Ningdong Li

696 total citations
59 papers, 489 citations indexed

About

Ningdong Li is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Ophthalmology. According to data from OpenAlex, Ningdong Li has authored 59 papers receiving a total of 489 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 16 papers in Pathology and Forensic Medicine and 12 papers in Ophthalmology. Recurrent topics in Ningdong Li's work include Ophthalmology and Eye Disorders (16 papers), Retinal Development and Disorders (12 papers) and Retinal Diseases and Treatments (8 papers). Ningdong Li is often cited by papers focused on Ophthalmology and Eye Disorders (16 papers), Retinal Development and Disorders (12 papers) and Retinal Diseases and Treatments (8 papers). Ningdong Li collaborates with scholars based in China, United States and Taiwan. Ningdong Li's co-authors include Kanxing Zhao, Chong Pang, Tengyue Zhang, Ming Ying, J. Fielding Hejtmancik, Xiaodong Jiao, Liming Wang, Ruifang Han, Ian M. MacDonald and Mei Han and has published in prestigious journals such as PLoS ONE, Scientific Reports and American Journal of Ophthalmology.

In The Last Decade

Ningdong Li

57 papers receiving 485 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ningdong Li China	10	187	97	64	54	45	59	489
Sean T. Berkowitz United States	11	447 2.4×	141 1.5×	115 1.8×	49 0.9×	71 1.6×	36	848
Arcadi Gual Spain	16	260 1.4×	169 1.7×	27 0.4×	91 1.7×	73 1.6×	50	795
Dong Hoon Shin South Korea	13	99 0.5×	58 0.6×	16 0.3×	23 0.4×	29 0.6×	44	480
Michael DeCuypere United States	12	73 0.4×	22 0.2×	47 0.7×	107 2.0×	48 1.1×	39	696
Rachel L. Taylor United Kingdom	16	358 1.9×	110 1.1×	10 0.2×	60 1.1×	45 1.0×	27	682
H Lippman United States	13	240 1.3×	54 0.6×	15 0.2×	32 0.6×	21 0.5×	36	786
Zujaja Tauqeer United States	8	94 0.5×	51 0.5×	28 0.4×	15 0.3×	54 1.2×	21	326
Lisa Turner United States	10	148 0.8×	32 0.3×	13 0.2×	32 0.6×	23 0.5×	19	462
Iva Lloyd United Kingdom	13	176 0.9×	129 1.3×	5 0.1×	33 0.6×	73 1.6×	40	574

Countries citing papers authored by Ningdong Li

Since Specialization

Citations

This map shows the geographic impact of Ningdong Li'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 Ningdong Li with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ningdong Li more than expected).

Fields of papers citing papers by Ningdong Li

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ningdong Li. 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 Ningdong Li. The network helps show where Ningdong Li may publish in the future.

Co-authorship network of co-authors of Ningdong Li

This figure shows the co-authorship network connecting the top 25 collaborators of Ningdong Li. A scholar is included among the top collaborators of Ningdong Li 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 Ningdong Li. Ningdong Li is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Huang, Lijuan, Yan Xie, Wen Liu, et al.. (2024). Clinical and genetic studies for a cohort of patients with Leber congenital amaurosis. Graefe s Archive for Clinical and Experimental Ophthalmology. 262(9). 3029–3038. 2 indexed citations

Huang, Lijuan, et al.. (2024). Clinical and genetic studies for a cohort of patients with congenital stationary night blindness. Orphanet Journal of Rare Diseases. 19(1). 101–101. 3 indexed citations

Huang, Lijuan, et al.. (2023). Diversity of clinical phenotypes in a cohort of Han Chinese patients with PAX6 variants. Frontiers in Genetics. 14. 1011060–1011060. 1 indexed citations

Zhang, Chengyue, et al.. (2023). Thicknesses of the retina and choroid in children with retinitis pigmentosa. BMC Ophthalmology. 23(1). 25–25.

