Xinjun Zhu

949 total citations
18 papers, 615 citations indexed

About

Xinjun Zhu is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Xinjun Zhu has authored 18 papers receiving a total of 615 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Neurology and 4 papers in Genetics. Recurrent topics in Xinjun Zhu's work include Ion Transport and Channel Regulation (4 papers), Neuroinflammation and Neurodegeneration Mechanisms (4 papers) and Tuberous Sclerosis Complex Research (2 papers). Xinjun Zhu is often cited by papers focused on Ion Transport and Channel Regulation (4 papers), Neuroinflammation and Neurodegeneration Mechanisms (4 papers) and Tuberous Sclerosis Complex Research (2 papers). Xinjun Zhu collaborates with scholars based in United States, Japan and Sweden. Xinjun Zhu's co-authors include Yunfei Huang, Xiaofeng Zhao, Ramkumar Mathur, Yuan Liao, Joseph E. Mazurkiewicz, Jun Yang, Mahabub Alam, John J. McMahon, Paul J. Feustel and Matthew A. Adamo and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and SHILAP Revista de lepidopterología.

In The Last Decade

Xinjun Zhu

18 papers receiving 613 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xinjun Zhu United States 12 209 169 120 120 115 18 615
Wei Shan China 16 172 0.8× 132 0.8× 55 0.5× 107 0.9× 143 1.2× 45 737
Xiaofeng Zhao United States 11 154 0.7× 161 1.0× 109 0.9× 88 0.7× 48 0.4× 24 458
Sean D. Hurley United States 14 205 1.0× 323 1.9× 142 1.2× 266 2.2× 139 1.2× 17 986
Zengli Zhang China 11 226 1.1× 162 1.0× 65 0.5× 81 0.7× 80 0.7× 18 544
Christian Schmeer Germany 23 575 2.8× 274 1.6× 116 1.0× 237 2.0× 167 1.5× 38 1.1k
Jaegwon Chung United States 13 205 1.0× 274 1.6× 138 1.1× 144 1.2× 153 1.3× 17 709
Zhigang Zhou China 13 207 1.0× 176 1.0× 88 0.7× 296 2.5× 204 1.8× 31 790
Khurshed A. Katki United States 13 242 1.2× 96 0.6× 69 0.6× 209 1.7× 108 0.9× 16 693
Elena Di Daniel United Kingdom 16 483 2.3× 165 1.0× 149 1.2× 275 2.3× 157 1.4× 29 934
Hans‐Georg König Ireland 15 525 2.5× 141 0.8× 100 0.8× 226 1.9× 128 1.1× 29 877

Countries citing papers authored by Xinjun Zhu

Since Specialization
Citations

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

Fields of papers citing papers by Xinjun Zhu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xinjun Zhu

