Ben Scheres

32.4k total citations · 12 hit papers
152 papers, 23.5k citations indexed

About

Ben Scheres is a scholar working on Plant Science, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Ben Scheres has authored 152 papers receiving a total of 23.5k indexed citations (citations by other indexed papers that have themselves been cited), including 144 papers in Plant Science, 123 papers in Molecular Biology and 4 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Ben Scheres's work include Plant Molecular Biology Research (131 papers), Plant Reproductive Biology (100 papers) and Plant nutrient uptake and metabolism (59 papers). Ben Scheres is often cited by papers focused on Plant Molecular Biology Research (131 papers), Plant Reproductive Biology (100 papers) and Plant nutrient uptake and metabolism (59 papers). Ben Scheres collaborates with scholars based in Netherlands, United States and United Kingdom. Ben Scheres's co-authors include Viola Willemsen, Renze Heidstra, Ikram Blilou, Jian Xu, Jiřı́ Friml, Peter Weisbeek, Marjolein Wildwater, Philip N. Benfey, Klaus Palme and Sabrina Sabatini and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Ben Scheres

148 papers receiving 23.1k citations

Hit Papers

The PIN auxin efflux facilitator network controls growt... 1993 2026 2004 2015 2005 1993 1999 2004 2007 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
Ben Scheres Netherlands 76 22.2k 17.1k 710 574 433 152 23.5k
Hiroo Fukuda Japan 68 14.8k 0.7× 12.5k 0.7× 827 1.2× 634 1.1× 315 0.7× 255 17.1k
Philip N. Benfey United States 87 23.7k 1.1× 17.7k 1.0× 467 0.7× 597 1.0× 521 1.2× 215 27.4k
Christian Fankhauser Switzerland 70 14.6k 0.7× 11.8k 0.7× 865 1.2× 435 0.8× 153 0.4× 113 16.8k
Eva Benková Austria 59 15.7k 0.7× 11.2k 0.7× 334 0.5× 458 0.8× 302 0.7× 102 16.3k
Masao Tasaka Japan 66 13.7k 0.6× 12.9k 0.8× 960 1.4× 618 1.1× 129 0.3× 165 16.5k
Dolf Weijers Netherlands 61 13.9k 0.6× 11.8k 0.7× 325 0.5× 504 0.9× 149 0.3× 150 15.1k
José M. Alonso United States 65 18.1k 0.8× 12.5k 0.7× 390 0.5× 446 0.8× 180 0.4× 115 20.1k
Ykä Helariutta Finland 59 11.4k 0.5× 8.9k 0.5× 183 0.3× 466 0.8× 218 0.5× 116 13.0k
Zhenbiao Yang United States 65 11.3k 0.5× 10.4k 0.6× 1.3k 1.9× 706 1.2× 125 0.3× 162 13.7k
Mark Estelle United States 85 25.6k 1.2× 19.9k 1.2× 742 1.0× 971 1.7× 294 0.7× 156 28.9k

