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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Skeletal Muscle Satellite Cells, Mitochondria, and MicroRNAs: Their Involvement in the Pathogenesis of ALS
Stavroula Tsitkanou, Paul A. Della Gatta, Aaron P. Russell
Frontiers in Physiology (2016) Vol. 7
Open Access | Times Cited: 53

Showing 1-25 of 53 citing articles:

Mitochondria: It is all about energy
Amaloha Casanova, Anne Wevers, Santiago Navarro‐Ledesma, et al.
Frontiers in Physiology (2023) Vol. 14
Open Access | Times Cited: 111
Mitochondria-Targeted Antioxidants, an Innovative Class of Antioxidant Compounds for Neurodegenerative Diseases: Perspectives and Limitations
Matteo Fields, Annalisa Marcuzzi, Arianna Gonelli, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 3739-3739
Open Access | Times Cited: 50
Long non-coding and coding RNAs characterization in Peripheral Blood Mononuclear Cells and Spinal Cord from Amyotrophic Lateral Sclerosis patients
Stella Gagliardi, Susanna Zucca, Cecilia Pandini, et al.
Scientific Reports (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 84
Skeletal-Muscle Metabolic Reprogramming in ALS-SOD1G93A Mice Predates Disease Onset and Is A Promising Therapeutic Target
Silvia Scaricamazza, I. Salvatori, Giacomo Giacovazzo, et al.
iScience (2020) Vol. 23, Iss. 5, pp. 101087-101087
Open Access | Times Cited: 76
Skeletal muscle dysfunction in amyotrophic lateral sclerosis: a mitochondrial perspective and therapeutic approaches
Gökhan Burçin Kubat, Pasquale Picone
Neurological Sciences (2024) Vol. 45, Iss. 9, pp. 4121-4131
Open Access | Times Cited: 10
What is “Hyper” in the ALS Hypermetabolism?
Alberto Ferri, Roberto Coccurello
Mediators of Inflammation (2017) Vol. 2017, pp. 1-11
Open Access | Times Cited: 71
The Role of Exercise as a Non-pharmacological Therapeutic Approach for Amyotrophic Lateral Sclerosis: Beneficial or Detrimental?
Stavroula Tsitkanou, Paul A. Della Gatta, Victoria C. Foletta, et al.
Frontiers in Neurology (2019) Vol. 10
Open Access | Times Cited: 66
The effects of diet and sex in amyotrophic lateral sclerosis
Jenny A. Pape, Julianne H. Grose
Revue Neurologique (2020) Vol. 176, Iss. 5, pp. 301-315
Open Access | Times Cited: 56
Screening the expression characteristics of several miRNAs in G93A‐SOD1 transgenic mouse: altered expression of miRNA‐124 is associated with astrocyte differentiation by targeting Sox2 and Sox9
Fenghua Zhou, Cai‐Xia Zhang, Yingjun Guan, et al.
Journal of Neurochemistry (2017) Vol. 145, Iss. 1, pp. 51-67
Open Access | Times Cited: 61
Histone deacetylase 4 protects from denervation and skeletal muscle atrophy in a murine model of amyotrophic lateral sclerosis
Eva Pigna, Elena Simonazzi, Krizia Sanna, et al.
EBioMedicine (2019) Vol. 40, pp. 717-732
Open Access | Times Cited: 52
Dysregulated mitochondrial Ca2+ and ROS signaling in skeletal muscle of ALS mouse model
Jingsong Zhou, Ang Li, Xuejun Li, et al.
Archives of Biochemistry and Biophysics (2019) Vol. 663, pp. 249-258
Open Access | Times Cited: 51
miR126-5p Downregulation Facilitates Axon Degeneration and NMJ Disruption via a Non–Cell-Autonomous Mechanism in ALS
Roy Maimon, Ariel Ionescu, Avichai Bonnie, et al.
