Advances of NOTCH2NLC Repeat Expansions and Associated Diseases: A Bibliometric and Meta-analysis-Reference-Cited by-同舟云学术

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Advances of NOTCH2NLC Repeat Expansions and Associated Diseases: A Bibliometric and Meta-analysis

Published:2024-05-06 Issue: Volume: Page:
ISSN:0893-7648
Container-title:Molecular Neurobiology
language:en
Short-container-title:Mol Neurobiol

Author:

Lu Yangguang,Chen Yiqun,Huang Jiaqi,Jiang Zihan,Ge Yaoying,Yao Ruotong,Zhang Jinxiu,Geng Shangze,Chen Feng,Jin Qiaoqiao,Chen Guangyong,Yang Dehao

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Natural Science Foundation of Zhejiang Province

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s12035-024-04193-6.pdf

Reference50 articles.

1. Fiddes IT, Lodewijk GA, Mooring M, Bosworth CM, Ewing AD, Mantalas GL, Novak AM, van den Bout A et al (2018) Human-specific NOTCH2NL genes affect notch signaling and cortical neurogenesis. Cell 173(6):1356-1369.e1322. https://doi.org/10.1016/j.cell.2018.03.051

2. Suzuki IK, Gacquer D, Van Heurck R, Kumar D, Wojno M, Bilheu A, Herpoel A, Lambert N et al (2018) Human-specific NOTCH2NL genes expand cortical neurogenesis through delta/notch regulation. Cell 173(6):1370-1384.e1316. https://doi.org/10.1016/j.cell.2018.03.067

3. Tian Y, Wang JL, Huang W, Zeng S, Jiao B, Liu Z, Chen Z, Li Y et al (2019) Expansion of human-specific GGC repeat in neuronal intranuclear inclusion disease-related disorders. Am J Hum Genet 105(1):166–176. https://doi.org/10.1016/j.ajhg.2019.05.013

4. Ishiura H, Shibata S, Yoshimura J, Suzuki Y, Qu W, Doi K, Almansour MA, Kikuchi JK et al (2019) Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease. Nat Genet 51(8):1222–1232. https://doi.org/10.1038/s41588-019-0458-z

5. Deng J, Gu M, Miao Y, Yao S, Zhu M, Fang P, Yu X, Li P et al (2019) Long-read sequencing identified repeat expansions in the 5’UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease. J Med Genet 56(11):758–764. https://doi.org/10.1136/jmedgenet-2019-106268

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