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 2022-06-01 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
Xenotransplantation Clinical Trials and the Need for Community Engagement13
Home Care in America: The Urgent Challenge of Putting Ethical Care into Practice13
Trust in Crises and Crises of Trust13
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
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
Clinician Moral Distress: Toward an Ethics of Agent‐Regret9
Errata9
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
Stef M. Shuster and Meredithe McNamara reply:8
Contributors8
Moral Humility for a Complex World8
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
What Is the Aim of Pediatric “Gender‐Affirming” Care?7
Rethinking the Burden of Traditional Informed Consent Prior to Prenatal Genetic Screening6
Is Food Medicine?6
Neither Ethical nor Prudent: Why Not to Choose Normothermic Regional Perfusion6
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
Rethinking Decision Quality: Measures, Meaning, and Bioethics5
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
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
Stories and Shame in Front‐Line Medicine3
Love Your Patient as Yourself: On Reviving the Broken Heart of American Medical Ethics3
Editors and Authors3
Living in the Shadow of Uncertainty: Rethinking Cancer as Chronic Illness3
Locked In3
Public Engagement as a Form of Moral Leadership3
Experiential Training in Psychedelic‐Assisted Therapy: A Risk‐Benefit Analysis3
Daoist Views on Disability and Genetic Intervention3
Science and Justice3
Arguments and Analogies: Do Children Have a Right to Know Their Genetic Origins?3
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
Opening the Door: Rethinking “Difficult Conversations” about Living and Dying with Dementia3
Participant Engagement, Epistemic Injustice, and Early‐Phase Implanted Neural Device Research3
A Timely Pursuit: Disability Justice in Pandemic Planning3
Contributors3
Editors and Authors3
About the Special Report3
Contributors3
Telemedicine and Healing Relationships2
2
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
The Dead Unborn, Postmortem Privacy Cases, and Abortion Rights2
The Bioethicist as Healer2
Issue Information and About the Cover Art2
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