Miroslav Repčák

1.7k total citations
60 papers, 1.3k citations indexed

About

Miroslav Repčák is a scholar working on Plant Science, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Miroslav Repčák has authored 60 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Plant Science, 27 papers in Molecular Biology and 11 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Miroslav Repčák's work include Phytochemistry and Biological Activities (14 papers), Plant tissue culture and regeneration (8 papers) and Plant biochemistry and biosynthesis (8 papers). Miroslav Repčák is often cited by papers focused on Phytochemistry and Biological Activities (14 papers), Plant tissue culture and regeneration (8 papers) and Plant biochemistry and biosynthesis (8 papers). Miroslav Repčák collaborates with scholars based in Slovakia, Czechia and Belarus. Miroslav Repčák's co-authors include Jozef Kováčik, Martin Bačkor, Pavol Mártonfi, Ján Imrich, Bořivoj Klejdus, Jiřı́ Grúz, Miroslav Strnad, Adriana Eliašová, Mária Vilková and Zuzana Dučaiová and has published in prestigious journals such as SHILAP Revista de lepidopterología, Food Chemistry and Molecules.

In The Last Decade

Miroslav Repčák

58 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Miroslav Repčák Slovakia 20 983 437 215 189 133 60 1.3k
Yashbir S. Bedi India 16 612 0.6× 557 1.3× 211 1.0× 104 0.6× 87 0.7× 39 1.3k
Iker Hernández Spain 16 1.1k 1.1× 598 1.4× 171 0.8× 296 1.6× 92 0.7× 22 1.6k
Sang‐Uk Chon South Korea 17 940 1.0× 275 0.6× 259 1.2× 221 1.2× 97 0.7× 75 1.3k
D. Štajner Serbia 22 764 0.8× 326 0.7× 318 1.5× 390 2.1× 65 0.5× 54 1.2k
Maciej Strzemski Poland 21 502 0.5× 277 0.6× 206 1.0× 108 0.6× 75 0.6× 76 1.0k
Sofia Caretto Italy 22 752 0.8× 624 1.4× 184 0.9× 262 1.4× 41 0.3× 42 1.4k
Dobrosława Białońska Poland 11 475 0.5× 222 0.5× 126 0.6× 246 1.3× 95 0.7× 16 1.1k
Madhu Sharma India 21 1.1k 1.1× 1.0k 2.4× 247 1.1× 161 0.9× 249 1.9× 108 1.9k
Badraldin Ebrahim Sayed Tabatabaei Iran 17 833 0.8× 385 0.9× 381 1.8× 200 1.1× 93 0.7× 37 1.2k
Md. Romij Uddin Bangladesh 19 743 0.8× 560 1.3× 192 0.9× 158 0.8× 46 0.3× 122 1.2k

