Lijian Hui

9.9k total citations · 2 hit papers
88 papers, 6.1k citations indexed

About

Lijian Hui is a scholar working on Molecular Biology, Hepatology and Surgery. According to data from OpenAlex, Lijian Hui has authored 88 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 31 papers in Hepatology and 30 papers in Surgery. Recurrent topics in Lijian Hui's work include Liver physiology and pathology (27 papers), Pancreatic function and diabetes (20 papers) and Pluripotent Stem Cells Research (11 papers). Lijian Hui is often cited by papers focused on Liver physiology and pathology (27 papers), Pancreatic function and diabetes (20 papers) and Pluripotent Stem Cells Research (11 papers). Lijian Hui collaborates with scholars based in China, United States and Austria. Lijian Hui's co-authors include Erwin F. Wagner, Pengyu Huang, Ewa Stępniak-Konieczna, Yiping Hu, Harald Scheuch, Latifa Bakiri, Dao Xiang, Chang‐Cheng Liu, Jin Cen and Xin Wang and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Lijian Hui

86 papers receiving 6.0k citations

Hit Papers

Induction of functional hepatocyte-like cells from mouse ... 2011 2026 2016 2021 2011 2014 200 400 600

Peers

Lijian Hui
Jean S. Campbell United States
Vincent W. Yang United States
Fanyin Meng United States
Jean S. Campbell United States
Lijian Hui
Citations per year, relative to Lijian Hui Lijian Hui (= 1×) peers Jean S. Campbell

Countries citing papers authored by Lijian Hui

Since Specialization
Citations

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

Fields of papers citing papers by Lijian Hui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lijian Hui

This figure shows the co-authorship network connecting the top 25 collaborators of Lijian Hui. A scholar is included among the top collaborators of Lijian Hui 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 Lijian Hui. Lijian Hui 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.
Yuan, Xiang, et al.. (2024). Cell therapy for liver diseases: From hepatocyte transplantation to bioartificial livers. Current Opinion in Biomedical Engineering. 30. 100530–100530. 2 indexed citations
2.
Fang, Zhaoyuan, Xiangkun Han, Yueqing Chen, et al.. (2023). Oxidative stress-triggered Wnt signaling perturbation characterizes the tipping point of lung adeno-to-squamous transdifferentiation. Signal Transduction and Targeted Therapy. 8(1). 16–16. 17 indexed citations
3.
Zhang, Kun, Ning Wu, Jing Cen, et al.. (2023). Ex vivo factor VIII‐modified proliferating human hepatocytes therapy for haemophilia A. Cell Proliferation. 56(5). e13467–e13467. 6 indexed citations
4.
Wang, Xujun, Zhengtao Zhang, Wenyi Qin, et al.. (2021). RePhine: An Integrative Method for Identification of Drug Response-Related Transcriptional Regulators. Genomics Proteomics & Bioinformatics. 19(4). 534–548. 3 indexed citations
5.
He, Lingli, Liang Yuan, Wentao Yu, et al.. (2020). A Regulation Loop between YAP and NR4A1 Balances Cell Proliferation and Apoptosis. Cell Reports. 33(3). 108284–108284. 76 indexed citations
6.
Li, Weiping, Liguang Yang, Qiang He, et al.. (2019). A Homeostatic Arid1a-Dependent Permissive Chromatin State Licenses Hepatocyte Responsiveness to Liver-Injury-Associated YAP Signaling. Cell stem cell. 25(1). 54–68.e5. 88 indexed citations
7.
Deng, Xing, Xin Zhang, Weiping Li, et al.. (2018). Chronic Liver Injury Induces Conversion of Biliary Epithelial Cells into Hepatocytes. Cell stem cell. 23(1). 114–122.e3. 213 indexed citations
8.
Xiao, Fei, Yajie Guo, Jiali Deng, et al.. (2018). Hepatic c-Jun regulates glucose metabolism via FGF21 and modulates body temperature through the neural signals. Molecular Metabolism. 20. 138–148. 16 indexed citations
9.
Jing, Renwei, Quan Rao, Ludi Zhang, et al.. (2018). Immortalized common marmoset (Callithrix jacchus) hepatic progenitor cells possess bipotentiality in vitro and in vivo. Cell Discovery. 4(1). 23–23. 9 indexed citations
10.
Sheng, Xiangpeng, Qing You, ZeNan Chang, et al.. (2017). Bacterial effector NleL promotes enterohemorrhagic E. coli-induced attaching and effacing lesions by ubiquitylating and inactivating JNK. PLoS Pathogens. 13(7). e1006534–e1006534. 26 indexed citations
11.
Tüysüz, Nesrin, Louis van Bloois, Stieneke van den Brink, et al.. (2017). Lipid-mediated Wnt protein stabilization enables serum-free culture of human organ stem cells. Nature Communications. 8(1). 14578–14578. 59 indexed citations
12.
Hui, Lijian, et al.. (2017). Chemical Cocktails Enable Hepatic Reprogramming of Mouse Fibroblasts with a Single Transcription Factor. Stem Cell Reports. 9(2). 499–512. 31 indexed citations
13.
Wang, Lihua, Tong Zhang, Lin Wang, et al.. (2017). Fatty acid synthesis is critical for stem cell pluripotency via promoting mitochondrial fission. The EMBO Journal. 36(10). 1330–1347. 108 indexed citations
14.
Wu, Zhitao, Dan Yao, Shuyi Ji, et al.. (2016). Optimized Hepatocyte-Like Cells with Functional Drug Transporters Directly-Reprogrammed from Mouse Fibroblasts and their Potential in Drug Disposition and Toxicology. Cellular Physiology and Biochemistry. 38(5). 1815–1830. 3 indexed citations
15.
Li, Lu, Dan Li, Feng Tian, et al.. (2016). Hepatic Loss of Borealin Impairs Postnatal Liver Development, Regeneration, and Hepatocarcinogenesis. Journal of Biological Chemistry. 291(40). 21137–21147. 12 indexed citations
16.
Zhang, Ludi, Yanjiao Shao, Lu Li, et al.. (2016). Efficient liver repopulation of transplanted hepatocyte prevents cirrhosis in a rat model of hereditary tyrosinemia type I. Scientific Reports. 6(1). 31460–31460. 22 indexed citations
17.
Qiu, Zhixin, Liping Zhuang, Jianjie Qin, et al.. (2016). Hepatocellular carcinoma cell lines retain the genomic and transcriptomic landscapes of primary human cancers. Scientific Reports. 6(1). 27411–27411. 55 indexed citations
18.
Zang, Aiping, Min Du, Dapeng Ma, et al.. (2015). mTOR regulates TLR-induced c-fos and Th1 responses to HBV and HCV vaccines. Virologica Sinica. 30(3). 174–189. 13 indexed citations
19.
Zeng, Liyong, Yihan Wan, Dan Li, et al.. (2013). The m Subunit of Murine Translation Initiation Factor eIF3 Maintains the Integrity of the eIF3 Complex and Is Required for Embryonic Development, Homeostasis, and Organ Size Control. Journal of Biological Chemistry. 288(42). 30087–30093. 27 indexed citations
20.
Huang, Pengyu, Jiahuai Han, & Lijian Hui. (2010). MAPK signaling in inflammation-associated cancer development. Protein & Cell. 1(3). 218–226. 215 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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