Panfeng Wang

2.9k total citations · 1 hit paper
109 papers, 2.1k citations indexed

About

Panfeng Wang is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Panfeng Wang has authored 109 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Molecular Biology, 49 papers in Ophthalmology and 29 papers in Genetics. Recurrent topics in Panfeng Wang's work include Retinal Development and Disorders (36 papers), Retinal Diseases and Treatments (31 papers) and Glaucoma and retinal disorders (17 papers). Panfeng Wang is often cited by papers focused on Retinal Development and Disorders (36 papers), Retinal Diseases and Treatments (31 papers) and Glaucoma and retinal disorders (17 papers). Panfeng Wang collaborates with scholars based in China, United States and France. Panfeng Wang's co-authors include Qingjiong Zhang, Shiqiang Li, Xueshan Xiao, Xiangming Guo, Xiaoyun Jia, Wenmin Sun, Yuntong Zhang, Zichen Hao, Shuo Fang and Yan Xia and has published in prestigious journals such as Journal of Clinical Oncology, Blood and PLoS ONE.

In The Last Decade

Panfeng Wang

105 papers receiving 2.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Umbilical Mesenchymal Stem Cell-Derived Exosome-Encapsulated Hydrogels Accelerate Bone Repair by Enhancing Angiogenesis

2021 200 citations Panfeng Wang et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Panfeng Wang China	24	1.5k	748	406	386	259	109	2.1k
Hardeep Singh Mudhar United Kingdom	21	563 0.4×	622 0.8×	125 0.3×	463 1.2×	264 1.0×	122	2.0k
Jane Ashworth United Kingdom	28	630 0.4×	712 1.0×	658 1.6×	334 0.9×	337 1.3×	87	2.2k
Clyde Guidry United States	25	1.0k 0.7×	994 1.3×	169 0.4×	783 2.0×	42 0.2×	41	2.4k
Martin P. Snead United Kingdom	29	522 0.3×	1.0k 1.4×	1.1k 2.8×	1.1k 3.0×	228 0.9×	94	2.5k
J.C. Murray United States	17	1.1k 0.7×	134 0.2×	747 1.8×	131 0.3×	77 0.3×	24	1.9k
Nicole Dünker Germany	20	944 0.6×	183 0.2×	153 0.4×	103 0.3×	56 0.2×	60	1.8k
Gary S. L. Peh Singapore	32	890 0.6×	597 0.8×	100 0.2×	2.1k 5.4×	79 0.3×	83	3.2k
Oliver Brandau Germany	19	906 0.6×	135 0.2×	286 0.7×	73 0.2×	87 0.3×	38	1.9k
Ben Mead United Kingdom	20	1.3k 0.8×	511 0.7×	72 0.2×	397 1.0×	38 0.1×	39	2.0k
Robert D. Sampson United Kingdom	18	1.0k 0.7×	149 0.2×	130 0.3×	95 0.2×	158 0.6×	28	1.5k

Countries citing papers authored by Panfeng Wang

Since Specialization

Citations

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

Fields of papers citing papers by Panfeng Wang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Panfeng Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Panfeng Wang. A scholar is included among the top collaborators of Panfeng 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 Panfeng Wang. Panfeng Wang 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

Zhen, Yi, Yingwei Wang, Jie Liu, et al.. (2025). Retinitis Pigmentosa‐Associated Gene TRIM49 Regulates ULK1‐Mediated Autophagy and Photoreceptor Phagocytosis by the Retinal Pigment Epithelium. Advanced Science. 12(43). e12305–e12305.

Yang, Min, Lin Zhuo, Peng Wang, et al.. (2024). Development of a prediction model for predicting the prevalence of nonalcoholic fatty liver disease in Chinese nurses: the first-year follow data of a web-based ambispective cohort study. BMC Gastroenterology. 24(1). 72–72. 2 indexed citations

Xiao, Xueshan, Wenmin Sun, Shiqiang Li, et al.. (2024). Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia. Journal of Translational Medicine. 22(1). 75–75. 7 indexed citations

Wang, Panfeng, Shiqiang Li, Yi Jiang, et al.. (2024). Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genes. Brain. 148(5). 1604–1620. 2 indexed citations

