Link

Ethical Challenges in ICU Research, Critical Care Canada Forum (2009)

Link

When Can Physicians Say “No” to Families and Patients?, Critical Care Canada Forum (2009)

Link

Providing Research Results to Participants: Attitudes and Needs of Adolescents and Parents of Children with Cancer (with Conrad Vincent Fernandez, Jun Gao, Caron Strahlendorf, Albert Moghrabi, Rebecca Davis Pentz, Raymond Carlton Barfield, Justin Nathaniel Baker, Darcy Santor, and Eric Kodish), Journal of Clinical Oncology (2009)

Link

Care of an Unresponsive Patient with a Poor Prognosis (with Arthur S. Slutsky, Leonard D. Hudson, Nancy N. Dubler, and Mark R. Tonelli), New England Journal of Medicine (2009)

Ethics and Schizophrenia (with A. Rudnick), The Clinical Handbook of Schizophrenia (2008)

Link

Trust-based Obligations of the State and Physician-researchers to Patient-subjects (with Paul B. Miller), Journal of Medical Ethics (2006)

Link

Fiduciary Obligation in Clinical Research (with Paul B. Miller), Journal of Law, Medicine & Ethics (2006)

Link

The Balm of Gilead: Is the Provision of Treatment to those Who Seroconvert in HIV Prevention Trials a Matter of Moral Obligation or Moral Negotiation? (with Guy J. Leblanc), Journal of Law, Medicine & Ethics (2006)

Link

A Death in the Family: Reflections on the Terri Schiavo Case, Canadian Medical Association Journal (2005)

Link

Importance of Informed Consent in Offering to Return Research Results to Research Participants (with Conrad V. Fernandez and Eric Kodish), Medical and Pediatric Oncology (2003)

Link

Will the Real Charles Fried Please Stand Up? (with Paul B. Miller), Kennedy Institute of Ethics Journal (2003)

Link

Disclosure of the Right of Research Participants to Receive Research Results: An Analysis of Consent Forms in the Children's Oncology Group (with Conrad V. Fernandez, Eric Kodish, Shaureen Taweel, and Susan Shurin), Cancer (2003)

Link

Rehabilitating Equipoise (with Paul B. Miller), Kennedy Institute of Ethics Journal (2003)

Ethical Issues in Palliative Care Research (with Neil MacDonald), Oxford Textbook of Palliative Medicine (2003)

Link

Should Physicians Accept Gifts from Their Patients? No: Gifts Debase the True Value of Care, Western Journal of Medicine (2001)

Link

Hospital Policy on Appropriate Use of Life-sustaining Treatment (with Peter A. Singer, Geoff Barker, Kerry W. Bowman, Christine Harrison, Philip Kernerman, Judy Kopelow, Neil Lazar, and Stephen Workman), Critical Care Medicine (2001)

Misrepresenting Research: Commentary, Ward Ethics: Dilemmas for Medical Students and Doctors in Training (2001)

Link

An Historical Take on the Physician's Charter (with Nuala Kenny), Canadian Medical Association Journal (2000)

Legal and Ethical Issues in Geriatric Medicine (with Heather MacDonald and Peter Singer), Oxford Textbook of Geriatric Medicine (2000)

Link

Voting Ourselves Rights: A Critique of the Canadian Medical Association Charter for Physicians (with Nuala Kenny and Francoise Baylis), Canadian Medical Association Journal (1999)

Link

Getting Doctors to Listen: Ethics and Outcomes Data in Context, Journal of the American Medical Association (1999)

Link

Medical Futility: Physicians, not Patients, Call the Shots, Western Journal of Medicine (1999)

Link

CPR for Patients in a Persistent Vegetative State?, Canadian Medical Association Journal (1998)

Link

Self Interest Is Not the Sole Legitimate Basis for Making Decisions, British Medical Journal (1998)

Link

Cardiopulmonary Resuscitation for Patients in a Persistent Vegetative State: Futile or Acceptable?, Canadian Medical Association Journal (1998)

Democracy in Medicine?, The Sciences (1995)

Link

Pulling the Plug on Futility (with Carl Elliott), British Medical Journal (1995)

Learning from the Dutch: Physician-assisted Death, Slippery Slopes and the Nazi Analogy, Health Law Review (1995)

Euthanasia, Assisted Suicide and the Family Physician, L'Actualité médicale (1993)

Link

When Can Physicians Say “No” to Families and Patients?, Critical Care Canada Forum (2009)

Link

Providing Research Results to Participants: Attitudes and Needs of Adolescents and Parents of Children with Cancer (with Conrad Vincent Fernandez, Jun Gao, Caron Strahlendorf, Albert Moghrabi, Rebecca Davis Pentz, Raymond Carlton Barfield, Justin Nathaniel Baker, Darcy Santor, and Eric Kodish), Journal of Clinical Oncology (2009)

Link

Care of an Unresponsive Patient with a Poor Prognosis (with Arthur S. Slutsky, Leonard D. Hudson, Nancy N. Dubler, and Mark R. Tonelli), New England Journal of Medicine (2009)

Link

The Limits of Consent: A Socio-ethical Approach to Human Subject Research in Medicine (with Oonagh Corrigan, John McMillan, Kathleen Liddell, and Martin Richards) (2009)

Ethics and Schizophrenia (with A. Rudnick), The Clinical Handbook of Schizophrenia (2008)

Link

The Return of Research Results to Participants: Pilot Questionnaire of Adolescents and Parents of Children with Cancer (with Conrad V. Fernandez, Darcy Santor, Caron Strahlendorf, Albert Moghrabi, Rebecca Pentz, Jun Gao, and Eric Kodish), Pediatric Blood & Cancer (2007)

Link

Disclosure of Research Result to Research Participants: Needs and Attitudes of Adolescents and Parents (with Conrad Vincent Fernandez, Shaureen Taweel, and Eric D. Kodish), Pediatrics and Child Health (2005)

Link

A Death in the Family: Reflections on the Terri Schiavo Case, Canadian Medical Association Journal (2005)

Link

Is Clinical Research and Ethics a Zero-sum Game?, Critical Care Medicine (2005)

Link

A Critical History of Individual and Collective Ethics in the Lineage of Lellouch and Schwartz (with Charles M. Heilig), Clinical Trials (2005)

Link

Disclosure of the Right of Research Participants to Receive Research Results: An Analysis of Consent Forms in the Children's Oncology Group (with Conrad V. Fernandez, Eric Kodish, Shaureen Taweel, and Susan Shurin), Cancer (2003)

Ethical Issues in Palliative Care Research (with Neil MacDonald), Oxford Textbook of Palliative Medicine (2003)

Link

Hospital Policy on Appropriate Use of Life-sustaining Treatment (with Peter A. Singer, Geoff Barker, Kerry W. Bowman, Christine Harrison, Philip Kernerman, Judy Kopelow, Neil Lazar, and Stephen Workman), Critical Care Medicine (2001)

Misrepresenting Research: Commentary, Ward Ethics: Dilemmas for Medical Students and Doctors in Training (2001)

Link

Family Duty Is More Important than Rights, British Medical Journal (2000)

Link

An Historical Take on the Physician's Charter (with Nuala Kenny), Canadian Medical Association Journal (2000)

Legal and Ethical Issues in Geriatric Medicine (with Heather MacDonald and Peter Singer), Oxford Textbook of Geriatric Medicine (2000)

Link

Voting Ourselves Rights: A Critique of the Canadian Medical Association Charter for Physicians (with Nuala Kenny and Francoise Baylis), Canadian Medical Association Journal (1999)

Link

Getting Doctors to Listen: Ethics and Outcomes Data in Context, Journal of the American Medical Association (1999)

Link

Medical Futility: Physicians, not Patients, Call the Shots, Western Journal of Medicine (1999)

Link

Monitoring Informed Consent in an Oncology Study Posing Serious Risk to Subjects (with Myrian Skrutkowski, Stan Shapiro, Abraham Fuks, Adrian Langleben, and Benjamin Freedman), IRB: A Review of Human Subjects Research (1998)

Link

CPR for Patients in a Persistent Vegetative State?, Canadian Medical Association Journal (1998)

Link

Self Interest Is Not the Sole Legitimate Basis for Making Decisions, British Medical Journal (1998)

Link

A Study in Contrasts: Eligibility Criteria in a Twenty-Year Sample of NSABP and POG Clinical Trials (with Abraham Fuks, Benjamin Freedman, Stanley Shapiro, Myriam Skrutkowska, and Amina Riaz), Journal of Clinical Epidemiology (1998)

Democracy in Medicine?, The Sciences (1995)

Learning from the Dutch: Physician-assisted Death, Slippery Slopes and the Nazi Analogy, Health Law Review (1995)

Euthanasia, Assisted Suicide and the Family Physician, L'Actualité médicale (1993)

Link

The Return of Research Results to Participants: Pilot Questionnaire of Adolescents and Parents of Children with Cancer (with Conrad V. Fernandez, Darcy Santor, Caron Strahlendorf, Albert Moghrabi, Rebecca Pentz, Jun Gao, and Eric Kodish), Pediatric Blood & Cancer (2007)

Link

Obligations in Offering to Disclose Genetic Research Results (with Conrad V. Fernandez), The American Journal of Bioethics (2006)

Link

Disclosure of Research Result to Research Participants: Needs and Attitudes of Adolescents and Parents (with Conrad Vincent Fernandez, Shaureen Taweel, and Eric D. Kodish), Pediatrics and Child Health (2005)

Link

Considerations and Costs of Disclosing Study Findings to Research Participants (with Conrad V. Fernandez and Chris Skedgel), Canadian Medical Association Journal (2004)

Link

Importance of Informed Consent in Offering to Return Research Results to Research Participants (with Conrad V. Fernandez and Eric Kodish), Medical and Pediatric Oncology (2003)

Link

Offering to Return Results to Research Participants: Attitudes and Needs of Principal Investigators in the Children's Oncology Group (with Conrad V. Fernandez, Eric Kodish, and Susan Shurin), Journal of Pediatric Hematology/Oncology (2003)

Link

Disclosure of the Right of Research Participants to Receive Research Results: An Analysis of Consent Forms in the Children's Oncology Group (with Conrad V. Fernandez, Eric Kodish, Shaureen Taweel, and Susan Shurin), Cancer (2003)

Ethical Issues in Palliative Care Research (with Neil MacDonald), Oxford Textbook of Palliative Medicine (2003)

Link

Informing Patients of Uncertainty in Clinical Trials (with S. D. Halpern and J. H. Karlawish), Journal of the American Medical Association (2001)

Link

Protecting Communities in Biomedical Research (with E. J. Emanuel), Science (2000)

Legal and Ethical Issues in Geriatric Medicine (with Heather MacDonald and Peter Singer), Oxford Textbook of Geriatric Medicine (2000)

