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-ing' from rare to common neurodegenerative disease mechanisms
Mengqi Ma, Matthew J. Moulton, Shenzhao Lu, et al.
Trends in Genetics (2022) Vol. 38, Iss. 9, pp. 972-984
Open Access | Times Cited: 23

Showing 23 citing articles:

Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans
Shinya Yamamoto, Oguz Kanca, Michael F. Wangler, et al.
Nature Reviews Genetics (2023) Vol. 25, Iss. 1, pp. 46-60
Closed Access | Times Cited: 42

Sphingolipids in neurodegenerative diseases
Xueyang Pan, Debdeep Dutta, Shenzhao Lu, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 24

Advanced Cellular Models for Rare Disease Study: Exploring Neural, Muscle and Skeletal Organoids
Cristina Bombieri, Andrea Corsi, Elisabetta Trabetti, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 2, pp. 1014-1014
Open Access | Times Cited: 9

Drosophila melanogaster as a versatile model organism to study genetic epilepsies: An overview
Florian P. Fischer, Robin A. Karge, Yvonne G. Weber, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 20

SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia
Siddharth Srivastava, Hagar Mor Shaked, Kenneth Gable, et al.
Brain (2023) Vol. 146, Iss. 4, pp. 1420-1435
Open Access | Times Cited: 17

De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement
Shenzhao Lu, Mengqi Ma, Xiao Mao, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 10, pp. 1932-1943
Open Access | Times Cited: 24

Restoration of Shal/KV4 proteostasis and motor function in a Drosophila model of spinocerebellar ataxia type 19/22
Cheng-Tsung Hsiao, Ssu‐Ju Fu, K. Cheng, et al.
Cellular and Molecular Life Sciences (2025) Vol. 82, Iss. 1
Open Access

Integrated regulation of dopaminergic and epigenetic effectors of neuroprotection in Parkinson’s disease models
J. Brucker Nourse, Shannon N. Russell, Nathan A. Moniz, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 7
Open Access | Times Cited: 8

Drosophila as a Model for Human Disease: Insights into Rare and Ultra-Rare Diseases
Sergio Casas‐Tintó
Insects (2024) Vol. 15, Iss. 11, pp. 870-870
Open Access | Times Cited: 2

Modeling neurodegenerative and neurodevelopmental disorders in theDrosophilamushroom body
Aaron Stahl, Seth M. Tomchik
Learning & Memory (2024) Vol. 31, Iss. 5, pp. a053816-a053816
Open Access | Times Cited: 2

Back to the future through the wormhole: Caenorhabditis elegans as a preclinical model
Guy A. Caldwell
Disease Models & Mechanisms (2023) Vol. 16, Iss. 6
Open Access | Times Cited: 4

Integrating massive RNA-seq data to elucidate transcriptome dynamics in Drosophila melanogaster
Sheng Hu Qian, Mengwei Shi, Dan‐Yang Wang, et al.
Briefings in Bioinformatics (2023) Vol. 24, Iss. 4
Open Access | Times Cited: 3

C9orf72 Toxic Species Affect ArfGAP-1 Function
Simona Rossi, Michela Di Salvio, Marilisa Balì, et al.
Cells (2023) Vol. 12, Iss. 15, pp. 2007-2007
Open Access | Times Cited: 2

Exploiting fly models to investigate rare human neurological disorders
Tomomi TANAKA, Hyunglok Chung
Neural Regeneration Research (2024) Vol. 20, Iss. 1, pp. 21-28
Open Access

Challenges and opportunities in neurodegenerative diseases management
Jehath Syed, S. C. Nemichandra, Sathvik Belagodu Sridhar, et al.
Elsevier eBooks (2024), pp. 559-586
Closed Access

Model organisms for investigating the functional involvement of NRF2 in non-communicable diseases.
Ana I. Rojo, Brigitta Buttari, Susana Cadenas, et al.
Redox Biology (2024) Vol. 79, pp. 103464-103464
Open Access

Genetic modifiers of synucleinopathies—lessons from experimental models
Rachel Min Qi Lee, Tong‐Wey Koh
Oxford Open Neuroscience (2023) Vol. 2
Open Access | Times Cited: 1

Intrinsic determinants of prion protein neurotoxicity in Drosophila: from sequence to (dys)function
Alessandro Cembran, Pedro Fernández-Fúnez
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 1

Unraveling the link between Neuropathy Target Esterase NTE/SWS, lysosomal storage diseases, inflammation, and abnormal fatty acid metabolism
Mariana I Tsap, Andriy S. Yatsenko, Jan Hegermann, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access

Neuronal LRP4 directs the development, maturation, and cytoskeletal organization of peripheral synapses
Alison T. DePew, Joseph Bruckner, Kate M. O’Connor-Giles, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access

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