OOIR: Observatory of International Research

Papers

(The TQCC of Skeletal Muscle is 10. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-08-01 to 2025-08-01.)

Article	Citations
Abnormalities in the genioglossus muscle and its neuromuscular synapse in leptin-deficient male mice	121
Metabolic signatures and potential biomarkers of sarcopenia in suburb-dwelling older Chinese: based on untargeted GC–MS and LC–MS	90
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy	81
Golodirsen restores DMD transcript imbalance in Duchenne Muscular Dystrophy patient muscle cells	39
The SarcoEndoplasmic Reticulum Calcium ATPase (SERCA) pump: a potential target for intervention in aging and skeletal muscle pathologies	39
Fibro-adipogenic progenitor cells in skeletal muscle unloading: metabolic and functional impairments	37
ASM is a therapeutic target in dermatomyositis by regulating the differentiation of naive CD4 + T cells into Th17 and Treg subsets	27
Pilot investigations into the mechanistic basis for adverse effects of glucocorticoids in dysferlinopathy	25
Zebrafish and cellular models of SELENON-Congenital myopathy exhibit novel embryonic and metabolic phenotypes	23
SIX transcription factors are necessary for the activation of DUX4 expression in facioscapulohumeral muscular dystrophy	22
A knock down strategy for rapid, generic, and versatile modelling of muscular dystrophies in 3D-tissue-engineered-skeletal muscle	20
Spiny mice are primed but fail to regenerate volumetric skeletal muscle loss injuries	19
Comparative lipidomic and metabolomic profiling of mdx and severe mdx-apolipoprotein e-null mice	19
AAV-NRIP gene therapy ameliorates motor neuron degeneration and muscle atrophy in ALS model mice	17
Effect of chronic intermittent hypoxia (CIH) on neuromuscular junctions and mitochondria in slow- and fast-twitch skeletal muscles of mice—the role of iNOS	14
Extensive striated muscle damage in a rat model of Duchenne muscular dystrophy with Dmd exons 10–17 duplication	13
Expression of Myomaker and Myomerger in myofibers causes muscle pathology	13
Improved CRISPR/Cas9 gene editing in primary human myoblasts using low confluency cultures on Matrigel	13
High-throughput muscle fiber typing from RNA sequencing data	13
New tools for the investigation of muscle fiber-type spatial distributions across histological sections	13
Metabolomic signatures for the longitudinal reduction of muscle strength over 10 years	12
Pannexin 1 dysregulation in Duchenne muscular dystrophy and its exacerbation of dystrophic features in mdx mice	12
Decreased number of satellite cells-derived myonuclei in both fast- and slow-twitch muscles in HeyL-KO mice during voluntary running exercise	12
Generation of a novel mouse model of nemaline myopathy due to recurrent NEB exon 55 deletion	12
Wnt7a is required for regeneration of dystrophic skeletal muscle	11

Fusion of myofibre branches is a physiological feature of healthy human skeletal muscle regeneration	11
Macroglossia and less advanced dystrophic change in the tongue muscle of the Duchenne muscular dystrophy rat	11
The Myotube Analyzer: how to assess myogenic features in muscle stem cells	10
Role and mechanism of myonectin in severe acute pancreatitis: a crosstalk between skeletal muscle and pancreas	10
Endurance exercise with reduced muscle glycogen content influences substrate utilization and attenuates acute mTORC1- and autophagic signaling in human type I and type II muscle fibers	10
Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1G93A amyotrophic lateral sclerosis (ALS) mouse model	10