Ján Imrich

1.9k total citations
110 papers, 1.6k citations indexed

About

Ján Imrich is a scholar working on Organic Chemistry, Molecular Biology and Toxicology. According to data from OpenAlex, Ján Imrich has authored 110 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Organic Chemistry, 52 papers in Molecular Biology and 20 papers in Toxicology. Recurrent topics in Ján Imrich's work include Synthesis and biological activity (43 papers), Cancer therapeutics and mechanisms (30 papers) and Bioactive Compounds and Antitumor Agents (20 papers). Ján Imrich is often cited by papers focused on Synthesis and biological activity (43 papers), Cancer therapeutics and mechanisms (30 papers) and Bioactive Compounds and Antitumor Agents (20 papers). Ján Imrich collaborates with scholars based in Slovakia, Czechia and Finland. Ján Imrich's co-authors include Pavol Kristián, Ladislav Janovec, Mária Vilková, Mária Kožurková, Danica Sabolová, Miroslav Repčák, Karel D. Klika, Helena Paulíková, Kalevi Pihlaja and Slávka Hamuľaková and has published in prestigious journals such as SHILAP Revista de lepidopterología, Food Chemistry and Journal of Colloid and Interface Science.

In The Last Decade

Ján Imrich

108 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ján Imrich Slovakia 22 921 762 223 216 174 110 1.6k
Sammer Yousuf Pakistan 28 1.5k 1.6× 655 0.9× 277 1.2× 113 0.5× 386 2.2× 251 2.6k
Alberto Leoni Italy 31 1.9k 2.1× 777 1.0× 265 1.2× 180 0.8× 213 1.2× 105 2.6k
Jean‐Luc Bernier France 22 788 0.9× 627 0.8× 163 0.7× 164 0.8× 426 2.4× 55 1.9k
Κonstantinos E. Litinas Greece 22 2.1k 2.3× 461 0.6× 752 3.4× 207 1.0× 89 0.5× 92 2.8k
Hany E. A. Ahmed Saudi Arabia 29 1.2k 1.3× 680 0.9× 263 1.2× 82 0.4× 150 0.9× 66 1.8k
Abdullah Mohammed Al‐Majid Saudi Arabia 27 1.9k 2.0× 471 0.6× 180 0.8× 208 1.0× 276 1.6× 154 2.4k
Nima Razzaghi‐Asl Iran 17 695 0.8× 312 0.4× 138 0.6× 59 0.3× 111 0.6× 67 1.2k
Hussein I. El‐Subbagh Egypt 33 2.6k 2.8× 979 1.3× 265 1.2× 115 0.5× 158 0.9× 120 3.2k
Joaquı́n Tamariz Mexico 27 1.8k 2.0× 422 0.6× 178 0.8× 63 0.3× 83 0.5× 174 2.5k
Aldo Andreani Italy 27 2.0k 2.1× 563 0.7× 261 1.2× 228 1.1× 127 0.7× 120 2.4k

Countries citing papers authored by Ján Imrich

Since Specialization
Citations

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

Fields of papers citing papers by Ján Imrich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ján Imrich

