D. Willison

C. Levy, Michelle L. Marcinow, S. Guilcher, 2020, Health expectations : an international journal of public participation in health care and health policy.

Seroprevalence of Pandemic Influenza H1N1 in Ontario from January 2009–May 2010

L. Rosella, A. Rebbapragada, S. Deeks, 2011, PloS one.

What do Canadians think about physician-pharmaceutical industry interactions?

C. Weijer, A. Holbrook, J. Lexchin, 2013, Health policy.

Survey of Awareness and Perceptions of Canadians on the Benefits and Risks of Clinical Trials

D. Willison, D. Richards, Alison Orth, 2018, Therapeutic innovation & regulatory science.

Cost Effectiveness of Multi-Therapy Treatment Strategies in the Prevention of Vertebral Fractures in Postmenopausal Women with Osteoporosis

G. Torrance, J. Adachi, D. Willison, 1998, PharmacoEconomics.

Assessing the Relative Timeliness of Ontario’s Syndromic Surveillance Systems for Early Detection of the 2009 Influenza H1N1 Pandemic Waves

L. Rosella, N. Crowcroft, D. Willison, 2013, Canadian Journal of Public Health.

The Effect of Comorbidity on Use of Thrombolysis or Aspirin in Patients with Acute Myocardial Infarction Eligible for Treatment

J. Gurwitz, S. Soumerai, D. Willison, 2006, Journal of General Internal Medicine.

Artificial intelligence for good health: a scoping review of the ethics literature

E. Di Ruggiero, N. Malhotra, Ross Upshur, 2020, BMC medical ethics.

Consultation between cardiologists and generalists in the management of acute myocardial infarction: implications for quality of care.

J. Gurwitz, E. Guadagnoli, S. Soumerai, 1998, Archives of internal medicine.

Participatory governance over research in an academic research network: the case of Diabetes Action Canada

D. Willison, Karim Keshavjee, F. Sullivan, 2019, BMJ Open.

Privacy and Health Information Systems: a Guide to Protecting Patient Confidentiality: By J. Goldman and D. Mulligan. Foundation for Health Care Quality, Seattle, 1996, $25, 45pp.

D. Willison, Don Willison, 1999 .

Privacy and confidentiality concerns--are we up to the challenge?

D. Willison, 2000, International journal for quality in health care : journal of the International Society for Quality in Health Care.

The use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution

K. Lajkosz, C. Virtanen, A. Heesters, 2021, BMC medical ethics.

Camouflaged sampling and contacting of people from administrative databases: reaching target patients without knowing who they are

M. Maclure, D. Willison, Leanne Warren, 2008, Pharmacoepidemiology and drug safety.

Patient consent preferences on sharing personal health information during the COVID-19 pandemic: “the more informed we are, the more likely we are to help”

K. Lajkosz, C. Virtanen, A. Heesters, 2022, BMC medical ethics.

Who's minding the shop? The role of Canadian research ethics boards in the creation and uses of registries and biobanks

K. Brazil, L. Schwartz, D. Willison, 2008, BMC medical ethics.

Impracticability of informed consent in the Registry of the Canadian Stroke Network.

Jack V Tu, Andreas Laupacis, Jiming Fang, 2004, The New England journal of medicine.

Perceptions of immunization information systems for collecting pandemic H1N1 immunization data within Canada's public health community: A qualitative study

D. Buckeridge, C. Heidebrecht, S. Deeks, 2010, BMC public health.

Intravenous fluids and the hospitalized dying: a medical last rite?

F. Burge, D. Willison, D. King, 1990, Canadian family physician Medecin de famille canadien.

Alternatives to project-specific consent for access to personal information for health research: what is the opinion of the Canadian public?

Lehana Thabane, Donald J. Willison, Cathy Charles, 2007, Journal of the American Medical Informatics Association : JAMIA.

Coding accuracy of administrative drug claims in the Ontario Drug Benefit database.

Paul Grootendorst, Bernie J O'Brien, Adrian R Levy, 2003, The Canadian journal of clinical pharmacology = Journal canadien de pharmacologie clinique.

Association of Physician and Hospital Volume With Use of Aspirin and Reperfusion Therapy in Acute Myocardial Infarction

S. Soumerai, D. Willison, R. Palmer, 2000, Medical care.

Adherence to national guidelines for drug treatment of suspected acute myocardial infarction: evidence for undertreatment in women and the elderly.

E. Antman, J. Gurwitz, E. Guadagnoli, 1996, Archives of internal medicine.

Effect of Local Medical Opinion Leaders on Quality of Care for Acute Myocardial Infarction: A Randomized Controlled Trial

Stephen B. Soumerai, Jerry H. Gurwitz, Donald J. Willison, 1999 .

The Influence of Age, Sex, and Socioeconomic Status on Glycemic Control Among People with Type 1 and Type 2 Diabetes in Canada: A Patient-Led Longitudinal Retrospective Cohort Study

Selma Chipenda Dansokho, H. Witteman, D. Willison, 2021, medRxiv.

If you build it, they will come: unintended future uses of organised health data collections

W. Burke, B. Koenig, N. Hallowell, 2016, BMC medical ethics.

Privacy and the secondary use of data for health research: experience in Canada and suggested directions forward

D. Willison, 2003, Journal of health services research & policy.

Written informed consent and selection bias in observational studies using medical records: systematic review

Melissa C Brouwers, Michelle E Kho, Mark Duffett, 2009, BMJ : British Medical Journal.

