Martin Genčík

1.6k total citations
48 papers, 1.0k citations indexed

About

Martin Genčík is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Martin Genčík has authored 48 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Martin Genčík's work include Genetic Neurodegenerative Diseases (8 papers), Mitochondrial Function and Pathology (6 papers) and Sleep and Wakefulness Research (6 papers). Martin Genčík is often cited by papers focused on Genetic Neurodegenerative Diseases (8 papers), Mitochondrial Function and Pathology (6 papers) and Sleep and Wakefulness Research (6 papers). Martin Genčík collaborates with scholars based in Germany, Austria and Slovakia. Martin Genčík's co-authors include Jörg T. Epplen, Claudia Gundacker, Stefan Wieczorek, Norbert Dahmen, Markus Hengstschläger, Harald Fricke, Stefan Borgmann, Peter Jagiello, Stephan Meller and Karl J. Wittmann and has published in prestigious journals such as The Science of The Total Environment, Neurology and Kidney International.

In The Last Decade

Martin Genčík

47 papers receiving 986 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 Genčík Germany 16 243 242 238 144 135 48 1.0k
Bin Zhu China 16 231 1.0× 447 1.8× 134 0.6× 139 1.0× 10 0.1× 58 1.4k
Shoko Murakami Japan 14 54 0.2× 186 0.8× 99 0.4× 42 0.3× 24 0.2× 40 643
Marco Faustini‐Fustini Italy 23 65 0.3× 450 1.9× 100 0.4× 39 0.3× 15 0.1× 45 2.2k
Keisuke Kobayashi Japan 16 33 0.1× 205 0.8× 151 0.6× 33 0.2× 48 0.4× 54 1.1k
Graziella Pinto France 26 22 0.1× 1.0k 4.1× 126 0.5× 130 0.9× 42 0.3× 65 2.1k
Svetlana Ghimbovschi United States 18 77 0.3× 431 1.8× 37 0.2× 71 0.5× 12 0.1× 34 828
İsmail Üstünel Türkiye 19 28 0.1× 256 1.1× 31 0.1× 134 0.9× 19 0.1× 74 920
Maki Sakuma Japan 16 19 0.1× 227 0.9× 36 0.2× 26 0.2× 46 0.3× 41 935
Joseph M. Valdez United States 14 37 0.2× 431 1.8× 131 0.6× 78 0.5× 17 0.1× 20 949
Mafalda Cacciottolo United States 17 447 1.8× 480 2.0× 45 0.2× 119 0.8× 11 0.1× 29 1.4k

