Klára Hlouchová

1.2k total citations
25 papers, 722 citations indexed

About

Klára Hlouchová is a scholar working on Molecular Biology, Astronomy and Astrophysics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Klára Hlouchová has authored 25 papers receiving a total of 722 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 5 papers in Astronomy and Astrophysics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Klára Hlouchová's work include RNA and protein synthesis mechanisms (12 papers), Protein Structure and Dynamics (10 papers) and Origins and Evolution of Life (5 papers). Klára Hlouchová is often cited by papers focused on RNA and protein synthesis mechanisms (12 papers), Protein Structure and Dynamics (10 papers) and Origins and Evolution of Life (5 papers). Klára Hlouchová collaborates with scholars based in Czechia, United States and Japan. Klára Hlouchová's co-authors include Jan Konvalinka, Cyril Bařinka, Petra Mlčochová, Pavel Šácha, J. Łubkowski, Pavel Majer, Johannes Rudolph, Shelley D. Copley, Kosuke Fujishima and Josef Zámečnı́k and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Klára Hlouchová

24 papers receiving 711 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Klára Hlouchová Czechia 16 429 146 145 135 91 25 722
E. A. Krasavin Russia 15 462 1.1× 214 1.5× 114 0.8× 49 0.4× 14 0.2× 70 736
Gloria Fuentes Singapore 15 757 1.8× 21 0.1× 60 0.4× 103 0.8× 22 0.2× 32 1.0k
D J Lundell United States 20 923 2.2× 66 0.5× 33 0.2× 114 0.8× 150 1.6× 27 1.3k
J.C. Fontecilla-Camps France 14 509 1.2× 10 0.1× 45 0.3× 47 0.3× 73 0.8× 26 852
Stephen G. Chamberlin United Kingdom 14 549 1.3× 37 0.3× 64 0.4× 136 1.0× 31 0.3× 23 746
Steven J. Robles United States 10 625 1.5× 25 0.2× 21 0.1× 116 0.9× 151 1.7× 13 913
Marina Gay Spain 16 454 1.1× 78 0.5× 38 0.3× 93 0.7× 66 0.7× 36 859
Zhiyuan Zhang China 16 516 1.2× 25 0.2× 47 0.3× 95 0.7× 35 0.4× 43 836
Anne Reynaud-Angelin France 7 376 0.9× 129 0.9× 39 0.3× 51 0.4× 14 0.2× 9 642
Edward L. Ezell United States 14 300 0.7× 60 0.4× 65 0.4× 46 0.3× 51 0.6× 35 620

Countries citing papers authored by Klára Hlouchová

Since Specialization
Citations

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

Fields of papers citing papers by Klára Hlouchová

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Klára Hlouchová

This figure shows the co-authorship network connecting the top 25 collaborators of Klára Hlouchová. A scholar is included among the top collaborators of Klára Hlouchová 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 Klára Hlouchová. Klára Hlouchová 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.
Kolář, Michal H. & Klára Hlouchová. (2025). Evolution of protein-RNA interactions. Current Opinion in Structural Biology. 94. 103109–103109.
2.
Bornberg‐Bauer, Erich, et al.. (2024). High-throughput Selection of Human de novo -emerged sORFs with High Folding Potential. Genome Biology and Evolution. 16(4). 3 indexed citations
3.
Pravda, Lukáš, et al.. (2024). Coenzyme-protein interactions since early life. eLife. 13. 1 indexed citations
4.
Yamaguchi, Tomoko, et al.. (2024). The interplay between peptides and RNA is critical for protoribosome compartmentalization and stability. Nucleic Acids Research. 52(20). 12689–12700. 3 indexed citations
5.
Loginov, Dmitry S., et al.. (2023). Experimental characterization of de novo proteins and their unevolved random-sequence counterparts. Nature Ecology & Evolution. 7(4). 570–580. 23 indexed citations
6.
Dzmitruk, Volha, Anneliese M. Faustino, Michal Lebl, et al.. (2023). Early Selection of the Amino Acid Alphabet Was Adaptively Shaped by Biophysical Constraints of Foldability. Journal of the American Chemical Society. 145(9). 5320–5329. 30 indexed citations
7.
Fried, Stephen D., et al.. (2022). Peptides before and during the nucleotide world: an origins story emphasizing cooperation between proteins and nucleic acids. Journal of The Royal Society Interface. 19(187). 20210641–20210641. 41 indexed citations
8.
Vymětal, Jiří, et al.. (2022). Modern and prebiotic amino acids support distinct structural profiles in proteins. Open Biology. 12(6). 220040–220040. 14 indexed citations
9.
Fujishima, Kosuke, et al.. (2022). In Vitro Evolution Reveals Noncationic Protein–RNA Interaction Mediated by Metal Ions. Molecular Biology and Evolution. 39(3). 19 indexed citations
10.
Bornberg‐Bauer, Erich, Klára Hlouchová, & Andreas Lange. (2021). Structure and function of naturally evolved de novo proteins. Current Opinion in Structural Biology. 68. 175–183. 37 indexed citations
11.
Meng, Jingwei, Pavel Srb, Lucie Bednářová, et al.. (2021). Enzyme catalysis prior to aromatic residues: Reverse engineering of a dephospho‐CoA kinase. Protein Science. 30(5). 1022–1034. 15 indexed citations
12.
Vymětal, Jiří, Lucie Bednářová, Vladimı́r Kopecký, et al.. (2017). Random protein sequences can form defined secondary structures and are well-tolerated in vivo. Scientific Reports. 7(1). 15449–15449. 59 indexed citations
13.
Tykvart, Jan, Jiří Schimer, Petr Pachl, et al.. (2016). Comparison of human glutamate carboxypeptidases II and III reveals their divergent substrate specificities. FEBS Journal. 283(13). 2528–2545. 20 indexed citations
14.
Hlouchová, Klára, et al.. (2012). GCPII Variants, Paralogs and Orthologs. Current Medicinal Chemistry. 19(9). 1316–1322. 13 indexed citations
15.
Hlouchová, Klára, Cyril Bařinka, Jan Konvalinka, & J. Łubkowski. (2009). Structural insight into the evolutionary and pharmacologic homology of glutamate carboxypeptidases II and III. FEBS Journal. 276(16). 4448–4462. 29 indexed citations
16.
Bařinka, Cyril, Klára Hlouchová, Pavel Majer, et al.. (2008). Structural Basis of Interactions between Human Glutamate Carboxypeptidase II and Its Substrate Analogs. Journal of Molecular Biology. 376(5). 1438–1450. 72 indexed citations
17.
Hlouchová, Klára, Pavel Šácha, Petra Mlčochová, et al.. (2007). Tissue expression and enzymologic characterization of human prostate specific membrane antigen and its rat and pig orthologs. The Prostate. 68(2). 171–182. 34 indexed citations
18.
Bařinka, Cyril, Petra Mlčochová, Klára Hlouchová, et al.. (2007). Structural Insight into the Pharmacophore Pocket of Human Glutamate Carboxypeptidase II. Journal of Medicinal Chemistry. 50(14). 3267–3273. 64 indexed citations
19.
Hlouchová, Klára, Cyril Bařinka, Vojtěch Klusák, et al.. (2006). Biochemical characterization of human glutamate carboxypeptidase III. Journal of Neurochemistry. 101(3). 682–696. 48 indexed citations
20.
Šácha, Pavel, Josef Zámečnı́k, Cyril Bařinka, et al.. (2006). Expression of glutamate carboxypeptidase II in human brain. Neuroscience. 144(4). 1361–1372. 100 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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