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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:

Reduced P53 levels ameliorate neuromuscular junction loss without affecting motor neuron pathology in a mouse model of spinal muscular atrophy
Natalie L. Courtney, Alannah J. Mole, Alison K. Thomson, et al.
Cell Death and Disease (2019) Vol. 10, Iss. 7
Open Access | Times Cited: 30

Showing 1-25 of 30 citing articles:

Curing SMA: Are we there yet?
Aoife Reilly, Lucia Chehadé, Rashmi Kothary
Gene Therapy (2022) Vol. 30, Iss. 1-2, pp. 8-17
Open Access | Times Cited: 43
Alterations in cardiac function correlate with a disruption in fatty acid metabolism in a mouse model of SMA
Nandini Nair, Rachel Kline, I. E. Boyd, et al.
Human Molecular Genetics (2025)
Open Access | Times Cited: 1
Diving into progress: a review on current therapeutic advancements in spinal muscular atrophy
P. S. Bagga, Sudhakar Singh, Gobind Ram, et al.
Frontiers in Neurology (2024) Vol. 15
Open Access | Times Cited: 7
TDP-43 induces p53-mediated cell death of cortical progenitors and immature neurons
Miriam A. Vogt, Zahra Ehsaei, Philip Knuckles, et al.
Scientific Reports (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 52
Emerging Gene Therapy Approaches in the Management of Spinal Muscular Atrophy (SMA): An Overview of Clinical Trials and Patent Landscape
Aleksei S. Ponomarev, Daria S. Chulpanova, Lina M. Yanygina, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 18, pp. 13743-13743
Open Access | Times Cited: 15
Central synaptopathy is the most conserved feature of motor circuit pathology across spinal muscular atrophy mouse models
Jannik M. Buettner, Josiane K. Sime Longang, Florian Gerstner, et al.
iScience (2021) Vol. 24, Iss. 11, pp. 103376-103376
Open Access | Times Cited: 27
MiR34 contributes to spinal muscular atrophy and AAV9-mediated delivery of MiR34a ameliorates the motor deficits in SMA mice
Tai‐Heng Chen, Shih-Hsin Chang, Yu-Fu Wu, et al.
Molecular Therapy — Nucleic Acids (2023) Vol. 32, pp. 144-160
Open Access | Times Cited: 11
Neuromuscular junction instability with inactivity: morphological and functional changes after 10 days of bed rest in older adults
Evgeniia Motanova, Fabio Sarto, Samuele Negro, et al.
The Journal of Physiology (2025)
Open Access
In Search of a Cure: The Development of Therapeutics to Alter the Progression of Spinal Muscular Atrophy
Kristine S. Ojala, Emily J. Reedich, Christine J. DiDonato, et al.
Brain Sciences (2021) Vol. 11, Iss. 2, pp. 194-194
Open Access | Times Cited: 25
Motor transmission defects with sex differences in a new mouse model of mild spinal muscular atrophy
Marc‐Olivier Deguise, Yves De Repentigny, Alexandra Tierney, et al.
EBioMedicine (2020) Vol. 55, pp. 102750-102750
Open Access | Times Cited: 26
Harmony Lost: Cell–Cell Communication at the Neuromuscular Junction in Motor Neuron Disease
Anastasia Gromova, Albert R. La Spada
Trends in Neurosciences (2020) Vol. 43, Iss. 9, pp. 709-724
Open Access | Times Cited: 25
Axonal Transport and Local Translation of mRNA in Neurodegenerative Diseases
Seiichi Nagano, Toshiyuki Araki
Frontiers in Molecular Neuroscience (2021) Vol. 14
Open Access | Times Cited: 21
Mouse models of SMA show divergent patterns of neuronal vulnerability and resilience
Victoria Woschitz, Irene Mei, Eva Hedlund, et al.
Skeletal Muscle (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 14
Cytoskeleton saga: Its regulation in normal physiology and modulation in neurodegenerative disorders
Santimoy Sen, Sheetal Lagas, Abhishek Roy, et al.
European Journal of Pharmacology (2022) Vol. 925, pp. 175001-175001
Closed Access | Times Cited: 13
Motor unit recovery following Smn restoration in mouse models of spinal muscular atrophy
Laura H. Comley, Rachel Kline, Alison K. Thomson, et al.
Human Molecular Genetics (2022) Vol. 31, Iss. 18, pp. 3107-3119
Open Access | Times Cited: 12
Suppression of the necroptotic cell death pathways improves survival in Smn2B/− mice
Lucia Chehadé, Marc‐Olivier Deguise, Yves De Repentigny, et al.
Frontiers in Cellular Neuroscience (2022) Vol. 16
Open Access | Times Cited: 11
Spinal motor neuron loss occurs through a p53-and-p21-independent mechanism in the Smn mouse model of spinal muscular atrophy
Emily J. Reedich, Martin Kalski, Nicholas Armijo, et al.
Experimental Neurology (2020) Vol. 337, pp. 113587-113587
Open Access | Times Cited: 10
Axonal mRNA localization and local translation in neurodegenerative disease
Haiying Li, Zhengquan Yu, Jinxin Lü, et al.
Neural Regeneration Research (2021) Vol. 16, Iss. 10, pp. 1950-1950
Open Access | Times Cited: 8
Neuromuscular denervation and deafferentation but not motor neuron death are disease features in the Smn2B/- mouse model of SMA
María J. Carlini, Marina K. Triplett, Livio Pellizzoni
PLoS ONE (2022) Vol. 17, Iss. 8, pp. e0267990-e0267990
Open Access | Times Cited: 5
Differential effect of Fas activation on spinal muscular atrophy motoneuron death and induction of axonal growth
Salim Benlefki, Richard Younes, Désiré Challuau, et al.
Cellular and Molecular Biology (2023) Vol. 69, Iss. 10, pp. 1-8
Open Access | Times Cited: 2
SMA Type II Skeletal Muscle Treated with Nusinersen shows SMN Restoration but Mitochondrial Deficiency.
Fiorella C. Grandi, Stéphanie Astord, Elèna Gidaja, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Loss of Synaptic Munc13-1 Underlies Neurotransmission Abnormalities in Spinal Muscular Atrophy
Mehri Moradi, Chunchu Deng, Michael Sendtner
Research Square (Research Square) (2024)
Open Access
Synaptic withdrawal following nerve injury is influenced by postnatal maturity, muscle‐specific properties, and the presence of underlying pathology in mice
Alannah J. Mole, S.C. Bell, Alison K. Thomson, et al.
Journal of Anatomy (2020) Vol. 237, Iss. 2, pp. 263-274
Open Access | Times Cited: 3
Low-dose brain radiation: lowering hyperphosphorylated-tau without increasing DNA damage or oncogenic activation
Diego Iacono, Erin K. Murphy, Cheryl D. Stimpson, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 1
Emerging concepts underlying selective neuromuscular dysfunction in infantile-onset spinal muscular atrophy
U. R. Monani, Kishore Gollapalli, Jeong-Ki Kim
Neural Regeneration Research (2021) Vol. 16, Iss. 10, pp. 1978-1978
Open Access | Times Cited: 3
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