Jan E. Backhausen

1.4k total citations
26 papers, 1.2k citations indexed

About

Jan E. Backhausen is a scholar working on Molecular Biology, Plant Science and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jan E. Backhausen has authored 26 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 16 papers in Plant Science and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jan E. Backhausen's work include Photosynthetic Processes and Mechanisms (20 papers), Plant Stress Responses and Tolerance (7 papers) and Mitochondrial Function and Pathology (6 papers). Jan E. Backhausen is often cited by papers focused on Photosynthetic Processes and Mechanisms (20 papers), Plant Stress Responses and Tolerance (7 papers) and Mitochondrial Function and Pathology (6 papers). Jan E. Backhausen collaborates with scholars based in Germany, United Kingdom and Hungary. Jan E. Backhausen's co-authors include Renate Scheibe, Simone Holtgrefe, Leonid E. Fridlyand, Peter Horton, Antje von Schaewen, Michael Klocke, Klaus P. Bader, Bernd Müller‐Röber, Ingo Voß and Christina Wunrau and has published in prestigious journals such as PLANT PHYSIOLOGY, Journal of Experimental Botany and Applied Microbiology and Biotechnology.

In The Last Decade

Jan E. Backhausen

26 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jan E. Backhausen Germany 20 935 677 103 81 75 26 1.2k
Teruhiro Takabe Japan 18 725 0.8× 1.0k 1.5× 68 0.7× 80 1.0× 27 0.4× 38 1.4k
Gary Gardner United States 23 988 1.1× 1.2k 1.7× 84 0.8× 73 0.9× 19 0.3× 53 1.7k
Eve‐Marie Josse United Kingdom 18 1.4k 1.5× 1.4k 2.0× 113 1.1× 200 2.5× 35 0.5× 20 1.8k
Jinkui Guo China 15 1.2k 1.2× 1.1k 1.7× 77 0.7× 179 2.2× 35 0.5× 21 1.8k
Adrian M. Lennon Trinidad and Tobago 14 666 0.7× 521 0.8× 57 0.6× 62 0.8× 30 0.4× 23 952
Bartolomé Sabater Spain 25 1.6k 1.7× 1.2k 1.7× 92 0.9× 139 1.7× 16 0.2× 74 2.1k
Dominique Rumeau France 23 1.8k 2.0× 1.4k 2.1× 216 2.1× 276 3.4× 97 1.3× 32 2.4k
Sergey Khorobrykh Russia 20 668 0.7× 535 0.8× 143 1.4× 124 1.5× 47 0.6× 28 1.0k
Günter F. Wildner Germany 16 523 0.6× 293 0.4× 72 0.7× 142 1.8× 66 0.9× 39 822
Tingyun Kuang China 19 670 0.7× 845 1.2× 87 0.8× 132 1.6× 17 0.2× 51 1.3k

Countries citing papers authored by Jan E. Backhausen

Since Specialization
Citations

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

Fields of papers citing papers by Jan E. Backhausen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jan E. Backhausen. 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 Jan E. Backhausen. The network helps show where Jan E. Backhausen may publish in the future.