Link

Structuring the Review of Human Genetics Protocols: Gene Localization and Identification Studies (with Kathleen Cranley Glass, Roberta M. Palmour, Stanley H. Shapiro, Trudo M. Lemmens, and Karen Lebacqz), IRB: A Review of Human Subjects Research (1996)

Link

Minimal Risk Remains an Open Question (with Ariella Binik and Mark Sheehan), The American Journal of Bioethics (2011)

Link

Refuting the Net Risks Test: A Response to Wendler and Miller's "Assessing Research Risks Systematically" (with Paul B. Miller), Journal of Medical Ethics (2007)

Link

Evaluating Risks of Non-therapeutic Research in Children (with Paul B. Miller), Ethics and Research with Children: A Case-based Approach (2005)

Link

Will the Real Charles Fried Please Stand Up? (with Paul B. Miller), Kennedy Institute of Ethics Journal (2003)

Link

When Argument Fails, The American Journal of Bioethics (2002)

Link

I Need a Placebo like I Need a Hole in the Head, Journal of Law, Medicine & Ethics (2002)

Link

The Ethics of Placebo-controlled Trials (with Kathleen Cranley Glass), New England Journal of Medicine (2002)

Link

Moral Solutions in Assessing Research Risk (with Paul B. Miller), IRB: Ethics and Human Research (2000)

Link

Thinking Clearly about Research Risk: Implications of the Work of Benjamin Freedman, IRB: Ethics and Human Research (1999)

Link

Research Involving the Vulnerable Sick, Accountability in Research (1999)

Link

The IRB's Role in Assessing the Generalizability of Non-NIH-Funded Clinical Trials, IRB: A Review of Human Subjects Research (1998)

Demarcating Research and Treatment: A Systematic Approach for the Analysis of the Ethics of Clinical Research (with Benjamin Freedman and Abraham Fuks), Clinical Research (1992)

Link

Minimal Risk and Large-scale Biobank and Cohort Research (with Timothy Caulfield), Health Law Review (2009)

Link

Helsinki Discords: FDA, Ethics, and International Drug Trials (with Jonathan Kimmelman and Eric M. Meslin), Lancet (2009)

Link

The Limits of Consent: A Socio-ethical Approach to Human Subject Research in Medicine (with Oonagh Corrigan, John McMillan, Kathleen Liddell, and Martin Richards) (2009)

Link

Evaluating Benefits and Harms in Intensive Care Research (with Paul B. Miller), Intensive Care Medicine (2007)

Link

Heads or Tails: Randomized Placebo-Controlled Trials, Virtual Mentor (2004)

Link

Waiver of Consent for Emergency Research (with Andrew D. McRae), Annals of Emergency Medicine (2004)

Link

The Quest for Legitimacy: Comment on Cox Macpherson's 'to Strengthen Consensus, Consult the Stakeholders', Bioethics (2004)

Link

Protecting Communities in Pharmacogenetic and Pharmacogenomic Research (with P. B. Miller), The Pharmacogenomics Journal (2004)

Link

Is the Use of Placebo Controls Ethically Permissible in Clinical Trials of Agents Intended to Reduce Fractures in Osteoporosis? (with Baruch A. Brody, Nancy Dickey, Susan S. Ellenberg, Robert P. Heaney, Robert J. Levine, Richard L. O'Brien, and Ruth B. Purtilo), Journal of Bone and Mineral Research (2003)

Link

The Ethics of Placebo-Controlled Trials, Journal of Bone and Mineral Research (2003)

Link

Informing Study Participants of Research Results: An Ethical Imperative (with Conrad V. Fernandez and Eric Kodish), IRB: Ethics and Human Research (2003)

Link

Lessons from Everyday Lives: A Moral Justification for Acute Care Research (with Andrew D. McRae), Critical Care Medicine (2002)

Link

Placebo Trials and Tribulations, Canadian Medical Association Journal (2002)

Link

I Need a Placebo like I Need a Hole in the Head, Journal of Law, Medicine & Ethics (2002)

Link

A Critical Appraisal of Protections for Aboriginal Communities in Biomedical Research (with James A. Anderson), Jurimetrics (2002)

Link

Continuing Review of Research Approved by Canadian Research Ethics Boards, Canadian Medical Association Journal (2001)

Link

The Ethics Wars: Disputes over International Research (with James A. Anderson), The Hastings Center Report (2001)

Link

The Research Subject as Entrepreneur (with James A. Anderson), The American Journal of Bioethics (2001)

Link

The Ethical Analysis of Risk, Journal of Law, Medicine & Ethics (2000)

Link

Moral Solutions in Assessing Research Risk (with Paul B. Miller), IRB: Ethics and Human Research (2000)

Link

Protecting Communities in Biomedical Research (with E. J. Emanuel), Science (2000)

Link

The Ethical Analysis of Risks and Potential Benefits in Human Subjects Research: History, Theory, and Implications for U.S. Regulation (2000)

Link

What's the Price of a Research Subject?, New England Journal of Medicine (1999)

Link

Thinking Clearly about Research Risk: Implications of the Work of Benjamin Freedman, IRB: Ethics and Human Research (1999)

Link

Protecting Communities in Research: Philosophical and Pragmatic Challenges, Cambridge Quarterly of Healthcare Ethics (1999)

Link

Research Involving the Vulnerable Sick, Accountability in Research (1999)

Link

Structuring the Review of Human Genetics Protocols Part-III: Gene Therapy Studies (with Kathleen C. Glass, Denis Cournoyer, Trudo Lemmens, Roberta M. Palmour, Stanley H. Shapiro, and Benjamin Freedman), IRB: A Review of Human Subjects Research (1999)

Link

Monitoring Informed Consent in an Oncology Study Posing Serious Risk to Subjects (with Myrian Skrutkowski, Stan Shapiro, Abraham Fuks, Adrian Langleben, and Benjamin Freedman), IRB: A Review of Human Subjects Research (1998)

Link

The IRB's Role in Assessing the Generalizability of Non-NIH-Funded Clinical Trials, IRB: A Review of Human Subjects Research (1998)

Link

Assessing the Interpretation of Criteria for Clinical Trial Eligibility: A Survey of Oncology Investigators (with Benjamin Freedman, Stanley Shapiro, Abraham Fuks, Myriam Skrutkowska, and Maria Sigurjonsdottir), Clinical and Investigative Medicine (1998)

Link

The Human Radiation Experiments: Final Report of the Advisory Committee on Human Radiation Experiments, Canadian Medical Association Journal (1997)

Link

Structuring the Review of Human Genetics Protocols Part II: Diagnostic and Screening Studies (with Kathleen Cranley Glass, Trudo Lemmens, Roberta M. Palmour, and Stanley H. Shapiro), IRB: A Review of Human Subjects Research (1997)

Link

Structuring the Review of Human Genetics Protocols: Gene Localization and Identification Studies (with Kathleen Cranley Glass, Roberta M. Palmour, Stanley H. Shapiro, Trudo M. Lemmens, and Karen Lebacqz), IRB: A Review of Human Subjects Research (1996)

Link

Evolving Ethical Issues in Selection of Subjects for Clinical Research, Cambridge Quarterly of Healthcare Ethics (1996)

Link

Cruel and Unusual Treatment (with Carl Elliott), Saturday Night (1995)

Link

The Ethics and Politics of Human Experimentation, Religious Studies Review (1995)

Link

In Loco Parentis: Minimal Risk as an Ethical Threshold for Research upon Children (with Benjamin Freedman and Abraham Fuks), The Hastings Center Report (1993)

Demarcating Research and Treatment: A Systematic Approach for the Analysis of the Ethics of Clinical Research (with Benjamin Freedman and Abraham Fuks), Clinical Research (1992)

Link

[Demarcating Research and Treatment Interventions: A Case Illustration]: Commentary (with Benjamin Freedman), IRB: A Review of Human Subjects Research (1992)

Link

Ethical Issues Posed by Cluster Randomized Trials in Health Research (with Jeremy M. Grimshaw, Monica Taljaard, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Antonio Gallo, Andrew D. McRae, Raphael Saginur, and Merrick Zwarenstein), Trials (2011)

Link

Conceptual Problems in Research Ethics, Research Day (Arts & Humanities, FIMS, and Education) (2010)

Link

Ethics in Conduct of Trials in Developing Countries, British Medical Journal (2010)

Ethical Considerations in the Conduct of Vaccine Trials in Developing Countries (with C. Lanata and C. Plowe), New Generation Vaccines (2009)

Link

Ethical and Policy Issues in Cluster Randomized Trials: Rationale and Design of a Mixed Methods Research Study (with Monica Taljaard, Jeremy M. Grimshaw, Judith Belle Brown, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Shazia H. Chaudhry, Martin P. Eccles, Andrew McRae, Raphael Saginur, Merrick Zwarenstein, and Allan Donner), Trials (2009)

Link

Ethics of Surgical Training in Developing Countries (with Kevin M. Ramsey), World Journal of Surgery (2007)

Link

Revisiting the Ethics of HIV Prevention Research in Developing Countries (with Guy LeBlanc), XVI International AIDS Conference (2006)

Link

The Balm of Gilead: Is the Provision of Treatment to those Who Seroconvert in HIV Prevention Trials a Matter of Moral Obligation or Moral Negotiation? (with Guy J. Leblanc), Journal of Law, Medicine & Ethics (2006)

Link

The Quest for Legitimacy: Comment on Cox Macpherson's 'to Strengthen Consensus, Consult the Stakeholders', Bioethics (2004)

Link

The Importance of Context in International Research (with Fern Brunger), Ethics & Behavior (2002)

Link

The Ethics Wars: Disputes over International Research (with James A. Anderson), The Hastings Center Report (2001)

Link

The Future of Research into Rotavirus Vaccine, British Medical Journal (2000)

Link

Ethics in Conduct of Trials in Developing Countries, British Medical Journal (2010)

Ethical Considerations in the Conduct of Vaccine Trials in Developing Countries (with C. Lanata and C. Plowe), New Generation Vaccines (2009)

Link

Research Governance Lessons from the National Placebo Initiative (with Heather Sampson and Daryl Pullman), Health Law Review (2009)

Link

Helsinki Discords: FDA, Ethics, and International Drug Trials (with Jonathan Kimmelman and Eric M. Meslin), Lancet (2009)

Link

Introduction (with Oonagh Corrigan and John McMillan), The Limits of Consent: A Socio-ethical Approach to Human Subject Research in Medicine (2009)

Link

The Limits of Consent: A Socio-ethical Approach to Human Subject Research in Medicine (with Oonagh Corrigan, John McMillan, Kathleen Liddell, and Martin Richards) (2009)

Link

Trust and Exploitation in Clinical Research (with Paul B. Miller), The Limits of Consent: A Socio-ethical Approach to Human Subject Research in Medicine (2009)

