- St. Michael's Hospital (Toronto)
- Nedd4 Regulation of Skeletal Muscle Atrophy and Regeneration
- Centre Hospitalier de l'Université de Montréal (CHUM)
- Developing molecular, cellular and mice models for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS)
- Co-applicants: Gehring, Kalle; McPherson, Peter
- University of Ottawa
- Mutation of the mouse NaV1.4 muscle sodium channel: Understanding hyperkalemic periodic paralysis (HyperKPP)
- University of Western Ontario
- Nesca, a novel signaling adapter that regulates neuronal growth and regeneration
- McGill University
- Molecular therapies for dystrophin deficiency
- Université Laval
- The role of inflammation in pathogenesis and immunotherapy of ALS
- Co-applicant: Dupré, Nicolas
- University of Calgary
- Understanding the molecular defects and treatment of human malignant hyperthermia and central core disease
- University of Toronto
- The TAR-DNA-binding protein-43 and amyotrophic lateral sclerosis
- Co-applicants: Zinman, Lorne; Hazrati, Lili-Naz
- University of Windsor
- Molecular mechanisms regulating myotubularin-related lipid phosphatases mutated in neuromuscular diseases
- University of Western Ontario
- The role of TDP-43 in regulating NFL mRNA metabolism
- Centre Hospitalier de l'Université de Montréal (CHUM)
- Cellular and biochemical impact of TDP-43 mutants in ALS
- Co-Applicants: Van de Velde, Christine; Parker, Jodey; Julien, Jean-Pierre
