among psychotherapists in Switzerland
- “I haven’t had to bare my soul but now I kind of have to”: describing how voluntary assisted dying conscientious objectors anticipated approaching conversations with patients in Victoria, Australia
- The Swedish translation and cultural adaptation of the Measure of Moral Distress for Healthcare Professionals (MMD-HP)
- Reporting violations of European Charter of Patients’ Rights: analysis of patient complaints in Croatia
- Governance frameworks for COVID-19 research ethics review and oversight in Latin America: an exploratory study
- When is it considered reasonable to start a risky and uncomfortable treatment in critically ill patients? A random sample online questionnaire study
- The impact of reporting magnetic resonance imaging incidental findings in the Canadian alliance for healthy hearts and minds cohort
- The association between perceived hospital ethical climate and self-evaluated care quality for COVID-19 patients: the mediating role of ethical sensitivity among Chinese anti-pandemic nurses
- The COVID-19 pandemic and organ donation and transplantation: ethical issues
- Uses of equipoise in discussions of the ethics of randomized controlled trials of COVID-19 therapies
- Goods, causes and intentions: problems with applying the doctrine of double effect to palliative sedation
- How to navigate the application of ethics norms in global health research: reflections based on qualitative research conducted with people with disabilities in Uganda
- Presumed post-mortem donors: the degree of information among university students
- Assessment of the appropriateness of the i-CONSENT guidelines recommendations for improving understanding of the informed consent process in clinical studies
- Advance research directives: avoiding double standards
- Equitable data sharing in epidemics and pandemics
- Defining ethical challenge(s) in healthcare research: a rapid review
- Cross-cultural validation of the IRB Researcher Assessment Tool: Chinese Version
- Factors influencing practitioners’ who do not participate in ethically complex, legally available care: scoping review
- A situation analysis of competences of research ethics committee members regarding review of research protocols with complex and emerging study designs in Uganda
- Neonatologists’ decision-making for resuscitation and non-resuscitation of extremely preterm infants: ethical principles, challenges, and strategies—a qualitative study
- Biomedical engineering and ethics: reflections on medical devices and PPE during the first wave of COVID-19
- COVID-19 underscores the important role of Clinical Ethics Committees in Africa
- Cross-sectional survey of surrogate decision-making in Japanese medical practice
- Ethical considerations for involving adolescents in biomedical HIV prevention research
- Reframing cancer: challenging the discourse on cancer and cancer drugs—a Norwegian perspective
- Polygenic risk scoring of human embryos: a qualitative study of media coverage
- Forensic mental health professionals’ perceptions of their dual loyalty conflict: findings from a qualitative study
- Developing new ways to listen: the value of narrative approaches in empirical (bio)ethics
- Privacy and artificial intelligence: challenges for protecting health information in a new era
- The ethics of explantation
- Attitudes toward withholding antibiotics from people with dementia lacking decisional capacity: findings from a survey of Canadian stakeholders
- Organ donation after euthanasia starting at home in a patient with multiple system atrophy
- Achieving inclusive research priority-setting: what do people with lived experience and the public think is essential?
- The ethical implications of verbal autopsy: responding to emotional and moral distress
- Patients’ and professionals’ views related to ethical issues in precision medicine: a mixed research synthesis
- Are investigators’ access to trial data and rights to publish restricted and are potential trial participants informed about this? A comparison of trial protocols and informed consent materials
- Practice variation in the informed consent procedure for thrombolysis in acute ischemic stroke: a survey among neurologists and neurology residents
- Collective forward-looking responsibility of patient advocacy organizations: conceptual and ethical analysis
- The ethics of machine learning-based clinical decision support: an analysis through the lens of professionalisation theory
- South African traditional values and beliefs regarding informed consent and limitations of the principle of respect for autonomy in African communities: a cross-cultural qualitative study
- The social licence for data-intensive health research: towards co-creation, public value and trust
- Does teaching medical ethics ensure good knowledge, attitude, and reported practice? An ethical vignette-based cross-sectional survey among doctors in a tertiary teaching hospital in Nepal
- Personalized and long-term electronic informed consent in clinical research: stakeholder views
- Health care ethics programs in U.S. Hospitals: results from a National Survey
- Motivation to participate and experiences of the informed consent process for randomized clinical trials in emergency obstetric care in Uganda
- Effectiveness of data auditing as a tool to reinforce good research data management (RDM) practice: a Singapore study
- Caregiver reactions to neuroimaging evidence of covert consciousness in patients with severe brain injury: a qualitative interview study
- Preprints in times of COVID19: the time is ripe for agreeing on terminology and good practices
- To disclose, or not to disclose? Perspectives of clinical genomics professionals toward returning incidental findings from genomic research
- A scoping review of considerations and practices for benefit sharing in biobanking
- Gurus and Griots: Revisiting the research informed consent process in rural African contexts
- Clinical ethics case consultation in a university department of cardiology and intensive care: a descriptive evaluation of consultation protocols
- Undisclosed probing into decision-making capacity: a dilemma in secondary care
- Scarcity of resources and inequity in access are frequently reported ethical issues for physiotherapists internationally: an observational study
- Challenges and proposed solutions in making clinical research on COVID-19 ethical: a status quo analysis across German research ethics committees
- The CORBEL matrix on informed consent in clinical studies: a multidisciplinary approach of Research Infrastructures Building Enduring Life-science Services
- Consent to research participation: understanding and motivation among German pupils
- Nurses’ ethical decision-making during end of life care in South Korea: a cross-sectional descriptive survey
- Reporting ethical approval in health and social science articles: an audit of adherence to GDPR and national legislation
- Non-medical risk factors associated with postponing elective surgery: a prospective observational study
- Pushing poverty off limits: quality improvement and the architecture of healthcare values
- Solitary death and new lifestyles during and after COVID-19: wearable devices and public health ethics
- Analyzing the paradigmatic cases of two persons with a disorder of consciousness: reflections on the legal and ethical perspectives
- The ethics of practicing defensive medicine in Jordan: a diagnostic study
- Trends in Swedish physicians’ attitudes towards physician-assisted suicide: a cross-sectional study
- Stakeholder perspectives on the ethico-legal dimensions of biobanking in South Africa
- How ethics committees and requirements are structuring health research in the Philippines: a qualitative study
- Documentation of ethically relevant information in out-of-hospital resuscitation is rare: a Danish nationwide observational study of 16,495 out-of-hospital cardiac arrests
- Ethics of HIV cure research: an unfinished agenda
- Meta-consent for the secondary use of health data within a learning health system: a qualitative study of the public’s perspective
- Adherence with reporting of ethical standards in COVID-19 human studies: a rapid review
- Why should HCWs receive priority access to vaccines in a pandemic?
