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:

The Role of Nucleocytoplasmic Transport Defects in Amyotrophic Lateral Sclerosis
J. Vanneste, Ludo Van Den Bosch
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 22, pp. 12175-12175
Open Access | Times Cited: 23

Showing 23 citing articles:

Genetics of amyotrophic lateral sclerosis: seeking therapeutic targets in the era of gene therapy
Naoki Suzuki, Ayumi Nishiyama, Hitoshi Warita, et al.
Journal of Human Genetics (2022) Vol. 68, Iss. 3, pp. 131-152
Open Access | Times Cited: 92

Current State and Future Directions in the Therapy of ALS
Laura Tzeplaeff, Sibylle Wilfling, Maria Viktoria Requardt, et al.
Cells (2023) Vol. 12, Iss. 11, pp. 1523-1523
Open Access | Times Cited: 55

Molecular Chaperones’ Potential against Defective Proteostasis of Amyotrophic Lateral Sclerosis
Sumit Kinger, Ankur Rakesh Dubey, Prashant Kumar, et al.
Cells (2023) Vol. 12, Iss. 9, pp. 1302-1302
Open Access | Times Cited: 13

Genetic Risk of Axonal Neuropathy Following Infection
J. Robert Harkness, John McDermott, Shea Marsden, et al.
(2025)
Open Access

Emerging Connections between Nuclear Pore Complex Homeostasis and ALS
Sunandini Chandra, C. Patrick Lusk
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 3, pp. 1329-1329
Open Access | Times Cited: 21

VRK1 variants at the cross road of Cajal body neuropathogenic mechanisms in distal neuropathies and motor neuron diseases
Pedro A. Lazo, Patricia Morejón‐García
Neurobiology of Disease (2023) Vol. 183, pp. 106172-106172
Open Access | Times Cited: 11

Mitochondrial Dysfunction in Sporadic Amyotrophic Lateral Sclerosis Patients: Insights from High-Resolution Respirometry
Petra Parvanovova, Andrea Evinová, Milan Grofik, et al.
Biomedicines (2024) Vol. 12, Iss. 6, pp. 1294-1294
Open Access | Times Cited: 3

Understanding Amyotrophic Lateral Sclerosis: Pathophysiology, Diagnosis, and Therapeutic Advances
Radu Eugen Rizea, Antonio-Daniel Corlatescu, Horia Petre Costin, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 18, pp. 9966-9966
Open Access | Times Cited: 3

Nucleoporin Nsp1 surveils the phase state of FG-Nups
Tegan A. Otto, Tessa Bergsma, Maurice Dekker, et al.
Cell Reports (2024) Vol. 43, Iss. 10, pp. 114793-114793
Open Access | Times Cited: 3

Nucleoporin Nsp1 surveils the phase state of FG-Nups
Tegan A. Otto, Tessa Bergsma, Maurice Dekker, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 8

Pathological mechanisms of amyotrophic lateral sclerosis
Yushu Hu, Wenzhi Chen, Caihui Wei, et al.
Neural Regeneration Research (2023) Vol. 19, Iss. 5, pp. 1036-1044
Open Access | Times Cited: 7

Unraveling the Multifaceted Insights into Amyotrophic Lateral Sclerosis: Genetic Underpinnings, Pathogenesis, and Therapeutic Horizons
Ramaish Sharma, Zuber Khan, Sidharth Mehan, et al.
Mutation Research/Reviews in Mutation Research (2024) Vol. 794, pp. 108518-108518
Closed Access | Times Cited: 2

Nuclear transport under stress phenocopies transport defects in models of C9Orf72 ALS
Marije F. W. Semmelink, Hamidreza Jafarinia, Justina C. Wolters, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 9

Measuring and Interpreting Nuclear Transport in Neurodegenerative Disease—The Example of C9orf72 ALS
Marije F. W. Semmelink, Anton Steen, Liesbeth M. Veenhoff
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 17, pp. 9217-9217
Open Access | Times Cited: 12

Evidence of mitochondrial dysfunction in ALS and methods for measuring in model systems
James Lee, Natalie Pye, Laura V. Ellis, et al.
International review of neurobiology (2024), pp. 269-325
Closed Access | Times Cited: 1

Cellular Stress Induces Nucleocytoplasmic Transport Deficits Independent of Stress Granules
J. Vanneste, Thomas Vercruysse, Steven Boeynaems, et al.
Biomedicines (2022) Vol. 10, Iss. 5, pp. 1057-1057
Open Access | Times Cited: 6

A comparison study of pathological features and drug efficacy between Drosophila models of C9orf72 ALS/FTD
Davin Lee, Hae Chan Jeong, Seung Yeol Kim, et al.
Molecules and Cells (2023) Vol. 47, Iss. 1, pp. 100005-100005
Open Access | Times Cited: 2

Genetic Risk of Axonal Neuropathy Following Infection
J. Robert Harkness, John McDermott, Shea Marsden, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access

Ibetazol, a novel inhibitor of importin β1-mediated nuclear import
Thomas Vercruysse, Els Vanstreels, Maarten Jacquemyn, et al.
Communications Biology (2024) Vol. 7, Iss. 1
Closed Access

SUMO modification in Huntington's disease: Unraveling complex mechanisms for therapeutic insights
Charlene Smith, Joan S. Steffan, Leslie M. Thompson
Elsevier eBooks (2024), pp. 259-283
Closed Access

Proteomics Analysis of Lymphoblastoid Cell Lines from Patients with Amyotrophic Lateral Sclerosis
Danielle Whitham, Eugene Belenkiy, Costel C. Darie, et al.
Molecules (2023) Vol. 28, Iss. 5, pp. 2014-2014
Open Access

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