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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:

The neurodegenerative diseases ALS and SMA are linked at the molecular level via the ASC-1 complex
Binkai Chi, Jeremy D. O’Connell, Alexander D Iocolano, et al.
Nucleic Acids Research (2018) Vol. 46, Iss. 22, pp. 11939-11951
Open Access | Times Cited: 45

Showing 1-25 of 45 citing articles:

The role of astrocytic glutamate transporters GLT-1 and GLAST in neurological disorders: Potential targets for neurotherapeutics
Edward Pajarillo, Asha Rizor, Jayden Lee, et al.
Neuropharmacology (2019) Vol. 161, pp. 107559-107559
Open Access | Times Cited: 342
Nuclear RNA binding regulates TDP-43 nuclear localization and passive nuclear export
Lauren Duan, Benjamin L. Zaepfel, Vasilisa Aksenova, et al.
Cell Reports (2022) Vol. 40, Iss. 3, pp. 111106-111106
Open Access | Times Cited: 69
Aberrant interaction of FUS with the U1 snRNA provides a molecular mechanism of FUS induced amyotrophic lateral sclerosis
Daniel Jutzi, Sébastien Campagne, Ralf Schmidt, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 60
Failure to Degrade CAT-Tailed Proteins Disrupts Neuronal Morphogenesis and Cell Survival
Tsuyoshi Udagawa, Moeka Seki, Taku Okuyama, et al.
Cell Reports (2021) Vol. 34, Iss. 1, pp. 108599-108599
Open Access | Times Cited: 51
Matrin3 mediates differentiation through stabilizing chromatin loop-domain interactions and YY1 mediated enhancer-promoter interactions
Tianxin Liu, Qian Zhu, Kai Yan, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 8
Role of RNA Binding Proteins with prion-like domains in muscle and neuromuscular diseases
Gina Picchiarelli, Luc Dupuis
Cell Stress (2020) Vol. 4, Iss. 4, pp. 76-91
Open Access | Times Cited: 48
High content screening and proteomic analysis identify a kinase inhibitor that rescues pathological phenotypes in a patient-derived model of Parkinson’s disease
Nasia Antoniou, Kanella Prodromidou, Georgia Kouroupi, et al.
npj Parkinson s Disease (2022) Vol. 8, Iss. 1
Open Access | Times Cited: 23
CRISPR and iPSCs: Recent Developments and Future Perspectives in Neurodegenerative Disease Modelling, Research, and Therapeutics
Tirthankar Sen, Rajkumar P. Thummer
Neurotoxicity Research (2022) Vol. 40, Iss. 5, pp. 1597-1623
Open Access | Times Cited: 23
ASCC1 structures and bioinformatics reveal a novel Helix-Clasp-Helix RNA-binding motif linked to a two-histidine phosphodiesterase
Naga Babu Chinnam, Roopa Thapar, Andy Arvai, et al.
Journal of Biological Chemistry (2024) Vol. 300, Iss. 6, pp. 107368-107368
Open Access | Times Cited: 4
Muscleblind acts as a modifier of FUS toxicity by modulating stress granule dynamics and SMN localization
Ian Casci, Karthik Krishnamurthy, Sukhleen Kour, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 35
A novel role of U1 snRNP: Splice site selection from a distance
Ravindra Singh, Natalia N. Singh
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms (2019) Vol. 1862, Iss. 6, pp. 634-642
Open Access | Times Cited: 32
Glial Subtype-Specific Modulation of Disease Pathogenesis in Drosophila Models of ALS
Yanan Wei, Hak Young Rhee, Hadi Najafi, et al.
Genes & Diseases (2025), pp. 101631-101631
Open Access
Protein kinase inhibitors as therapeutics in neurodegenerative and psychiatric disorders
Giuseppe Tridente, Ankit Jana, Arnab Nath, et al.
Elsevier eBooks (2023), pp. 403-573
Closed Access | Times Cited: 7
Detecting differential transcript usage in complex diseases with SPIT
Beril Erdogdu, Ales Varabyou, Stephanie C. Hicks, et al.
Cell Reports Methods (2024) Vol. 4, Iss. 3, pp. 100736-100736
Open Access | Times Cited: 2
CircFndc3b Mediates Exercise‐Induced Neuroprotection by Mitigating Microglial/Macrophage Pyroptosis via the ENO1/KLF2 Axis in Stroke Mice
Yun Zhao, Xiaofei He, Xiaofeng Yang, et al.
Advanced Science (2024)
Open Access | Times Cited: 2
ASC‐1 Is a Cell Cycle Regulator Associated with Severe and Mild Forms of Myopathy
Rocío N. Villar‐Quiles, Fabio Catervi, Éva Cabet, et al.
Annals of Neurology (2019) Vol. 87, Iss. 2, pp. 217-232
Open Access | Times Cited: 17
Characteristics of circular RNAs generated by human Survival Motor Neuron genes
Eric W. Ottesen, Ravindra Singh
Cellular Signalling (2020) Vol. 73, pp. 109696-109696
Open Access | Times Cited: 16
How Inflammation Pathways Contribute to Cell Death in Neuro-Muscular Disorders
Sara Salucci, Anna Bartoletti Stella, Michela Battistelli, et al.
Biomolecules (2021) Vol. 11, Iss. 8, pp. 1109-1109
Open Access | Times Cited: 14
The role of excitatory amino acid transporter 2 (EAAT2) in epilepsy and other neurological disorders
Sahar Alijanpour, Mohammad Miryounesi, Soudeh Ghafouri‐Fard
Metabolic Brain Disease (2022) Vol. 38, Iss. 1, pp. 1-16
Closed Access | Times Cited: 10
Suboptimal RNA–RNA interaction limits U1 snRNP inhibition of canonical mRNA 3’ processing
Junjie Shi, Yanhui Deng, Shanshan Huang, et al.
RNA Biology (2019) Vol. 16, Iss. 10, pp. 1448-1460
Open Access | Times Cited: 14
U1 snRNP proteins promote proximal alternative polyadenylation sites by directly interacting with 3′ end processing core factors
Zhijie Hu, Mengxia Li, Zhanfeng Huo, et al.
Journal of Molecular Cell Biology (2022) Vol. 14, Iss. 8
Open Access | Times Cited: 9
Noncoding RNAs Set the Stage for RNA Polymerase II Transcription
Cécilia Studniarek, Sylvain Egloff, Shona Murphy
Trends in Genetics (2020) Vol. 37, Iss. 3, pp. 279-291
Open Access | Times Cited: 11
MATR3’s Role beyond the Nuclear Matrix: From Gene Regulation to Its Implications in Amyotrophic Lateral Sclerosis and Other Diseases
Jhune Rizsan Santos, Jeehye Park
Cells (2024) Vol. 13, Iss. 11, pp. 980-980
Open Access | Times Cited: 1
A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita
Xénia Latypova, Stefan Giovanni Creadore, Noémi Dahan‐Oliel, et al.
Genes (2021) Vol. 12, Iss. 7, pp. 1052-1052
Open Access | Times Cited: 9
Inherited Defects of the ASC-1 Complex in Congenital Neuromuscular Diseases
Justine Meunier, Rocío‐Nur Villar‐Quiles, Isabelle Duband‐Goulet, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 11, pp. 6039-6039
Open Access | Times Cited: 8
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