Zoltán Maróti

1.0k total citations
53 papers, 431 citations indexed

About

Zoltán Maróti is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Zoltán Maróti has authored 53 papers receiving a total of 431 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 23 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Zoltán Maróti's work include Forensic and Genetic Research (11 papers), Genomics and Phylogenetic Studies (6 papers) and Genetic diversity and population structure (5 papers). Zoltán Maróti is often cited by papers focused on Forensic and Genetic Research (11 papers), Genomics and Phylogenetic Studies (6 papers) and Genetic diversity and population structure (5 papers). Zoltán Maróti collaborates with scholars based in Hungary, United States and Germany. Zoltán Maróti's co-authors include Tibor Kalmár, Csaba Bereczki, István Nagy, István Raskó, Emõke Endreffy, Endre Neparáczki, Tibor Tőrők, M Snyder, Zsolt Boldogkői and Dóra Tombácz and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Zoltán Maróti

49 papers receiving 422 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zoltán Maróti Hungary 13 157 140 37 36 35 53 431
Nathan Harris United States 11 54 0.3× 203 1.4× 60 1.6× 19 0.5× 13 0.4× 15 603
Olga Derbeneva United States 15 461 2.9× 1.0k 7.4× 20 0.5× 149 4.1× 21 0.6× 21 1.5k
Fedor Gusev United States 11 61 0.4× 160 1.1× 94 2.5× 11 0.3× 6 0.2× 22 406
Jean‐François Deleuze France 15 192 1.2× 412 2.9× 2 0.1× 12 0.3× 13 0.4× 26 740
B. M. Lewis United Kingdom 12 62 0.4× 171 1.2× 7 0.2× 7 0.2× 9 0.3× 25 425
Tomaz Berisa United States 5 701 4.5× 378 2.7× 13 0.4× 4 0.1× 29 0.8× 5 1.1k
Sophie Hackinger United Kingdom 8 153 1.0× 123 0.9× 39 1.1× 6 0.2× 8 0.2× 15 380
Antònia Flaquer Germany 14 173 1.1× 197 1.4× 14 0.4× 4 0.1× 12 0.3× 23 515
Mari Nelis Estonia 13 306 1.9× 183 1.3× 2 0.1× 22 0.6× 16 0.5× 35 567
Alenka Hodžić Slovenia 12 124 0.8× 154 1.1× 15 0.4× 2 0.1× 18 0.5× 27 455

Countries citing papers authored by Zoltán Maróti

Since Specialization
Citations

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

Fields of papers citing papers by Zoltán Maróti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zoltán Maróti

This figure shows the co-authorship network connecting the top 25 collaborators of Zoltán Maróti. A scholar is included among the top collaborators of Zoltán Maróti 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 Zoltán Maróti. Zoltán Maróti 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.
Maróti, Zoltán, et al.. (2024). Archaeogenetic analysis revealed East Eurasian paternal origin to the Aba royal family of Hungary. iScience. 27(10). 110892–110892.
2.
Kalmár, Tibor, et al.. (2024). Phenotypic and Genotypic Features of the FAN1 Mutation-Related Disease in a Large Hungarian Family. International Journal of Molecular Sciences. 25(11). 5907–5907. 1 indexed citations
3.
Fehér, Tamás, et al.. (2024). Cone dysfunction in ARR3-mutation-associated early-onset high myopia: an electrophysiological study. Orphanet Journal of Rare Diseases. 19(1). 385–385. 1 indexed citations
4.
5.
Farkas, Klára, Zsuzsanna Szalai, Judit Bene, et al.. (2023). Co-occurrence of neurofibromatosis type 1 and pseudoachondroplasia – a first case report. BMC Pediatrics. 23(1). 110–110. 3 indexed citations
6.
Kalmár, Tibor, et al.. (2023). Phenotype–Genotype Correlations in Three Different Cases of Adult-Onset Genetic Focal Segmental Glomerulosclerosis. International Journal of Molecular Sciences. 24(24). 17489–17489. 3 indexed citations
7.
Maróti, Zoltán, et al.. (2023). Adaptive Savitzky–Golay Filters for Analysis of Copy Number Variation Peaks from Whole-Exome Sequencing Data. Information. 14(2). 128–128. 5 indexed citations
8.
Boros, Fanni Annamária, László Szpisjak, Dénes Zádori, et al.. (2023). Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the CCDC88C Gene. International Journal of Molecular Sciences. 24(3). 2617–2617. 2 indexed citations
9.
Kalmár, Tibor, et al.. (2023). correctKin: an optimized method to infer relatedness up to the 4th degree from low-coverage ancient human genomes. Genome biology. 24(1). 38–38. 9 indexed citations
10.
Maár, Kitti, et al.. (2022). Multi-disciplinary analysis of an elite Xiongnu tomb from Belkhin Am cemetery, Ulaanbaatar. SZTE Publicatio Repozitórium (University of Szeged). 2(2). 101–113. 1 indexed citations
11.
Neparáczki, Endre, Zoltán Maróti, Horolma Pamjav, et al.. (2022). The genetic legacy of the Hunyadi descendants. Heliyon. 8(11). e11731–e11731. 2 indexed citations
12.
Maár, Kitti, et al.. (2022). Maternal Lineages of Gepids from Transylvania. Genes. 13(4). 563–563. 1 indexed citations
13.
Maár, Kitti, et al.. (2021). An archaeogenetic approach to identify the remains of the Hungarian Kings. Working Plan. SZTE Publicatio Repozitórium (University of Szeged). 1(2). 333–342. 1 indexed citations
14.
Zádori, Dénes, Anikó Újfalusi, László Szpisjak, et al.. (2021). Hereditary and non-hereditary etiologies associated with extensive brain calcification: case series. Metabolic Brain Disease. 36(7). 2131–2139. 1 indexed citations
15.
Fehér, Tamás, Zoltán Maróti, Tibor Kalmár, et al.. (2021). Myopia-26, the female-limited form of early-onset high myopia, occurring in a European family. Orphanet Journal of Rare Diseases. 16(1). 45–45. 18 indexed citations
16.
Maróti, Zoltán, Dóra Tombácz, Norbert Moldován, et al.. (2021). Time course profiling of host cell response to herpesvirus infection using nanopore and synthetic long-read transcriptome sequencing. Scientific Reports. 11(1). 14219–14219. 5 indexed citations
17.
Kalmár, Tibor, Zoltán Maróti, Alíz Zimmermann, & László Sztriha. (2020). Tremor as an early sign of hereditary spastic paraplegia due to mutations in ALDH18A1. Brain and Development. 43(1). 144–151. 5 indexed citations
18.
Tombácz, Dóra, Zoltán Maróti, Tibor Kalmár, et al.. (2019). Whole-exome sequencing data of suicide victims who had suffered from major depressive disorder. Scientific Data. 6(1). 190010–190010. 3 indexed citations
19.
Szpisjak, László, Dénes Zádori, Zoltán Maróti, et al.. (2017). Neurocognitive Characterization of an SCA28 Family Caused by a Novel AFG3L2 Gene Mutation. The Cerebellum. 16(5-6). 979–985. 6 indexed citations
20.
László, Aranka, et al.. (2003). Clinical and genetical aspects of autosomal dominantly inherited osteogenesis imperfecta tarda. Acta Biologica Szegediensis. 47. 41–45. 1 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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