Martin Bayer

2.8k total citations
43 papers, 2.1k citations indexed

About

Martin Bayer is a scholar working on Molecular Biology, Plant Science and Cell Biology. According to data from OpenAlex, Martin Bayer has authored 43 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 29 papers in Plant Science and 5 papers in Cell Biology. Recurrent topics in Martin Bayer's work include Plant Molecular Biology Research (26 papers), Plant Reproductive Biology (24 papers) and Photosynthetic Processes and Mechanisms (12 papers). Martin Bayer is often cited by papers focused on Plant Molecular Biology Research (26 papers), Plant Reproductive Biology (24 papers) and Photosynthetic Processes and Mechanisms (12 papers). Martin Bayer collaborates with scholars based in Germany, United States and Belgium. Martin Bayer's co-authors include Andreas Mayer, Christopher M. Peters, Wolfgang Lukowitz, Jens Andersen, Matthias Mann, Tal Nawy, Thomas Musielak, Carmela Giglione, Thierry Meinnel and Mary Galli and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Martin Bayer

41 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin Bayer Germany 23 1.7k 1.3k 417 83 75 43 2.1k
Chieko Saito Japan 20 1.2k 0.7× 762 0.6× 501 1.2× 63 0.8× 198 2.6× 45 1.7k
Kazuo Ebine Japan 25 1.6k 1.0× 1.5k 1.2× 908 2.2× 120 1.4× 124 1.7× 51 2.3k
Corrado Viotti Germany 19 1.2k 0.7× 1.1k 0.9× 696 1.7× 99 1.2× 191 2.5× 26 1.9k
Cláudia Rato United Kingdom 16 772 0.5× 344 0.3× 497 1.2× 37 0.4× 211 2.8× 16 1.2k
Allan D. Shapiro United States 14 665 0.4× 797 0.6× 557 1.3× 121 1.5× 45 0.6× 17 1.5k
Ken-ichi Noma United States 27 4.1k 2.5× 1.6k 1.2× 130 0.3× 40 0.5× 144 1.9× 55 4.7k
Michael J. Deeks United Kingdom 21 1.2k 0.7× 1.1k 0.9× 533 1.3× 28 0.3× 37 0.5× 35 1.6k
Ann M. Rose Canada 34 2.6k 1.5× 638 0.5× 612 1.5× 13 0.2× 64 0.9× 86 3.4k
Monika Dieterle Luxembourg 22 1.2k 0.7× 1.2k 0.9× 190 0.5× 11 0.1× 45 0.6× 30 1.7k
Tomoyasu Sugiyama United States 18 3.0k 1.8× 1.2k 0.9× 149 0.4× 10 0.1× 63 0.8× 23 3.3k

Countries citing papers authored by Martin Bayer

Since Specialization
Citations

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

Fields of papers citing papers by Martin Bayer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Bayer

