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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:

Glial cells in the driver seat of leukodystrophy pathogenesis
Luis Garcia, Julia Hacker, Sunetra Sase, et al.
Neurobiology of Disease (2020) Vol. 146, pp. 105087-105087
Open Access | Times Cited: 22

Showing 22 citing articles:

White matter microglia heterogeneity in the CNS
Sandra Amor, Niamh B. McNamara, Emma Gerrits, et al.
Acta Neuropathologica (2021) Vol. 143, Iss. 2, pp. 125-141
Closed Access | Times Cited: 65
Role of glial cells in the generation of sex differences in neurodegenerative diseases and brain aging
Julie A. Chowen, Luis Miguel García‐Segura
Mechanisms of Ageing and Development (2021) Vol. 196, pp. 111473-111473
Open Access | Times Cited: 55
Human post-mortem organotypic brain slice cultures: a tool to study pathomechanisms and test therapies
Bonnie C. Plug, Ilma M. Revers, Marjolein Breur, et al.
Acta Neuropathologica Communications (2024) Vol. 12, Iss. 1
Open Access | Times Cited: 6
The Primary Microglial Leukodystrophies: A Review
Isidró Ferrer
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 11, pp. 6341-6341
Open Access | Times Cited: 19
Neuroglia in leukodystrophies
Elly M. Hol, Werner Dykstra, J. Chevalier, et al.
Handbook of clinical neurology (2025), pp. 159-175
Closed Access
Epigenetics and Neuroinflammation Associated With Neurodevelopmental Disorders: A Microglial Perspective
Munekazu Komada, Yuhei Nishimura
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 18
Modeling Developmental Brain Diseases Using Human Pluripotent Stem Cells-Derived Brain Organoids – Progress and Perspective
Afrin Bhattacharya, Wendy W. Y. Choi, Julien Muffat, et al.
Journal of Molecular Biology (2021) Vol. 434, Iss. 3, pp. 167386-167386
Closed Access | Times Cited: 23
Promoting remyelination in central nervous system diseases: potentials and prospects of natural products and herbal medicine
Hongru Zhu, En Hu, Xin Guo, et al.
Pharmacological Research (2024), pp. 107533-107533
Open Access | Times Cited: 2
The multicellular interplay of microglia in health and disease: lessons from leukodystrophy
Woutje M. Berdowski, Leslie E. Sanderson, Tjakko J. van Ham
Disease Models & Mechanisms (2021) Vol. 14, Iss. 8
Open Access | Times Cited: 13
Renewal of oligodendrocyte lineage reverses dysmyelination and CNS neurodegeneration through corrected N-acetylaspartate metabolism
Anoushka Lotun, Danning Li, Hongxia Xu, et al.
Progress in Neurobiology (2023) Vol. 226, pp. 102460-102460
Open Access | Times Cited: 5
Developmental regulation of zinc homeostasis in differentiating oligodendrocytes
Christopher M. Elitt, Madeline M. Ross, Jianlin Wang, et al.
Neuroscience Letters (2024) Vol. 831, pp. 137727-137727
Open Access | Times Cited: 1
Hematopoietic stem cell transplantation in leukodystrophies
Caroline Sevin, Fanny Mochel
Handbook of clinical neurology (2024), pp. 355-366
Closed Access | Times Cited: 1
Emerging Concepts in Vector Development for Glial Gene Therapy: Implications for Leukodystrophies
Georg von Jonquières, Caroline Rae, Gary D. Housley
Frontiers in Cellular Neuroscience (2021) Vol. 15
Open Access | Times Cited: 8
Human iPSC-Derived Astrocytes: A Powerful Tool to Study Primary Astrocyte Dysfunction in the Pathogenesis of Rare Leukodystrophies
Angela Lanciotti, Maria Stefania Brignone, Pompeo Macioce, et al.
International Journal of Molecular Sciences (2021) Vol. 23, Iss. 1, pp. 274-274
Open Access | Times Cited: 8
SCA34 caused by ELOVL4 L168F mutation is a lysosomal lipid storage disease sharing pathology features with neuronal ceroid lipofuscinosis and peroxisomal disorders
Benjamin Ellezam, Matsanga Leyila Kaseka, Dang Khoa Nguyen, et al.
Acta Neuropathologica (2023) Vol. 146, Iss. 2, pp. 337-352
Closed Access | Times Cited: 3
Delineating the epilepsy phenotype of NRROS-related microgliopathy: A case report and literature review
Priyanka Madaan, Yashovardhan Kaushal, Priyanka Srivastava, et al.
Seizure (2022) Vol. 100, pp. 15-20
Open Access | Times Cited: 5
Lethal adulthood myelin breakdown by oligodendrocyte-specific Ddx54 knockout
Hiroaki Oizumi, Yuki Miyamoto, Chika Seiwa, et al.
iScience (2023) Vol. 26, Iss. 10, pp. 107448-107448
Open Access | Times Cited: 2
Démarche diagnostique devant une leucodystrophie métabolique de l’adulte
Fanny Mochel
Pratique Neurologique - FMC (2024) Vol. 15, Iss. 1, pp. 9-21
Open Access
Neuropathology of white matter disorders
Zane Jaunmuktane
Handbook of clinical neurology (2024), pp. 3-20
Closed Access
Other diseases of the CNS
Alexei Verkhratsky, Arthur M. Butt
Neuroglia (2023), pp. 629-672
Open Access
Developmental regulation of zinc homeostasis in differentiating oligodendrocytes
Christopher M. Elitt, Madeline M. Ross, Jianlin Wang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
X-linked adrenoleukodystrophy in a pediatric patient: A case report
Graciela Arelí López Uriarte, Leonor G. Hinojosa-Amaya, Laura Gabriela Pena Baolboa, et al.
Medicina Universitaria (2021) Vol. 23, Iss. 2
Open Access
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