Zhongjun Zhou

8.4k total citations · 1 hit paper
121 papers, 5.7k citations indexed

About

Zhongjun Zhou is a scholar working on Molecular Biology, Cancer Research and Cell Biology. According to data from OpenAlex, Zhongjun Zhou has authored 121 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 78 papers in Molecular Biology, 16 papers in Cancer Research and 14 papers in Cell Biology. Recurrent topics in Zhongjun Zhou's work include Nuclear Structure and Function (27 papers), RNA Research and Splicing (20 papers) and Genomics and Chromatin Dynamics (18 papers). Zhongjun Zhou is often cited by papers focused on Nuclear Structure and Function (27 papers), RNA Research and Splicing (20 papers) and Genomics and Chromatin Dynamics (18 papers). Zhongjun Zhou collaborates with scholars based in Hong Kong, China and United States. Zhongjun Zhou's co-authors include Karl Tryggvason, Baohua Liu, Renhai Cao, Yihai Cao, Jianming Wang, Shrestha Ghosh, Raija Soininen, Suneel Apte, Zimei Wang and Richard W. Rauser and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Zhongjun Zhou

118 papers receiving 5.6k citations

Hit Papers

Impaired endochondral ossification and angiogenesis in mi... 2000 2026 2008 2017 2000 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zhongjun Zhou Hong Kong 39 3.4k 1.1k 1.1k 666 594 121 5.7k
Susan E. Crawford United States 31 3.7k 1.1× 832 0.8× 1.1k 1.0× 554 0.8× 442 0.7× 92 5.9k
Peggy Myung United States 23 3.6k 1.1× 1.2k 1.1× 785 0.7× 702 1.1× 323 0.5× 40 6.9k
Guillem Genové Sweden 27 3.4k 1.0× 1.1k 1.0× 868 0.8× 661 1.0× 689 1.2× 42 7.5k
Annika Armulik Sweden 19 3.9k 1.2× 1.2k 1.1× 846 0.8× 919 1.4× 1.0k 1.7× 20 8.7k
Anna Dimberg Sweden 38 4.5k 1.3× 2.2k 2.0× 1.5k 1.4× 630 0.9× 281 0.5× 92 7.8k
Mats Hellström Sweden 24 4.6k 1.4× 978 0.9× 1.0k 0.9× 937 1.4× 303 0.5× 42 7.2k
Yoshiaki Kubota Japan 42 3.1k 0.9× 1.0k 1.0× 1.1k 1.0× 817 1.2× 555 0.9× 110 6.7k
Friedemann Kiefer Germany 43 2.8k 0.8× 2.0k 1.8× 582 0.5× 999 1.5× 506 0.9× 98 5.9k
Stefania Mitola Italy 36 2.8k 0.8× 799 0.7× 729 0.7× 606 0.9× 253 0.4× 111 4.9k
Franklin Peale United States 36 3.8k 1.1× 1.9k 1.7× 1.3k 1.2× 395 0.6× 454 0.8× 70 7.6k