- What does engagement mean to participants in longitudinal cohort studies? A qualitative study
- Principles for pandemics: COVID-19 and professional ethical guidance in England and Wales
- Association between knowledge and attitudes towards advance directives in emergency services
- Who should be tested in a pandemic? Ethical considerations
- Assessing research misconduct in Iran: a perspective from Iranian medical faculty members
- Consent for withholding life-sustaining treatment in cancer patients: a retrospective comparative analysis before and after the enforcement of the Life Extension Medical Decision law
- Moral distress and ethical climate in intensive care medicine during COVID-19: a nationwide study
- A policy Delphi study to validate the key implications of data sharing (KIDS) framework for pediatric genomics in Canada
- The theorisation of ‘best interests’ in bioethical accounts of decision-making
- Correction to: Under consent: participation of people with HIV in an Ebola vaccine trial in Canada
- Ethical factors determining ECMO allocation during the COVID-19 pandemic
- Stakeholders’ perspectives on research integrity training practices: a qualitative study
- Knowledge and attitudes about end-of-life decisions, good death and principles of medical ethics among doctors in tertiary care hospitals in Sri Lanka: a cross-sectional study
- Development and validation of an instrument to measure physician awareness of bioethics and medical law in Oman
- Study protocol: the Australian genetics and life insurance moratorium—monitoring the effectiveness and response (A-GLIMMER) project
- Current wishes to die; characteristics of middle-aged and older Dutch adults who are ready to give up on life: a cross-sectional study
- Citizens’ views on sharing their health data: the role of competence, reliability and pursuing the common good
- On intimate relationships between healthcare professionals and patients: a nationwide cohort analysis of medical tribunal decisions in the Netherlands
- Cultures and cures: neurodiversity and brain organoids
- Cultural sensitivity in brain death determination: a necessity in end-of-life decisions in Japan
- The path toward ectogenesis: looking beyond the technical challenges
- Something must happen before first breath
- Precision medicine and the principle of equal treatment: a conjoint analysis
- Taking stock of the availability and functions of National Ethics Committees worldwide
- Priority setting at the clinical level: the case of nusinersen and the Norwegian national expert group
- Normative framework of informed consent in clinical research in Germany, Poland, and Russia
- Ethics review of big data research: What should stay and what should be reformed?
- A scoping review of the literature featuring research ethics and research integrity cases
- Correction to: Regulatory, scientific, and ethical issues arising from institutional activity in one of the 90 Italian Research Ethics Committees
- Ethical and procedural issues for applying researcher-driven multi-national paediatric clinical trials in and outside the European Union: the challenging experience of the DEEP project
- Recognising values and engaging communities across cultures: towards developing a cultural protocol for researchers
- A Q methodology study on divergent perspectives on CRISPR-Cas9 in the Netherlands
- Unapproved clinical trials in Russia: exception or norm?
- Trust and professionalism in science: medical codes as a model for scientific negligence?
- Inter-physician variability in strategies linked to treatment limitations after severe traumatic brain injury; proactivity or wait-and-see
- Identifying disincentives to ethics consultation requests among physicians, advance practice providers, and nurses: a quality improvement all staff survey at a tertiary academic medical center
- Under consent: participation of people with HIV in an Ebola vaccine trial in Canada
- Regulatory, scientific, and ethical issues arising from institutional activity in one of the 90 Italian Research Ethics Committees
- Ethical concerns in suicide research: thematic analysis of the views of human research ethics committees in Australia
- A scoping review of genetics and genomics research ethics policies and guidelines for Africa
- What does it take to consent to islet cell xenotransplantation?: Insights from an interview study with type 1 diabetes patients and review of the literature
- Ethical considerations for research involving pregnant women living with HIV and their young children: a systematic review of the empiric literature and discussion
- Ethical challenges of the healthcare transition to adult antiretroviral therapy (ART) clinics for adolescents and young people with HIV in Uganda
- Among equity and dignity: an argument-based review of European ethical guidelines under COVID-19
- Do-not-attempt-resuscitation orders: attitudes, perceptions and practices of Swedish physicians and nurses
- Health workers’ perspectives on informed consent for caesarean section in Southern Malawi
- The full spectrum of ethical issues in dementia research: findings of a systematic qualitative review
- Pharmacy stakeholder reports on ethical and logistical considerations in anti-opioid vaccine development
- Considerations for applying bioethics norms to a biopharmaceutical industry setting
- The use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution
- Prioritising ‘already-scarce’ intensive care unit resources in the midst of COVID-19: a call for regional triage committees in South Africa
- Perceptions of important outcomes of moral case deliberations: a qualitative study among healthcare professionals in childhood cancer care
- Experts’ moral views on gene drive technologies: a qualitative interview study
- Enhancing patient safety by integrating ethical dimensions to Critical Incident Reporting Systems
- Dialysis decisions concerning cognitively impaired adults: a scoping literature review
- Québec health care professionals’ perspectives on organ donation after medical assistance in dying
- Systematic review: bioethical implications for COVID-19 research in low prevalence countries, a distinctly different set of problems
- Is there a need for a clear advice? A retrospective comparative analysis of ethics consultations with and without recommendations in a maximum-care university hospital
- Facing new challenges to informed consent processes in the context of translational research: the case in CARPEM consortium
- Digital tools in the informed consent process: a systematic review
- Knowledge, attitudes, ethical and social perspectives towards fecal microbiota transplantation (FMT) among Jordanian healthcare providers
- Frankenstein; or, the modern Prometheus: a classic novel to stimulate the analysis of complex contemporary issues in biomedical sciences
- Using practical wisdom to facilitate ethical decision-making: a major empirical study of phronesis in the decision narratives of doctors
- Should biomedical research with great apes be restricted? A systematic review of reasons
- Artificial intelligence for good health: a scoping review of the ethics literature
- Ethical challenges of caring for burn patients: a qualitative study
- Adding dynamic consent to a longitudinal cohort study: A qualitative study of EXCEED participant perspectives
- “It’s all about delivery”: researchers and health professionals’ views on the moral challenges of accessing neurobiological information in the context of psychosis
- The anatomy of electronic patient record ethics: a framework to guide design, development, implementation, and use
- Enhancing the ethical conduct of a longitudinal cluster-randomized trial of psychosocial stimulation intervention for children with complicated severe acute malnutrition through Rapid Ethical Assessment: a qualitative study
- Patient privacy and autonomy: a comparative analysis of cases of ethical dilemmas in China and the United States
- Health data research on sudden cardiac arrest: perspectives of survivors and their next-of-kin
- HIV prevention research and COVID-19: putting ethics guidance to the test
- Grounds for surrogate decision-making in Japanese clinical practice: a qualitative survey
- Improving pharmacy practice in relation to complementary medicines: a qualitative study evaluating the acceptability and feasibility of a new ethical framework in Australia
- Women’s viewpoints on egg freezing in Austria: an online Q-methodology study
- Perceptions of and barriers to ethical promotion of pharmaceuticals in Pakistan: perspectives of medical representatives and doctors
- Lay persons’ perception of the requirements for research in emergency obstetric and newborn care
- Barriers in implementing the dying patient law: the Israeli experience – a qualitative study
- Communication patterns in the doctor–patient relationship: evaluating determinants associated with low paternalism in Mexico
- Attitudes towards organ donation in Syria: a cross-sectional study
- Qualitative study of comprehension of heritability in genomics studies among the Yoruba in Nigeria
- Moral structuring of children during the process of obtaining informed consent in clinical and research settings
- Physicians’ attitudes in relation to end-of-life decisions in Neonatal Intensive Care Units: a national multicenter survey
- Correction to: South Africa’s new standard material transfer agreement: proposals for improvement and pointers for implementation
- Intensive and pharmacological care in times of COVID-19: A “special ethics” for emergency?
