Alexander Dovzhenko

3.1k total citations
17 papers, 736 citations indexed

About

Alexander Dovzhenko is a scholar working on Plant Science, Molecular Biology and Physiology. According to data from OpenAlex, Alexander Dovzhenko has authored 17 papers receiving a total of 736 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Plant Science, 13 papers in Molecular Biology and 2 papers in Physiology. Recurrent topics in Alexander Dovzhenko's work include Plant Molecular Biology Research (12 papers), Plant Reproductive Biology (9 papers) and Plant nutrient uptake and metabolism (5 papers). Alexander Dovzhenko is often cited by papers focused on Plant Molecular Biology Research (12 papers), Plant Reproductive Biology (9 papers) and Plant nutrient uptake and metabolism (5 papers). Alexander Dovzhenko collaborates with scholars based in Germany, Italy and United States. Alexander Dovzhenko's co-authors include Klaus Palme, Cristina Dal Bosco, Franck Anicet Ditengou, Benedetto Ruperti, H. -U. Koop, Ivan A. Paponov, William Teale, Jörg Meurer, Taras Pasternak and Arthur J. Molendijk and has published in prestigious journals such as The EMBO Journal, Scientific Reports and The Plant Journal.

In The Last Decade

Alexander Dovzhenko

17 papers receiving 719 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexander Dovzhenko Germany 16 644 525 34 32 28 17 736
Chihiro Nakamori Japan 9 371 0.6× 652 1.2× 20 0.6× 6 0.2× 38 1.4× 9 798
Elodie Boucheron‐Dubuisson France 8 523 0.8× 433 0.8× 60 1.8× 58 1.8× 67 2.4× 13 626
Elizabeth Rosen United States 6 853 1.3× 654 1.2× 18 0.5× 58 1.8× 29 1.0× 7 910
Myung Ki Min South Korea 16 656 1.0× 429 0.8× 11 0.3× 14 0.4× 13 0.5× 25 821
Hugues Nziengui Germany 10 547 0.8× 394 0.8× 21 0.6× 24 0.8× 19 0.7× 11 667
Yongqing Yang China 11 803 1.2× 482 0.9× 16 0.5× 28 0.9× 11 0.4× 16 976
Laura Luoni Italy 18 661 1.0× 419 0.8× 12 0.4× 31 1.0× 6 0.2× 25 827
Sabine Grat France 11 246 0.4× 245 0.5× 15 0.4× 25 0.8× 36 1.3× 13 373
Huiqiong Zheng China 14 411 0.6× 227 0.4× 16 0.5× 87 2.7× 123 4.4× 36 577
Tiffanie Girault France 8 393 0.6× 209 0.4× 34 1.0× 14 0.4× 28 1.0× 9 453

Countries citing papers authored by Alexander Dovzhenko

Since Specialization
Citations

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

Fields of papers citing papers by Alexander Dovzhenko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander Dovzhenko

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

All Works

17 of 17 papers shown
1.
Teale, William, Taras Pasternak, Cristina Dal Bosco, et al.. (2020). Flavonol‐mediated stabilization of PIN efflux complexes regulates polar auxin transport. The EMBO Journal. 40(1). e104416–e104416. 71 indexed citations
2.
Middleton, A., Cristina Dal Bosco, Phillip Chlap, et al.. (2018). Data-Driven Modeling of Intracellular Auxin Fluxes Indicates a Dominant Role of the ER in Controlling Nuclear Auxin Uptake. Cell Reports. 22(11). 3044–3057. 23 indexed citations
3.
Johnson, Gregory R., Joshua Kangas, Alexander Dovzhenko, et al.. (2017). A method for characterizing phenotypic changes in highly variable cell populations and its application to high content screening of Arabidopsis thaliana protoplasts. Cytometry Part A. 91(4). 326–335. 2 indexed citations
4.
Panigrahi, Kishore C. S., et al.. (2016). Hydrolases of the ILR1-like family of Arabidopsis thaliana modulate auxin response by regulating auxin homeostasis in the endoplasmic reticulum. Scientific Reports. 6(1). 24212–24212. 55 indexed citations
5.
Wang, Hui, Xugang Li, Lars Krause, et al.. (2015). 2-D Clinostat for Simulated Microgravity Experiments with Arabidopsis Seedlings. Microgravity Science and Technology. 28(1). 59–66. 21 indexed citations
6.
Schmidt, Thorsten, Taras Pasternak, Kun Liu, et al.. (2014). The iRoCS Toolbox – 3D analysis of the plant root apical meristem at cellular resolution. The Plant Journal. 77(5). 806–814. 51 indexed citations
7.
Bosco, Cristina Dal, Michael M. Kämpf, Klaus Palme, et al.. (2013). A quantitative ratiometric sensor for time-resolved analysis of auxin dynamics. Scientific Reports. 3(1). 2052–2052. 62 indexed citations
8.
Begheldo, Maura, Taras Pasternak, Monica Zermiani, et al.. (2013). The Arabidopsis thaliana Mob1A gene is required for organ growth and correct tissue patterning of the root tip. Annals of Botany. 112(9). 1803–1814. 16 indexed citations
9.
Nziengui, Hugues, Ivan A. Paponov, Yong Li, et al.. (2013). Analysis of gene expression during parabolic flights reveals distinct early gravity responses in Arabidopsis roots. Plant Biology. 16(s1). 129–141. 28 indexed citations
10.
Bosco, Cristina Dal, Alexander Dovzhenko, Xing Liu, et al.. (2012). The endoplasmic reticulum localized PIN8 is a pollen‐specific auxin carrier involved in intracellular auxin homeostasis. The Plant Journal. 71(5). 860–870. 123 indexed citations
11.
Bosco, Cristina Dal, Alexander Dovzhenko, & Klaus Palme. (2012). Intracellular auxin transport in pollen. Plant Signaling & Behavior. 7(11). 1504–1505. 28 indexed citations
12.
Teale, William, Franck Anicet Ditengou, Alexander Dovzhenko, et al.. (2008). Auxin as a Model for the Integration of Hormonal Signal Processing and Transduction. Molecular Plant. 1(2). 229–237. 55 indexed citations
13.
Molendijk, Arthur J., Benedetto Ruperti, Manoj Kumar Singh, et al.. (2007). A cysteine‐rich receptor‐like kinase NCRK and a pathogen‐induced protein kinase RBK1 are Rop GTPase interactors. The Plant Journal. 53(6). 909–923. 54 indexed citations
14.
Palme, Klaus, Alexander Dovzhenko, & Franck Anicet Ditengou. (2006). Auxin transport and gravitational research: perspectives. PROTOPLASMA. 229(2-4). 175–181. 42 indexed citations
15.
Dovzhenko, Alexander, Cristina Dal Bosco, Jörg Meurer, & H. -U. Koop. (2003). Efficient regeneration from cotyledon protoplasts in Arabidopsis thaliana. PROTOPLASMA. 222(1-2). 107–111. 52 indexed citations
16.
Dovzhenko, Alexander & Hans‐Ulrich Koop. (2003). Sugarbeet ( Beta vulgaris L.): shoot regeneration from callus and callus protoplasts. Planta. 217(3). 374–381. 19 indexed citations
17.
Dovzhenko, Alexander, et al.. (1998). Thin-alginate-layer technique for protoplast culture of tobacco leaf protoplasts: Shoot formation in less than two weeks. PROTOPLASMA. 204(1-2). 114–118. 34 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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