Countries citing papers authored by Zhongjun Zhou

Since Specialization
Citations

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

Fields of papers citing papers by Zhongjun Zhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zhongjun Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Zhongjun Zhou. A scholar is included among the top collaborators of Zhongjun 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 Zhongjun Zhou. Zhongjun 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.
Suter, Thomas, et al.. (2026). A Histone Code Functionally Linked to Replicative Senescence. Aging Cell. 25(1). e70343–e70343.
2.
Fu, Tao & Zhongjun Zhou. (2025). Senescent cells as a target for anti-aging interventions: From senolytics to immune therapies. Journal of Translational Internal Medicine. 13(1). 33–47. 9 indexed citations
3.
Jiang, Shaoshuai, Xinyi Liu, Yi He, et al.. (2024). Disorganized chromatin hierarchy and stem cell aging in a male patient of atypical laminopathy-based progeria mandibuloacral dysplasia type A. Nature Communications. 15(1). 10046–10046. 1 indexed citations
4.
Wang, Longyue, Linlin Zhuo, Xiangzheng Fu, et al.. (2024). BloodPatrol: Revolutionizing Blood Cancer Diagnosis - Advanced Real-Time Detection Leveraging Deep Learning & Cloud Technologies. IEEE Journal of Biomedical and Health Informatics. PP. 1–11. 2 indexed citations
5.
Gao, Ge, Xiaoping Li, Zhixin Jiang, et al.. (2023). Isthmin-1 (Ism1) modulates renal branching morphogenesis and mesenchyme condensation during early kidney development. Nature Communications. 14(1). 2378–2378. 3 indexed citations
6.
Zhang, Lian, et al.. (2023). RAGA prevents tumor immune evasion of LUAD by promoting CD47 lysosome degradation. Communications Biology. 6(1). 211–211. 7 indexed citations
7.
Wang, Yan, Xiaoxu Liu, Ge Gao, et al.. (2022). ZFP281-BRCA2 prevents R-loop accumulation during DNA replication. Nature Communications. 13(1). 25 indexed citations
8.
He, Yi, Li Tuo, Fei Long, et al.. (2022). Rapid and robust derivation of mesenchymal stem cells from human pluripotent stem cells via temporal induction of neuralized ectoderm. Cell & Bioscience. 12(1). 31–31. 8 indexed citations
9.
Tuo, Li, et al.. (2020). Generation of PRMT6 homozygous knockout human embryonic stem cell lines. Stem Cell Research. 50. 102136–102136. 1 indexed citations
10.
Wu, Xuewei, et al.. (2014). Distinct spatiotemporal expression ofISM1during mouse and chick development. Cell Cycle. 13(10). 1571–1582. 33 indexed citations
11.
Liu, Jia, Baohua Liu, Huiling Zheng, et al.. (2014). HP1α mediates defective heterochromatin repair and accelerates senescence inZmpste24-deficient cells. Cell Cycle. 13(8). 1237–1247. 14 indexed citations
12.
Liu, Baohua, et al.. (2012). Chromatin Remodeling, DNA Damage Repair and Aging. Current Genomics. 13(7). 533–547. 55 indexed citations
13.
Lau, Edward, Maggie P. Y. Lam, S. O. Siu, et al.. (2011). Combinatorial use of offline SCX and online RP–RP liquid chromatography for iTRAQ-based quantitative proteomics applications. Molecular BioSystems. 7(5). 1399–1408. 31 indexed citations
14.
Liu, Baohua, et al.. (2011). Quantitative nucleolar proteomics reveals nuclear re-organization during stress- induced senescence in mouse fibroblast. BMC Cell Biology. 12(1). 33–33. 30 indexed citations
15.
Liu, Baohua & Zhongjun Zhou. (2008). Lamin A/C, laminopathies and premature ageing.. PubMed. 23(6). 747–63. 48 indexed citations
16.
Neumann, Sascha, Wenshu Lu, Martina Munck, et al.. (2007). Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells. Human Molecular Genetics. 16(23). 2944–2959. 58 indexed citations
17.
Religa, Piotr, Renhai Cao, Meit A. Björndahl, et al.. (2005). Presence of bone marrow–derived circulating progenitor endothelial cells in the newly formed lymphatic vessels. Blood. 106(13). 4184–4190. 108 indexed citations
18.
Varela, Ignacio, Juan Cadiñanos, Alberto M. Pendás, et al.. (2005). Accelerated ageing in mice deficient in Zmpste24 protease is linked to p53 signalling activation. Nature. 437(7058). 564–568. 367 indexed citations
19.
Zhou, Zhongjun, Masayuki Doi, Jianming Wang, et al.. (2004). Deletion of Laminin-8 Results in Increased Tumor Neovascularization and Metastasis in Mice. Cancer Research. 64(12). 4059–4063. 31 indexed citations
20.
Oblander, Samantha A., Zhongjun Zhou, Beatriz G. Gálvez, et al.. (2004). Distinctive functions of membrane type 1 matrix-metalloprotease (MT1-MMP or MMP-14) in lung and submandibular gland development are independent of its role in pro-MMP-2 activation. Developmental Biology. 277(1). 255–269. 109 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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