Hastings Center Report

Papers
(The TQCC of Hastings Center Report is 2. 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 2022-05-01 to 2026-05-01.)
ArticleCitations
An Ecostructural Lens for Health Ethics46
Guiding the Future: Rethinking the Role of Advance Directives in the Care of People with Dementia37
Deciding with Others: Interdependent Decision‐Making31
What Patient‐Experience Data Reveal about Trust25
On the Authority of Advance Euthanasia Directives for People with Severe Dementia: Reflections on a Dutch Case23
About the Special Report20
Cultivating Peace and Health at Community Health Centers19
Contributors19
Moral Status and the Oversight of Research Involving Chimeric Animals16
Digital Mental Health Tools and AI Therapy Chatbots: A Balanced Approach to Regulation15
Contributors15
From Eugenics to Human Genome Editing: Bionationalism and Instrumentalizing Life in China within a Global Context14
Abortion Access Persists, but So Do the Threats14
Xenotransplantation Clinical Trials and the Need for Community Engagement13
Moving toward Equity through Embedded ELSI Ethnography13
Trust in Crises and Crises of Trust12
Contributors12
Home Care in America: The Urgent Challenge of Putting Ethical Care into Practice12
Challenging Disability Discrimination in the Clinical Use of PDMP Algorithms11
The Pandemic of Invisible Victims in American Mental Health11
How Seeking Transfer Often Fails to Help Define Medically Inappropriate Treatment11
Contributors10
Reevaluating the Ethical Issues in Porcine‐to‐Human Heart Xenotransplantation10
Facilitating Ukrainian Refugees’ Continued Participation in Clinical Trials10
Lockdowns, Bioethics, and the Public: Policy‐Making in a Liberal Democracy10
Errata9
Identity Theft, Deep Brain Stimulation, and the Primacy of Post‐trial Obligations9
Enhancing Equity in Genomics: Incorporating Measures of Structural Racism, Discrimination, and Social Determinants of Health9
Who Carries the Responsibility for Health Care Carbon Reduction?9
Moral Humility for a Complex World9
Clinician Moral Distress: Toward an Ethics of Agent‐Regret8
Choice in the Context of Dementia: Emerging Issues for Health Care Practice in Aging Societies8
Contributors8
“You have to trust yourself”: The Overlooked Role of Self‐Trust in Coping with Chronic Illness8
Accountability for Reasonableness as a Framework for the Promotion of Fair and Equitable Research8
Defining Death Anew: Reexamining the Twentieth‐Century Brain Death Debates and the Uniform Determination of Death Act8
Complex Decisions8
8
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
Stef M. Shuster and Meredithe McNamara reply:7
Neither Ethical nor Prudent: Why Not to Choose Normothermic Regional Perfusion7
Learning Health Care and the Obligation to Participate in Research7
The Case for Baptizing a Dying, Unconscious Atheist7
Is Food Medicine?7
Why Aren't There More Whistleblowers?7
What Is the Aim of Pediatric “Gender‐Affirming” Care?6
Rethinking the Burden of Traditional Informed Consent Prior to Prenatal Genetic Screening5
Dementia and Concurrent Consent to Sexual Relations5
In Defense of Openness—Genetic Knowledge and Gamete Donation5
Contributors5
The Microethics of Communication in Health Care: A New Framework for the Fast Thinking of Everyday Clinical Encounters5
The Problem Is Not (Merely) Mass Incarceration: Incarceration as a Bioethical Crisis and Abolition as a Moral Obligation5
Issue Information and About the Cover Art5
Global Efforts to Protect Healthy Volunteers5
Deception, Pain, and Placebo: Applying the Brummett‐Salter Deception Framework4
The Values That Influence Psychiatric Diagnosis and Accountability4
Principled Conscientious Provision: Referral Symmetry and Its Implications for Protecting Secular Conscience4
Forgotten and without Protections: Older Adults in Prison Settings4
Dementia, Narrative, and Place: What Can Be Learned from the Age‐Friendly Movement?4
