Su Zhou

5.2k total citations · 2 hit papers
48 papers, 3.1k citations indexed

About

Su Zhou is a scholar working on Pulmonary and Respiratory Medicine, Surgery and Molecular Biology. According to data from OpenAlex, Su Zhou has authored 48 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Pulmonary and Respiratory Medicine, 21 papers in Surgery and 19 papers in Molecular Biology. Recurrent topics in Su Zhou's work include Neonatal Respiratory Health Research (23 papers), Congenital Diaphragmatic Hernia Studies (17 papers) and Congenital heart defects research (7 papers). Su Zhou is often cited by papers focused on Neonatal Respiratory Health Research (23 papers), Congenital Diaphragmatic Hernia Studies (17 papers) and Congenital heart defects research (7 papers). Su Zhou collaborates with scholars based in United States, China and United Kingdom. Su Zhou's co-authors include Edward E. Morrisey, Michael P. Morley, David B. Frank, Jarod A. Zepp, William J. Zacharias, Jun Kong, Edward Cantu, Apoorva Babu, Minmin Lu and Min Lü and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Su Zhou

46 papers receiving 3.0k citations

Hit Papers

Regeneration of the lung alveolus by an evolutionarily co... 2017 2026 2020 2023 2018 2017 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Su Zhou United States 22 1.5k 1.3k 1.1k 265 187 48 3.1k
Kyu Sang Song South Korea 26 464 0.3× 1.0k 0.8× 640 0.6× 364 1.4× 118 0.6× 80 2.4k
Lixin Jia China 32 685 0.5× 890 0.7× 454 0.4× 250 0.9× 117 0.6× 63 2.7k
Xavier Houard France 35 867 0.6× 889 0.7× 894 0.8× 502 1.9× 53 0.3× 67 3.6k
Xin Yi China 28 837 0.6× 1.4k 1.1× 279 0.2× 675 2.5× 123 0.7× 122 2.6k
Ken‐ichi Mukaisho Japan 25 504 0.3× 583 0.4× 760 0.7× 229 0.9× 225 1.2× 130 1.8k
Xinguo Jiang United States 27 629 0.4× 569 0.4× 431 0.4× 254 1.0× 110 0.6× 51 2.1k
Richard Seonghun Nho United States 24 809 0.5× 975 0.7× 175 0.2× 218 0.8× 105 0.6× 43 2.2k
Ting Xie China 27 1.1k 0.7× 1.0k 0.8× 447 0.4× 347 1.3× 109 0.6× 92 2.6k
Marie‐Paule Jacob France 28 510 0.3× 458 0.3× 607 0.5× 385 1.5× 63 0.3× 56 2.4k

