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 2021-02-01 to 2025-02-01.)
ArticleCitations
Opening the Door: Rethinking “Difficult Conversations” about Living and Dying with Dementia32
Guiding the Future: Rethinking the Role of Advance Directives in the Care of People with Dementia23
Editors and Authors19
About The Hastings Center and the Cover Art17
Issue Information (About the Cover Art)15
An Ecostructural Lens for Health Ethics15
Issue Information (About the Cover Art)13
Stories and Shame in Front‐Line Medicine12
About the Special Report11
History and Bioethics11
Editors and Authors10
10
Pediatric Off‐Label Use of Covid‐19 Vaccines: Ethical and Legal Considerations10
Bioethics Rooted in Justice: Community‐Expert Reflections10
Contributors10
What Patient‐Experience Data Reveal about Trust10
Living Out a Life's Meaning10
A Realpolitik for Presidential Health: A Psychiatrist's Perspective9
Virginia A. Brown replies9
ICU Care in a Pandemic8
Authenticity and Clinical Decision‐Making8
Teneille Brown, Leslie Francis, and James Tabery respond8
Essential Reading for Bioethicists in the Anthropocene Era8
On Ethicists and Their Diets7
Contributors7
Disability Affirmative Action Requirements for the U.S. HHS and Academic Medical Centers7
What Do Genomics Studies Really Mean? A New Resource7
Resisting Transhumanist Fantasies7
Public Engagement and the Social Risks of Science7
The Decision Phases Framework for Public Engagement:Engaging Stakeholders about Gene Editing in the Wild6
Bioethics' Conceptual Tool Kit6
Ending One's Life in Advance6
Restructuring Deliberation Using a Cultural Theory Lens6
About the Special Report6
The Business of Medicine Fails Many American Patients6
Social Equality in an Alternate World6
Issue Information (About the Cover Art)6
Public Attitudes toward Consent When Research Is Integrated into Care—Any “Ought” from All the “Is”?6
Holding the Guardrails on Involuntary Commitment5
Science and Justice5
Understanding Organ Stewardship5
Deciding with Others: Interdependent Decision‐Making5
Love Your Patient as Yourself: On Reviving the Broken Heart of American Medical Ethics5
How to Diagnose Abhorrent Science5
Strategic Ethics: Physician Associations and Their Roles in Pursuing Racial Equity5
A Risk Is Not a Harm: Abortion Exceptions in State Laws5
Material Insecurity, Racial Capitalism, and Public Health5
Deficits of Public Deliberation in U.S. Oversight for Gene Edited Organisms5
Making the World Safer and Fairer in Pandemics5
Fifty Years of U.S. Mass Incarceration and What It Means for Bioethics5
It Is Time to Abandon the Dogma That Brain Death Is Biological Death5
Experiential Training in Psychedelic‐Assisted Therapy: A Risk‐Benefit Analysis5
Centering Home Care in Bioethics Scholarship, Education, and Practice5
The Bioethics of Built Space: Health Care Architecture as a Medical Intervention4
How Chimeric Animal Research Impacts Animal Welfare: A Conversation with Animal Welfare Experts4
Contributors4
Colonial and Neocolonial Barriers to Companion Digital Humans in Africa4
If Not Now, Then When? Taking Disability Seriously in Bioethics4
About The Hastings Center and the Cover Art4
Health Justice and Rawls's Theory at Fifty: Will New Thinking about Health and Inequality Influence the Most Influential Account of Justice?4
Facing Progress with Pragmatism: Telemedicine and Family Medicine4
About The Hastings Center, the Department of Bioethics at Case Western Reserve University, and the Cover Art4
Testimonies and Healing: Anti‐oppressive Research with Black Women and the Implications for Compassionate Ethical Care4
Editors and Authors4
Editors’ Statement on the Responsible Use of Generative AI Technologies in Scholarly Journal Publishing4
Genomics and Health Data Governance in Africa: Democratize the Use of Big Data and Popularize Public Engagement4
Do Health Care Organizations Have Legitimate Responsibilities beyond the Delivery of Health Care? Insights from Citizenship Theory4
Black and Waiting: Bioethics and Care during the Covid‐19 Pandemic4
Composite Animals: Then and Now4
4
Genomics and Biodiversity: Applications and Ethical Considerations for Climate‐Just Conservation4
Erratum4
Giving Voice to the Voiceless in Environmental Gene Editing4
Wrestling with Public Input on an Ethical Analysis of Scientific Research3
Too Soon or Too Late: Rethinking the Significance of Six Months When Dementia Is a Primary Diagnosis3
Issue Information (About the Cover Art)3
Dementia, Sex, and Consent: Beyond the Uncomplicated Cases3
Locked In3
Contributors3
3
Related Developments and Debates in Canada: Time Line and Publications3
