Mark Estelle

41.5k total citations · 17 hit papers
156 papers, 28.9k citations indexed

About

Mark Estelle is a scholar working on Plant Science, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Mark Estelle has authored 156 papers receiving a total of 28.9k indexed citations (citations by other indexed papers that have themselves been cited), including 139 papers in Plant Science, 131 papers in Molecular Biology and 4 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Mark Estelle's work include Plant Molecular Biology Research (131 papers), Plant Reproductive Biology (79 papers) and Ubiquitin and proteasome pathways (33 papers). Mark Estelle is often cited by papers focused on Plant Molecular Biology Research (131 papers), Plant Reproductive Biology (79 papers) and Ubiquitin and proteasome pathways (33 papers). Mark Estelle collaborates with scholars based in United States, United Kingdom and Germany. Mark Estelle's co-authors include Sunethra Dharmasiri, Nihal Dharmasiri, Aaron Santner, William M. Gray, Chris Somerville, Luz Irina A. Calderón Villalobos, Lawrence Hobbie, Ottoline Leyser, Cynthia Lincoln and Geraint Parry and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Mark Estelle

154 papers receiving 28.4k citations

Hit Papers

The F-box protein TIR1 is an auxin receptor 1987 2026 2000 2013 2005 2006 2007 2001 2005 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark Estelle United States 85 25.6k 19.9k 971 764 742 156 28.9k
Jen Sheen United States 85 33.5k 1.3× 21.0k 1.1× 841 0.9× 679 0.9× 1.1k 1.5× 148 38.3k
Andrew F. Bent United States 51 23.4k 0.9× 16.5k 0.8× 433 0.4× 600 0.8× 1.2k 1.7× 97 27.6k
Xing Wang Deng China 93 21.9k 0.9× 17.7k 0.9× 444 0.5× 289 0.4× 448 0.6× 285 25.6k
Tai‐ping Sun United States 52 12.9k 0.5× 10.4k 0.5× 673 0.7× 466 0.6× 279 0.4× 77 15.8k
Dae‐Jin Yun South Korea 74 12.3k 0.5× 10.0k 0.5× 377 0.4× 443 0.6× 625 0.8× 265 16.4k
Steven J. Clough United States 28 18.7k 0.7× 15.0k 0.8× 451 0.5× 601 0.8× 921 1.2× 60 22.1k
Jörg Kudla Germany 71 17.7k 0.7× 11.3k 0.6× 432 0.4× 331 0.4× 665 0.9× 137 21.0k
Blake C. Meyers United States 80 18.7k 0.7× 11.1k 0.6× 572 0.6× 420 0.5× 832 1.1× 269 22.3k
Gynheung An South Korea 96 22.3k 0.9× 15.7k 0.8× 1000 1.0× 566 0.7× 514 0.7× 376 26.8k
Zhixiang Chen United States 69 14.8k 0.6× 9.8k 0.5× 329 0.3× 708 0.9× 787 1.1× 164 18.0k

Countries citing papers authored by Mark Estelle

Since Specialization
Citations

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

Fields of papers citing papers by Mark Estelle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Estelle

