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:

Stage-specific control of oligodendrocyte survival and morphogenesis by TDP-43
Dongeun Heo, Jonathan P. Ling, Gian C Molina-Castro, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 29

Showing 1-25 of 29 citing articles:

The era of cryptic exons: implications for ALS-FTD
Puja R. Mehta, Anna‐Leigh Brown, Michael E. Ward, et al.
Molecular Neurodegeneration (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 60

TDP-43 and other hnRNPs regulate cryptic exon inclusion of a key ALS/FTD risk gene, UNC13A
Yuka Koike, Sarah Pickles, Virginia Estades Ayuso, et al.
PLoS Biology (2023) Vol. 21, Iss. 3, pp. e3002028-e3002028
Open Access | Times Cited: 28

White matter injury across neurodegenerative disease
Lindsay Festa, Judith B. Grinspan, Kelly L. Jordan‐Sciutto
Trends in Neurosciences (2023) Vol. 47, Iss. 1, pp. 47-57
Closed Access | Times Cited: 23

A transient protein folding response targets aggregation in the early phase of TDP-43-mediated neurodegeneration
Rebecca San Gil, Dana Pascovici, Juliana Venturato, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 12

TDP-43 dysregulation and neuromuscular junction disruption in amyotrophic lateral sclerosis
Sarah Lépine, María José Castellanos‐Montiel, Thomas M. Durcan
Translational Neurodegeneration (2022) Vol. 11, Iss. 1
Open Access | Times Cited: 25

TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43
Juan M. Godoy-Corchuelo, Zeinab Ali, José Miguel Brito Armas, et al.
Neurobiology of Disease (2024) Vol. 193, pp. 106437-106437
Open Access | Times Cited: 5

Challenges of modelling TDP-43 pathology in mice
José Miguel Brito Armas, Lucas Taoro-González, Elizabeth Fisher, et al.
Mammalian Genome (2025)
Open Access

TDP‐43 Cryptic RNAs in Perry Syndrome: Differences across Brain Regions and TDP‐43 Proteinopathies
Sarah Pickles, Jesús González Bejarano, Anusha Narayan, et al.
Movement Disorders (2025)
Open Access

pTDP-43 levels correlate with cell type–specific molecular alterations in the prefrontal cortex of C9orf72 ALS/FTD patients
Hsiao‐Lin V. Wang, Jian‐Feng Xiang, Chenyang Yuan, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 9
Open Access

Neuropathology and neuroanatomy of TDP-43 amyotrophic lateral sclerosis
Kelly Del Tredici, Heiko Braak
Current Opinion in Neurology (2022) Vol. 35, Iss. 5, pp. 660-671
Closed Access | Times Cited: 16

Pathological mechanisms of amyotrophic lateral sclerosis
Yushu Hu, Wenzhi Chen, Caihui Wei, et al.
Neural Regeneration Research (2023) Vol. 19, Iss. 5, pp. 1036-1044
Open Access | Times Cited: 8

Abundant transcriptomic alterations in the human cerebellum of patients with a C9orf72 repeat expansion
Evan Udine, Mariely DeJesus‐Hernandez, Shulan Tian, et al.
Acta Neuropathologica (2024) Vol. 147, Iss. 1
Open Access | Times Cited: 3

Understanding age-related pathologic changes in TDP-43 functions and the consequence on RNA splicing and signalling in health and disease
Flora Cheng, Tyler Chapman, Selina Zhang, et al.
Ageing Research Reviews (2024) Vol. 96, pp. 102246-102246
Open Access | Times Cited: 2

ALS-linked mutant TDP-43 in oligodendrocytes induces oligodendrocyte damage and exacerbates motor dysfunction in mice
Mai Horiuchi, Seiji Watanabe, Okiru Komine, et al.
Acta Neuropathologica Communications (2024) Vol. 12, Iss. 1
Open Access | Times Cited: 2

RNA-binding proteins as a common ground for neurodegeneration and inflammation in amyotrophic lateral sclerosis and multiple sclerosis
Isabel Acosta-Galeana, Ricardo Hernández, Tania Reyes-Cruz, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 6

Single nucleus multiome analysis of the prefrontal cortex fromC9orf72ALS/FTD patients illuminates pathways affected during disease progression
Hsiao‐Lin V. Wang, Jian‐Feng Xiang, Chenyang Yuan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5

Decoding TDP-43: the molecular chameleon of neurodegenerative diseases
Jixiang Zeng, Can Luo, Yang Jiang, et al.
Acta Neuropathologica Communications (2024) Vol. 12, Iss. 1
Open Access | Times Cited: 1

Implications of TDP-43 in non-neuronal systems
Ke Hao, Kang Liu, Baowei Jiao, et al.
Cell Communication and Signaling (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 3

Glia in FTLD-GRN: from supporting cast to leading role
Emile Pinarbasi, Sami J. Barmada
Journal of Clinical Investigation (2023) Vol. 133, Iss. 6
Open Access | Times Cited: 2

The role of glial cells in amyotrophic lateral sclerosis
Virenkumar A. Pandya, Rickie Patani
International review of neurobiology (2024), pp. 381-450
Closed Access

Towards an integrated approach for understanding glia in Amyotrophic Lateral Sclerosis
Stanisław Majewski, Pierre Klein, Séverine Boillée, et al.
Glia (2024)
Open Access

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