Zhao Su

3.4k total citations
30 papers, 2.6k citations indexed

About

Zhao Su is a scholar working on Molecular Biology, Plant Science and Oncology. According to data from OpenAlex, Zhao Su has authored 30 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 10 papers in Plant Science and 7 papers in Oncology. Recurrent topics in Zhao Su's work include Plant Stress Responses and Tolerance (7 papers), Plant Molecular Biology Research (6 papers) and RNA modifications and cancer (5 papers). Zhao Su is often cited by papers focused on Plant Stress Responses and Tolerance (7 papers), Plant Molecular Biology Research (6 papers) and RNA modifications and cancer (5 papers). Zhao Su collaborates with scholars based in United States, China and Belgium. Zhao Su's co-authors include Paul B. Fisher, Sarah M. Assmann, Devanand Sarkar, Seok‐Geun Lee, Philip C. Bevilacqua, Laura E. Ritchey, Neil I. Goldstein, Hong Mā, Pankaj Gupta and Luni Emdad and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Zhao Su

30 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zhao Su United States 23 1.5k 709 567 375 335 30 2.6k
Drew E. Van Dyk United States 10 2.4k 1.6× 274 0.4× 527 0.9× 154 0.4× 221 0.7× 11 3.5k
Jill D. Haag United States 22 1.5k 1.0× 320 0.5× 406 0.7× 118 0.3× 553 1.7× 50 2.5k
Joan Bertran Spain 23 1.0k 0.7× 126 0.2× 372 0.7× 297 0.8× 238 0.7× 41 2.4k
Ernest Martinez United States 29 3.0k 2.0× 195 0.3× 384 0.7× 93 0.2× 1.0k 3.0× 49 3.8k
Wen Wei China 28 1.9k 1.2× 267 0.4× 277 0.5× 99 0.3× 584 1.7× 68 2.6k
Attila Reményi Hungary 26 2.7k 1.8× 257 0.4× 225 0.4× 114 0.3× 292 0.9× 50 3.3k
Toshihiko Eki Japan 29 2.1k 1.4× 433 0.6× 545 1.0× 58 0.2× 451 1.3× 106 2.9k
Andreas Klingenhoff Germany 12 2.4k 1.6× 262 0.4× 254 0.4× 86 0.2× 513 1.5× 14 3.3k
Marc Blondel France 30 2.1k 1.4× 162 0.2× 311 0.5× 113 0.3× 186 0.6× 75 2.7k
Joanne M. Yeakley United States 27 2.0k 1.3× 507 0.7× 149 0.3× 66 0.2× 327 1.0× 43 2.9k

