Fang Shen

1.1k total citations
38 papers, 740 citations indexed

About

Fang Shen is a scholar working on Molecular Biology, Epidemiology and Hepatology. According to data from OpenAlex, Fang Shen has authored 38 papers receiving a total of 740 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Epidemiology and 8 papers in Hepatology. Recurrent topics in Fang Shen's work include Hepatitis B Virus Studies (9 papers), Hepatitis C virus research (8 papers) and Epigenetics and DNA Methylation (4 papers). Fang Shen is often cited by papers focused on Hepatitis B Virus Studies (9 papers), Hepatitis C virus research (8 papers) and Epigenetics and DNA Methylation (4 papers). Fang Shen collaborates with scholars based in China, Australia and United States. Fang Shen's co-authors include Miguel C. Seabra, Jieliang Chen, Zhenghong Yuan, Lu Bai, Baocun Li, Min Wu, Jianhua Li, Guang Yang, Jiangxia Liu and Xiaonan Zhang and has published in prestigious journals such as Journal of Biological Chemistry, Hepatology and Journal of Virology.

In The Last Decade

Fang Shen

32 papers receiving 729 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fang Shen China 13 414 333 283 111 92 38 740
Charles R. Madden United States 12 596 1.4× 224 0.7× 375 1.3× 72 0.6× 132 1.4× 13 933
You‐Yu Lin Taiwan 15 397 1.0× 430 1.3× 254 0.9× 86 0.8× 45 0.5× 47 898
Marie-Anne Petit France 18 612 1.5× 198 0.6× 589 2.1× 102 0.9× 135 1.5× 35 968
Zhongliang Shen China 16 246 0.6× 258 0.8× 167 0.6× 61 0.5× 104 1.1× 39 582
Helenia Ansuini Italy 8 801 1.9× 264 0.8× 983 3.5× 71 0.6× 122 1.3× 8 1.3k
Shau‐Feng Chang Germany 11 334 0.8× 206 0.6× 196 0.7× 66 0.6× 46 0.5× 17 650
Yongxin Mu China 19 235 0.6× 480 1.4× 103 0.4× 68 0.6× 185 2.0× 33 905
Cheng-Fu Kuo United States 8 584 1.4× 255 0.8× 265 0.9× 60 0.5× 246 2.7× 10 1.0k
Sanami Takada Japan 12 431 1.0× 262 0.8× 240 0.8× 43 0.4× 80 0.9× 26 640
Nathalie Callens France 12 467 1.1× 218 0.7× 589 2.1× 93 0.8× 59 0.6× 16 881

Countries citing papers authored by Fang Shen

Since Specialization
Citations

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

Fields of papers citing papers by Fang Shen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fang Shen

This figure shows the co-authorship network connecting the top 25 collaborators of Fang Shen. A scholar is included among the top collaborators of Fang Shen 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 Fang Shen. Fang Shen 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.
Deng, Mei, Fang Shen, Yu Zheng, et al.. (2025). Synostosis of joints caused by mutant FBN2 is linked to the abnormalities and misdifferentiation of articular surface cells. Genetics in Medicine. 27(10). 101537–101537.
2.
3.
Liu, Cheng, Fang Shen, Mei Deng, et al.. (2025). AUTS2 disruption underlies radioulnar synostosis and skeletal dysmorphogenesis: evidence from four unrelated cases. Journal of Medical Genetics. 62(11). 677–681.
4.
5.
Yang, Min, et al.. (2024). Lysine demethylase KDM3A alleviates hyperoxia-induced bronchopulmonary dysplasia in mice by promoting ETS1 expression. Experimental Cell Research. 435(2). 113945–113945. 2 indexed citations
6.
Shen, Fang, Yongjia Yang, Yu Zheng, et al.. (2022). MECOM-related disorder: Radioulnar synostosis without hematological aberration due to unique variants. Genetics in Medicine. 24(5). 1139–1147. 12 indexed citations
7.
Yang, Min, et al.. (2022). Lef1 is transcriptionally activated by Klf4 and suppresses hyperoxia-induced alveolar epithelial cell injury. Experimental Lung Research. 48(7-8). 213–223.
8.
Duan, Xiaojun, Fang Shen, Yafei Deng, et al.. (2022). Novel Loss of Function (G15D) Mutation on RAC2 in a Family with Combined Immunodeficiency and Increased Levels of Immunoglobulin G, A, and E. Journal of Clinical Immunology. 43(3). 604–614. 2 indexed citations
9.
Shen, Fang, et al.. (2022). Testicular infarction and spontaneous scrotal rupture secondary to acute epididymo-orchitis. BMJ Case Reports. 15(3). e247028–e247028.
10.
Shen, Fang, Yongjia Yang, Yu Zheng, et al.. (2022). Mutant B3GALT6 in a Multiplex Family: A Dominant Variant Co-Segregated With Moderate Malformations. Frontiers in Genetics. 13. 824445–824445. 2 indexed citations
11.
Shen, Fang, Yongjia Yang, Pengcheng Li, et al.. (2021). A genotype and phenotype analysis of SMAD6 mutant patients with radioulnar synostosis. Molecular Genetics & Genomic Medicine. 10(1). e1850–e1850. 10 indexed citations
12.
Yang, Yue, Fang Shen, Nu Zhang, et al.. (2021). Case Report: Whole-Exome Sequencing of Hypothalamic Hamartoma From an Infant With Pallister-Hall Syndrome Revealed Novel de novo Mutation in the GLI3. Frontiers in Surgery. 8. 734757–734757. 4 indexed citations
13.
14.
Sheng, Hansong, Fang Shen, Nu Zhang, et al.. (2019). <p>Whole exome sequencing of multiple meningiomas with varying histopathological presentation in one patient revealed distinctive somatic mutation burden and independent clonal origins</p>. Cancer Management and Research. Volume 11. 4085–4095. 12 indexed citations
15.
Lu, Tianbao, Peter J. Connolly, Ulrike Philippar, et al.. (2019). Discovery and optimization of a series of small-molecule allosteric inhibitors of MALT1 protease. Bioorganic & Medicinal Chemistry Letters. 29(23). 126743–126743. 9 indexed citations
16.
Sozzi, Vitina, Fang Shen, Jieliang Chen, et al.. (2018). In vitro studies identify a low replication phenotype for hepatitis B virus genotype H generally associated with occult HBV and less severe liver disease. Virology. 519. 190–196. 21 indexed citations
17.
Li, Xiaofang, Jieliang Chen, Jiahui Ding, et al.. (2018). Exosomes Exploit the Virus Entry Machinery and Pathway To Transmit Alpha Interferon-Induced Antiviral Activity. Journal of Virology. 92(24). 107 indexed citations
18.
Shen, Fang, Yaming Li, Yang Wang, et al.. (2017). Hepatitis B virus sensitivity to interferon‐α in hepatocytes is more associated with cellular interferon response than with viral genotype. Hepatology. 67(4). 1237–1252. 50 indexed citations
19.
Shen, Fang, et al.. (2017). Transmission Capability of the Grid Cross Section Considering the Interruptible Load Management. DEStech Transactions on Environment Energy and Earth Science. 4 indexed citations
20.
Li, Hua, et al.. (2006). Two novel missense mutations of GATA4 gene in Chinese patients with sporadic congenital heart defects.. PubMed. 23(2). 134–7. 15 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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