Tamás Sohajda

1.5k total citations · 1 hit paper
50 papers, 1.2k citations indexed

About

Tamás Sohajda is a scholar working on Spectroscopy, Biomedical Engineering and Molecular Biology. According to data from OpenAlex, Tamás Sohajda has authored 50 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Spectroscopy, 26 papers in Biomedical Engineering and 9 papers in Molecular Biology. Recurrent topics in Tamás Sohajda's work include Analytical Chemistry and Chromatography (27 papers), Microfluidic and Capillary Electrophoresis Applications (19 papers) and Innovative Microfluidic and Catalytic Techniques Innovation (15 papers). Tamás Sohajda is often cited by papers focused on Analytical Chemistry and Chromatography (27 papers), Microfluidic and Capillary Electrophoresis Applications (19 papers) and Innovative Microfluidic and Catalytic Techniques Innovation (15 papers). Tamás Sohajda collaborates with scholars based in Hungary, Spain and Czechia. Tamás Sohajda's co-authors include Lajos Szente, Szabolcs Béni, Julianna Szemán, Éva Fenyvesi, Béla Noszál, Erzsébet Varga, Milo Malanga, Ida Fejős, István Puskás and Gábor Benkovics and has published in prestigious journals such as International Journal of Molecular Sciences, Biophysical Journal and Carbohydrate Polymers.

In The Last Decade

Tamás Sohajda

50 papers receiving 1.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Removal of emerging contaminants from wastewater using advanced treatments. A review

2022 260 citations Nadia Morin‐Crini, Éric Lichtfouse et al. Environmental Chemistry Letters profile →

Peers

Tamás Sohajda

SPECT

Paweł K. Zarzycki Poland

Muhammad Ali Sheraz Pakistan

Ting Huang China

Constantinos K. Zacharis Greece

Salman S. Alharthi Saudi Arabia

Rajaram Rajamohan India

Panagiotis Manesiotis United Kingdom

Tânia E. Sintra Portugal

Li Zhu China

Joanna Kurczewska Poland

Paweł K. Zarzycki Poland

Tamás Sohajda

525 ×1.1

SPECT

525 ×1.3

297 ×1.5

225 ×1.3

397 ×2.4

Citations per year, relative to Tamás Sohajda Tamás Sohajda (= 1×) peers Paweł K. Zarzycki

Countries citing papers authored by Tamás Sohajda

Since Specialization

Citations

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

Fields of papers citing papers by Tamás Sohajda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tamás Sohajda

This figure shows the co-authorship network connecting the top 25 collaborators of Tamás Sohajda. A scholar is included among the top collaborators of Tamás Sohajda 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 Tamás Sohajda. Tamás Sohajda 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

Faudzi, Siti Munirah Mohd, et al.. (2025). Mechanisms and Therapeutic Applications of β‐Cyclodextrin in Drug Solubilisation and Delivery Systems. Chemistry & Biodiversity. 22(11). e00359–e00359. 1 indexed citations

O’Connor, Matthew S., J.D. Pipkin, Milo Malanga, et al.. (2025). A comprehensive nomenclature system for cyclodextrins. Carbohydrate Polymers. 360. 123600–123600. 1 indexed citations

Morin‐Crini, Nadia, Éric Lichtfouse, Marc Fourmentin, et al.. (2022). Removal of emerging contaminants from wastewater using advanced treatments. A review. Environmental Chemistry Letters. 20(2). 1333–1375. 260 indexed citations breakdown →

Szente, Lajos, et al.. (2022). Comparative bioavailability study following a single dose intravenous and buccal administration of remdesivir in rabbits. International Journal of Pharmaceutics. 620. 121739–121739. 5 indexed citations

Malanga, Milo, et al.. (2022). Sugammadex analogue cyclodextrins as chiral selectors for enantioseparation of cathinone derivatives by capillary electrophoresis. Journal of Chromatography A. 1683. 463506–463506. 12 indexed citations

Fenyvesi, Éva & Tamás Sohajda. (2022). Cyclodextrin-enabled green environmental biotechnologies. Environmental Science and Pollution Research. 29(14). 20085–20097. 24 indexed citations

