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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:

Hypoexcitability precedes denervation in the large fast-contracting motor units in two unrelated mouse models of ALS
María de Lourdes Martínez-Silva, Rebecca D Imhoff-Manuel, Aarti Sharma, et al.
eLife (2018) Vol. 7
Open Access | Times Cited: 142

Showing 1-25 of 142 citing articles:

Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
Sai Zhang, Johnathan Cooper‐Knock, Annika K. Weimer, et al.
Neuron (2022) Vol. 110, Iss. 6, pp. 992-1008.e11
Open Access | Times Cited: 98
Neuromuscular Junction Dysfunction in Amyotrophic Lateral Sclerosis
Sagar Verma, Shiffali Khurana, Kavita Vats, et al.
Molecular Neurobiology (2022) Vol. 59, Iss. 3, pp. 1502-1527
Closed Access | Times Cited: 73
Homozygous ALS-linked mutations in TARDBP/TDP-43 lead to hypoactivity and synaptic abnormalities in human iPSC-derived motor neurons
Sarah Lépine, Angela Nauleau-Javaudin, Éric Deneault, et al.
iScience (2024) Vol. 27, Iss. 3, pp. 109166-109166
Open Access | Times Cited: 11
How do we get from hyperexcitability to excitotoxicity in amyotrophic lateral sclerosis?
G. Lorenzo Odierna, Steve Vucic, Marcus S. Dyer, et al.
Brain (2024) Vol. 147, Iss. 5, pp. 1610-1621
Open Access | Times Cited: 9
Driven to decay: Excitability and synaptic abnormalities in amyotrophic lateral sclerosis
Matthew J. Fogarty
Brain Research Bulletin (2018) Vol. 140, pp. 318-333
Closed Access | Times Cited: 72
Direct Electrical Stimulation in Electrocorticographic Brain–Computer Interfaces: Enabling Technologies for Input to Cortex
David J. Caldwell, Jeffrey G. Ojemann, Rajesh P. N. Rao
Frontiers in Neuroscience (2019) Vol. 13
Open Access | Times Cited: 69
Multimaterial and multifunctional neural interfaces: from surface-type and implantable electrodes to fiber-based devices
Changhoon Sung, Woojin Jeon, Kum Seok Nam, et al.
Journal of Materials Chemistry B (2020) Vol. 8, Iss. 31, pp. 6624-6666
Closed Access | Times Cited: 62
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
Synaptic restoration by cAMP/PKA drives activity-dependent neuroprotection to motoneurons in ALS
Marcin Bączyk, Najwa Ouali Alami, Nicolas Delestrée, et al.
The Journal of Experimental Medicine (2020) Vol. 217, Iss. 8
Open Access | Times Cited: 52
Human amyotrophic lateral sclerosis excitability phenotype screen: Target discovery and validation
Xuan Huang, Kasper C. D. Roet, Liying Zhang, et al.
Cell Reports (2021) Vol. 35, Iss. 10, pp. 109224-109224
Open Access | Times Cited: 50
Adaptable P body physical states differentially regulate bicoid mRNA storage during early Drosophila development
Mugesh Sankaranarayanan, Ryan J. Emenecker, Elise L. Wilby, et al.
Developmental Cell (2021) Vol. 56, Iss. 20, pp. 2886-2901.e6
Open Access | Times Cited: 42
The Role of DNA Damage in Neural Plasticity in Physiology and Neurodegeneration
Anna Konopka, Julie D. Atkin
Frontiers in Cellular Neuroscience (2022) Vol. 16
Open Access | Times Cited: 37
Synaptic dysfunction in ALS and FTD: anatomical and molecular changes provide insights into mechanisms of disease
Pauline A. Gelon, Paul A. Dutchak, Chantelle F. Sephton
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 37
Detecting motor unit abnormalities in amyotrophic lateral sclerosis using high-density surface EMG
Yuichi Nishikawa, Aleš Holobar, Kohei Watanabe, et al.
Clinical Neurophysiology (2022) Vol. 142, pp. 262-272
Closed Access | Times Cited: 31
Spinal motoneurones are intrinsically more responsive in the adult G93A SOD1 mouse model of amyotrophic lateral sclerosis
Dennis Bo Jensen, Marion Kadlecova, Ilary Allodi, et al.
The Journal of Physiology (2020) Vol. 598, Iss. 19, pp. 4385-4403
Open Access | Times Cited: 40
Synaptic disruption and CREB‐regulated transcription are restored by K + channel blockers in ALS
Alberto Catanese, Sandeep Rajkumar, Doron D. Sommer, et al.
EMBO Molecular Medicine (2021) Vol. 13, Iss. 7
Open Access | Times Cited: 34
Aberrant axon initial segment plasticity and intrinsic excitability of ALS hiPSC motor neurons
Peter Harley, Caoimhe Kerins, Ariana Gatt, et al.
Cell Reports (2023) Vol. 42, Iss. 12, pp. 113509-113509
Open Access | Times Cited: 16
Regulation of cortical hyperexcitability in amyotrophic lateral sclerosis: focusing on glial mechanisms
Manling Xie, Praveen N. Pallegar, Sebastian Parusel, et al.
Molecular Neurodegeneration (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 14
Scaling of Motor Output, From Mouse to Humans
Marin Manuel, Matthieu K. Chardon, Vicki M. Tysseling, et al.
Physiology (2018) Vol. 34, Iss. 1, pp. 5-13
Open Access | Times Cited: 43
Dynamic interplay between H-current and M-current controls motoneuron hyperexcitability in amyotrophic lateral sclerosis
Yossi Buskila, Orsolya Kékesi, Alba Bellot-Saez, et al.
Cell Death and Disease (2019) Vol. 10, Iss. 4
Open Access | Times Cited: 39
Object-Displacement-Sensitive Visual Neurons Drive Freezing in Drosophila
Ryosuke Tanaka, Damon A. Clark
Current Biology (2020) Vol. 30, Iss. 13, pp. 2532-2550.e8
Open Access | Times Cited: 39
Multiplexed chemogenetics in astrocytes and motoneurons restore blood–spinal cord barrier in ALS
Najwa Ouali Alami, Linyun Tang, Diana Wiesner, et al.
Life Science Alliance (2020) Vol. 3, Iss. 11, pp. e201900571-e201900571
Open Access | Times Cited: 33
Mathematical relationships between spinal motoneuron properties
Arnault H. Caillet, Andrew Phillips, Dario Farina, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 22
Pharmacological inhibition of the integrated stress response accelerates disease progression in an amyotrophic lateral sclerosis mouse model
Elías Marlin, Miguel Valencia, Nuria Peregrín, et al.
British Journal of Pharmacology (2023) Vol. 181, Iss. 3, pp. 495-508
Open Access | Times Cited: 13
Longitudinal changes in intrinsic motoneuron excitability in amyotrophic lateral sclerosis are dependent on disease progression
Gabriel S. Trajano, Lucas B. R. Orssatto, Pamela McCombe, et al.
The Journal of Physiology (2023) Vol. 601, Iss. 21, pp. 4723-4735
Open Access | Times Cited: 11
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