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
2022–2023 · research · Idea Award
Combining oxytocin with corticosteroid therapy in DMD patients
Sabine De La Porte Hdr · Institut National de Recherche en Santé Publique
2022–2024 · research · Research Grant
Engineering CAR-Tregs for the induction of immune tolerance in gene therapy
Armando Villalta · University of California, Irvine
2022–2023 · research · Idea Award
Ultrasound-induced access of therapeutics to peripheral nerves
Alexia Kagiava · The Cyprus Foundation For Muscular Dystrophy Research
2022–2023 · research · Idea Award
Metabolic imaging of muscular dystrophy and cardiomyopathy
Jae Mo Park · The University Of Texas Southwestern Medical Center (ut Southwestern)
2022–2025 · research · Development Grant
DMD-Related Cardiomyopathy Beyond Dystrophin Deficiency in Skeletal Muscle
Luca Caputo · Sanford Burnham Prebys Medical Discovery Institute
2022–2025 · research · Research Grant
Developing Gene Therapy Approaches for mtDNA Deletions
Carlos Moraes · University of Miami
2022–2025 · research · Clinical Research Network Grant
Advanced Heart Failure Therapy Outcomes in Neuromuscular Cardiomyopathy
Forum Kamdar · Twin Cities Orthopedics
2022–2023 · award
10th Annual UC Irvine Neuromuscular Colloquium
Tahseen Mozaffar · University of California, Irvine
2022–2025 · research · Research Grant
A Designer HMGB1 as a Drug Candidate for Duchenne Muscular Dystrophy
Emilie Venereau · IRCCS Ospedale San Raffaele
2022–2023 · research · Clinical Trial Travel Grant
Advancing equitable access to clinical trials in rare diseases
Mathula Thangarajh · Virginia Commonwealth University
2022–2025 · research · Development Grant
ASM-AAV Gene Therapy as a Treatment for Limb Girdle Muscular Dystrophy 2B
Daniel Bittel · Children's Research Institute (cnmc)
2022–2025 · research · Development Grant
Leveraging microglia states to understand ALS disease
Martine Therrien · Broad Institute
2022 · award
Development of SPY-DYS45-55, a CRISPR therapy for Duchenne muscular dystrophy
Courtney Young · Myogene Bio Llc
2022–2025 · research · Development Grant
Microdystrophin Design for the Treatment of Dystrophin-Deficient Cardiomyocytes
Asuka Eguchi · The Board Of Trustees Of The Leland Stanford Junior University
2022–2025 · research · Research Grant
Mirabegron in Treating Muscle Dystrophy
Xuhui Liu · Regent University
2022–2025 · research · Research Grant
Fetal and neonatal gene therapy for DMD through homology directed repair
William Pu · Boston Children's Hospital
2022 · award
ENMC Workshop # 261 on AAV gene therapy
Franziska Ott · European Neuro Muscular Centre
2022–2025 · research · Research Grant
Nucleocytoplasmic GU-RNA gradients and TDP-43 mislocalization in ALS
Lindsey Hayes · Johns Hopkins University
2022–2025 · research · Research Grant
Long-read genome sequencing to diagnose neuromuscular disorders
Greg Cooper · HudsonAlpha Institute for Biotechnology
2022 · award
29th Annual International Research Congress on FSHD
June Kinoshita · FSH Society
2022 · award
Skeletal Muscle Stem Cells and Regeneration
Addolorata Pisconti · Federation of American Societies for Experimental Biology
2022–2025 · research · Research Grant
Cannabidiol for the treatment of Duchenne Muscular Dystrophy
George Rodney · Baylor College of Medicine
2022–2025 · research · Research Grant
Developing a bioassay for GJB1 variants causing CMTX1
Charles Abrams · The Board Of Trustees Of The University Of Illinois - University Of Illinois At Chicago
2022 · research · Restricted Research Grant
Maximizing dystrophin functionality
Jeffrey Chamberlain · University of Washington
2022–2025 · research · Clinical Research Grant
Advancing clinical trial readiness in TRPV4 neuropathy
Brett Mccray · Johns Hopkins University
2022–2025 · research · Research Grant
SARM1 antagonism as adjunct therapy in SMA
Charlotte Sumner · Johns Hopkins University
2022–2023 · research · Idea Award
Gene therapy for large muscle disease genes
James Dowling · Hospital for Sick Children
2022–2025 · research · Development Grant
Unveiling the pivotal disease-associated mechanisms in TPM3-related myopathy
Matthias Lambert · Boston Children's Hospital
2022–2025 · research · Development Grant
NF-kB signaling in muscle regeneration and disease
Neena Lala-Tabbert · Children's Hospital of Eastern Ontario
2022–2023 · award
2023 Gordon Myogenesis Conference
Clarissa Henry · University of Maine System
2022–2025 · research · Research Grant
tRNA sequestration as a pathogenic mechanism of tRNA synthetase-associated CMT
Erik Storkebaum · Stichting Radboud Universiteit
2022–2025 · research · Research Grant
Contribution of metabolic abnormalities to spinal muscular atrophy
Rashmi Kothary · Ottawa Hospital Research Institute
2022–2025 · research · Research Grant
CSF1R inhibitors as therapeutics for Duchenne Muscular Dystrophy
Fabio Rossi · University of British Columbia
2022–2023 · research · Idea Award
Development of lipid nanoparticles for antisense delivery to dystrophic muscle
James Novak · Children's Research Institute (cnmc)
2022–2025 · research · Research Grant
AMPK signaling defect in DM1 and its potential as a novel therapeutic target
Bernard Jasmin · University of Ottawa
2022–2025 · research · Development Grant
Identification of genetic modifiers for C9ORF72-ALS/FTD
Zhe Zhang · Johns Hopkins University
2022–2025 · research · Development Grant
Improving interpretation of variants in Sarcoglycanopathies
Shushu Huang · Yale University
2022–2025 · research · Research Grant
Genetic and metabolic strategies for mutant CHCHD10 neuromuscular disorders
Hibiki Fujita · Weill Cornell Medicine
2022–2023 · research · Idea Award
Molecular characterization of hippocampal neurons in Duchenne Muscular Dystrophy
Mathula Thangarajh · Virginia Commonwealth University
2022–2025 · research · Research Grant
Calcium regulation of ER stress and protein degradation in congenital myopathy
Amy Hanna · The University of Queensland