Zoltán Grosz
- Co-authors
- Mária Judit MolnárAnikó GálViktor MolnárEdina VargaPéter KlivènyiAndrás GézsiLéna SzabóPéter Diószeghy
- Topics
- Hereditary Neurological Disorders (6 papers)Neurological diseases and metabolism (5 papers)Genetic Neurodegenerative Diseases (4 papers)
In The Last Decade
Zoltán Grosz
18 papers receiving 168 citations
Peers
Comparison fields: 5 of 51
- Molecular Biology 81
- Cellular and Molecular Neuroscience 57
- Genetics 50
- Neurology 44
- Neurology 33
Countries citing papers authored by Zoltán Grosz
This map shows the geographic impact of Zoltán Grosz'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 Grosz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zoltán Grosz more than expected).
Fields of papers citing papers by Zoltán Grosz
This network shows the impact of papers produced by Zoltán Grosz. 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 Grosz. The network helps show where Zoltán Grosz may publish in the future.
Co-authorship network of co-authors of Zoltán Grosz
This figure shows the co-authorship network connecting the top 25 collaborators of Zoltán Grosz. A scholar is included among the top collaborators of Zoltán Grosz 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 Grosz. Zoltán Grosz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 4 | |
| 3 | 5 | |
| 4 | 13 | |
| 5 | 3 | |
| 6 | 1 | |
| 7 | 5 | |
| 8 | 0 | |
| 9 | 2 | |
| 10 | 38 | |
| 11 | 9 | |
| 12 | 15 | |
| 13 | 10 | |
| 14 | 14 | |
| 15 | 1 | |
| 16 | 1 | |
| 17 | A teljesexom-szekvenálás jelentősége a ritka neurológiai betegségek diagnosztikájában – saját tapasztalatok egy ataxiás eset kapcsán = Significance of whole exome sequencing in the diagnostics of rare neurological diseases – own experiences through a case presenting with ataxia | 1 |
| 18 | 18 | |
| 19 | 24 | |
| 20 | 6 |
About Zoltán Grosz
Zoltán Grosz is a scholar working on Neurology, Cellular and Molecular Neuroscience and Clinical Biochemistry, having authored 20 papers that have together received 170 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (6 papers), Neurological diseases and metabolism (5 papers) and Genetic Neurodegenerative Diseases (4 papers). The work is most often cited by research in Neurology (44 citations), Genetics (50 citations) and Cellular and Molecular Neuroscience (57 citations). Zoltán Grosz has collaborated with scholars based in Hungary, Sweden and Canada. Frequent co-authors include Mária Judit Molnár, Anikó Gál, Viktor Molnár, Edina Varga, Péter Klivènyi, András Gézsi, Léna Szabó, Péter Diószeghy, Judit Boczán and Dorottya Czövek. Their work appears in journals such as Journal of the Neurological Sciences, Frontiers in Psychiatry and Frontiers in Genetics.
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.