J Zeman

7.5k citations

253 papers · 4.8k · h-index 34

Impact in

Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
Physiology top 2%
- Lysosomal Storage Disorders Research

Papers in

Molecular Biology 152
- Mitochondrial Function and Pathology 101
- ATP Synthase and ATPases Research 57
- Biochemical and Molecular Research 15
Clinical Biochemistry 94
- Metabolism and Genetic Disorders 94

Co-authors: Hana Hansíková (86 shared papers)J Houštěk (42 shared papers)Tomáš Honzík (67 shared papers)Markéta Tesařová (67 shared papers)Lukáš Stibůrek (15 shared papers)Martin Magner (44 shared papers)László Wenchich (24 shared papers)H Houst'ková (18 shared papers)
Journals: Journal of Inherited Metabolic Disease (24 papers)Acta Paediatrica (9 papers)Molecular Genetics and Metabolism (8 papers)Biochimica et Biophysica Acta (BBA) - Bioenergetics (8 papers)Physiological Research (7 papers)
Partner nations: Czechia United States Netherlands

In The Last Decade

J Zeman

241 papers receiving 4.7k citations

Peers

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-authors

The 25 scholars most cited alongside J Zeman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with J Zeman Line = papers co-authored together J Zeman links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 253 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy European Journal of Pediatrics ·J. E. Wraith, Maurizio Scarpa, Michael Beck, Olaf A. Bodamer, Linda De Meırleır, Nathalie Guffon, Allan M. Lund, Gunilla Malm, Ans T. van der Ploeg, J Zeman	2007	365
2	New insights in cardiac structural changes in patients with Fabry’s disease American Heart Journal ·Aleš Linhart, Tomáš Paleček, Jan Bultas, James J. Ferguson, J Hrudová, Debora Karetová, J Zeman, J. Ledvinová, Helena Poupětová, M. Elleder, Michael Aschermann	2000	189
3	YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation Molecular Biology of the Cell ·Lukáš Stibůrek, Jana Cesnekova, Olga Kostková, Daniela Fornůsková, Kamila Vinšová, László Wenchich, J Houštěk, J Zeman	2012	140
4	Inborn Metabolic Diseases: Diagnosis and Treatment Acta Paediatrica ·J Zeman	2012	119
5	Clinical presentation and metabolic consequences in 40 breastfed infants with nutritional vitamin B12 deficiency – What have we learned? European Journal of Paediatric Neurology ·Tomáš Honzík, Miriam Adamovičová, Vratislav Smolka, Martin Magner, Eva Hrubá, J Zeman	2010	116
6	Mutation of Nogo-B Receptor, a Subunit of cis-Prenyltransferase, Causes a Congenital Disorder of Glycosylation Cell Metabolism ·Eon Joo Park, Kariona A. Grabińska, Ziqiang Guan, Viktor Stránecký, Hana Hartmannová, Kateřina Hodaňová, Veronika Barešová, Jana Sovová, Levente József, Nina Ondrušková, Hana Hansíková, Tomáš Honzík, J Zeman, Helena Hůlková, Rong Wen, Stanislav Kmoch, William C. Sessa	2014	99
7	Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1 Biochemical Journal ·Lukáš Stibůrek, Kateřina Veselá, Hana Hansı́ková, Petr Pecina, Markéta Tesařová, Leona Černá, J Houštěk, J Zeman	2005	88
8	Retrospective, Multicentric Study of 180 Children with Cytochrome c Oxidase Deficiency Pediatric Research ·Marek Böhm, Ewa Pronicka, Elżbieta Karczmarewicz, Maciej Pronicki, Dorota Piekutowska‐Abramczuk, Jolanta Sykut‐Cegielska, Hanna Mierzewska, Hana Hansı́ková, Kateřina Veselá, Markéta Tesařová, H Houst'ková, J Houštěk, J Zeman	2005	87
9	Altered properties of mitochondrial ATP-synthase in patients with a T → G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNA Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·J Houštěk, Petr Klement, Jana Heřmanská, H Houst'ková, Hana Hansı́ková, Coby Van den Bogert, J Zeman	1995	85
10	Genetic defects of cytochrome c oxidase assembly Physiological Research ·Petr Pecina, H Houst'ková, J Zeman, J Houštěk	2004	84
11	Loss of function of Sco1 and its interaction with cytochrome c oxidase American Journal of Physiology-Cell Physiology ·Lukáš Stibůrek, Kateřina Veselá, Hana Hansı́ková, Helena Hůlková, J Zeman	2009	83