Link

Revisiting Equipoise: A Response to Gifford (with Paul B. Miller), Kennedy Institute of Ethics Journal (2007)

Link

Refuting the Net Risks Test: A Response to Wendler and Miller's "Assessing Research Risks Systematically" (with Paul B. Miller), Journal of Medical Ethics (2007)

Link

The Return of Research Results to Participants: Pilot Questionnaire of Adolescents and Parents of Children with Cancer (with Conrad V. Fernandez, Darcy Santor, Caron Strahlendorf, Albert Moghrabi, Rebecca Pentz, Jun Gao, and Eric Kodish), Pediatric Blood & Cancer (2007)

Link

Equipoise and the Duty of Care in Clinical Research: A Philosophical Response to Our Critics (with Paul B. Miller), Journal of Medicine and Philosophy (2007)

Link

Evaluating Benefits and Harms in Clinical Research (with Paul B. Miller), Principles of Health Care Ethics (2007)

Link

Fiduciary Obligation in Clinical Research (with Paul B. Miller), Journal of Law, Medicine & Ethics (2006)

Link

The Balm of Gilead: Is the Provision of Treatment to those Who Seroconvert in HIV Prevention Trials a Matter of Moral Obligation or Moral Negotiation? (with Guy J. Leblanc), Journal of Law, Medicine & Ethics (2006)

Link

Is Clinical Research and Ethics a Zero-sum Game?, Critical Care Medicine (2005)

Link

A Critical History of Individual and Collective Ethics in the Lineage of Lellouch and Schwartz (with Charles M. Heilig), Clinical Trials (2005)

Clinical Trials, Encyclopedia of Science, Technology, and Ethics (2005)

Link

Heads or Tails: Randomized Placebo-Controlled Trials, Virtual Mentor (2004)

Link

Waiver of Consent for Emergency Research (with Andrew D. McRae), Annals of Emergency Medicine (2004)

Link

When Are Research Risks Reasonable in Relation to Anticipated Benefits? (with Paul B. Miller), Nature Medicine (2004)

Link

Importance of Informed Consent in Offering to Return Research Results to Research Participants (with Conrad V. Fernandez and Eric Kodish), Medical and Pediatric Oncology (2003)

Link

Disclosure of the Right of Research Participants to Receive Research Results: An Analysis of Consent Forms in the Children's Oncology Group (with Conrad V. Fernandez, Eric Kodish, Shaureen Taweel, and Susan Shurin), Cancer (2003)

Link

Is the Use of Placebo Controls Ethically Permissible in Clinical Trials of Agents Intended to Reduce Fractures in Osteoporosis? (with Baruch A. Brody, Nancy Dickey, Susan S. Ellenberg, Robert P. Heaney, Robert J. Levine, Richard L. O'Brien, and Ruth B. Purtilo), Journal of Bone and Mineral Research (2003)

Link

Therapeutic Obligation in Clinical Research (with Paul B. Miller), The Hastings Center report (2003)

Link

The Research Subject as Wage Earner (with James A. Anderson), Theoretical Medicine and Bioethics (2002)

Link

Continuing Review of Clinical Research Canadian-style, Clinical and Investigative Medicine (2002)

Link

Lessons from Everyday Lives: A Moral Justification for Acute Care Research (with Andrew D. McRae), Critical Care Medicine (2002)

Ethics in Clinical Research, The Clinical Research Survival Guide (2002)

Link

Minimal Risk and Its Implications, NCEHR Communiqué (2001)

Link

The Research Subject as Entrepreneur (with James A. Anderson), The American Journal of Bioethics (2001)

Link

Trial by Error, The Hastings Center Report (2001)

Link

The Ethical Analysis of Risk, Journal of Law, Medicine & Ethics (2000)

Link

Clinical Equipoise and Not the Uncertainty Principle Is the Moral Underpinning of the Randomised Controlled Trial (with Stanley H. Shapiro and Kathleen Cranley Glass), British Medical Journal (2000)

Link

Reporting the Study Populations of Clinical Trials. Clear Transmission or Static on the Line? (with Stanley H. Shapiro and Benjamin Freedman), Journal of Clinical Epidemiology (2000)

Link

What's the Price of a Research Subject?, New England Journal of Medicine (1999)

Link

Selecting Subjects for Participation in Clinical Research: One Sphere of Justice, Journal of Medical Ethics (1999)

Link

Consensus-seeking Roundtable on Placebos in Clinical Research, NCEHR Communiqué (1999)

Link

Bioethics for Clinicians: 16. Dealing with Demands for Inappropriate Treatment (with Peter A. Singer, Bernard M. Dickens, and Stephen Workman), Canadian Medical Association Journal (1998)

Link

A Study in Contrasts: Eligibility Criteria in a Twenty-Year Sample of NSABP and POG Clinical Trials (with Abraham Fuks, Benjamin Freedman, Stanley Shapiro, Myriam Skrutkowska, and Amina Riaz), Journal of Clinical Epidemiology (1998)

Link

REB Review of Research Proposals Involving Placebo Controls, NCEHR Communiqué (1998)

Link

The Placebo Effect, Canadian Medical Association Journal (1997)

Do Patients with Breast Cancer Participating in Clinical Trials Receive Better Nursing Care? (with Myriam Skrutkowska), Oncology Nursing Forum (1997)

Link

Spilker's Guide to Clinical Trials on CD-ROM, Journal of the American Medical Association (1997)

Link

Selecting Subjects for Participation in Clinical Research: An Empirical Inquiry and Ethical Analysis (1997)

Link

Bioethics for Clinicians: 10. Research Ethics (with Bernard Dickens and Eric M. Meslin), Canadian Medical Association Journal (1997)

Link

Evolving Ethical Issues in Selection of Subjects for Clinical Research, Cambridge Quarterly of Healthcare Ethics (1996)

Link

What Difference Does It Make to Be Treated in a Clinical Trial? A Pilot Study (with Benjamin Freedman, Abraham Fuks, James Robbins, Stanley Shapiro, and Myriam Skrutkowska), Clinical and Investigative Medicine (1996)

Link

Down with Placebolatry (with Carl Elliott), New Scientist (1996)

Link

Characterizing the Population in Clinical Trials: Barriers, Comparability, and Implications for Review (1995)

Link

Monitoring Clinical Research: An Obligation Unfulfilled (with Stanley Shapiro, Abraham Fuks, Kathleen Cranley Glass, and Myriam Skrutkowska), Canadian Medical Association Journal (1995)

Link

The Duty to Exclude: Excluding People at Undue Risk from Research (with Abraham Fuks), Clinical and Investigative Medicine (1994)

The Revolution in Clinical Trials: From Burden to Benefit and back Again, Future Health (1994)

Link

In Loco Parentis: Minimal Risk as an Ethical Threshold for Research upon Children (with Benjamin Freedman and Abraham Fuks), The Hastings Center Report (1993)

Demarcating Research and Treatment: A Systematic Approach for the Analysis of the Ethics of Clinical Research (with Benjamin Freedman and Abraham Fuks), Clinical Research (1992)

Link

When Are Research Risks Reasonable in Relation to Anticipated Benefits? (with Paul B. Miller), Nature Medicine (2004)

Link

Will the Real Charles Fried Please Stand Up? (with Paul B. Miller), Kennedy Institute of Ethics Journal (2003)

Link

Therapeutic Obligation in Clinical Research (with Paul B. Miller), The Hastings Center report (2003)

Link

I Need a Placebo like I Need a Hole in the Head, Journal of Law, Medicine & Ethics (2002)

Link

Moral Solutions in Assessing Research Risk (with Paul B. Miller), IRB: Ethics and Human Research (2000)

Link

Thinking Clearly about Research Risk: Implications of the Work of Benjamin Freedman, IRB: Ethics and Human Research (1999)

Link

Research Involving the Vulnerable Sick, Accountability in Research (1999)

Link

Selecting Subjects for Participation in Clinical Research: One Sphere of Justice, Journal of Medical Ethics (1999)

Link

The IRB's Role in Assessing the Generalizability of Non-NIH-Funded Clinical Trials, IRB: A Review of Human Subjects Research (1998)

Link

Placebo Orthodoxy in Clinical Research I: Empirical and Methodological Myths (with Benjamin Freedman and Kathleen Cranley Glass), Journal of Law, Medicine & Ethics (1996)

Link

Placebo Orthodoxy in Clinical Research II: Ethical, Legal, and Regulatory Myths (with Benjamin Freedman and Kathleen Cranley Glass), Journal of Law, Medicine & Ethics (1996)

Link

The Duty to Exclude: Excluding People at Undue Risk from Research (with Abraham Fuks), Clinical and Investigative Medicine (1994)

Link

In Loco Parentis: Minimal Risk as an Ethical Threshold for Research upon Children (with Benjamin Freedman and Abraham Fuks), The Hastings Center Report (1993)

Demarcating Research and Treatment: A Systematic Approach for the Analysis of the Ethics of Clinical Research (with Benjamin Freedman and Abraham Fuks), Clinical Research (1992)

Link

[Demarcating Research and Treatment Interventions: A Case Illustration]: Commentary (with Benjamin Freedman), IRB: A Review of Human Subjects Research (1992)

Link

Is the Use of Placebo Controls Ethically Permissible in Clinical Trials of Agents Intended to Reduce Fractures in Osteoporosis? (with Baruch A. Brody, Nancy Dickey, Susan S. Ellenberg, Robert P. Heaney, Robert J. Levine, Richard L. O'Brien, and Ruth B. Purtilo), Journal of Bone and Mineral Research (2003)

Link

The Ethics of Placebo-Controlled Trials, Journal of Bone and Mineral Research (2003)

Link

The Ethics of Placebo-controlled Trials (with Kathleen Cranley Glass), New England Journal of Medicine (2002)

Link

Thinking Clearly about Research Risk: Implications of the Work of Benjamin Freedman, IRB: Ethics and Human Research (1999)

Link

Placebo-controlled Studies in Schizophrenia: Ethical and Scientific Perspectives. Panel Discussion (with T. M. Lemmens, P. S. Appelbaum, W. Carpenter, C. McCarthy, C. Peterson, and D. Streiner), Schizophrenia Research (1999)

Link

Placebo-controlled Trials in Schizophrenia: Are They Ethical? Are They Necessary?, Schizophrenia Research (1999)

Link

Placebo Orthodoxy in Clinical Research I: Empirical and Methodological Myths (with Benjamin Freedman and Kathleen Cranley Glass), Journal of Law, Medicine & Ethics (1996)

Link

Placebo Orthodoxy in Clinical Research II: Ethical, Legal, and Regulatory Myths (with Benjamin Freedman and Kathleen Cranley Glass), Journal of Law, Medicine & Ethics (1996)

