This journal focuses on neuromuscular disorders, including genetic conditions like spinal muscular atrophy, Pompe disease, facioscapulohumeral muscular dystrophy, and limb girdle muscular dystrophy. It also covers mitochondrial disorders and inflammatory myopathies. The scope includes clinical presentations, genetic and phenotypic spectrums, diagnostic approaches, and therapeutic interventions such as gene therapy and outcome assessments.
Based on the Think.Check.Submit framework by DOAJ, COPE & OASPA. All data from verified open sources.
Publication & Citation Trend
Articles published
Times cited
2019
2020
2021
2022
2023
2024
2025
2026
Source: OpenAlex · Note: citations accumulate over time so older years appear higher
SJR Quartile by Discipline
Scimago ranks this journal separately in each subject category — its quartile can differ by discipline.
Pediatrics, Perinatology and Child HealthQ1
Genetics (clinical)Q2
NeurologyQ2
Neurology (clinical)Q2
Subject Classification
Web of Science Categories
Clinical NeurologyNeurosciences
Scopus Categories
Neurology (clinical)Pediatrics, Perinatology and Child HealthGenetics (clinical)Neurology
Research Topics (OpenAlex)
Muscle Physiology and DisordersNeurogenetic and Muscular Disorders ResearchGenetic Neurodegenerative DiseasesCardiomyopathy and Myosin StudiesMitochondrial Function and PathologyInflammatory Myopathies and DermatomyositisRNA modifications and cancerMyasthenia Gravis and ThymomaRNA Research and SplicingNuclear Structure and Function