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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:

Downregulation of PMP22 ameliorates myelin defects in iPSC-derived human organoid cultures of CMT1A
Jonas Van Lent, Leen Vendredy, Elias Adriaenssens, et al.
Brain (2022) Vol. 146, Iss. 7, pp. 2885-2896
Open Access | Times Cited: 19

Showing 19 citing articles:

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: 11
Advances and challenges in modeling inherited peripheral neuropathies using iPSCs
Jonas Van Lent, Robert Prior, Gonzalo Pérez Siles, et al.
Experimental & Molecular Medicine (2024) Vol. 56, Iss. 6, pp. 1348-1364
Open Access | Times Cited: 8
PMP22 duplication dysregulates lipid homeostasis and plasma membrane organization in developing human Schwann cells
Robert Prior, Alessio Silva, Tim Vangansewinkel, et al.
Brain (2024) Vol. 147, Iss. 9, pp. 3113-3130
Open Access | Times Cited: 7
Charcot–Marie–Tooth neuropathies: Current gene therapy advances and the route toward translation
Marina Stavrou, Alexia Kagiava, Irene Sargiannidou, et al.
Journal of the Peripheral Nervous System (2023) Vol. 28, Iss. 2, pp. 150-168
Open Access | Times Cited: 16
Addressing Myelination Disorders: Novel Strategies using human 3D peripheral nerve model
Camille Loret, Camille Scherrer, Amandine Rovini, et al.
Brain Research Bulletin (2025) Vol. 222, pp. 111252-111252
Open Access
From in vivo models to in vitro bioengineered neuromuscular junctions for the study of Charcot-Marie-Tooth disease
Camille Scherrer, Camille Loret, Nicolas Védrenne, et al.
Journal of Tissue Engineering (2025) Vol. 16
Open Access
Advances in modeling the Charcot-Marie-Tooth disease: Human induced pluripotent stem cell-derived Schwann cells harboring SH3TC2 variants
Camille Loret, Camille Scherrer, Amandine Rovini, et al.
European Journal of Cell Biology (2025), pp. 151485-151485
Open Access
Unleashing the Power of Multiomics: Unraveling the Molecular Landscape of Peripheral Neuropathy
Julie Choi, Zitian Tang, Wendy Dong, et al.
Annals of Clinical and Translational Neurology (2025)
Open Access
Role of glial cells in motor neuron degeneration in hereditary spastic paraplegias
Manaswini Vijayaraghavan, S. R. Murali, Gitika Thakur, et al.
Frontiers in Cellular Neuroscience (2025) Vol. 19
Open Access
Brain organoids engineered to give rise to glia and neural networks after 90 days in culture exhibit human-specific proteoforms
Tyler J. Wenzel, Darrell D. Mousseau
Frontiers in Cellular Neuroscience (2024) Vol. 18
Open Access | Times Cited: 3
Schwann cells are axo-protective after injury irrespective of myelination status in mouse Schwann cell–neuron cocultures
Clara Mutschler, Shaline V. Fazal, Nathalie Schumacher, et al.
Journal of Cell Science (2023) Vol. 136, Iss. 18
Open Access | Times Cited: 6
Addressing Key Questions in Organoid Models: Who, Where, How, and Why?
María Gómez‐Álvarez, Marcos Agustina‐Hernández, Emilio Francés‐Herrero, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 21, pp. 16014-16014
Open Access | Times Cited: 4
Navigating the Landscape of CMT1B: Understanding Genetic Pathways, Disease Models, and Potential Therapeutic Approaches
Mary Kate McCulloch, Fatemeh Mehryab, Afrooz Rashnonejad
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 17, pp. 9227-9227
Open Access | Times Cited: 1
Distinct axo-protective and axo-destructive roles for Schwann cells after injury in a novel compartmentalised mouse myelinating coculture system
Clara Mutschler, Shaline V. Fazal, Nathalie Schumacher, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Using Human iPSC-Derived Peripheral Nervous System Disease Models for Drug Discovery
Yuan Gao
Handbook of experimental pharmacology (2023), pp. 191-205
Closed Access | Times Cited: 1
hESC- and hiPSC-derived Schwann cells are molecularly comparable and functionally equivalent
Kathryn R. Moss, Ruifa Mi, Riki Kawaguchi, et al.
iScience (2024) Vol. 27, Iss. 6, pp. 109855-109855
Open Access
Current Treatment Methods for Charcot–Marie–Tooth Diseases
Hongxian Dong, Boquan Qin, Hui Zhang, et al.
Biomolecules (2024) Vol. 14, Iss. 9, pp. 1138-1138
Open Access
Biomedical applications of organoids in genetic diseases
Wenhua Huang, Seogsong Jeong, Won‐Ho Kim, et al.
Medical Review (2024) Vol. 5, Iss. 2, pp. 152-163
Open Access
Protein expression profiles in brain organoids are more similar to those in human brain parenchyma than in mouse brain parenchyma
Tyler J. Wenzel, Darrell D. Mousseau
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
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