Link

Placebo Controls Are Not Good Science, IRB: A Review of Human Subjects Research (1996)

Link

Reporting of patient consent in healthcare cluster randomised trials is associated with the type of study interventions and publication characteristics (with Andrew McRae, Monica Taljaard, Carol Bennett, Zoe Skea, Robert Boruch, Jamie Brehaut, Martin Eccles, Jeremy Grimshaw, and Allan Donner), Journal of Medical Ethics (2013)

Link

When Is Informed Consent Required in Cluster Randomized Trials in Health Research? (with Andrew D. McRae, Ariella Binik, Jeremy M. Grimshaw, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P Eccles, Raphael Saginur, Angela White, and Monica Taljaard), Trials (2011)

Link

Inadequate Reporting of Research Ethics Review and Informed Consent in Cluster Randomised Trials: Review of Random Sample of Published Trials (with Monica Taljaard, Andrew D. McRae, Carol Bennett, Stephanie Dixon, Julia Taleban, Zoe Skea, Martin P Eccles, Jamie C. Brehaut, Allan Donner, Raphael Saginur, Robert F. Boruch, and Jeremy M. Grimshaw), British Medical Journal (2011)

Link

Ethical Issues Posed by Cluster Randomized Trials in Health Research (with Jeremy M. Grimshaw, Monica Taljaard, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Antonio Gallo, Andrew D. McRae, Raphael Saginur, and Merrick Zwarenstein), Trials (2011)

Link

Decision-making by Adolescents and Parents of Children with Cancer Regarding Health Research Participation (with Kate Read, Conrad Vincent Fernandez, Jun Gao, Caron Strahlendorf, Albert Moghrabi, Rebecca Davis Pentz, Raymond Carlton Barfield, Justin Nathaniel Baker, Darcy Santor, and Eric Kodish), Pediatrics (2009)

Link

Ethical and Policy Issues in Cluster Randomized Trials: Rationale and Design of a Mixed Methods Research Study (with Monica Taljaard, Jeremy M. Grimshaw, Judith Belle Brown, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Shazia H. Chaudhry, Martin P. Eccles, Andrew McRae, Raphael Saginur, Merrick Zwarenstein, and Allan Donner), Trials (2009)

Link

Introduction (with Oonagh Corrigan and John McMillan), The Limits of Consent: A Socio-ethical Approach to Human Subject Research in Medicine (2009)

Link

The Limits of Consent: A Socio-ethical Approach to Human Subject Research in Medicine (with Oonagh Corrigan, John McMillan, Kathleen Liddell, and Martin Richards) (2009)

Link

Risk in Emergency Research Using a Waiver of/Exception from Consent: Implications of a Structured Approach for Institutional Review Board Review (with Andrew D. McRae and Stacy Ackroyd-Stolarz), Academic Emergency Medicine (2005)

Link

Is Clinical Research and Ethics a Zero-sum Game?, Critical Care Medicine (2005)

Link

Waiver of Consent for Emergency Research (with Andrew D. McRae), Annals of Emergency Medicine (2004)

Link

Protecting Communities in Pharmacogenetic and Pharmacogenomic Research (with P. B. Miller), The Pharmacogenomics Journal (2004)

Link

Importance of Informed Consent in Offering to Return Research Results to Research Participants (with Conrad V. Fernandez and Eric Kodish), Medical and Pediatric Oncology (2003)

Link

Will the Real Charles Fried Please Stand Up? (with Paul B. Miller), Kennedy Institute of Ethics Journal (2003)

Link

Informing Study Participants of Research Results: An Ethical Imperative (with Conrad V. Fernandez and Eric Kodish), IRB: Ethics and Human Research (2003)

Community Consent for Genetic Research, Nature Encyclopedia of the Human Genome (2003)

Link

The Importance of Context in International Research (with Fern Brunger), Ethics & Behavior (2002)

Link

Lessons from Everyday Lives: A Moral Justification for Acute Care Research (with Andrew D. McRae), Critical Care Medicine (2002)

Link

I Need a Placebo like I Need a Hole in the Head, Journal of Law, Medicine & Ethics (2002)

Link

A Critical Appraisal of Protections for Aboriginal Communities in Biomedical Research (with James A. Anderson), Jurimetrics (2002)

Link

Informing Patients of Uncertainty in Clinical Trials (with S. D. Halpern and J. H. Karlawish), Journal of the American Medical Association (2001)

Link

Family Duty Is More Important than Rights, British Medical Journal (2000)

Link

Benefit-sharing and Other Protections for Communities in Genetic Research, Clinical Genetics (2000)

Link

Protecting Communities in Biomedical Research (with E. J. Emanuel), Science (2000)

Link

Protecting Communities in Research: Current Guidelines and Limits of Extrapolation (with Gary Goldsand and Ezekiel J. Emanuel), Nature Genetics (1999)

Link

Thinking Clearly about Research Risk: Implications of the Work of Benjamin Freedman, IRB: Ethics and Human Research (1999)

Link

Protecting Communities in Research: Philosophical and Pragmatic Challenges, Cambridge Quarterly of Healthcare Ethics (1999)

Link

Research Involving the Vulnerable Sick, Accountability in Research (1999)

Link

Another Tuskegee?, American Journal of Tropical Medicine and Hygiene (1999)

Link

Structuring the Review of Human Genetics Protocols Part-III: Gene Therapy Studies (with Kathleen C. Glass, Denis Cournoyer, Trudo Lemmens, Roberta M. Palmour, Stanley H. Shapiro, and Benjamin Freedman), IRB: A Review of Human Subjects Research (1999)

Link

Monitoring Informed Consent in an Oncology Study Posing Serious Risk to Subjects (with Myrian Skrutkowski, Stan Shapiro, Abraham Fuks, Adrian Langleben, and Benjamin Freedman), IRB: A Review of Human Subjects Research (1998)

Research Methods and Policies, Encyclopedia of Applied Ethics (1998)

Link

Structuring the Review of Human Genetics Protocols Part II: Diagnostic and Screening Studies (with Kathleen Cranley Glass, Trudo Lemmens, Roberta M. Palmour, and Stanley H. Shapiro), IRB: A Review of Human Subjects Research (1997)

Link

Placebo Orthodoxy in Clinical Research II: Ethical, Legal, and Regulatory Myths (with Benjamin Freedman and Kathleen Cranley Glass), Journal of Law, Medicine & Ethics (1996)

Link

Structuring the Review of Human Genetics Protocols: Gene Localization and Identification Studies (with Kathleen Cranley Glass, Roberta M. Palmour, Stanley H. Shapiro, Trudo M. Lemmens, and Karen Lebacqz), IRB: A Review of Human Subjects Research (1996)

Democracy in Medicine?, The Sciences (1995)

Link

Monitoring Clinical Research: An Obligation Unfulfilled (with Stanley Shapiro, Abraham Fuks, Kathleen Cranley Glass, and Myriam Skrutkowska), Canadian Medical Association Journal (1995)

Link

The Duty to Exclude: Excluding People at Undue Risk from Research (with Abraham Fuks), Clinical and Investigative Medicine (1994)

Link

[Demarcating Research and Treatment Interventions: A Case Illustration]: Commentary (with Benjamin Freedman), IRB: A Review of Human Subjects Research (1992)

Link

Ethical Issues Posed by Cluster Randomized Trials in Health Research (with Jeremy M. Grimshaw, Monica Taljaard, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Antonio Gallo, Andrew D. McRae, Raphael Saginur, and Merrick Zwarenstein), Trials (2011)

Link

Ethical and Policy Issues in Cluster Randomized Trials: Rationale and Design of a Mixed Methods Research Study (with Monica Taljaard, Jeremy M. Grimshaw, Judith Belle Brown, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Shazia H. Chaudhry, Martin P. Eccles, Andrew McRae, Raphael Saginur, Merrick Zwarenstein, and Allan Donner), Trials (2009)

Link

Research Governance Lessons from the National Placebo Initiative (with Heather Sampson and Daryl Pullman), Health Law Review (2009)

Link

Heads or Tails: Randomized Placebo-Controlled Trials, Virtual Mentor (2004)

Link

When Are Research Risks Reasonable in Relation to Anticipated Benefits? (with Paul B. Miller), Nature Medicine (2004)

Link

Is the Use of Placebo Controls Ethically Permissible in Clinical Trials of Agents Intended to Reduce Fractures in Osteoporosis? (with Baruch A. Brody, Nancy Dickey, Susan S. Ellenberg, Robert P. Heaney, Robert J. Levine, Richard L. O'Brien, and Ruth B. Purtilo), Journal of Bone and Mineral Research (2003)

Link

Rehabilitating Equipoise (with Paul B. Miller), Kennedy Institute of Ethics Journal (2003)

Link

The Ethics of Placebo-Controlled Trials, Journal of Bone and Mineral Research (2003)

Link

Placebo Tribulations, Canadian Medical Association Journal (2002)

Link

When Argument Fails, The American Journal of Bioethics (2002)

Link

Placebo Trials and Tribulations, Canadian Medical Association Journal (2002)

Link

I Need a Placebo like I Need a Hole in the Head, Journal of Law, Medicine & Ethics (2002)

Link

The Ethics of Placebo-controlled Trials (with Kathleen Cranley Glass), New England Journal of Medicine (2002)

Link

Research Involving the Vulnerable Sick, Accountability in Research (1999)

Link

Placebo-controlled Studies in Schizophrenia: Ethical and Scientific Perspectives. Panel Discussion (with T. M. Lemmens, P. S. Appelbaum, W. Carpenter, C. McCarthy, C. Peterson, and D. Streiner), Schizophrenia Research (1999)

Link

Placebo-controlled Trials in Schizophrenia: Are They Ethical? Are They Necessary?, Schizophrenia Research (1999)

Link

Consensus-seeking Roundtable on Placebos in Clinical Research, NCEHR Communiqué (1999)

Link

REB Review of Research Proposals Involving Placebo Controls, NCEHR Communiqué (1998)

Link

The Placebo Effect, Canadian Medical Association Journal (1997)

Link

CCNP Position Paper on the Use of Placebos in Psychiatry (with William C. Friend), Journal of Psychiatry & Neuroscience (1996)

Link

Placebo Orthodoxy in Clinical Research I: Empirical and Methodological Myths (with Benjamin Freedman and Kathleen Cranley Glass), Journal of Law, Medicine & Ethics (1996)

Link

Placebo Orthodoxy in Clinical Research II: Ethical, Legal, and Regulatory Myths (with Benjamin Freedman and Kathleen Cranley Glass), Journal of Law, Medicine & Ethics (1996)

Link

Placebo Controls Are Not Good Science, IRB: A Review of Human Subjects Research (1996)

Link

Down with Placebolatry (with Carl Elliott), New Scientist (1996)

