- Not a matter of parental choice but of social justice obligation: Children are owed measles vaccination
- Ethical issues in research on substance‐dependent parents: The risk of implicit normative judgements by researchers
- Suffering at the end of life
- The value of work: Addressing the future of work through the lens of solidarity
- From protectionism to inclusion: A New Zealand perspective on health‐related research involving adults incapable of giving informed consent
- Ethics and HIV prevention research: An analysis of the early tenofovir PrEP trial in Nigeria
- Cosmetic dentistry: A socioethical evaluation
- In vitro gametogenesis and reproductive cloning: Can we allow one while banning the other?
- Illegitmate authorship and flawed procedures: Fundamental, formal criticisms of the Declaration of Helsinki
- Why pro‐life arguments still are not convincing: A reply to my critics
- Financing uterus transplants: The United States context
- Compulsory moral bioenhancement should be covert
- Transcranial electrical stimulation for human enhancement and the risk of inequality: Prohibition or compensation?
- Enriching the concept of vulnerability in research ethics: An integrative and functional account
- The Unabomber’s ethics
- Robot Sex: Social and Ethical Implications. John Danaher Neil MacArthur (Eds.) The MIT Press: Cambridge, MA, and London, 2017. 314 pp., includes index. ISBN 9780262036689. $40 (Hardcover).
- Political legitimacy and research ethics
- In vitro gametogenesis: The end of egg donation?
- Empathy is a poor foundation on which to base legislative medical policy
- Precaution, threshold risk and public deliberation
- Is infertility a disease and does it matter?
- Self‐admission in psychiatry: The ethics
- Mechanistic reasoning and informed consent
- An ecological approach to modeling disability
- Return to childhood? Against the infantilization of people with dementia
- Parents’ posthumous use of daughter’s ovarian tissue: Ethical dimensions
- Should human germ line editing be allowed? Some suggestions on the basis of the existing regulatory framework
- Genetic research and consent: On the crossroads of human and data research
- Discussing rights and wrongs: Three suggestions for moving forward with the migrant health rights debate
- Companions or patients? The impact of family presence in genetic consultations for inherited breast cancer: Relational autonomy in practice
- Clinical Research Involving Pregnant Women. F. Baylis A. Ballantyne (Eds.) Springer, Research Ethics Forum 3, 2016. 301 pp. US$ 149.00 e-book, US$ 199.00 hb. ISBN 978‐3‐319‐26510‐0, $189.
- From self‐interest to solidarity: One path towards delivering refugee health
- Migration, health, and ethics
- Social value, clinical equipoise, and research in a public health emergency
- Positioning uterus transplantation as a ‘more ethical’ alternative to surrogacy: Exploring symmetries between uterus transplantation and surrogacy through analysis of a Swedish government white paper
- Solidarity and the problem of structural injustice in healthcare
- A conception of genetic parenthood
- Community engagement in global health research that advances health equity
- The ethics of ordinary and exact justification in blood donation deferral categories for men who have sex with men
- Deceased‐directed donation: Considering the ethical permissibility in a multicultural setting
- Uterus transplantation as radical reproduction: Taking the adoption alternative more seriously
- Our flawed approach to undue inducement in medical research
- Trust and responsibility in molecular tumour boards
- Conscientious objection in healthcare: How much discretionary space best supports good medicine?
- Mandatory sex selection and mitochondrial transfer
- Humanitarian medical aid to the Syrian people: Ethical implications and dilemmas
- Tu Youyou winning the Nobel Prize: Ethical research on the value and safety of traditional Chinese medicine
- Conscientious objection and compromising the patient: Response to Hughes
- Self‐ownership, relational dignity, and organ sales
- Informed consent and nudging
- Should consent be required for organ procurement?
- There is no right to the death of the fetus
- When is coercive methadone therapy justified?