Why the Gene Was (Mis)Placed at the Center of American Health Policy3
Contributors3
About the Special Report3
Cultivating Peace and Health at Community Health Centers3
Can I Hold That Thought for You? Dementia and Shared Relational Agency3
What Makes a Better Life for People Facing Dementia? Toward Dementia‐Friendly Health and Social Policy, Medical Care, and Community Support in the United States3
3
Contributors3
3
Activism and the Clinical Ethicist3
Conscience, Caricatures, and Catholic Identities3
Big Mistake: Knowing and Doing Better in Patient Engagement2
Contributors2
Another Defense of Abortion: What Transplant Ethics Tells Us about the Ethics of Abortion after Dobbs2
2
Care or Complicity? Medical Personnel in Prisons2
Issue Information and About the Cover Art2
Can Open Science Advance Health Justice? Genomic Research Dissemination in the Evolving Data‐Sharing Landscape2
Empowering Indigenous Knowledge in Deliberations on Gene Editing in the Wild2
About The Hastings Center, the Center for ELSI Resources and Analysis, and the Cover Art2
The Crisis in Standards of Care2
Contributors2
Vulnerability, Autonomy, and the Living Organ Donor2
The Open Donor View and Procreative Beneficence2
Breaking Binaries: The Critical Need for Feminist Bioethics in Pediatric Gender‐Affirming Care2
Contributors2
Contributors2
A Coeditors' Note2
The Public Performativity of Trust2
Contributors2
Moving toward Equity through Embedded ELSI Ethnography2
Advance Directives: The Principle of Determining Authenticity2
Risk Trade‐Offs and Equitable Decision‐Making in the Covid‐19 Pandemic2
Hope to the End2
A Developing Timeline for Bioethics2
Learning Health Systems, Informed Consent, and Respect for Persons2
Not Just for Nurses2
Toward Justice and Community Empowerment in Genomics Studies on Sensitive Traits2
The UN Challenge to Guardianship and Surrogate Decision‐Making2
Challenging Disability Discrimination in the Clinical Use of PDMP Algorithms2
A Call for Solidarity in Bioethics: Confronting Anti‐Black Racism Together2
From Eugenics to Human Genome Editing: Bionationalism and Instrumentalizing Life in China within a Global Context2
Legal and Ethical Issues in the Report Heritable Human Genome Editing2
Nothing about Us without Us in Precision Medicine: A Call to Reframe Disability Difference in Genetics and Genomics2
Ethics of a Mandatory Waiting Period for Female Sterilization2
Lessons from Biomedical Innovation during World War II2
Zoonoses and Animal Culling: The Need for One Health Policy2
Structural Inequities, Fair Opportunity, and the Allocation of Scarce ICU Resources1
Antiracist Activism in Clinical Ethics: What's Stopping Us?1
Hope and Exploitation in Commercial Provision of Assisted Reproductive Technologies1
Justice through a Wide‐Angle Lens1
On the Authority of Advance Euthanasia Directives for People with Severe Dementia: Reflections on a Dutch Case1
Erratum1
Issue Information (About the Cover Art)1
Home Care in America: The Urgent Challenge of Putting Ethical Care into Practice1
Moral Status and the Oversight of Research Involving Chimeric Animals1
Removing a Disabled Person from Her Treasured Independent Living1
Moral Humility for a Complex World1
Public Trust and Medical Ethics1
Issue Information1
Cruzan after Dobbs: What Remains of the Constitutional Right to Refuse Treatment?1
From a Reckoning to Racial Concordance: A Strategy to Protect Black Mothers, Children, and Infants1
The Case for Ethical Efficiency: A System That Has Run Out of Time1
Thinking about Moral Progress1
Equal Access to Organ Transplantation for People with Disabilities1
Contributors1
1
Contributors1
Expanding Paid Sick Leave Laws: The Public Health Imperative1
Community‐Based Organizations as Trusted Messengers in Health1
New Findings on Unconsented Intimate Exams Suggest Racial Bias and Gender Parity1
Trust in Crises and Crises of Trust1
Justice, Bioethics, and Covid‐191
On Normothermic Regional Perfusion1
Issue Information and About the Cover Art1
Climates of Distrust in Medicine1
Care Ethics versus the CARES Act1
When People Facing Dementia Choose to Hasten Death: The Landscape of Current Ethical, Legal, Medical, and Social Considerations in the United States1
Physician Perspectives on Building Trust with Patients1
Narratives in Public Deliberation: Empowering Gene Editing Debate with Storytelling1
The Problem of Clinical Deception and Why We Cannot Begin in the Middle1
Securing the Trustworthiness of the FDA to Build Public Trust in Vaccines1
Ethics Big and Small, Thinking Fast and Slow1
Why Clinical Ethicists Are Not Activists1
Contributors1
Facilitating Ukrainian Refugees’ Continued Participation in Clinical Trials1