- “Who is watching the watchdog?”: ethical perspectives of sharing health-related data for precision medicine in Singapore
- Sharing genomic data from clinical testing with researchers: public survey of expectations of clinical genomic data management in Queensland, Australia
- Clinical Ethics Committees in Africa: lost in the shadow of RECs/IRBs?
- Ethics framework for treatment use of investigational drugs
- Moral neutralization: Nurses’ evolution in unethical climate workplaces
- Why have Advance Directives failed in Spain?
- Do solidarity and reciprocity obligations compel African researchers to feedback individual genetic results in genomics research?
- Sharing whilst caring: solidarity and public trust in a data-driven healthcare system
- US medical and surgical society position statements on physician-assisted suicide and euthanasia: a review
- Just say “no”: Can dentists refuse care on the basis of finances? A survey using an ethical vignette in an Iranian Dental School
- A principled ethical approach to intersex paediatric surgeries
- Redundant trials can be prevented, if the EU clinical trial regulation is applied duly
- Ethics and the marketing authorization of pharmaceuticals: what happens to ethical issues discovered post-trial and pre-marketing authorization?
- “It gets people through the door”: a qualitative case study of the use of incentives in the care of people at risk or living with HIV in British Columbia, Canada
- The relationship between the perception of open disclosure of patient safety incidents, perception of patient safety culture, and ethical awareness in nurses
- An ethical issue: nurses’ conscientious objection regarding induced abortion in South Korea
- A qualitative study of big data and the opioid epidemic: recommendations for data governance
- Genetic testing for breast cancer risk, from BRCA1/2 to a seven gene panel: an ethical analysis
- Potential research ethics violations against an indigenous tribe in Ecuador: a mixed methods approach
- Forgoing life-sustaining treatment – a comparative analysis of regulations in Japan, Korea, Taiwan, and England
- Challenges to effective and autonomous genetic testing and counseling for ethno-cultural minorities: a qualitative study
- Nocebo effects by providing informed consent in shared decision making? Not necessarily: a randomized pilot-trial using an open-label placebo approach
- Bioethics and the use of social media for medical crowdfunding
- Human genome editing: how to prevent rogue actors
- Researchers’ views on, and experiences with, the requirement to obtain informed consent in research involving human participants: a qualitative study
- An ethics analysis of the rationale for publicly funded plastic surgery
- Correction to: Implementing clinical ethics committees as a complex intervention: presentation of a feasibility study in community care
- Ethical and human rights considerations in public health in low and middle-income countries: an assessment using the case of Uganda’s responses to COVID-19 pandemic
- Structural coercion in the context of community engagement in global health research conducted in a low resource setting in Africa
- A practical approach to the ethical use of memory modulating technologies
- Human germline editing in the era of CRISPR-Cas: risk and uncertainty, inter-generational responsibility, therapeutic legitimacy
- Study of laboratory staff’ knowledge of biobanking in Côte d’Ivoire
- South Africa’s new standard material transfer agreement: proposals for improvement and pointers for implementation
- White lie during patient care: a qualitative study of nurses’ perspectives
- Ethics parallel research: an approach for (early) ethical guidance of biomedical innovation
- The obstacles to organ donation following brain death in Iran: a qualitative study
- Implementing clinical ethics committees as a complex intervention: presentation of a feasibility study in community care
- The challenges of ethical behaviors for drug supply in pharmacies in Iran by a principle-based approach
- Withholding and withdrawal of life-sustaining treatments in intensive care units in Lebanon: a cross-sectional survey of intensivists and interviews of professional societies, legal and religious leaders
- Theory and practice of integrative clinical ethics support: a joint experience within gender affirmative care
- “You would not be in a hurry to go back home”: patients’ willingness to participate in HIV/AIDS clinical trials at a clinical and research facility in Kampala, Uganda
- Examination and diagnosis of electronic patient records and their associated ethics: a scoping literature review
- Street research market: dealing with scientific misconduct in Iran
- Disclosure of medical errors: physicians’ knowledge, attitudes and practices (KAP) in an oncology center
- In Defence of informed consent for health record research – why arguments from ‘easy rescue’, ‘no harm’ and ‘consent bias’ fail
- Public trust and global biobank networks
- Patient distrust in pharmaceutical companies: an explanation for women under-representation in respiratory clinical trials?
- Withdrawal of treatment in a pediatric intensive care unit at a Children’s Hospital in China: a 10-year retrospective study
- Conscientious objection to abortion: why it should be a specified legal right for doctors in South Korea
- Medical ethics: knowledge, attitude and practice among doctors in three teaching hospitals in Sri Lanka
- Ethical practice in my work: community health workers’ perspectives using photovoice in Wakiso district, Uganda
- Usage of do-not-attempt-to-resuscitate orders in a Swedish community hospital – patient involvement, documentation and compliance
- Public awareness of and attitudes towards research biobanks in Latvia
- The ethics of DNR-decisions in oncology and hematology care: a qualitative study
- Ethical and social implications of approaching death prediction in humans – when the biology of ageing meets existential issues
- Motives of contributing personal data for health research: (non-)participation in a Dutch biobank
- Changing medical education scenario: a wakeup call for reforms in Anatomy Act
- A qualitative study exploring stakeholder perspectives on the use of biological samples for future unspecified research in Malawi
- Bin it or pin it? Which professional ethical guidance on managing COVID-19 should I follow?
- Will my patients get their residence permit? A critical analysis of the ethical dilemmas involved in writing medical certificates for residence permits in France
- The patient and clinician experience of informed consent for surgery: a systematic review of the qualitative evidence
- Family discussions and demographic factors influence adolescent’s knowledge and attitude towards organ donation after brain death: a questionnaire study
- Making researchers responsible: attributions of responsibility and ambiguous notions of culture in research codes of conduct
- The polysemy of psychotropic drugs: continuity and overlap between neuroenhancement, treatment, prevention, pain relief, and pleasure-seeking in a clinical setting
- Evaluation of decision-making capacity in patients with dementia: challenges and recommendations from a secondary analysis of qualitative interviews
- Moral competence, moral teamwork and moral action – the European Moral Case Deliberation Outcomes (Euro-MCD) Instrument 2.0 and its revision process
- Evaluating assessment tools of the quality of clinical ethics consultations: a systematic scoping review from 1992 to 2019
- The law and problematic marketing by private umbilical cord blood banks
- Relational autonomy in end-of-life care ethics: a contextualized approach to real-life complexities
- Egyptians’ social acceptance and consenting options for posthumous organ donation; a cross sectional study
- A qualitative study on aspects of consent for genomic research in communities with low literacy
- No research for the decisionally-impaired mentally ill: a view from Montenegro
- Exploring the evolution of a dental code of ethics: a critical discourse analysis
- Ethical arguments against coercing provider participation in MAiD (medical assistance in dying) in Ontario, Canada
- Perceptions of plagiarism by biomedical researchers: an online survey in Europe and China
- Self-evaluated ethical competence of a practicing physiotherapist: a national study in Finland
- Medical and midwifery students’ views on the use of conscientious objection in abortion care, following legal reform in Chile: a cross-sectional study
- Prioritising access to pandemic influenza vaccine: a review of the ethics literature
- Knowledge and attitudes of physicians toward research ethics and scientific misconduct in Lebanon
- What passive euthanasia is
- Ethical issues and practical barriers in internet-based suicide prevention research: a review and investigator survey
- Too much safety? Safeguards and equal access in the context of voluntary assisted dying legislation
- Ethical challenges regarding the use of stem cells: interviews with researchers from Saudi Arabia
- How do 66 European institutional review boards approve one protocol for an international prospective observational study on traumatic brain injury? Experiences from the CENTER-TBI study
- Addressing ethical challenges of disclosure in dementia prediction: limitations of current guidelines and suggestions to proceed
- Partnering with patients in healthcare research: a scoping review of ethical issues, challenges, and recommendations for practice
- COVID-19: where is the national ethical guidance?
