Groupe de Recherche Interdisciplinaire sur les Maladies Neuromusculaires

Homepage: grimn.ca

ROR: 00p6tra76

OpenAlex ID: I4405273906

CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy

2017 · Lise Barbé, Stella Lanni, et al. · The American Journal of Human Genetics · 107

Cognitive decline over time in adults with myotonic dystrophy type 1: A 9-year longitudinal study

2016 · Benjamin Gallais, Cynthia Gagnon, et al. · Neuromuscular Disorders · 97

An Update of Comprehensive Evidence-Based Guidelines for Interventional Techniques in Chronic Spinal Pain. Part I: Introduction and General Considerations

2013 · Laxmaiah Manchikanti, Frank J E Falco, et al. · Pain Physician · 97

Impact of Inflammation and Anti-inflammatory Modalities on Skeletal Muscle Healing: From Fundamental Research to the Clinic

2017 · Elise Duchesne, Sébastien S. Dufresne, et al. · Physical Therapy · 85

Prevalence and correlates of apathy in myotonic dystrophy type 1

2015 · Benjamin Gallais, Michèle Montreuil, et al. · BMC Neurology · 84

A 9-year follow-up study of quantitative muscle strength changes in myotonic dystrophy type 1

2018 · Cynthia Gagnon, Émilie Petitclerc, et al. · Journal of Neurology · 55

Strength-training effectively alleviates skeletal muscle impairments in myotonic dystrophy type 1

2020 · Marie-Pier Roussel, Luc J. Hébert, et al. · Neuromuscular Disorders · 50

Further evidence for the reliability and validity of the Fatigue and Daytime Sleepiness Scale

2017 · Benjamin Gallais, Cynthia Gagnon, et al. · Journal of the Neurological Sciences · 48

Report of the second Outcome Measures in Myotonic Dystrophy type 1 (OMMYD-2) international workshop San Sebastian, Spain, October 16, 2013

2015 · Cynthia Gagnon, Giovanni Meola, et al. · Neuromuscular Disorders · 47

Report of the first Outcome Measures in Myotonic Dystrophy type 1 (OMMYD-1) international workshop

2013 · Cynthia Gagnon, Giovanni Meola, et al. · Neuromuscular Disorders · 46

What is known about the effects of exercise or training to reduce skeletal muscle impairments of patients with myotonic dystrophy type 1? A scoping review

2019 · Marie-Pier Roussel, Marika Morin, et al. · BMC Musculoskeletal Disorders · 44

Report of the third outcome measures in myotonic dystrophy type 1 (OMMYD-3) international workshop Paris, France, June 8, 2015

2018 · Cynthia Gagnon, Chad Heatwole, et al. · Journal of Neuromuscular Diseases · 43

Clearance of defective muscle stem cells by senolytics restores myogenesis in myotonic dystrophy type 1

2023 · Talita C. Conte, Gilberto Duran-Bishop, et al. · Nature Communications · 41

Predicting daytime sleepiness and fatigue: a 9-year prospective study in myotonic dystrophy type 1

2019 · Luc Laberge, Benjamin Gallais, et al. · Journal of Neurology · 40

Comparison of two methods to categorize thickened liquids for dysphagia management in a clinical care setting context: The Bostwick consistometer and the IDDSI Flow Test. Are we talking about the same concept?

2018 · Claudia Côté, Isabelle Germain, et al. · Journal of Texture Studies · 40

A 9-year follow-up study of the natural progression of upper limb performance in myotonic dystrophy type 1: A similar decline for phenotypes but not for gender

2017 · Kateri Raymond, Mélanie Levasseur, et al. · Neuromuscular Disorders · 40

A Review of Psychopathology Features, Personality, and Coping in Myotonic Dystrophy Type 1

2018 · Lisa Minier, Baptiste Lignier, et al. · Journal of Neuromuscular Diseases · 37

DMPK gene DNA methylation levels are associated with muscular and respiratory profiles in DM1

2019 · Cécilia Légaré, Gayle Overend, et al. · Neurology Genetics · 36

Rehabilitation needs of youth with arthrogryposis multiplex congenita: Perspectives from key stakeholders

2019 · Caroline Elfassy, Vasiliki Betty Darsaklis, et al. · Disability and Rehabilitation · 36

Prevalence of Lifestyle Risk Factors in Myotonic Dystrophy Type 1

2013 · Cynthia Gagnon, Maud-Christine Chouinard, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 36

Psychometric properties of a standardized protocol of muscle strength assessment by hand-held dynamometry in healthy adults: a reliability study

2023 · Marika Morin, Luc J. Hébert, et al. · BMC Musculoskeletal Disorders · 35

Progressive Decline in Daily and Social Activities: A 9-year Longitudinal Study of Participation in Myotonic Dystrophy Type 1

2019 · Kateri Raymond, Mélanie Levasseur, et al. · Archives of Physical Medicine and Rehabilitation · 35

A study of impairments in oculopharyngeal muscular dystrophy

2020 · Jean‐Denis Brisson, Cynthia Gagnon, et al. · Muscle & Nerve · 34

The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care

2019 · the Filnemus Myotonic Dystrophy Study Group, Marie De Antonio, et al. · Orphanet Journal of Rare Diseases · 33

Expanding the clinical description of autosomal recessive spastic ataxia of Charlevoix-Saguenay

2019 · Marie-Michèle Briand, Xavier Rodrigue, et al. · Journal of the Neurological Sciences · 33

Works count: 139

Citation count: 6,614