Countries citing papers authored by Martin Genčík

Since Specialization
Citations

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

Fields of papers citing papers by Martin Genčík

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Genčík

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Genčík. A scholar is included among the top collaborators of Martin Genčík 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 Genčík. Martin Genčík 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.
Gundacker, Claudia, Martin Genčík, Markus Hengstschläger, et al.. (2021). Gene Variants Determine Placental Transfer of Perfluoroalkyl Substances (PFAS), Mercury (Hg) and Lead (Pb), and Birth Outcome: Findings From the UmMuKi Bratislava-Vienna Study. Frontiers in Genetics. 12. 664946–664946. 17 indexed citations
2.
Mansour, Hicham, Sandra Sabbagh, Stephany El‐Hayek, et al.. (2019). The Lebanese Allele in the PET100 Gene: Report on Two New Families with Cytochrome c Oxidase Deficiency. Journal of Pediatric Genetics. 8(3). 172–178. 5 indexed citations
3.
Milenković, Ivan, et al.. (2018). A novel nonsense autosomal dominant mutation in the GLRA1 gene causing hyperekplexia. Journal of Neural Transmission. 125(12). 1877–1883. 3 indexed citations
4.
Finsterer, Josef, Claudia Stöllberger, Hans Keller, & Martin Genčík. (2016). Familial accumulation of sudden cardiac deaths and the LMNA variant c.868G > A (p.Glu290Lys). International Journal of Cardiology. 215. 84–86. 1 indexed citations
5.
Knopp, Cordula, Sabine Rudnik‐Schöneborn, Klaus Zerres, et al.. (2014). Twenty‐one years to the right diagnosis – clinical overlap of Simpson–Golabi–Behmel and Beckwith–Wiedemann syndrome. American Journal of Medical Genetics Part A. 167(1). 151–155. 13 indexed citations
6.
Minić, Snežana, et al.. (2012). Dental and oral anomalies in incontinentia pigmenti: a systematic review. Clinical Oral Investigations. 17(1). 1–8. 43 indexed citations
7.
Kiefer, Alexander, et al.. (2011). Rapidly Progressive Phenotype of Lafora Disease Associated With a Novel NHLRC1 Mutation. Pediatric Neurology. 44(6). 475–477. 12 indexed citations
8.
9.
Gundacker, Claudia, Martin Genčík, & Markus Hengstschläger. (2010). The relevance of the individual genetic background for the toxicokinetics of two significant neurodevelopmental toxicants: Mercury and lead. Mutation Research/Reviews in Mutation Research. 705(2). 130–140. 109 indexed citations
10.
Gundacker, Claudia, et al.. (2007). Glutathione-S-transferase polymorphism, metallothionein expression, and mercury levels among students in Austria. The Science of The Total Environment. 385(1-3). 37–47. 78 indexed citations
11.
Brune, N., J. Andrich, Martin Genčík, et al.. (2004). Methyltetrahydrofolate reductase polymorphism influences onset of Huntington’s disease. Journal of neural transmission. Supplementum. 105–110. 8 indexed citations
12.
Wieczorek, Stefan, Norbert Dahmen, Meike Kasten, Jörg T. Epplen, & Martin Genčík. (2004). A rare form of narcolepsy (HLA-DR2???) shows possible association with (functionally relevant) alpha-interferon gene polymorphisms. Psychiatric Genetics. 14(1). 47–51. 9 indexed citations
13.
Wieczorek, Stefan, Norbert Dahmen, Peter Jagiello, Jörg T. Epplen, & Martin Genčík. (2003). Polymorphisms of the tumor necrosis factor receptors: no association with narcolepsy in German patients. Journal of Molecular Medicine. 81(2). 87–90. 11 indexed citations
14.
Jagiello, Peter, Stefan Wieczorek, Larissa Arning, et al.. (2003). A novel splice site mutation in theTRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity. Human Mutation. 21(6). 630–635. 21 indexed citations
15.
Meller, Stephan, Peter Jagiello, Stefan Borgmann, et al.. (2001). Novel SNPs in the CD18 gene validate the association with MPO-ANCA + vasculitis. Genes and Immunity. 2(5). 269–272. 26 indexed citations
16.
Genčík, Martin, et al.. (2000). Novel mutation in theRYR1gene (R2454C) in a patient with malignant hyperthermia. Human Mutation. 15(1). 122–122. 4 indexed citations
17.
Genčík, Martin, Stephan Meller, Stefan Borgmann, & Harald Fricke. (2000). Proteinase 3 gene polymorphisms and Wegener's granulomatosis. Kidney International. 58(6). 2473–2477. 71 indexed citations
18.
Genčík, Martin, Stephan Meller, Stefan Borgmann, et al.. (2000). The Association of CD18 Alleles with Anti-myeloperoxidase Subtypes of ANCA-Associated Systemic Vasculitides. Clinical Immunology. 94(1). 9–12. 37 indexed citations
19.
Genčík, Martin, Stefan Borgmann, R. Zahn, et al.. (1999). Immunogenetic risk factors for anti-neutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitis. Clinical & Experimental Immunology. 117(2). 412–417. 53 indexed citations
20.
Genčík, Martin, et al.. (1993). Multistep transformation in low-grade lymphoproliferative diseases. Annals of Oncology. 4(10). 825–830. 25 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Bin Zhu Breakdown of academic impact, for papers by Shoko Murakami Breakdown of academic impact, for papers by Marco Faustini‐Fustini Breakdown of academic impact, for papers by Keisuke Kobayashi Breakdown of academic impact, for papers by Graziella Pinto Breakdown of academic impact, for papers by Svetlana Ghimbovschi Breakdown of academic impact, for papers by İsmail Üstünel Breakdown of academic impact, for papers by Maki Sakuma Breakdown of academic impact, for papers by Joseph M. Valdez Breakdown of academic impact, for papers by Mafalda Cacciottolo
Rankless by CCL
2026