- Autonomous decisions by couples in reproductive care
- Community perspectives on the benefits and risks of technologically enhanced communicable disease surveillance systems: a report on four community juries
- A palliative care approach in psychiatry: clinical implications
- Perspectives regarding privacy in clinical research among research professionals from the Arab region: an exploratory qualitative study
- Development and psychometric evaluation of a new tool for measuring the attitudes of patients with progressive neurological diseases to ethical aspects of end-of-life care
- An interprofessional cohort analysis of student interest in medical ethics education: a survey-based quantitative study
- Impact of legislation and public funding on oncofertility: a survey of Canadian, French and Moroccan pediatric hematologists/oncologists
- Ethical arguments concerning human-animal chimera research: a systematic review
- Clarifying how to deploy the public interest criterion in consent waivers for health data and tissue research
- Dishonesty and research misconduct within the medical profession
- Disease awareness or subtle product placement? Orphan diseases featured in the television series “House, M.D.” – a cross-sectional analysis
- Developing a toolkit for engagement practice: sharing power with communities in priority-setting for global health research projects
- Is it morally permissible for general practitioners to disclose their opinion on a woman’s decision on abortion?
- A systematic review of patient access to medical records in the acute setting: practicalities, perspectives and ethical consequences
- Structural racism in precision medicine: leaving no one behind
- Still a moral dilemma: how Ethiopian professionals providing abortion come to terms with conflicting norms and demands
- Implementation challenges for an ethical introduction of noninvasive prenatal testing: a qualitative study of healthcare professionals’ views from Lebanon and Quebec
- Stakeholder views on the acceptability of human infection studies in Malawi
- Disclosure to genetic relatives without consent – Australian genetic professionals’ awareness of the health privacy law
- Data Access Committees
- Why genomics researchers are sometimes morally required to hunt for secondary findings
- Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing: a qualitative study
- Addressing harm in moral case deliberation: the views and experiences of facilitators
- Legal and ethical framework for global health information and biospecimen exchange – an international perspective
- Do patients and research subjects have a right to receive their genomic raw data? An ethical and legal analysis
- Important situations that capture moral distress in paediatric oncology
- Researcher and study participants’ perspectives of consent in clinical studies in four referral hospitals in Vietnam
- Refusals to perform ritual circumcision: a qualitative study of doctors’ professional and ethical reasoning
- Digital pills: a scoping review of the empirical literature and analysis of the ethical aspects
- Informed consent procedure in a double blind randomized anthelminthic trial on Pemba Island, Tanzania: do pamphlet and information session increase caregivers knowledge?
- What is it like to use a BCI? – insights from an interview study with brain-computer interface users
- Dying too soon or living too long? Withdrawing treatment from patients with prolonged disorders of consciousness after Re Y
- Assessing attitudes towards medical assisted dying in Canadian family medicine residents: a cross-sectional study
- Culture and personal influences on cardiopulmonary resuscitation- results of international survey
- Research approvals iceberg: helping it melt away
- Response to Correspondence from Kolstoe and colleagues concerning our paper entitled, Research approvals iceberg: How a ‘low-key’ study in England needed 89 professionals to approve it and how we can do better
- Community perspectives on randomisation and fairness in a cluster randomised controlled trial in Zambia
- Can clinical ethics committees be legitimate actors in bedside rationing?
- Ethical concerns with the use of intelligent assistive technology: findings from a qualitative study with professional stakeholders
- When patient advocacy organizations meet industry: a novel approach to dealing with financial conflicts of interest
- Engaging people with lived experience in the grant review process
- Experience of oncology residents with death: a qualitative study in Mexico
- Reporting of ethical approval and informed consent in clinical research published in leading nursing journals: a retrospective observational study
- Are physicians on the same page about do-not-resuscitate? To examine individual physicians’ influence on do-not-resuscitate decision-making: a retrospective and observational study
- Dual consent? Donors’ and recipients’ views about involvement in decision-making on the use of embryos created by gamete donation in research
- Reprogenetics, reproductive risks and cultural awareness: what may we learn from Israeli and Croatian medical students?
- Mapping, framing, shaping: a framework for empirical bioethics research projects
- Ethical considerations in prehospital ambulance based research: qualitative interview study of expert informants
- Vulnerability identified in clinical practice: a qualitative analysis
- Disability, vulnerability and assisted death: commentary on Tuffrey-Wijne, Curfs, Finlay and Hollins
- Is selecting better than modifying? An investigation of arguments against germline gene editing as compared to preimplantation genetic diagnosis
- Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?
- How to tackle the conundrum of quality appraisal in systematic reviews of normative literature/information? Analysing the problems of three possible strategies (translation of a German paper)
- Analysis of official deceased organ donation data casts doubt on the credibility of China’s organ transplant reform
- Compensation of subjects for participation in biomedical research in resource – limited settings: a discussion of practices in Malawi
- What do patients with unmet medical needs want? A qualitative study of patients’ views and experiences with expanded access to unapproved, investigational treatments in the Netherlands
- Lessons learned from implementing a responsive quality assessment of clinical ethics support
- Infringement of the right to surgical informed consent: negligent disclosure and its impact on patient trust in surgeons at public general hospitals – the voice of the patient
- Relational autonomy: what does it mean and how is it used in end-of-life care? A systematic review of argument-based ethics literature
- Hospital ethics reflection groups: a learning and development resource for clinical practice
- Effect of written outcome information on attitude of perinatal healthcare professionals at the limit of viability: a randomized study
- Engaging research ethics committees to develop an ethics and governance framework for best practices in genomic research and biobanking in Africa: the H3Africa model
- Forming and implementing community advisory boards in low- and middle-income countries: a scoping review
- How do researchers acquire and develop notions of research integrity? A qualitative study among biomedical researchers in Switzerland
- Broad consent for biobanks is best – provided it is also deep
- Legal medicine implications in fibrinolytic therapy of acute ischemic stroke
- Why research ethics should add retrospective review
- Ethical issues associated with HIV molecular epidemiology: a qualitative exploratory study using inductive analytic approaches
- Euthanasia requests in dementia cases; what are experiences and needs of Dutch physicians? A qualitative interview study
- The effects of industry funding and positive outcomes in the interpretation of clinical trial results: a randomized trial among Dutch psychiatrists
- Secularity, abortion, assisted dying and the future of conscientious objection: modelling the relationship between attitudes
- Clinical ethics dilemmas in a low-income setting – a national survey among physicians in Ethiopia
- Influence of response shift and disposition on patient-reported outcomes may lead to suboptimal medical decisions: a medical ethics perspective
- Public and physicians’ support for euthanasia in people suffering from psychiatric disorders: a cross-sectional survey study
- When the law makes doors slightly open: ethical dilemmas among abortion service providers in Addis Ababa, Ethiopia
- Ghent University Hospital’s protocol regarding the procedure concerning euthanasia and psychological suffering
- Umbrella and basket trials in oncology: ethical challenges
- What Egyptians think. Knowledge, attitude, and opinions of Egyptian patients towards biobanking issues
- 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
- Regulatory and policy tools to address unproven stem cell interventions in Canada: the need for action
- Model consent clauses for rare disease research
- Informed consent and community engagement in open field research: lessons for gene drive science
- Global health ethics: critical reflections on the contours of an emerging field, 1977–2015
- Do codes of ethics and position statements help guide ethical decision making in Australian immigration detention centres?