12	Novel insights into the assembly and function of human nuclear-encoded cytochromecoxidase subunits 4, 5a, 6a, 7a and 7b Biochemical Journal ·Daniela Fornůsková, Lukáš Stibůrek, László Wenchich, Kamila Vinšová, Hana Hansíková, J Zeman	2010	83
13	Knockdown of Human Oxa1l Impairs the Biogenesis of F1Fo-ATP Synthase and NADH:Ubiquinone Oxidoreductase Journal of Molecular Biology ·Lukáš Stibůrek, Daniela Fornůsková, László Wenchich, Martina Pejznochová, Hana Hansíková, J Zeman	2007	73
14	Acid sphingomyelinase deficiency. Phenotype variability with prevalence of intermediate phenotype in a series of twenty‐five Czech and Slovak patients. A multi‐approach study Journal of Inherited Metabolic Disease ·Hana Pavlú-Pereira, Befekadu Asfaw, H. Poupčtová, J. Ledvinová, Jakub Sikora, M. T. Vanier, Konrad Sandhoff, J Zeman, Zorka Novotna, D Chudoba, M. Elleder	2005	70
15	Neonatal onset of mitochondrial disorders in 129 patients: clinical and laboratory characteristics and a new approach to diagnosis Journal of Inherited Metabolic Disease ·Tomáš Honzík, Markéta Tesařová, Martin Magner, Johannes A. Mayr, Pavel Ješina, Kateřina Veselá, László Wenchich, K Szentiványi, Hana Hansíková, Wolfgang Sperl, J Zeman	2012	63
16	Deficiency of mitochondrial ATP synthase of nuclear genetic origin Neuromuscular Disorders ·Wolfgang Sperl, Pavel Ješina, J Zeman, Johannes A. Mayr, L. DeMeirleir, R. Vancoster, Andrea Pı́cková, Hana Hansíková, H Houst'ková, Zdeněk Krejčík, Johannes Koch, Joél Smet, Wolfgang Muss, E. Holme, J Houštěk	2006	56
17	Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation Archives of Disease in Childhood ·Tomáš Honzík, Markéta Tesařová, Johannes A. Mayr, Hana Hansíková, Pavel Ješina, Olaf A. Bodamer, Johannes Koch, Martin Magner, Peter Freisinger, Martina Huemer, Olga Kostková, Rudy Van Coster, Stanislav Kmoch, J Houštěk, Wolfgang Sperl, J Zeman	2010	54
18	Bone mineral density in patients with phenylketonuria Acta Paediatrica ·J Zeman, M Bayer, J Štěpán	1999	54
19	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 Biochemical Journal ·Pavel Ješina, Markéta Tesařová, Daniela Fornůsková, Alena Vojtı́šková, Petr Pecina, Vilma Kaplanová, Hana Hansı́ková, J Zeman, J Houštěk	2004	53
20	Mitochondrial DNA content and expression of genes involved in mtDNA transcription, regulation and maintenance during human fetal development Mitochondrion ·Martina Pejznochová, Markéta Tesařová, Hana Hansíková, Martin Magner, Tomáš Honzík, Kamila Vinšová, Zuzana Hájková, Vendula Havlíčková, J Zeman	2010	51

About J Zeman

J Zeman is a scholar working on Molecular Biology, Clinical Biochemistry, Physiology, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 253 papers that have together received 4.8k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (101 papers), Metabolism and Genetic Disorders (94 papers), ATP Synthase and ATPases Research (57 papers), Lysosomal Storage Disorders Research (30 papers), Biochemical and Molecular Research (15 papers), Neonatal Health and Biochemistry (15 papers), Folate and B Vitamins Research (14 papers) and Carbohydrate Chemistry and Synthesis (11 papers). The work is most often cited by research in Clinical Biochemistry (1.4k citations), Physiology (1.3k citations), Rheumatology (666 citations), Molecular Biology (2.9k citations) and Biochemistry (219 citations). J Zeman has collaborated with scholars based in Czechia, United States and Netherlands. Frequent co-authors include Hana Hansíková, J Houštěk, Tomáš Honzík, Markéta Tesařová, Lukáš Stibůrek, Martin Magner, László Wenchich, H Houst'ková, Hana Hansı́ková and Kateřina Veselá. Their work appears in journals such as Journal of Inherited Metabolic Disease, Acta Paediatrica, Molecular Genetics and Metabolism, Biochimica et Biophysica Acta (BBA) - Bioenergetics and Physiological Research.

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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