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:

Pathogenesis of FUS-associated ALS and FTD: insights from rodent models
Matthew Nolan, Kevin Talbot, Olaf Ansorge
Acta Neuropathologica Communications (2016) Vol. 4, Iss. 1
Open Access | Times Cited: 117

Showing 1-25 of 117 citing articles:

ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?
Rita Mejzini, Loren L. Flynn, Ianthe Pitout, et al.
Frontiers in Neuroscience (2019) Vol. 13
Open Access | Times Cited: 658

Animal models of neurodegenerative diseases
Ted M. Dawson, Todd E. Golde, Clotilde Lagier‐Tourenne
Nature Neuroscience (2018) Vol. 21, Iss. 10, pp. 1370-1379
Open Access | Times Cited: 491

RNA-binding proteins in neurodegeneration: mechanisms in aggregate
Erin G. Conlon, James L. Manley
Genes & Development (2017) Vol. 31, Iss. 15, pp. 1509-1528
Open Access | Times Cited: 204

Genetic mutations in RNA-binding proteins and their roles in ALS
Katannya Kapeli, Fernando J. Martínez, G Yeo
Human Genetics (2017) Vol. 136, Iss. 9, pp. 1193-1214
Open Access | Times Cited: 190

Mutant FUS causes DNA ligation defects to inhibit oxidative damage repair in Amyotrophic Lateral Sclerosis
Haibo Wang, Wenting Guo, Joy Mitra, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 180

Modelling amyotrophic lateral sclerosis: progress and possibilities
Philip Van Damme, Wim Robberecht, Ludo Van Den Bosch
Disease Models & Mechanisms (2017) Vol. 10, Iss. 5, pp. 537-549
Open Access | Times Cited: 177

FUS-ALS hiPSC-derived astrocytes impair human motor units through both gain-of-toxicity and loss-of-support mechanisms
Katarina Stoklund Dittlau, Lisanne Terrie, Pieter Baatsen, et al.
Molecular Neurodegeneration (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 45

Amyotrophic lateral sclerosis caused by FUS mutations: advances with broad implications
Thomas G. Moens, Sandrine Da Cruz, Manuela Neumann, et al.
The Lancet Neurology (2025) Vol. 24, Iss. 2, pp. 166-178
Closed Access | Times Cited: 4

Loss of Dynamic RNA Interaction and Aberrant Phase Separation Induced by Two Distinct Types of ALS/FTD-Linked FUS Mutations
Amirhossein Ghanbari Niaki, Jaya Sarkar, Xinyi Cai, et al.
Molecular Cell (2019) Vol. 77, Iss. 1, pp. 82-94.e4
Open Access | Times Cited: 143

Mouse models of ALS: Past, present and future
Cathleen Lutz
Brain Research (2018) Vol. 1693, pp. 1-10
Closed Access | Times Cited: 109

Linking hnRNP Function to ALS and FTD Pathology
Maria D. Purice, J. Paul Taylor
Frontiers in Neuroscience (2018) Vol. 12
Open Access | Times Cited: 109

Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in ‘FUSDelta14’ knockin mice
Anny Devoy, Bernadett Kalmár, Michelle Stewart, et al.
Brain (2017) Vol. 140, Iss. 11, pp. 2797-2805
Open Access | Times Cited: 104

The role of hnRNPs in frontotemporal dementia and amyotrophic lateral sclerosis
Alexander Bampton, Lauren M. Gittings, Pietro Fratta, et al.
Acta Neuropathologica (2020) Vol. 140, Iss. 5, pp. 599-623
Open Access | Times Cited: 97

Synapses in neurodegenerative diseases
Jae Ryul Bae, Sung Hyun Kim
BMB Reports (2017) Vol. 50, Iss. 5, pp. 237-246
Open Access | Times Cited: 96

Inhibiting p38 MAPK alpha rescues axonal retrograde transport defects in a mouse model of ALS
Katherine L. Gibbs, Bernadett Kalmár, Elena R. Rhymes, et al.
Cell Death and Disease (2018) Vol. 9, Iss. 6
Open Access | Times Cited: 94

RNA-binding proteins in neurological development and disease
Shavanie Prashad, Pallavi P. Gopal
RNA Biology (2020) Vol. 18, Iss. 7, pp. 972-987
Open Access | Times Cited: 94

The role of amyloid oligomers in neurodegenerative pathologies
Cameron I. Wells, Samuel Brennan, Matt Keon, et al.
International Journal of Biological Macromolecules (2021) Vol. 181, pp. 582-604
Open Access | Times Cited: 83

Nearly 30 Years of Animal Models to Study Amyotrophic Lateral Sclerosis: A Historical Overview and Future Perspectives
Tiziana Bonifacino, Roberta Arianna Zerbo, Matilde Balbi, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 22, pp. 12236-12236
Open Access | Times Cited: 64

Direct and Indirect Protein Interactions Link FUS Aggregation to Histone Post-Translational Modification Dysregulation and Growth Suppression in an ALS/FTD Yeast Model
Seth A. Bennett, Samantha N. Cobos, Raven M. A. Fisher, et al.
Journal of Fungi (2025) Vol. 11, Iss. 1, pp. 58-58
Open Access | Times Cited: 1

Implications of Microglia in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
Henriette Haukedal, Kristine Freude
Journal of Molecular Biology (2019) Vol. 431, Iss. 9, pp. 1818-1829
Closed Access | Times Cited: 62

Nucleocytoplasmic Transport: Regulatory Mechanisms and the Implications in Neurodegeneration
Baojin Ding, Masood Sepehrimanesh
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 8, pp. 4165-4165
Open Access | Times Cited: 53

The RGG motif proteins: Interactions, functions, and regulations
Mashiat N. Chowdhury, Hong Jin
Wiley Interdisciplinary Reviews - RNA (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 37

Towards Personalized Allele-Specific Antisense Oligonucleotide Therapies for Toxic Gain-of-Function Neurodegenerative Diseases
Jacob Helm, Lüdger Schöls, Stefan Hauser
Pharmaceutics (2022) Vol. 14, Iss. 8, pp. 1708-1708
Open Access | Times Cited: 34

Drug Discovery and Development Targeting Dementia
Agnieszka Zagórska, Anna Czopek, Monika Fryc, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 2, pp. 151-151
Open Access | Times Cited: 20

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