Countries citing papers authored by Miroslav Repčák

Since Specialization
Citations

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

Fields of papers citing papers by Miroslav Repčák

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miroslav Repčák

This figure shows the co-authorship network connecting the top 25 collaborators of Miroslav Repčák. A scholar is included among the top collaborators of Miroslav Repčák 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 Miroslav Repčák. Miroslav Repčák 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.
García‐Calderón, Margarita, Peter Paľove-Balang, Mária Vilková, et al.. (2015). Modulation of phenolic metabolism under stress conditions in a Lotus japonicus mutant lacking plastidic glutamine synthetase. Frontiers in Plant Science. 6. 760–760. 40 indexed citations
2.
Repčák, Miroslav, et al.. (2013). Coumarins of Matricaria chamomilla L.: Aglycones and glycosides. Food Chemistry. 141(1). 54–59. 64 indexed citations
3.
Repčák, Miroslav, et al.. (2009). Circadian rhythm of (Z)- and (E)-2-β-d-glucopyranosyloxy-4-methoxy cinnamic acids and herniarin in leaves of Matricaria chamomilla. Plant Cell Reports. 28(7). 1137–1143. 10 indexed citations
4.
Repčák, Miroslav, et al.. (2009). Phenolic glucosides in the course of ligulate flower development in diploid and tetraploid Matricaria chamomilla. Food Chemistry. 116(1). 19–22. 27 indexed citations
5.
Kováčik, Jozef, Jiřı́ Grúz, Martin Bačkor, Miroslav Strnad, & Miroslav Repčák. (2008). Salicylic acid-induced changes to growth and phenolic metabolism in Matricaria chamomilla plants. Plant Cell Reports. 28(1). 135–143. 144 indexed citations
6.
Kováčik, Jozef & Miroslav Repčák. (2008). Accumulation of coumarin-related compounds in leaves of Matricaria chamomilla related to sample processing. Food Chemistry. 111(3). 755–757. 10 indexed citations
7.
Kováčik, Jozef, Bořivoj Klejdus, Martin Bačkor, & Miroslav Repčák. (2006). Phenylalanine ammonia-lyase activity and phenolic compounds accumulation in nitrogen-deficient Matricaria chamomilla leaf rosettes. Plant Science. 172(2). 393–399. 151 indexed citations
8.
Repčák, Miroslav, et al.. (2005). Comparative evaluation of different valerian (Valeriana officinalis L.) lines. SHILAP Revista de lepidopterología. 11(2). 1 indexed citations
9.
Mártonfi, Pavol, Miroslav Repčák, & Peter Zanvit. (2005). Secondary metabolites variation in Hypericum maculatum and its relatives. Biochemical Systematics and Ecology. 34(1). 56–59. 21 indexed citations
10.
Repčák, Miroslav, et al.. (2001). Effect of cadmium on active principle contents of Matricaria recutita L.. Herba Polonica. 47(3). 5 indexed citations
11.
Mártonfi, Pavol, Miroslav Repčák, Daniela Ciccarelli, & Fabio Garbari. (2001). Hypericum perforatum L. — chemotype without rutin from Italy. Biochemical Systematics and Ecology. 29(6). 659–661. 29 indexed citations
12.
Galambosi, Bertalan, et al.. (2000). The effect of regular collection of Drosera rotundifolia in natural peatlands in Finland: plant density, yield and regeneration.. Jukuri (Natural Resources Institute Finland (Luke)). 51(2). 37–46. 1 indexed citations
13.
Galambosi, Bertalan, et al.. (2000). Growth, yield and secondary metabolite production of Drosera species cultivated in peat beds in Finland.. Jukuri (Natural Resources Institute Finland (Luke)). 51(2). 47–57. 5 indexed citations
14.
Bačkor, Martin, et al.. (1998). The Influence of pH and Lichen Metabolites (Vulpinic Acid and (+) Usnic Acid) on the Growth of the Lichen Photobiont Trebouxia Irregularis. The Lichenologist. 30(6). 577–582. 27 indexed citations
15.
Repčák, Miroslav, et al.. (1998). 9-(Methylsulphinyl)nonanenitrile, a stress metabolite of Rorippa sylvestris. Phytochemistry. 47(7). 1219–1221. 2 indexed citations
16.
Repčák, Miroslav, et al.. (1998). The influence of soil cadmium eliminating sorbents on Chamomilla recutita. Journal of Environmental Science and Health Part B. 33(3). 307–316. 4 indexed citations
17.
Mártonfi, Pavol, et al.. (1996). Apomixis and hybridity inHypericum perforatum. Folia Geobotanica et Phytotaxonomica. 31(3). 389–396. 28 indexed citations
18.
Mártonfi, Pavol, et al.. (1996). Soil chemistry of Thymus species stands in Carpathians and Pannonia. 6. 39–48. 6 indexed citations
19.
Mártonfi, Pavol, et al.. (1994). Chemotype pattern differentiation of Thymus pulegioides on different substrates. Biochemical Systematics and Ecology. 22(8). 819–825. 36 indexed citations
20.
Čellárová, Eva, et al.. (1982). Morphogenesis in callus tissue cultures of someMatricaria andAchillea Species. Biologia Plantarum. 24(6). 430–433. 11 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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