Li Yuan

449 total citations
13 papers, 322 citations indexed

About

Li Yuan is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, Li Yuan has authored 13 papers receiving a total of 322 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Cellular and Molecular Neuroscience, 7 papers in Molecular Biology and 3 papers in Cell Biology. Recurrent topics in Li Yuan's work include Neuroscience and Neuropharmacology Research (4 papers), Wnt/β-catenin signaling in development and cancer (4 papers) and Axon Guidance and Neuronal Signaling (3 papers). Li Yuan is often cited by papers focused on Neuroscience and Neuropharmacology Research (4 papers), Wnt/β-catenin signaling in development and cancer (4 papers) and Axon Guidance and Neuronal Signaling (3 papers). Li Yuan collaborates with scholars based in United States, China and India. Li Yuan's co-authors include Jyothi Arikkath, Eunju Seong, Yu Cai, Shilpa Buch, Lu Yang, Huangui Xiong, Fang Niu, Xufeng Chen, Guoku Hu and Han Liu and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and The Journal of Cell Biology.

In The Last Decade

Li Yuan

13 papers receiving 319 citations

Peers

Li Yuan

MB

CMN

PHYSI

GENET

NEURO

Héctor Albert‐Gascó Spain

Akito Nakao Japan

Vera Medvedeva United States

Juan Esteban Oyarzún Chile

Dove Keith United States

Juliann D. Jaumotte United States

Carla Montecinos-Oliva Chile

Huantong Wu China

Livia La Barbera Italy

Margaret E. Maes United States

Héctor Albert‐Gascó Spain

Li Yuan

109 ×0.8

MB

57 ×0.6

CMN

48 ×0.8

PHYSI

29 ×0.6

GENET

39 ×0.9

NEURO

Citations per year, relative to Li Yuan Li Yuan (= 1×) peers Héctor Albert‐Gascó

Countries citing papers authored by Li Yuan

Since Specialization

Citations

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

Fields of papers citing papers by Li Yuan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Li Yuan

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

All Works

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13 of 13 papers shown

1.

Yuan, Li, et al.. (2024). Massive multiplexing of spatially resolved single neuron projections with axonal BARseq. Nature Communications. 15(1). 8371–8371. 3 indexed citations

2.

Seong, Eunju, Li Yuan, Yu Cai, et al.. (2020). δ-Catenin engages the autophagy pathway to sculpt the developing dendritic arbor. Journal of Biological Chemistry. 295(32). 10988–11001. 7 indexed citations

3.

Chen, Jinlong, Lining Liang, Li Yuan, et al.. (2020). Naloxone regulates the differentiation of neural stem cells via a receptor‐independent pathway. The FASEB Journal. 34(4). 5917–5930. 11 indexed citations

4.

Yuan, Li, et al.. (2018). Neuron-Type Specific Loss of CDKL5 Leads to Alterations in mTOR Signaling and Synaptic Markers. Molecular Neurobiology. 56(6). 4151–4162. 17 indexed citations

5.

Kumar, Sushil, et al.. (2018). Intracellular amyloid beta expression leads to dysregulation of the mitogen-activated protein kinase and bone morphogenetic protein-2 signaling axis. PLoS ONE. 13(2). e0191696–e0191696. 15 indexed citations

6.

Yuan, Li, Quan Li, Chun‐Shui Pan, et al.. (2018). Bushen Huoxue Attenuates Diabetes-Induced Cognitive Impairment by Improvement of Cerebral Microcirculation: Involvement of RhoA/ROCK/moesin and Src Signaling Pathways. Frontiers in Physiology. 9. 527–527. 20 indexed citations

7.

Yuan, Li, et al.. (2018). A role for proteolytic regulation of δ-catenin in remodeling a subpopulation of dendritic spines in the rodent brain. Journal of Biological Chemistry. 293(29). 11625–11638. 3 indexed citations

8.

Yuan, Li & Jyothi Arikkath. (2017). Functional roles of p120ctn family of proteins in central neurons. Seminars in Cell and Developmental Biology. 69. 70–82. 19 indexed citations

9.

Cai, Yu, Lu Yang, Guoku Hu, et al.. (2016). Regulation of morphine-induced synaptic alterations: Role of oxidative stress, ER stress, and autophagy. The Journal of Cell Biology. 215(2). 245–258. 83 indexed citations

10.

Yuan, Yang, et al.. (2015). Differential regulation of apical–basolateral dendrite outgrowth by activity in hippocampal neurons. Frontiers in Cellular Neuroscience. 9. 314–314. 4 indexed citations

11.

Yuan, Li, et al.. (2015). δ-Catenin Regulates Spine Architecture via Cadherin and PDZ-dependent Interactions. Journal of Biological Chemistry. 290(17). 10947–10957. 26 indexed citations

12.

Seong, Eunju, Li Yuan, & Jyothi Arikkath. (2015). Cadherins and catenins in dendrite and synapse morphogenesis. Cell Adhesion & Migration. 9(3). 202–213. 76 indexed citations

13.

Duysen, Ellen G., et al.. (2010). Visualization of exogenous delivery of nanoformulated butyrylcholinesterase to the central nervous system. Chemico-Biological Interactions. 187(1-3). 295–298. 38 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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