Jiangxia Li

990 total citations
40 papers, 755 citations indexed

About

Jiangxia Li is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jiangxia Li has authored 40 papers receiving a total of 755 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jiangxia Li's work include MicroRNA in disease regulation (4 papers), RNA Research and Splicing (4 papers) and interferon and immune responses (3 papers). Jiangxia Li is often cited by papers focused on MicroRNA in disease regulation (4 papers), RNA Research and Splicing (4 papers) and interferon and immune responses (3 papers). Jiangxia Li collaborates with scholars based in China, United States and Russia. Jiangxia Li's co-authors include Qiji Liu, Yaoqin Gong, Shan Shan, Xianli Bian, Changshun Shao, Jie Dang, Fei Gao, Qianqian Yuan, Xiaochun Ma and Xi Li and has published in prestigious journals such as The Journal of Immunology, Biomaterials and Scientific Reports.

In The Last Decade

Jiangxia Li

37 papers receiving 749 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jiangxia Li China	18	478	145	123	119	85	40	755
Baichun Jiang China	21	783 1.6×	167 1.2×	147 1.2×	85 0.7×	62 0.7×	51	1.1k
Takahide Tohmonda Japan	20	598 1.3×	81 0.6×	90 0.7×	137 1.2×	58 0.7×	24	905
Eva M. Monsalve Spain	13	342 0.7×	247 1.7×	152 1.2×	62 0.5×	32 0.4×	18	668
Roberto Paredes Chile	16	610 1.3×	74 0.5×	105 0.9×	160 1.3×	55 0.6×	30	913
Sophie Godard France	11	632 1.3×	121 0.8×	320 2.6×	196 1.6×	117 1.4×	17	1.3k
Keith W. McLarren Canada	11	763 1.6×	270 1.9×	136 1.1×	138 1.2×	56 0.7×	12	1.1k
Alexa Burger Switzerland	17	902 1.9×	111 0.8×	132 1.1×	140 1.2×	38 0.4×	30	1.2k
Zunyi Zhang China	22	847 1.8×	77 0.5×	260 2.1×	217 1.8×	83 1.0×	58	1.3k
Akio Mantani Japan	9	445 0.9×	157 1.1×	67 0.5×	138 1.2×	36 0.4×	12	779
C. Herbert Pratt United States	12	295 0.6×	113 0.8×	38 0.3×	113 0.9×	43 0.5×	20	898

Countries citing papers authored by Jiangxia Li

Since Specialization

Citations

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

Fields of papers citing papers by Jiangxia Li

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jiangxia Li

This figure shows the co-authorship network connecting the top 25 collaborators of Jiangxia Li. A scholar is included among the top collaborators of Jiangxia Li 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 Jiangxia Li. Jiangxia Li is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Song, Yu, Zhengbin Li, Shang Gao, et al.. (2024). SMEK1 ablation promotes glucose uptake and improves obesity-related metabolic dysfunction via AMPK signaling pathway. American Journal of Physiology-Endocrinology and Metabolism. 326(6). E776–E790. 2 indexed citations

Xu, Zhiliang, Yecheng Jin, Wenjie Sun, et al.. (2024). Near-infrared light induces neurogenesis and modulates anxiety-like behavior. Stem Cell Research & Therapy. 15(1). 494–494. 1 indexed citations

Ai, Liu, Shang Gao, Yiming Liu, et al.. (2024). Loss of Smek1 Induces Tauopathy and Triggers Neurodegeneration by Regulating Microtubule Stability. Advanced Science. 11(40). e2400584–e2400584. 3 indexed citations

Gao, Shang, et al.. (2022). Ppp4r3a deficiency leads to depression-like behaviors in mice by modulating the synthesis of synaptic proteins. Disease Models & Mechanisms. 15(6). 6 indexed citations

Li, Yan, Anran Wang, Fei Gao, et al.. (2021). Lack of WDFY4 Aggravates Ovalbumin-Induced Asthma via Enhanced Th2 Cell Differentiation. International Archives of Allergy and Immunology. 182(11). 1089–1096. 4 indexed citations