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Bayer. A scholar is included among the top collaborators of Martin Bayer 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 Martin Bayer. Martin Bayer 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.
Xiao, Wei, Houming Chen, Dagmar Ripper, et al.. (2025). An AINTEGUMENTA phosphoswitch controls bilateral stem cell activity during secondary growth. Proceedings of the National Academy of Sciences. 122(47). e2510538122–e2510538122.
2.
Chen, Houming, Feng Xiong, Daniel Slane, et al.. (2024). Phosphorylation‐dependent activation of the bHLH transcription factor ICE1 / SCRM promotes polarization of the Arabidopsis zygote. New Phytologist. 245(3). 1029–1039. 3 indexed citations
3.
Wang, Kai, Houming Chen, Yanfei Ma, et al.. (2021). Independent parental contributions initiate zygote polarization in Arabidopsis thaliana. Current Biology. 31(21). 4810–4816.e5. 22 indexed citations
4.
Chen, Houming, et al.. (2021). Zygotic Embryogenesis in Flowering Plants. Methods in molecular biology. 2288. 73–88. 7 indexed citations
5.
Hohmann, Ulrich, Priya Ramakrishna, Laura Lorenzo‐Orts, et al.. (2020). Constitutive Activation of Leucine-Rich Repeat Receptor Kinase Signaling Pathways by BAK1-INTERACTING RECEPTOR-LIKE KINASE3 Chimera. The Plant Cell. 32(10). 3311–3323. 27 indexed citations
6.
Slane, Daniel, Martina Kolb, Craig Dent, et al.. (2020). The integral spliceosomal component CWC15 is required for development in Arabidopsis. Scientific Reports. 10(1). 13336–13336. 8 indexed citations
7.
Wijnker, Erik, Hirofumi Harashima, C. Bastiaan de Snoo, et al.. (2019). The Cdk1/Cdk2 homolog CDKA;1 controls the recombination landscape in Arabidopsis. Proceedings of the National Academy of Sciences. 116(25). 12534–12539. 28 indexed citations
8.
Chen, Houming, et al.. (2019). Square one: zygote polarity and early embryogenesis in flowering plants. Current Opinion in Plant Biology. 53. 128–133. 16 indexed citations
9.
Park, Misoon, Cornélia Krause, Ilka Reichardt, et al.. (2018). Concerted Action of Evolutionarily Ancient and Novel SNARE Complexes in Flowering-Plant Cytokinesis. Developmental Cell. 44(4). 500–511.e4. 35 indexed citations
10.
Slane, Daniel, et al.. (2017). Staining and Clearing of Arabidopsis Reproductive Tissue for Imaging of Fluorescent Proteins. Methods in molecular biology. 1669. 87–94. 4 indexed citations
11.
Bayer, Martin, Daniel Slane, & Gerd Jürgens. (2016). Early plant embryogenesis — dark ages or dark matter?. Current Opinion in Plant Biology. 35. 30–36. 28 indexed citations
12.
Musielak, Thomas, Daniel Slane, Christian Liebig, & Martin Bayer. (2016). A Versatile Optical Clearing Protocol for Deep Tissue Imaging of Fluorescent Proteins in Arabidopsis thaliana. PLoS ONE. 11(8). e0161107–e0161107. 38 indexed citations
13.
Rademacher, Eike H., Annemarie S. Lokerse, Alexandra Schlereth, et al.. (2012). Different Auxin Response Machineries Control Distinct Cell Fates in the Early Plant Embryo. Developmental Cell. 22(1). 211–222. 170 indexed citations
14.
Jeong, Sang-Ho, Martin Bayer, & Wolfgang Lukowitz. (2010). Taking the very first steps: from polarity to axial domains in the early Arabidopsis embryo. Journal of Experimental Botany. 62(5). 1687–1697. 32 indexed citations
15.
Nawy, Tal, Martin Bayer, Jozef Mravec, et al.. (2010). The GATA Factor HANABA TARANU Is Required to Position the Proembryo Boundary in the Early Arabidopsis Embryo. Developmental Cell. 19(1). 103–113. 63 indexed citations
16.
Bayer, Martin, Tal Nawy, Carmela Giglione, et al.. (2009). Paternal Control of Embryonic Patterning in Arabidopsis thaliana. Science. 323(5920). 1485–1488. 268 indexed citations
17.
Schwab, Rebecca, Alexis Maizel, Virginia Ruíz‐Ferrer, et al.. (2009). Endogenous TasiRNAs Mediate Non-Cell Autonomous Effects on Gene Regulation in Arabidopsis thaliana. PLoS ONE. 4(6). e5980–e5980. 79 indexed citations
18.
Nawy, Tal, Wolfgang Lukowitz, & Martin Bayer. (2007). Talk global, act local—patterning the Arabidopsis embryo. Current Opinion in Plant Biology. 11(1). 28–33. 34 indexed citations
19.
Müller, Oliver, Martin Bayer, Christopher M. Peters, et al.. (2002). The Vtc proteins in vacuole fusion: coupling NSF activity to V 0 trans -complex formation. The EMBO Journal. 21(3). 259–269. 116 indexed citations
20.
Peters, Christopher M., et al.. (2001). Trans-complex formation by proteolipid channels in the terminal phase of membrane fusion. Nature. 409(6820). 581–588. 407 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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