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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:

Abnormal RNA stability in amyotrophic lateral sclerosis
EM Tank, Claudia Figueroa‐Romero, Lucy M. Hinder, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 136

Showing 1-25 of 136 citing articles:

Genetics of amyotrophic lateral sclerosis: A review
Stéphane Mathis, Cyril Goizet, Antoine Soulages, et al.
Journal of the Neurological Sciences (2019) Vol. 399, pp. 217-226
Open Access | Times Cited: 223
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
RNAs undergo phase transitions with lower critical solution temperatures
Gable M. Wadsworth, Walter J. Zahurancik, Xiangze Zeng, et al.
Nature Chemistry (2023) Vol. 15, Iss. 12, pp. 1693-1704
Open Access | Times Cited: 72
RNA methylation influences TDP43 binding and disease pathogenesis in models of amyotrophic lateral sclerosis and frontotemporal dementia
Michael McMillan, Nicolás Gómez, Caroline Hsieh, et al.
Molecular Cell (2023) Vol. 83, Iss. 2, pp. 219-236.e7
Open Access | Times Cited: 61
TDP-43-stratified single-cell proteomics of postmortem human spinal motor neurons reveals protein dynamics in amyotrophic lateral sclerosis
Amanda J. Guise, Santosh A. Misal, Richard H. Carson, et al.
Cell Reports (2024) Vol. 43, Iss. 1, pp. 113636-113636
Open Access | Times Cited: 23
RNA dysregulation in neurodegenerative diseases
Yini Li, Shuying Sun
The EMBO Journal (2025) Vol. 44, Iss. 3, pp. 613-638
Open Access | Times Cited: 3
Structural insights and milestones in TDP-43 research: A comprehensive review of its pathological and therapeutic advances
Mei Dang, Longjiang Wu, Xiaoying Zhang
International Journal of Biological Macromolecules (2025), pp. 141677-141677
Open Access | Times Cited: 2
Genetic Convergence Brings Clarity to the Enigmatic Red Line in ALS
Casey Cook, Leonard Petrucelli
Neuron (2019) Vol. 101, Iss. 6, pp. 1057-1069
Open Access | Times Cited: 125
Structural Properties and Interaction Partners of Familial ALS-Associated SOD1 Mutants
Jisen Huai, Zhongjian Zhang
Frontiers in Neurology (2019) Vol. 10
Open Access | Times Cited: 91
An Intramolecular Salt Bridge Linking TDP43 RNA Binding, Protein Stability, and TDP43-Dependent Neurodegeneration
Brittany Flores, Xingli Li, Ahmed M. Malik, et al.
Cell Reports (2019) Vol. 27, Iss. 4, pp. 1133-1150.e8
Open Access | Times Cited: 86
Nucleocytoplasmic Proteomic Analysis Uncovers eRF1 and Nonsense-Mediated Decay as Modifiers of ALS/FTD C9orf72 Toxicity
Juan A. Ortega, Elizabeth L. Daley, Sukhleen Kour, et al.
Neuron (2020) Vol. 106, Iss. 1, pp. 90-107.e13
Open Access | Times Cited: 78
TDP-43 mutations link Amyotrophic Lateral Sclerosis with R-loop homeostasis and R loop-mediated DNA damage
Marta Giannini, Aleix Bayona‐Feliú, Daisy Sproviero, et al.
PLoS Genetics (2020) Vol. 16, Iss. 12, pp. e1009260-e1009260
Open Access | Times Cited: 78
Loss of Tdp-43 disrupts the axonal transcriptome of motoneurons accompanied by impaired axonal translation and mitochondria function
Michael Briese, Lena Saal-Bauernschubert, Patrick Lüningschrör, et al.
Acta Neuropathologica Communications (2020) Vol. 8, Iss. 1
Open Access | Times Cited: 75
ALS/FTD-associated protein FUS induces mitochondrial dysfunction by preferentially sequestering respiratory chain complex mRNAs
Yueh-Lin Tsai, Tristan H. Coady, Lei Lü, et al.
Genes & Development (2020) Vol. 34, Iss. 11-12, pp. 785-805
Open Access | Times Cited: 71
Molecular Mechanisms Underlying TDP-43 Pathology in Cellular and Animal Models of ALS and FTLD
Alistair Wood, Yuval Gurfinkel, Nicole Polain, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 9, pp. 4705-4705
Open Access | Times Cited: 70
Nuclear RNA binding regulates TDP-43 nuclear localization and passive nuclear export
Lauren Duan, Benjamin L. Zaepfel, Vasilisa Aksenova, et al.
Cell Reports (2022) Vol. 40, Iss. 3, pp. 111106-111106
Open Access | Times Cited: 69
The Link between Oxidative Stress, Redox Status, Bioenergetics and Mitochondria in the Pathophysiology of ALS
Elena Obrador, Rosario Salvador‐Palmer, Rafael López‐Blanch, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 12, pp. 6352-6352
Open Access | Times Cited: 68
TDP-43 pathology: From noxious assembly to therapeutic removal
Sean S. Keating, Rebecca San Gil, Molly E. V. Swanson, et al.
Progress in Neurobiology (2022) Vol. 211, pp. 102229-102229
Closed Access | Times Cited: 55
Cryptic exon detection and transcriptomic changes revealed in single-nuclei RNA sequencing of C9ORF72 patients spanning the ALS-FTD spectrum
Lauren M. Gittings, Eric Alsop, Jerry Antone, et al.
Acta Neuropathologica (2023) Vol. 146, Iss. 3, pp. 433-450
Open Access | Times Cited: 28
Unraveling the Genetic Landscape of Neurological Disorders: Insights into Pathogenesis, Techniques for Variant Identification, and Therapeutic Approaches
Zeba Firdaus, Xiaogang Li
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2320-2320
Open Access | Times Cited: 14
FDA-approved disulfiram inhibits the NLRP3 inflammasome by regulating NLRP3 palmitoylation
Jie Xu, Joseph M. Pickard, Gabriel Núñez
Cell Reports (2024) Vol. 43, Iss. 8, pp. 114609-114609
Open Access | Times Cited: 11
TDP-43 proteinopathy in ALS is triggered by loss of ASRGL1 and associated with HML-2 expression
Marta García‐Montojo, Saeed Fathi, Cyrus Rastegar, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 10
RNA methylation modifications in neurodegenerative diseases: Focus on their enzyme system
Lu Liu, Yujia Zhao, Feng Zhang
Journal of Advanced Research (2025)
Open Access | Times Cited: 1
Amyotrophic lateral sclerosis caused by TARDBP mutations: from genetics to TDP-43 proteinopathy
Rubika Balendra, Jemeen Sreedharan, Martina Hallegger, et al.
The Lancet Neurology (2025) Vol. 24, Iss. 5, pp. 456-470
Closed Access | Times Cited: 1
Proteomics Approaches for Biomarker and Drug Target Discovery in ALS and FTD
Thomas J. Hedl, Rebecca San Gil, Flora Cheng, et al.
Frontiers in Neuroscience (2019) Vol. 13
Open Access | Times Cited: 75
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