Cynthia Gagnon
Investigator
Professor, Rehabilitation, Université de Sherbrooke; Researcher, FRQS Centre de recherche du CRCHUS
Visiting Professor, uOttawa and CHEO-RI
NMD4C Involvement: Pillar 2: Clinical Research, Pillar 3: Clinical Practice Research, Theme 5: Open Science
Email CynthiaBiography
Cynthia is a senior career-award researcher specializing in adult genetic neuromuscular disorders. She holds a professorial appointment at the School of Rehabilitation at the University of Sherbrooke. She is the scientific director of the Groupe de recherche interdisciplinaire sur les maladies neuromusculaires (GRIMN) and is a researcher at the Centre de recherche Charles-Le Moyne-Saguenay-Lac-St-Jean sur les innovations en santé.
Cynthia trained as an occupational therapist at McGill University. She has a doctoral degree in experimental medicine from Laval University and pursued a postdoctoral fellowship in program evaluation at Montreal University. Her work aims at improving clinical care and speeding up trial readiness in the most prevalent neuromuscular diseases in Canada. Her main interest is to document the natural history of the disease through an interdisciplinary perspective to be able to document the progression of the disease and to identify significant predictor and explanatory factors related to participation in daily activities and social roles of patients such as work and autonomous living. Her other interest is to define the best outcome measures to assess potential therapeutic targets such as muscle strength, fatigue or cognitive functions. She also works on developing knowledge translation strategies related to rare diseases to ensure effective and just-in-time knowledge translation to the interdisciplinary team through different strategies including wiki, articles, clinical practice guidelines to improve clinical care for patients and their families.
She is involved in several international projects in relation to myotonic dystrophy type 1 (DM1), oculopharyngeal muscular dystrophy (OPMD) and autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS).
Within NMD4C, Cynthia is lead for knowledge translation.
Recent Publications
Osman, H, Masnata, M, Adamji, Z, Rodrigue, X, Nguyen, CÉ, Slayter, J et al.. Strengthening clinical capacity in spinal muscular atrophy: Developing and implementing training on clinical outcome assessments. J Neuromuscul Dis. 2026. 22143602261416298 PMID:41564276
Laberge, L, Turcotte, O, Angeard, N, Maltais, A, Martin, JS, Gagnon, C et al.. Endogenous circadian rhythm sleep disorders through the lens of nonparametric variables of actigraphy: an exploratory study in myotonic dystrophy type 1. Sleep Med. 2026.140 108781 PMID:41547321
van As, D, Claeys, T, Salz, R, Haver, DV, Dufour, S, Deelen, AV et al.. Large-scale proteomics profiling of peripheral blood of DM1 patients identifies biomarkers for disease severity and functional capacity. J Neuromuscul Dis. 2026. 22143602251410443 PMID:41544176
Bélair, N, Gagnon, C, Duchesne, E. What is known about muscle weakness, balance impairments and indoor mobility limitations in oculopharyngeal muscular dystrophy? A scoping review. J Neuromuscul Dis. 2025. 22143602251397052 PMID:41467981
Osman, H, Adamji, Z, Lintern, S, Smith, IC, Grant, A, Lessard, LER et al.. Counting the Cost: The Hidden Financial Realities of Neuromuscular Disease Through Patient and Family Perspectives. Health Expect. 2025.28 (6)e70529 PMID:41405177
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