Markéta Tesařová

2.6k citations

86 papers · 1.3k indexed · h-index 22

Co-authors: J Zeman Hana Hansíková Tomáš Honzík J Houštěk Martin Magner Kateřina Veselá Hana Hansı́ková Lukáš Stibůrek
Topics: Mitochondrial Function and Pathology (53 papers)Metabolism and Genetic Disorders (40 papers)ATP Synthase and ATPases Research (34 papers)
Cited by: Clinical Biochemistry Molecular Biology Biochemistry
Journals: SHILAP Revista de lepidopterologíaAnalytical Biochemistry Biochemical Journal
Partner nations: Czechia Slovakia United Kingdom

In The Last Decade

Markéta Tesařová

83 papers receiving 1.3k citations

Peers

Countries citing papers authored by Markéta Tesařová

Since Specialization

Citations

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

Fields of papers citing papers by Markéta Tesařová

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Markéta Tesařová

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

#	Work	Indexed citations
1	ATAD3A-related pontocerebellar hypoplasia: new patients and insights into phenotypic variability 2023 ·Orphanet Journal of Rare Diseases ·Martina Škopková,(unknown),(unknown),Viktor Stránecký,(unknown),Miriam Kolníková,(unknown),Miloslav Karhánek,Lenka Nosková,Markéta Tesařová,Hana Hansíková,Daniela Gašperíková	6
2	A Novel MTTK Gene Variant m.8315A>C as a Cause of MERRF Syndrome 2022 ·Genes ·(unknown),(unknown),(unknown),Tomáš Honzík,J Zeman,Hana Hansíková,Markéta Tesařová	3
3	Microarray and qPCR Analysis of Mitochondrial Metabolism Activation during Prenatal and Early Postnatal Development in Rats and Humans with Emphasis on CoQ10 Biosynthesis 2021 ·Biology ·Jana Křížová,(unknown),Václav Čapek,Petr Mlejnek,Jan Šilhavý,Markéta Tesařová,J Zeman,Hana Hansíková	3
4	Homozygous missense mutation in UQCRC2 associated with severe encephalomyopathy, mitochondrial complex III assembly defect and activation of mitochondrial protein quality control 2021 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·(unknown),Lukáš Stibůrek,Jana Křížová,(unknown),Václav Martínek,(unknown),Josef Zámečnı́k,Tomáš Honzík,J Zeman,Hana Hansíková,Markéta Tesařová	16
5	Severe phenotype of ATP6AP1‐CDG in two siblings with a novel mutation leading to a differential tissue‐specific ATP6AP1 protein pattern, cellular oxidative stress and hepatic copper accumulation 2020 ·Journal of Inherited Metabolic Disease ·Nina Ondrušková,Tomáš Honzík,(unknown),Viktor Stránecký,Markéta Tesařová,J Zeman,Hana Hansíková	13
6	The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions 2020 ·Brain Sciences ·(unknown),(unknown),(unknown),(unknown),(unknown),Petra Lišková,Martin Magner,Josef Zámečnı́k,Hana Hansíková,J Zeman,Markéta Tesařová,Tomáš Honzík	13
7	Review of SRD5A3 Disease-Causing Sequence Variants and Ocular Findings in Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation, and a Detailed New Case 2019 ·Folia Biologica ·Bohdan Kousal,Tomáš Honzík,Hana Hansíková,Nina Ondrušková,(unknown),Markéta Tesařová,Viktor Stránecký,(unknown),Michel Michaelides,Petra Lišková	10
8	Attenuated Type of Asphyxiating Thoracic Dysplasia due to Mutations in DYNC2H1 Gene 2019 ·SHILAP Revista de lepidopterología ·Anna Čechová,A Baxová,J Zeman,Lukáš Lambert,Tomáš Honzík,(unknown),(unknown),Markéta Tesařová	1
9	Hereditary Multiple Exostoses: Clinical, Molecular and Radiologic Survey in 9 Families 2017 ·Prague Medical Report ·(unknown),J Zeman,Tomáš Honzík,Hana Hansíková,(unknown),(unknown),(unknown),(unknown),J Chomiak,Markéta Tesařová	3
