Lingfei Luo

3.3k total citations
91 papers, 2.1k citations indexed

About

Lingfei Luo is a scholar working on Molecular Biology, Surgery and Cell Biology. According to data from OpenAlex, Lingfei Luo has authored 91 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 23 papers in Surgery and 21 papers in Cell Biology. Recurrent topics in Lingfei Luo's work include Pancreatic function and diabetes (19 papers), Congenital heart defects research (16 papers) and Zebrafish Biomedical Research Applications (16 papers). Lingfei Luo is often cited by papers focused on Pancreatic function and diabetes (19 papers), Congenital heart defects research (16 papers) and Zebrafish Biomedical Research Applications (16 papers). Lingfei Luo collaborates with scholars based in China, Germany and Bangladesh. Lingfei Luo's co-authors include Jianbo He, Huiqiang Lu, Qifen Yang, Jingying Chen, Michael Kessel, Rui Ni, Sizhou Huang, Hendrik Knoetgen, Xiaoping Yang and Yoshihiro Takihara and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Lingfei Luo

85 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lingfei Luo China	23	1.0k	452	443	306	276	91	2.1k
Emma Andersson Sweden	25	1.7k 1.7×	270 0.6×	239 0.5×	116 0.4×	197 0.7×	61	2.6k
Hitomi Aoki Japan	24	1.2k 1.2×	395 0.9×	239 0.5×	105 0.3×	131 0.5×	90	2.2k
Younès Achouri Belgium	26	1.8k 1.7×	317 0.7×	569 1.3×	280 0.9×	230 0.8×	53	3.3k
Marina Macı́as-Silva Mexico	23	2.3k 2.2×	229 0.5×	220 0.5×	146 0.5×	254 0.9×	74	3.1k
Donghun Shin United States	22	1.2k 1.1×	436 1.0×	880 2.0×	579 1.9×	77 0.3×	46	2.2k
Anna-Pavlina G. Haramis Netherlands	15	2.8k 2.7×	526 1.2×	426 1.0×	108 0.4×	170 0.6×	20	3.8k
Christophe Fuerer Switzerland	18	1.7k 1.6×	224 0.5×	257 0.6×	92 0.3×	79 0.3×	30	2.1k
Jian‐Zhong Shao China	29	1.2k 1.1×	109 0.2×	413 0.9×	201 0.7×	296 1.1×	51	2.3k
Giovanni Di Bernardo Italy	29	1.0k 1.0×	91 0.2×	345 0.8×	159 0.5×	122 0.4×	125	2.6k

Countries citing papers authored by Lingfei Luo

Since Specialization

Citations

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

Fields of papers citing papers by Lingfei Luo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lingfei Luo

This figure shows the co-authorship network connecting the top 25 collaborators of Lingfei Luo. A scholar is included among the top collaborators of Lingfei Luo 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 Lingfei Luo. Lingfei Luo 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

Cai, Pengcheng, et al.. (2026). PDGF signaling drives bipotential progenitor cell re-differentiation during zebrafish biliary-mediated liver regeneration. Development. 153(6).

He, Jianbo, Shuang Li, Jianlong Ma, et al.. (2025). Gallbladder-derived retinoic acid signalling drives reconstruction of the damaged intrahepatic biliary ducts. Nature Cell Biology. 27(1). 39–47. 3 indexed citations

Ruan, Hua, Dan Wu, Pengfei Jiang, et al.. (2024). An animal model recapitulates human hepatic diseases associated with GATA6 mutations. Proceedings of the National Academy of Sciences. 122(1). e2317801121–e2317801121. 1 indexed citations

Liu, Shengnan, Ming Su, Chen‐Yu Lin, et al.. (2024). TANGO6 regulates cell proliferation via COPI vesicle-mediated RPB2 nuclear entry. Nature Communications. 15(1). 2371–2371. 1 indexed citations