Li, Xueqing, Hui Xiao, Xueshan Xiao, et al.. (2024). Clinical features of patients with mutations in genes for nanophthalmos. British Journal of Ophthalmology. 108(12). 1679–1687. 1 indexed citations

Zhen, Yi, Xueshan Xiao, Shiqiang Li, et al.. (2023). Clinical and Genetic Features of NR2E3-Associated Retinopathy: A Report of Eight Families with a Longitudinal Study and Literature Review. Genes. 14(8). 1525–1525. 3 indexed citations

Zhen, Yi, Yingwei Wang, Yi Jiang, et al.. (2023). FDXR-Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population. Genes. 14(4). 952–952. 8 indexed citations

Wang, Yingwei, Yi Jiang, Yi Zhen, et al.. (2023). New Insight into the Genotype-Phenotype Correlation of PRPH2-Related Diseases Based on a Large Chinese Cohort and Literature Review. International Journal of Molecular Sciences. 24(7). 6728–6728. 6 indexed citations

Li, Shiqiang, Yi Jiang, Zhen Yi, et al.. (2023). Pathogenic Variants in CEP290 or IQCB1 Cause Earlier-Onset Retinopathy in Senior-Loken Syndrome Compared to Those in INVS, NPHP3, or NPHP4. American Journal of Ophthalmology. 252. 188–204. 8 indexed citations

10.

Zhou, Wenhui, et al.. (2023). Defect of TIMP4 Is Associated with High Myopia and Participates in Rat Ocular Development in a Dose-Dependent Manner. International Journal of Molecular Sciences. 24(23). 16928–16928. 4 indexed citations

11.

Wang, Jingpin, Siwei Zhang, Lin Zhuo, et al.. (2023). Relationship between night shift and sleep problems, risk of metabolic abnormalities of nurses: a 2 years follow-up retrospective analysis in the National Nurse Health Study (NNHS). International Archives of Occupational and Environmental Health. 96(10). 1361–1371. 13 indexed citations

12.

Wang, Yingwei, Yi Jiang, Shiqiang Li, et al.. (2023). Variant Landscape of 15 Genes Involved in Corneal Dystrophies: Report of 30 Families and Comprehensive Analysis of the Literature. International Journal of Molecular Sciences. 24(5). 5012–5012.

13.

Wang, Yingwei, Xueshan Xiao, Xueqing Li, et al.. (2022). Genetic and clinical landscape ofARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance. British Journal of Ophthalmology. 107(10). 1545–1553. 19 indexed citations

14.

Sun, Wenmin, Xueshan Xiao, Shiqiang Li, et al.. (2021). Clinical and genetic features of retinoschisis in 120 families withRS1mutations. British Journal of Ophthalmology. 107(3). 367–372. 11 indexed citations

15.

Wang, Panfeng, Xiaoyun Jia, Wenmin Sun, et al.. (2021). Pathogenicity evaluation and the genotype–phenotype analysis of OPA1 variants. Molecular Genetics and Genomics. 296(4). 845–862. 5 indexed citations

16.

Xiao, Xueshan, Shiqiang Li, Xiaoyun Jia, et al.. (2021). Severe Exudative Vitreoretinopathy as a Common Feature for CTNNB1, KIF11 and NDP Variants Plus Sector Degeneration for KIF11. American Journal of Ophthalmology. 235. 178–187. 5 indexed citations

17.

Sun, Wenmin, Shiqiang Li, Xiaoyun Jia, et al.. (2020). Structural variations in a non-coding region at 1q32.1 are responsible for the NYS7 locus in two large families. Human Genetics. 139(8). 1057–1064. 4 indexed citations

18.

Huang, Li, Limei Sun, Zhirong Wang, et al.. (2020). Clinical manifestation and genetic analysis in Chinese early onset X‐linked retinoschisis. Molecular Genetics & Genomic Medicine. 8(10). e1421–e1421. 14 indexed citations

19.

Li, Shiqiang, et al.. (2012). Identification of FZD4 and LRP5 mutations in 11 of 49 families with familial exudative vitreoretinopathy.. PubMed Central. 36 indexed citations

20.

Wang, Panfeng, Zhikuan Yang, Shiqiang Li, et al.. (2009). Evaluation of MFRP as a candidate gene for high hyperopia.. PubMed. 15. 181–6. 12 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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