Yiguo Zhang

4.4k total citations · 1 hit paper
100 papers, 3.4k citations indexed

About

Yiguo Zhang is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Yiguo Zhang has authored 100 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Molecular Biology, 18 papers in Cell Biology and 10 papers in Oncology. Recurrent topics in Yiguo Zhang's work include Genomics, phytochemicals, and oxidative stress (46 papers), Endoplasmic Reticulum Stress and Disease (15 papers) and Glutathione Transferases and Polymorphisms (12 papers). Yiguo Zhang is often cited by papers focused on Genomics, phytochemicals, and oxidative stress (46 papers), Endoplasmic Reticulum Stress and Disease (15 papers) and Glutathione Transferases and Polymorphisms (12 papers). Yiguo Zhang collaborates with scholars based in China, United States and United Kingdom. Yiguo Zhang's co-authors include John D. Hayes, Zigang Dong, Ann M. Bode, Sudhir Chowdhry, Calum Sutherland, Michael McMahon, Antonio Cuadrado, Yuancai Xiang, Masayuki Yamamoto and Weiya Ma and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Yiguo Zhang

93 papers receiving 3.3k citations

Hit Papers

Nrf2 is controlled by two distinct β-TrCP recognition mot... 2012 2026 2016 2021 2012 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yiguo Zhang China 33 2.4k 534 303 292 263 100 3.4k
Zhiguo Zhang China 36 2.4k 1.0× 171 0.3× 498 1.6× 159 0.5× 332 1.3× 133 4.6k
Haifeng Chen China 29 1.3k 0.6× 107 0.2× 183 0.6× 173 0.6× 135 0.5× 190 2.8k
Xiaofeng Tian China 30 1.8k 0.8× 145 0.3× 874 2.9× 192 0.7× 313 1.2× 110 3.5k
Xiong Li China 24 1.3k 0.6× 157 0.3× 410 1.4× 301 1.0× 73 0.3× 45 1.9k
Sanjay Pandey India 19 960 0.4× 229 0.4× 252 0.8× 240 0.8× 242 0.9× 44 2.3k
Sabu Abraham India 27 1.5k 0.6× 464 0.9× 261 0.9× 365 1.3× 98 0.4× 53 2.5k
Zhongfa Liu United States 31 2.7k 1.1× 59 0.1× 1.1k 3.7× 311 1.1× 165 0.6× 106 4.3k
Minghan Wang China 29 1.5k 0.6× 139 0.3× 98 0.3× 168 0.6× 460 1.7× 147 3.3k
Jun Xia China 35 2.1k 0.9× 101 0.2× 794 2.6× 362 1.2× 413 1.6× 123 3.4k
Xu Ma China 26 963 0.4× 55 0.1× 206 0.7× 206 0.7× 46 0.2× 93 2.0k

Countries citing papers authored by Yiguo Zhang

Since Specialization
Citations

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

Fields of papers citing papers by Yiguo Zhang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yiguo Zhang

