Faculty profile

Brenda Wilson

ResearcherEpidemiology and Community MedicineUniversity of Ottawa

This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a University of Ottawa directory, so their courses and email address may be missing. Find their university profile.

Brenda Wilson

Researcher

Epidemiology and Community Medicine

Health Sciences

University of Ottawa

Ottawa, Ontario, Canada

Supervision signals

Has led research grants, which requires an independent research appointment. Ask their department whether they supervise graduate students.
1 publication in the last five years, latest in 2022.
Principal investigator on 1 research grant (1 CIHR), most recently in 2013.
Supervised 1 trainee who won CIHR awards, most recently in 2011.

These signals come from public records, including CIHR, NSERC and SSHRC funding decisions. Ask the professor or the graduate program whether they are taking new students.

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Citations

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Collaborators

Grants

Publications by year

Counts cover the works listed on the university profile; citation counts come from Dimensions.

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Signals and details

Research

Equity Experience Healthcare Professionals Informed Consent Interviews Latent Class Analysis Mixed Methods Newborn Screening

Latest papers

Recommendation on instrument-based screening for depression during pregnancy and the postpartum period
CANADIAN MEDICAL ASSOCIATION JOURNAL · 2022
Australians' views and experience of personal genomic testing: survey findings from the Genioz study.
European journal of human genetics : EJHG · 2019
Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz study.
European journal of medical genetics · 2019

All 15 publications

Latest funding

An innovative registry-based trials platform to improve clinical care, outcomes, and health policy for children with treatable rare diseases
CIHR · 2019 · Co-investigator
$2,754,009
Designing interventions to improve delivery of health care for children with inherited metabolic diseases: family and provider perspectives
CIHR · 2016 · Co-investigator
$738,224
Promoting implementation of evidence-based care
CIHR · 2014 · Co-investigator
$2,128,006

All 11 grants and awards

15 publications.

Recommendation on instrument-based screening for depression during pregnancy and the postpartum period

Lang E, Colquhoun H, LeBlanc JC, Riva JJ, Moore A, Traversy G, Wilson B, Grad R

CANADIAN MEDICAL ASSOCIATION JOURNAL202248 citationsOpen Access

DOI: 10.1503/cmaj.220290 PMID: W4287092733

Australians' views and experience of personal genomic testing: survey findings from the Genioz study.

Savard J, Hickerton C, Tytherleigh R, Terrill B, Turbitt E, Newson AJ, Wilson B, Gray K, Gaff C, Middleton A, Stackpoole E, Metcalfe SA

European journal of human genetics : EJHG2019

DOI: 10.1038/s41431-018-0325-x PMID: 30666046

Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz study.

Metcalfe SA, Hickerton C, Savard J, Stackpoole E, Tytherleigh R, Tutty E, Terrill B, Turbitt E, Gray K, Middleton A, Wilson B, Newson AJ, Gaff C

European journal of medical genetics2019

DOI: 10.1016/j.ejmg.2018.11.002 PMID: 30439534

Australians' views on personal genomic testing: focus group findings from the Genioz study.

Metcalfe SA, Hickerton C, Savard J, Terrill B, Turbitt E, Gaff C, Gray K, Middleton A, Wilson B, Newson AJ

European journal of human genetics : EJHG2018

DOI: 10.1038/s41431-018-0151-1 PMID: 29706641

A blueprint for the next generation of ELSI research, training, and outreach in regenerative medicine.

Illes J, Sipp D, Kleiderman E, Benjaminy S, Isasi R, Lomax G, Master Z, McCormick J, Ogbogu U, Ravitsky V, Robillard JM, Rossi F, Wilson B, Zarzeczny A

NPJ Regenerative medicine2017

DOI: 10.1038/s41536-017-0026-z PMID: 29302357

Consumer Health Informatics Aspects of Direct-to-Consumer Personal Genomic Testing.

Gray K, Stephen R, Terrill B, Wilson B, Middleton A, Tytherleigh R, Turbitt E, Gaff C, Savard J, Hickerton C, Newson A, Metcalfe S

Studies in health technology and informatics2017

PMID: 29295058

Consent for newborn screening: parents' and health-care professionals' experiences of consent in practice.

Etchegary H, Nicholls SG, Tessier L, Simmonds C, Potter BK, Brehaut JC, Pullman D, Hayeems R, Zelenietz S, Lamoureux M, Milburn J, Turner L, Chakraborty P, Wilson B

European journal of human genetics : EJHG2016Senior author

DOI: 10.1038/ejhg.2016.55 PMID: 27302842

Using Newborn Screening Bloodspots for Research: Public Preferences for Policy Options.

Hayeems RZ, Miller FA, Barg CJ, Bombard Y, Cressman C, Painter-Main M, Wilson B, Little J, Allanson J, Avard D, Giguere Y, Chakraborty P, Carroll JC

Pediatrics2016

DOI: 10.1542/peds.2015-4143 PMID: 27244855

Multigene panels in prostate cancer risk assessment: a systematic review

Little J, Wilson B, Carter R, Walker K, Santaguida P, Tomiak E, Beyene J, Usman Ali M, Raina P

Genetics in Medicine201613 citationsOpen Access

DOI: 10.1038/gim.2015.125 PMID: W2253585993

Analyzing communication in genetic consultations--a systematic review.

