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Items: 1 to 20 of 35

1.

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

Ondrusek NK, Willison DJ, Haroun V, Bell JA, Bornbaum CC.

BMC Med Ethics. 2015 Jul 7;16:47. doi: 10.1186/s12910-015-0039-3.

2.

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

Willison DJ, Ondrusek N, Dawson A, Emerson C, Ferris LE, Saginur R, Sampson H, Upshur R.

BMC Med Ethics. 2014 Aug 8;15:61. doi: 10.1186/1472-6939-15-61.

3.

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

Laurie KL, Huston P, Riley S, Katz JM, Willison DJ, Tam JS, Mounts AW, Hoschler K, Miller E, Vandemaele K, Broberg E, Van Kerkhove MD, Nicoll A.

Influenza Other Respir Viruses. 2013 Mar;7(2):211-24. doi: 10.1111/j.1750-2659.2012.0370a.x. Epub 2012 Apr 30.

4.

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

Perera G, Holbrook A, Thabane L, Foster G, Willison DJ.

Int J Med Inform. 2011 Feb;80(2):94-101. doi: 10.1016/j.ijmedinf.2010.11.005. Epub 2010 Dec 16.

PMID:
21167771
5.

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

Heidebrecht CL, Foisy J, Pereira JA, Quan SD, Willison DJ, Deeks SL, Finkelstein M, Crowcroft NS, Buckeridge DL, Guay M, Sikora CA, Kwong JC; Public Health Agency of Canada/Canadian Institutes of Health Research Influenza Research Network Vaccine Coverage Theme Group.

BMC Public Health. 2010 Aug 31;10:523. doi: 10.1186/1471-2458-10-523.

6.

Association between the 2008-09 seasonal influenza vaccine and pandemic H1N1 illness during Spring-Summer 2009: four observational studies from Canada.

Skowronski DM, De Serres G, Crowcroft NS, Janjua NZ, Boulianne N, Hottes TS, Rosella LC, Dickinson JA, Gilca R, Sethi P, Ouhoummane N, Willison DJ, Rouleau I, Petric M, Fonseca K, Drews SJ, Rebbapragada A, Charest H, Hamelin ME, Boivin G, Gardy JL, Li Y, Kwindt TL, Patrick DM, Brunham RC; Canadian SAVOIR Team.

PLoS Med. 2010 Apr 6;7(4):e1000258. doi: 10.1371/journal.pmed.1000258.

7.

ICES reports: Canada's response to pandemic H1N1 influenza: the collection of individual-level data at the point of vaccination.

Kwong JC, Foisy J, Quan S, Heidebrecht C, Kolbe F, Bettinger JA, Buckeridge DL, Chambers LW, Crowcroft NS, Dhalla IA, Sikora CA, Willison DJ, Pereira JA; Pubic Health Agency of Canada/Canadian Institutes of Health Research Influenza Research Network (PCIRN).

Healthc Q. 2010;13(2):18-20. No abstract available.

PMID:
20357539
8.

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

Willison DJ, Steeves V, Charles C, Schwartz L, Ranford J, Agarwal G, Cheng J, Thabane L.

BMC Med Ethics. 2009 Jul 24;10:10. doi: 10.1186/1472-6939-10-10.

9.

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

Kho ME, Duffett M, Willison DJ, Cook DJ, Brouwers MC.

BMJ. 2009 Mar 12;338:b866. doi: 10.1136/bmj.b866. Review.

10.

Alternatives to project-specific consent for access to personal information for health research: insights from a public dialogue.

Willison DJ, Swinton M, Schwartz L, Abelson J, Charles C, Northrup D, Cheng J, Thabane L.

BMC Med Ethics. 2008 Nov 19;9:18. doi: 10.1186/1472-6939-9-18.

11.

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

Gibson E, Brazil K, Coughlin MD, Emerson C, Fournier F, Schwartz L, Szala-Meneok KV, Weisbaum KM, Willison DJ.

BMC Med Ethics. 2008 Nov 14;9:17. doi: 10.1186/1472-6939-9-17.

12.

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

Willison DJ, Emerson C, Szala-Meneok KV, Gibson E, Schwartz L, Weisbaum KM, Fournier F, Brazil K, Coughlin MD.

J Med Ethics. 2008 Apr;34(4):308-14. doi: 10.1136/jme.2006.020032.

PMID:
18375687
13.

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

Willison DJ, Schwartz L, Abelson J, Charles C, Swinton M, Northrup D, Thabane L.

J Am Med Inform Assoc. 2007 Nov-Dec;14(6):706-12. Epub 2007 Aug 21.

14.

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

Marshall DA, Willison DJ, Grootendorst P, LeLorier J, Maclure M, Kulin NA, Sheehy OE, Warren L, Sykora K, Rahme E.

Health Policy. 2007 Nov;84(1):1-13. Epub 2007 Jun 13.

PMID:
17570558
16.

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

Willison DJ, Kapral MK, Peladeau P, Richards JA, Fang J, Silver FL.

BMC Med Ethics. 2006 May 23;7:E6.

17.
18.

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

Lynd LD, Taylor J, Dobson R, Willison DJ.

CMAJ. 2005 Sep 27;173(7):775-7. Epub 2005 Sep 12. No abstract available.

19.

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

Morgan SG, Willison DJ.

Healthc Pap. 2004;4(3):10-20.

PMID:
15114064
20.

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

Tu JV, Willison DJ, Silver FL, Fang J, Richards JA, Laupacis A, Kapral MK; Investigators in the Registry of the Canadian Stroke Network.

N Engl J Med. 2004 Apr 1;350(14):1414-21.

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