Ines Kreuzer

1.5k total citations
19 papers, 1.0k citations indexed

About

Ines Kreuzer is a scholar working on Plant Science, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ines Kreuzer has authored 19 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Plant Science, 8 papers in Molecular Biology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ines Kreuzer's work include Plant and Biological Electrophysiology Studies (14 papers), Plant Molecular Biology Research (7 papers) and Photosynthetic Processes and Mechanisms (5 papers). Ines Kreuzer is often cited by papers focused on Plant and Biological Electrophysiology Studies (14 papers), Plant Molecular Biology Research (7 papers) and Photosynthetic Processes and Mechanisms (5 papers). Ines Kreuzer collaborates with scholars based in Germany, Saudi Arabia and Australia. Ines Kreuzer's co-authors include Rainer Hedrich, Sönke Scherzer, Khaled A. S. Al‐Rasheid, Heinz Rennenberg, Waltraud X. Schulze, Elżbieta Król, Dietmar Geiger, Dirk Becker, Erwin Neher and Jennifer Böhm and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Current Biology and Scientific Reports.

In The Last Decade

Ines Kreuzer

18 papers receiving 1.0k citations

Peers

Ines Kreuzer

EEBS

CMN

PHYSI

Richard Hilleary United States

Erwan Michard United States

Ken Yokawa Japan

Virginia A. Shepherd Australia

Kai R. Konrad Germany

Marten Staal Netherlands

Su‐Hwa Kim United States

Maria Teresa Portes United States

Thomas J. Kleist United States

Sönke Scherzer Germany

Richard Hilleary United States

Ines Kreuzer

966 ×1.1

350 ×1.2

59 ×0.4

EEBS

78 ×0.5

CMN

58 ×1.4

PHYSI

Citations per year, relative to Ines Kreuzer Ines Kreuzer (= 1×) peers Richard Hilleary

Countries citing papers authored by Ines Kreuzer

Since Specialization

Citations

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

Fields of papers citing papers by Ines Kreuzer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ines Kreuzer

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

All Works

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19 of 19 papers shown

Kreuzer, Ines, Federico Scossa, Takayuki Tohge, Alisdair R. Fernie, & Rainer Hedrich. (2025). Venus flytraps' metabolome analysis discloses the metabolic fate of prey animal foodstock. The Plant Journal. 123(3). e70391–e70391.

Hedrich, Rainer & Ines Kreuzer. (2023). Demystifying the Venus flytrap action potential. New Phytologist. 239(6). 2108–2112. 12 indexed citations

Scherzer, Sönke, Sonja Bauer, Dirk Becker, et al.. (2023). DYSCALCULIA, a Venus flytrap mutant without the ability to count action potentials. Current Biology. 33(3). 589–596.e5. 6 indexed citations

Scherzer, Sönke, Jennifer Böhm, Shouguang Huang, et al.. (2022). A unique inventory of ion transporters poises the Venus flytrap to fast-propagating action potentials and calcium waves. Current Biology. 32(19). 4255–4263.e5. 33 indexed citations

Scherzer, Sönke, Shouguang Huang, Ines Kreuzer, et al.. (2022). Ether anesthetics prevents touch-induced trigger hair calcium-electrical signals excite the Venus flytrap. Scientific Reports. 12(1). 2851–2851. 28 indexed citations

Böhm, Jennifer, Sönke Scherzer, Khaled A. S. Al‐Rasheid, et al.. (2020). The Venus flytrap trigger hair–specific potassium channel KDM1 can reestablish the K+ gradient required for hapto-electric signaling. PLoS Biology. 18(12). e3000964–e3000964. 28 indexed citations

Scherzer, Sönke, Lana Shabala, Jörg Fromm, et al.. (2017). Insect haptoelectrical stimulation of Venus flytrap triggers exocytosis in gland cells. Proceedings of the National Academy of Sciences. 114(18). 4822–4827. 39 indexed citations

Kreuzwieser, Jürgen, Ines Kreuzer, Waltraud X. Schulze, et al.. (2017). The carnivorous Venus flytrap uses prey‐derived amino acid carbon to fuel respiration. New Phytologist. 214(2). 597–606. 23 indexed citations

Böhm, Jennifer, Sönke Scherzer, Elżbieta Król, et al.. (2016). The Venus Flytrap Dionaea muscipula Counts Prey-Induced Action Potentials to Induce Sodium Uptake. Current Biology. 26(3). 286–295. 117 indexed citations

10.

Bemm, Felix, Dirk Becker, Ines Kreuzer, et al.. (2016). Venus flytrap carnivorous lifestyle builds on herbivore defense strategies. Genome Research. 26(6). 812–825. 76 indexed citations

11.

Lind, Christof, Ingo Drèyer, Kimitsune Ishizaki, et al.. (2015). Stomatal Guard Cells Co-opted an Ancient ABA-Dependent Desiccation Survival System to Regulate Stomatal Closure. Current Biology. 25(7). 928–935. 127 indexed citations

12.

Scherzer, Sönke, Jennifer Böhm, Elżbieta Król, et al.. (2015). Calcium sensor kinase activates potassium uptake systems in gland cells of Venus flytraps. Proceedings of the National Academy of Sciences. 112(23). 7309–7314. 84 indexed citations

13.

Kreuzwieser, Jürgen, Jörg Kruse, Tim Burzlaff, et al.. (2014). The Venus flytrap attracts insects by the release of volatile organic compounds. Journal of Experimental Botany. 65(2). 755–766. 71 indexed citations

14.

Kruse, Jörg, Elżbieta Król, Sönke Scherzer, et al.. (2014). Integration of trap‐ and root‐derived nitrogen nutrition of carnivorous Dionaea muscipula. New Phytologist. 205(3). 1320–1329. 21 indexed citations

15.

Demir, Fatih, Sönke Scherzer, Yvonne Reinders, et al.. (2013). Arabidopsis nanodomain-delimited ABA signaling pathway regulates the anion channel SLAH3. Proceedings of the National Academy of Sciences. 110(20). 8296–8301. 174 indexed citations

16.

Scherzer, Sönke, Elżbieta Król, Ines Kreuzer, et al.. (2013). The Dionaea muscipula Ammonium Channel DmAMT1 Provides NH4+ Uptake Associated with Venus Flytrap’s Prey Digestion. Current Biology. 23(17). 1649–1657. 41 indexed citations

17.

Escalante‐Pérez, María, Henrik Karring, Ida B. Thøgersen, et al.. (2013). Secreted major Venus flytrap chitinase enables digestion of Arthropod prey. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1844(2). 374–383. 34 indexed citations

18.

Demir, Fatih, et al.. (2012). Methods of staining and visualization of sphingolipid enriched and non-enriched plasma membrane regions of Arabidopsis thaliana with fluorescent dyes and lipid analogues. Plant Methods. 8(1). 28–28. 23 indexed citations

19.

Schulze, Waltraud X., Kristian W. Sanggaard, Ines Kreuzer, et al.. (2012). The Protein Composition of the Digestive Fluid from the Venus Flytrap Sheds Light on Prey Digestion Mechanisms. Molecular & Cellular Proteomics. 11(11). 1306–1319. 79 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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