Paul J, Metcalfe S, Stirling L, Wilson B, Hodgson J

Patient education and counseling2015

DOI: 10.1016/j.pec.2014.09.017 PMID: 25312331

An innovative registry-based trials platform to improve clinical care, outcomes, and health policy for children with treatable rare diseases

Co-investigatorCIHR2019Operating Grant: SPOR Innovative Clinical Trial Multi-Year Grant

Principal investigators: Potter, Elizabeth K; McCabe, Christopher; Smith, Maureen M; Binik, Ariella; Chakraborty, Pranesh K; Inbar-Feigenberg, Michal; Mitchell, John J; Offringa, Martin; Oskoui, Maryam; Stockler, Sylvia

Keywords: Comparative Effectiveness; Core Outcomes; Genetic Disease; Innovative Clinical Trial; Orphan Therapy; Patient Partnership; Patient-Oriented Outcomes; Pediatrics; Rare Disease; Registry-Based Randomized Trial

$2,754,009

Designing interventions to improve delivery of health care for children with inherited metabolic diseases: family and provider perspectives

Co-investigatorCIHR2016Project Grant

Principal investigators: Potter, Elizabeth K; Chakraborty, Pranesh K

Keywords: Health Care Coordination; Inherited Metabolic Diseases; Patient Centred Care; Patient-Oriented Research; Pediatrics; Rare Diseases

$738,224

Promoting implementation of evidence-based care

Co-investigatorCIHR2014Foundation Grant

Principal investigators: Grimshaw, Jeremy M

Keywords: Behavioural Science; Cluster Randomised Trials; Complex Interventions; Health Services Research; Implementation Research; Integrated Knowledge Translation; Knowledge Synthesis; Knowledge Translation; Quality Improvement; Quasi Experimental Studies

$2,128,006

A shared understanding? Attitudes and experiences of stakeholders to newborn screening consent practices and implications for policy and practice

Nominated PICIHR2013Operating Grant - Priority Announcement: Ethics

Principal investigators: Wilson, Brenda J; Brehaut, Jamie C; Etchegary, Holly

Keywords: Equity; Experience; Healthcare Professionals; Informed Consent; Interviews; Latent Class Analysis; Mixed Methods; Newborn Screening; Parents; Policy

$271,733

Governing the Use of Genetic Tests and Technologies

Co-investigatorCIHR2012Evidence on Tap - Expedited Knowledge Synthesis (EIHR)

Principal investigators: Wilson, Michael G; Lavis, John N

Keywords: Evidence Brief; Knowledge Synthesis; Stakeholder Dialogue

$99,790

Emerging team in rare diseases: achieving the "triple aim" for inborn errors of metabolism

Co-investigatorCIHR2011Emerging Team Grant: Rare Diseases - Health Services/GELS

Principal investigators: Potter, Elizabeth K; Chakraborty, Pranesh K; Coyle, Douglas A; Kronick, Jonathan B; Wilson, Kumanan

Keywords: "Triple Aim"; Comparative Effectiveness; Health Service Delivery Models; Inborn Errors Of Metabolism; Newborn Screening; Patient-Oriented Research; Personalized Medicine; Rare Diseases; Reimbursement Policy

$1,490,492

An analysis of stakeholder attitudes towards the role and application of informed consent for expanded newborn bloodspot screening

SupervisorCIHR2011CIHR Fellowship

Principal investigators: Nicholls, Stuart G

Keywords: Attitudes; Focus Groups; Informed Consent; Interviews; Newborn Screening; Questionnaire; Stakeholder

$135,000

New directions for the use of genetic information by Aboriginal communities: Lessons learned from Québec First Nations with specific monogenic diseases.

Co-investigatorCIHR2011Operating Grant - Aboriginal Health Intervention - full application

Principal investigators: Laberge, Anne-Marie

Keywords: Carrier Screening; Cultural Issues; First Nations; Genetic Counseling; Genetic Information; Health Services Research; Needs Assessment; Program Evaluation; Recessive Diseases

$576,103

Development and Dissemination of a Knowledge Support Service in Genetics for Primary Care Providers

Co-investigatorCIHR2010Knowledge Translation Supplement

Principal investigators: Carroll, June C

Keywords: Continuing Medical Education; Email Alerts; Genetics; Knowledge Translation; Primary Care

$40,000

Training in Statistical Genetics and Epidemiological Research (TRIGGER)

Co-investigatorCIHR2009Training Grant in Genetic Epidemiology - Letter of Intent

Principal investigators: Little, Julian

Keywords: Bioinformatics; Collaborative; Ethics; Genetic Epidemiology; Graduate Education; Interdisciplinary; Legal Issues; Public Health Genomics; Social Implications; Statistical Genetics

From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.

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Brenda Wilson

Research

Latest papers

Latest funding

Recommendation on instrument-based screening for depression during pregnancy and the postpartum period

Australians' views and experience of personal genomic testing: survey findings from the Genioz study.

Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz study.

Australians' views on personal genomic testing: focus group findings from the Genioz study.

A blueprint for the next generation of ELSI research, training, and outreach in regenerative medicine.

Consumer Health Informatics Aspects of Direct-to-Consumer Personal Genomic Testing.

Consent for newborn screening: parents' and health-care professionals' experiences of consent in practice.

Using Newborn Screening Bloodspots for Research: Public Preferences for Policy Options.

Multigene panels in prostate cancer risk assessment: a systematic review

Analyzing communication in genetic consultations--a systematic review.

Frequent collaborators

Holly Etchegary

Julian Little

Pranesh Chakraborty

Beth Potter

Fabio Rossi

Ian Graham

Mario Cappelli

Eva Tomiak

Doug Coyle

Eddy Lang

Holly Etchegary

Mark Walker

Heather Colquhoun

Yvonne Bombard

Joseph Beyene

Parminder Raina

Pasqualina Santaguida

John Riva

Ubaka Ogbogu

Vardit Ravitsky

Yves Giguere

Denise Avard

Jamie Brehaut

Judy Illes