Shijing Wu

524 total citations
31 papers, 306 citations indexed

About

Shijing Wu is a scholar working on Molecular Biology, Ophthalmology and Physiology. According to data from OpenAlex, Shijing Wu has authored 31 papers receiving a total of 306 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 15 papers in Ophthalmology and 4 papers in Physiology. Recurrent topics in Shijing Wu's work include Retinal Development and Disorders (17 papers), Retinal Diseases and Treatments (12 papers) and CRISPR and Genetic Engineering (5 papers). Shijing Wu is often cited by papers focused on Retinal Development and Disorders (17 papers), Retinal Diseases and Treatments (12 papers) and CRISPR and Genetic Engineering (5 papers). Shijing Wu collaborates with scholars based in China, United States and Poland. Shijing Wu's co-authors include Ruifang Sui, Zixi Sun, Xuan Zou, Tian Zhu, Xing Wei, Hui Li, Liang Zheng, Yujie Sun, Julin Wang and Bingran Yu and has published in prestigious journals such as Advanced Functional Materials, Scientific Reports and British Journal of Ophthalmology.

In The Last Decade

Shijing Wu

30 papers receiving 300 citations

Peers

Shijing Wu
Suqian Wu China
Risa Sato Japan
Yashar Seyed‐Razavi United States
Juan Wu China
Ann Cooper United States
Christopher May United States
Ahruem Baek South Korea
Shijing Wu
Citations per year, relative to Shijing Wu Shijing Wu (= 1×) peers Beatriz Jiménez

Countries citing papers authored by Shijing Wu

Since Specialization
Citations

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

Fields of papers citing papers by Shijing Wu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shijing Wu

This figure shows the co-authorship network connecting the top 25 collaborators of Shijing Wu. A scholar is included among the top collaborators of Shijing Wu 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 Shijing Wu. Shijing Wu 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.
Liu, Jiayang, et al.. (2024). A novel multiscale adaptive graph adversarial network for mechanical fault diagnosis. Knowledge-Based Systems. 309. 112787–112787. 9 indexed citations
3.
Wu, Shijing, Yinhui Yu, Yao Wang, et al.. (2024). Novel ATF6 homozygous variant in a Chinese patient with achromatopsia. Ophthalmic Genetics. 45(2). 153–158. 1 indexed citations
4.
Li, Huajin, Xing Wei, Shijing Wu, et al.. (2023). Clinical and genetic characterization of a large cohort of Chinese patients with Bietti crystalline retinopathy. Graefe s Archive for Clinical and Experimental Ophthalmology. 262(1). 337–351. 4 indexed citations
5.
Wei, Xing, Hui Li, Shijing Wu, Tian Zhu, & Ruifang Sui. (2022). Genetic analysis and clinical features of three Chinese patients with Oguchi disease. Documenta Ophthalmologica. 146(1). 17–32. 4 indexed citations
6.
Sun, Zixi, Shijing Wu, Tian Zhu, et al.. (2022). Generation of a human induced pluripotent stem cell line PUMCHi019-A from a dominant optic atrophy patient with an OPA1 mutation. Stem Cell Research. 60. 102705–102705. 2 indexed citations
7.
Wu, Shijing, Tian Zhu, Zixi Sun, et al.. (2021). Generation of a human induced pluripotent stem cell line from a Bietti crystalline corneoretinal dystrophy patient with CYP4V2 mutations. Stem Cell Research. 53. 102330–102330. 5 indexed citations
8.
Zhu, Tian, Shijing Wu, Zixi Sun, et al.. (2021). Generation of two human induced pluripotent stem cell lines from patients with biallelic USH2A variants. Stem Cell Research. 55. 102502–102502. 2 indexed citations
9.
Zhong, Linqing, et al.. (2021). Thalidomide may be an effective drug for Blau syndrome: a case report. Annals of Palliative Medicine. 11(7). 2538–2543. 6 indexed citations
10.
Wu, Shijing, Zixi Sun, Tian Zhu, et al.. (2021). A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophy. Graefe s Archive for Clinical and Experimental Ophthalmology. 260(2). 645–653. 3 indexed citations
11.
Qu, Bin, Shijing Wu, Xuan Zou, et al.. (2020). Treating Bietti crystalline dystrophy in a high-fat diet-exacerbated murine model using gene therapy. Gene Therapy. 27(7-8). 370–382. 23 indexed citations
12.
Zhu, Tian, Defu Chen, Lei Wang, et al.. (2020). USH2A variants in Chinese patients with Usher syndrome type II and non-syndromic retinitis pigmentosa. British Journal of Ophthalmology. 105(5). 694–703. 28 indexed citations
13.
Sun, Zixi, Lizhu Yang, Hui Li, et al.. (2020). Clinical and genetic analysis of the ABCA4 gene associated retinal dystrophy in a large Chinese cohort. Experimental Eye Research. 202. 108389–108389. 6 indexed citations
14.
Zou, Xuan, Shijing Wu, Hui Li, et al.. (2020). Detailed comparison of phenotype between male patients carrying variants in exons 1–14 and ORF15 of RPGR. Experimental Eye Research. 198. 108147–108147. 5 indexed citations
15.
Wu, Shijing, Zixi Sun, Tian Zhu, et al.. (2020). Novel variants in PNPLA6 causing syndromic retinal dystrophy. Experimental Eye Research. 202. 108327–108327. 10 indexed citations
16.
Han, Xiaoxu, et al.. (2018). Study of natural history of Chinese patients with choroideremia. Zhonghua shiyan yanke zazhi. 36(7). 519–525. 1 indexed citations
17.
Li, Huajin, et al.. (2018). A novel small deletion in the NHS gene associated with Nance-Horan syndrome. Scientific Reports. 8(1). 2398–2398. 10 indexed citations
19.
Sun, Zixi, Qi Zhou, Huajin Li, et al.. (2017). Mutations in crystallin genes result in congenital cataract associated with other ocular abnormalities.. PubMed. 23. 977–986. 20 indexed citations
20.
Yamaguchi, Michio, et al.. (1991). Cranial Computed Tomography of Psychiatric Patients - Analysis of 130 cases. Kobe University Repository Kernel (Kobe University). 7. 103–108.

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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