Faculty profile
Elise Duchesne
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Research
Latest papers
Individual transcriptomic response to strength training for patients with myotonic dystrophy type 1.
JCI insight · 2023
Psychometric properties of a standardized protocol of muscle strength assessment by hand-held dynamometry in healthy adults: a reliability study.
BMC musculoskeletal disorders · 2023 · senior author
A rehabilitation program to increase balance and mobility in ataxia of Charlevoix-Saguenay: An exploratory study.
PloS one · 2022 · senior author
Latest funding
- $820,846
A comprehensive study of the natural history of OPMD: An essential step towards clinical trial readiness and evidence-based interventions
CIHR · 2021 · Principal investigator
- $569,925
A comprehensive study of the natural history of ARSACS: An essential step towards clinical trial readiness and evidence-based interventions
CIHR · 2018 · Co-investigator
9 publications.
Individual transcriptomic response to strength training for patients with myotonic dystrophy type 1.
Davey EE, Légaré C, Planco L, Shaughnessy S, Lennon CD, Roussel MP, Shorrock HK, Hung M, Cleary JD, Duchesne E, Berglund JA
Psychometric properties of a standardized protocol of muscle strength assessment by hand-held dynamometry in healthy adults: a reliability study.
Morin M, Hébert LJ, Perron M, Petitclerc É, Lake SR, Duchesne E
A rehabilitation program to increase balance and mobility in ataxia of Charlevoix-Saguenay: An exploratory study.
Lessard I, Masterman V, Côté I, Gagnon C, Duchesne E
Explanatory factors of dynamic balance impairment in myotonic dystrophy type 1.
Bélair N, Côté I, Gagnon C, Mathieu J, Duchesne E
Impact of a 12-week Strength Training Program on Fatigue, Daytime Sleepiness, and Apathy in Men with Myotonic Dystrophy Type 1.
Gallais B, Roussel MP, Laberge L, Hébert LJ, Duchesne E
Assessment of muscular strength and functional capacity in the juvenile and adult myotonic dystrophy type 1 population: a 3-year follow-up study.
Roussel MP, Fiset MM, Gauthier L, Lavoie C, McNicoll É, Pouliot L, Gagnon C, Duchesne E
Effects and Acceptability of an Individualized Home-Based 10-Week Training Program in Adults with Myotonic Dystrophy Type 1.
Lessard I, Gaboury S, Gagnon C, Bouchard K, Chapron K, Lavoie M, Lapointe P, Duchesne E
Validity of the Mini-BESTest in adults with myotonic dystrophy type 1.
Duchesne E, Hébert LJ, Mathieu J, Côté I, Roussel MP, Gagnon C
Strength-training effectively alleviates skeletal muscle impairments in myotonic dystrophy type 1.
Roussel MP, Hébert LJ, Duchesne E
A comprehensive study of the natural history of OPMD: An essential step towards clinical trial readiness and evidence-based interventions
Principal investigators: Gagnon, Cynthia; Brais, Bernard; Duchesne, Elise; Hébert, Luc J
Keywords: Dysphagia; Metrological Properties; Mobility; Muscle Strength; Natural History Study; Oculopharyngeal Muscular Dystrophy; Participation Restrictions; Physical Impairments; Walking Capacities
A comprehensive study of the natural history of ARSACS: An essential step towards clinical trial readiness and evidence-based interventions
Principal investigators: Gagnon, Cynthia; Brais, Bernard; Hébert, Luc J
Keywords: Cognitive Impairments; Longitudinal Study; Mobility; Natural History Study; Participation Restriction; Physical Impairments; Recessive Ataxia
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
- Cynthia Gagnon and Cynthia Gagnon: 93 shared papers
- Cynthia Gagnon and Elise Duchesne: 18 shared papers
- Elise Duchesne and Cynthia Gagnon: 18 shared papers
- Elise Duchesne and Elise Duchesne: 9 shared papers
- Cynthia Gagnon and Elise Duchesne: 5 shared papers
- Elise Duchesne and Cynthia Gagnon: 5 shared papers
- Ecole de réadaptation
- Other
Co-authors at Université de Sherbrooke, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
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