László Kozma‐Bognár

4.9k total citations
47 papers, 3.8k citations indexed

About

László Kozma‐Bognár is a scholar working on Plant Science, Molecular Biology and Endocrine and Autonomic Systems. According to data from OpenAlex, László Kozma‐Bognár has authored 47 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Plant Science, 37 papers in Molecular Biology and 5 papers in Endocrine and Autonomic Systems. Recurrent topics in László Kozma‐Bognár's work include Light effects on plants (43 papers), Plant Molecular Biology Research (40 papers) and Photosynthetic Processes and Mechanisms (33 papers). László Kozma‐Bognár is often cited by papers focused on Light effects on plants (43 papers), Plant Molecular Biology Research (40 papers) and Photosynthetic Processes and Mechanisms (33 papers). László Kozma‐Bognár collaborates with scholars based in Hungary, United Kingdom and Germany. László Kozma‐Bognár's co-authors include Ferenc Nagy, Andrew J. Millar, Éva Ádám, Anthony Hall, Eberhard Schäfer, Stefan Kircher, James Locke, Éva Kevei, Matthew S. Turner and Megan M. Southern and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Plant Cell.

In The Last Decade

László Kozma‐Bognár

45 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
László Kozma‐Bognár Hungary 30 3.5k 2.7k 330 138 95 47 3.8k
Isabelle A. Carré United Kingdom 27 3.1k 0.9× 2.2k 0.8× 566 1.7× 172 1.2× 99 1.0× 46 3.6k
Norihito Nakamichi Japan 32 3.9k 1.1× 2.7k 1.0× 320 1.0× 52 0.4× 181 1.9× 69 4.2k
Michael F. Covington United States 20 3.0k 0.9× 1.9k 0.7× 250 0.8× 53 0.4× 199 2.1× 25 3.4k
Ute Hoecker Germany 38 4.2k 1.2× 3.6k 1.3× 83 0.3× 98 0.7× 70 0.7× 64 4.6k
Henry D. Priest United States 19 2.2k 0.6× 2.1k 0.8× 166 0.5× 53 0.4× 179 1.9× 24 3.0k
David Alabadı́ Spain 34 4.6k 1.3× 3.3k 1.2× 208 0.6× 32 0.2× 83 0.9× 61 4.9k
Carl A. Strayer United States 10 1.8k 0.5× 1.4k 0.5× 685 2.1× 220 1.6× 85 0.9× 12 2.4k
Rossana Henriques Spain 23 3.7k 1.1× 2.8k 1.0× 120 0.4× 42 0.3× 68 0.7× 32 4.3k
Rachel M. Green Israel 16 1.4k 0.4× 962 0.4× 360 1.1× 102 0.7× 92 1.0× 22 1.7k
Shoji Sugano Japan 24 2.9k 0.8× 1.7k 0.6× 158 0.5× 34 0.2× 143 1.5× 32 3.3k

Countries citing papers authored by László Kozma‐Bognár

Since Specialization
Citations

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

Fields of papers citing papers by László Kozma‐Bognár

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by László Kozma‐Bognár. 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 László Kozma‐Bognár. The network helps show where László Kozma‐Bognár may publish in the future.

