Variation in recruitment across sites in a consent-based clinical data registry: lessons from the Canadian Stroke Network by Richards Janice A, Peladeau Pierrot, Kapral Moira K, Willison Donald J, Fang Jiming, Silver Frank L

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

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Who's minding the shop? The role of Canadian research ethics boards in the creation and uses of registries and biobanks by Schwartz Lisa, Fournier Francois, Emerson Claudia, Coughlin Michael D, Brazil Kevin, Gibson Elaine, Szala-Meneok Karen V, Weisbaum Karen M, Willison Donald J

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Perceptions of immunization information systems for collecting pandemic H1N1 immunization data within Canada's public health community: A qualitative study by Heidebrecht Christine L, Foisy Julie, Pereira Jennifer A, Quan Sherman D, Willison Donald J, Deeks Shelley L, Finkelstein Michael, Crowcroft Natasha S, Buckeridge David L, Guay Maryse, Sikora Christopher A, Kwong Jeffrey C

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