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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:

Fly for ALS: Drosophila modeling on the route to amyotrophic lateral sclerosis modifiers
Francesco Liguori, Susanna Amadio, Cinzia Volonté
Cellular and Molecular Life Sciences (2021) Vol. 78, Iss. 17-18, pp. 6143-6160
Open Access | Times Cited: 30

Showing 1-25 of 30 citing articles:

Human stem cell models of neurodegeneration: From basic science of amyotrophic lateral sclerosis to clinical translation
Elisa Giacomelli, Björn F. Vahsen, Elizabeth L. Calder, et al.
Cell stem cell (2022) Vol. 29, Iss. 1, pp. 11-35
Open Access | Times Cited: 66
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: 63
ALS ‐linked KIF5A ΔExon27 mutant causes neuronal toxicity through gain‐of‐function
Devesh C. Pant, Janani Parameswaran, Lu Rao, et al.
EMBO Reports (2022) Vol. 23, Iss. 8
Open Access | Times Cited: 42
PP2A and GSK3 act as modifiers of FUS-ALS by modulating mitochondrial transport
Paraskevi Tziortzouda, Jolien Steyaert, Wendy Scheveneels, et al.
Acta Neuropathologica (2024) Vol. 147, Iss. 1
Open Access | Times Cited: 5
Patient-derived induced pluripotent stem cell organoids for amyotrophic lateral sclerosis drug discovery
Wenyan Li, Jinqi Liu, Wenting Li, et al.
Acta Materia Medica (2025) Vol. 4, Iss. 1
Open Access
Precise measurement of motor neuron dysfunction in Drosophila ALS model via climbing assay and leg imaging
Yanan Wei, Hongyu Miao, Hadi Najafi, et al.
Methods in cell biology (2025)
Closed Access
CRISPR and iPSCs: Recent Developments and Future Perspectives in Neurodegenerative Disease Modelling, Research, and Therapeutics
Tirthankar Sen, Rajkumar P. Thummer
Neurotoxicity Research (2022) Vol. 40, Iss. 5, pp. 1597-1623
Open Access | Times Cited: 21
Pan-neuronal expression of human mutant SOD1 in Drosophila impairs survival and motor performance, induces early neuroinflammation and chromosome aberrations
Francesco Liguori, Francesca Alberti, Susanna Amadio, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2024) Vol. 1870, Iss. 5, pp. 167192-167192
Open Access | Times Cited: 4
Black chokeberry (×Sorbaronia mitschurinii) fruit extract affects the survival of Drosophila melanogaster with the model of amyotrophic lateral sclerosis depending on the concentration
Nadezhda Zemskaya, E. Platonova, N. Pakshina, et al.
Proceedings of the Komi Science Centre of the Ural Division of the Russian Academy of Sciences (2025), Iss. 9, pp. 84-91
Closed Access
The Genetics of Diabetes: What We Can Learn from Drosophila
Francesco Liguori, Elisa Mascolo, Fiammetta Vernı̀
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 20, pp. 11295-11295
Open Access | Times Cited: 20
IL-33/ST2 Axis: A Potential Therapeutic Target in Neurodegenerative Diseases
Zexi Jia, Mengtian Guo, Xintong Ge, et al.
Biomolecules (2023) Vol. 13, Iss. 10, pp. 1494-1494
Open Access | Times Cited: 7
In Vivo Animal Models Development and Their Limitations for Brain Research
Shubhada Mangrulkar, Shalakha V. Dabhekar, Pankaj Neje, et al.
(2024), pp. 315-339
Closed Access | Times Cited: 2
Small molecules targeting different cellular pathologies for the treatment of amyotrophic lateral sclerosis
Mohamed F. El‐Mansy, Cory T. Reidl, Mizzanoor Rahaman, et al.
Medicinal Research Reviews (2023) Vol. 43, Iss. 6, pp. 2260-2302
Open Access | Times Cited: 6
A Novel Drosophila-based Drug Repurposing Platform Identified Fingolimod As a Potential Therapeutic for TDP-43 Proteinopathy
Luca Lo Piccolo, Takanari Umegawachi, Ranchana Yeewa, et al.
Neurotherapeutics (2023) Vol. 20, Iss. 5, pp. 1330-1346
Open Access | Times Cited: 4
A comprehensive review of electrophysiological techniques in amyotrophic lateral sclerosis research
Keyuan Ren, Qinglong Wang, Douglas Jiang, et al.
Frontiers in Cellular Neuroscience (2024) Vol. 18
Open Access | Times Cited: 1
Inter-Species Rescue of Mutant Phenotype—The Standard for Genetic Analysis of Human Genetic Disorders in Drosophila melanogaster Model
Alexandru Al. Ecovoiu, Attila Cristian Rațiu, Miruna Mihaela Micheu, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 5, pp. 2613-2613
Open Access | Times Cited: 6
ALS-linked KIF5A ΔExon27 mutant causes neuronal toxicity through gain of function
Devesh C. Pant, Janani Parameswaran, Lu Rao, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Closed Access | Times Cited: 6
The international exchange of Drosophila melanogaster strains
Kevin R Cook, Annette L. Parks
Revue Scientifique et Technique de l OIE (2022) Vol. 41, Iss. 1, pp. 82-90
Open Access | Times Cited: 6
Drosophila as a Model for Human Viral Neuroinfections
Ilena Benoit, Domenico Di Curzio, Alberto Civetta, et al.
Cells (2022) Vol. 11, Iss. 17, pp. 2685-2685
Open Access | Times Cited: 5
Functional characterisation of the ACE2 orthologues in Drosophila provides insights into the neuromuscular complications of COVID-19
P. Herrera, Ruben J. Cauchi
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2023) Vol. 1869, Iss. 8, pp. 166818-166818
Open Access | Times Cited: 2
Animal Models of FUS-Proteinopathy: A Systematic Review
Alexander P. Rezvykh, Daniil Shteinberg, Evgeny V. Bronovitsky, et al.
Biochemistry (Moscow) (2024) Vol. 89, Iss. S1, pp. S34-S56
Closed Access
Boosting life sciences research in Brazil: building a case for a local Drosophila stock center
Marcos T. Oliveira, Lucas Anhezini, Helena Araujo, et al.
Genetics and Molecular Biology (2024) Vol. 47, Iss. 1
Open Access
Analysis of asymptomatic Drosophila models for ALS and SMA reveals convergent impact on functional protein complexes linked to neuro-muscular degeneration
Marina L. García‐Vaquero, M. Heim, Barbara Flix, et al.
BMC Genomics (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 1
Hereditary motor and sensory neuropathy with SOD1-mutant: A case report
Zhong Luo, Linhai Zhang, Juan Yang, et al.
Medicine (2022) Vol. 101, Iss. 43, pp. e31378-e31378
Open Access | Times Cited: 2
Surface glia predominantly contribute to the development of ALS/FTD in Drosophila model
Brittany Anne Snow, Ciara Crowley Stevenson, Jasdeep Kaur, et al.
Research Square (Research Square) (2022)
Open Access | Times Cited: 2
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