Chen, Yuanyuan, Wen Liu, Di Hu, et al.. (2023). Alterations of large‐scale functional network connectivity in patients with infantile esotropia before and after surgery. Brain and Behavior. 13(8). e3154–e3154. 1 indexed citations

Oke, Isdin, Birgit Lorenz, Birsen Gökyiğit, et al.. (2022). Nasal Transposition of the Split Lateral Rectus Muscle for Strabismus Associated With Bilateral 3rd-Nerve Palsy. American Journal of Ophthalmology. 242. 165–172. 2 indexed citations

Chen, Yuanyuan, Wen Liu, Di Hu, et al.. (2022). Abnormal developmental trends of functional connectivity in young children with infantile esotropia. Frontiers in Neuroscience. 16. 972882–972882. 2 indexed citations

Huang, Lijuan, et al.. (2022). Case report: Exotropia in waardenburg syndrome with novel variations. Frontiers in Genetics. 13. 969680–969680. 2 indexed citations

Huang, Lijuan, Yan Xie, Kaiwen He, et al.. (2022). Correlations of FRMD7 gene mutations with ocular oscillations. Scientific Reports. 12(1). 9914–9914. 5 indexed citations

10.

Huang, Lijuan, et al.. (2022). Clinical features and genotypes of six patients from four families with horizontal gaze palsy with progressive scoliosis. Frontiers in Pediatrics. 10. 949565–949565. 3 indexed citations

11.

Huang, Lijuan & Ningdong Li. (2022). Augmented lateral rectus muscle recession for treatment of infantile exotropia. International Ophthalmology. 42(5). 1589–1594. 1 indexed citations

12.

Jiang, Jingjing, Likun Yang, Hui Li, Lijuan Huang, & Ningdong Li. (2019). Evaluation of the iris thickness changes for the Chinese families with GPR143 gene mutations. Experimental Eye Research. 189. 107819–107819. 4 indexed citations

13.

Wang, Xiaojuan, Ming Ying, Changbo Fu, Yuchuan Wang, & Ningdong Li. (2017). TGFBI gene mutations analysis in Chinese families with corneal dystrophies. Molecular Medicine Reports. 15(5). 3198–3202. 3 indexed citations

14.

Yang, Likun & Ningdong Li. (2016). Therapeutic evaluation of lateral rectus super-recession surgery for large angle divergence excess exotropia. Zhonghua shiyan yanke zazhi. 34(5). 438–442. 1 indexed citations

15.

Han, Ruifang, Xiaojuan Wang, Dongjie Wang, et al.. (2015). GPR143 Gene Mutations in Five Chinese Families with X-linked Congenital Nystagmus. Scientific Reports. 5(1). 12031–12031. 17 indexed citations

16.

Ying, Ming, Kai Wang, Liming Wang, et al.. (2015). Two Novel NYX Gene Mutations in the Chinese Families with X-linked Congenital Stationary Night Blindness. Scientific Reports. 5(1). 12679–12679. 6 indexed citations

17.

Lu, Yongyue, Lei Wang, Yijuan Xu, Ling Zeng, & Ningdong Li. (2014). Correlation of the Nest Density and the Number of Workers in Bait Traps for Fire Ants (Solenopsis invicta) in Southern China. Sociobiology. 59(4). 1197–1204. 2 indexed citations

18.

Ying, Ming, Ruifang Han, Hao Peng, Liming Wang, & Ningdong Li. (2013). Inherited KIF21A and PAX6 gene mutations in a boy with congenital Fibrosis of extraocular muscles and aniridia. BMC Medical Genetics. 14(1). 63–63. 5 indexed citations

19.

Peng, Hao, Xin Tang, Hui Song, et al.. (2010). [Screening of FBN1 gene mutations in a family with Marfan syndrome].. PubMed. 46(11). 984–8. 2 indexed citations

20.

Li, Ningdong, et al.. (2010). A novel mutation of RPGR gene in an X-Linked Chinese family with retinitis pigmentosa. Molecular Genetics and Metabolism. 102(4). 488–493. 4 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.

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