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 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
Clotilde Lagier‐Tourenne, Magdalini Polymenidou, Don W. Cleveland
Human Molecular Genetics (2010) Vol. 19, Iss. R1, pp. R46-R64
Open Access | Times Cited: 947

Showing 26-50 of 947 citing articles:

Pre-mRNA splicing in disease and therapeutics
Ravi K. Singh, Thomas A. Cooper
Trends in Molecular Medicine (2012) Vol. 18, Iss. 8, pp. 472-482
Open Access | Times Cited: 414

TDP-43 promotes microRNA biogenesis as a component of the Drosha and Dicer complexes
Yukio Kawahara, Ai Mieda-Sato
Proceedings of the National Academy of Sciences (2012) Vol. 109, Iss. 9, pp. 3347-3352
Open Access | Times Cited: 400

RNA-binding proteins with prion-like domains in health and disease
Alice Ford Harrison, James Shorter
Biochemical Journal (2017) Vol. 474, Iss. 8, pp. 1417-1438
Open Access | Times Cited: 384

Phase Separation and Neurodegenerative Diseases: A Disturbance in the Force
Aurélie Zbinden, Manuela Pérez‐Berlanga, Pierre De Rossi, et al.
Developmental Cell (2020) Vol. 55, Iss. 1, pp. 45-68
Open Access | Times Cited: 384

A yeast functional screen predicts new candidate ALS disease genes
Julien Couthouis, Michael P. Hart, James Shorter, et al.
Proceedings of the National Academy of Sciences (2011) Vol. 108, Iss. 52, pp. 20881-20890
Open Access | Times Cited: 381

Risk factors for amyotrophic lateral sclerosis
Fang Fang, Caroline Ingre, Per M. Roos, et al.
Clinical Epidemiology (2015), pp. 181-181
Open Access | Times Cited: 381

Autophagy activators rescue and alleviate pathogenesis of a mouse model with proteinopathies of the TAR DNA-binding protein 43
I‐Fang Wang, Bo-Shen Guo, Yu‐Chih Liu, et al.
Proceedings of the National Academy of Sciences (2012) Vol. 109, Iss. 37, pp. 15024-15029
Open Access | Times Cited: 359

The Seeds of Neurodegeneration: Prion-like Spreading in ALS
Magdalini Polymenidou, Don W. Cleveland
Cell (2011) Vol. 147, Iss. 3, pp. 498-508
Open Access | Times Cited: 357

Therapeutic modulation of eIF2α phosphorylation rescues TDP-43 toxicity in amyotrophic lateral sclerosis disease models
Hyung‐Jun Kim, Alya R. Raphael, Eva LaDow, et al.
Nature Genetics (2013) Vol. 46, Iss. 2, pp. 152-160
Open Access | Times Cited: 356

TDP-43 represses cryptic exon inclusion in the FTD–ALS gene UNC13A
X. Rosa, Mercedes Prudencio, Yuka Koike, et al.
Nature (2022) Vol. 603, Iss. 7899, pp. 124-130
Open Access | Times Cited: 342

Understanding the role of TDP-43 and FUS/TLS in ALS and beyond
Sandrine Da Cruz, Don W. Cleveland
Current Opinion in Neurobiology (2011) Vol. 21, Iss. 6, pp. 904-919
Open Access | Times Cited: 341

TDP-43 Is Directed to Stress Granules by Sorbitol, a Novel Physiological Osmotic and Oxidative Stressor
Colleen M. Dewey, Basar Cenik, Chantelle F. Sephton, et al.
Molecular and Cellular Biology (2010) Vol. 31, Iss. 5, pp. 1098-1108
Open Access | Times Cited: 332

Evidence for an oligogenic basis of amyotrophic lateral sclerosis
Marka van Blitterswijk, Michael A. van Es, Eric A. M. Hennekam, et al.
Human Molecular Genetics (2012) Vol. 21, Iss. 17, pp. 3776-3784
Open Access | Times Cited: 324

Mutant induced pluripotent stem cell lines recapitulate aspects of TDP-43 proteinopathies and reveal cell-specific vulnerability
Bilada Bilican, Andrea Serio, Sami J. Barmada, et al.
Proceedings of the National Academy of Sciences (2012) Vol. 109, Iss. 15, pp. 5803-5808
Open Access | Times Cited: 324

The role of FUS gene variants in neurodegenerative diseases
Hao Deng, Kai Gao, Joseph Jankovic
Nature Reviews Neurology (2014) Vol. 10, Iss. 6, pp. 337-348
Closed Access | Times Cited: 317

The neurogenetics of alternative splicing
Celine K. Vuong, Douglas L. Black, Sika Zheng
Nature reviews. Neuroscience (2016) Vol. 17, Iss. 5, pp. 265-281
Open Access | Times Cited: 310

ALS Genetics: Gains, Losses, and Implications for Future Therapies
Garam Kım, Olivia Gautier, Eduardo Tassoni-Tsuchida, et al.
Neuron (2020) Vol. 108, Iss. 5, pp. 822-842
Open Access | Times Cited: 301

Motor neuron vulnerability and resistance in amyotrophic lateral sclerosis
Jik Nijssen, Laura H. Comley, Eva Hedlund
Acta Neuropathologica (2017) Vol. 133, Iss. 6, pp. 863-885
Open Access | Times Cited: 300

Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUS
Dorothee Dormann, Tobias Madl, Chiara F. Valori, et al.
The EMBO Journal (2012) Vol. 31, Iss. 22, pp. 4258-4275
Open Access | Times Cited: 294

An ALS-associated mutation affecting TDP-43 enhances protein aggregation, fibril formation and neurotoxicity
Weirui Guo, Yanbo Chen, Xiaohong Zhou, et al.
Nature Structural & Molecular Biology (2011) Vol. 18, Iss. 7, pp. 822-830
Open Access | Times Cited: 294

An acetylation switch controls TDP-43 function and aggregation propensity
Todd J. Cohen, Andrew Hwang, Clark R. Restrepo, et al.
Nature Communications (2015) Vol. 6, Iss. 1
Open Access | Times Cited: 293

MicroRNA biogenesis: regulating the regulators
Emily F. Finnegan, Amy E. Pasquinelli
Critical Reviews in Biochemistry and Molecular Biology (2012) Vol. 48, Iss. 1, pp. 51-68
Open Access | Times Cited: 286

Local RNA Translation at the Synapse and in Disease: Figure 1.
Liqun Liu‐Yesucevitz, Gary J. Bassell, Aaron D. Gitler, et al.
Journal of Neuroscience (2011) Vol. 31, Iss. 45, pp. 16086-16093
Open Access | Times Cited: 285

Genetics of familial amyotrophic lateral sclerosis
Paul N. Valdmanis, Guy A. Rouleau
Neurology (2008) Vol. 70, Iss. 2, pp. 144-152
Closed Access | Times Cited: 281

Emerging mechanisms of molecular pathology in ALS
Owen M. Peters, Mehdi Ghasemi, Robert H. Brown
Journal of Clinical Investigation (2015) Vol. 125, Iss. 5, pp. 1767-1779
Open Access | Times Cited: 279

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