1
Antiracist Praxis in Public Health: A Call for Ethical Reflections1
Divided Loyalties: Fire and ICE1
Threats to Benefits: Assessing Knowledge Production in Nonhuman Models of Human Neuropsychiatric Disorders1
Looking Closely at Health Inequities1
Earning Mistrust through Fake Compromises and Broken Promises1
Contributors1
Disability Access and Digital Platforms1
About the Special Report1
How Seeking Transfer Often Fails to Help Define Medically Inappropriate Treatment1
Past: Imperfect; Future: Tense1
Handle with Care: The WHO Report on Human Genome Editing1
About The Hastings, the American Board of Internal Medicine Foundation, and the Cover Art1
Gene Editing: How Can You Ask “Whether” If You Don't Know “How”?1
In the Name of Racial Justice: Why Bioethics Should Care about Environmental Toxins1
Distressed Work: Chronic Imperatives and Distress in Covid‐19 Critical Care1
Disability, Bioethics, and the Problem of Prejudice1
Digital Humans to Combat Loneliness and Social Isolation: Ethics Concerns and Policy Recommendations1
Contributors1
John Rawls, Godfather of Bioethics1
Reevaluating the Ethical Issues in Porcine‐to‐Human Heart Xenotransplantation1
To Understand Inequity, Bioethics Needs to Sort Things Out1
1
Coming to Terms with the Black Box Problem: How to Justify AI Systems in Health Care1
The Bleak Future of Reproductive Rights for Queer Indians1
Choice in the Context of Dementia: Emerging Issues for Health Care Practice in Aging Societies1
Adam Omelianchuk, Alexander Morgan Capron, Lainie Friedman Ross, Arthur R. Derse, James L. Bernat, and David Magnus reply:1
1
Clarifying the Ethics and Oversight of Chimeric Research1
Synthetic Health Data: Real Ethical Promise and Peril1
BeforeThe Birth of Bioethics: James M. Gustafson at Yale1
The Pandemic of Invisible Victims in American Mental Health1
Lockdowns, Bioethics, and the Public: Policy‐Making in a Liberal Democracy1
Life‐Years & Rationing in the Covid‐19 Pandemic: A Critical Analysis1
Holding Them Accountable: Organizational Commitments to Ending Systemic Anti‐Black Racism in Medicine and Public Health1
Pediatric Authenticity: Hiding in Plain Sight1
Xenotransplantation Clinical Trials and the Need for Community Engagement1
Issue Information and About the Cover Art0
Mapping the Moral Terrain of Clinical Deception0
0
Demonstrating Trustworthiness to Patients in Data‐Driven Health Care0
Govind Persad replies0
Editors and Authors0
Parity, Poverty, and Physician Aid in Dying: Policy Recommendations for PAD in Light of Social Injustices0
Speaking Truthfully about Provider‐Assisted Death0
Henri Wijsbek and Thomas Nys Respond0
Erratum0
A “Surprise” Health Policy Legislative Victory0
Nancy S. Jecker, Zohar Lederman, and Anita Ho reply0
Contributors0
Activism and Bioethics: Taking a Stand on Things That Matter0
Leah Z. Rand, Daniel P. Carpenter, Aaron S. Kesselheim, Anushka Bhaskar, Jonathan J. Darrow, and William B. Feldman Reply0
Expanding the Agenda for a More Just Genomics0
Dementia and Concurrent Consent to Sexual Relations0
Issue Information and About the Cover Art0
The Sociotechnical Construction of Distrust during the Covid‐19 Pandemic0
Minors Lack the Autonomy to Consent to Gender‐Affirming Care: Best Interests Must Be Primary0
Refusal of Representation in Advance Care Planning: A Case‐Inspired Ethical Analysis0
Choosing to Die0
0
Exploring the Ethics of the Parental Role in Parent‐Clinician Conflict0
Troubling Trends in Health Misinformation Related to Gender‐Affirming Care0
Brain Pioneers and Moral Entanglement: An Argument for Post‐trial Responsibilities in Neural‐Device Trials0
The Center's Highest Award0
Deliberative Public Consultation via Deliberative Polling:Criteria and Methods0
Values across Ages0
Confronting the “Weaponization” of Genetics by Racists Online and Elsewhere0
The Ethic of Accompaniment0
Genetic Control in Historical Perspective:The Legacy of India's Genetic Control of Mosquitoes Unit0
Expanding Boundaries0
Reproductive Embryo Editing: Attending to Justice0
Values and Evidence in Gender‐Affirming Care0
The Dead Unborn, Postmortem Privacy Cases, and Abortion Rights0
Issue Information0
0
Contributors0
Erratum0
Deception and Distress0
Regulating AI in Health Care: The Challenges of Informed User Engagement0
The Surrogation of Surrogacy: The Perils and Pitfalls of Epistemic Authority0
Beneath the Sword of Damocles: Moral Obligations of Physicians in a Post‐Dobbs Landscape0
What Do Prospective Parents Owe to Their Children?0
Rectifying or Reinforcing? The (In)Equity Implications of Recontacting Practices in Genomic Medicine0
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