OpenAlex Citation Counts

OpenAlex Citations Logo

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:

TDP-43 Accumulation Within Intramuscular Nerve Bundles of Patients With Amyotrophic Lateral Sclerosis
Takashi Kurashige, Hiroyuki Morino, Tomomi Murao, et al.
JAMA Neurology (2022) Vol. 79, Iss. 7, pp. 693-693
Open Access | Times Cited: 25

Showing 25 citing articles:

Polystyrene nanoparticles trigger aberrant condensation of TDP-43 and amyotrophic lateral sclerosis-like symptoms
Hang Sun, Bingwei Yang, Qiong Li, et al.
Nature Nanotechnology (2024) Vol. 19, Iss. 9, pp. 1354-1365
Closed Access | Times Cited: 23

Lost in local translation: TDP-43 and FUS in axonal/neuromuscular junction maintenance and dysregulation in amyotrophic lateral sclerosis
Diana Piol, Tessa Robberechts, Sandrine Da Cruz
Neuron (2023) Vol. 111, Iss. 9, pp. 1355-1380
Open Access | Times Cited: 26

Intramuscular Nerve Bundles Reflect TDP‐43 Pathology in the Medulla and Spinal Cord of ALS Patients
Takashi Kurashige, Tomomi Murao, Yuhei Kanaya, et al.
Neuropathology and Applied Neurobiology (2025) Vol. 51, Iss. 2
Open Access | Times Cited: 1

Amyotrophic lateral sclerosis caused by TARDBP mutations: from genetics to TDP-43 proteinopathy
Rubika Balendra, Jemeen Sreedharan, Martina Hallegger, et al.
The Lancet Neurology (2025) Vol. 24, Iss. 5, pp. 456-470
Closed Access | Times Cited: 1

Molecular Dissection of TDP-43 as a Leading Cause of ALS/FTLD
Yoshitaka Tamaki, Makoto Urushitani
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 20, pp. 12508-12508
Open Access | Times Cited: 36

CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis
Kodai Kume, Takashi Kurashige, Keiko Muguruma, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 7, pp. 1086-1097
Open Access | Times Cited: 14

In vivo diagnosis of TDP-43 proteinopathies: in search of biomarkers of clinical use
Juan I. López-Carbonero, Irene García-Toledo, Laura Fernández-Hernández, et al.
Translational Neurodegeneration (2024) Vol. 13, Iss. 1
Open Access | Times Cited: 5

Peripheral proteinopathy in neurodegenerative diseases
Bin Xu, Lei Xia, Ying Yang, et al.
Translational Neurodegeneration (2025) Vol. 14, Iss. 1
Open Access

Improved detection of pre-symptomatic, non-central nervous system TDP-43 pathology in amyotrophic lateral sclerosis using RNA aptamer
Fergal M. Waldron, Tatiana Langerová, Fiona L. Read, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Looking for answers far away from the soma—the (un)known axonal functions of TDP-43, and their contribution to early NMJ disruption in ALS
Ariel Ionescu, Topaz Altman, Eran Perlson
Molecular Neurodegeneration (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 9

Detection of pTDP‐43 via routine muscle biopsy: A promising diagnostic biomarker for amyotrophic lateral sclerosis
Qi‐Jie Zhang, Jie Lin, Youliang Wang, et al.
Brain Pathology (2024) Vol. 34, Iss. 6
Open Access | Times Cited: 3

Brain imaging signatures in amyotrophic lateral sclerosis: Correlation with peripheral motor degeneration
Sung‐Ju Hsueh, Chi‐Chao Chao, Ta‐Fu Chen, et al.
Annals of Clinical and Translational Neurology (2023) Vol. 10, Iss. 8, pp. 1456-1466
Open Access | Times Cited: 6

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

Axonopathy Underlying Amyotrophic Lateral Sclerosis: Unraveling Complex Pathways and Therapeutic Insights
Tongshu Luan, Qing Li, Zhi Huang, et al.
Neuroscience Bulletin (2024) Vol. 40, Iss. 11, pp. 1789-1810
Closed Access | Times Cited: 1

Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosis
Mónica Zufiría, Oihane Pikatza-Menoio, Maddi Garciandia-Arcelus, et al.
Acta Neuropathologica (2024) Vol. 148, Iss. 1
Open Access | Times Cited: 1

Decoding the Cellular Trafficking of Prion-like Proteins in Neurodegenerative Diseases
Chenjun Hu, Yiqun Yan, Yanhong Jin, et al.
Neuroscience Bulletin (2023) Vol. 40, Iss. 2, pp. 241-254
Closed Access | Times Cited: 3

Neuromuscular disease: 2023 update.
Marta Margeta
PubMed (2023) Vol. 4
Closed Access | Times Cited: 1

Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosis.
Mónica Zufiría, Oihane Pikatza-Menoio, Maddi Garciandia-Arcelus, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access

Intrinsic Templates for Neurodegenerations Featuring Disease-Specific Axonal or Dendritic Vulnerability
Toshiki Uchihara
Oxford University Press eBooks (2024), pp. 81-104
Closed Access

A bibliometric analysis of gene editing and amyotrophic lateral sclerosis (from 2004 to 2024)
Hejia Wan, Wenli Qian, Bing-qi Wei, et al.
Frontiers in Neuroscience (2024) Vol. 18
Open Access

Phosphorylated CRMP1, axon guidance protein, is a component of spheroids and is involved in axonal pathology in amyotrophic lateral sclerosis
Yuko Kawamoto, Mikiko Tada, Tetsuya Asano, et al.
Frontiers in Neurology (2022) Vol. 13
Open Access | Times Cited: 2

Error in Figure
Richard Gray, Crispin Jenkinson, Carl E Clarke
JAMA Neurology (2022) Vol. 79, Iss. 7, pp. 727-727
Open Access

Misfolding at the synapse: A role in amyotrophic lateral sclerosis pathogenesis?
Jeremy S. Lum, Justin J. Yerbury
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access

Page 1

Scroll to top