Research funder · United States
Muscular Dystrophy Association
American organization which combats muscular dystrophy
- Grants since 2016
- 438
- Awarded, last 5 years (where amounts are published)
- $37.7M + 1.5M
- Funded works, last 5 years
- 1 011
- Funded works, all time
- 9 236
Grants
2023–2026 · research · Research Grant
Targeting inflamma-miRs in DMD
Alyson Fiorillo · Virginia Commonwealth University
2023–2026 · research · Research Grant
Longitudinal Endpoint Optimization to Provide an Assessment of Relevant Drugs
Chad Heatwole · University of Rochester
2023–2026 · research · Research Grant
Contributions of genetic variation to LMNA-associated muscular dystrophy
Lori Wallrath · University of Iowa
2023–2026 · research · Research Grant
Mobile App to Overcome Barriers and Increase Level of Exercise in DM1 (MOBILE)
Kate Eichinger · University of Rochester
2023–2026 · research · Research Grant
Targeting the Mitoribosome to Treat Mitochondrial Myopathies
Pere Puigserver · Dana-Farber Cancer Institute
2023–2026 · research · Research Grant
Nanoparticle-based gene delivery to Schwann cells for treating CMT disease
Alexia Kagiava · The Cyprus Foundation For Muscular Dystrophy Research
2023–2026 · research · Research Grant
Repressing Adipogenesis in LGMD2B
Marshall Hogarth · Children's Research Institute (cnmc)
2023–2024 · research · Clinical Research Grant
Clinical Study of Anti-AAV Antibody Depletion using Efgartigimod alfa-fcab in Boys with DMD Prior to and Following AAV Gene Therapy
Barry Byrne · University of Florida
2023–2026 · research · Research Grant
Repair of the ALS Nuclear Pore and associated TDP-43 misregulation by CHMP7 ASO
Jeffrey Rothstein · Johns Hopkins University
2023–2024 · research · Restricted Research Grant
NYS-DM: Building the next generation of DM therapeutics and researchers
Andy Berglund · Research Foundation for the State University of New York
2023–2026 · research · Development Grant
Mouse Dmpk CTG expansion knockin models for myotonic dystrophy
Curtis Nutter · University of Florida
2023–2026 · research · Research Grant
Targeting the RNA Repeat Expansion that Causes Myotonic Dystrophy Type 2
Matthew Disney · University of Florida
2023–2026 · research · Development Grant
Pathomechanism of motor neuron degeneration and myopathy in MICU1 deficiency
Raghavendra Singh · Thomas Jefferson University
2023–2026 · research · Development Grant
Dissecting lysosomal signals to fight Pompe disease
Andrea Armani · University of Zurich
2022–2026 · research · Clinical Research Network Grant
Muscular Dystrophy Clinical Trial Research Network
Jeffrey Statland · University Of Kansas Medical Center Research Institute, Inc
2022–2024 · research · MDA Request for Applications
Single cell transcriptomics to assess transgene related responses in DMD
Carrie Miceli · The Regents Of The University Of California, Los Angeles
2022–2023 · research · Idea Award
Modulating ER-phagy thwart muscle diseases
Paolo Grumati · Fondazione Telethon
2022–2025 · research · Clinical Research Grant
Phase-2 Trial of 5m/kg/week Prednisolone in Young Boys with DMD
Anne Connolly · Nationwide Children's Hospital
2022–2025 · research · Infrastructure Grant
Inherited Neuropathy Consortium
Michael Shy · University of Iowa
2022–2025 · research · Development Grant
LEMS-induced disruption of the nanoscale organization of the active zone
Tyler Tarr · University of Pittsburgh
2022–2025 · research · Research Grant
Linker-based gene therapy of LAMA2-related muscular dystrophy using AAVMYO
Markus Ruegg · University of Basel
2022–2025 · research · Research Grant
Assessing the role of Fibro-Adipogenic Progenitors in EDMD
Chiara Mozzetta · Institute of Molecular Biology and Pathology
2022–2024 · research · MDA Request for Applications
Expression of enhanced dystrophins via AAV
Jeffrey Chamberlain · University of Washington
2022–2025 · research · Development Grant
Restoration of motor neuron function via potassium channels in SMA mice
Nandhini Sivakumar · Columbia University Irving Medical Center
2022–2025 · research · Research Grant
Antigen-Specific Treatment of Myasthenia: Chimeric Autoantibody Receptor T Cells
David Richman · University of California System
2022–2025 · research · Research Grant
Unraveling the contribution of local translation to ALS pathogenesis
Sandrine Da Cruz · Vibvzw
2022 · research · Restricted Research Grant
Clinical Research in ALS (CRiALS)
Jonathan Glass · Emory University
2022 · award
Stanford University 4th Annual Spinal Muscular Atrophy Continuing Medical Education Conference
Deanna Hudspeth · Stanford University
2022 · award
Eleventh Annual NCH/OSU/CORT Myology Course
Kevin Flanigan · Nationwide Children's Hospital
2022–2025 · research · Research Grant
HSPB3: a promising candidate for the maintenance of the neuromuscular system
Serena Carra · University of Modena and Reggio Emilia
2022–2025 · research · Research Grant
Manipulating muscle growth and oxidative metabolism to improve pathology in DMD
Gordon Lynch · The University of Melbourne
2022–2025 · research · Research Grant
Restoring membrane trafficking in CMT neuropathies with aberrant myelin
Alessandra Bolino · IRCCS Ospedale San Raffaele
2022–2025 · research · Research Grant
Obesity as a modifier of disease progression caused by dystrophin deficiency
Joshua Selsby · Iowa State University
2022–2023 · award
RYR-1-Related Diseases International Research Workshop: From Mechanisms to Treatment
Michael Goldberg · RYR 1 Foundation
2022–2025 · research · Development Grant
Design and evaluation of drug-like small molecules targeting repeat expansion
Amirhossein Taghavi · University of Florida
2022 · award
Support for 2022 New Directions in Biology and Disease of Skeletal Muscle Conference
Lee Sweeney · University of Florida
2022–2025 · research · Research Grant
Pathophysiology and Treatment of Tubular Aggregate Myopathy
Robert Dirksen · University of Rochester
2022–2025 · research · Research Grant
Utrophin Genome Editing for Duchenne's Muscular Dystrophy (DMD) Therapy
Tejvir Khurana · The Trustees Of The University Of Pennsylvania
2022–2025 · research · Research Grant
Contribution of variable number tandem repeats to Amyotrophic Lateral Sclerosis
Paul Valdmanis · University of Washington
2022–2025 · research · Research Grant
Developing treatments for Duchenne Muscular Dystrophy
Peter Noakes · The University of Queensland