Countries citing papers authored by Su Zhou

Since Specialization
Citations

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

Fields of papers citing papers by Su Zhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Su Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Su Zhou. A scholar is included among the top collaborators of Su Zhou 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 Su Zhou. Su Zhou 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.
Shestov, Maksim, Joseph D. Planer, Andrew R. Peterson, et al.. (2025). Shared roles of immune and stromal cells in the pathogenesis of human bronchiolitis obliterans syndrome. JCI Insight. 10(10). 1 indexed citations
2.
Li, Yuan, Zhiyan Li, Chao Jia, et al.. (2025). Global, Regional and National Burden of Chronic Hepatitis C, 1990–2021: A Systematic Analysis for the GBD Study 2021. Journal of Viral Hepatitis. 32(8). e70053–e70053.
3.
Zhou, Su, Xuanji He, Fei Mao, & Ying Chu. (2025). Mitochondrial targeting of coenzyme Q10 in inflammatory bowel disease: mechanisms, challenges, and prospects for clinical application. International Immunopharmacology. 166. 115529–115529. 1 indexed citations
4.
Niethamer, Terren K., Joseph D. Planer, Michael P. Morley, et al.. (2025). Longitudinal single-cell profiles of lung regeneration after viral infection reveal persistent injury-associated cell states. Cell stem cell. 32(2). 302–321.e6. 6 indexed citations
5.
Morley, Michael P., Dakota L. Jones, Gan Zhao, et al.. (2024). Airway epithelial cell identity and plasticity are constrained by Sox2 during lung homeostasis, tissue regeneration, and in human disease. npj Regenerative Medicine. 9(1). 2–2. 3 indexed citations
6.
Jones, Dakota L., Michael P. Morley, Yun Ying, et al.. (2024). An injury-induced mesenchymal-epithelial cell niche coordinates regenerative responses in the lung. Science. 386(6727). eado5561–eado5561. 12 indexed citations
7.
Zhou, Su, Zhiying Li, Haizhao Song, et al.. (2023). Recent advances in tea seeds (Camellia Sinensis (L.) O. Kuntze): Active ingredients, health effects, and potential applications. Trends in Food Science & Technology. 141. 104192–104192. 18 indexed citations
8.
Niethamer, Terren K., et al.. (2023). Atf3 defines a population of pulmonary endothelial cells essential for lung regeneration. eLife. 12. 19 indexed citations
9.
10.
Liberti, Derek C., William A. Liberti, Madison M. Kremp, et al.. (2022). Klf5 defines alveolar epithelial type 1 cell lineage commitment during lung development and regeneration. Developmental Cell. 57(14). 1742–1757.e5. 14 indexed citations
11.
Penkala, Ian J., Derek C. Liberti, Aravind Sivakumar, et al.. (2021). Age-dependent alveolar epithelial plasticity orchestrates lung homeostasis and regeneration. Cell stem cell. 28(10). 1775–1789.e5. 87 indexed citations
12.
Zepp, Jarod A., Michael P. Morley, Claudia Loebel, et al.. (2021). Genomic, epigenomic, and biophysical cues controlling the emergence of the lung alveolus. Science. 371(6534). 99 indexed citations
13.
Niethamer, Terren K., Collin T. Stabler, John P. Leach, et al.. (2020). Defining the role of pulmonary endothelial cell heterogeneity in the response to acute lung injury. eLife. 9. 157 indexed citations
14.
Windmueller, Rebecca, John P. Leach, Apoorva Babu, et al.. (2020). Direct Comparison of Mononucleated and Binucleated Cardiomyocytes Reveals Molecular Mechanisms Underlying Distinct Proliferative Competencies. Cell Reports. 30(9). 3105–3116.e4. 46 indexed citations
15.
Alapati, Deepthi, William J. Zacharias, Heather A. Hartman, et al.. (2019). In utero gene editing for monogenic lung disease. Science Translational Medicine. 11(488). 79 indexed citations
16.
Liberti, Derek C., Jarod A. Zepp, Su Zhou, et al.. (2019). Dnmt1 is required for proximal-distal patterning of the lung endoderm and for restraining alveolar type 2 cell fate. Developmental Biology. 454(2). 108–117. 19 indexed citations
17.
Swarr, Daniel T., William H. Peranteau, Jennifer Pogoriler, et al.. (2018). Novel Molecular and Phenotypic Insights into Congenital Lung Malformations. American Journal of Respiratory and Critical Care Medicine. 197(10). 1328–1339. 32 indexed citations
18.
Li, Shanru, Michael P. Morley, Minmin Lu, et al.. (2016). Foxp transcription factors suppress a non-pulmonary gene expression program to permit proper lung development. Developmental Biology. 416(2). 338–346. 19 indexed citations
19.
Peng, Tien, David B. Frank, Rachel S. Kadzik, et al.. (2015). Hedgehog actively maintains adult lung quiescence and regulates repair and regeneration. Nature. 526(7574). 578–582. 157 indexed citations
20.
Zhou, Su. (2010). Photodynamic inhibition of hematoporphyrin monomethyl ether in hepatoma cells. Jiguang zazhi. 1 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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