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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:

Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms
Hyunglok Chung, Michael F. Wangler, Paul C. Marcogliese, et al.
Neuron (2020) Vol. 106, Iss. 4, pp. 589-606.e6
Open Access | Times Cited: 104

Showing 1-25 of 104 citing articles:

Peroxisomal β-oxidation acts as a sensor for intracellular fatty acids and regulates lipolysis
Lianggong Ding, Wenfei Sun, Miroslav Baláž, et al.
Nature Metabolism (2021) Vol. 3, Iss. 12, pp. 1648-1661
Open Access | Times Cited: 145
Neuronal ROS-induced glial lipid droplet formation is altered by loss of Alzheimer’s disease–associated genes
Matthew J. Moulton, Scott Barish, Isha Ralhan, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 52
Open Access | Times Cited: 120
Antioxidant Therapy in Cancer: Rationale and Progress
Maochao Luo, Li Zhou, Zhao Huang, et al.
Antioxidants (2022) Vol. 11, Iss. 6, pp. 1128-1128
Open Access | Times Cited: 115
Peroxisomes as cellular adaptors to metabolic and environmental stress
Anyuan He, John M. Dean, Irfan J. Lodhi
Trends in Cell Biology (2021) Vol. 31, Iss. 8, pp. 656-670
Open Access | Times Cited: 106
Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision
Dustin Baldridge, Michael F. Wangler, Angela N. Bowman, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 72
Ensheathment and Myelination of Axons: Evolution of Glial Functions
Klaus‐Armin Nave, Hauke Werner
Annual Review of Neuroscience (2021) Vol. 44, Iss. 1, pp. 197-219
Closed Access | Times Cited: 68
Myelin lipid metabolism and its role in myelination and myelin maintenance
Joseph A. Barnes-Vélez, Fatma Betul Aksoy Yasar, Jian Hu
The Innovation (2022) Vol. 4, Iss. 1, pp. 100360-100360
Open Access | Times Cited: 46
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
Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases
Paul C. Marcogliese, Samantha L. Deal, Jonathan C. Andrews, et al.
Cell Reports (2022) Vol. 38, Iss. 11, pp. 110517-110517
Open Access | Times Cited: 39
Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation
Hyunglok Chung, Qi Ye, Ye-Jin Park, et al.
Cell Metabolism (2023) Vol. 35, Iss. 5, pp. 855-874.e5
Open Access | Times Cited: 34
Sphingolipids in neurodegenerative diseases
Xueyang Pan, Debdeep Dutta, Shenzhao Lu, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 24
Colonization of root endophytic fungus Serendipita indica improves drought tolerance of Pinus taeda seedlings by regulating metabolome and proteome
Chu Wu, Yujie Yang, Yun Wang, et al.
Frontiers in Microbiology (2024) Vol. 15
Open Access | Times Cited: 11
Senolytic combination of dasatinib and quercetin attenuates renal damage in diabetic kidney disease
Guo-Xiu Li, Wen Si, Jiao Wang, et al.
Phytomedicine (2024) Vol. 130, pp. 155705-155705
Open Access | Times Cited: 11
Role of peroxisomes in the pathogenesis and therapy of renal fibrosis
Dan Zhang, Yang-He Zhang, Bin Liu, et al.
Metabolism (2025) Vol. 166, pp. 156173-156173
Closed Access | Times Cited: 1
Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures
Shenzhao Lu, Rebecca Hernan, Paul C. Marcogliese, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 4, pp. 571-586
Open Access | Times Cited: 31
Clinical genetics of Charcot–Marie–Tooth disease
Yujiro Higuchi, Hiroshi Takashima
Journal of Human Genetics (2022) Vol. 68, Iss. 3, pp. 199-214
Closed Access | Times Cited: 30
LC3-associated phagocytosis promotes glial degradation of axon debris after injury in Drosophila models
Áron Szabó, Virág Vincze, Aishwarya Chhatre, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 17
Using Drosophila to drive the diagnosis and understand the mechanisms of rare human diseases
Nichole Link, Hugo J. Bellen
Development (2020) Vol. 147, Iss. 21
Open Access | Times Cited: 48
'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: 24
Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling
Paul C. Marcogliese, Debdeep Dutta, Shrestha Sinha Ray, et al.
Science Advances (2022) Vol. 8, Iss. 3
Open Access | Times Cited: 23
The Astrocyte: Metabolic Hub of the Brain
L. Felipe Barros, Stefanie Schirmeier, Bruno Weber
Cold Spring Harbor Perspectives in Biology (2024) Vol. 16, Iss. 9, pp. a041355-a041355
Closed Access | Times Cited: 6
A novel missense variant in ACAA1 contributes to early-onset Alzheimer’s disease, impairs lysosomal function, and facilitates amyloid-β pathology and cognitive decline
Rongcan Luo, Yu Fan, Jing Yang, et al.
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 30
Downregulation of glial genes involved in synaptic function mitigates Huntington's disease pathogenesis
Tarik Seref Onur, Andrew Laitman, Zhao He, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 29
The murine retinal pigment epithelium requires peroxisomal β-oxidation to maintain lysosomal function and prevent dedifferentiation
Sai Kocherlakota, Yannick Das, Daniëlle Swinkels, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 43
Open Access | Times Cited: 12
Metabolic reprogramming: a new option for the treatment of spinal cord injury
Jiangjie Chen, Jinyang Chen, Chao Yu, et al.
Neural Regeneration Research (2024) Vol. 20, Iss. 4, pp. 1042-1057
Open Access | Times Cited: 4
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