- Implementing ethics reflection groups in hospitals: an action research study evaluating barriers and promotors
- Experiences from a community advisory Board in the Implementation of early access to ART for all in Eswatini: a qualitative study
- Do we understand the intervention? What complex intervention research can teach us for the evaluation of clinical ethics support services (CESS)
- A reflection on ethical and methodological challenges of using separate interviews with adolescent-older carer dyads in rural South Africa
- Is the non-identity problem relevant to public health and policy? An online survey
- Bioethical reflexivity and requirements of valid consent: conceptual tools
- Trust and the ethical challenges in the use of whole genome sequencing for tuberculosis surveillance: a qualitative study of stakeholder perspectives
- The challenge of community engagement and informed consent in rural Zambia: an example from a pilot study
- Ethical challenges of integration across primary and secondary care: a qualitative and normative analysis
- Who should decide about children’s and adolescents’ participation in health research? The views of children and adults in rural Kenya
- Mention of ethical review and informed consent in the reports of research undertaken during the armed conflict in Darfur (2004–2012): a systematic review
- A survey in Mexico about ethics dumping in clinical research
- Huge variation in obtaining ethical permission for a non-interventional observational study in Europe
- Achieving Self-Directed Integrated Cancer Aftercare (ASICA) in melanoma: protocol for a randomised patient-focused pilot trial of delivering the ASICA intervention as a means to earlier detection of recurrent and second primary melanoma
- Evaluating the safety and feasibility of a new surgical treatment for forearm fractures in older children: study protocol for a randomised controlled trial
- A randomised controlled trial assessing the use of citalopram, sertraline, fluoxetine and mirtazapine in preventing relapse in primary care patients who are taking long-term maintenance antidepressants (ANTLER: ANTidepressants to prevent reLapse in dEpRession): study protocol for a randomised controlled trial
- LLIN Evaluation in Uganda Project (LLINEUP) – Impact of long-lasting insecticidal nets with, and without, piperonyl butoxide on malaria indicators in Uganda: study protocol for a cluster-randomised trial
- High drug-loading gold nanoclusters for responsive glucose control in type 1 diabetes
- Social norms, misperceptions, and mosquito net use: a population-based, cross-sectional study in rural Uganda
- Porcine parvovirus VP1/VP2 on a time series epitope mapping: exploring the effects of high hydrostatic pressure on the immune recognition of antigens
- Detection of HPV RNA molecules in stratified mucin-producing intraepithelial lesion (SMILE) with concurrent cervical intraepithelial lesion: a case report
- Dynamics of gene regulatory networks and their dependence on network topology and quantitative parameters – the case of phage λ
- Competent with patients and populations: integrating public health into a medical program
- Certainty-based marking in a formative assessment improves student course appreciation but not summative examination scores
- Combination of problem-based learning with high-fidelity simulation in CPR training improves short and long-term CPR skills: a randomised single blinded trial
- Expression dynamics of repetitive DNA in early human embryonic development
- Global transcriptome profiling and functional analysis reveal that tissue-specific constitutive overexpression of cytochrome P450s confers tolerance to imidacloprid in palm weevils in date palm fields
- Biochemical functionality of magnetic particles as nanosensors: how far away are we to implement them into clinical practice?
- The acquisition of long-lived memory B cell responses to merozoite surface protein-8 in individuals with Plasmodium vivax infection
- Pairwise efficiency: a new mathematical approach to qPCR data analysis increases the precision of the calibration curve assay
- Student progress decision-making in programmatic assessment: can we extrapolate from clinical decision-making and jury decision-making?
- “Princess and the pea” – an assessment tool for palpation skills in postgraduate education
- High-resolution mapping of quantitative trait loci controlling main floral stalk length in Chinese cabbage (Brassica rapa L. ssp. pekinensis)
- Phylogeny, Divergent Evolution, and Speciation of Sulfur-Oxidizing Acidithiobacillus Populations
- Neuronal methylome reveals CREB-associated neuro-axonal impairment in multiple sclerosis
- Using mid-infrared spectroscopy and supervised machine-learning to identify vertebrate blood meals in the malaria vector, Anopheles arabiensis
- Ethical issues in denial of church wedding based on couple’s hemoglobin genotype in Enugu, south eastern Nigeria
- Conventionally used reference genes are not outstanding for normalization of gene expression in human cancer research
- Computational determination of hERG-related cardiotoxicity of drug candidates
- Is automatic detection of hidden knowledge an anomaly?
- Correction to: Whole genome sequencing Mycobacterium tuberculosis directly from sputum identifies more genetic diversity than sequencing from culture
- HEVC double compression detection under different bitrates based on TU partition type
- Combination treatment strategy for pancreatic cancer involving the novel HDAC inhibitor MPT0E028 with a MEK inhibitor beyond K-Ras status
- Novel sporozoite-based ELISpot assay to assess frequency of parasite-specific B cells after vaccination with irradiated sporozoites
- Attitudes of Iranian students about organ donation: a qualitative study
- Coronary calcification as a predictor of cardiovascular mortality in advanced chronic kidney disease: a prospective long-term follow-up study
- Capturing the differences between humoral immunity in the normal and tumor environments from repertoire-seq of B-cell receptors using supervised machine learning
- Comparison of kNN and k-means optimization methods of reference set selection for improved CNV callers performance
- Batch correction evaluation framework using a-priori gene-gene associations: applied to the GTEx dataset
- Assessment of food insecurity and its determinants in the rural households in Damot Gale Woreda, Wolaita zone, southern Ethiopia
- Estimation of gait normality index based on point clouds through deep auto-encoder
- Efficient single image dehazing by modifying the dark channel prior
- Acute Dysnatremias – a dangerous and overlooked clinical problem
- Response to letter to the editor: “comment on unplanned out-of-hospital birth and risk factors of adverse perinatal outcome: findings from a prospective cohort”
- Promoter methylation changes and vascular dysfunction in pre-eclamptic umbilical vein
- Correction to: Ten years malaria trend at Arjo-Didessa sugar development site and its vicinity, Southwest Ethiopia: a retrospective study
- ‘You can give them wings to fly’: a qualitative study on values-based leadership in health care
- Rare variant phasing using paired tumor:normal sequence data
- Utilization of maternal health services and its determinants: a cross-sectional study among women in rural Uttar Pradesh, India
- Microfluidics for studying metastatic patterns of lung cancer
- Extracellular vesicles from regenerative human cardiac cells act as potent immune modulators by priming monocytes
- A novel camera path planning algorithm for real-time video stabilization
- Angiopoietin-like-3 knockout protects against glomerulosclerosis in murine adriamycin-induced nephropathy by attenuating podocyte loss
- Impact of blood glucose levels on the accuracy of urinary N-acety-β-D-glucosaminidase for acute kidney injury detection in critically ill adults: a multicenter, prospective, observational study
- Association between vitamin D level and hematuria from a dipstick test in a large scale population based study: Korean National Health and nutrition examination survey
- Characterization of the non-glandular gastric region microbiota in Helicobacter suis-infected versus non-infected pigs identifies a potential role for Fusobacterium gastrosuis in gastric ulceration
- The CpxR regulates type VI secretion system 2 expression and facilitates the interbacterial competition activity and virulence of avian pathogenic Escherichia coli
- Reconstruction for block-based compressive sensing of image with reweighted double sparse constraint