This figure shows the co-authorship network connecting the top 25 collaborators of Yiguo Zhang. A scholar is included among the top collaborators of Yiguo Zhang 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 Yiguo Zhang. Yiguo Zhang 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.
Liu, Keli, Shiqun Chen, Shaofan Hu, et al.. (2025). Inhibition of NFE2L1 Enables the Tumor‐Associated Macrophage Polarization and Enhances Anti‐PD1 Immunotherapy in Glioma. CNS Neuroscience & Therapeutics. 31(7). e70488–e70488.
3.
Chen, Xi, Ping Sheng, Jian Song, et al.. (2025). A bright lipid drop-targeted probe for dual channel visualizing of colorectal cancer. Sensors and Actuators B Chemical. 440. 137936–137936.
6.
Zheng, Ze, Shaofan Hu, Jing Feng, et al.. (2023). Loss of Nrf1 rather than Nrf2 leads to inflammatory accumulation of lipids and reactive oxygen species in human hepatoma cells, which is alleviated by 2-bromopalmitate. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1871(2). 119644–119644. 7 indexed citations
7.
Zhang, Xuemei, Yi Guo, Changhaoyue Xu, et al.. (2023). Chemical and electrochemical synergistic weaving stable interface enabling longevous zinc plating/stripping process. Chemical Engineering Journal. 457. 141305–141305. 21 indexed citations
8.
Zhang, Yiguo, Liu X, Guojie Zhang, et al.. (2020). Barriers and Strategies: A Review of Access to Affordable Multi-Drug Resistant Tuberculosis Medication in China. SHILAP Revista de lepidopterología. 1 indexed citations
9.
Zhu, Yuping, Ze Zheng, Yuancai Xiang, & Yiguo Zhang. (2020). Glucose Starvation-Induced Rapid Death of Nrf1 α -Deficient, but Not Nrf2-Deficient, Hepatoma Cells Results from Its Fatal Defects in the Redox Metabolism Reprogramming. Oxidative Medicine and Cellular Longevity. 2020. 1–20. 12 indexed citations
10.
Chen, Jiayu, Meng Wang, Yuancai Xiang, et al.. (2020). Nrf1 Is Endowed with a Dominant Tumor-Repressing Effect onto the Wnt/ β -Catenin-Dependent and Wnt/ β -Catenin-Independent Signaling Networks in the Human Liver Cancer. Oxidative Medicine and Cellular Longevity. 2020. 1–28. 15 indexed citations
11.
Zhang, Wei, Suyi Liu, Yong Gong, et al.. (2020). A facile strategy for observation of helical carbon nanofiber fillers in polymer matrix under different stresses. Polymer Testing. 93. 106977–106977. 1 indexed citations
12.
Zhang, Yiguo, et al.. (2020). A New Method for Ultra-Low Permeability Reservoir Characterization After Water Flooding Development. Journal of Energy Resources Technology. 142(11). 6 indexed citations
13.
Hou, Yongyong, Zhiyuan Liu, Zhuo Zuo, et al.. (2018). Adipocyte-specific deficiency of Nfe2l1 disrupts plasticity of white adipose tissues and metabolic homeostasis in mice. Biochemical and Biophysical Research Communications. 503(1). 264–270. 33 indexed citations
14.
Ren, Yonggang, Lu Qiu, Feng-Lin Lu, et al.. (2016). TALENs-directed knockout of the full-length transcription factor Nrf1α that represses malignant behaviour of human hepatocellular carcinoma (HepG2) cells. Scientific Reports. 6(1). 23775–23775. 35 indexed citations
15.
Xiang, Yuancai, et al.. (2016). The Proceedings of IscA That Functions as a Biomagnetic Receptor Protein (MagR). 43(12). 1128. 7 indexed citations
16.
Zhang, Yiguo, Shaojun Li, Yuancai Xiang, et al.. (2015). The selective post-translational processing of transcription factor Nrf1 yields distinct isoforms that dictate its ability to differentially regulate gene expression. Scientific Reports. 5(1). 12983–12983. 42 indexed citations
17.
Dong, Yunpeng, Xiaoming Liu, Franz Neubauer, et al.. (2012). Timing of Paleozoic amalgamation between the North China and South China Blocks: Evidence from detrital zircon U–Pb ages. Tectonophysics. 586. 173–191. 223 indexed citations
18.
Chowdhry, Sudhir, Yiguo Zhang, Michael McMahon, et al.. (2012). Nrf2 is controlled by two distinct β-TrCP recognition motifs in its Neh6 domain, one of which can be modulated by GSK-3 activity. Oncogene. 32(32). 3765–3781. 550 indexed citations breakdown →
19.
Wu, Yongjun, WU Yi-ming, WU Yi-ming, et al.. (2011). An optimal tumor marker group-coupled artificial neural network for diagnosis of lung cancer. Expert Systems with Applications. 38(9). 11329–11334. 27 indexed citations
20.
Zhang, Yiguo, Ziming Dong, Ann M. Bode, et al.. (2001). Induction of EGFR-Dependent and EGFR-Independent Signaling Pathways by Ultraviolet A Irradiation. DNA and Cell Biology. 20(12). 769–779. 23 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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