Co-authorship network of co-authors of Jan E. Backhausen

This figure shows the co-authorship network connecting the top 25 collaborators of Jan E. Backhausen. A scholar is included among the top collaborators of Jan E. Backhausen 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 Jan E. Backhausen. Jan E. Backhausen 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.
Voß, Ingo, et al.. (2008). Knockout of major leaf ferredoxin reveals new redox‐regulatory adaptations in Arabidopsis thaliana. Physiologia Plantarum. 133(3). 584–598. 55 indexed citations
2.
Holtgrefe, Simone, et al.. (2007). Transcriptional Regulation of NADP-Dependent Malate Dehydrogenase: Comparative Genetics and Identification of DNA-Binding Proteins. Journal of Molecular Evolution. 65(4). 437–455. 24 indexed citations
3.
Holtgrefe, Simone, Christina Wunrau, Andrea Kandlbinder, et al.. (2006). Influence of the photoperiod on redox regulation and stress responses in Arabidopsis thaliana L. (Heynh.) plants under long- and short-day conditions. Planta. 224(2). 380–393. 63 indexed citations
4.
5.
Scheibe, Renate, et al.. (2005). Strategies to maintain redox homeostasis during photosynthesis under changing conditions. Journal of Experimental Botany. 56(416). 1481–1489. 191 indexed citations
6.
Holtgrefe, Simone, Klaus P. Bader, Peter Horton, et al.. (2003). Decreased Content of Leaf Ferredoxin Changes Electron Distribution and Limits Photosynthesis in Transgenic Potato Plants. PLANT PHYSIOLOGY. 133(4). 1768–1778. 65 indexed citations
7.
Backhausen, Jan E., et al.. (2000). Electron acceptors in isolated intact spinach chloroplasts act hierarchically to prevent over-reduction and competition for electrons. Photosynthesis Research. 64(1). 1–13. 87 indexed citations
8.
Reichert, Angelika, et al.. (2000). Activation properties of the redox-modulated chloroplast enzymes glyceraldehyde 3-phosphate dehydrogenase and fructose-1,6-bisphosphatase. Physiologia Plantarum. 110(3). 330–341. 14 indexed citations
9.
Reichert, Angelika, et al.. (2000). Activation properties of the redox‐modulated chloroplast enzymes glyceraldehyde 3‐phosphate dehydrogenase and fructose‐1,6‐bisphosphatase. Physiologia Plantarum. 110(3). 330–341. 16 indexed citations
10.
Fridlyand, Leonid E., Jan E. Backhausen, & Renate Scheibe. (1999). Homeostatic regulation upon changes of enzyme activities in the Calvin cycle as an example for general mechanisms of flux control. What can we expect from transgenic plants?. Photosynthesis Research. 61(3). 227–239. 33 indexed citations
11.
Fridlyand, Leonid E., Jan E. Backhausen, & Renate Scheibe. (1998). Flux Control of the Malate Valve in Leaf Cells. Archives of Biochemistry and Biophysics. 349(2). 290–298. 60 indexed citations
12.
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14.
Fridlyand, Leonid E., et al.. (1997). Quantitative Evaluation of the Rate of 3-Phosphoglycerate Reduction in Chloroplasts. Plant and Cell Physiology. 38(11). 1177–1186. 18 indexed citations
15.
Backhausen, Jan E., et al.. (1997). Competitive inhibition of spinach leaf phosphoglucose isomerase isoenzymes by erythrose 4-phosphate. Plant Science. 130(2). 121–131. 19 indexed citations
16.
Scheibe, Renate, et al.. (1996). C-terminal truncation of spinach chloroplast NAD(P)-dependent glyceraldehyde-3-phosphate dehydrogenase prevents inactivation and reaggregation. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1296(2). 228–234. 28 indexed citations
17.
Holtgrefe, Simone, et al.. (1995). Redox equilibria between the regulatory thiols of light/dark-modulated chloroplast enzymes and dithiothreitol: fine-tuning by metabolites. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1247(1). 135–142. 44 indexed citations
18.
Backhausen, Jan E., et al.. (1995). Reductive Modification and Nonreductive Activation of Purified Spinach Chloroplast NADP-Dependent Glyceraldehyde-3-phosphate Dehydrogenase. Archives of Biochemistry and Biophysics. 324(2). 201–208. 75 indexed citations
19.
Backhausen, Jan E., et al.. (1994). Competition between electron acceptors in photosynthesis: Regulation of the malate valve during CO2 fixation and nitrite reduction. Photosynthesis Research. 42(1). 75–86. 70 indexed citations
20.
Backhausen, Jan E., et al.. (1994). Regulation of NADP‐Dependent Glyceraldehyde 3‐Phosphate Dehydrogenase Activity in Spinach Chloroplasts*. Botanica Acta. 107(5). 313–320. 43 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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