Hastings Center Report

Papers
(The median citation count of Hastings Center Report is 0. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-06-01 to 2026-06-01.)
ArticleCitations
An Ecostructural Lens for Health Ethics48
Guiding the Future: Rethinking the Role of Advance Directives in the Care of People with Dementia38
Deciding with Others: Interdependent Decision‐Making32
What Patient‐Experience Data Reveal about Trust26
On the Authority of Advance Euthanasia Directives for People with Severe Dementia: Reflections on a Dutch Case24
About the Special Report20
Cultivating Peace and Health at Community Health Centers19
Contributors19
Moral Status and the Oversight of Research Involving Chimeric Animals18
Abortion Access Persists, but So Do the Threats16
Contributors16
From Eugenics to Human Genome Editing: Bionationalism and Instrumentalizing Life in China within a Global Context15
Moving toward Equity through Embedded ELSI Ethnography14
Trust in Crises and Crises of Trust13
Xenotransplantation Clinical Trials and the Need for Community Engagement13
Home Care in America: The Urgent Challenge of Putting Ethical Care into Practice13
The Pandemic of Invisible Victims in American Mental Health12
Making the Move to a Learning System of Research Ethics12
How Seeking Transfer Often Fails to Help Define Medically Inappropriate Treatment11
Contributors11
Digital Mental Health Tools and AI Therapy Chatbots: A Balanced Approach to Regulation10
Challenging Disability Discrimination in the Clinical Use of PDMP Algorithms10
Reevaluating the Ethical Issues in Porcine‐to‐Human Heart Xenotransplantation10
Choice in the Context of Dementia: Emerging Issues for Health Care Practice in Aging Societies10
Clinician Moral Distress: Toward an Ethics of Agent‐Regret9
Errata9
Contributors9
Enhancing Equity in Genomics: Incorporating Measures of Structural Racism, Discrimination, and Social Determinants of Health9
Identity Theft, Deep Brain Stimulation, and the Primacy of Post‐trial Obligations9
Stef M. Shuster and Meredithe McNamara reply:8
Contributors8
Moral Humility for a Complex World8
Why Aren't There More Whistleblowers?8
Complex Decisions8
Who Carries the Responsibility for Health Care Carbon Reduction?8
Lockdowns, Bioethics, and the Public: Policy‐Making in a Liberal Democracy8
8
“You have to trust yourself”: The Overlooked Role of Self‐Trust in Coping with Chronic Illness8
Defining Death Anew: Reexamining the Twentieth‐Century Brain Death Debates and the Uniform Determination of Death Act8
What Is the Aim of Pediatric “Gender‐Affirming” Care?7
The Case for Baptizing a Dying, Unconscious Atheist7
Risk‐Sensitive Assessment of Decision‐Making Capacity: A Comprehensive Defense7
Errors in Converting Principles to Protocols: Where the Bioethics of U.S. Covid‐19 Vaccine Allocation Went Wrong7
Neither Ethical nor Prudent: Why Not to Choose Normothermic Regional Perfusion6
Rethinking the Burden of Traditional Informed Consent Prior to Prenatal Genetic Screening6
Is Food Medicine?6
Rethinking Decision Quality: Measures, Meaning, and Bioethics5
The Problem Is Not (Merely) Mass Incarceration: Incarceration as a Bioethical Crisis and Abolition as a Moral Obligation5
In Defense of Openness—Genetic Knowledge and Gamete Donation5
5
Accountability for Reasonableness as a Framework for the Promotion of Fair and Equitable Research5
Dementia and Concurrent Consent to Sexual Relations5
The Values That Influence Psychiatric Diagnosis and Accountability5
Issue Information and About the Cover Art5
Global Efforts to Protect Healthy Volunteers5
The Microethics of Communication in Health Care: A New Framework for the Fast Thinking of Everyday Clinical Encounters4
What Do Prospective Parents Owe to Their Children?4
Moral Nuances in Broad Policies4
Dementia, Narrative, and Place: What Can Be Learned from the Age‐Friendly Movement?4
Finding Disability in Everyday Life4
Exploring the Ethics of the Parental Role in Parent‐Clinician Conflict4
Editors and Authors4
Principled Conscientious Provision: Referral Symmetry and Its Implications for Protecting Secular Conscience4
Recalibrating Bioethics for the Reality of Interdependence: The Challenge of Collective‐Impact Problems4
Justifying Clinical Deception: Some Amendments to Brummett and Salter4
Policy, Politics, and Impact4
Deception, Pain, and Placebo: Applying the Brummett‐Salter Deception Framework4
Gender and Sport4
Intersecting Narratives in the Lives of Black Women Aging with Dementia4
Rethinking Theory in Bioethics4
Forgotten and without Protections: Older Adults in Prison Settings4
Editors and Authors3
About the Special Report3
Contributors3
Love Your Patient as Yourself: On Reviving the Broken Heart of American Medical Ethics3
Stories and Shame in Front‐Line Medicine3