- The effect of a terrorist attack on emergency department inflow: an observation study using difference-in-differences methodology
- Serum osteoprotegerin is an independent marker of central arterial stiffness as assessed using carotid–femoral pulse wave velocity in hemodialysis patients: a cross sectional study
- Identification of dynamic glucocorticoid-induced methylation changes at the FKBP5 locus
- Longitudinal field studies reveal early infection and persistence of influenza A virus in piglets despite the presence of maternally derived antibodies
- Hemagglutinin-neuraminidase and fusion proteins of virulent Newcastle disease virus cooperatively disturb fusion–fission homeostasis to enhance mitochondrial function by activating the unfolded protein response of endoplasmic reticulum and mitochondrial stress
- Correlation between footpad lesions and systemic bacterial infections in broiler breeders
- NeoPredPipe: high-throughput neoantigen prediction and recognition potential pipeline
- Correction to: Alaska’s Next Generation of Potential Fishermen: a Survey of Youth Attitudes Towards Fishing and Community in Bristol Bay and the Kodiak Archipelago
- A prospective pilot study using metabolomics discloses specific fatty acid, catecholamine and tryptophan metabolic pathways as possible predictors for a negative outcome after severe trauma
- Polyanionic carbosilane dendrimers as a new adjuvant in combination with latency reversal agents for HIV treatment
- Use and completion of partograph during labour is associated with a reduced incidence of birth asphyxia: a retrospective study at a peri-urban setting in Ghana
- Epigenetics in cancer therapy and nanomedicine
- How general practitioners decide on maxims of action in response to demands from conflicting sets of norms: a grounded theory study
- How should assent to research be sought in low income settings? Perspectives from parents and children in Southern Malawi
- A qualitative study on existential suffering and assisted suicide in Switzerland
- Polymer coil–globule phase transition is a universal folding principle of Drosophila epigenetic domains
- Ovarian dysfunction following prenatal exposure to an insecticide, chlordecone, associates with altered epigenetic features
- Multi-channel waveform clustering: a first look at microseismic multiplets from coalbed methane stimulation
- The notion of free will and its ethical relevance for decision-making capacity
- Live video footage from scene to aid helicopter emergency medical service dispatch: a feasibility study
- Methodological challenges in European ethics approvals for a genetic epidemiology study in critically ill patients: the GenOSept experience
- Ethics preparedness: facilitating ethics review during outbreaks – recommendations from an expert panel
- Prediction of life-story narrative for end-of-life surrogate’s decision-making is inadequate: a Q-methodology study
- Ezh2-dCas9 and KRAB-dCas9 enable engineering of epigenetic memory in a context-dependent manner
- Profiling of chromatin accessibility and identification of general cis-regulatory mechanisms that control two ocular lens differentiation pathways
- A probabilistic approach to the seismic hazard in Kashmir basin, NW Himalaya
- A fortnightly atmospheric ‘tide’ at Bali caused by oceanic tidal mixing in Lombok Strait
- Ethical tensions in the informed consent process for randomized clinical trials in emergency obstetric and newborn care in low and middle-income countries
- Nursing and midwifery students’ attitudes towards principles of medical ethics in Kermanshah, Iran
- Values and value conflicts in implementation and use of preconception expanded carrier screening – an expert interview study
- Urban heat island modelling of a tropical city: case of Kuala Lumpur
- Correction to: Consent requirements for research with human tissue: Swiss ethics committee members disagree
- Tat inhibition by didehydro-Cortistatin A promotes heterochromatin formation at the HIV-1 long terminal repeat
- Postoperative nutritional support of the patient with gut gangrene—a case report
- The involvement of family in the Dutch practice of euthanasia and physician assisted suicide: a systematic mixed studies review
- Perceptions and intentions toward medical assistance in dying among Canadian medical students
- First-time mothers’ experiences of pregnancy and birth following assisted reproductive technology treatment in Taiwan
- Responsible data sharing in international health research: a systematic review of principles and norms
- Coping strategies of families of persons with learning disability in Imo state of Nigeria
- A survey of submesoscale currents
- Men and women’s perception of yellow-root cassava among rural farmers in eastern Uganda
- Ethical failings of CPSO policy and the health care consent act: case review
- Advance directives in France: do junior general practitioners want to improve their implementation and usage? A nationwide survey
- Comparing cisplatin-Chemoradiotherapy to Cetuximab-radiotherapy in HPV+ “low-risk” locally advanced oropharyngeal squamous cell carcinoma: lessons from De-escalate study
- Using brain-computer interfaces: a scoping review of studies employing social research methods
- A review and analysis of new Italian law 219/2017: ‘provisions for informed consent and advance directives treatment’
- Physician workload associated with do-not-resuscitate decision-making in intensive care units: an observational study using Cox proportional hazards analysis
- Recent efforts to elucidate the scientific validity of animal-based drug tests by the pharmaceutical industry, pro-testing lobby groups, and animal welfare organisations
- Truth-telling and doctor-assisted death as perceived by Israeli physicians
- Using animal-derived constituents in anaesthesia and surgery: the case for disclosing to patients
- Conscientious objection to abortion, the law and its implementation in Victoria, Australia: perspectives of abortion service providers
- The picture talk project: Aboriginal community input on consent for research
- Research approvals iceberg: how a ‘low-key’ study in England needed 89 professionals to approve it and how we can do better
- A framework for the ethical assessment of chimeric animal research involving human neural tissue
- The psychology of “cure” – unique challenges to consent processes in HIV cure research in South Africa
- How to effectively obtain informed consent in trauma patients: a systematic review
- Assessment of Ficus thonningii tree production and utilization for livestock feed by smallholder farmers in northwestern Ethiopia
- Comparative analysis of technical efficiency of catfish farms using different technologies in Lagos State, Nigeria: a Data Envelopment Analysis (DEA) approach
- Bioactive compounds, health benefits and utilization of Rhododendron: a comprehensive review
- Circumcision registry promotes precise research and fosters informed parental decisions
- Illness and disease: an empirical-ethical viewpoint
- Shall parent / patient wishes be fulfilled in any case? A series of 32 ethics consultations: from reproductive medicine to neonatology
- Kenyan health stakeholder views on individual consent, general notification and governance processes for the re-use of hospital inpatient data to support learning on healthcare systems
- Participants’ awareness of ethical compliance, safety and protection during participation in pharmaceutical industry clinical trials: a controlled survey
- Does written informed consent adequately inform surgical patients? A cross sectional study
- HPV-driven oropharyngeal cancer: current knowledge of molecular biology and mechanisms of carcinogenesis
- Seed dormancy, germination and seedling characteristics of Elaeocarpus prunifolius Wall. ex Müll. Berol.: a threatened tree species of north-eastern India
- Assessment of genetic diversity of Saraca asoca (Roxb.) De Wilde: a commercially important, but endangered, forest tree species in Western Ghats, India
- Invasive alien plant species, fragmentation and scale effects on urban forest community composition in Durban, South Africa
- Potential use of hyperspectral data to classify forest tree species
- Plantation species-specific adjustment functions for the Forest Carbon Predictor in New Zealand
- African bioethics: methodological doubts and insights
- Developing an ethics support tool for dealing with dilemmas around client autonomy based on moral case deliberations
- Participation in a single-blinded pediatric therapeutic strategy study for juvenile idiopathic arthritis: are parents and patient-participants in equipoise?
