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

by Willison, Donald J, Kapral, Moira K, Peladeau, Pierrot, Richards, Janice A, Fang, Jiming, Silver, Frank L
Published 2006

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

by Ondrusek, Nancy K., Willison, Donald J., Haroun, Vinita, Bell, Jennifer A. H., Bornbaum, Catherine C.
Published 2015

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

by Willison, Donald J, Steeves, Valerie, Charles, Cathy, Schwartz, Lisa, Ranford, Jennifer, Agarwal, Gina, Cheng, Ji, Thabane, Lehana
Published 2009

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

by Willison, Donald J, Ondrusek, Nancy, Dawson, Angus, Emerson, Claudia, Ferris, Lorraine E, Saginur, Raphael, Sampson, Heather, Upshur, Ross
Published 2014

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

by O’Doherty, Kieran C., Christofides, Emily, Yen, Jeffery, Bentzen, Heidi Beate, Burke, Wylie, Hallowell, Nina, Koenig, Barbara A., Willison, Donald J.
Published 2016