Countries citing papers authored by Zhao Su

Since Specialization
Citations

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

Fields of papers citing papers by Zhao Su

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zhao Su

This figure shows the co-authorship network connecting the top 25 collaborators of Zhao Su. A scholar is included among the top collaborators of Zhao Su 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 Zhao Su. Zhao Su 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, Dan, et al.. (2025). Rethinking MYC inhibition: a multi-dimensional approach to overcome cancer’s master regulator. Frontiers in Cell and Developmental Biology. 13. 1601975–1601975. 1 indexed citations
2.
Ma, Xinwei, Jun Wang, Zhao Su, & Hong Mā. (2024). Developmentally dependent reprogramming of the Arabidopsis floral transcriptome under sufficient and limited water availability. BMC Plant Biology. 24(1). 273–273. 3 indexed citations
3.
Tack, David C., Zhao Su, Yunqing Yu, Philip C. Bevilacqua, & Sarah M. Assmann. (2020). Tissue-specific changes in the RNA structurome mediate salinity response in Arabidopsis. RNA. 26(4). 492–511. 20 indexed citations
4.
Sukiran, Noor Liyana, Cécile Julia, Hong Mā, & Zhao Su. (2019). ANAC019 is required for recovery of reproductive development under drought stress in Arabidopsis. Plant Molecular Biology. 99(1-2). 161–174. 38 indexed citations
5.
Ritchey, Laura E., Zhao Su, Sarah M. Assmann, & Philip C. Bevilacqua. (2019). In Vivo Genome-Wide RNA Structure Probing with Structure-seq. Methods in molecular biology. 1933. 305–341. 7 indexed citations
6.
Su, Zhao, Yin Tang, Laura E. Ritchey, et al.. (2018). Genome-wide RNA structurome reprogramming by acute heat shock globally regulates mRNA abundance. Proceedings of the National Academy of Sciences. 115(48). 12170–12175. 79 indexed citations
7.
Ma, Xuan, Noor Liyana Sukiran, Hong Mā, & Zhao Su. (2014). Moderate drought causes dramatic floral transcriptomic reprogramming to ensure successful reproductive development in Arabidopsis. BMC Plant Biology. 14(1). 164–164. 37 indexed citations
8.
Lee, Seok‐Geun, Timothy P. Kegelman, Rupesh Dash, et al.. (2011). Oncogene AEG-1 Promotes Glioma-Induced Neurodegeneration by Increasing Glutamate Excitotoxicity. Cancer Research. 71(20). 6514–6523. 89 indexed citations
9.
Su, Zhao, et al.. (2011). Operator splitting implicit integration factor methods for stiff reaction–diffusion–advection systems. Journal of Computational Physics. 230(15). 5996–6009. 52 indexed citations
10.
Emdad, Luni, Devanand Sarkar, Seok‐Geun Lee, et al.. (2010). Astrocyte Elevated Gene-1: A Novel Target for Human Glioma Therapy. Molecular Cancer Therapeutics. 9(1). 79–88. 87 indexed citations
11.
Lee, Seok‐Geun, Zhao Su, Joanna E. Richards, et al.. (2009). Astrocyte elevated gene-1 contributes to the pathogenesis of neuroblastoma. Oncogene. 28(26). 2476–2484. 94 indexed citations
12.
Lee, Seok‐Geun, Zhao Su, Luni Emdad, et al.. (2008). Mechanism of Ceftriaxone Induction of Excitatory Amino Acid Transporter-2 Expression and Glutamate Uptake in Primary Human Astrocytes. Journal of Biological Chemistry. 283(19). 13116–13123. 252 indexed citations
13.
An, Rui, Qijun Chen, Maofeng Chai, et al.. (2007). AtNHX8, a member of the monovalent cation:proton antiporter‐1 family in Arabidopsis thaliana, encodes a putative Li+/H+ antiporter. The Plant Journal. 49(4). 718–728. 105 indexed citations
14.
Su, Zhao, Maofeng Chai, Pingli Lu, et al.. (2007). AtMTM1, a novel mitochondrial protein, may be involved in activation of the manganese-containing superoxide dismutase in Arabidopsis. Planta. 226(4). 1031–1039. 22 indexed citations
15.
Su, Zhao. (2006). Effects of Rehmannia glutinosa polysaccharide on immune function of mice. 3 indexed citations
16.
17.
Fisher, Paul G., Devanand Sarkar, Irina V. Lebedeva, et al.. (2006). Melanoma differentiation associated gene-7/interleukin-24 (mda-7/IL-24): Novel gene therapeutic for metastatic melanoma. Toxicology and Applied Pharmacology. 224(3). 300–307. 65 indexed citations
18.
Gupta, Pankaj, Zhao Su, Irina V. Lebedeva, et al.. (2006). mda-7/IL-24: Multifunctional cancer-specific apoptosis-inducing cytokine. Pharmacology & Therapeutics. 111(3). 596–628. 152 indexed citations
19.
Su, Zhao, Jian Lin, R Shen, et al.. (1996). Surface-epitope masking and expression cloning identifies the human prostate carcinoma tumor antigen gene PCTA-1 a member of the galectin gene family.. Proceedings of the National Academy of Sciences. 93(14). 7252–7257. 115 indexed citations
20.
Su, Zhao, Bernard Avalosse, J.G. Vos, Johnny Cornelis, & Jean Rommelaere. (1985). Mutagenesis at putative apurinic sites in alkylated single-stranded DNA of parvovirus H-1 propagated in human cells. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 149(1). 1–8. 4 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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