The effects of coxib formulary restrictions on analgesic use and cost: regional evidence from Canada.

E. Rahme, M. Maclure, D. Marshall, 2007, Health policy.

A Review of the Comprehensiveness of Provincial Drug Coverage for Canadian Seniors*

J. Hurley, P. Grootendorst, D. Willison, 2003, Canadian Journal on Aging / La Revue canadienne du vieillissement.

Influenza serological studies to inform public health action: best practices to optimise timing, quality and reporting

S. Riley, M. V. Van Kerkhove, K. Laurie, 2012, Influenza and other respiratory viruses.

Informing Governance through Evidence-Based Research on REBs: Challenges and Opportunities

P. Kolopack, D. Willison, C. Emerson, 2009 .

Post-Romanow pharmacare: last-dollar first...first-dollar lost?

S. Morgan, D. Willison, 2004, HealthcarePapers.

Outpatient pharmaceuticals and the elderly: policies in seven nations.

J. Cosby, D. Willison, D. Freund, 2000, Health affairs.

Evaluating Unpaid Time Contributions by Seniors: A Conceptual Framework

A. Gafni, M. Denton, Jason Lian, 1997 .

Preparations for Independence and Financial Security in Later Life: A Conceptual Framework and Application to Canada

A. Gafni, M. Denton, Anju Joshi, 1998 .

International Society for Disease Surveillance Conference 2011: Building the Future of Public Health Surveillance

Roman Garnett, Ricardo H. C. Takahashi, Rumi Chunara, 2011, Emerging health threats journal.

Perceived usefulness of syndromic surveillance in Ontario during the H1N1 pandemic

Norman G. Vinson, Laura C Rosella, Monali Varia, 2011, Journal of public health.

Access to medical records for research purposes: varying perceptions across research ethics boards

K. Brazil, L. Schwartz, D. Willison, 2008, Journal of Medical Ethics.

A risk screening tool for ethical appraisal of evidence-generating initiatives

V. Haroun, Catherine Bornbaum, D. Willison, 2015, BMC medical ethics.

The role of research evidence in pharmaceutical policy making: evidence when necessary but not necessarily evidence.

D. Willison, S. M. MacLeod, 1999, Journal of evaluation in clinical practice.

The use of syndromic surveillance for decision-making during the H1N1 pandemic: A qualitative study

Laura C Rosella, Natasha S Crowcroft, Anna Chu, 2012, BMC Public Health.

Prescription to over-the-counter deregulation in Canada: Are we ready for it, or do we need to be?

L. Lynd, D. Willison, R. Dobson, 2005, Canadian Medical Association Journal.

The Role of Health and Age in Financial Preparations for Later Life

P. Raina, A. Gafni, M. Denton, 1997 .

Experience in The Development of a Postmarketing Surveillance Network: The Pharmacy Medication Monitoring Program

C. Goldsmith, M. Levine, D. Willison, 1995, The Annals of pharmacotherapy.

The use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution

K. Lajkosz, C. Virtanen, A. Heesters, 2021, BMC medical ethics.

Patenting of genetic material: are the benefits to society being realized?

D. Willison, S. M. MacLeod, 2002, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.

Workload, Data Gathering, and Quality of Community Pharmacists' Advice

L J Muzzin, D. Willison, L. Muzzin, 1995, Medical care.

The Influence of Age, Sex, and Socioeconomic Status on Glycemic Control Among People With Type 1 and Type 2 Diabetes in Canada: Patient-Led Longitudinal Retrospective Cross-sectional Study With Multiple Time Points of Measurement

H. Witteman, J. McGavock, D. Willison, 2023, JMIR Diabetes.

Views on health information sharing and privacy from primary care practices using electronic medical records

Anne Holbrook, Lehana Thabane, Donald J. Willison, 2011, Int. J. Medical Informatics.

Pandemic H1N1 in Canada and the use of evidence in developing public health policies – A policy analysis

Ross Upshur, K. Wilson, L. Rosella, 2013, Social Science & Medicine.

Who's minding the shop? The role of Canadian research ethics boards in the creation and uses of registries and biobanks

K. Brazil, L. Schwartz, D. Willison, 2008, BMC Medical Ethics.

Human study participants

Donald Willison, Nancy Ondrusek, John McLaughlin, 2015, Canadian Medical Association Journal.

Research Ethics Broadly Writ: Beyond REB Review

James A. Anderson, D. Pullman, D. Willison, 2011 .

Variation in recruitment across sites in a consent-based clinical data registry: lessons from the Canadian Stroke Network

Jiming Fang, F. Silver, D. Willison, 2006, BMC medical ethics.

What makes public health studies ethical? Dissolving the boundary between research and practice

Claudia Emerson, Lorraine E Ferris, Angus Dawson, 2014, BMC medical ethics.

Valuation of Unpaid Help by Seniors in Canada: An Empirical Analysis

A. Gafni, M. Denton, Jason Lian, 1997, Canadian Journal on Aging / La Revue canadienne du vieillissement.

Consent for use of personal information for health research: Do people with potentially stigmatizing health conditions and the general public differ in their opinions?

C. Charles, G. Agarwal, V. Steeves, 2009, BMC medical ethics.