Ning Wang

3.6k total citations · 1 hit paper
137 papers, 2.5k citations indexed

About

Ning Wang is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Ning Wang has authored 137 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Molecular Biology, 47 papers in Cellular and Molecular Neuroscience and 29 papers in Neurology. Recurrent topics in Ning Wang's work include Genetic Neurodegenerative Diseases (25 papers), Mitochondrial Function and Pathology (21 papers) and Muscle Physiology and Disorders (20 papers). Ning Wang is often cited by papers focused on Genetic Neurodegenerative Diseases (25 papers), Mitochondrial Function and Pathology (21 papers) and Muscle Physiology and Disorders (20 papers). Ning Wang collaborates with scholars based in China, United States and Taiwan. Ning Wang's co-authors include Zhi‐Ying Wu, Wan‐Jin Chen, David M. Stern, Xi Chen, Jun Yao, Joyce W. Lustbader, Shi Du Yan, Casper Caspersen, Hong Xu and Guy M. McKhann and has published in prestigious journals such as Nature Communications, Neuron and Nature Genetics.

In The Last Decade

Ning Wang

124 papers receiving 2.5k citations

Hit Papers

Mitochondrial Aβ: a potential focal point for neuronal me... 2005 2026 2012 2019 2005 200 400 600

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ning Wang China 21 1.2k 727 638 406 350 137 2.5k
Cezary Żekanowski Poland 24 1.1k 0.9× 256 0.4× 622 1.0× 364 0.9× 270 0.8× 96 1.9k
Bart Dermaut Belgium 31 1.9k 1.6× 540 0.7× 1.3k 2.1× 872 2.1× 373 1.1× 64 3.3k
Maurizio De Fusco Italy 19 1.3k 1.1× 770 1.1× 315 0.5× 351 0.9× 319 0.9× 32 2.8k
Akiko Furuta Japan 26 1.3k 1.1× 1.1k 1.6× 459 0.7× 474 1.2× 114 0.3× 57 2.8k
Alessandro Simonati Italy 28 959 0.8× 488 0.7× 864 1.4× 279 0.7× 186 0.5× 94 2.2k
Charalampos Tzoulis Norway 31 1.8k 1.5× 656 0.9× 429 0.7× 896 2.2× 200 0.6× 95 3.0k
Benoît Funalot France 26 1.1k 0.9× 813 1.1× 239 0.4× 657 1.6× 127 0.4× 87 2.3k
Roman Chrast Switzerland 35 1.8k 1.5× 1.1k 1.5× 560 0.9× 356 0.9× 275 0.8× 70 3.3k
Tomoko Kurata Japan 27 1.2k 1.0× 355 0.5× 396 0.6× 752 1.9× 136 0.4× 87 2.5k
Eiichiro Nagata Japan 30 2.1k 1.8× 1.2k 1.7× 588 0.9× 485 1.2× 208 0.6× 117 4.0k

Countries citing papers authored by Ning Wang

Since Specialization
Citations

This map shows the geographic impact of Ning Wang's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ning Wang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ning Wang more than expected).

Fields of papers citing papers by Ning Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ning Wang. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ning Wang. The network helps show where Ning Wang may publish in the future.

