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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:

NGLY1 mutations cause protein aggregation in human neurons
Andreea Manole, Thomas L. Wong, Amanda Rhee, et al.
Cell Reports (2023) Vol. 42, Iss. 12, pp. 113466-113466
Open Access | Times Cited: 10

Showing 10 citing articles:

Review: Utility of mass spectrometry in rare disease research and diagnosis
Teresa Zhao, Daniella H. Hock, James Pitt, et al.
npj Genomic Medicine (2025) Vol. 10, Iss. 1
Open Access
Increased Oxidative Stress and Autophagy in NGLY1 Patient iPSC-derived Neural Stem Cells
Zeenat A. Shyr, Soukaina Amniouel, Kofi Owusu-Ansah, et al.
Experimental Cell Research (2025), pp. 114540-114540
Open Access
NFE2L1 as a central regulator of proteostasis in neurodegenerative diseases: interplay with autophagy, ferroptosis, and the proteasome
Hossein Khodadadi, Kamila Łuczyńska, Dawid Winiarczyk, et al.
Frontiers in Molecular Neuroscience (2025) Vol. 18
Open Access
Prader-Willi syndrome: Genetics, clinical symptoms, and model systems
Mayssa Saade, Wote Amelo Rike, Omveer Sharma, et al.
Genomic psychiatry : (2025), pp. 1-21
Closed Access
Case Report: A Case of a Patient with Smith–Magenis Syndrome and Early-Onset Parkinson’s Disease
Tchelet Stern, Yara Hussein, Diogo Cordeiro, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 15, pp. 8447-8447
Open Access | Times Cited: 1
Genetic Overlap Between Inflammatory Bowel Disease and Neurological Disorders: Insights from GWAS and Gene Expression Analysis
Utkarsh Tripathi, Yam Stern, Inbal Dagan, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Systemic gene therapy corrects neurological phenotype in a mouse model of NGLY1 deficiency
Ailing Du, Kun Yang, Xuntao Zhou, et al.
JCI Insight (2024) Vol. 9, Iss. 19
Open Access
SAK3 confers neuroprotection in the neurodegeneration model of X-linked Dystonia-Parkinsonism
Shivani Aryal, Shawei Chen, Kyle F. Burbach, et al.
Research Square (Research Square) (2024)
Open Access
Mutations in nucleotide metabolism genes bypass proteasome defects in png-1/NGLY1-deficient Caenorhabditis elegans
Katherine S. Yanagi, Briar E. Jochim, Sheikh Omar Kunjo, et al.
PLoS Biology (2024) Vol. 22, Iss. 7, pp. e3002720-e3002720
Open Access
A commentary on ‘Patient-derived gene and protein expression signatures of NGLY1 deficiency’
Tadashi Suzuki
The Journal of Biochemistry (2023) Vol. 175, Iss. 3, pp. 221-223
Open Access
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