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Research
Latest papers
"It's an Uphill Battle. We Have a Long Way to Go": Perspectives of Canadian Individuals Living with Genetic Conditions Detectable by Prenatal Cell-Free DNA Screening.
AJOB empirical bioethics · 2026 · senior author
A multi-ancestry genetic reference for the Quebec population.
Nature communications · 2026
How variants of uncertain significance affect clinical decisions: A systematic review.
Genetics in medicine : official journal of the American College of Medical Genetics · 2026
Latest funding
- $397,800
Vivre avec une maladie complexe, multisystémique et douloureuse : Cartographier le parcours de vie avec un trouble héréditaire du tissu conjonctif pour développer un parcours d'apprentissage patients
CIHR · 2025 · Co-investigator
- $248,625
The Clinician-reported Genetic testing Utility InDEx (C-GUIDE): Development and validation for neonatal intensive care
CIHR · 2024 · Co-investigator
- $508,725
Defining and measuring the value of genetic testing from patients' perspectives: Developing the Patient-reported Genetic testing Utility InDEx (P-GUIDE)
CIHR · 2020 · Co-investigator
50 publications.
"It's an Uphill Battle. We Have a Long Way to Go": Perspectives of Canadian Individuals Living with Genetic Conditions Detectable by Prenatal Cell-Free DNA Screening.
Cassou M, Ravitsky V, Laberge AM
A multi-ancestry genetic reference for the Quebec population.
McClelland P, Femerling G, Laflamme R, Mejia-Garcia A, Sayahian Dehkordi M, Xiao H, Diaz-Papkovich A, Pelletier J, Grenier JC, Lo KS, Anderson-Trocmé L, Bellavance J, Chapdelaine V, Gagnon G, De Mori A, Martinez G, Mohler K, de Malliard T, Labbé C, Labrecque M, Montpetit A, Spiegelman D, Rouleau GA, Théroux JF, Zhou H, Girard SL, Hussin JG, Laberge AM, Bhérer C, Tetreault M, Gagliano Taliun SA, Taliun D, Gravel S, Lettre G
How variants of uncertain significance affect clinical decisions: A systematic review.
Ayappa S, Joffe S, Laberge AM, Nye RT, Hess M, Callahan KP
The Patient-reported Genetic testing Utility InDEx: A novel measure of personal utility.
Poole E, Xiao B, Luca S, Assamad D, Abbott LS, Armstrong L, Boycott KM, Carroll JC, Chad L, De Bie I, Denburg A, Deyell RJ, Elliott AM, Goudie C, Laberge AM, Mucha BE, Peltekova IT, Quinlan B, Sawyer SL, Smith M, Villani A, Ungar WJ, Hayeems RZ, P-GUIDE Study Team
Forced resilience: Indigenous perspectives on systemic barriers and humanizing genomic medicine in British Columbia, Canada.
Ehman M, Montour L, Pollard S, Weymann D, Kirk D, Brown K, Epp S, Wadsworth D, Garrison NA, Laberge AM, Caron NR, Arbour L, Regier DA
Macrothrombocytopaenia: More to Fear Than Just Low Platelet Count.
Rivard GE, Merlen C, Rouette A, Mathews N, Bonnefoy A, Nava T, Leduc L, Laberge AM, Lavallée VP
Mainstreaming of clinical genetic testing: A conceptual framework.
Mackley MP, Richer J, Guerin A, Caluseriu O, Armstrong L, Blood KA, Bernier F, Boswell-Patterson C, Chard M, Costain G, Dyment D, Eaton A, Faghfoury H, Frosk P, Gillespie MK, Goh ES, Hayeems RZ, Hashemi B, Innes AM, Jackson M, Laberge AM, Limoges J, Marshall C, McMillan H, Nelson TN, Osmond M, Parboosingh J, Penney L, Prince B, Sawyer SL, Siu VM, Thomas MA, Turner L, Villeneuve-Cloutier N, Hartley T, Boycott KM
Canadian College of Medical Geneticists (CCMG) position statement on the storage of patient genetic and genomic information in electronic health records.
Laberge AM, D'Souza N, Penney LS, Jessa K, Chad L
Training competencies and recommendations for the next generation of public health genetics: Reflections from current leaders in the field.
Xue D, Blue EE, Fullerton SM, Henrikson NB, Knerr S, Laberge AM, Parker LS, Sabatello M, Shridhar NN, Smith JA, Wilfond BS, Wojcik GL, Yu JH, Fohner AE
Reproductive carrier screening for genetic disorders: position statement of the Canadian College of Medical Geneticists.