Editors and Authors3
Living in the Shadow of Uncertainty: Rethinking Cancer as Chronic Illness3
Locked In3
Public Engagement as a Form of Moral Leadership3
Daoist Views on Disability and Genetic Intervention3
Experiential Training in Psychedelic‐Assisted Therapy: A Risk‐Benefit Analysis3
Arguments and Analogies: Do Children Have a Right to Know Their Genetic Origins?3
Science and Justice3
Fifty Years of U.S. Mass Incarceration and What It Means for Bioethics3
Editors’ Statement on the Responsible Use of Generative AI Technologies in Scholarly Journal Publishing3
Xenotransplantation: Injustice, Harm, and Alternatives for Addressing the Organ Crisis3
Issue Information and About the Cover Art3
Participant Engagement, Epistemic Injustice, and Early‐Phase Implanted Neural Device Research3
Opening the Door: Rethinking “Difficult Conversations” about Living and Dying with Dementia3
A Timely Pursuit: Disability Justice in Pandemic Planning3
Contributors3
The Dead Unborn, Postmortem Privacy Cases, and Abortion Rights2
The Bioethicist as Healer2
Issue Information and About the Cover Art2
2
Telemedicine and Healing Relationships2
Issue Information2
Talking with Each Other about Science2
Food and Drug Administration v. Alliance for Hippocratic Medicine: How Conscience Protections Preserved Mifepristone Access2
Knowing the Mind from Brain Data: The Challenge of Prediction and the Fairness of Relying on Objective Data about the Mind2
Parity, Poverty, and Physician Aid in Dying: Policy Recommendations for PAD in Light of Social Injustices2
About the Special Report2
Choosing to Die2
When Mistakes Multiply: How Inadequate Responses to Medical Mishaps Erode Trust in American Medicine2
Neuroscience and Society: Supporting and Unsettling Public Engagement2
Contributors2
Rethinking the Ethics of the Covid‐19 Pandemic Lockdowns2
Can Caregivers Ever Say No?2
Should Parents of the Deceased Have Standing to Initiate Posthumous Sperm Retrieval? Analyzing Developments in Israel2
A Life Worth Sustaining? Bestowed Worth and Pediatric Care2
Can Open Science Advance Health Justice? Genomic Research Dissemination in the Evolving Data‐Sharing Landscape2
Dignity and the Founding Myth of Bioethics2
2
Genetics and Scientific Values: Aaron Panofsky, Kushan Dasgupta, Nicole Iturriaga, and Bernard Koch Reply2
Implicit Narratives in Participatory Arts Collaborations with People with Lived Experience of Dementia2
Gender‐Affirming Care for Cisgender People2
The Need for Bioethics Departments in HBCU Medical Schools2
Residency Requirements for Medical Aid in Dying2
The Ethic of Accompaniment2
2
Bright‐Line Policy and the Future of the Fourteen‐Day Rule2
What Makes a Better Life for People Facing Dementia? Toward Dementia‐Friendly Health and Social Policy, Medical Care, and Community Support in the United States2
Dementia as a Critical Lens on the Role of Narrative in Medical Training and Practice2
A Prescriptive Metaphysics of DEATH2
Editors and Authors2
Smuggled Doughnuts and Forbidden Fried Chicken: Addressing Tensions around Family and Food Restrictions in Hospitals2
Managing Dependence: Assistive Technologies in Dementia Care2
Leah Z. Rand, Daniel P. Carpenter, Aaron S. Kesselheim, Anushka Bhaskar, Jonathan J. Darrow, and William B. Feldman Reply1
Holding the Guardrails on Involuntary Commitment1
The Problem of Clinical Deception and Why We Cannot Begin in the Middle1
The Case for Prescribing Metformin Off‐Label for a Child in Remission from Ependymoma1
Musical Performance and Biomedical Human Enhancement: Ethnographic Perspectives on Bioethical Questions1
Issue Information and About the Cover Art1
Issue Information and About the Cover Art1
Confronting the “Weaponization” of Genetics by Racists Online and Elsewhere1
Contributors1
Conscience, Caricatures, and Catholic Identities1
Protecting Health after Dobbs1
Can I Hold That Thought for You? Dementia and Shared Relational Agency1
Issue Information (About the Cover Art)1
Rectifying or Reinforcing? The (In)Equity Implications of Recontacting Practices in Genomic Medicine1
Zoonoses and Animal Culling: The Need for One Health Policy1
Inferring Mental States from Brain Data: Ethico‐legal Questions about Social Uses of Brain Data1
Implications for All Animal Research1
Carbon Emissions from Overuse of U.S. Health Care: Medical and Ethical Problems1
Erratum1
1
Making the World Safer and Fairer in Pandemics1
Strategic Ethics: Physician Associations and Their Roles in Pursuing Racial Equity1
History and the Challenges of Dementia1
Unfolding Hidden Narratives: Glimpses of an Ethos of Senses in a Dementia‐Care Facility1
Spiritual Care Ethics1
Banning Gender‐Affirming Treatment for Minors: The Supreme Court Speaks1
Thinking about Moral Progress1
Issue Information and About the Cover Art1
