Vilma Kaplanová

760 total citations
13 papers, 340 citations indexed

About

Vilma Kaplanová is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Vilma Kaplanová has authored 13 papers receiving a total of 340 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 1 paper in Physiology. Recurrent topics in Vilma Kaplanová's work include Mitochondrial Function and Pathology (13 papers), ATP Synthase and ATPases Research (12 papers) and Metabolism and Genetic Disorders (6 papers). Vilma Kaplanová is often cited by papers focused on Mitochondrial Function and Pathology (13 papers), ATP Synthase and ATPases Research (12 papers) and Metabolism and Genetic Disorders (6 papers). Vilma Kaplanová collaborates with scholars based in Czechia, United States and Slovakia. Vilma Kaplanová's co-authors include J Houštěk, Hana Nůsková, Pavel Ješina, Vendula Havlíčková, Petr Pecina, J Zeman, Tomáš Mráček, Markéta Tesařová, Wolfgang Sperl and Alena Pecinová and has published in prestigious journals such as Biochemical Journal, The FASEB Journal and Human Molecular Genetics.

In The Last Decade

Vilma Kaplanová

13 papers receiving 339 citations

Peers

Countries citing papers authored by Vilma Kaplanová

Since Specialization

Citations

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

Fields of papers citing papers by Vilma Kaplanová

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vilma Kaplanová

This figure shows the co-authorship network connecting the top 25 collaborators of Vilma Kaplanová. A scholar is included among the top collaborators of Vilma Kaplanová 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 Vilma Kaplanová. Vilma Kaplanová is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Haplotype variability in mitochondrial rRNA predisposes to metabolic syndrome 2024 ·Communications Biology ·Petr Pecina, (unknown), Vilma Kaplanová, (unknown), Jan Šilhavý, (unknown), Marek Vrbacký, Tomáš Čajka, Ondřej Gahura, Markéta Hlaváčková, Viktor Stránecký, Stanislav Kmoch, Michal Pravenec, J Houštěk, Tomáš Mráček, Alena Pecinová	2
2	Genetic Complementation of ATP Synthase Deficiency Due to Dysfunction of TMEM70 Assembly Factor in Rat 2022 ·Biomedicines ·Aleksandra Pavlović Marković, (unknown), Miroslava Šimáková, Petr Mlejnek, Vilma Kaplanová, Petr Pecina, Alena Pecinová, F Papoušek, František Liška, Jan Šilhavý, Jana Mikešová, Jan Neckář, J Houštěk, Michal Pravenec, Tomáš Mráček	4
3	TMEM70 facilitates biogenesis of mammalian ATP synthase by promoting subunit c incorporation into the rotor structure of the enzyme 2019 ·The FASEB Journal ·(unknown), Marek Vrbacký, Petr Pecina, (unknown), Hana Nůsková, Vilma Kaplanová, Andrea Brázdová, Lukáš Alán, Jan Eliáš, (unknown), Vladimír Kořínek, Radislav Sedláček, Tomáš Mráček, J Houštěk	22
4	Role of the mitochondrial ATP synthase central stalk subunits γ and δ in the activity and assembly of the mammalian enzyme 2018 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Petr Pecina, Hana Nůsková, (unknown), Vilma Kaplanová, Tomáš Mráček, J Houštěk	17
5	Alteration of structure and function of ATP synthase and cytochromecoxidase by lack of Fo-a and Cox3 subunits caused by mitochondrial DNA 9205delTA mutation 2015 ·Biochemical Journal ·Kateřina Hejzlarová, Vilma Kaplanová, Hana Nůsková, (unknown), Pavel Ješina, Z Drahota, Tomáš Mráček, Sara Seneca, J Houštěk	15
6	Nuclear Genetic Defects of Mitochondrial ATP Synthase 2014 ·Physiological Research ·Kateřina Hejzlarová, Tomáš Mráček, Marek Vrbacký, Vilma Kaplanová, (unknown), Hana Nůsková, Petr Pecina, J Houštěk	36
7	Localization and orientation of TMEM70 protein in the inner mitochondrial membrane 2012 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Kateřina Hejzlarová, (unknown), Tomáš Mráček, Markéta Tesařová, (unknown), Marek Vrbacký, Hana Hartmannová, Vilma Kaplanová, Lenka Nosková, Jana Buzková, (unknown), J Zeman, Stanislav Kmoch, J Houštěk	1
8	Expression and processing of the TMEM70 protein 2010 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Kateřina Hejzlarová, Markéta Tesařová, (unknown), Marek Vrbacký, Hana Hartmannová, Vilma Kaplanová, Lenka Nosková, (unknown), Jana Buzková, Vendula Havlíčková, J Zeman, Stanislav Kmoch, J Houštěk	23
9	Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 subunit 2010 ·Human Molecular Genetics ·Johannes A. Mayr, Vendula Havlíčková, Franz Zimmermann, (unknown), Vilma Kaplanová, Pavel Ješina, Alena Pecinová, Hana Nůsková, Johannes Koch, Wolfgang Sperl, J Houštěk	95
10	Knockdown of F1 epsilon subunit decreases mitochondrial content of ATP synthase and leads to accumulation of subunit c 2009 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Vendula Havlíčková, Vilma Kaplanová, Hana Nůsková, Z Drahota, J Houštěk	39
11	Mitochondrial Membrane Potential and ATP Production in Primary Disorders of ATP Synthase 2004 ·Toxicology Mechanisms and Methods ·Alena Vojtı́šková, Pavel Ješina, Martin Kalous, Vilma Kaplanová, J Houštěk, Markéta Tesařová, Daniela Fornůsková, J Zeman, (unknown), Catherine Godinot	18
12	Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family 2004 ·Journal of the Neurological Sciences ·Vilma Kaplanová, J Zeman, Hana Hansı́ková, (unknown), H Houst'ková, (unknown), J Houštěk	15
13	Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206 2004 ·Biochemical Journal ·Pavel Ješina, Markéta Tesařová, Daniela Fornůsková, Alena Vojtı́šková, Petr Pecina, Vilma Kaplanová, Hana Hansı́ková, J Zeman, J Houštěk	53

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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