Kateřina Veselá

964 total citations
34 papers, 722 citations indexed

About

Kateřina Veselá is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Kateřina Veselá has authored 34 papers receiving a total of 722 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Kateřina Veselá's work include Mitochondrial Function and Pathology (12 papers), ATP Synthase and ATPases Research (10 papers) and Metabolism and Genetic Disorders (6 papers). Kateřina Veselá is often cited by papers focused on Mitochondrial Function and Pathology (12 papers), ATP Synthase and ATPases Research (10 papers) and Metabolism and Genetic Disorders (6 papers). Kateřina Veselá collaborates with scholars based in Czechia, Poland and United Kingdom. Kateřina Veselá's co-authors include J Zeman, Hana Hansı́ková, Markéta Tesařová, Lukáš Stibůrek, J Houštěk, Hana Hansíková, Helena Hůlková, Tomáš Honzík, Martin Magner and M. Cristina Magli and has published in prestigious journals such as Biochemical Journal, American Journal of Physiology-Cell Physiology and Archives of Disease in Childhood.

In The Last Decade

Kateřina Veselá

32 papers receiving 695 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kateřina Veselá Czechia 15 493 188 124 101 79 34 722
R. Charles Netherlands 18 367 0.7× 164 0.9× 58 0.5× 51 0.5× 27 0.3× 34 812
Gaia Bistulfi United States 11 372 0.8× 42 0.2× 28 0.2× 78 0.8× 18 0.2× 13 498
Henry N. Fukui United States 14 519 1.1× 138 0.7× 103 0.8× 56 0.6× 80 1.0× 22 783
Helmut Baitsch Germany 13 209 0.4× 50 0.3× 110 0.9× 255 2.5× 21 0.3× 50 653
Rieko Kojima Japan 15 605 1.2× 102 0.5× 27 0.2× 30 0.3× 45 0.6× 26 931
Xue Lü China 15 419 0.8× 14 0.1× 38 0.3× 37 0.4× 30 0.4× 60 692
Cavatina K. Truong United States 10 531 1.1× 288 1.5× 35 0.3× 131 1.3× 4 0.1× 10 659
Patricia Lenhart United States 11 267 0.5× 21 0.1× 36 0.3× 41 0.4× 16 0.2× 17 500
Patrick W. Turk United States 7 397 0.8× 13 0.1× 50 0.4× 57 0.6× 31 0.4× 9 545
Elayanambi Sundaramoorthy United States 12 661 1.3× 27 0.1× 33 0.3× 92 0.9× 13 0.2× 15 873

Countries citing papers authored by Kateřina Veselá

Since Specialization
Citations

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

Fields of papers citing papers by Kateřina Veselá

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kateřina Veselá

This figure shows the co-authorship network connecting the top 25 collaborators of Kateřina Veselá. A scholar is included among the top collaborators of Kateřina Veselá 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 Kateřina Veselá. Kateřina Veselá 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.
Veselá, Kateřina, et al.. (2016). [Mutations in genes affecting fertility of men - current routine laboratory genetic diagnostics and searching for more DNA segments and genes influencing spermatogenesis].. PubMed. 81(6). 437–443. 2 indexed citations
2.
3.
Veselá, Kateřina, et al.. (2012). High-resolution melting analysis of 15 genes in 60 patients with cytochrome-c oxidase deficiency. Journal of Human Genetics. 57(7). 442–448. 14 indexed citations
4.
Handyside, Alan H., Markus Montag, M. Cristina Magli, et al.. (2012). Multiple meiotic errors caused by predivision of chromatids in women of advanced maternal age undergoing in vitro fertilisation. European Journal of Human Genetics. 20(7). 742–747. 107 indexed citations
5.
Guillard, Maïlys, Yoshinao Wada, Hana Hansíková, et al.. (2011). Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I. Journal of Inherited Metabolic Disease. 34(4). 901–906. 30 indexed citations
6.
Veselá, Kateřina, et al.. (2009). Cytosine-Adenosine (CA)n repeats polymorphism in IGF-I gene and early growth in infants born appropriate and small for gestational age.. PubMed. 30(4). 501–5. 1 indexed citations
7.
Piekutowska‐Abramczuk, Dorota, Martin Magner, Ewa Popowska, et al.. (2009). SURF1 missense mutations promote a mild Leigh phenotype. Clinical Genetics. 76(2). 195–204. 29 indexed citations
8.
Stibůrek, Lukáš, Kateřina Veselá, Hana Hansı́ková, Helena Hůlková, & J Zeman. (2009). Loss of function of Sco1 and its interaction with cytochrome c oxidase. American Journal of Physiology-Cell Physiology. 296(5). C1218–C1226. 83 indexed citations
9.
Asfaw, Befekadu, Helena Poupětová, Martin Magner, et al.. (2009). Ultrastructural and functional abnormalities of mitochondria in cultivated fibroblasts from α-mannosidosis patients. Biologia. 64(2). 394–401. 3 indexed citations
10.
Zeman, J, Hana Hansíková, Markéta Tesařová, et al.. (2008). CYTOCHROME C OXIDASE DEFICIENCY IN CHILDHOOD. Archives of Disease in Childhood. 93. 2 indexed citations
11.
Veselá, Kateřina, Helena Hůlková, Hana Hansíková, J Zeman, & M. Elleder. (2008). Structural analysis of tissues affected by cytochrome C oxidase deficiency due to mutations in the SCO2 gene. Apmis. 116(1). 41–49. 14 indexed citations
12.
Veselá, Kateřina, et al.. (2005). Topic-focus articulation and anaphoric relations: corpus based probe.. ˜The œPrague Bulletin of Mathematical Linguistics. 84. 5–12. 2 indexed citations
13.
Hromadníková, Ilona, et al.. (2005). Non-invasive fetal RHD and RHCE genotyping from maternal plasma in alloimmunized pregnancies. Prenatal Diagnosis. 25(12). 1079–1083. 17 indexed citations
14.
Böhm, Marek, Ewa Pronicka, Elżbieta Karczmarewicz, et al.. (2005). Retrospective, Multicentric Study of 180 Children with Cytochrome c Oxidase Deficiency. Pediatric Research. 59(1). 21–26. 87 indexed citations
15.
Stibůrek, Lukáš, Kateřina Veselá, Hana Hansı́ková, et al.. (2005). Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1. Biochemical Journal. 392(3). 625–632. 88 indexed citations
16.
Hajičová, Eva, et al.. (2004). Issues of Projectivity in the Prague Dependency Treebank.. ˜The œPrague Bulletin of Mathematical Linguistics. 81. 5–22. 20 indexed citations
17.
Veselá, Kateřina, et al.. (2004). Annotators' Agreement: The Case of Topic-Focus Articulation.. Language Resources and Evaluation. 2 indexed citations
18.
Veselá, Kateřina, Hana Hansíková, Markéta Tesařová, et al.. (2004). Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the SCO2 gene. Acta Paediatrica. 93(10). 1312–1317. 10 indexed citations
19.
Veselá, Kateřina, et al.. (2003). Topic-Focus Articulation in PDT: Prosodic Characteristics of Contrastive Topic.. ˜The œPrague Bulletin of Mathematical Linguistics. 5–22. 5 indexed citations
20.
Hajičová, Eva, Petr Pajas, & Kateřina Veselá. (2002). Corpus Annotation on the Tectogrammatical Layer: Summarizing of the First Stages of Evaluations.. ˜The œPrague Bulletin of Mathematical Linguistics. 77. 5–18. 2 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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