Contributors1
Contributors1
Where the Genetic Code Meets the Zip Code: Advancing Equity in Rare Disease Genomics1
Physician Perspectives on Building Trust with Patients1
1
Big Mistake: Knowing and Doing Better in Patient Engagement1
Do Suicide Attempters Have a Right Not to Be Stabilized in an Emergency?1
On Old Age: A Relational Account of Agency and Meaning in Later Life1
Henri Wijsbek and Thomas Nys Respond1
Transformed but Not Cured: The Ethics of Describing Gene‐Editing Therapy for Sickle Cell Disease1
In Defense of Normothermic Regional Perfusion1
Issue Information (About the Cover Art)1
Composite Animals: Then and Now1
Tyler Tate replies1
How Should Clinical Ethics Evolve to Ensure Moral Use of AI?1
Editors and Authors1
U.S. Lawsuit Claims Federal Law Can Require Emergency Abortions1
Care or Complicity? Medical Personnel in Prisons1
Expanding the Agenda for a More Just Genomics1
1
1
Issue Information and About the Cover Art1
Breaking Binaries: The Critical Need for Feminist Bioethics in Pediatric Gender‐Affirming Care1
Conscientious Provision of Care1
Contributors1
Contributors1
The Ethics of Humanlikeness in AI Therapy Chatbots1
Epistemic Humility in the Age of Assisted Dying0
Climates of Distrust in Medicine0
Legal Discrepancies and Expectations of Women: Abortion, Fetal Therapy, and NICU Care0
Issue Information and About the Cover Art0
Editors and Authors0
Too Soon or Too Late: Rethinking the Significance of Six Months When Dementia Is a Primary Diagnosis0
0
Facing Progress with Pragmatism: Telemedicine and Family Medicine0
Brain Pioneers and Moral Entanglement: An Argument for Post‐trial Responsibilities in Neural‐Device Trials0
0
Demonstrating Trustworthiness to Patients in Data‐Driven Health Care0
Expanding Boundaries0
Governance of Direct‐to‐User Digital Mental Health Tools: Emphasizing Transparency over Paternalism0
Genome Engineering, Chemical Exposure, and the Germline: An Ethical Synthesis0
Ethical Challenges of Advances in Vaccine Delivery Technologies0
Contributors0
Values and Evidence in Gender‐Affirming Care0
Abigail Levin replies0
Human, Nonhuman, and Chimeric Research: Considering Old Issues with New Research0
Contributors0
Past: Imperfect; Future: Tense0
Euthanasia as Medical Therapy in Canada0
The Moral Value of Telemedicine to the Physician‐Patient Relationship0
Disability, Relational Equality, and the Expressivist Objection0
On Normothermic Regional Perfusion0
0
Related Developments and Debates in Canada: Time Line and Publications0
Synthetic Health Data: Real Ethical Promise and Peril0
Dignity, Personhood, or Sacred Selves? Complicating Medical Literature and Caregiver Narratives in Dementia Care0
Troubling Trends in Health Misinformation Related to Gender‐Affirming Care0
About The Hastings Center and the Cover Art0
Speaking Truthfully about Provider‐Assisted Death0
Centering Home Care in Bioethics Scholarship, Education, and Practice0
Mapping the Moral Terrain of Clinical Deception0
The Pitfalls of Genomic Data Diversity0
Interweaving Indigenous and Western Concepts of Dementia0
Preventive Human Genome Editing and Enhancement: Candidate Criteria for Governance0
Dependence0
Reliable Narrators of Experience: Rethinking Dementia Narratives from Insider Perspectives0
Nancy S. Jecker, Zohar Lederman, and Anita Ho reply0
In Defense of Post Hoc Explanations in Medical AI0
Love Is Good, but Does It Have Teeth?0
The Third Person in the Room0
Clarifying the Ethics and Oversight of Chimeric Research0
0
Hidden Ethical Challenges in Health Data Infrastructure0
0
Issue Information (About the Cover Art)0
Issue Information and About the Cover Art0
About The Hastings Center, the Center for ELSI Resources and Analysis, and the Cover Art0
0
Contributors0
Raising the Dead? Limits of CPR and Harms of Defensive Practices0
Colonial and Neocolonial Barriers to Companion Digital Humans in Africa0
Issue Information and About the Cover Art0
0
The Hennepin Healthcare Forced Ketamine Studies, Excited Delirium, and Police Violence0
Why We Can Thrive past Seventy‐Five: In Favor of Efforts to Extend the Human Lifespan0
Genomics and Biodiversity: Applications and Ethical Considerations for Climate‐Just Conservation0
Issue Information and About the Cover Art0
An Ambitious Goal: A Grounded, Informed, and Compelling Theological Bioethics0
What Does Moral Agency Mean for Nurses in the Era of Artificial Intelligence?0
Contributors0
Hope and Exploitation in Commercial Provision of Assisted Reproductive Technologies0
Reproductive Embryo Editing: Attending to Justice0
Rethinking Mandated Drug Treatment: Why Expanding Freedom Requires Structural Drug Policy Reform0
Offering “Faux Codes”: An Ethical Option for the Patient Who Can't Tell Their Family No0
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