J Zeman

7.5k total citations
253 papers, 4.8k citations indexed

About

J Zeman is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, J Zeman has authored 253 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 152 papers in Molecular Biology, 94 papers in Clinical Biochemistry and 44 papers in Physiology. Recurrent topics in J Zeman's work include Mitochondrial Function and Pathology (101 papers), Metabolism and Genetic Disorders (94 papers) and ATP Synthase and ATPases Research (57 papers). J Zeman is often cited by papers focused on Mitochondrial Function and Pathology (101 papers), Metabolism and Genetic Disorders (94 papers) and ATP Synthase and ATPases Research (57 papers). J Zeman collaborates with scholars based in Czechia, United States and Netherlands. J Zeman's co-authors include Hana Hansíková, J Houštěk, Tomáš Honzík, Markéta Tesařová, Lukáš Stibůrek, Martin Magner, László Wenchich, H Houst'ková, Hana Hansı́ková and M. Elleder and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Journal of Molecular Biology.

In The Last Decade

J Zeman

241 papers receiving 4.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J Zeman Czechia 34 2.9k 1.4k 1.3k 666 579 253 4.8k
Fernando Scaglia United States 50 4.8k 1.7× 3.0k 2.1× 1.0k 0.8× 495 0.7× 399 0.7× 168 7.1k
Gregory M. Enns United States 36 2.5k 0.9× 2.0k 1.4× 687 0.5× 433 0.7× 203 0.4× 133 4.4k
Scott W. Ballinger United States 43 5.1k 1.8× 1.7k 1.2× 1.4k 1.1× 160 0.2× 693 1.2× 97 8.2k
Lambert P. van den Heuvel Netherlands 40 3.3k 1.2× 1.3k 0.9× 361 0.3× 1.2k 1.8× 224 0.4× 78 5.3k
Charles P. Venditti United States 37 2.2k 0.8× 1.6k 1.2× 554 0.4× 891 1.3× 240 0.4× 102 4.1k
Paul M. Fernhoff United States 32 1.9k 0.7× 658 0.5× 377 0.3× 504 0.8× 487 0.8× 66 4.0k
Shamima Rahman United Kingdom 44 4.7k 1.6× 2.8k 2.0× 561 0.4× 319 0.5× 158 0.3× 160 6.3k
C. R. Scriver Canada 39 1.8k 0.6× 1.5k 1.1× 740 0.6× 516 0.8× 123 0.2× 128 4.3k
V. Reid Sutton United States 41 2.5k 0.9× 916 0.7× 730 0.6× 313 0.5× 414 0.7× 146 4.7k
Balakuntalam S. Kasinath United States 40 2.4k 0.8× 337 0.2× 628 0.5× 232 0.3× 343 0.6× 125 4.8k

Countries citing papers authored by J Zeman

Since Specialization
Citations

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

Fields of papers citing papers by J Zeman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J Zeman