Countries citing papers authored by Ben Scheres

Since Specialization
Citations

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

Fields of papers citing papers by Ben Scheres

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ben Scheres

This figure shows the co-authorship network connecting the top 25 collaborators of Ben Scheres. A scholar is included among the top collaborators of Ben Scheres 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 Ben Scheres. Ben Scheres 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.
Scheres, Ben. (2025). Plant development: from sessile to fertile. Development. 152(21).
2.
Rajagopalan, K.V., Brendan Lane, Seung Hyeun Ka, et al.. (2025). Wound repair in plants guided by cell geometry. Current Biology. 35(16). 3851–3868.e7. 2 indexed citations
3.
Hofhuis, Hugo, Robert Sévenier, Bjorn Kloosterman, et al.. (2025). Rational design of induced regeneration via somatic embryogenesis in the absence of exogenous phytohormones. The Plant Cell. 37(11). 1 indexed citations
5.
Scheres, Ben, et al.. (2023). SCHIZORIZA domain–function analysis identifies requirements for its specific role in cell fate segregation. PLANT PHYSIOLOGY. 193(3). 1866–1879. 1 indexed citations
6.
Kareem, Abdul, Mohammed Aiyaz, Anil Shaji, et al.. (2020). A coherent feed-forward loop drives vascular regeneration in damaged aerial organs of plants growing in a normal developmental context. Development. 147(6). 26 indexed citations
7.
Lokdarshi, Ansul, Csaba Papdi, Aladár Pettkó‐Szandtner, et al.. (2019). ErbB-3 BINDING PROTEIN 1 Regulates Translation and Counteracts RETINOBLASTOMA RELATED to Maintain the Root Meristem. PLANT PHYSIOLOGY. 182(2). 919–932. 12 indexed citations
8.
Horváth, Beatrix, Szilvia K. Nagy, Edit Németh, et al.. (2017). Arabidopsis RETINOBLASTOMA RELATED directly regulates DNA damage responses through functions beyond cell cycle control. The EMBO Journal. 36(9). 1261–1278. 85 indexed citations
9.
Porco, Silvana, Antoine Larrieu, Yujuan Du, et al.. (2016). Lateral root emergence in Arabidopsis is dependent on transcription factor LBD29 regulating auxin influx carrier LAX3. Development. 143(18). 3340–9. 97 indexed citations
10.
Long, Yuchen, Joachim Goedhart, Martinus Schneijderberg, et al.. (2015). SCARECROWLIKE 23 and SCARECROW jointly specify endodermal cell fate but distinctly control SHORTROOT movement. The Plant Journal. 84(4). 773–784. 46 indexed citations
11.
Long, Yuchen, Ben Scheres, & Ikram Blilou. (2015). The logic of communication: roles for mobile transcription factors in plants. Journal of Experimental Botany. 66(4). 1133–1144. 17 indexed citations
12.
Riccardo, Siligato, Xin Wang, Shri Ram Yadav, et al.. (2015). MultiSite Gateway-Compatible Cell Type-Specific Gene-Inducible System for Plants. PLANT PHYSIOLOGY. 170(2). 627–641. 100 indexed citations
13.
Hassan, Hala, Ben Scheres, & Ikram Blilou. (2010). JACKDAW controls epidermal patterning in the Arabidopsis root meristem through a non-cell-autonomous mechanism. Development. 137(9). 1523–1529. 84 indexed citations
14.
Bennett, Tom, A. van den Toorn, Gabino Sanchez‐Perez, et al.. (2010). SOMBRERO, BEARSKIN1, and BEARSKIN2 Regulate Root Cap Maturation in Arabidopsis    . The Plant Cell. 22(3). 640–654. 153 indexed citations
16.
Willemsen, Viola, Marion Bauch, Tom Bennett, et al.. (2008). The NAC Domain Transcription Factors FEZ and SOMBRERO Control the Orientation of Cell Division Plane in Arabidopsis Root Stem Cells. Developmental Cell. 15(6). 913–922. 186 indexed citations
17.
Laskowski, Marta, Verônica A. Grieneisen, Hugo Hofhuis, et al.. (2008). Root System Architecture from Coupling Cell Shape to Auxin Transport. PLoS Biology. 6(12). e307–e307. 322 indexed citations
18.
Cui, Hongchang, Mitchell P. Levesque, Teva Vernoux, et al.. (2007). An Evolutionarily Conserved Mechanism Delimiting SHR Movement Defines a Single Layer of Endodermis in Plants. Science. 316(5823). 421–425. 446 indexed citations
19.
Xu, Jian, Hugo Hofhuis, Renze Heidstra, et al.. (2006). A Molecular Framework for Plant Regeneration. Science. 311(5759). 385–388. 291 indexed citations
20.
Willemsen, Viola, Jiřı́ Friml, Markus Grebe, et al.. (2003). Cell Polarity and PIN Protein Positioning in Arabidopsis Require STEROL METHYLTRANSFERASE1 Function. The Plant Cell. 15(3). 612–625. 216 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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