Li, Pengyu, et al.. (2021). COL2A1 Mutation (c.611G>C) Leads to Early-Onset Osteoarthritis in a Chinese Family. International Journal of General Medicine. Volume 14. 2569–2574. 5 indexed citations

Li, Yan, Jiangxia Li, Qianqian Yuan, et al.. (2021). Deficiency in WDFY4 reduces the number of CD8+ T cells via reactive oxygen species-induced apoptosis. Molecular Immunology. 139. 131–138. 10 indexed citations

Xia, Yangyang, Jianfeng Cui, Yong Wang, et al.. (2021). Berberine suppresses bladder cancer cell proliferation by inhibiting JAK1-STAT3 signaling via upregulation of miR-17-5p. Biochemical Pharmacology. 188. 114575–114575. 35 indexed citations

Li, Pengyu, Yan Li, Fei Gao, et al.. (2020). A SMOC2 variant inhibits BMP signaling by competitively binding to BMPR1B and causes growth plate defects. Bone. 142. 115686–115686. 17 indexed citations

10.

Bian, Xianli, Pengfei Lin, Jiangxia Li, et al.. (2018). Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in NEFH in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in NEFH for Charcot-Marie-Tooth 2. Neurodegenerative Diseases. 18(2-3). 74–83. 7 indexed citations

11.

Dang, Jie, Xianli Bian, Xiaochun Ma, et al.. (2017). ORMDL3 Facilitates the Survival of Splenic B Cells via an ATF6α–Endoplasmic Reticulum Stress–Beclin1 Autophagy Regulatory Pathway. The Journal of Immunology. 199(5). 1647–1659. 27 indexed citations

12.

Guo, Hui, Jisheng Li, Fei Gao, et al.. (2015). Whole-exome sequencing reveals a novel CHM gene mutation in a family with choroideremia initially diagnosed as retinitis pigmentosa. BMC Ophthalmology. 15(1). 85–85. 19 indexed citations

13.

Dang, Jie, Jiangxia Li, Shan Shan, et al.. (2015). Gene–gene interaction of ATG5, ATG7, BLK and BANK1 in systemic lupus erythematosus. International Journal of Rheumatic Diseases. 19(12). 1284–1293. 30 indexed citations

14.

Wang, Xue, Lin Li, Jiangxia Li, et al.. (2014). Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation. European Journal of Human Genetics. 22(9). 1105–1110. 27 indexed citations

15.

Qiu, Rongfang, Yang Yang, Hailing Zhao, et al.. (2013). Signal transducer and activator of transcription 6 directly regulates human ORMDL3 expression. FEBS Journal. 280(9). 2014–2026. 25 indexed citations

16.

Liu, Yongchao, Hua Zhang, Jiangxia Li, et al.. (2013). Association of common variants in KIF21B and ankylosing spondylitis in a Chinese Han population: a replication study. Immunogenetics. 65(12). 835–839. 3 indexed citations

17.

Li, Jiangxia, Yang Yang, Baichun Jiang, et al.. (2010). Sp1 and KLF15 regulate basal transcription of the human LRP5 gene. BMC Genetics. 11(1). 12–12. 20 indexed citations

18.

Zou, Yongxin, Qiji Liu, Bingxi Chen, et al.. (2007). Mutation in CUL4B, Which Encodes a Member of Cullin-RING Ubiquitin Ligase Complex, Causes X-Linked Mental Retardation. The American Journal of Human Genetics. 80(3). 561–566. 123 indexed citations

19.

Zhang, Xiyu, Qiji Liu, Bingxi Chen, et al.. (2004). A locus for nonspecific X‐linked mental retardation mapped to a 22.3 cM region of Xp11.3‐q22.3. American Journal of Medical Genetics Part A. 129A(3). 286–289. 3 indexed citations

20.

Liu, Qiji, et al.. (2002). [Linkage analysis of X-linked nuclear protein gene in Smith-Fineman-Myers syndrome].. PubMed. 19(1). 22–5. 2 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.

Explore authors with similar magnitude of impact