Co-authorship network of co-authors of László Kozma‐Bognár

This figure shows the co-authorship network connecting the top 25 collaborators of László Kozma‐Bognár. A scholar is included among the top collaborators of László Kozma‐Bognár 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 László Kozma‐Bognár. László Kozma‐Bognár 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.
Mérai, Zsuzsanna, et al.. (2025). Phytochrome A is required for light‐inhibited germination of Aethionema arabicum seed. New Phytologist. 247(5). 2134–2146.
2.
Ádám, Éva, Cornelia Klose, Gábor Grézal, et al.. (2024). Phytochrome C and Low Temperature Promote the Protein Accumulation and Red-Light Signaling of Phytochrome D. Plant and Cell Physiology. 65(10). 1717–1735. 1 indexed citations
3.
4.
Pettkó‐Szandtner, Aladár, László Kozma‐Bognár, Eve‐Marie Josse, et al.. (2020). SUMOylation of PHYTOCHROME INTERACTING FACTOR 3 promotes photomorphogenesis in Arabidopsis thaliana. New Phytologist. 229(4). 2050–2061. 17 indexed citations
5.
Domijan, Mirela, et al.. (2018). ELONGATED HYPOCOTYL 5 mediates blue light signalling to the Arabidopsis circadian clock. The Plant Journal. 96(6). 1242–1254. 54 indexed citations
6.
Gould, Peter, Mirela Domijan, Mark Greenwood, et al.. (2018). Coordination of robust single cell rhythms in the Arabidopsis circadian clock via spatial waves of gene expression. eLife. 7. 78 indexed citations
7.
Gierczik, Krisztián, Mohamed Ahres, Alexandra Soltész, et al.. (2017). Circadian and Light Regulated Expression of CBFs and their Upstream Signalling Genes in Barley. International Journal of Molecular Sciences. 18(8). 1828–1828. 23 indexed citations
8.
Boldizsár, Ákos, Éva Ádám, László Kozma‐Bognár, et al.. (2015). Light-quality and temperature-dependentCBF14gene expression modulates freezing tolerance in cereals. Journal of Experimental Botany. 67(5). 1285–1295. 39 indexed citations
9.
Sadanandom, Ari, Éva Ádám, Beatriz Orosa‐Puente, et al.. (2015). SUMOylation of phytochrome-B negatively regulates light-induced signaling in Arabidopsis thaliana. Proceedings of the National Academy of Sciences. 112(35). 11108–11113. 66 indexed citations
10.
Ádám, Éva, et al.. (2015). High‐level expression and phosphorylation of phytochrome B modulates flowering time in Arabidopsis. The Plant Journal. 83(5). 794–805. 33 indexed citations
11.
Dixon, Laura E., Kirsten Knox, László Kozma‐Bognár, et al.. (2011). Temporal Repression of Core Circadian Genes Is Mediated through EARLY FLOWERING 3 in Arabidopsis. Current Biology. 21(2). 120–125. 184 indexed citations
12.
Fehér, Balázs, László Kozma‐Bognár, Éva Kevei, et al.. (2011). Functional interaction of the circadian clock and UV RESISTANCE LOCUS 8‐controlled UV‐B signaling pathways in Arabidopsis thaliana. The Plant Journal. 67(1). 37–48. 103 indexed citations
13.
Aleksić, J., Andrew J. Millar, László Kozma‐Bognár, et al.. (2007). Development of a novel biosensor for the detection of arsenic in drinking water. 1(1). 87–90. 23 indexed citations
14.
Kevei, Éva, Péter Gyula, Balázs Fehér, et al.. (2007). Arabidopsis thaliana Circadian Clock Is Regulated by the Small GTPase LIP1. Current Biology. 17(17). 1456–1464. 34 indexed citations
15.
Locke, James, László Kozma‐Bognár, Peter Gould, et al.. (2006). Experimental validation of a predicted feedback loop in the multi‐oscillator clock of Arabidopsis thaliana. Molecular Systems Biology. 2(1). 59–59. 329 indexed citations
16.
Viczián, András, Stefan Kircher, Erzsébet Fejes, et al.. (2005). Functional Characterization of Phytochrome Interacting Factor 3 for the Arabidopsis thaliana Circadian Clockwork. Plant and Cell Physiology. 46(10). 1591–1602. 35 indexed citations
17.
Hall, Anthony, László Kozma‐Bognár, Ruth Bastow, Ferenc Nagy, & Andrew J. Millar. (2002). Distinct regulation of CAB and PHYB gene expression by similar circadian clocks. The Plant Journal. 32(4). 529–537. 63 indexed citations
18.
Doyle, Mark R., Seth J Davis, Ruth Bastow, et al.. (2002). The ELF4 gene controls circadian rhythms and flowering time in Arabidopsis thaliana. Nature. 419(6902). 74–77. 389 indexed citations
19.
Tóth, Réka, Éva Kevei, Anthony Hall, et al.. (2001). Circadian Clock-Regulated Expression of Phytochrome and Cryptochrome Genes in Arabidopsis. PLANT PHYSIOLOGY. 127(4). 1607–1616. 198 indexed citations
20.
Ádám, Éva, László Kozma‐Bognár, Carol Kolar, E. Schäfer, & Ferenc Nagy. (1996). The Tissue-Specific Expression of a Tobacco Phytochrome B Gene. PLANT PHYSIOLOGY. 110(4). 1081–1088. 30 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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