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:

Circuit-Specific Early Impairment of Proprioceptive Sensory Neurons in the SOD1G93AMouse Model for ALS
S Seki, Toru Yamamoto, Kiara N. Quinn, et al.
Journal of Neuroscience (2019) Vol. 39, Iss. 44, pp. 8798-8815
Open Access | Times Cited: 30

Showing 1-25 of 30 citing articles:

Advances in Applying Computer-Aided Drug Design for Neurodegenerative Diseases
Mootaz M. Salman, Zaid Al-Obaidi, Philip Kitchen, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 9, pp. 4688-4688
Open Access | Times Cited: 99

Muscle spindle function in healthy and diseased muscle
Stephan Kröger, Bridgette Watkins
Skeletal Muscle (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 82

Single-cell RNA-seq analysis of the brainstem of mutant SOD1 mice reveals perturbed cell types and pathways of amyotrophic lateral sclerosis
Wenting Liu, Sharmila Venugopal, Sana Majid, et al.
Neurobiology of Disease (2020) Vol. 141, pp. 104877-104877
Open Access | Times Cited: 68

Exciting Complexity: The Role of Motor Circuit Elements in ALS Pathophysiology
Zeynep I. Gunes, Vanessa W. Y. Kan, XiaoQian Ye, et al.
Frontiers in Neuroscience (2020) Vol. 14
Open Access | Times Cited: 56

Sensory Involvement in Amyotrophic Lateral Sclerosis
M.Á. Rubio, Mireia Herrando‐Grabulosa, Xavier Navarro
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 24, pp. 15521-15521
Open Access | Times Cited: 21

Sensory Dysfunction in ALS and Other Motor Neuron Diseases: Clinical Relevance, Histopathology, Neurophysiology, and Insights from Neuroimaging
Jana Kleinerová, Rangariroyashe H. Chipika, Ee Ling Tan, et al.
Biomedicines (2025) Vol. 13, Iss. 3, pp. 559-559
Open Access

How Degeneration of Cells Surrounding Motoneurons Contributes to Amyotrophic Lateral Sclerosis
Roxane Crabé, Franck Aimond, Philippe Gosset, et al.
Cells (2020) Vol. 9, Iss. 12, pp. 2550-2550
Open Access | Times Cited: 31

Chronic Pharmacological Increase of Neuronal Activity Improves Sensory-Motor Dysfunction in Spinal Muscular Atrophy Mice
Christian M. Simon, Beatriz Blanco-Redondo, Jannik M. Buettner, et al.
Journal of Neuroscience (2020) Vol. 41, Iss. 2, pp. 376-389
Open Access | Times Cited: 24

Early deficits in GABA inhibition parallels an increase in L-type Ca2+ currents in the jaw motor neurons of SOD1G93A mouse model for ALS
Sharmila Venugopal, Zohal Ghulam-Jelani, In Sook Ahn, et al.
Neurobiology of Disease (2023) Vol. 177, pp. 105992-105992
Open Access | Times Cited: 8

Clinical and preclinical evidence of somatosensory involvement in amyotrophic lateral sclerosis
Javier Riancho, Lucía Paz‐Fajardo, Adolfo López de Munaín
British Journal of Pharmacology (2020) Vol. 178, Iss. 6, pp. 1257-1268
Open Access | Times Cited: 19

Motoneuronal Spinal Circuits in Degenerative Motoneuron Disease
Mélanie Falgairolle, Michael J. O’Donovan
Frontiers in Molecular Neuroscience (2020) Vol. 13
Open Access | Times Cited: 18

Characteristics of Sensory Neuron Dysfunction in Amyotrophic Lateral Sclerosis (ALS): Potential for ALS Therapy
S Seki, Y. Kitaoka, Sou Kawata, et al.
Biomedicines (2023) Vol. 11, Iss. 11, pp. 2967-2967
Open Access | Times Cited: 5

Altered Sensory Neuron Development in CMT2D Mice Is Site-Specific and Linked to Increased GlyRS Levels
James N. Sleigh, Aleksandra M. Mech, Tahmina Aktar, et al.
Frontiers in Cellular Neuroscience (2020) Vol. 14
Open Access | Times Cited: 12

Satellite Glial Cells of the Dorsal Root Ganglion: A New “Guest/Physiopathological Target” in ALS
María Ruiz‐Soto, Javier Riancho, O. Tapia, et al.
Frontiers in Aging Neuroscience (2020) Vol. 12
Open Access | Times Cited: 12

Multifaceted superoxide dismutase 1 expression in amyotrophic lateral sclerosis patients: a rare occurrence?
Ilaria Martinelli, Jessica Mandrioli, Andrea Ghezzi, et al.
Neural Regeneration Research (2024) Vol. 20, Iss. 1, pp. 130-138
Open Access | Times Cited: 1

Synaptic imbalance and increased inhibition impair motor function in SMA
Emily V. Fletcher, Joshua I. Chalif, Travis M. Rotterman, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1

In vitro modelling of human proprioceptive sensory neurons in the neuromuscular system
Maider Badiola-Mateos, Tatsuya Osaki, Roger D. Kamm, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 4

Altered sensory neuron development in CMT2D mice is site-specific and linked to increased GlyRS levels
James N. Sleigh, Aleksandra M. Mech, Tahmina Aktar, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 4

Synaptic Transmission and Motoneuron Excitability Defects in Amyotrophic Lateral Sclerosis
Frédérique Scamps, Franck Aimond, Cécile Hilaire, et al.
Amyotrophic Lateral Sclerosis (2021), pp. 55-94
Open Access | Times Cited: 4

Preservation of masseter muscle until the end stage in the SOD1G93A mouse model for ALS
Sou Kawata, S Seki, Akira Nishiura, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access

Pathomechanistic Networks of Motor System Injury in Amyotrophic Lateral Sclerosis
B.R. Dey, Arvind Kumar, Anant B. Patel
Current Neuropharmacology (2023) Vol. 22, Iss. 11, pp. 1778-1806
Open Access | Times Cited: 1

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