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 2022-06-01 to 2026-06-01.)

Article	Citations
iPSC-derived skeletal muscle spheroids for Duchenne Muscular Dystrophy modeling	64
Caloric restriction reprograms skeletal muscle molecular pathways in non-human primates: potential relevance to human aging biology	58
The paradox of hnRNPK: both absence and excess impair skeletal muscle function in mice	53
Abnormalities in the genioglossus muscle and its neuromuscular synapse in leptin-deficient male mice	42
Metabolic signatures and potential biomarkers of sarcopenia in suburb-dwelling older Chinese: based on untargeted GC–MS and LC–MS	41
Non-regenerative myogenesis in adult skeletal muscles: myofiber death-independent muscle satellite cell expansion	31
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy	27
Pirfenidone treatment improves ischemic muscle function in mice with chronic kidney disease	25
Golodirsen restores DMD transcript imbalance in Duchenne Muscular Dystrophy patient muscle cells	24
Pilot investigations into the mechanistic basis for adverse effects of glucocorticoids in dysferlinopathy	23
Zebrafish and cellular models of SELENON-Congenital myopathy exhibit novel embryonic and metabolic phenotypes	21
SIX transcription factors are necessary for the activation of DUX4 expression in facioscapulohumeral muscular dystrophy	21
A knock down strategy for rapid, generic, and versatile modelling of muscular dystrophies in 3D-tissue-engineered-skeletal muscle	17
ASM is a therapeutic target in dermatomyositis by regulating the differentiation of naive CD4 + T cells into Th17 and Treg subsets	17
Comparative lipidomic and metabolomic profiling of mdx and severe mdx-apolipoprotein e-null mice	15
Spiny mice are primed but fail to regenerate volumetric skeletal muscle loss injuries	15
Integrin αVβ5 regulates myoblast proliferation and differentiation in sarcopenia mice treated with FNDC5 gene delivery	15
Fibro-adipogenic progenitor cells in skeletal muscle unloading: metabolic and functional impairments	15
AAV-NRIP gene therapy ameliorates motor neuron degeneration and muscle atrophy in ALS model mice	15
New tools for the investigation of muscle fiber-type spatial distributions across histological sections	14
The contribution of skeletal muscle interstitial cells to myogenesis	14
Extensive striated muscle damage in a rat model of Duchenne muscular dystrophy with Dmd exons 10–17 duplication	14
High-throughput muscle fiber typing from RNA sequencing data	13
Expression of Myomaker and Myomerger in myofibers causes muscle pathology	13
Functional and structural pathologies in skeletal muscle of a rat model of Duchenne muscular dystrophy	12

Necessity of Notch3 signaling in myofiber maturation in a pluripotent stem cell transplant model	12
Macroglossia and less advanced dystrophic change in the tongue muscle of the Duchenne muscular dystrophy rat	12
Generation of a novel mouse model of nemaline myopathy due to recurrent NEB exon 55 deletion	11
Pannexin 1 dysregulation in Duchenne muscular dystrophy and its exacerbation of dystrophic features in mdx mice	11
Decreased number of satellite cells-derived myonuclei in both fast- and slow-twitch muscles in HeyL-KO mice during voluntary running exercise	10
The Myotube Analyzer: how to assess myogenic features in muscle stem cells	10
Wnt7a is required for regeneration of dystrophic skeletal muscle	10
A 3D skeletal muscle system for disease modelling and secretome profiling of Duchenne muscular dystrophy	10
Fusion of myofibre branches is a physiological feature of healthy human skeletal muscle regeneration	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