Journal of Neuroscience (2018) Vol. 38, Iss. 24, pp. 5478-5494
Open Access | Times Cited: 48
Enhanced oxidative stress and the treatment by edaravone in mice model of amyotrophic lateral sclerosis
Yasuyuki Ohta, Emi Nomura, Jingwei Shang, et al.
Journal of Neuroscience Research (2018) Vol. 97, Iss. 5, pp. 607-619
Closed Access | Times Cited: 47
The Skeletal Muscle Emerges as a New Disease Target in Amyotrophic Lateral Sclerosis
Oihane Pikatza-Menoio, Amaia Elicegui, Xabier Bengoetxea, et al.
Journal of Personalized Medicine (2021) Vol. 11, Iss. 7, pp. 671-671
Open Access | Times Cited: 34
Permittivity of ex vivo healthy and diseased murine skeletal muscle from 10 kHz to 1 MHz
Janice A. Nagy, Christine J. DiDonato, Seward B. Rutkove, et al.
Scientific Data (2019) Vol. 6, Iss. 1
Open Access | Times Cited: 36
Role of Mitophagy in neurodegenerative Diseases and potential tagarts for Therapy
Lingling Jiao, Xixun Du, Yong Li, et al.
Molecular Biology Reports (2022) Vol. 49, Iss. 11, pp. 10749-10760
Closed Access | Times Cited: 20
Current view and perspectives in amyotrophic lateral sclerosis
Stéphane Mathis, Philippe Couratier, Adrien Julian, et al.
Neural Regeneration Research (2017) Vol. 12, Iss. 2, pp. 181-181
Open Access | Times Cited: 37
P2X7 activation enhances skeletal muscle metabolism and regeneration in SOD1G93A mouse model of amyotrophic lateral sclerosis
Paola Fabbrizio, Savina Apolloni, Andrea Bianchi, et al.
Brain Pathology (2019) Vol. 30, Iss. 2, pp. 272-282
Open Access | Times Cited: 32
Functional skeletal muscle model derived from SOD1-mutant ALS patient iPSCs recapitulates hallmarks of disease progression
Agnes Badu-Mensah, Xiufang Guo, Christopher W. McAleer, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 32
ALS mutations in both human skeletal muscle and motoneurons differentially affects neuromuscular junction integrity and function
Agnes Badu-Mensah, Xiufang Guo, Siddharth Nimbalkar, et al.
Biomaterials (2022) Vol. 289, pp. 121752-121752
Closed Access | Times Cited: 17
Comparative Study of Structural and Functional Rearrangements in Skeletal Muscle Mitochondria of SOD1-G93A Transgenic Mice at Pre-, Early-, and Late-Symptomatic Stages of ALS Progression
Natalia V. Belosludtseva, Anna I. Ilzorkina, Mikhail V. Dubinin, et al.
Frontiers in Bioscience-Landmark (2025) Vol. 30, Iss. 3
Open Access
The effect of exercise intervention on amyotrophic lateral sclerosis: a systematic review and meta-analysis
Shijie Ren, X.L. Che, Shunding Hu, et al.
Frontiers in Neurology (2025) Vol. 16
Open Access
Clinical Research on Traditional Chinese Medicine compounds and their preparations for Amyotrophic Lateral Sclerosis
Jiayi Zhu, Lan Shen, Xiao Lin, et al.
Biomedicine & Pharmacotherapy (2017) Vol. 96, pp. 854-864
Closed Access | Times Cited: 29
Long non coding RNAs and ALS: Still much to do
Stella Gagliardi, Cecilia Pandini, Maria Garofalo, et al.
Non-coding RNA Research (2018) Vol. 3, Iss. 4, pp. 226-231
Open Access | Times Cited: 29
Biological Indicators of Oxidative Stress [Malondialdehyde, Catalase, Glutathione Peroxidase, and Superoxide Dismutase] and Their Application in Nutrition
Maria do Carmo de Carvalho e Martins, Amanda Suellenn da Silva Santos Oliveira, Liriane Andressa Alves da Silva, et al.
Biomarkers in disease (2022), pp. 833-856
Closed Access | Times Cited: 15
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