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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:

Lysosomal cholesterol accumulation contributes to the movement phenotypes associated with NUS1 haploinsufficiency
Seok‐Ho Yu, Tong Wang, Kali Wiggins, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 7, pp. 1305-1314
Open Access | Times Cited: 30

Showing 1-25 of 30 citing articles:

Advances of Zebrafish in Neurodegenerative Disease: From Models to Drug Discovery
Xiaobo Wang, Jinbao Zhang, Kaijie He, et al.
Frontiers in Pharmacology (2021) Vol. 12
Open Access | Times Cited: 76
Novel Copy Number Deletion Involving NUS1 Associated With Epilepsy, Tremor, and Intellectual Disability
Jing Y. Hsu, Daniah H. Ibrahim, Riza Ali, et al.
Clinical Case Reports (2025) Vol. 13, Iss. 1
Open Access | Times Cited: 1
Tracer metabolomics reveals the role of aldose reductase in glycosylation
Silvia Radenkovic, Anna N. Ligezka, Sneha S. Mokashi, et al.
Cell Reports Medicine (2023) Vol. 4, Iss. 6, pp. 101056-101056
Open Access | Times Cited: 18
The evolving genetic landscape of congenital disorders of glycosylation
Matthew P. Wilson, Gert Matthijs
Biochimica et Biophysica Acta (BBA) - General Subjects (2021) Vol. 1865, Iss. 11, pp. 129976-129976
Open Access | Times Cited: 29
Genome sequencing reanalysis increases the diagnostic yield in dystonia
Avi Fellner, Gurusidheshwar M. Wali, Neil Mahant, et al.
Parkinsonism & Related Disorders (2024) Vol. 124, pp. 107010-107010
Open Access | Times Cited: 4
Heterozygous pathogenic STT3A variation leads to dominant congenital glycosylation disorders and functional validation in zebrafish
Linxue Meng, Zhixu Fang, Li Jiang, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Niemann-Pick C-like Endolysosomal Dysfunction in DHDDS Patient Cells, a Congenital Disorder of Glycosylation, Can Be Treated with Miglustat
Hannah L. Best, Sophie R. Cook, Helen Waller‐Evans, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 4, pp. 1471-1471
Open Access
The Therapeutic Future for Congenital Disorders of Glycosylation
Irena Muffels, Tamás Kozicz, Ethan Perlstein, et al.
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Closed Access
Loss of NgBR causes neuronal damage through decreasing KAT7-mediated RFX1 acetylation and FGF1 expression
Yuwei Hu, Yanni Ma, Lele Liu, et al.
Cellular and Molecular Life Sciences (2025) Vol. 82, Iss. 1
Open Access
De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus
Serena Galosi, Ban H. Edani, Simone Martinelli, et al.
Brain (2021) Vol. 145, Iss. 1, pp. 208-223
Open Access | Times Cited: 24
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review
Emma N. M. M. von Scheibler, Agnies M. van Eeghen, Tom J. de Koning, et al.
Movement Disorders Clinical Practice (2022) Vol. 10, Iss. 1, pp. 17-31
Open Access | Times Cited: 15
DHDDS and NUS1: A Converging Pathway and Common Phenotype
Laura Williams, Sophie Waller, Jessica Qiu, et al.
Movement Disorders Clinical Practice (2023) Vol. 11, Iss. 1, pp. 76-85
Open Access | Times Cited: 8
NUS1 and Epilepsy-myoclonus-ataxia Syndrome: An Under-recognized Entity?
Giulietta Riboldi, Edoardo Monfrini, Christine E. Stahl, et al.
Tremor and Other Hyperkinetic Movements (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 11
Genomic insights into the comorbidity between type 2 diabetes and schizophrenia
Ana Luiza Arruda, Golam M. Khandaker, Andrew P. Morris, et al.
Schizophrenia (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 2
Overexpression of NgBR inhibits high-fat diet–induced atherosclerosis in ApoE-deficiency mice
Ke Gong, Mengyao Wang, Dandan Wang, et al.
Hepatology Communications (2023) Vol. 7, Iss. 4
Open Access | Times Cited: 6
Novel NUS1 variant in a Chinese patient with progressive myoclonus epilepsy: a case report and systematic review
Caihong Ji, Jiajia Zhao, Jianfang Zhang, et al.
Neurological Sciences (2023) Vol. 44, Iss. 10, pp. 3495-3498
Closed Access | Times Cited: 4
Novel Copy Number Deletion involving NUS1 associated with Epilepsy, Tremor, and Intellectual Disability
Gholson J. Lyon, Jing Y. Hsu, Daniah H. Ibrahim, et al.
Authorea (Authorea) (2024)
Open Access | Times Cited: 1
Loss of Drosophila NUS1 results in cholesterol accumulation and Parkinson’s disease‐related neurodegeneration
Jin Xue, Yingbao Zhu, Liyi Wei, et al.
The FASEB Journal (2022) Vol. 36, Iss. 7
Closed Access | Times Cited: 7
Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings
Matthew P. Wilson, Alejandro Garanto, Filippo Pinto e Vairo, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 11, pp. 2130-2144
Open Access | Times Cited: 8
Zebrafish as a comprehensive model of neurological diseases
Shahnawaz Ahmed, Gayathri Venkatesan, Deshapathi Sai Prapul, et al.
International Journal of Science and Research Archive (2023) Vol. 10, Iss. 1, pp. 018-052
Open Access | Times Cited: 3
Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease
Jiang Li, Junpu Mei, Yuwen Zhao, et al.
Neurobiology of Aging (2021) Vol. 110, pp. 106-112
Closed Access | Times Cited: 6
Case report: splicing effect of a novel heterozygous variant of the NUS1 gene in a child with epilepsy
Yan Hu, Mingwei Huang, Jialun Wen, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 2
Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome
Emma Nicolette Maximiliane Maria Boersma- von Scheibler
(2023)
Open Access | Times Cited: 2
NUS1 Variants Cause Lennox-Gastaut Syndrome Related to Unfolded Protein Reaction Activation
Nan-Xiang Shen, Xiao-Chong Qu, Jing Yu, et al.
Molecular Neurobiology (2024) Vol. 61, Iss. 11, pp. 8518-8530
Closed Access
Identification of two novel variants in NUS1 gene in two unrelated Chinese families with intellectual disorder and epilepsy
Yuling Kan, Haiyan Zhao, Hongxing Li, et al.
Research Square (Research Square) (2024)
Open Access
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