Jian‐Xiu Shang

1.1k total citations · 1 hit paper
16 papers, 836 citations indexed

About

Jian‐Xiu Shang is a scholar working on Plant Science, Molecular Biology and Genetics. According to data from OpenAlex, Jian‐Xiu Shang has authored 16 papers receiving a total of 836 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Plant Science, 10 papers in Molecular Biology and 1 paper in Genetics. Recurrent topics in Jian‐Xiu Shang's work include Plant Stress Responses and Tolerance (10 papers), Plant nutrient uptake and metabolism (10 papers) and Plant Molecular Biology Research (8 papers). Jian‐Xiu Shang is often cited by papers focused on Plant Stress Responses and Tolerance (10 papers), Plant nutrient uptake and metabolism (10 papers) and Plant Molecular Biology Research (8 papers). Jian‐Xiu Shang collaborates with scholars based in China, United States and Hong Kong. Jian‐Xiu Shang's co-authors include Wenqiang Tang, Yu Sun, Zhiping Deng, Alma L. Burlingame, Ying Sun, Zhiyong Wang, Tae‐Wuk Kim, Shenheng Guan, Ruijiao Xin and Yang Bai and has published in prestigious journals such as Nature Cell Biology, New Phytologist and International Journal of Molecular Sciences.

In The Last Decade

Jian‐Xiu Shang

14 papers receiving 831 citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Brassinosteroid signal transduction from cell-surface receptor kinases to nuclear transcription factors

2009 550 citations Tae‐Wuk Kim, Shenheng Guan et al. Nature Cell Biology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jian‐Xiu Shang China	8	736	486	25	21	19	16	836
Philipp Gaugler Germany	5	289 0.4×	142 0.3×	7 0.3×	79 3.8×	10 0.5×	6	382
A. V. Roberts United Kingdom	11	379 0.5×	357 0.7×	21 0.8×	48 2.3×	49 2.6×	16	523
Jill Stevenson-Paulik United States	6	512 0.7×	302 0.6×	34 1.4×	103 4.9×	4 0.2×	6	600
Béatrice Godin France	9	384 0.5×	170 0.3×	10 0.4×	9 0.4×		14	448
Wim Reidt Germany	7	669 0.9×	334 0.7×	16 0.6×	8 0.4×		7	737
Clayton T. Larue United States	7	556 0.8×	543 1.1×	2 0.1×	33 1.6×	3 0.2×	8	751
Meng Ma China	12	389 0.5×	338 0.7×	2 0.1×	10 0.5×	4 0.2×	26	616
Timothy C. Howton United States	7	382 0.5×	233 0.5×	2 0.1×	16 0.8×	2 0.1×	17	494
L F Dickey United States	9	300 0.4×	482 1.0×	124 5.0×	12 0.6×	21 1.1×	10	615
Zhong‐Tian Xue Sweden	11	268 0.4×	291 0.6×	2 0.1×	16 0.8×	10 0.5×	18	446

Countries citing papers authored by Jian‐Xiu Shang

Since Specialization

Citations

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

Fields of papers citing papers by Jian‐Xiu Shang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jian‐Xiu Shang. 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 Jian‐Xiu Shang. The network helps show where Jian‐Xiu Shang may publish in the future.

Co-authorship network of co-authors of Jian‐Xiu Shang

This figure shows the co-authorship network connecting the top 25 collaborators of Jian‐Xiu Shang. A scholar is included among the top collaborators of Jian‐Xiu Shang 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 Jian‐Xiu Shang. Jian‐Xiu Shang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Zhang, Jiaojiao, Xiaoying Li, Xiaotong Liu, et al.. (2025). CaM4 Functions as a Positive Regulator of the SOS Pathway in Response to Salt Stress. Plant Cell & Environment. 48(10). 7317–7331. 1 indexed citations

Liu, Xiaoqian, Liang Gao, Xinye Liu, et al.. (2025). Protein tyrosine phosphatase IBR5 positively affects salt stress response by modulating CAT2 activity. Plant Science. 359. 112615–112615.

