Martin Magner

1.6k total citations
64 papers, 892 citations indexed

About

Martin Magner is a scholar working on Molecular Biology, Physiology and Clinical Biochemistry. According to data from OpenAlex, Martin Magner has authored 64 papers receiving a total of 892 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 23 papers in Physiology and 18 papers in Clinical Biochemistry. Recurrent topics in Martin Magner's work include Lysosomal Storage Disorders Research (20 papers), Metabolism and Genetic Disorders (18 papers) and Mitochondrial Function and Pathology (15 papers). Martin Magner is often cited by papers focused on Lysosomal Storage Disorders Research (20 papers), Metabolism and Genetic Disorders (18 papers) and Mitochondrial Function and Pathology (15 papers). Martin Magner collaborates with scholars based in Czechia, Germany and Slovakia. Martin Magner's co-authors include J Zeman, Tomáš Honzík, Markéta Tesařová, Hana Hansíková, Eva Hrubá, Vratislav Smolka, Miriam Adamovičová, Pavel Ješina, Kateřina Veselá and Johannes A. Mayr and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Martin Magner

61 papers receiving 875 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin Magner Czechia 17 493 287 188 180 103 64 892
Paula Garcia Portugal 16 344 0.7× 272 0.9× 106 0.6× 162 0.9× 195 1.9× 49 774
Parayil Sankaran Bindu India 19 386 0.8× 177 0.6× 108 0.6× 170 0.9× 80 0.8× 92 1.1k
Mohammed Almannai Saudi Arabia 17 597 1.2× 381 1.3× 60 0.3× 125 0.7× 137 1.3× 43 935
François Feillet France 15 248 0.5× 251 0.9× 97 0.5× 212 1.2× 152 1.5× 45 685
Hélène Ogier France 13 443 0.9× 415 1.4× 113 0.6× 292 1.6× 86 0.8× 16 877
Cheryl Garganta United States 15 249 0.5× 212 0.7× 114 0.6× 158 0.9× 90 0.9× 28 745
Chike Bellarmine Item Austria 17 348 0.7× 360 1.3× 132 0.7× 179 1.0× 108 1.0× 38 879
Luísa Diogo Portugal 20 790 1.6× 622 2.2× 183 1.0× 185 1.0× 304 3.0× 71 1.4k
Ann Bowron United Kingdom 13 424 0.9× 303 1.1× 255 1.4× 100 0.6× 79 0.8× 29 997
V. Barash Israel 22 483 1.0× 229 0.8× 236 1.3× 239 1.3× 172 1.7× 49 1.1k

Countries citing papers authored by Martin Magner

Since Specialization
Citations

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

Fields of papers citing papers by Martin Magner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Magner

