Fu Xiong

1.7k total citations
82 papers, 1.1k citations indexed

About

Fu Xiong is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Fu Xiong has authored 82 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 31 papers in Genetics and 21 papers in Genetics. Recurrent topics in Fu Xiong's work include Hemoglobinopathies and Related Disorders (18 papers), Muscle Physiology and Disorders (16 papers) and Iron Metabolism and Disorders (9 papers). Fu Xiong is often cited by papers focused on Hemoglobinopathies and Related Disorders (18 papers), Muscle Physiology and Disorders (16 papers) and Iron Metabolism and Disorders (9 papers). Fu Xiong collaborates with scholars based in China, United States and Macao. Fu Xiong's co-authors include Xiangmin Xu, Xuan Shang, Cheng Zhang, Ren Cai, Xiaofeng Wei, Yanchang Shang, Manna Sun, Yuqiu Zhou, Jiwu Lou and Chang Zhou and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Brain Research.

In The Last Decade

Fu Xiong

77 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fu Xiong China 16 556 415 296 147 142 82 1.1k
Shahram Teimourian Iran 19 197 0.4× 385 0.9× 164 0.6× 55 0.4× 164 1.2× 78 1.1k
M Kobayashi Japan 17 160 0.3× 412 1.0× 307 1.0× 210 1.4× 85 0.6× 69 1.2k
Wuyi Kong United States 16 492 0.9× 330 0.8× 607 2.1× 203 1.4× 82 0.6× 36 1.4k
Antonella Conforti Italy 17 376 0.7× 356 0.9× 151 0.5× 174 1.2× 98 0.7× 31 1.0k
Emmanuel Olivier United States 20 255 0.5× 915 2.2× 109 0.4× 282 1.9× 152 1.1× 33 1.3k
Li Ding China 22 204 0.4× 713 1.7× 151 0.5× 118 0.8× 102 0.7× 80 1.3k
Maciej Hałasa Poland 11 331 0.6× 487 1.2× 81 0.3× 213 1.4× 51 0.4× 35 913
Marjolein van Driel Netherlands 22 89 0.2× 602 1.5× 146 0.5× 92 0.6× 112 0.8× 32 1.5k
Hidetoshi Tsuda Japan 20 235 0.4× 279 0.7× 28 0.1× 356 2.4× 34 0.2× 58 1.2k
Hiroko Tsuji Japan 13 184 0.3× 215 0.5× 89 0.3× 184 1.3× 44 0.3× 38 717

Countries citing papers authored by Fu Xiong

Since Specialization
Citations

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

Fields of papers citing papers by Fu Xiong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fu Xiong

This figure shows the co-authorship network connecting the top 25 collaborators of Fu Xiong. A scholar is included among the top collaborators of Fu Xiong 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 Fu Xiong. Fu Xiong 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
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Li, Xiaoyong, et al.. (2024). Uncovering the Role of Anoikis-Related Genes in Modulating Immune Infiltration and Pathogenesis of Diabetic Kidney Disease. Journal of Inflammation Research. Volume 17. 4975–4991. 2 indexed citations
3.
Gao, Jinyu, Chaochao Luo, Junxiao Zhang, et al.. (2024). Impact of genomic and epigenomic alterations of multigene on a multicancer pedigree. Cancer Medicine. 13(13). e7394–e7394. 1 indexed citations
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Li, Hang, et al.. (2024). Four novel mutations identified in the COL4A3, COL4A4 and COL4A5 genes in 10 families with Alport syndrome. BMC Medical Genomics. 17(1). 181–181. 2 indexed citations
7.
Zhang, Yanxia, et al.. (2023). A novel gain‐of‐function PIP4K2A mutation elevates the expression of β‐globin and aggravates the severity of α‐thalassemia. British Journal of Haematology. 202(5). 1018–1023. 1 indexed citations
8.
Li, Xiaoyong, et al.. (2023). Unveiling FOS as a Potential Diagnostic Biomarker and Emetine as a Prospective Therapeutic Agent for Diabetic Nephropathy. Journal of Inflammation Research. Volume 16. 6139–6153. 1 indexed citations
9.
Lou, Jiwu, Manna Sun, Aiping Mao, et al.. (2023). Molecular spectrum and prevalence of thalassemia investigated by third-generation sequencing in the Dongguan region of Guangdong Province, Southern China. Clinica Chimica Acta. 551. 117622–117622. 7 indexed citations
10.
Zhang, Guilian, et al.. (2023). The loss of function GBA1 c.231C > G mutation associated with Parkinson disease. Journal of Neural Transmission. 130(7). 905–913. 3 indexed citations
11.
Li, Meiyi, Fei He, Zhikui Wang, et al.. (2023). Intravenous Administration of an AAV9 Vector Ubiquitously Expressing C1orf194 Gene Improved CMT-Like Neuropathy in C1orf194-/- Mice. Neurotherapeutics. 20(6). 1835–1846.
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Guo, Xiaoling, Yue Liu, Tingting Yang, et al.. (2021). Case Report: A Novel Compound Heterozygous Mutation of the FRMD4A Gene Identified in a Chinese Family With Global Developmental Delay, Intellectual Disability, and Ataxia. Frontiers in Pediatrics. 9. 775488–775488. 2 indexed citations
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Zheng, Hua, Qi Yang, Qiuxia Yu, et al.. (2015). A Double Heterozygous Mutation of <b><i>TNNI3</i></b> Causes Hypertrophic Cardiomyopathy in a Han Chinese Family. Cardiology. 133(2). 91–96. 7 indexed citations
16.
Huang, Jiwei, Xuan Shang, Ying Zhao, et al.. (2013). A novel fusion gene and a common α0-thalassemia deletion cause hemoglobin H disease in a Chinese family. Blood Cells Molecules and Diseases. 51(1). 31–34. 13 indexed citations
17.
Xiong, Fu, Qian Li, Cuimei Zhang, et al.. (2012). Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease. Cardiovascular Pathology. 22(2). 141–145. 33 indexed citations
18.
Xiong, Fu, Yong Xu, Hui Zheng, et al.. (2010). Microdystrophin Delivery in Dystrophin-Deficient (mdx) Mice by Genetically-Corrected Syngeneic MSCs Transplantation. Transplantation Proceedings. 42(7). 2731–2739. 9 indexed citations
19.
Li, Yong, et al.. (2008). Comparative study of mesenchymal stem cells from C57BL/10 and mdx mice. BMC Cell Biology. 9(1). 24–24. 33 indexed citations
20.
Xiong, Fu, Shaobo Xiao, Hui Zheng, et al.. (2007). Herpes Simplex Virus VP22 Enhances Adenovirus-Mediated Microdystrophin Gene Transfer to Skeletal Muscles in Dystrophin-Deficient ( mdx ) Mice. Human Gene Therapy. 18(6). 490–501. 8 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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