Zhang, Ya, Liyuan Han, Miao Chang, et al.. (2025). Two E-clade protein phosphatase 2Cs enhance ABA signaling by dephosphorylating ABI1 in Arabidopsis. Molecular Plant. 18(5). 783–796. 3 indexed citations

Shang, Jian‐Xiu, et al.. (2025). Nitric Oxide Regulates Multiple Signal Pathways in Plants via Protein S-Nitrosylation. Current Issues in Molecular Biology. 47(6). 407–407. 1 indexed citations

Liu, Xiaoqian, et al.. (2024). Emerging Functions of Protein Tyrosine Phosphatases in Plants. International Journal of Molecular Sciences. 25(22). 12050–12050.

Wang, Yuehua, Xiaoying Li, Xiahe Huang, et al.. (2023). S‐nitrosylation of RABG3E positively regulates vesicle trafficking to promote salt tolerance. Plant Cell & Environment. 46(12). 3858–3870. 9 indexed citations

Li, Xuetong, Zhiping Deng, Xinye Liu, et al.. (2023). EGR1 and EGR2 positively regulate plant ABA signaling by modulating the phosphorylation of SnRK2.2. New Phytologist. 241(4). 1492–1509. 7 indexed citations

Shang, Jian‐Xiu, et al.. (2022). The Role of Nitric Oxide in Plant Responses to Salt Stress. International Journal of Molecular Sciences. 23(11). 6167–6167. 48 indexed citations

Guo, Shanshan, et al.. (2021). AtPFA-DSP5 interacts with MPK3/MPK6 and negatively regulates plant salt responses. Plant Signaling & Behavior. 16(12). 2000808–2000808. 3 indexed citations

10.

Shang, Jian‐Xiu, et al.. (2021). Plastid-Localized EMB2726 Is Involved in Chloroplast Biogenesis and Early Embryo Development in Arabidopsis. Frontiers in Plant Science. 12. 675838–675838. 5 indexed citations

11.

Shang, Jian‐Xiu, et al.. (2021). AtPFA‐DSP3, an atypical dual‐specificity protein tyrosine phosphatase, affects salt stress response by modulating MPK3 and MPK6 activity. Plant Cell & Environment. 44(5). 1534–1548. 22 indexed citations

12.

Wang, Yuehua, et al.. (2021). OsWAK112, A Wall-Associated Kinase, Negatively Regulates Salt Stress Responses by Inhibiting Ethylene Production. Frontiers in Plant Science. 12. 751965–751965. 23 indexed citations

13.

Yang, Xiaorui, Yang Bai, Jian‐Xiu Shang, Ruijiao Xin, & Wenqiang Tang. (2016). The antagonistic regulation of abscisic acid‐inhibited root growth by brassinosteroids is partially mediated via direct suppression of ABSCISIC ACID INSENSITIVE 5 expression by BRASSINAZOLE RESISTANT 1. Plant Cell & Environment. 39(9). 1994–2003. 79 indexed citations

14.

Wang, Chunming, Jian‐Xiu Shang, Juan A. Osés-Prieto, et al.. (2013). Identification of BZR1-interacting Proteins as Potential Components of the Brassinosteroid Signaling Pathway in Arabidopsis Through Tandem Affinity Purification. Molecular & Cellular Proteomics. 12(12). 3653–3665. 59 indexed citations

15.

Kim, Tae‐Wuk, Shenheng Guan, Yu Sun, et al.. (2009). Brassinosteroid signal transduction from cell-surface receptor kinases to nuclear transcription factors. Nature Cell Biology. 11(10). 1254–1260. 550 indexed citations breakdown →

16.

Kong, Weina, et al.. (2008). Effect of erythropoietin on hepcidin, DMT1 with IRE, and hephaestin gene expression in duodenum of rats. Journal of Gastroenterology. 43(2). 136–143. 26 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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