Link

Providing Research Results to Participants: Attitudes and Needs of Adolescents and Parents of Children with Cancer (with Conrad Vincent Fernandez, Jun Gao, Caron Strahlendorf, Albert Moghrabi, Rebecca Davis Pentz, Raymond Carlton Barfield, Justin Nathaniel Baker, Darcy Santor, and Eric Kodish), Journal of Clinical Oncology (2009)

Link

Trust and Exploitation in Clinical Research (with Paul B. Miller), The Limits of Consent: A Socio-ethical Approach to Human Subject Research in Medicine (2009)

Link

Evaluating Benefits and Harms in Clinical Research (with Paul B. Miller), Principles of Health Care Ethics (2007)

Link

Obligations in Offering to Disclose Genetic Research Results (with Conrad V. Fernandez), The American Journal of Bioethics (2006)

Link

Trust-based Obligations of the State and Physician-researchers to Patient-subjects (with Paul B. Miller), Journal of Medical Ethics (2006)

Link

Revisiting the Ethics of HIV Prevention Research in Developing Countries (with Guy LeBlanc), XVI International AIDS Conference (2006)

Link

Fiduciary Obligation in Clinical Research (with Paul B. Miller), Journal of Law, Medicine & Ethics (2006)

Link

The Balm of Gilead: Is the Provision of Treatment to those Who Seroconvert in HIV Prevention Trials a Matter of Moral Obligation or Moral Negotiation? (with Guy J. Leblanc), Journal of Law, Medicine & Ethics (2006)

Link

Disclosure of Research Result to Research Participants: Needs and Attitudes of Adolescents and Parents (with Conrad Vincent Fernandez, Shaureen Taweel, and Eric D. Kodish), Pediatrics and Child Health (2005)

Protecting Communities in Research: From a New Principle to Rational Protections (with Ezekiel J. Emanuel), Belmont Revisited: Ethical Principles for Research with Human Subjects (2005)

Link

When Are Research Risks Reasonable in Relation to Anticipated Benefits? (with Paul B. Miller), Nature Medicine (2004)

Link

Considerations and Costs of Disclosing Study Findings to Research Participants (with Conrad V. Fernandez and Chris Skedgel), Canadian Medical Association Journal (2004)

Link

The Ethical Analysis of Risk in Intensive Care Unit Research, Critical Care (2004)

Link

Protecting Communities in Pharmacogenetic and Pharmacogenomic Research (with P. B. Miller), The Pharmacogenomics Journal (2004)

Link

Offering to Return Results to Research Participants: Attitudes and Needs of Principal Investigators in the Children's Oncology Group (with Conrad V. Fernandez, Eric Kodish, and Susan Shurin), Journal of Pediatric Hematology/Oncology (2003)

Link

Informing Study Participants of Research Results: An Ethical Imperative (with Conrad V. Fernandez and Eric Kodish), IRB: Ethics and Human Research (2003)

Link

Therapeutic Obligation in Clinical Research (with Paul B. Miller), The Hastings Center report (2003)

Community Consent for Genetic Research, Nature Encyclopedia of the Human Genome (2003)

Link

The Research Subject as Wage Earner (with James A. Anderson), Theoretical Medicine and Bioethics (2002)

Link

A Critical Appraisal of Protections for Aboriginal Communities in Biomedical Research (with James A. Anderson), Jurimetrics (2002)

Ethics in Clinical Research, The Clinical Research Survival Guide (2002)

Link

The Research Subject as Entrepreneur (with James A. Anderson), The American Journal of Bioethics (2001)

REC Approval, Clinical Researcher (2001)

Link

Reporting the Study Populations of Clinical Trials. Clear Transmission or Static on the Line? (with Stanley H. Shapiro and Benjamin Freedman), Journal of Clinical Epidemiology (2000)

Link

What's the Price of a Research Subject?, New England Journal of Medicine (1999)

Link

Protecting Communities in Research: Current Guidelines and Limits of Extrapolation (with Gary Goldsand and Ezekiel J. Emanuel), Nature Genetics (1999)

Link

Protecting Communities in Research: Philosophical and Pragmatic Challenges, Cambridge Quarterly of Healthcare Ethics (1999)

Link

Another Tuskegee?, American Journal of Tropical Medicine and Hygiene (1999)

Link

Placebo-controlled Studies in Schizophrenia: Ethical and Scientific Perspectives. Panel Discussion (with T. M. Lemmens, P. S. Appelbaum, W. Carpenter, C. McCarthy, C. Peterson, and D. Streiner), Schizophrenia Research (1999)

Link

Placebo-controlled Trials in Schizophrenia: Are They Ethical? Are They Necessary?, Schizophrenia Research (1999)

Link

Selecting Subjects for Participation in Clinical Research: One Sphere of Justice, Journal of Medical Ethics (1999)

Protecting Human Research Subjects: Case-Based Learning for Canadian Research Ethics Boards and Researchers (with Françoise Baylis, A. Ireland, and David Kaufman) (1999)

Link

Bioethics for Clinicians: 16. Dealing with Demands for Inappropriate Treatment (with Peter A. Singer, Bernard M. Dickens, and Stephen Workman), Canadian Medical Association Journal (1998)

Link

Assessing the Interpretation of Criteria for Clinical Trial Eligibility: A Survey of Oncology Investigators (with Benjamin Freedman, Stanley Shapiro, Abraham Fuks, Myriam Skrutkowska, and Maria Sigurjonsdottir), Clinical and Investigative Medicine (1998)

Research Methods and Policies, Encyclopedia of Applied Ethics (1998)

Do Patients with Breast Cancer Participating in Clinical Trials Receive Better Nursing Care? (with Myriam Skrutkowska), Oncology Nursing Forum (1997)

Link

Bioethics for Clinicians: 10. Research Ethics (with Bernard Dickens and Eric M. Meslin), Canadian Medical Association Journal (1997)

Link

Evolving Ethical Issues in Selection of Subjects for Clinical Research, Cambridge Quarterly of Healthcare Ethics (1996)

Link

Cruel and Unusual Treatment (with Carl Elliott), Saturday Night (1995)

Link

When Can Physicians Say “No” to Families and Patients?, Critical Care Canada Forum (2009)

Link

Family Duty Is More Important than Rights, British Medical Journal (2000)

Link

Benefit-sharing and Other Protections for Communities in Genetic Research, Clinical Genetics (2000)

Link

Reporting the Study Populations of Clinical Trials. Clear Transmission or Static on the Line? (with Stanley H. Shapiro and Benjamin Freedman), Journal of Clinical Epidemiology (2000)

Link

An Historical Take on the Physician's Charter (with Nuala Kenny), Canadian Medical Association Journal (2000)

Link

Protecting Communities in Research: Current Guidelines and Limits of Extrapolation (with Gary Goldsand and Ezekiel J. Emanuel), Nature Genetics (1999)

Link

Protecting Communities in Research: Philosophical and Pragmatic Challenges, Cambridge Quarterly of Healthcare Ethics (1999)

Research Methods and Policies, Encyclopedia of Applied Ethics (1998)

Link

Structuring the Review of Human Genetics Protocols Part II: Diagnostic and Screening Studies (with Kathleen Cranley Glass, Trudo Lemmens, Roberta M. Palmour, and Stanley H. Shapiro), IRB: A Review of Human Subjects Research (1997)

Link

Structuring the Review of Human Genetics Protocols: Gene Localization and Identification Studies (with Kathleen Cranley Glass, Roberta M. Palmour, Stanley H. Shapiro, Trudo M. Lemmens, and Karen Lebacqz), IRB: A Review of Human Subjects Research (1996)

Democracy in Medicine?, The Sciences (1995)

Link

Heads or Tails: Randomized Placebo-Controlled Trials, Virtual Mentor (2004)

Link

The Quest for Legitimacy: Comment on Cox Macpherson's 'to Strengthen Consensus, Consult the Stakeholders', Bioethics (2004)

Link

Will the Real Charles Fried Please Stand Up? (with Paul B. Miller), Kennedy Institute of Ethics Journal (2003)

Link

Rehabilitating Equipoise (with Paul B. Miller), Kennedy Institute of Ethics Journal (2003)

Link

When Argument Fails, The American Journal of Bioethics (2002)

Link

Placebo Trials and Tribulations, Canadian Medical Association Journal (2002)

Link

I Need a Placebo like I Need a Hole in the Head, Journal of Law, Medicine & Ethics (2002)

Link

Informing Patients of Uncertainty in Clinical Trials (with S. D. Halpern and J. H. Karlawish), Journal of the American Medical Association (2001)

Link

Clinical Equipoise and Not the Uncertainty Principle Is the Moral Underpinning of the Randomised Controlled Trial (with Stanley H. Shapiro and Kathleen Cranley Glass), British Medical Journal (2000)

Link

The Future of Research into Rotavirus Vaccine, British Medical Journal (2000)

Link

Clinical Equipoise and RCT Design, Ethical Issues in Clinical Trials Conference (2000)

Ethical Challenges of the Randomized Controlled Trial (2000)

Why Should We Include Women and Minorities in Randomized Controlled Trials? (with R. A. Crouch), Journal of Clinical Ethics (1999)

Link

Assessing the Interpretation of Criteria for Clinical Trial Eligibility: A Survey of Oncology Investigators (with Benjamin Freedman, Stanley Shapiro, Abraham Fuks, Myriam Skrutkowska, and Maria Sigurjonsdottir), Clinical and Investigative Medicine (1998)

Link

The Breast Cancer Research Scandal: Addressing the Issues, Canadian Medical Association Journal (1995)

Link

Does Clinical Equipoise Apply to Cluster Randomized Trials in Health Research? (with Ariella Binik, Andrew D. McRae, Jeremy M. Grimshaw, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Raphael Saginur, Monica Taljaard, and Merrick Zwarenstein), Trials (2011)

Link

Ethical Issues Posed by Cluster Randomized Trials in Health Research (with Jeremy M. Grimshaw, Monica Taljaard, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Antonio Gallo, Andrew D. McRae, Raphael Saginur, and Merrick Zwarenstein), Trials (2011)

Link

Ethical and Policy Issues in Cluster Randomized Trials: Rationale and Design of a Mixed Methods Research Study (with Monica Taljaard, Jeremy M. Grimshaw, Judith Belle Brown, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Shazia H. Chaudhry, Martin P. Eccles, Andrew McRae, Raphael Saginur, Merrick Zwarenstein, and Allan Donner), Trials (2009)

Link

Minimal Risk and Large-scale Biobank and Cohort Research (with Timothy Caulfield), Health Law Review (2009)