Co-authorship network of co-authors of Ning Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Ning Wang. A scholar is included among the top collaborators of Ning Wang based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ning Wang. Ning Wang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Zhang, Tongtong, Hui‐Zhen Su, Shuyuan Wang, et al.. (2025). Lysosomal and mTORC1 signaling dysregulation underpin the pathology of spastic paraplegia type 80. Nature Communications. 16(1). 9833–9833.
2.
Wang, Ming, Richard Cheng, Yuhai Gao, et al.. (2025). Correlation of computed fractional flow and in-stent restenosis in patients with intracranial atherosclerotic stenosis. Journal of NeuroInterventional Surgery. 18(3). 868–875.
4.
Chen, Xuan-Yu, Xintong Yu, Chunyu Huang, et al.. (2024). Apolipoprotein E epsilon4 allele is associated with better performance language and visual memory in spinocerebellar ataxia type 3. European Journal of Neurology. 32(1). e70017–e70017.
5.
Jiang, Junyi, et al.. (2024). A pseudo‐homozygous missense variant and Alu‐mediated exon 5 deletion in FARS2 causing spastic paraplegia 77. Annals of Clinical and Translational Neurology. 11(11). 3019–3024.
6.
Su, Hui‐Zhen, Xiang Lin, Yan Shi, et al.. (2024). ESCRT-I protein UBAP1 controls ventricular expansion and cortical neurogenesis via modulating adherens junctions of radial glial cells. Cell Reports. 43(3). 113818–113818. 2 indexed citations
7.
Chen, Long, Ying Zheng, Xiaodan Lin, et al.. (2023). Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy. Neurology. 101(3). e225–e237. 9 indexed citations
8.
Lin, Xiang, Junyi Jiang, Daojun Hong, et al.. (2023). Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization. Movement Disorders. 39(1). 152–163. 3 indexed citations
9.
Wu, Zhiwei, Shulong Li, Ning Wang, & Tao Zhou. (2023). Microstructure and electrochemical properties of Cr– Si–C–N coatings as biological dry electrode. Materials Chemistry and Physics. 307. 128212–128212. 3 indexed citations
10.
Feng, Lin, et al.. (2023). The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy. Annals of Clinical and Translational Neurology. 10(3). 426–439. 2 indexed citations
11.
Chen, Yijun, Mengwen Wang, En‐Lin Dong, et al.. (2019). Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia. Parkinsonism & Related Disorders. 65. 256–260. 10 indexed citations
12.
Li, Hong‐Fu, Liqin Yang, Dazhi Yin, et al.. (2019). Associations between neuroanatomical abnormality and motor symptoms in paroxysmal kinesigenic dyskinesia. Parkinsonism & Related Disorders. 62. 134–140. 15 indexed citations
13.
Yao, Xiang‐Ping, Xuewen Cheng, Chong Wang, et al.. (2018). Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification. Neuron. 98(6). 1116–1123.e5. 97 indexed citations
14.
Chen, Sheng, Ni Wang, Xinzhen Yin, et al.. (2017). Clinical features and mutation spectrum in Chinese patients with CADASIL: A multicenter retrospective study. CNS Neuroscience & Therapeutics. 23(9). 707–716. 48 indexed citations
15.
Wei, Wei, et al.. (2012). [Prevalence of CYP2C19 polymorphisms involved in clopidogrel metabolism in Fujian Han population].. PubMed. 29(4). 420–5. 6 indexed citations
16.
Zhang, Xiong, et al.. (2012). Screening for FMR1 expanded alleles in patients with parkinsonism in mainland China. Neuroscience Letters. 514(1). 16–21. 7 indexed citations
17.
Gan, Shi‐Rui, et al.. (2010). The reliability of cloning-sequencing to detect the number of trinucleotide repeats. Chin J Neurol. 43(9). 659–663. 1 indexed citations
18.
Wang, Ning, et al.. (2009). Mutation and polymorphism analysis of SPG4 and SPG3A in Chinese patients with hereditary spastic paraplegia. Chin J Neurol. 42(4). 253–257. 1 indexed citations
19.
Wang, Jingjing, Ning Wang, & Liuwang Nie. (2009). Cloning and analysis of the HMG domains of ten Sox genes from Bombina maxima (Amphibia: Anura). AFRICAN JOURNAL OF BIOTECHNOLOGY. 8(8). 1441–1448. 1 indexed citations
20.
Chen, Dachun, Xiangyang Zhang, Yanli Li, et al.. (2008). Adjunctive celecoxib treatment with risperidone in first-episode schizophrenia: a double blind,randomized and placebo controlled trial. Chin J Psychiatry. 41(3). 160–164. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Rankless by CCL
2026