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

All Works

18 of 18 papers shown
1.
Wu, Yanan, Shengyu Gao, Linlin Li, et al.. (2023). Multifunctional optical tomography system combining surface extraction and 3D fluorescence reconstruction. 26–26. 1 indexed citations
2.
Alam, Mahabub, Xiaofeng Zhao, Yuan Liao, et al.. (2021). Deficiency of Microglial Autophagy Increases the Density of Oligodendrocytes and Susceptibility to Severe Forms of Seizures. eNeuro. 8(1). ENEURO.0183–20.2021. 15 indexed citations
3.
Zhao, Xiaofeng, Yuan Liao, Mahabub Alam, et al.. (2020). Microglial mTOR is Neuronal Protective and Antiepileptogenic in the Pilocarpine Model of Temporal Lobe Epilepsy. Journal of Neuroscience. 40(40). 7593–7608. 43 indexed citations
4.
Mathur, Ramkumar, Mahabub Alam, Xiaofeng Zhao, Yunfei Huang, & Xinjun Zhu. (2019). Mechanistic Insight into the Development of TNBS-Mediated Intestinal Fibrosis and Evaluating the Inhibitory Effects of Rapamycin. Journal of Visualized Experiments. 3 indexed citations
5.
Mathur, Ramkumar, Mahabub Alam, Xiaofeng Zhao, et al.. (2019). Induction of autophagy in Cx3cr1+ mononuclear cells limits IL-23/IL-22 axis-mediated intestinal fibrosis. Mucosal Immunology. 12(3). 612–623. 53 indexed citations
6.
Zhao, Xiaofeng, Mahabub Alam, Yuan Liao, et al.. (2019). Targeting Microglia Using Cx3cr1-Cre Lines: Revisiting the Specificity. eNeuro. 6(4). ENEURO.0114–19.2019. 61 indexed citations
7.
Zhu, Xinjun, Shanti S. D’Souza, Reynold I. Lopez‐Soler, et al.. (2019). IFN-γ and IL-17A regulate intestinal crypt production of CXCL10 in the healthy and inflamed colon. American Journal of Physiology-Gastrointestinal and Liver Physiology. 318(3). G479–G489. 25 indexed citations
8.
Zhao, Xiaofeng, Yuan Liao, Ramkumar Mathur, et al.. (2018). Noninflammatory Changes of Microglia Are Sufficient to Cause Epilepsy. Cell Reports. 22(8). 2080–2093. 145 indexed citations
9.
Yin, Jianyi, Chung‐Ming Tse, Boyoung Cha, et al.. (2017). A common NHE3 single-nucleotide polymorphism has normal function and sensitivity to regulatory ligands. American Journal of Physiology-Gastrointestinal and Liver Physiology. 313(2). G129–G137. 4 indexed citations
10.
Yang, Jun, Xiaofeng Zhao, Michael T. Dolinger, et al.. (2015). Rapamycin Inhibition of mTOR Reduces Levels of the Na+/H+ Exchanger 3 in Intestines of Mice and Humans, Leading to Diarrhea. Gastroenterology. 149(1). 151–162. 31 indexed citations
11.
Padala, Santosh K., et al.. (2015). Acute Coronary Syndrome: An Unusual Consequence of GERD. SHILAP Revista de lepidopterología. 2015. 1–4. 1 indexed citations
12.
Zhu, Xinjun, Rafiquel Sarker, J.R. Horton, et al.. (2015). Nonsynonymous single nucleotide polymorphisms of NHE3 differentially decrease NHE3 transporter activity. American Journal of Physiology-Cell Physiology. 308(9). C758–C766. 9 indexed citations
13.
McMahon, John J., Wilson Yu, Jun Yang, et al.. (2014). Seizure-dependent mTOR activation in 5-HT neurons promotes autism-like behaviors in mice. Neurobiology of Disease. 73. 296–306. 19 indexed citations
14.
McMahon, John J., Xiaoxing Huang, Jun Yang, et al.. (2012). Impaired Autophagy in Neurons after Disinhibition of Mammalian Target of Rapamycin and Its Contribution to Epileptogenesis. Journal of Neuroscience. 32(45). 15704–15714. 123 indexed citations
15.
Yang, Jun, Michael T. Dolinger, Joseph E. Mazurkiewicz, et al.. (2012). Leucine Stimulates Insulin Secretion via Down-regulation of Surface Expression of Adrenergic α2A Receptor through the mTOR (Mammalian Target of Rapamycin) Pathway. Journal of Biological Chemistry. 287(29). 24795–24806. 47 indexed citations
16.
Yang, Jun, et al.. (2012). Inhibition of the mTOR Pathway Alleviates Intestinal Fibrosis Via Suppression of Myofibroblast Proliferation. Inflammatory Bowel Diseases. 18. S95–S95. 1 indexed citations
17.
Zhu, Xinjun, Boyoung Cha, Nicholas C. Zachos, et al.. (2011). Elevated Calcium Acutely Regulates Dynamic Interactions of NHERF2 and NHE3 Proteins in Opossum Kidney (OK) Cell Microvilli. Journal of Biological Chemistry. 286(40). 34486–34496. 15 indexed citations
18.
Cha, Boyoung, Xinjun Zhu, Weiping Chen, et al.. (2010). NHE3 mobility in brush borders increases upon NHERF2-dependent stimulation by lyophosphatidic acid. Journal of Cell Science. 123(14). 2434–2443. 19 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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