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Dr. Wilson's
major interest is public health genetics. This covers a wide spectrum of
activities - from establishing the contribution that genetic predisposition
makes to disease burden in populations, through evaluating potential
interventions to prevent illness and death from genetic disease, to assessing
how health services may be appropriately and efficiently organized to deliver
such interventions. A key element of such work as understanding the
perspectives and values of the general public, service users, health
professionals and decision makers.
She applies
her public health training to questions of emerging health technologies,
particularly genomics in medicine and public health. Her interdisciplinary
research program spans a broad questions pertaining to the evidence base for
genome-based tests and health interventions, effective service delivery models,
and social and family implications of genomics.
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Researcher Information
Associate Professor
Epidemiology and Community Medicine
Website
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Dr. Wilson is an Associate Professor in the Department of Epidemiology
and Community Medicine at the University of Ottawa. She trained in medicine at
the universities of St Andrews (BSc) and Edinburgh (MB ChB), with postgraduate
training in internal medicine and public health medicine. She worked as a
public health physician in the UK National Health Service until 1991, when she
joined Aberdeen University as a lecturer in public health where she became
interested in public health and health system aspects of emerging genetic technologies.
She moved to Ottawa in 2002, and was Director of Graduate Studies in
Epidemiology and Director of the Community Medicine Residency program as well
as teaching graduate courses in epidemiology and establishing a research
program. From 2002-08 she was lead PI of a CIHR-ICE team in genetics health
services research (GeneSens), which transformed into a CIHR Emerging Team of
Genomics in Screening in 2009.
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Researcher Information
Associate Professor
Epidemiology and Community Medicine
Website
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Wilson BJ, Qureshi N, Santaguida P, Little J, Carroll JC, Allanson J, Raina P. Systematic review: family history in risk assessment for common diseases. Ann Intern Med 2009;151:878-885.
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Heshka J, Dunn C, Howley H, Wilson B, Wells PS. A systematic review of perceived risks, psychological and behavioural impacts of genetic testing. Genet Med 2008; 10: 19-32.
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Wilson BJ, Torrance N, Mollison J, Watson MS, Douglas A, Miedzybrodzka Z, Gordon R, Wordsworth S, Campbell M, Haites N, Grant A. Cluster randomized trial of a multifaceted primary care decision-support intervention for inherited breast cancer risk. Fam Pract 2006; 23: 537-44.
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Wilson BJ. The challenge of developing evidence-based genetics health care in practice. Fam Cancer 2006; 5:55-9.
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Wilson BJ, Forrest K, van Teijlingen E, McKee L, Haites N, Matthews E, Simpson SA. Family communication about genetic risk: the little they know. Comm Genet 2004; 7: 15-24.
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Researcher Information
Associate Professor
Epidemiology and Community Medicine
Website
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