- Hit but not down. The substance view in light of the criticism of Lovering and Simkulet
- A rights‐based proposal for managing faith‐based values and expectations of migrants at end‐of‐life illustrated by an empirical study involving South Asians in the UK
- Bioethics culture wars – 2018 edition: Alfie Evans
- Framing the ethical and legal issues of human artificial gametes in research, therapy, and assisted reproduction: A German perspective
- Union’s inspiration: Universal health care and the essential partiality of solidarity
- Language barriers and epistemic injustice in healthcare settings
- Will cognitive enhancement create post‐persons? The use(lessness) of induction in determining the likelihood of moral status enhancement
- Solidarity as a national health care strategy
- Health worker migration and migrant healthcare: Seeking cosmopolitanism in the NHS
- Physician‐Assisted Death: What Everyone Needs to Know. L. W. Sumner, Oxford University Press, New York, NY, 2017. xv + 243 pp. US$ 16.95 pbk, ISBN 978‐0‐19‐049017‐1. US$ 74.00 hbk. ISBN 978‐0‐19‐049018‐8.
- Educational pelvic exams on anesthetized women: Why consent matters
- Regret, shame, and denials of women’s voluntary sterilization
- Conscience claims, metaphysics, and avoiding an LGBT eugenic
- The ethics of ageing
- The canary in the coal mine: Continence care for people with dementia in acute hospital wards as a crisis of dehumanization
- Toward a global geroethics – gerontology and the theory of the good human life
- Responsibility and age‐related dementia
- Are older people a vulnerable group? Philosophical and bioethical perspectives on ageing and vulnerability
- Indignity and Old Age
- Empathy, social media, and directed altruistic living organ donation
- Reproductive cloning revisited
- Fostering caring relationships: Suggestions to rethink liberal perspectives on the ethics of newborn screening
- Fragile lives with fragile rights: Justice for babies born at the limit of viability
- Effective altruists ought to be allowed to sell their kidneys
- Melanoma in the shopping mall: A utilitarian argument for offering unsolicited medical opinions in informal settings
- Relational autonomy, care, and Jehovah’s Witnesses in Germany
- Why arguments against infanticide remain convincing: A reply to Räsänen
- Influencing relatives to respect donor autonomy: Should we nudge families to consent to organ donation?
- The future-like-ours argument, animalism, and mereological universalism
- The trouble with public health: HIV/AIDS in Canada as a case in point
- Manipulation, salience, and nudges
- From applied ethics to empirical ethics to contextual ethics
- The epistemic costs of compromise in bioethics
- Reproductive autonomy and responsibility: current trends
- Queer reproduction revisited and why race, class and citizenship still matters: A response to Cristina Richie
- Different games of moral bioenhancement
- Who gets the gametes? An argument for a points system for fertility patients
- Enthusiastic portrayal of 3D bioprinting in the media: Ethical side effects
- Judgments of moral responsibility in tissue donation cases
- The parenthood argument
- Conscientious objection, professional duty and compromise: A response to Savulescu and Schuklenk
- A dubious defense of ‘after-birth abortion’: A reply to Räsänen
- Ectogenesis, abortion and a right to the death of the fetus
- Many thanks to Bioethics reviewers
- A Bioethics Editor’s Summer 2017 Conference Season: Conscientious Objection and Research Ethics
- Books Received September 2016 – August 2017
- The ethics of public policy RCTs: The principle of policy equipoise
- A Prospectus for ethical analysis of ageing individuals’ responsibility to prevent cognitive decline
- Scanning the body, sequencing the genome: Dealing with unsolicited findings
- Moral bioenhancement and agential risks: Good and bad outcomes
- Autism, theory of mind, and the reactive attitudes
- Public health agencies’ obligations and the case of Zika
- IAB Presidential address: “Searching for Justice”
- The limits of the treatment-enhancement distinction as a guide to public policy
- Balancing bioethics by sensing the aesthetic
- Ethical issues raised by thyroid cancer overdiagnosis: A matter for public health?
- Family interests and medical decisions for children
- Merging arts and bioethics: An interdisciplinary experiment in cultural and scientific mediation
- Fertility, immigration, and the fight against climate change
- Does benefit justify research with children?