- Experiences of pre-hospital emergency medical personnel in ethical decision-making: a qualitative study
- Time abides long enough for those who make use of it
- Exploring the ethics of global health research priority-setting
- Consent requirements for research with human tissue: Swiss ethics committee members disagree
- Parents’ attitudes towards and perceptions of involving minors in medical research from the Japanese perspective
- A qualitative study on the voluntariness of counselling and testing for HIV amongst antenatal clinic attendees: do women have a choice?
- A comprehensive systematic review of stakeholder attitudes to alternatives to prospective informed consent in paediatric acute care research
- Stakeholder views regarding ethical issues in the design and conduct of pragmatic trials: study protocol
- Defining and categorizing outcomes of Moral Case Deliberation (MCD): concept mapping with experienced MCD participants
- Nodal disease predicts recurrence whereas other traditional factors affect survival in a cohort of South African patients with differentiated thyroid carcinoma
- Application of the rapid ethical assessment approach to enhance the ethical conduct of longitudinal population based female cancer research in an urban setting in Ethiopia
- Correction to: Alaska’s next generation of potential fishermen: a survey of youth attitudes towards fishing and community in Bristol Bay and the Kodiak Archipelago
- Challenges arising when seeking broad consent for health research data sharing: a qualitative study of perspectives in Thailand
- Impact of moral case deliberation in healthcare settings: a literature review
- Survival and associated factors among patients with oral squamous cell carcinoma (OSCC) in Mulago hospital, Kampala, Uganda
- Addressing vaccine hesitancy requires an ethically consistent health strategy
- Ethical considerations for HIV cure-related research at the end of life
- Conscientious objection to intentional killing: an argument for toleration
- Correction to: Beyond the cooperative: the story of collective action in North Carolina’s small-scale fisheries
- Exploring neurologists’ perspectives on the return of next generation sequencing results to their patients: a needed step in the development of guidelines
- Attitudes to prenatal screening among Norwegian citizens: liberality, ambivalence and sensitivity
- Correction to: Building fisheries institutions through collective action in Norway
- What information and the extent of information research participants need in informed consent forms: a multi-country survey
- The last cowboys: keeping open access in the Aleut groundfish fishery of the Gulf of Alaska
- A bioethical framework to guide the decision-making process in the care of seriously ill patients
- Reuse of cardiac organs in transplantation: an ethical analysis
- Frequency of use of the religious exemption in New Jersey cases of determination of brain death
- The values and ethical commitments of doctors engaging in macroallocation: a qualitative and evaluative analysis
- Beyond ‘health and safety’ – the challenges facing students asked to work outside of their comfort, qualification level or expertise on medical elective placement
- A systematic review of the literature on ethical aspects of transitional care between child- and adult-orientated health services
- Setting standards for empirical bioethics research: a response to Carter and Cribb
- Debating diversity: a commentary on Standards of practice in empirical bioethics research
- Predictors of consent to cell line creation and immortalisation in a South African schizophrenia genomics study
- Let’s talk about standards: a commentary on standards of practice in empirical bioethics
- Standards of practice in empirical bioethics research: towards a consensus
- Their view: difficulties and challenges of patients and physicians in cross-cultural encounters and a medical ethics perspective
- 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
- Management of financial conflicts of interests in clinical practice guidelines in Germany: results from the public database GuidelineWatch
- Good health checks according to the general public; expectations and criteria: a focus group study
- Ethical challenges assessed in the clinical ethics Committee of Psychiatry in the region of Southern Denmark in 2010–2015: a qualitative content analyses
- Ethical competence in DNR decisions –a qualitative study of Swedish physicians and nurses working in hematology and oncology care
- Ethical concerns on sharing genomic data including patients’ family members
- A reflection on the challenge of protecting confidentiality of participants while disseminating research results locally
- Introduction to Ethics and Global Health
- Commodification of care and its effects on maternal health in the Noun division (West Region – Cameroon)
- Integrated primary health care in low- and middle-income countries: a double challenge
- In pursuit of goodness in bioethics: analysis of an exemplary article
- Evaluation as institution: a contractarian argument for needs-based economic evaluation
- Advance directive: does the GP know and address what the patient wants? Advance directive in primary care
- Opening the debate on deep brain stimulation for Alzheimer disease – a critical evaluation of rationale, shortcomings, and ethical justification
- Identification of ethics committees based on authors’ disclosures: cross-sectional study of articles published in the European Journal of Anaesthesiology and a survey of ethics committees
- The patient perspective in health care networks
- The significance of ethics reflection groups in mental health care: a focus group study among health care professionals
- Medicine, market and communication: ethical considerations in regard to persuasive communication in direct-to-consumer genetic testing services
- The dual use of research ethics committees: why professional self-governance falls short in preserving biosecurity
- Leadership in palliative medicine: moral, ethical and educational
- Changes in attitudes towards hastened death among Finnish physicians over the past sixteen years
- Surgical informed consent in obstetric and gynecologic surgeries: experience from a comprehensive teaching hospital in Southern Ethiopia
- Research ethics review at University Eduardo Mondlane (UEM)/Maputo Central Hospital, Mozambique (2013–2016): a descriptive analysis of the start-up of a new research ethics committee (REC)
- A scoping review of reporting ‘Ethical Research Practices’ in research conducted among refugees and war-affected populations in the Arab world
- Translating and culturally adapting the shortened version of the Hospital Ethical Climate Survey (HECS-S) – retaining or modifying validated instruments
- Involvement in decisions about intravenous treatment for nursing home patients: nursing homes versus hospital wards
- Complexity of consenting for medical termination of pregnancy: prospective and longitudinal study in Paris
- The involvement of Canadian physicians in promoting and providing unproven and unapproved stem cell interventions
- Conscientious objection to participation in abortion by midwives and nurses: a systematic review of reasons
- ‘Screening audit’ as a quality assurance tool in good clinical practice compliant research environments
- Patenting human genes: Chinese academic articles’ portrayal of gene patents
- Rationing elective surgery for smokers and obese patients: responsibility or prognosis?