Justifying Clinical Deception: Some Amendments to Brummett and Salter4
Covid‐19: Medical Decisions, Mandates, and High‐Risk Minors4
4
Gender and Sport4
Editors and Authors4
A Timely Pursuit: Disability Justice in Pandemic Planning4
Intersecting Narratives in the Lives of Black Women Aging with Dementia4
Policy, Politics, and Impact4
Exploring the Ethics of the Parental Role in Parent‐Clinician Conflict4
Rethinking Decision Quality: Measures, Meaning, and Bioethics4
What Do Prospective Parents Owe to Their Children?4
Moral Nuances in Broad Policies4
Recalibrating Bioethics for the Reality of Interdependence: The Challenge of Collective‐Impact Problems4
Rethinking Theory in Bioethics4
Fifty Years of U.S. Mass Incarceration and What It Means for Bioethics3
Living in the Shadow of Uncertainty: Rethinking Cancer as Chronic Illness3
Science and Justice3
Love Your Patient as Yourself: On Reviving the Broken Heart of American Medical Ethics3
Experiential Training in Psychedelic‐Assisted Therapy: A Risk‐Benefit Analysis3
Editors’ Statement on the Responsible Use of Generative AI Technologies in Scholarly Journal Publishing3
Bright‐Line Policy and the Future of the Fourteen‐Day Rule3
Arguments and Analogies: Do Children Have a Right to Know Their Genetic Origins?3
Editors and Authors3
Participant Engagement, Epistemic Injustice, and Early‐Phase Implanted Neural Device Research3
Daoist Views on Disability and Genetic Intervention3
Issue Information and About the Cover Art3
Xenotransplantation: Injustice, Harm, and Alternatives for Addressing the Organ Crisis3
Erratum3
Finding Disability in Everyday Life3
Opening the Door: Rethinking “Difficult Conversations” about Living and Dying with Dementia3
Contributors3
Stories and Shame in Front‐Line Medicine3
Public Engagement as a Form of Moral Leadership3
Locked In3
Gender‐Affirming Care for Cisgender People2
Smuggled Doughnuts and Forbidden Fried Chicken: Addressing Tensions around Family and Food Restrictions in Hospitals2
2
The Need for Bioethics Departments in HBCU Medical Schools2
2
2
Should Parents of the Deceased Have Standing to Initiate Posthumous Sperm Retrieval? Analyzing Developments in Israel2
Dementia as a Critical Lens on the Role of Narrative in Medical Training and Practice2
Editors and Authors2
Knowing the Mind from Brain Data: The Challenge of Prediction and the Fairness of Relying on Objective Data about the Mind2
Rethinking the Ethics of the Covid‐19 Pandemic Lockdowns2
Genetics and Scientific Values: Aaron Panofsky, Kushan Dasgupta, Nicole Iturriaga, and Bernard Koch Reply2
Managing Dependence: Assistive Technologies in Dementia Care2
The Dead Unborn, Postmortem Privacy Cases, and Abortion Rights2
Parity, Poverty, and Physician Aid in Dying: Policy Recommendations for PAD in Light of Social Injustices2
Dignity and the Founding Myth of Bioethics2
Residency Requirements for Medical Aid in Dying2
Issue Information2
Can Caregivers Ever Say No?2
Food and Drug Administration v. Alliance for Hippocratic Medicine: How Conscience Protections Preserved Mifepristone Access2
A Life Worth Sustaining? Bestowed Worth and Pediatric Care2
Can Open Science Advance Health Justice? Genomic Research Dissemination in the Evolving Data‐Sharing Landscape2
Telemedicine and Healing Relationships2
Choosing to Die2
When Mistakes Multiply: How Inadequate Responses to Medical Mishaps Erode Trust in American Medicine2
Implicit Narratives in Participatory Arts Collaborations with People with Lived Experience of Dementia2
The Ethic of Accompaniment2
The Bioethicist as Healer2
Neuroscience and Society: Supporting and Unsettling Public Engagement2
Contributors2
Talking with Each Other about Science2
About the Special Report2
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
A Prescriptive Metaphysics of DEATH2
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