- Bioethics, children, and the environment
- Medical Innovation in a Children’s Hospital: ‘Diseases desperate grown by desperate appliance are relieved, or not at all’
- A Kantian ethics approach to moral bioenhancement
- Presuming patient autonomy in the face of therapeutic misconception
- Reconsidering paternalism in clinical research
- The indispensability of labelled groups to vulnerability in bioethics
- When doctors deny drugs: Sexism and contraception access in the medical field
- Shame and HIV: Strategies for addressing the negative impact shame has on public health and diagnosis and treatment of HIV
- Two kinds of physician-assisted death
- First, do no harm: Generalized procreative non-maleficence
- A pragmatic analysis of vulnerability in clinical research
- Human organisms begin to exist at fertilization
- Euthanasia and cryothanasia
- Ways of showing respect for life
- Defending the social value of knowledge as a safeguard for public trust
- Response to Vogelstein: How the 2012 AAP Task Force on circumcision went wrong
- Tying oneself to the mast: One necessary cost to morally enhancing oneself biomedically
- ‘You are inferior!’ Revisiting the expressivist argument
- New Frontiers in End-of-Life Ethics (and Policy): Scope, Advance Directives and Conscientious Objection
- The experiences of pregnant women in an interventional clinical trial: Research In Pregnancy Ethics (RIPE) study
- The Ethics of Clinical Trials Research in Severe Mood Disorders
- The Voluntary Nature of Decision-Making in Addiction: Static Metaphysical Views Versus Epistemologically Dynamic Views
- Respect for Autonomy in Light of Neuropsychiatry
- Can Neuroscience Contribute to Practical Ethics? A Critical Review and Discussion of the Methodological and Translational Challenges of the Neuroscience of Ethics
- Moral Enhancement Meets Normative and Empirical Reality: Assessing the Practical Feasibility of Moral Enhancement Neurotechnologies
- Neuroethics: Neuroscience’s Contributions to Bioethics
- Assisted Dying & Disability
- What Outcomes do Dutch Healthcare Professionals Perceive as Important Before Participation in Moral Case Deliberation?
- Evaluating Clinical Ethics Support: A Participatory Approach
- Methodological Reflections on the Contribution of Qualitative Research to the Evaluation of Clinical Ethics Support Services
- Discovering What Matters: Interrogating Clinician Responses to Ethics Consultation
- Integrating Theory and Data in Evaluating Clinical Ethics Support. Still a Long Way to Go
- Evaluating the Quality of the Deliberation in Moral Case Deliberations: A Coding Scheme
- Fair Resource Allocation to Health Research: Priority Topics for Bioethics Scholarship
- Wrongness, Responsibility, and Conscientious Refusals in Health Care
- Ethical Considerations of Triage Following Natural Disasters: The IDF Experience in Haiti as a Case Study
- Moral Hard-Wiring and Moral Enhancement
- Is Consent Based on Trust Morally Inferior to Consent Based on Information?
- Alcohol Use Disorder, Liver Transplantation and Ethics
- Bioethics in a Post-Truth Era
- Human Dignity and Human Enhancement: A Multidimensional Approach
- The Place of Crowdfunding in the Discovery of Scientific and Social Value of Medical Research
- Is There a Right to the Death of the Foetus?
- Ways Out of the Patenting Prohibition? Human Parthenogenetic and Induced Pluripotent Stem Cells
- Epistemic Authority and Genuine Ethical Controversies
- In Defense of Artificial Replacement
- The Mitochondrial Replacement ‘Therapy’ Myth
- The Consequences of Vagueness in Consent to Organ Donation
- The human genome as public: Justifications and implications
- Permanence can be Defended
- When is a Choice not a Choice? ‘Sham Offers’ and the Asymmetry of Adolescent Consent and Refusal
- The Substance View: A Critique (Part 3)
- Objection to Conscience: An Argument Against Conscience Exemptions in Healthcare
- Conscientious Objection to Vaccination
- The Invisible Discrimination Before Our Eyes: A Bioethical Analysis
- The Edge of Human? The Problem with the Posthuman as the ‘Beyond’
- Bioethics, General Ethics and CAM
- Misplaced Paternalism and other Mistakes in the Debate over Kidney Sales
- Assisted Suicide in Switzerland: Clarifying Liberties and Claims
- Doctors Have no Right to Refuse Medical Assistance in Dying, Abortion or Contraception