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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 Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review
XiuRong Huang, Beisha Tang, Peng Jin, et al.
Molecular Neurobiology (2021) Vol. 59, Iss. 1, pp. 523-534
Closed Access | Times Cited: 35

Showing 1-25 of 35 citing articles:

Sequence composition changes in short tandem repeats: heterogeneity, detection, mechanisms and clinical implications
Indhu‐Shree Rajan‐Babu, Egor Dolzhenko, Michael A. Eberle, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 7, pp. 476-499
Closed Access | Times Cited: 27
CGG repeat expansion in NOTCH2NLC causes mitochondrial dysfunction and progressive neurodegeneration in Drosophila model
Jiaxi Yu, Tongling Liufu, Yilei Zheng, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 41
Open Access | Times Cited: 29
Review of Phenotypic Heterogeneity of Neuronal Intranuclear Inclusion Disease and NOTCH2NLC -Related GGC Repeat Expansion Disorders
Tao Zhang, Lei Bao, Hao Chen
Neurology Genetics (2024) Vol. 10, Iss. 2
Open Access | Times Cited: 6
Clinical and mechanism advances of neuronal intranuclear inclusion disease
Yueqi Liu, Hao Li, Xuan Liu, et al.
Frontiers in Aging Neuroscience (2022) Vol. 14
Open Access | Times Cited: 26
Expression of expanded GGC repeats within NOTCH2NLC causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease
Qiong Liu, Kailin Zhang, Yunhee Kang, et al.
Science Advances (2022) Vol. 8, Iss. 47
Open Access | Times Cited: 22
Current advances in neuronal intranuclear inclusion disease
Lei Bao, Dandan Zuo, Qingjie Li, et al.
Neurological Sciences (2023) Vol. 44, Iss. 6, pp. 1881-1889
Closed Access | Times Cited: 13
A case report of oculopharyngodistal myopathy with 126 CGG repeat expansions in RILPL1
Wenjing Wang, Tielun Yin, Xinyu Zhang, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
Oculopharyngodistal myopathy
Jiaxi Yu, Jianwen Deng, Zhaoxia Wang
Current Opinion in Neurology (2022) Vol. 35, Iss. 5, pp. 637-644
Closed Access | Times Cited: 17
Clinical features of neuronal intranuclear inclusion disease with seizures: a systematic literature review
Jinwei Zhang, Ling Ling, Lei Xiang, et al.
Frontiers in Neurology (2024) Vol. 15
Open Access | Times Cited: 3
Non-coding CGG repeat expansion inLOC642361/NUTM2B-AS1is associated with a phenotype of oculopharyngodistal myopathy
Xinyu Gu, Jiaxi Yu, Kexin Jiao, et al.
Journal of Medical Genetics (2023) Vol. 61, Iss. 4, pp. 340-346
Closed Access | Times Cited: 9
Neuronal Intranuclear Inclusion Disease with NOTCH2NLC GGC Repeat Expansion: A Systematic Review and Challenges of Phenotypic Characterization
Tian Zeng, Yiqun Chen, Honghao Huang, et al.
Aging and Disease (2024)
Open Access | Times Cited: 3
Subclinical peripheral neuropathy is common in neuronal intranuclear inclusion disease with dominant encephalopathy
Daojun Hong, Hui Wang, Min Zhu, et al.
European Journal of Neurology (2022) Vol. 30, Iss. 2, pp. 527-537
Closed Access | Times Cited: 12
The clinical characteristics of neuronal intranuclear inclusion disease and its relation with inflammation
Yaping Yan, Lanxiao Cao, Luyan Gu, et al.
Neurological Sciences (2023) Vol. 44, Iss. 9, pp. 3189-3197
Closed Access | Times Cited: 6
Recent advances in novel mutation genes of Parkinson's disease
Jie Yang, Xinyu Wu, Yuning Song
Journal of Neurology (2023) Vol. 270, Iss. 8, pp. 3723-3732
Closed Access | Times Cited: 5
The role of tandem repeat expansions in brain disorders
Mary Anne Panoyan, Frank R. Wendt
Emerging Topics in Life Sciences (2023) Vol. 7, Iss. 3, pp. 249-263
Closed Access | Times Cited: 5
A case of unusual renal manifestation in a patient with neuronal intranuclear inclusion disease treated with steroids
Keisuke Morita, Takahiro Shinzato, Yuzo Endo, et al.
Clinical Case Reports (2023) Vol. 11, Iss. 8
Open Access | Times Cited: 5
Intermediate-Length GGC Repeat Expansion in NOTCH2NLC Was Identified in Chinese Patients with Amyotrophic Lateral Sclerosis
Mengxia Wan, Ji He, Junyan Huo, et al.
Brain Sciences (2023) Vol. 13, Iss. 1, pp. 85-85
Open Access | Times Cited: 4
Expression of expanded GGC repeats within NOTCH2NLC causes cardiac dysfunction in mouse models
Yongcheng Pan, Ying Jiang, Juan Wan, et al.
Cell & Bioscience (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 4
CGG Repeat Expansion in NOTCH2NLC Causing Overlapping Oculopharyngodistal Myopathy and Neuronal Intranuclear Inclusion Disease With Diffusion Weighted Imaging Abnormality in the Cerebellum
Jing Ma, Huiqiu Zhang, Bing Meng, et al.
Journal of Clinical Neurology (2024) Vol. 20, Iss. 6, pp. 580-580
Open Access | Times Cited: 1
Clinical features and reclassification of essential tremor with NOTCH2NLC GGC repeat expansions based on a long‐term follow‐up
Xun Zhou, Hongyan Huang, Runcheng He, et al.
European Journal of Neurology (2022) Vol. 29, Iss. 12, pp. 3600-3610
Closed Access | Times Cited: 6
Skin biopsy and neuronal intranuclear inclusion disease
Xiao Ren, Dandan Tan, Jianwen Deng, et al.
The Journal of Dermatology (2023) Vol. 50, Iss. 11, pp. 1367-1372
Open Access | Times Cited: 3
GGC expansions in NOTCH2NLC contribute to Parkinson disease and dopaminergic neuron degeneration
Qiong Liu, Juan Chen, Jin Xue, et al.
European Journal of Neurology (2023) Vol. 31, Iss. 2
Open Access | Times Cited: 3
Patients with biallelic GGC repeat expansions in NOTCH2NLC exhibiting a typical neuronal intranuclear inclusion disease phenotype
Shinichi Kameyama, Takeshi Mizuguchi, Hiroshi Doi, et al.
Genomics (2022) Vol. 114, Iss. 5, pp. 110469-110469
Open Access | Times Cited: 5
Urine cytological study in patients with clinicopathologically confirmed neuronal intranuclear inclusion disease
Yiyi Zhou, Pengcheng Huang, Zhaojun Huang, et al.
Frontiers in Aging Neuroscience (2022) Vol. 14
Open Access | Times Cited: 4
NOTCH2NLC mutation-positive neuronal intranuclear inclusion disease with retinal dystrophy: A case report and literature review
Takayuki Katayama, Kae Takahashi, Osamu Yahara, et al.
Medicine (2023) Vol. 102, Iss. 19, pp. e33789-e33789
Open Access | Times Cited: 2
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