Salgado, Antonio, Milo Malanga, Tamás Sohajda, et al.. (2021). Structural characterization of methyl-β-cyclodextrins by high-performance liquid chromatography and nuclear magnetic resonance spectroscopy and effect of their isomeric composition on the capillary electrophoresis enantioseparation of daclatasvir. Journal of Chromatography A. 1661. 462675–462675. 11 indexed citations

Fábián, Ákos, et al.. (2021). Carboxymethyl-γ-cyclodextrin, a novel selective relaxant binding agent for the reversal of neuromuscular block induced by aminosteroid neuromuscular blockers: an ex vivo laboratory study. BMC Anesthesiology. 21(1). 206–206. 2 indexed citations

Grabarics, Márkó, Zoltán Szakács, Kevin Pagel, et al.. (2021). Structural characterization of fondaparinux interaction with per-6-amino-beta-cyclodextrin: An NMR and MS study. Journal of Pharmaceutical and Biomedical Analysis. 197. 113947–113947. 4 indexed citations

10.

Malanga, Milo, et al.. (2021). Molecular interactions in remdesivir-cyclodextrin systems. Journal of Pharmaceutical and Biomedical Analysis. 209. 114482–114482. 19 indexed citations

11.

Zákány, Florina, Tamás Kovács, Tamás Sohajda, et al.. (2020). Characterization of Direct Cyclodextrin Effects on Voltage-Gated Potassium Channels. Biophysical Journal. 118(3). 263a–264a. 1 indexed citations

12.

Dargó, Gergő, László Péter, Milo Malanga, et al.. (2018). Novel medium-throughput technique for investigating drug-cyclodextrin complexation by pH-metric titration using the partition coefficient method. International Journal of Pharmaceutics. 542(1-2). 100–107. 5 indexed citations

13.

Chankvetadze, Lali, Tamás Sohajda, Julianna Szemán, et al.. (2018). Separation of terbutaline enantiomers in capillary electrophoresis with cyclodextrin-type chiral selectors and investigation of structure of selector-selectand complexes. Journal of Chromatography A. 1571. 231–239. 38 indexed citations

14.

Benkovics, Gábor, Ida Fejős, András Darcsi, et al.. (2016). Single-isomer carboxymethyl-γ-cyclodextrin as chiral resolving agent for capillary electrophoresis. Journal of Chromatography A. 1467. 445–453. 29 indexed citations

15.

Fejős, Ida, Erzsébet Varga, Gábor Benkovics, et al.. (2016). Comparative evaluation of the chiral recognition potential of single-isomer sulfated beta-cyclodextrin synthesis intermediates in non-aqueous capillary electrophoresis. Journal of Chromatography A. 1467. 454–462. 16 indexed citations

16.

Szabó, Zoltán‐István, Gergő Tóth, Gergely Völgyi, et al.. (2015). Chiral separation of asenapine enantiomers by capillary electrophoresis and characterization of cyclodextrin complexes by NMR spectroscopy, mass spectrometry and molecular modeling. Journal of Pharmaceutical and Biomedical Analysis. 117. 398–404. 44 indexed citations

17.

Jicsinszky, László, et al.. (2014). Synthesis of modified cyclic and acyclic dextrins and comparison of their complexation ability. Beilstein Journal of Organic Chemistry. 10. 2836–2843. 2 indexed citations

18.

Malanga, Milo, István Puskás, Tamás Sohajda, et al.. (2014). Synthetic strategies for the fluorescent labeling of epichlorohydrin-branched cyclodextrin polymers. Beilstein Journal of Organic Chemistry. 10. 3007–3018. 22 indexed citations

19.

Sohajda, Tamás, András Darcsi, Gergő Tóth, et al.. (2012). Chiral recognition of dapoxetine enantiomers with methylated-gamma-cyclodextrin: A validated capillary electrophoresis method. Journal of Pharmaceutical and Biomedical Analysis. 62. 42–47. 27 indexed citations

20.

Sohajda, Tamás, Szabolcs Béni, Erzsébet Varga, et al.. (2009). Characterization of aspartame–cyclodextrin complexation. Journal of Pharmaceutical and Biomedical Analysis. 50(5). 737–745. 33 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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