This map shows the geographic impact of Chongfei Jin'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 Chongfei Jin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chongfei Jin more than expected).
This network shows the impact of papers produced by Chongfei Jin. 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 Chongfei Jin. The network helps show where Chongfei Jin may publish in the future.
Co-authorship network of co-authors of Chongfei Jin
This figure shows the co-authorship network connecting the top 25 collaborators of Chongfei Jin.
A scholar is included among the top collaborators of Chongfei Jin 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 Chongfei Jin. Chongfei Jin is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Li, David, Chongfei Jin, Xiaodong Jiao, et al.. (2014). AIPL1 implicated in the pathogenesis of two cases of autosomal recessive retinal degeneration.. PubMed. 20. 1–14.5 indexed citations
8.
Bennett, Thomas M., Giovanni Maraini, Chongfei Jin, et al.. (2013). Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataract.. PubMed. 19. 835–44.9 indexed citations
Yao, Ke, Jinyu Li, Chongfei Jin, et al.. (2011). Characterization of a novel mutation in the CRYBB2 gene associated with autosomal dominant congenital posterior subcapsular cataract in a Chinese family.. PubMed. 17. 144–52.19 indexed citations
12.
Yao, Ke, et al.. (2011). [Clinical evaluation on the coaxial 1.8 mm microincision cataract surgery].. PubMed. 47(10). 903–7.4 indexed citations
13.
Wang, Wei, Jin Jiang, Yanan Zhu, et al.. (2010). A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese family.. PubMed. 16. 534–9.29 indexed citations
14.
Jin, Chongfei, Jin Jiang, Wei Wang, & Ke Yao. (2010). Identification of a MIP mutation that activates a cryptic acceptor splice site in the 3' untranslated region.. PubMed. 16. 2253–8.5 indexed citations
15.
Shentu, Xingchao, et al.. (2009). [Computer construction and analysis of protein models of mutant fibrillin-1 gene in Marfan's syndrome].. PubMed. 45(8). 699–702.1 indexed citations
16.
Jiang, Jin, Chongfei Jin, Wei Wang, et al.. (2009). Identification of a novel splice-site mutation in MIP in a Chinese congenital cataract family.. PubMed. 15. 38–44.26 indexed citations
17.
Zhang, Zhiyong, Ke Yao, & Chongfei Jin. (2009). Apoptosis of lens epithelial cells induced by high concentration of glucose is associated with a decrease in caveolin-1 levels.. PubMed. 15. 2008–17.11 indexed citations
Yao, Ke, Chongfei Jin, Ning Zhu, et al.. (2008). A nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese family.. PubMed. 14. 1272–6.27 indexed citations
20.
Jin, Chongfei, Ke Yao, Jin Jiang, et al.. (2007). Novel FBN1 mutations associated with predominant ectopia lentis and marfanoid habitus in Chinese patients.. PubMed. 13. 1280–4.22 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.