Link

Ethical Issues Associated With the Introduction of New Surgical Devices, or Just Because We Can, Doesn’t Mean We Should (with Sue Ross, Magali Robert, Marie-Andrée Harvey, Scott Farrell, Jane Schulz, David Wilkie, Danny Lovatsis, Annette Epp, Bill Easton, Barry McMillan, Joyce Schachter, and Chander Gupta), Journal of Obstetrics and Gynaecology Canada (2008)

Link

Ethics of Surgical Training in Developing Countries (with Kevin M. Ramsey), World Journal of Surgery (2007)

Link

Evaluating Benefits and Harms in Intensive Care Research (with Paul B. Miller), Intensive Care Medicine (2007)

Link

Refuting the Net Risks Test: A Response to Wendler and Miller's "Assessing Research Risks Systematically" (with Paul B. Miller), Journal of Medical Ethics (2007)

Link

Evaluating Benefits and Harms in Clinical Research (with Paul B. Miller), Principles of Health Care Ethics (2007)

Politics, Risk, and Community in the Maya ICBG Case (with Fern Brunger), Ethical Issues in International Biomedical Research: A Casebook (2007)

Link

Risk in Emergency Research Using a Waiver of/Exception from Consent: Implications of a Structured Approach for Institutional Review Board Review (with Andrew D. McRae and Stacy Ackroyd-Stolarz), Academic Emergency Medicine (2005)

Link

Evaluating Risks of Non-therapeutic Research in Children (with Paul B. Miller), Ethics and Research with Children: A Case-based Approach (2005)

Link

When Are Research Risks Reasonable in Relation to Anticipated Benefits? (with Paul B. Miller), Nature Medicine (2004)

Link

The Ethical Analysis of Risk in Intensive Care Unit Research, Critical Care (2004)

Link

Informing Study Participants of Research Results: An Ethical Imperative (with Conrad V. Fernandez and Eric Kodish), IRB: Ethics and Human Research (2003)

Link

Lessons from Everyday Lives: A Moral Justification for Acute Care Research (with Andrew D. McRae), Critical Care Medicine (2002)

Link

When Argument Fails, The American Journal of Bioethics (2002)

Link

I Need a Placebo like I Need a Hole in the Head, Journal of Law, Medicine & Ethics (2002)

Link

Minimal Risk and Its Implications, NCEHR Communiqué (2001)

Link

The Ethical Analysis of Risk, Journal of Law, Medicine & Ethics (2000)

Link

Moral Solutions in Assessing Research Risk (with Paul B. Miller), IRB: Ethics and Human Research (2000)

Link

The Ethical Analysis of Risks and Potential Benefits in Human Subjects Research: History, Theory, and Implications for U.S. Regulation (2000)

Link

Research Involving the Vulnerable Sick, Accountability in Research (1999)

Link

The Analysis of Risks and Potential Benefits in Research, NCEHR Communiqué (1999)

Why Should We Include Women and Minorities in Randomized Controlled Trials? (with R. A. Crouch), Journal of Clinical Ethics (1999)

Link

Structuring the Review of Human Genetics Protocols Part-III: Gene Therapy Studies (with Kathleen C. Glass, Denis Cournoyer, Trudo Lemmens, Roberta M. Palmour, Stanley H. Shapiro, and Benjamin Freedman), IRB: A Review of Human Subjects Research (1999)

Link

Monitoring Informed Consent in an Oncology Study Posing Serious Risk to Subjects (with Myrian Skrutkowski, Stan Shapiro, Abraham Fuks, Adrian Langleben, and Benjamin Freedman), IRB: A Review of Human Subjects Research (1998)

Link

The IRB's Role in Assessing the Generalizability of Non-NIH-Funded Clinical Trials, IRB: A Review of Human Subjects Research (1998)

Link

Cardiopulmonary Resuscitation for Patients in a Persistent Vegetative State: Futile or Acceptable?, Canadian Medical Association Journal (1998)

Link

Structuring the Review of Human Genetics Protocols Part II: Diagnostic and Screening Studies (with Kathleen Cranley Glass, Trudo Lemmens, Roberta M. Palmour, and Stanley H. Shapiro), IRB: A Review of Human Subjects Research (1997)

Link

Bioethics for Clinicians: 10. Research Ethics (with Bernard Dickens and Eric M. Meslin), Canadian Medical Association Journal (1997)

Link

Placebo Orthodoxy in Clinical Research I: Empirical and Methodological Myths (with Benjamin Freedman and Kathleen Cranley Glass), Journal of Law, Medicine & Ethics (1996)

Link

Placebo Orthodoxy in Clinical Research II: Ethical, Legal, and Regulatory Myths (with Benjamin Freedman and Kathleen Cranley Glass), Journal of Law, Medicine & Ethics (1996)

Link

Structuring the Review of Human Genetics Protocols: Gene Localization and Identification Studies (with Kathleen Cranley Glass, Roberta M. Palmour, Stanley H. Shapiro, Trudo M. Lemmens, and Karen Lebacqz), IRB: A Review of Human Subjects Research (1996)

Link

Evolving Ethical Issues in Selection of Subjects for Clinical Research, Cambridge Quarterly of Healthcare Ethics (1996)

Link

The Duty to Exclude: Excluding People at Undue Risk from Research (with Abraham Fuks), Clinical and Investigative Medicine (1994)

Link

In Loco Parentis: Minimal Risk as an Ethical Threshold for Research upon Children (with Benjamin Freedman and Abraham Fuks), The Hastings Center Report (1993)

Demarcating Research and Treatment: A Systematic Approach for the Analysis of the Ethics of Clinical Research (with Benjamin Freedman and Abraham Fuks), Clinical Research (1992)

Link

[Demarcating Research and Treatment Interventions: A Case Illustration]: Commentary (with Benjamin Freedman), IRB: A Review of Human Subjects Research (1992)

Link

Who Is the Research Subject in Cluster Randomized Trials in Health Research? (with Andrew D. McRae, Ariella Binik, Angela White, Jeremy M. Grimshaw, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Raphael Saginur, Merrick Zwarenstein, and Monica Taljaard), Trials (2011)

Link

Ethical Issues Posed by Cluster Randomized Trials in Health Research (with Jeremy M. Grimshaw, Monica Taljaard, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Antonio Gallo, Andrew D. McRae, Raphael Saginur, and Merrick Zwarenstein), Trials (2011)

Link

Decision-making by Adolescents and Parents of Children with Cancer Regarding Health Research Participation (with Kate Read, Conrad Vincent Fernandez, Jun Gao, Caron Strahlendorf, Albert Moghrabi, Rebecca Davis Pentz, Raymond Carlton Barfield, Justin Nathaniel Baker, Darcy Santor, and Eric Kodish), Pediatrics (2009)

Link

Ethical and Policy Issues in Cluster Randomized Trials: Rationale and Design of a Mixed Methods Research Study (with Monica Taljaard, Jeremy M. Grimshaw, Judith Belle Brown, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Shazia H. Chaudhry, Martin P. Eccles, Andrew McRae, Raphael Saginur, Merrick Zwarenstein, and Allan Donner), Trials (2009)

Link

Providing Research Results to Participants: Attitudes and Needs of Adolescents and Parents of Children with Cancer (with Conrad Vincent Fernandez, Jun Gao, Caron Strahlendorf, Albert Moghrabi, Rebecca Davis Pentz, Raymond Carlton Barfield, Justin Nathaniel Baker, Darcy Santor, and Eric Kodish), Journal of Clinical Oncology (2009)

Link

Introduction (with Oonagh Corrigan and John McMillan), The Limits of Consent: A Socio-ethical Approach to Human Subject Research in Medicine (2009)

Link

The Limits of Consent: A Socio-ethical Approach to Human Subject Research in Medicine (with Oonagh Corrigan, John McMillan, Kathleen Liddell, and Martin Richards) (2009)

Link

Trust and Exploitation in Clinical Research (with Paul B. Miller), The Limits of Consent: A Socio-ethical Approach to Human Subject Research in Medicine (2009)

Link

Refuting the Net Risks Test: A Response to Wendler and Miller's "Assessing Research Risks Systematically" (with Paul B. Miller), Journal of Medical Ethics (2007)

Link

The Return of Research Results to Participants: Pilot Questionnaire of Adolescents and Parents of Children with Cancer (with Conrad V. Fernandez, Darcy Santor, Caron Strahlendorf, Albert Moghrabi, Rebecca Pentz, Jun Gao, and Eric Kodish), Pediatric Blood & Cancer (2007)

Link

Evaluating Benefits and Harms in Clinical Research (with Paul B. Miller), Principles of Health Care Ethics (2007)

Link

Obligations in Offering to Disclose Genetic Research Results (with Conrad V. Fernandez), The American Journal of Bioethics (2006)

Link

Trust-based Obligations of the State and Physician-researchers to Patient-subjects (with Paul B. Miller), Journal of Medical Ethics (2006)

Link

Revisiting the Ethics of HIV Prevention Research in Developing Countries (with Guy LeBlanc), XVI International AIDS Conference (2006)

Link

Risk in Emergency Research Using a Waiver of/Exception from Consent: Implications of a Structured Approach for Institutional Review Board Review (with Andrew D. McRae and Stacy Ackroyd-Stolarz), Academic Emergency Medicine (2005)

Link

Meaningful Work as Due Inducement, Theoretical Medicine and Bioethics (2005)

Link

Disclosure of Research Result to Research Participants: Needs and Attitudes of Adolescents and Parents (with Conrad Vincent Fernandez, Shaureen Taweel, and Eric D. Kodish), Pediatrics and Child Health (2005)

Link

A Critical History of Individual and Collective Ethics in the Lineage of Lellouch and Schwartz (with Charles M. Heilig), Clinical Trials (2005)

Protecting Communities in Research: From a New Principle to Rational Protections (with Ezekiel J. Emanuel), Belmont Revisited: Ethical Principles for Research with Human Subjects (2005)

Link

When Are Research Risks Reasonable in Relation to Anticipated Benefits? (with Paul B. Miller), Nature Medicine (2004)

Link

Considerations and Costs of Disclosing Study Findings to Research Participants (with Conrad V. Fernandez and Chris Skedgel), Canadian Medical Association Journal (2004)

Link

The Ethical Analysis of Risk in Intensive Care Unit Research, Critical Care (2004)

Link

Protecting Communities in Pharmacogenetic and Pharmacogenomic Research (with P. B. Miller), The Pharmacogenomics Journal (2004)

Link

Offering to Return Results to Research Participants: Attitudes and Needs of Principal Investigators in the Children's Oncology Group (with Conrad V. Fernandez, Eric Kodish, and Susan Shurin), Journal of Pediatric Hematology/Oncology (2003)

Link

Informing Study Participants of Research Results: An Ethical Imperative (with Conrad V. Fernandez and Eric Kodish), IRB: Ethics and Human Research (2003)

Community Consent for Genetic Research, Nature Encyclopedia of the Human Genome (2003)

