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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:

TDP-43 Proteinopathy and ALS: Insights into Disease Mechanisms and Therapeutic Targets
Emma L. Scotter, Han-Jou Chen, Christopher E. Shaw
Neurotherapeutics (2015) Vol. 12, Iss. 2, pp. 352-363
Open Access | Times Cited: 308

Showing 1-25 of 308 citing articles:

Alternative splicing as a regulator of development and tissue identity
Francisco E. Baralle, Jimena Giudice
Nature Reviews Molecular Cell Biology (2017) Vol. 18, Iss. 7, pp. 437-451
Open Access | Times Cited: 1116
Molecular Mechanisms of TDP-43 Misfolding and Pathology in Amyotrophic Lateral Sclerosis
A. Aditya Prasad, Vidhya Bharathi, Vishwanath Sivalingam, et al.
Frontiers in Molecular Neuroscience (2019) Vol. 12
Open Access | Times Cited: 636
RNA Binding Antagonizes Neurotoxic Phase Transitions of TDP-43
Jacob R. Mann, Amanda M. Gleixner, Jocelyn C. Mauna, et al.
Neuron (2019) Vol. 102, Iss. 2, pp. 321-338.e8
Open Access | Times Cited: 480
Remodeling of epigenome and transcriptome landscapes with aging in mice reveals widespread induction of inflammatory responses
Bérénice A. Benayoun, Elizabeth A. Pollina, Param Priya Singh, et al.
Genome Research (2019) Vol. 29, Iss. 4, pp. 697-709
Open Access | Times Cited: 299
Molecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision Medicine
Gábor G. Kovács
International Journal of Molecular Sciences (2016) Vol. 17, Iss. 2, pp. 189-189
Open Access | Times Cited: 279
Gene therapy for neurological disorders: progress and prospects
Benjamin E. Deverman, Bernard Ravina, Krystof S. Bankiewicz, et al.
Nature Reviews Drug Discovery (2018) Vol. 17, Iss. 9, pp. 641-659
Closed Access | Times Cited: 272
ALS Genes in the Genomic Era and their Implications for FTD
Hung Phuoc Nguyen, Christine Van Broeckhoven, Julie van der Zee
Trends in Genetics (2018) Vol. 34, Iss. 6, pp. 404-423
Open Access | Times Cited: 271
Erratum: Gene therapy for neurological disorders: progress and prospects
Benjamin E. Deverman, Bernard Ravina, Krystof S. Bankiewicz, et al.
Nature Reviews Drug Discovery (2018) Vol. 17, Iss. 10, pp. 767-767
Open Access | Times Cited: 251
2D versus 3D human induced pluripotent stem cell-derived cultures for neurodegenerative disease modelling
Eduarda Gervini Zampieri Centeno, Helena Cimarosti, Angela Bithell
Molecular Neurodegeneration (2018) Vol. 13, Iss. 1
Open Access | Times Cited: 212
Defective control of pre–messenger RNA splicing in human disease
Benoı̂t Chabot, Lulzim Shkreta
The Journal of Cell Biology (2016) Vol. 212, Iss. 1, pp. 13-27
Open Access | Times Cited: 203
TDP-43 activates microglia through NF-κB and NLRP3 inflammasome
Weihua Zhao, David R. Beers, Shaughn Bell, et al.
Experimental Neurology (2015) Vol. 273, pp. 24-35
Closed Access | Times Cited: 203
Functional Significance of TDP-43 Mutations in Disease
Emanuele Buratti
Advances in genetics (2015), pp. 1-53
Closed Access | Times Cited: 202
Autophagy Induction as a Therapeutic Strategy for Neurodegenerative Diseases
Alvin Djajadikerta, Swati Keshri, Mariana Pavel, et al.
Journal of Molecular Biology (2019) Vol. 432, Iss. 8, pp. 2799-2821
Open Access | Times Cited: 201
Astrocyte-derived extracellular vesicles: Neuroreparative properties and role in the pathogenesis of neurodegenerative disorders
Raghavendra Upadhya, Winston Zingg-De Jongh, Siddhant Shetty, et al.
Journal of Controlled Release (2020) Vol. 323, pp. 225-239
Open Access | Times Cited: 198
Functional roles and networks of non-coding RNAs in the pathogenesis of neurodegenerative diseases
Yi‐Ying Wu, Hung‐Chih Kuo
Journal of Biomedical Science (2020) Vol. 27, Iss. 1
Open Access | Times Cited: 186
Motor Neuron Susceptibility in ALS/FTD
Audrey Ragagnin, Sina Shadfar, Marta Vidal, et al.
Frontiers in Neuroscience (2019) Vol. 13
Open Access | Times Cited: 173
Lysosome dysfunction as a cause of neurodegenerative diseases: Lessons from frontotemporal dementia and amyotrophic lateral sclerosis
Jessica Root, Paola Merino, Austin Nuckols, et al.
Neurobiology of Disease (2021) Vol. 154, pp. 105360-105360
Open Access | Times Cited: 165
The debated toxic role of aggregated TDP-43 in amyotrophic lateral sclerosis: a resolution in sight?
Rudolf Hergesheimer, Anna A. Chami, Dênis Reis de Assis, et al.
Brain (2019) Vol. 142, Iss. 5, pp. 1176-1194
Open Access | Times Cited: 163
SQuIRE reveals locus-specific regulation of interspersed repeat expression
Wan Rou Yang, Daniel Ardeljan, Clarissa N. Pacyna, et al.
Nucleic Acids Research (2019) Vol. 47, Iss. 5, pp. e27-e27
Open Access | Times Cited: 159
Protein posttranslational modifications in health and diseases: Functions, regulatory mechanisms, and therapeutic implications
Qian Zhong, Xina Xiao, Yijie Qiu, et al.
MedComm (2023) Vol. 4, Iss. 3
Open Access | Times Cited: 125
Familial Amyotrophic Lateral Sclerosis
Khrista Boylan
Neurologic Clinics (2015) Vol. 33, Iss. 4, pp. 807-830
Open Access | Times Cited: 166
Disrupted neuronal trafficking in amyotrophic lateral sclerosis
Katja Burk, R. Jeroen Pasterkamp
Acta Neuropathologica (2019) Vol. 137, Iss. 6, pp. 859-877
Open Access | Times Cited: 141
TDP-43 regulates the alternative splicing of hnRNP A1 to yield an aggregation-prone variant in amyotrophic lateral sclerosis
Jade-Emmanuelle Deshaies, Lulzim Shkreta, Alexander J. Moszczynski, et al.
Brain (2018) Vol. 141, Iss. 5, pp. 1320-1333
Open Access | Times Cited: 126
Extracellular Vesicles: Packages Sent With Complement
Ebru Karasu, Steffen U. Eisenhardt, Julia Harant, et al.
Frontiers in Immunology (2018) Vol. 9
Open Access | Times Cited: 119
TRIM16 controls assembly and degradation of protein aggregates by modulating the p62‐NRF2 axis and autophagy
Kautilya Kumar Jena, Srinivasa Prasad Kolapalli, Subhash Mehto, et al.
The EMBO Journal (2018) Vol. 37, Iss. 18
Open Access | Times Cited: 118
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