# Muscular Dystrophy Association

**Type:** Institutions  
**Canonical URL:** https://scholariq.org/institutions/muscular-dystrophy-association/

## Facts

| Field | Value |
| --- | --- |
| Avg h-index | 85.5 |
| Citations | 72,415 |
| City | Chicago |
| Country | US |
| Description | Muscular Dystrophy Association is a research organisation in Chicago, US. OpenAlex records 642 works and 72,415 citations for it. 190 researchers list it as their most recent affiliation. |
| Homepage | http://www.mda.org/ |
| OpenAlex ID | https://openalex.org/I1303526167 |
| Region | Illinois |
| Researchers | 190 |
| ROR ID | https://ror.org/01frxsf98 |
| Type | nonprofit |
| Wikidata ID | https://www.wikidata.org/wiki/Q6940370 |
| Works | 642 |

## University papers

Showing 12 of 13.

- [Nuclear and Neuropil Aggregates in Huntington’s Disease: Relationship to Neuropathology](https://scholariq.org/papers/nuclear-and-neuropil-aggregates-in-huntington-s-disease-relationship-to/)
- [Localization of D1 and D2 dopamine receptors in brain with subtype-specific antibodies.](https://scholariq.org/papers/localization-of-d1-and-d2-dopamine-receptors-in-brain-with-subtype-specific/)
- [Movement Assessment Battery for Children](https://scholariq.org/papers/movement-assessment-battery-for-children/)
- [Cerebral cortex and the clinical expression of Huntington's disease: complexity and heterogeneity](https://scholariq.org/papers/cerebral-cortex-and-the-clinical-expression-of-huntington-s-disease-complexity/)
- [CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion](https://scholariq.org/papers/cag-repeat-expansion-in-huntington-disease-determines-age-at-onset-in-a-fully/)
- [Diffusion tensor imaging in presymptomatic and early Huntington's disease: Selective white matter pathology and its relationship to clinical measures](https://scholariq.org/papers/diffusion-tensor-imaging-in-presymptomatic-and-early-huntington-s-disease/)
- [Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations](https://scholariq.org/papers/mitochondrial-neurogastrointestinal-encephalomyopathy-an-autosomal-recessive/)
- [Mullen Scales of Early Learning](https://scholariq.org/papers/mullen-scales-of-early-learning/)
- [The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene](https://scholariq.org/papers/the-myopathic-form-of-coenzyme-q10-deficiency-is-caused-by-mutations-in-the/)
- [Creatine in Huntington disease is safe, tolerable, bioavailable in brain and reduces serum 8OH2′dG](https://scholariq.org/papers/creatine-in-huntington-disease-is-safe-tolerable-bioavailable-in-brain-and/)
- [Nuclear genome transfer in human oocytes eliminates mitochondrial DNA variants](https://scholariq.org/papers/nuclear-genome-transfer-in-human-oocytes-eliminates-mitochondrial-dna-variants/)
- [Big GABA: Edited MR spectroscopy at 24 research sites](https://scholariq.org/papers/big-gaba-edited-mr-spectroscopy-at-24-research-sites/)

## University top topics

Showing 8 of 25.

- [Muscle Physiology and Disorders](https://scholariq.org/topics/muscle-physiology-and-disorders/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [Virus-based gene therapy research](https://scholariq.org/topics/virus-based-gene-therapy-research/)
- [Cardiomyopathy and Myosin Studies](https://scholariq.org/topics/cardiomyopathy-and-myosin-studies/)
- [Metabolism and Genetic Disorders](https://scholariq.org/topics/metabolism-and-genetic-disorders/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.