Ingo Ensminger

3.6k total citations
60 papers, 2.6k citations indexed

About

Ingo Ensminger is a scholar working on Plant Science, Global and Planetary Change and Molecular Biology. According to data from OpenAlex, Ingo Ensminger has authored 60 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Plant Science, 35 papers in Global and Planetary Change and 21 papers in Molecular Biology. Recurrent topics in Ingo Ensminger's work include Plant Water Relations and Carbon Dynamics (33 papers), Plant responses to elevated CO2 (19 papers) and Plant Stress Responses and Tolerance (15 papers). Ingo Ensminger is often cited by papers focused on Plant Water Relations and Carbon Dynamics (33 papers), Plant responses to elevated CO2 (19 papers) and Plant Stress Responses and Tolerance (15 papers). Ingo Ensminger collaborates with scholars based in Canada, Germany and Switzerland. Ingo Ensminger's co-authors include Norman P. A. Hüner, Florian A. Busch, Christopher Y. S. Wong, C. Y. Chang, Jon Lloyd, Petra D’Odorico, Arthur Geßler, M. Altaf Arain, John A. Gamon and Josep Peñuelas and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and PLANT PHYSIOLOGY.

In The Last Decade

Ingo Ensminger

56 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ingo Ensminger Canada	28	1.4k	1.1k	815	677	410	60	2.6k
Onno Muller Germany	33	2.1k 1.5×	1.2k 1.0×	831 1.0×	775 1.1×	287 0.7×	92	3.1k
Albert Rivas‐Ubach United States	23	1.2k 0.9×	905 0.8×	949 1.2×	411 0.6×	375 0.9×	39	3.3k
Otmar Urban Czechia	34	2.8k 2.0×	1.9k 1.7×	776 1.0×	877 1.3×	1.0k 2.5×	170	4.6k
Markus Lange Germany	27	923 0.7×	583 0.5×	1.3k 1.6×	718 1.1×	224 0.5×	57	3.9k
Yusuke Onoda Japan	32	2.2k 1.6×	1.6k 1.4×	663 0.8×	518 0.8×	410 1.0×	76	3.9k
Albert Porcar‐Castell Finland	31	1.5k 1.1×	2.7k 2.4×	2.4k 2.9×	527 0.8×	514 1.3×	66	3.8k
Michal V. Marek Czechia	26	1.3k 0.9×	1.4k 1.2×	414 0.5×	292 0.4×	591 1.4×	101	2.3k
Yves Goulas France	26	1.6k 1.1×	1.5k 1.3×	1.6k 2.0×	479 0.7×	198 0.5×	48	3.1k
Laura Llorens Spain	24	1.2k 0.9×	1.1k 1.0×	606 0.7×	253 0.4×	352 0.9×	40	2.6k
Martina Pollastrini Italy	29	1.2k 0.9×	1.3k 1.1×	394 0.5×	263 0.4×	656 1.6×	75	2.5k

Countries citing papers authored by Ingo Ensminger

Since Specialization

Citations

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

Fields of papers citing papers by Ingo Ensminger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ingo Ensminger

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

All Works

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20 of 20 papers shown

Schneider, Adam C., et al.. (2025). Photosynthetic activity in the heterotrophic plant genus Cuscuta (Convolvulaceae) is modulated by phylogeny and ontogeny. Annals of Botany.

Chang, C. Y., Faride Unda, Shawn D. Mansfield, & Ingo Ensminger. (2023). Rapid response of nonstructural carbohydrate allocation and photosynthesis to short photoperiod, low temperature, or elevated CO₂ in Pinus strobus. Physiologia Plantarum. 175(6). e14095–e14095.

D’Odorico, Petra, Leonie Schönbeck, Valentina Vitali, et al.. (2021). Drone‐based physiological index reveals long‐term acclimation and drought stress responses in trees. Plant Cell & Environment. 44(11). 3552–3570. 45 indexed citations

Larama, Giovanni, et al.. (2020). A comparative gene co-expression analysis using self-organizing maps on two congener filmy ferns identifies specific desiccation tolerance mechanisms associated to their microhabitat preference. BMC Plant Biology. 20(1). 56–56. 8 indexed citations

Larama, Giovanni, Ana Gutiérrez‐Moraga, Ingo Ensminger, et al.. (2020). Decoding Gene Networks Modules That Explain the Recovery of Hymenoglossum cruentum Cav. After Extreme Desiccation. Frontiers in Plant Science. 11. 574–574. 4 indexed citations