Link

The Research Subject as Wage Earner (with James A. Anderson), Theoretical Medicine and Bioethics (2002)

Link

A Critical Appraisal of Protections for Aboriginal Communities in Biomedical Research (with James A. Anderson), Jurimetrics (2002)

Ethics in Clinical Research, The Clinical Research Survival Guide (2002)

Link

Continuing Review of Research Approved by Canadian Research Ethics Boards, Canadian Medical Association Journal (2001)

Link

The Ethics Wars: Disputes over International Research (with James A. Anderson), The Hastings Center Report (2001)

Link

The Research Subject as Entrepreneur (with James A. Anderson), The American Journal of Bioethics (2001)

REC Approval, Clinical Researcher (2001)

Link

Reporting the Study Populations of Clinical Trials. Clear Transmission or Static on the Line? (with Stanley H. Shapiro and Benjamin Freedman), Journal of Clinical Epidemiology (2000)

Link

The Ethical Analysis of Risks and Potential Benefits in Human Subjects Research: History, Theory, and Implications for U.S. Regulation (2000)

Link

What's the Price of a Research Subject?, New England Journal of Medicine (1999)

Link

Protecting Communities in Research: Current Guidelines and Limits of Extrapolation (with Gary Goldsand and Ezekiel J. Emanuel), Nature Genetics (1999)

Link

Protecting Communities in Research: Philosophical and Pragmatic Challenges, Cambridge Quarterly of Healthcare Ethics (1999)

Link

Research Involving the Vulnerable Sick, Accountability in Research (1999)

Link

Another Tuskegee?, American Journal of Tropical Medicine and Hygiene (1999)

Why Should We Include Women and Minorities in Randomized Controlled Trials? (with R. A. Crouch), Journal of Clinical Ethics (1999)

Link

Placebo-controlled Studies in Schizophrenia: Ethical and Scientific Perspectives. Panel Discussion (with T. M. Lemmens, P. S. Appelbaum, W. Carpenter, C. McCarthy, C. Peterson, and D. Streiner), Schizophrenia Research (1999)

Link

Placebo-controlled Trials in Schizophrenia: Are They Ethical? Are They Necessary?, Schizophrenia Research (1999)

Link

Selecting Subjects for Participation in Clinical Research: One Sphere of Justice, Journal of Medical Ethics (1999)

Protecting Human Research Subjects: Case-Based Learning for Canadian Research Ethics Boards and Researchers (with Françoise Baylis, A. Ireland, and David Kaufman) (1999)

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Bioethics for Clinicians: 16. Dealing with Demands for Inappropriate Treatment (with Peter A. Singer, Bernard M. Dickens, and Stephen Workman), Canadian Medical Association Journal (1998)

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The IRB's Role in Assessing the Generalizability of Non-NIH-Funded Clinical Trials, IRB: A Review of Human Subjects Research (1998)

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Assessing the Interpretation of Criteria for Clinical Trial Eligibility: A Survey of Oncology Investigators (with Benjamin Freedman, Stanley Shapiro, Abraham Fuks, Myriam Skrutkowska, and Maria Sigurjonsdottir), Clinical and Investigative Medicine (1998)

Research Methods and Policies, Encyclopedia of Applied Ethics (1998)

Do Patients with Breast Cancer Participating in Clinical Trials Receive Better Nursing Care? (with Myriam Skrutkowska), Oncology Nursing Forum (1997)

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Selecting Subjects for Participation in Clinical Research: An Empirical Inquiry and Ethical Analysis (1997)

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Structuring the Review of Human Genetics Protocols Part II: Diagnostic and Screening Studies (with Kathleen Cranley Glass, Trudo Lemmens, Roberta M. Palmour, and Stanley H. Shapiro), IRB: A Review of Human Subjects Research (1997)

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Bioethics for Clinicians: 10. Research Ethics (with Bernard Dickens and Eric M. Meslin), Canadian Medical Association Journal (1997)

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Placebo Orthodoxy in Clinical Research I: Empirical and Methodological Myths (with Benjamin Freedman and Kathleen Cranley Glass), Journal of Law, Medicine & Ethics (1996)

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Placebo Orthodoxy in Clinical Research II: Ethical, Legal, and Regulatory Myths (with Benjamin Freedman and Kathleen Cranley Glass), Journal of Law, Medicine & Ethics (1996)

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Structuring the Review of Human Genetics Protocols: Gene Localization and Identification Studies (with Kathleen Cranley Glass, Roberta M. Palmour, Stanley H. Shapiro, Trudo M. Lemmens, and Karen Lebacqz), IRB: A Review of Human Subjects Research (1996)

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Evolving Ethical Issues in Selection of Subjects for Clinical Research, Cambridge Quarterly of Healthcare Ethics (1996)

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Cruel and Unusual Treatment (with Carl Elliott), Saturday Night (1995)

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Characterizing the Population in Clinical Trials: Barriers, Comparability, and Implications for Review (1995)

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The Breast Cancer Research Scandal: Addressing the Issues, Canadian Medical Association Journal (1995)

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The Duty to Exclude: Excluding People at Undue Risk from Research (with Abraham Fuks), Clinical and Investigative Medicine (1994)

Link

In Loco Parentis: Minimal Risk as an Ethical Threshold for Research upon Children (with Benjamin Freedman and Abraham Fuks), The Hastings Center Report (1993)

Demarcating Research and Treatment: A Systematic Approach for the Analysis of the Ethics of Clinical Research (with Benjamin Freedman and Abraham Fuks), Clinical Research (1992)

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Researchers’ perceptions of ethical challenges in cluster randomized trials: a qualitative analysis (with Andrew D. McRae, Carol Bennett, Judith Belle Brown, Robert Boruch, Jamie Brehaut, Shazia Chaudhry, Allan Donner, Martin Eccles, Jeremy Grimshaw, Merrick Zwarenstein, and Monica Taljaard), Trials (2013)

Film and Narrative in Bioethics: Akira Kurosawa's Ikiru, Stories and Their Limits: Narrative Approaches to Bioethics (1997)

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Requirements for Ethics Committee Review for Studies Submitted to Implementation Science (with Martin P. Eccles and Brian Mittman), Implementation Science (2011)

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Ethics, Economics and the Regulation and Adoption of New Medical Devices: Case Studies in Pelvic Floor Surgery (with Sue Ross, Amiram Gafni, Ariel Ducey, Carmen Thompson, and Rene Lafreniere), BMC Medical Ethics (2010)

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Conceptual Problems in Research Ethics, Research Day (Arts & Humanities, FIMS, and Education) (2010)

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Decision-making by Adolescents and Parents of Children with Cancer Regarding Health Research Participation (with Kate Read, Conrad Vincent Fernandez, Jun Gao, Caron Strahlendorf, Albert Moghrabi, Rebecca Davis Pentz, Raymond Carlton Barfield, Justin Nathaniel Baker, Darcy Santor, and Eric Kodish), Pediatrics (2009)

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Providing Research Results to Participants: Attitudes and Needs of Adolescents and Parents of Children with Cancer (with Conrad Vincent Fernandez, Jun Gao, Caron Strahlendorf, Albert Moghrabi, Rebecca Davis Pentz, Raymond Carlton Barfield, Justin Nathaniel Baker, Darcy Santor, and Eric Kodish), Journal of Clinical Oncology (2009)

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Helsinki Discords: FDA, Ethics, and International Drug Trials (with Jonathan Kimmelman and Eric M. Meslin), Lancet (2009)

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A Comparison of Journal Instructions Regarding Institutional Review Board Approval and Conflict-of-interest Disclosure between 1995 and 2005 (with Anne Rowan-Legg, J. Gao, and C. Fernandez), Journal of Medical Ethics (2009)

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U.S. Federal Regulations for Emergency Research: A Practical Guide and Commentary (with Andrew McRae), Academic Emergency Medicine (2008)

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Evaluating Benefits and Harms in Intensive Care Research (with Paul B. Miller), Intensive Care Medicine (2007)

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Equipoise and the Duty of Care in Clinical Research: A Philosophical Response to Our Critics (with Paul B. Miller), Journal of Medicine and Philosophy (2007)

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Trust-based Obligations of the State and Physician-researchers to Patient-subjects (with Paul B. Miller), Journal of Medical Ethics (2006)

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Fiduciary Obligation in Clinical Research (with Paul B. Miller), Journal of Law, Medicine & Ethics (2006)

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The Balm of Gilead: Is the Provision of Treatment to those Who Seroconvert in HIV Prevention Trials a Matter of Moral Obligation or Moral Negotiation? (with Guy J. Leblanc), Journal of Law, Medicine & Ethics (2006)

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Meaningful Work as Due Inducement, Theoretical Medicine and Bioethics (2005)

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Disclosure of Research Result to Research Participants: Needs and Attitudes of Adolescents and Parents (with Conrad Vincent Fernandez, Shaureen Taweel, and Eric D. Kodish), Pediatrics and Child Health (2005)

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Considerations and Costs of Disclosing Study Findings to Research Participants (with Conrad V. Fernandez and Chris Skedgel), Canadian Medical Association Journal (2004)

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Bioethics in Social Context, edited by Barry Hoffmaster, Bioethics (2003)

Community Consent for Genetic Research, Nature Encyclopedia of the Human Genome (2003)

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Unethical Author Attribution (with Akira Akabayashi), Cambridge Quarterly of Healthcare Ethics (2003)

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The Importance of Context in International Research (with Fern Brunger), Ethics & Behavior (2002)

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Matters of Life and Death: Making Moral Theory Work in Medical Ethics and the Law (with James A. Anderson), Journal of the American Medical Association (2002)

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Continuing Review of Clinical Research Canadian-style, Clinical and Investigative Medicine (2002)

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Who Should Foot the Bill for Continuing Review of Research?, Canadian Medical Association Journal (2001)

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Continuing Review of Research Approved by Canadian Research Ethics Boards, Canadian Medical Association Journal (2001)

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The Ethics Wars: Disputes over International Research (with James A. Anderson), The Hastings Center Report (2001)

REC Approval, Clinical Researcher (2001)

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Benefit-sharing and Other Protections for Communities in Genetic Research, Clinical Genetics (2000)

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A Philosophical Disease: Bioethics, Culture, and Identity, Journal of the American Medical Association (2000)

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Bioethics: An Anthology, British Medical Journal (2000)

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Clinical Equipoise and RCT Design, Ethical Issues in Clinical Trials Conference (2000)

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Protecting Communities in Research: Current Guidelines and Limits of Extrapolation (with Gary Goldsand and Ezekiel J. Emanuel), Nature Genetics (1999)

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Another Tuskegee?, American Journal of Tropical Medicine and Hygiene (1999)

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The Analysis of Risks and Potential Benefits in Research, NCEHR Communiqué (1999)