This figure shows the co-authorship network connecting the top 25 collaborators of Ján Imrich. A scholar is included among the top collaborators of Ján Imrich 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 Ján Imrich. Ján Imrich 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.
Janovec, Ladislav, Jana Janočková, Eva Konkoľová, et al.. (2018). Proliferation inhibition of novel diphenylamine derivatives. Bioorganic Chemistry. 83. 487–499. 7 indexed citations
2.
Vilková, Mária, Rastislav Jendželovský, Jana Kašpárková, et al.. (2016). New spiro tria(thia)zolidineacridines as topoisomerase inhibitors, DNA binders and cytostatic compounds. International Journal of Biological Macromolecules. 86. 690–700. 29 indexed citations
3.
Bujňáková, Zdenka Lukáčová, Matěj Baláž, Erika Dutková, et al.. (2016). Mechanochemical approach for the capping of mixed core CdS/ZnS nanocrystals: Elimination of cadmium toxicity. Journal of Colloid and Interface Science. 486. 97–111. 22 indexed citations
4.
Hamuľaková, Slávka, Ján Imrich, Ladislav Janovec, et al.. (2014). Novel tacrine/acridine anticholinesterase inhibitors with piperazine and thiourea linkers. International Journal of Biological Macromolecules. 70. 435–439. 36 indexed citations
5.
Plšíková, Jana, Ladislav Janovec, Ján Kovaĺ, et al.. (2014). Novel trisubstituted acridines as human telomeric quadruplex binding ligands. Bioorganic Chemistry. 57. 13–29. 17 indexed citations
6.
Repčák, Miroslav, et al.. (2013). Coumarins of Matricaria chamomilla L.: Aglycones and glycosides. Food Chemistry. 141(1). 54–59. 64 indexed citations
7.
Paulíková, Helena, Ľuba Hunáková, Mária Čarná, et al.. (2012). DNA binding acridine–thiazolidinone agents affecting intracellular glutathione. Bioorganic & Medicinal Chemistry. 20(24). 7139–7148. 21 indexed citations
8.
Plšíková, Jana, Ladislav Janovec, Ján Kovaĺ, et al.. (2012). 3,6-Bis(3-alkylguanidino)acridines as DNA-intercalating antitumor agents. European Journal of Medicinal Chemistry. 57. 283–295. 42 indexed citations
9.
Janovec, Ladislav, Mária Kožurková, Danica Sabolová, et al.. (2011). Cytotoxic 3,6-bis((imidazolidinone)imino)acridines: Synthesis, DNA binding and molecular modeling. Bioorganic & Medicinal Chemistry. 19(5). 1790–1801. 83 indexed citations
10.
Antošová, Andrea, Beatrice Chelli, Eva Bystrenová, et al.. (2011). Structure-activity relationship of acridine derivatives to amyloid aggregation of lysozyme. Biochimica et Biophysica Acta (BBA) - General Subjects. 1810(4). 465–474. 32 indexed citations
11.
Potočňák, Ivan, et al.. (2010). 4-(9,10-Dihydroacridin-9-ylidene)thiosemicarbazide and its five-membered thiazole and six-membered thiazine derivatives. Acta Crystallographica Section C Crystal Structure Communications. 66(2). o87–o92. 1 indexed citations
12.
Imrich, Ján, Pavol Kristián, Stanislav Böhm, et al.. (2009). Spectroscopic, structural and theoretical studies of novel, potentially cytotoxic 4-acridonecarboxamide imines. Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy. 73(2). 238–248. 8 indexed citations
13.
Paulíková, Helena, Danica Sabolová, Mária Kožurková, et al.. (2009). Cytotoxic activity of acridin-3,6-diyl dithiourea hydrochlorides in human leukemia line HL-60 and resistant subline HL-60/ADR. International Journal of Biological Macromolecules. 45(2). 174–180. 20 indexed citations
14.
Gažová, Zuzana, Zuzana Daxnerová, Ján Imrich, et al.. (2008). Acridine derivatives inhibit lysozyme aggregation. European Biophysics Journal. 37(7). 1261–1270. 59 indexed citations
15.
Sabolová, Danica, et al.. (2006). Determination of the binding affinities of plasmid DNA using fluorescent intercalators possessing an acridine skeleton. International Journal of Biological Macromolecules. 38(2). 94–98. 22 indexed citations
16.
Balentová, Eva, Ján Imrich, Mária Vilková, et al.. (2006). Stereochemistry, Tautomerism, and Reactions of Acridinyl Thiosemicarbazides in the Synthesis of 1,3‐Thiazolidines.. ChemInform. 37(41). 2 indexed citations
17.
Imrich, Ján, Mária Vilková, & Juraj Černák. (2005). 2-(Acridin-9-ylimino)-3-dimethylamino-1,3-thiazolidin-4-one. Acta Crystallographica Section C Crystal Structure Communications. 61(4). o231–o233. 2 indexed citations
18.
Klika, Karel D., Ján Imrich, Stanislav Böhm, et al.. (2005). Configuration and E/Z interconversion mechanism of O(S)‐allyl‐S(O)‐methyl‐N‐(acridin‐9‐yl) iminothiocarbonate. Magnetic Resonance in Chemistry. 43(5). 380–388. 9 indexed citations
19.
20.
Gonda, Jozef, Pavol Kristián, & Ján Imrich. (1987). 2-Isothiocyanatobenzyltriphenylphosphonium bromides – new type of functionalized heterocumulenes suitable for synthesis of indole derivatives. Collection of Czechoslovak Chemical Communications. 52(10). 2508–2520. 1 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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