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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:

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 26-50 of 117 citing articles:

Artificial MicroRNAs Targeting C9orf72 Can Reduce Accumulation of Intra-nuclear Transcripts in ALS and FTD Patients
Raygene Martier, Jolanda M.P. Liefhebber, Jana Miniarikova, et al.
Molecular Therapy — Nucleic Acids (2019) Vol. 14, pp. 593-608
Open Access | Times Cited: 51
Lysine acetylation regulates the RNA binding, subcellular localization and inclusion formation of FUS
Alexandra Arenas, Jing Chen, Lisha Kuang, et al.
Human Molecular Genetics (2020) Vol. 29, Iss. 16, pp. 2684-2697
Open Access | Times Cited: 43
The FUS gene is dual‐coding with both proteins contributing to FUS ‐mediated toxicity
Marie A. Brunet, Jean‐François Jacques, Sonya Nassari, et al.
EMBO Reports (2020) Vol. 22, Iss. 1
Open Access | Times Cited: 41
Differential roles for DNAJ isoforms in HTT-polyQ and FUS aggregation modulation revealed by chaperone screens
Kinneret Rozales, Amal Younis, Naseeb Saida, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 25
Pathological insights from amyotrophic lateral sclerosis animal models: comparisons, limitations, and challenges
Longhong Zhu, Shihua Li, Xiao‐Jiang Li, et al.
Translational Neurodegeneration (2023) Vol. 12, Iss. 1
Open Access | Times Cited: 15
Amyotrophic lateral sclerosis represents corticomotoneuronal system failure
Andrew Eisen, Steve Vucic, Matthew C. Kiernan
Muscle & Nerve (2024)
Open Access | Times Cited: 6
A Review of Biomarkers of Amyotrophic Lateral Sclerosis: A Pathophysiologic Approach
Rawiah S. Alshehri, Ahmad R. Abuzinadah, Moafaq S. Alrawaili, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 20, pp. 10900-10900
Open Access | Times Cited: 5
Emerging small-molecule therapeutic approaches for amyotrophic lateral sclerosis and frontotemporal dementia
Dean G. Brown, James Shorter, Heike J. Wobst
Bioorganic & Medicinal Chemistry Letters (2019) Vol. 30, Iss. 4, pp. 126942-126942
Closed Access | Times Cited: 43
FUS-induced neurotoxicity in Drosophila is prevented by downregulating nucleocytoplasmic transport proteins
Jolien Steyaert, Wendy Scheveneels, J. Vanneste, et al.
Human Molecular Genetics (2018)
Open Access | Times Cited: 41
Synaptic FUS Localization During Motoneuron Development and Its Accumulation in Human ALS Synapses
Dhruva Deshpande, Julia Higelin, Michael Schoen, et al.
Frontiers in Cellular Neuroscience (2019) Vol. 13
Open Access | Times Cited: 38
The Need for Biomarkers in the ALS–FTD Spectrum: A Clinical Point of View on the Role of Proteomics
Francesca Vignaroli, Angelica Mele, Giacomo Tondo, et al.
Proteomes (2023) Vol. 11, Iss. 1, pp. 1-1
Open Access | Times Cited: 12
Regulation of DNA damage response by RNA/DNA-binding proteins: Implications for neurological disorders and aging
Manohar Kodavati, Vikas H. Maloji Rao, Vincent Provasek, et al.
Ageing Research Reviews (2024) Vol. 100, pp. 102413-102413
Closed Access | Times Cited: 4
Neuroinflammation in Amyotrophic Lateral Sclerosis: Role of Redox (dys)Regulation
Nadia D’Ambrosi, Mauro Cozzolino, Maria Teresa Carrı̀
Antioxidants and Redox Signaling (2017) Vol. 29, Iss. 1, pp. 15-36
Closed Access | Times Cited: 38
Biomarkers in Human Peripheral Blood Mononuclear Cells: The State of the Art in Amyotrophic Lateral Sclerosis
Orietta Pansarasa, Maria Garofalo, Eveljn Scarian, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 5, pp. 2580-2580
Open Access | Times Cited: 18
Interactions of amyloid coaggregates with biomolecules and its relevance to neurodegeneration
Kazuma Murakami, Kenjiro Ono
The FASEB Journal (2022) Vol. 36, Iss. 9
Open Access | Times Cited: 17
Neural circuit and synaptic dysfunctions in ALS-FTD pathology
Santiago Mora, Ilary Allodi
Frontiers in Neural Circuits (2023) Vol. 17
Open Access | Times Cited: 11
Investigation of the role of miRNA variants in neurodegenerative brain diseases
Alexandros Frydas, Rita Cacace, Julie van der Zee, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
Amyotrophic Lateral Sclerosis: Focus on Cytoplasmic Trafficking and Proteostasis
Shrilaxmi Ms, Saradindu Banerjee, Santosh R. D’Mello, et al.
Molecular Neurobiology (2025)
Open Access
Protein Misfolding and Aggregation as a Mechanistic Link Between Chronic Pain and Neurodegenerative Diseases
Nebojša Brezić, Strahinja Gligorevic, Aleksandar Sič, et al.
Current Issues in Molecular Biology (2025) Vol. 47, Iss. 4, pp. 259-259
Open Access
Molecular Mechanisms of Protein Aggregation in ALS-FTD: Focus on TDP-43 and Cellular Protective Responses
Enza Maria Verde, Valentina Secco, Andrea Ghezzi, et al.
Cells (2025) Vol. 14, Iss. 10, pp. 680-680
Open Access
Mistranslation and ageing unmask FUS and TDP-43 toxicity in yeast models of neurodegenerative diseases
David C. McDonald, Nikita Chugh, Rares Sava, et al.
(2025)
Closed Access
DNA nanoflower Oligo-PROTAC for targeted degradation of FUS to treat neurodegenerative diseases
Ruixin Ge, Miao Chen, Sijin Wu, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Genetic Basis of Motor Neuron Diseases: Insights, Clinical Management, and Future Directions
Apostolos Antonakoudis, Stella Aikaterini Kyriakoudi, Despoina Chatzi, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 10, pp. 4904-4904
Open Access
Overexpression of HSP70 in mice with mutant FUS protein is accompanied by a mitigated neurodegeneration in limbic system
Gennadii Piavchenko, K. S. Pokidova, E. A. Kuzmin, et al.
Sechenov Medical Journal (2025) Vol. 16, Iss. 1, pp. 4-19
Open Access
Functional interaction between FUS and SMN underlies SMA-like splicing changes in wild-type hFUS mice
Alessia Mirra, Simona Rossi, Silvia Scaricamazza, et al.
Scientific Reports (2017) Vol. 7, Iss. 1
Open Access | Times Cited: 31

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