Liu, Huijuan, et al.. (2024). Mdka produced by the activated HSCs drives bipotential progenitor cell redifferentiation during zebrafish biliary-mediated liver regeneration. Hepatology. 81(5). 1400–1415. 3 indexed citations

Song, Jingmei, Jianlong Ma, Xing Liu, et al.. (2023). The MRN complex maintains the biliary-derived hepatocytes in liver regeneration through ATR-Chk1 pathway. npj Regenerative Medicine. 8(1). 20–20. 7 indexed citations

Wu, Chao‐Ying, Wenfeng Zhang, Xinjuan Wang, et al.. (2023). Zebrafish ppp1r21 mutant as a model for the study of primary biliary cholangitis. Journal of genetics and genomics. 50(12). 1004–1013. 5 indexed citations

Luo, Lingfei, Sudipto Roy, Li Li, & Ming Ma. (2023). Polycystic kidney disease: novel insights into polycystin function. Trends in Molecular Medicine. 29(4). 268–281. 22 indexed citations

Yang, Yun, Yanfeng Li, Shuang Li, et al.. (2022). Intestinal precursors avoid being misinduced to liver cells by activating Cdx-Wnt inhibition cascade. Proceedings of the National Academy of Sciences. 119(45). e2205110119–e2205110119. 13 indexed citations

10.

Yang, Yun, Hao Wang, Jia He, et al.. (2021). A single-cell–resolution fate map of endoderm reveals demarcation of pancreatic progenitors by cell cycle. Proceedings of the National Academy of Sciences. 118(25). 20 indexed citations

11.

Zhang, Wenfeng, et al.. (2021). Formimidoyltransferase cyclodeaminase prevents the starvation-induced liver hepatomegaly and dysfunction through downregulating mTORC1. PLoS Genetics. 17(12). e1009980–e1009980. 13 indexed citations

12.

Chen, Jingying, Xiuhua Li, Rui Ni, et al.. (2021). Acute brain vascular regeneration occurs via lymphatic transdifferentiation. Developmental Cell. 56(22). 3115–3127.e6. 35 indexed citations

13.

Wang, Xinjuan, et al.. (2021). The Lysosomal Storage Disorder Due to fig4a Mutation Causes Robust Liver Vacuolation in Zebrafish. Zebrafish. 18(3). 175–183. 5 indexed citations

14.

Wang, Hao, et al.. (2020). Key Developmental Regulators Suggest Multiple Origins of Pancreatic Beta Cell Regeneration. Zebrafish. 17(3). 187–195. 5 indexed citations

15.

Dong, Guoping, Yueyue Huang, Lingfei Luo, et al.. (2019). Mypt1 regulates Bmp signaling to promote embryonic exocrine pancreas growth in zebrafish. genesis. 58(2). e23345–e23345. 1 indexed citations

16.

Yu, Jia, Chao Ma, Guoping Dong, et al.. (2019). The effector of Hippo signaling, Taz, is required for formation of the micropyle and fertilization in zebrafish. PLoS Genetics. 15(1). e1007408–e1007408. 15 indexed citations

17.

Gao, Ce, Weidong Huang, Li Jan Lo, et al.. (2018). Zebrafish hhex-null mutant develops an intrahepatic intestinal tube due to de-repression of cdx1b and pdx1. Journal of Molecular Cell Biology. 11(6). 448–462. 29 indexed citations

18.

Yu, Jia, Chao Ma, Li Li, et al.. (2018). Yap1/Taz are essential for the liver development in zebrafish. Biochemical and Biophysical Research Communications. 503(1). 131–137. 12 indexed citations

19.

Tian, Ye, Jin Xu, Sicong He, et al.. (2017). The first wave of T lymphopoiesis in zebrafish arises from aorta endothelium independent of hematopoietic stem cells. The Journal of Experimental Medicine. 214(11). 3347–3360. 68 indexed citations

20.

Lu, Huiqiang, et al.. (2013). EpCAM Is an Endoderm-Specific Wnt Derepressor that Licenses Hepatic Development. Developmental Cell. 24(5). 543–553. 127 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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