Thomas Greb

6.0k total citations
49 papers, 4.0k citations indexed

About

Thomas Greb is a scholar working on Plant Science, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Thomas Greb has authored 49 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Plant Science, 34 papers in Molecular Biology and 7 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Thomas Greb's work include Plant Molecular Biology Research (45 papers), Plant Reproductive Biology (23 papers) and Plant nutrient uptake and metabolism (14 papers). Thomas Greb is often cited by papers focused on Plant Molecular Biology Research (45 papers), Plant Reproductive Biology (23 papers) and Plant nutrient uptake and metabolism (14 papers). Thomas Greb collaborates with scholars based in Germany, Austria and United States. Thomas Greb's co-authors include Javier Agustí, Pablo Sánchez, Martina Schwarz, Caroline Dean, Pedro Crevillén, Klaus Theres, Jan U. Lohmann, Filomena De Lucia, Alexandra M. E. Jones and Oliver Clarenz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Genes & Development.

In The Last Decade

Thomas Greb

47 papers receiving 4.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Greb Germany 28 3.6k 2.6k 561 91 87 49 4.0k
Gwyneth Ingram France 32 3.6k 1.0× 2.8k 1.1× 210 0.4× 159 1.7× 41 0.5× 72 3.9k
Adrienne Roeder United States 28 3.1k 0.8× 2.6k 1.0× 299 0.5× 142 1.6× 64 0.7× 71 3.6k
Ari Pekka Mähönen Finland 30 5.3k 1.4× 4.0k 1.5× 139 0.2× 69 0.8× 45 0.5× 52 5.6k
Kenneth D. Birnbaum United States 34 4.4k 1.2× 3.5k 1.3× 120 0.2× 194 2.1× 96 1.1× 62 5.4k
Christian S. Hardtke Switzerland 45 7.9k 2.2× 6.0k 2.3× 405 0.7× 241 2.6× 56 0.6× 100 8.5k
Viola Willemsen Netherlands 26 7.6k 2.1× 6.0k 2.3× 192 0.3× 81 0.9× 33 0.4× 45 7.9k
Marja C.P. Timmermans United States 41 5.3k 1.4× 4.2k 1.6× 211 0.4× 497 5.5× 57 0.7× 80 6.1k
Thomas Berleth Canada 29 4.8k 1.3× 4.6k 1.7× 261 0.5× 164 1.8× 76 0.9× 54 5.4k
Therese Mandel Switzerland 29 4.9k 1.3× 4.4k 1.7× 693 1.2× 158 1.7× 57 0.7× 38 5.5k
Emmanuel Liscum United States 38 5.6k 1.5× 4.5k 1.7× 173 0.3× 109 1.2× 43 0.5× 58 6.0k