This figure shows the co-authorship network connecting the top 25 collaborators of J Zeman. A scholar is included among the top collaborators of J Zeman 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 J Zeman. J Zeman 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.
Zikánová, Marie, Kyra E. Stuurman, Veronika Barešová, et al.. (2025). Phosphoribosylformylglycinamidine Synthase ( PFAS ) Deficiency: Clinical, Genetic and Metabolic Characterisation of a Novel Defect in Purine de Novo Synthesis. Journal of Inherited Metabolic Disease. 48(3). e70041–e70041. 1 indexed citations
2.
Fajkusová, Lenka, Kamila Réblová, J Zeman, et al.. (2024). Large TRAPPC11 gene deletions as a cause of muscular dystrophy and their estimated genesis. Journal of Medical Genetics. 61(9). 908–913. 1 indexed citations
3.
Honzík, Tomáš, et al.. (2022). A Novel MTTK Gene Variant m.8315A>C as a Cause of MERRF Syndrome. Genes. 13(7). 1245–1245. 3 indexed citations
4.
Křížová, Jana, et al.. (2022). Mitochondrial organization and structure are compromised in fibroblasts from patients with Huntington’s disease. Ultrastructural Pathology. 46(5). 462–475. 7 indexed citations
5.
Křížová, Jana, Václav Čapek, Petr Mlejnek, et al.. (2021). Microarray and qPCR Analysis of Mitochondrial Metabolism Activation during Prenatal and Early Postnatal Development in Rats and Humans with Emphasis on CoQ10 Biosynthesis. Biology. 10(5). 418–418. 3 indexed citations
6.
Ondrušková, Nina, Tomáš Honzík, Viktor Stránecký, et al.. (2020). 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. Journal of Inherited Metabolic Disease. 43(4). 694–700. 13 indexed citations
7.
Lišková, Petra, Martin Magner, Josef Zámečnı́k, et al.. (2020). The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions. Brain Sciences. 10(11). 766–766. 13 indexed citations
8.
9.
Ježková, Jana, László Wenchich, Hana Hansíková, et al.. (2019). <p>The relationship of mitochondrial dysfunction and the development of insulin resistance in Cushing’s syndrome</p>. Diabetes Metabolic Syndrome and Obesity. Volume 12. 1459–1471. 5 indexed citations
10.
Koene, Saskia, Enrico Bertini, Cecilia Jimenez‐Moreno, et al.. (2018). Outcome measures for children with mitochondrial disease: consensus recommendations for future studies from a Delphi‐based international workshop. Journal of Inherited Metabolic Disease. 41(6). 1267–1273. 21 indexed citations
11.
Hansíková, Hana, et al.. (2017). Molecular Diagnostics of Copper-Transporting Protein Mutations Allows Early Onset Individual Therapy of Menkes Disease. Folia Biologica. 63(5-6). 165–173. 4 indexed citations
12.
Zeman, J, et al.. (2015). Late Neolithic circular enclosures: never entirely uncovered. SHILAP Revista de lepidopterología. 1 indexed citations
13.
Zeman, J, et al.. (2015). On the trail of Caesar and Vercingetorix: survey in the Bibracte oppidum, Mont Beuvray (France). SHILAP Revista de lepidopterología. 1 indexed citations
14.
Zeman, J, et al.. (2015). Průzkum mladoneolitického rondelu v Nových Bránicích, okr. Brno-venkov. 20(2). 1 indexed citations
15.
Tesařová, Markéta, Viktor Stránecký, Anna Přistoupilová, et al.. (2014). Lipoprotein Lipase Deficiency: Clinical, Biochemical and Molecular Characteristics in Three Patients with Novel Mutations in the LPL Gene. Folia Biologica. 60(5). 235–243. 9 indexed citations
16.
Helman, Karel, et al.. (2013). Sustainable Development Indicators at the Regional Level in the Czech Republic. SHILAP Revista de lepidopterología. 4 indexed citations
17.
Zeman, J. (2013). Recenze: James Wilson: Moravians in Prague: A Sociolinguistic Study of Dialect Contact in the Czech Republic. Digitalni Knihovna - Knihovna Akademie věd ČR. 74(4). 307–310. 4 indexed citations
18.
Zeman, J, Hana Hansíková, Markéta Tesařová, et al.. (2008). CYTOCHROME C OXIDASE DEFICIENCY IN CHILDHOOD. Archives of Disease in Childhood. 93. 2 indexed citations
19.
Sperl, Wolfgang, Pavel Ješina, J Zeman, et al.. (2005). Isolated defects of mitochondrial ATP synthase: overview of 15 cases.. Journal of Inherited Metabolic Disease. 134–134. 1 indexed citations
20.
Zeman, J, H Houst'ková, Hana Hansíková, et al.. (1999). [Various manifestations of the A8344G mtDNA heteroplasmic mutation in 4 families with the MERRF syndrome].. PubMed. 138(13). 401–5. 8 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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