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Magner. A scholar is included among the top collaborators of Martin Magner 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 Martin Magner. Martin Magner 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.
Klocperk, Adam, Markéta Bloomfield, Zuzana Paračková, et al.. (2023). B cell phenotype and serum levels of interferons, BAFF, and APRIL in multisystem inflammatory syndrome in children associated with COVID-19 (MIS-C). SHILAP Revista de lepidopterología. 10(1). 15–15. 3 indexed citations
2.
Malinová, Vĕra, et al.. (2023). Long-Term Evaluation of Biomarkers in the Czech Cohort of Gaucher Patients. International Journal of Molecular Sciences. 24(19). 14440–14440. 3 indexed citations
3.
Stawarski, Michał, Lenka Nosková, Martin Magner, et al.. (2022). GABBR1 monoallelic de novo variants linked to neurodevelopmental delay and epilepsy. The American Journal of Human Genetics. 109(10). 1885–1893. 14 indexed citations
4.
Mitchell, John J., Barbara K. Burton, Michael B. Bober, et al.. (2022). Findings from the Morquio A Registry Study (MARS) after 6 years: Long-term outcomes of MPS IVA patients treated with elosulfase alfa. Molecular Genetics and Metabolism. 137(1-2). 164–172. 4 indexed citations
5.
Nestrašil, Igor, Susanne A. Schneider, Helena Jahnová, et al.. (2021). Pontocerebellar atrophy is the hallmark neuroradiological finding in late-onset Tay-Sachs disease. Neurological Sciences. 43(5). 3273–3281. 3 indexed citations
6.
Saldarriaga, Wilmar, et al.. (2021). Hearing Loss in Patients With Morquio Syndrome: Protocol for a Scoping Review. JMIR Research Protocols. 11(6). e32986–e32986. 2 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.
Bloomfield, Markéta, et al.. (2020). Searching for COVID-19 Antibodies in Czech Children—A Needle in the Haystack. Frontiers in Pediatrics. 8. 597736–597736. 6 indexed citations
9.
Nestrašil, Igor, David Nascene, Troy C. Lund, et al.. (2020). White matter alteration and cerebellar atrophy are hallmarks of brain MRI in alpha-mannosidosis. Molecular Genetics and Metabolism. 132(3). 189–197. 7 indexed citations
10.
Frühauf, Pavel, et al.. (2019). Associations between breastfeeding rates and infant disease: A survey of 2338 Czech children. Nutrition & Dietetics. 77(3). 310–314. 2 indexed citations
11.
Magner, Martin, et al.. (2018). The Age Dependent Progression of Hajdu-Cheney Syndrome in Two Families. Prague Medical Report. 119(4). 156–164. 6 indexed citations
12.
Dobrovolný, Robert, Martin Hřebı́ček, J. Ledvinová, et al.. (2016). X-Chromosome Inactivation Analysis in Different Cell Types and Induced Pluripotent Stem Cells Elucidates the Disease Mechanism in a Rare Case of Mucopolysaccharidosis Type II in a Female. Folia Biologica. 62(2). 82–89. 21 indexed citations
13.
Magner, Martin, Viktor Stránecký, Anna Přistoupilová, et al.. (2016). Thymidine kinase 2 and alanyl-tRNA synthetase 2 deficiencies cause lethal mitochondrial cardiomyopathy: case reports and review of the literature. Cardiology in the Young. 27(5). 936–944. 27 indexed citations
14.
Tesařová, Markéta, Martin Magner, H Houst'ková, et al.. (2013). Novel Mutations in the TAZ Gene in Patients with Barth Syndrome. Prague Medical Report. 114(3). 139–153. 15 indexed citations
15.
Ondrušková, Nina, Kateřina Veselá, Hana Hansíková, et al.. (2012). RFT1-CDG in adult siblings with novel mutations. Molecular Genetics and Metabolism. 107(4). 760–762. 13 indexed citations
16.
Tesařová, Markéta, Hana Hansíková, Martin Magner, et al.. (2010). Developmental changes of mitochondrial DNA content and expression of genes involved in mtDNA transcription and maintenance in human fetal liver and muscle tissues. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1797. 108–109. 2 indexed citations
17.
Beesley, Clare, Linda Berná, Hana Vlášková, et al.. (2009). Mucopolysaccharidosis type I in 21 Czech and Slovak patients: Mutation analysis suggests a functional importance of C‐terminus of the IDUA protein. American Journal of Medical Genetics Part A. 149A(5). 965–974. 29 indexed citations
18.
Tesařová, Markéta, et al.. (2008). Mitochondrial DNA Haplogroups in the Czech Population Compared to Other European Countries. Human Biology. 80(6). 669–674. 6 indexed citations
19.
Tesařová, Markéta, et al.. (2008). The developmental changes in mitochondrial DNA content per cell in human cord blood leukocytes during gestation. Physiological Research. 57(6). 947–955. 29 indexed citations
20.
Tio, R. A., et al.. (1998). Intramyocardial injection with naked DNA encoding for VEGF causes local and systemic production of VEGF, and improves collateral flow to ischemic myocardial tissue.. Data Archiving and Networked Services (DANS). 3 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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