- Women’s perspectives on the ethical implications of non-invasive prenatal testing: a qualitative analysis to inform health policy decisions
- Skepticism towards the Swedish vision zero for suicide: interviews with 12 psychiatrists
- Forensic psychiatry, one subspecialty with two ethics? A systematic review
- Ethical principles and placebo-controlled trials – interpretation and implementation of the Declaration of Helsinki’s placebo paragraph in medical research
- Compassionate use programs in Italy: ethical guidelines
- Educational video-assisted versus conventional informed consent for trauma-related debridement surgery: a parallel group randomized controlled trial
- Patient data and patient rights: Swiss healthcare stakeholders’ ethical awareness regarding large patient data sets – a qualitative study
- Early-career researchers’ views on ethical dimensions of patient engagement in research
- Leaving patients to their own devices? Smart technology, safety and therapeutic relationships
- The ethics of using placebo in randomised controlled trials: a case study of a Plasmodium vivax antirelapse trial
- Euthanasia and assisted suicide for people with an intellectual disability and/or autism spectrum disorder: an examination of nine relevant euthanasia cases in the Netherlands (2012–2016)
- Objectivity applied to embodied subjects in health care and social security medicine: definition of a comprehensive concept of cognitive objectivity and criteria for its application
- Screening for infectious diseases of asylum seekers upon arrival: the necessity of the moral principle of reciprocity
- Rules of engagement: perspectives on stakeholder engagement for genomic biobanking research in South Africa
- Matters to address prior to introducing new life support technology in Japan: three serious ethical concerns related to the use of left ventricular assist devices as destination therapy and suggested policies to deal with them
- Ethical issues in pragmatic randomized controlled trials: a review of the recent literature identifies gaps in ethical argumentation
- 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)
- Moral dilemmas and conflicts concerning patients in a vegetative state/unresponsive wakefulness syndrome: shared or non-shared decision making? A qualitative study of the professional perspective in two moral case deliberations
- Advance directives as a tool to respect patients’ values and preferences: discussion on the case of Alzheimer’s disease
- Disparate compensation policies for research related injury in an era of multinational trials: a case study of Brazil, Russia, India, China and South Africa
- Benefit in liver transplantation: a survey among medical staff, patients, medical students and non-medical university staff and students
- An update on the “empirical turn” in bioethics: analysis of empirical research in nine bioethics journals
- Combining value of information analysis and ethical argumentation in decisions on participation of vulnerable patients in clinical research
- Fake facts and alternative truths in medical research
- Autonomy and couples’ joint decision-making in healthcare
- “Right to recommend, wrong to require”- an empirical and philosophical study of the views among physicians and the general public on smoking cessation as a condition for surgery
- Ethical aspects of diagnosis and interventions for children with fetal alcohol Spectrum disorder (FASD) and their families
- Balancing the local and the universal in maintaining ethical access to a genomics biobank
- The use of empirical research in bioethics: a survey of researchers in twelve European countries
- Participatory improvement of a template for informed consent documents in biobank research – study results and methodological reflections
- Ethical challenges experienced by UK military medical personnel deployed to Sierra Leone (operation GRITROCK) during the 2014–2015 Ebola outbreak: a qualitative study
- Experiences of community members and researchers on community engagement in an Ecohealth project in South Africa and Zimbabwe
- The ethics of caring for hospital-dependent patients
- Decision-making on therapeutic futility in Mexican adolescents with cancer: a qualitative study
- Transplant eligibility for patients with affective and psychotic disorders: a review of practices and a call for justice
- Must we remain blind to undergraduate medical ethics education in Africa? A cross-sectional study of Nigerian medical students
- Attitudes towards assisted suicide and euthanasia among care-dependent older adults (50+) in Austria: the role of socio-demographics, religiosity, physical illness, psychological distress, and social isolation
- Patient-targeted Googling and social media: a cross-sectional study of senior medical students
- Informed consent for clinical treatment in low-income setting: evaluating the relationship between satisfying consent and extent of recall of consent information
- Roles and responsibilities of clinical ethics committees in priority setting
- Ethical considerations in forensic genetics research on tissue samples collected post-mortem in Cape Town, South Africa
- Development and pilot testing of an informed consent video for patients with limb trauma prior to debridement surgery using a modified Delphi technique
- Measuring inconsistency in research ethics committee review
- The no correlation argument: can the morality of conscientious objection be empirically supported? the Italian case
- Biobanking in Israel 2016–17; expressed perceptions versus real life enrollment
- Gender and age disparity in the initiation of life-supporting treatments: a population-based cohort study
- The strange case of Mr. H. Starting dialysis at 90 years of age: clinical choices impact on ethical decisions
- Ethical aspects of brain computer interfaces: a scoping review
- The emergence of ethical issues in the provision of online sexual health outreach for gay, bisexual, two-spirit and other men who have sex with men: perspectives of online outreach workers
- This moral coil: a cross-sectional survey of Canadian medical student attitudes toward medical assistance in dying
- Collaborative partnership and the social value of clinical research: a qualitative secondary analysis
- Limits to human enhancement: nature, disease, therapy or betterment?
- What is a good health check? An interview study of health check providers’ views and practices
- Descriptive study of association between quality of care and empathy and burnout in primary care
- Informed consent and registry-based research – the case of the Danish circumcision registry
- Erratum to: The Liverpool Care Pathway: discarded in cancer patients but good enough for dying nursing home patients? A systematic review
- Eliciting meta consent for future secondary research use of health data using a smartphone application – a proof of concept study in the Danish population
- Ethical issues of informed consent in malaria research proposals submitted to a research ethics committee in Thailand: a retrospective document review
- Does growing up with a physician influence the ethics of medical students’ relationships with the pharmaceutical industry? The cases of the US and Poland
- The Liverpool Care Pathway: a systematic review discarded in cancer patients but good enough for dying nursing home patients?
- Healthcare professionals’ and patients’ perspectives on consent to clinical genetic testing: moving towards a more relational approach
- Pre- and post-testing counseling considerations for the provision of expanded carrier screening: exploration of European geneticists’ views
- Erratum to: Ethics review of studies during public health emergencies – the experience of the WHO ethics review committee during the Ebola virus disease epidemic
- Familiar ethical issues amplified: how members of research ethics committees describe ethical distinctions between disaster and non-disaster research
- Ethics review of studies during public health emergencies – the experience of the WHO ethics review committee during the Ebola virus disease epidemic
- Comparative effectiveness research: what to do when experts disagree about risks
- Development of a consensus operational definition of child assent for research
- Are advance directives helpful for good end of life decision making: a cross sectional survey of health professionals
- How Chinese clinicians face ethical and social challenges in fecal microbiota transplantation: a questionnaire study
- A 14-day limit for bioethics: the debate over human embryo research
- Staff’s normative attitudes towards coercion: the role of moral doubt and professional context—a cross-sectional survey study
- Written versus verbal consent: a qualitative study of stakeholder views of consent procedures used at the time of recruitment into a peripartum trial conducted in an emergency setting
- A qualitative study on acceptable levels of risk for pregnant women in clinical research
- The Picture Talk Project: Starting a Conversation with Community Leaders on Research with Remote Aboriginal Communities of Australia
- Self-tests for influenza: an empirical ethics investigation
- Assessment of knowledge about biobanking among healthcare students and their willingness to donate biospecimens
- On classifying the field of medical ethics
- Ethics of health research with prisoners in Canada
- Core information sets for informed consent to surgical interventions: baseline information of importance to patients and clinicians
- The elusive ideal of inclusiveness: lessons from a worldwide survey of neurologists on the ethical issues raised by whole-genome sequencing
- A critique of the regulation of data science in healthcare research in the European Union
- Fair is fair: We must re-allocate livers for transplant
- Smart homes, private homes? An empirical study of technology researchers’ perceptions of ethical issues in developing smart-home health technologies
- Factors affecting willingness to share electronic health data among California consumers