Countries citing papers authored by Thomas Greb

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Greb

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Greb

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Greb. A scholar is included among the top collaborators of Thomas Greb 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 Thomas Greb. Thomas Greb 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.
Zhao, Jiao, Dongbo Shi, Changzheng Song, et al.. (2025). Strigolactones optimise plant water usage by modulating vessel formation. Nature Communications. 16(1). 3854–3854. 2 indexed citations
2.
Li, Qingtian, Sun Hyun Chang, Lionel Faure, et al.. (2024). SMXL5 attenuates strigolactone signaling in Arabidopsis thaliana by inhibiting SMXL7 degradation. Molecular Plant. 17(4). 631–647. 16 indexed citations
3.
Wallner, Eva‐Sophie, Dongbo Shi, Friederike Wanke, et al.. (2023). OBERON3 and SUPPRESSOR OF MAX2 1-LIKE proteins form a regulatory module driving phloem development. Nature Communications. 14(1). 2128–2128. 9 indexed citations
5.
Xu, Xiaocai, Cezary Smaczniak, Wenhao Yan, et al.. (2022). A 3D gene expression atlas of the floral meristem based on spatial reconstruction of single nucleus RNA sequencing data. Nature Communications. 13(1). 2838–2838. 49 indexed citations
6.
Song, Changzheng, Jiao Zhao, Dongbo Shi, et al.. (2021). Strigo-D2—a bio-sensor for monitoring spatio-temporal strigolactone signaling patterns in intact plants. PLANT PHYSIOLOGY. 188(1). 97–110. 13 indexed citations
7.
Shi, Dongbo, Virginie Jouannet, Javier Agustí, et al.. (2020). Tissue-specific transcriptome profiling of the Arabidopsis inflorescence stem reveals local cellular signatures. The Plant Cell. 33(2). 200–223. 51 indexed citations
8.
Wallner, Eva‐Sophie, et al.. (2020). SUPPRESSOR OF MAX2 1‐LIKE 5 promotes secondary phloem formation during radial stem growth. The Plant Journal. 102(5). 903–915. 25 indexed citations
9.
Shi, Dongbo, et al.. (2019). Bifacial cambium stem cells generate xylem and phloem during radial plant growth. Development. 146(1). 72 indexed citations
10.
Ma, Yanfei, Christian Wenzl, Anna Medzihradszky, et al.. (2019). WUSCHEL acts as an auxin response rheostat to maintain apical stem cells in Arabidopsis. Nature Communications. 10(1). 5093–5093. 150 indexed citations
11.
Brackmann, Klaus, Jiyan Qi, Michael Gebert, et al.. (2018). Spatial specificity of auxin responses coordinates wood formation. Nature Communications. 9(1). 875–875. 119 indexed citations
12.
Schürholz, Ann-Kathrin, Vadir Lopéz-Salmerón, Joachim Forner, et al.. (2018). A Comprehensive Toolkit for Inducible, Cell Type-Specific Gene Expression in Arabidopsis. PLANT PHYSIOLOGY. 178(1). 40–53. 65 indexed citations
13.
Han, Soeun, Hyunwoo Cho, Jiyan Qi, et al.. (2018). BIL1-mediated MP phosphorylation integrates PXY and cytokinin signalling in secondary growth. Nature Plants. 4(8). 605–614. 70 indexed citations
14.
Ragni, Laura & Thomas Greb. (2017). Secondary growth as a determinant of plant shape and form. Seminars in Cell and Developmental Biology. 79. 58–67. 71 indexed citations
15.
Qi, Jiyan & Thomas Greb. (2016). Cell polarity in plants: the Yin and Yang of cellular functions. Current Opinion in Plant Biology. 35. 105–110. 17 indexed citations
16.
Jouannet, Virginie, Klaus Brackmann, & Thomas Greb. (2014). (Pro)cambium formation and proliferation: two sides of the same coin?. Current Opinion in Plant Biology. 23. 54–60. 62 indexed citations
17.
Agustí, Javier, Silvia Herold, Martina Schwarz, et al.. (2011). Strigolactone signaling is required for auxin-dependent stimulation of secondary growth in plants. Proceedings of the National Academy of Sciences. 108(50). 20242–20247. 307 indexed citations
18.
Agustí, Javier, Raffael Lichtenberger, Martina Schwarz, Lilian Nehlin, & Thomas Greb. (2011). Characterization of Transcriptome Remodeling during Cambium Formation Identifies MOL1 and RUL1 As Opposing Regulators of Secondary Growth. PLoS Genetics. 7(2). e1001312–e1001312. 116 indexed citations
19.
Lucia, Filomena De, Pedro Crevillén, Alexandra M. E. Jones, Thomas Greb, & Caroline Dean. (2008). A PHD-Polycomb Repressive Complex 2 triggers the epigenetic silencing of FLC during vernalization. Proceedings of the National Academy of Sciences. 105(44). 16831–16836. 395 indexed citations
20.
Greb, Thomas, Oliver Clarenz, Elisabeth Schäfer, et al.. (2003). Molecular analysis of the LATERAL SUPPRESSOR gene in Arabidopsis reveals a conserved control mechanism for axillary meristem formation. Genes & Development. 17(9). 1175–1187. 414 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026