Duty and Healing: Foundations of a Jewish Bioethic (with Benjamin Freedman) (1999)

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Society’s Choices: Social and Ethical Decision Making in Biomedicine, NCEHR Communiqué (1998)

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REB Review of Research Proposals Involving Placebo Controls, NCEHR Communiqué (1998)

Research Methods and Policies, Encyclopedia of Applied Ethics (1998)

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Duty and Healing: The Lifework of Benjamin Freedman, Canadian Medical Association Journal (1997)

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Remembering Benjamin Freedman (1951-1997) (with Françoise Baylis), The Hastings Center Report (1997)

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Queer Science: The Use and Abuse of Research into Homosexuality, British Medical Journal (1996)

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What Difference Does It Make to Be Treated in a Clinical Trial? A Pilot Study (with Benjamin Freedman, Abraham Fuks, James Robbins, Stanley Shapiro, and Myriam Skrutkowska), Clinical and Investigative Medicine (1996)

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Ethical Issues in Research, Religious Studies Review (1996)

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Do the Right Thing, McGill News (1996)

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Cruel and Unusual Treatment (with Carl Elliott), Saturday Night (1995)

Link

Monitoring Clinical Research: An Obligation Unfulfilled (with Stanley Shapiro, Abraham Fuks, Kathleen Cranley Glass, and Myriam Skrutkowska), Canadian Medical Association Journal (1995)

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Our Bodies, Our Science, The Sciences (1995)

Link

The Breast Cancer Research Scandal: Addressing the Issues, Canadian Medical Association Journal (1995)

Biomedical Research: Collaboration and Conflict of Interest, NCEHR Communiqué (1995)

Link

Biomedical Ethics in a Canadian Context, Religious Studies Review (1994)

Link

Thinking Clearly about Research Risk: Implications of the Work of Benjamin Freedman, IRB: Ethics and Human Research (1999)

Duty and Healing: Foundations of a Jewish Bioethic (with Benjamin Freedman) (1999)

Link

Duty and Healing: The Lifework of Benjamin Freedman, Canadian Medical Association Journal (1997)

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Remembering Benjamin Freedman (1951-1997) (with Françoise Baylis), The Hastings Center Report (1997)

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Why I Am Not a Futilitarian (Review of When Doctors Say No: The Battleground of Medical Futility), Canadian Medical Association Journal (1999)

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Wrong Medicine: Doctors, Patients, and Futile Treatment, British Medical Journal (1995)

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Pulling the Plug on Futility (with Carl Elliott), British Medical Journal (1995)

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Minimal Risk Remains an Open Question (with Ariella Binik and Mark Sheehan), The American Journal of Bioethics (2011)

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Does Clinical Equipoise Apply to Cluster Randomized Trials in Health Research? (with Ariella Binik, Andrew D. McRae, Jeremy M. Grimshaw, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Raphael Saginur, Monica Taljaard, and Merrick Zwarenstein), Trials (2011)

Link

Ethical Issues Posed by Cluster Randomized Trials in Health Research (with Jeremy M. Grimshaw, Monica Taljaard, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Antonio Gallo, Andrew D. McRae, Raphael Saginur, and Merrick Zwarenstein), Trials (2011)

Link

Ethical and Policy Issues in Cluster Randomized Trials: Rationale and Design of a Mixed Methods Research Study (with Monica Taljaard, Jeremy M. Grimshaw, Judith Belle Brown, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Shazia H. Chaudhry, Martin P. Eccles, Andrew McRae, Raphael Saginur, Merrick Zwarenstein, and Allan Donner), Trials (2009)

Link

The Ottawa Statement on the Ethical Design and Conduct of Cluster Randomized Trials (with Jeremy M. Grimshaw, Martin P. Eccles, Andrew D. McRae, Angela White, Jamie C. Brehaut, and Monica Taljaard), PLoS Medicine (2012)

Private Religious Schools and Public Reasons, Statistics, Science and Public Policy (2009)

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Reporting of patient consent in healthcare cluster randomised trials is associated with the type of study interventions and publication characteristics (with Andrew McRae, Monica Taljaard, Carol Bennett, Zoe Skea, Robert Boruch, Jamie Brehaut, Martin Eccles, Jeremy Grimshaw, and Allan Donner), Journal of Medical Ethics (2013)

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The publication of ethically uncertain research: attitudes and practices of journal editors (with Carla Angelski, Conrad V. Fernandez, and Jun Gao), BMC Medical Ethics (2012)

Link

Impact of CONSORT Extension for Cluster Randomised Trials on Quality of Reporting and Study Methodology: Review of Random Sample of 300 Trials, 2000-8 (with N. M. Ivers, M. Taljaard, Stephanie Dixon, C. Bennett, A. McRae, J. Taleban, Z. Skea, J. C. Brehaut, R. F. Boruch, M. P. Eccles, J. M. Grimshaw, M. Zwarenstein, and A. Donner), British Medical Journal (2011)

Link

Inadequate Reporting of Research Ethics Review and Informed Consent in Cluster Randomised Trials: Review of Random Sample of Published Trials (with Monica Taljaard, Andrew D. McRae, Carol Bennett, Stephanie Dixon, Julia Taleban, Zoe Skea, Martin P Eccles, Jamie C. Brehaut, Allan Donner, Raphael Saginur, Robert F. Boruch, and Jeremy M. Grimshaw), British Medical Journal (2011)

Link

Reporting of patient consent in healthcare cluster randomised trials is associated with the type of study interventions and publication characteristics (with Andrew McRae, Monica Taljaard, Carol Bennett, Zoe Skea, Robert Boruch, Jamie Brehaut, Martin Eccles, Jeremy Grimshaw, and Allan Donner), Journal of Medical Ethics (2013)

Link

Researchers’ perceptions of ethical challenges in cluster randomized trials: a qualitative analysis (with Andrew D. McRae, Carol Bennett, Judith Belle Brown, Robert Boruch, Jamie Brehaut, Shazia Chaudhry, Allan Donner, Martin Eccles, Jeremy Grimshaw, Merrick Zwarenstein, and Monica Taljaard), Trials (2013)

Link

The Ottawa Statement on the Ethical Design and Conduct of Cluster Randomized Trials (with Jeremy M. Grimshaw, Martin P. Eccles, Andrew D. McRae, Angela White, Jamie C. Brehaut, and Monica Taljaard), PLoS Medicine (2012)

Link

What is the role and authority of gatekeepers in cluster randomized trials in health research? (with Antonio Gallo, Angela White, Jeremy M. Grimshaw, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Andrew D. McRae, Raphael Saginur, Merrick Zwarenstein, and Monica Taljaard), Trials (2012)

Link

Impact of CONSORT Extension for Cluster Randomised Trials on Quality of Reporting and Study Methodology: Review of Random Sample of 300 Trials, 2000-8 (with N. M. Ivers, M. Taljaard, Stephanie Dixon, C. Bennett, A. McRae, J. Taleban, Z. Skea, J. C. Brehaut, R. F. Boruch, M. P. Eccles, J. M. Grimshaw, M. Zwarenstein, and A. Donner), British Medical Journal (2011)

Link

When Is Informed Consent Required in Cluster Randomized Trials in Health Research? (with Andrew D. McRae, Ariella Binik, Jeremy M. Grimshaw, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P Eccles, Raphael Saginur, Angela White, and Monica Taljaard), Trials (2011)

Link

Who Is the Research Subject in Cluster Randomized Trials in Health Research? (with Andrew D. McRae, Ariella Binik, Angela White, Jeremy M. Grimshaw, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Raphael Saginur, Merrick Zwarenstein, and Monica Taljaard), Trials (2011)

Link

Does Clinical Equipoise Apply to Cluster Randomized Trials in Health Research? (with Ariella Binik, Andrew D. McRae, Jeremy M. Grimshaw, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Raphael Saginur, Monica Taljaard, and Merrick Zwarenstein), Trials (2011)

Link

Inadequate Reporting of Research Ethics Review and Informed Consent in Cluster Randomised Trials: Review of Random Sample of Published Trials (with Monica Taljaard, Andrew D. McRae, Carol Bennett, Stephanie Dixon, Julia Taleban, Zoe Skea, Martin P Eccles, Jamie C. Brehaut, Allan Donner, Raphael Saginur, Robert F. Boruch, and Jeremy M. Grimshaw), British Medical Journal (2011)

Link

Ethical Issues Posed by Cluster Randomized Trials in Health Research (with Jeremy M. Grimshaw, Monica Taljaard, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Antonio Gallo, Andrew D. McRae, Raphael Saginur, and Merrick Zwarenstein), Trials (2011)

Link

Ethical and Policy Issues in Cluster Randomized Trials: Rationale and Design of a Mixed Methods Research Study (with Monica Taljaard, Jeremy M. Grimshaw, Judith Belle Brown, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Shazia H. Chaudhry, Martin P. Eccles, Andrew McRae, Raphael Saginur, Merrick Zwarenstein, and Allan Donner), Trials (2009)

Link

What is the role and authority of gatekeepers in cluster randomized trials in health research? (with Antonio Gallo, Angela White, Jeremy M. Grimshaw, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Andrew D. McRae, Raphael Saginur, Merrick Zwarenstein, and Monica Taljaard), Trials (2012)

Link

Is Philosophy Dead? Far from It, Western News (2010)

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Rotman Institute Opening (with Joseph Rotman, Janice Deakin, Jane Maienschein, and Philip Kitcher), Rotman Events and Speakers Series (2010)

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Terri Schiavo: Rest in Peace, Canadian Medical Association Journal (2006)

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The Sum of My Parts, British Medical Journal (2000)

Canada’s First Gene Therapy Death, Parkhurst Exchange (2000)

When Doctors Say "No", Hospital News (2000)

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We’re Alright Jack, Canadian Bioethics Society Newsletter (1999)

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Integrating Bioethics and Health Law Into the Canadian Institutes of Health Research (with Susan Sherwin, Françoise Baylis, Alan Bernstein, Timothy Caulfield, Bernard Dickens, Jocelyn Downie, Bartha Knoppers, Thérèse Leroux, Neil MacDonald, Michael McDonald, and Janet Storch) (1999)

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D'oh! An Analysis of the Medical Care Provided to the Family of Homer J. Simpson (with Robert Patterson), Canadian Medical Association Journal (1998)

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Full House: The Spread of Excellence from Plato to Darwin, British Medical Journal (1997)

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Kenneth V. Iserson. Death to Dust: What Happens to Dead Bodies?, Theoretical Medicine (1995)

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Mental Capacity, Responsibility, and Mental Health Legislation (with Carl Elliott), Current Opinion in Psychiatry (1994)

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Momento Mori, The Hastings Center Report (1994)

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Case Notes and Carting of Bioethical Case Consultations (with Benjamin Freedman and Eugene Bereza), HEC Forum (1993)