Aul RB, Canales KE, De Bie I, Laberge AM, Langlois S, Nelson TN, Walji S, Yu AC, Lazier J, Canadian College of Medical Geneticists, Canadian College of Medical Geneticists
Vivre avec une maladie complexe, multisystémique et douloureuse : Cartographier le parcours de vie avec un trouble héréditaire du tissu conjonctif pour développer un parcours d'apprentissage patients
Principal investigators: Page, Gabrielle; Grenier, Annie-Danielle
Keywords: Accès Aux Soins; Cartographie; Co-Construction; Douleur Chronique; Détresse Psychologique; Parcours De Vie; Partenariat; Qualitatif; Trouble Héréditaire Du Tissu Conjonctif
The Clinician-reported Genetic testing Utility InDEx (C-GUIDE): Development and validation for neonatal intensive care
Principal investigators: Hayeems, Robin Z
Keywords: Clinical Utility; Genomics; Neonatal Intensive Care; Outcome Measurement Development
Defining and measuring the value of genetic testing from patients' perspectives: Developing the Patient-reported Genetic testing Utility InDEx (P-GUIDE)
Principal investigators: Hayeems, Robin Z
Keywords: Genomic Medicine; Measurement Science; Patient Reported Outcome Measure
An innovative registry-based trials platform to improve clinical care, outcomes, and health policy for children with treatable rare diseases
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
Assessing Outcomes of Carrier Screening: Patient-Level Outcomes and Health Professionals' Preparedness to Provide Carrier Screening in Structured Programs and Routine Care
Principal investigators: Laberge, Anne-Marie
Keywords: Carrier Screening; Evaluative Research; Genetic Screening; Health Professional Training; Health Services Research; Indigenous Health; Program Evaluation
From the omics bench to personalized medicine: ethical and scientific challenges
Principal investigators: Godard, Beatrice
Keywords: Delphi Survey; End-Users; Personalized Medicine; Policy Framework; Research Ethics; Website Survey; Whole Genome Sequencing Technologies
Knowledge Transfer in Genetics: Evaluation of the Use of Genetic Tests in Clinical and Community Settings
Principal investigators: Laberge, Anne-Marie
Keywords: Clinical Utility; Ethical; Genetic Screening; Genetic Services; Genetic Tests; Health Services Research; Health Technology Assessment; Interdisciplinary; Legal And Social Issues; Program Evaluation; Qualitative Methods
Knowledge Transfer in Genetics: Evaluation of the Use of Genetic Tests in Clinical and Community Settings
Principal investigators: Laberge, Anne-Marie
Keywords: Program Evaluation
Use of genetic tests in practice: role of physicians, guidelines, and health policies and impacts on patients
Principal investigators: Laberge, Anne-Marie
Keywords: Clinical Practice Guidelines; Decision-Making; Health Policy; Health Services Research; Knowledge Translation; Public Health Genetics; Use Of Genetic Tests
New directions for the use of genetic information by Aboriginal communities: Lessons learned from Québec First Nations with specific monogenic diseases.
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
From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.
Frequent collaborators
- Pediatrics
- Médecine sociale et préventive
- School of Epidemiology and Public Health
- Li Ka Shing Knowledge
- Health Research Methods, Evidence, and Impact
- Psychiatry
- Department of Medicine
- Other
Co-authors at Université de Montréal, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Vardit Ravitsky
Médecine sociale et préventive
10 shared papers, latest 2026
Laurent Legault
Faculty
5 shared papers, latest 2025
Lauren Chad
Li Ka Shing Knowledge
5 shared papers, latest 2026
Laurent Legault
Faculty
5 shared papers, latest 2025
Katherine Morrison
Pediatrics
5 shared papers, latest 2025
Lehana Thabane
Health Research Methods, Evidence, and Impact
4 shared papers, latest 2022
Catherine Goudie
Faculty
3 shared papers, latest 2026
Pranesh Chakraborty
Pediatrics
3 shared papers, latest 2022
Sylvia Stockler
Pediatrics
3 shared papers, latest 2022
Kumanan Wilson
Department of Medicine
3 shared papers, latest 2022
Jill Hamilton
Psychiatry
3 shared papers, latest 2025
Julian Little
School of Epidemiology and Public Health
3 shared papers, latest 2022
Doug Coyle
School of Epidemiology and Public Health
3 shared papers, latest 2022
Charles Dupras
Médecine sociale et préventive
2 shared papers, latest 2021
Yvonne Bombard
Institute of Health Policy, Management, and Evaluation
2 shared papers, latest 2024
Gregory Costain
Faculty
2 shared papers, latest 2025
Simon Gravel
Human Genetics
2 shared papers, latest 2026
Mark Tremblay
Clinical Epidemiology
2 shared papers, latest 2019
Francois Bernier
Cell Biology and Anatomy
2 shared papers, latest 2025
Daniel Taliun
Faculty
2 shared papers, latest 2026
Daniel Taliun
Human Genetics
2 shared papers, latest 2026
Ian Zenlea
Pediatrics
2 shared papers, latest 2025
David Chitayat
Computer Science
2 shared papers, latest 2025
Guillaume Lettre
Faculty
2 shared papers, latest 2026
Meredith Vanstone
Family Medicine
2 shared papers, latest 2021
Murray Alexander Potter
Pathology & Molecular Medicine
2 shared papers, latest 2019
Patrick Mcphee
Rehabilitation Science
1 shared papers, latest 2022
Astrid Guttmann
Department of Paediatrics
1 shared papers, latest 2019
Linda Dodds
Pediatrics
1 shared papers, latest 2019
David Dyment
Faculty
1 shared papers, latest 2025
Jennifer MacKenzie
Pediatrics
1 shared papers, latest 2015
Hubert Labelle
Orthopédie
1 shared papers, latest 2025
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