Jansen, Kirstin, Henning Wildhagen, Moritz Hess, et al.. (2017). Variation in short-term and long-term responses of photosynthesis and isoprenoid-mediated photoprotection to soil water availability in four Douglas-fir provenances. Scientific Reports. 7(1). 40145–40145. 17 indexed citations

Gamon, John A., K. F. Huemmrich, Christopher Y. S. Wong, et al.. (2016). A remotely sensed pigment index reveals photosynthetic phenology in evergreen conifers. Proceedings of the National Academy of Sciences. 113(46). 13087–13092. 271 indexed citations

Ensminger, Ingo, et al.. (2016). Relationship between leaf optical properties, chlorophyll fluorescence and pigment changes in senescingAcer saccharumleaves. Tree Physiology. 36(6). 694–711. 68 indexed citations

Hess, Moritz, et al.. (2016). Transcriptome responses to temperature, water availability and photoperiod are conserved among mature trees of two divergent Douglas-fir provenances from a coastal and an interior habitat. BMC Genomics. 17(1). 682–682. 24 indexed citations

10.

Chang, C. Y., et al.. (2016). Photoperiod and temperature constraints on the relationship between the photochemical reflectance index and the light use efficiency of photosynthesis inPinus strobus. Tree Physiology. 36(3). 311–324. 30 indexed citations

11.

Chang, C. Y., et al.. (2016). Elevated temperature and CO2 stimulate late season photosynthesis but impair cold hardening in pine. PLANT PHYSIOLOGY. 172(2). pp.00753.2016–pp.00753.2016. 27 indexed citations

12.

Du, Baoguo, Kirstin Jansen, Monika Eiblmeier, et al.. (2015). A coastal and an interior Douglas fir provenance exhibit different metabolic strategies to deal with drought stress. Tree Physiology. 36(2). tpv105–tpv105. 42 indexed citations

13.

Flexas, Jaume, Thomas D. Sharkey, Christine H. Foyer, et al.. (2012). Terrestrial Photosynthesis in a Changing Environment. Cambridge University Press eBooks. 58 indexed citations

14.

Müller, T., Ingo Ensminger, & Karl Schmid. (2012). A catalogue of putative unique transcripts from Douglas-fir (Pseudotsuga menziesii) based on 454 transcriptome sequencing of genetically diverse, drought stressed seedlings. BMC Genomics. 13(1). 673–673. 30 indexed citations

15.

Herschbach, Cornelia, Luca Rizzini, Tanja Nicole Hartmann, et al.. (2010). Overexpression of bacterial γ-glutamylcysteine synthetase (GSH1) in plastids affects photosynthesis, growth and sulphur metabolism in poplar (Populus tremulaxP. alba) dependent on the resulting γ-EC and GSH levels. Plant Cell & Environment. 33(7). 1138–51. 14 indexed citations

16.

Porcar‐Castell, Albert, Eija Juurola, Ingo Ensminger, et al.. (2008). Seasonal acclimation of photosystem II in Pinus sylvestris. II. Using the rate constants of sustained thermal energy dissipation and photochemistry to study the effect of the light environment. Tree Physiology. 28(10). 1483–1491. 49 indexed citations

17.

Busch, Florian A., Norman P. A. Hüner, & Ingo Ensminger. (2007). Increased Air Temperature during Simulated Autumn Conditions Does Not Increase Photosynthetic Carbon Gain But Affects the Dissipation of Excess Energy in Seedlings of the Evergreen Conifer Jack Pine. PLANT PHYSIOLOGY. 143(3). 1242–1251. 61 indexed citations

18.

Ensminger, Ingo, et al.. (2007). Soil temperature and intermittent frost modulate the rate of recovery of photosynthesis in Scots pine under simulated spring conditions. New Phytologist. 177(2). 428–442. 60 indexed citations

19.

Ensminger, Ingo, Florian A. Busch, & Norman P. A. Hüner. (2006). Photostasis and cold acclimation: sensing low temperature through photosynthesis. Physiologia Plantarum. 126(1). 28–44. 442 indexed citations

20.

Sveshnikov, Dmitry, Ingo Ensminger, Alexander G. Ivanov, et al.. (2006). Excitation energy partitioning and quenching during cold acclimation in Scots pine. Tree Physiology. 26(3). 325–336. 55 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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