This figure shows the co-authorship network connecting the top 25 collaborators of Mark Estelle. A scholar is included among the top collaborators of Mark Estelle 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 Mark Estelle. Mark Estelle 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.
Ingram, Gwyneth, et al.. (2022). Heterologous expression of a lycophyte protein enhances angiosperm seedling vigor. Development. 149(21).
2.
Prigge, Michael J., Matthieu Pierre Platre, Nikita Kadakia, et al.. (2020). Genetic analysis of the Arabidopsis TIR1/AFB auxin receptors reveals both overlapping and specialized functions. eLife. 9. 114 indexed citations
3.
Katz, Ella, Rammyani Bagchi, Verena Jeschke, et al.. (2020). Diverse Allyl Glucosinolate Catabolites Independently Influence Root Growth and Development. PLANT PHYSIOLOGY. 183(3). 1376–1390. 34 indexed citations
4.
Prigge, Michael J., Kathleen Greenham, Yi Zhang, et al.. (2016). The Arabidopsis Auxin Receptor F-Box Proteins AFB4 and AFB5 Are Required for Response to the Synthetic Auxin Picloram. G3 Genes Genomes Genetics. 6(5). 1383–1390. 82 indexed citations
5.
Gao, Yangbin, Yi Zhang, Da Zhang, et al.. (2015). Auxin binding protein 1 (ABP1) is not required for either auxin signaling or Arabidopsis development. Proceedings of the National Academy of Sciences. 112(7). 2275–2280. 268 indexed citations
6.
Kelley, Dior R., et al.. (2015). Lysine Residues Are Not Required for Proteasome-Mediated Proteolysis of the Auxin/Indole Acidic Acid Protein IAA1. PLANT PHYSIOLOGY. 168(2). 708–720. 41 indexed citations
7.
Wu, Miin‐Feng, Nobutoshi Yamaguchi, Jun Xiao, et al.. (2015). Auxin-regulated chromatin switch directs acquisition of flower primordium founder fate. eLife. 4. e09269–e09269. 192 indexed citations
8.
Shani, Eilon, Roy Weinstain, Yi Zhang, et al.. (2013). Gibberellins accumulate in the elongating endodermal cells of Arabidopsis root. Proceedings of the National Academy of Sciences. 110(12). 4834–4839. 160 indexed citations
9.
Pěnčík, Aleš, Eva Hényková, Sibu Simon, et al.. (2013). Regulation of Auxin Homeostasis and Gradients in Arabidopsis Roots through the Formation of the Indole-3-Acetic Acid Catabolite 2-Oxindole-3-Acetic Acid. The Plant Cell. 25(10). 3858–3870. 121 indexed citations
10.
Sanz, Luis, Walter Dewitte, Céline Forzani, et al.. (2011). The Arabidopsis D-Type Cyclin CYCD2;1 and the Inhibitor ICK2/KRP2 Modulate Auxin-Induced Lateral Root Formation. The Plant Cell. 23(2). 641–660. 103 indexed citations
11.
Ge, Lei, Wendy Ann Peer, Stéphanie Robert, et al.. (2010). Arabidopsis ROOT UVB SENSITIVE2/WEAK AUXIN RESPONSE1 Is Required for Polar Auxin Transport  . The Plant Cell. 22(6). 1749–1761. 35 indexed citations
12.
Yamada, Masashi, Kathleen Greenham, Michael J. Prigge, Philip J. Jensen, & Mark Estelle. (2009). The TRANSPORT INHIBITOR RESPONSE2 Gene Is Required for Auxin Synthesis and Diverse Aspects of Plant Development. PLANT PHYSIOLOGY. 151(1). 168–179. 152 indexed citations
13.
Savaldi‐Goldstein, Sigal, T.J. Baiga, Florence Pojer, et al.. (2008). New auxin analogs with growth-promoting effects in intact plants reveal a chemical strategy to improve hormone delivery. Proceedings of the National Academy of Sciences. 105(39). 15190–15195. 87 indexed citations
14.
Navarro, Lionel, Patrice Dunoyer, Florence Jay, et al.. (2006). A Plant miRNA Contributes to Antibacterial Resistance by Repressing Auxin Signaling. Science. 312(5772). 436–439. 1435 indexed citations breakdown →
15.
Dharmasiri, Sunethra, Ranjan Swarup, Keithanne Mockaitis, et al.. (2006). AXR4 Is Required for Localization of the Auxin Influx Facilitator AUX1. Science. 312(5777). 1218–1220. 133 indexed citations
16.
Ljung, Karin, Anna K. Hull, John L. Celenza, et al.. (2005). Sites and Regulation of Auxin Biosynthesis in Arabidopsis Roots. The Plant Cell. 17(4). 1090–1104. 405 indexed citations
17.
Weber, Henriette, Anne Bernhardt, Monika Dieterle, et al.. (2004). Arabidopsis AtCUL3a and AtCUL3b Form Complexes with Members of the BTB/POZ-MATH Protein Family. PLANT PHYSIOLOGY. 137(1). 83–93. 118 indexed citations
18.
Yang, Xiaoqing, Sungsu Lee, Nihal Dharmasiri, et al.. (2004). The IAA1 protein is encoded by AXR5 and is a substrate of SCFTIR1. The Plant Journal. 40(5). 772–782. 177 indexed citations
19.
Parry, Geraint & Mark Estelle. (2004). Regulation of cullin-based ubiquitin ligases by the Nedd8/RUB ubiquitin-like proteins. Seminars in Cell and Developmental Biology. 15(2). 221–229. 70 indexed citations
20.
Estelle, Mark. (1996). Plant tropisms: The ins and outs of auxin. Current Biology. 6(12). 1589–1591. 57 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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