10	Thymidine kinase 2 and alanyl-tRNA synthetase 2 deficiencies cause lethal mitochondrial cardiomyopathy: case reports and review of the literature 2016 ·Cardiology in the Young ·(unknown),Martin Magner,(unknown),(unknown),Viktor Stránecký,Anna Přistoupilová,Josef Zámečnı́k,Hana Hansíková,J Zeman,Markéta Tesařová,Tomáš Honzík	27
11	Lipoprotein Lipase Deficiency: Clinical, Biochemical and Molecular Characteristics in Three Patients with Novel Mutations in the LPL Gene 2014 ·Folia Biologica ·(unknown),Markéta Tesařová,(unknown),Viktor Stránecký,Anna Přistoupilová,Tomáš Zima,Jana Uhrová,(unknown),J Zeman,Tomáš Honzík	9
12	Non-Invasive Screening of Cytochrome c Oxidase Deficiency in Children Using a Dipstick Immunocapture Assay 2014 ·Folia Biologica ·(unknown),(unknown),Tomáš Honzík,Markéta Tesařová,J Zeman,Hana Hansíková	4
13	Novel Mutations in the TAZ Gene in Patients with Barth Syndrome 2013 ·Prague Medical Report ·(unknown),Markéta Tesařová,Martin Magner,H Houst'ková,Hana Hansı́ková,(unknown),Viktor Tomek,(unknown),J Zeman,Tomáš Honzík	15
14	Novel Mutations in the Tyrosine Hydroxylase Gene in the First Czech Patient with Tyrosine Hydroxylase Deficiency 2012 ·Prague Medical Report ·(unknown),Hana Hansíková,Jakub Krijt,(unknown),Markéta Tesařová,(unknown),Petr Klement,J Zeman,Tomáš Honzík	3
15	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
16	Fumarate hydratase gene mutation in two young patients with sporadic uterine fibroids 2012 ·Journal of obstetrics and gynaecology research ·(unknown),Markéta Tesařová,Hana Hansíková,Kamila Veselá,D Kužel,Michal Mára	3
17	CYTOCHROME C OXIDASE DEFICIENCY IN CHILDHOOD 2008 ·Archives of Disease in Childhood ·J Zeman,Hana Hansíková,Markéta Tesařová,Kateřina Veselá,(unknown),Richard Plavka,Ewa Pronicka	2
18	Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the SCO2 gene 2004 ·Acta Paediatrica ·Kateřina Veselá,Hana Hansíková,Markéta Tesařová,Pavel Martásek,M. Elleder,J Houštěk,J Zeman	10
19	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
20	Polarographic evaluation of mitochondrial enzymes activity in isolated mitochondria and in permeabilized human muscle cells with inherited mitochondrial defects. 2003 ·Physiological Research ·László Wenchich,Z Drahota,Tomáš Honzík,Hana Hansíková,Markéta Tesařová,J Zeman,J Houštěk	22

About Markéta Tesařová

Markéta Tesařová is a scholar working on Clinical Biochemistry, Molecular Biology and Biochemistry, having authored 86 papers that have together received 1.3k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (53 papers), Metabolism and Genetic Disorders (40 papers) and ATP Synthase and ATPases Research (34 papers). The work is most often cited by research in Clinical Biochemistry (483 citations), Molecular Biology (1.0k citations) and Biochemistry (35 citations). Markéta Tesařová has collaborated with scholars based in Czechia, Slovakia and United Kingdom. Frequent co-authors include J Zeman, Hana Hansíková, Tomáš Honzík, J Houštěk, Martin Magner, Kateřina Veselá, Hana Hansı́ková, Lukáš Stibůrek, Pavel Ješina and Petr Pecina. Their work appears in journals such as SHILAP Revista de lepidopterología, Analytical Biochemistry and Biochemical Journal.

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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