Katalin Szakszon
- Co-authors
- Éva OláhIstván BaloghGuntram BorckAlida C. KnegtChristian KubischBruno DallapiccolaAnikó ÚjfalusiNaseebullah Kakar
- Topics
- Genomic variations and chromosomal abnormalities (7 papers)Genetics and Neurodevelopmental Disorders (4 papers)DNA Repair Mechanisms (3 papers)
- Partner nations
- HungaryNetherlandsGermany
In The Last Decade
Katalin Szakszon
28 papers receiving 272 citations
Peers
Comparison fields: 5 of 62
- Molecular Biology 178
- Genetics 103
- Cell Biology 30
- Clinical Biochemistry 27
- Physiology 26
Countries citing papers authored by Katalin Szakszon
This map shows the geographic impact of Katalin Szakszon'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 Katalin Szakszon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katalin Szakszon more than expected).
Fields of papers citing papers by Katalin Szakszon
This network shows the impact of papers produced by Katalin Szakszon. 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 Katalin Szakszon. The network helps show where Katalin Szakszon may publish in the future.
Co-authorship network of co-authors of Katalin Szakszon
This figure shows the co-authorship network connecting the top 25 collaborators of Katalin Szakszon. A scholar is included among the top collaborators of Katalin Szakszon 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 Katalin Szakszon. Katalin Szakszon 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 | 2 | |
| 3 | 1 | |
| 4 | 8 | |
| 5 | 7 | |
| 6 | 18 | |
| 7 | 3 | |
| 8 | 1 | |
| 9 | 11 | |
| 10 | 3 | |
| 11 | 16 | |
| 12 | 9 | |
| 13 | 7 | |
| 14 | 38 | |
| 15 | 26 | |
| 16 | 18 | |
| 17 | 7 | |
| 18 | 8 | |
| 19 | 4 | |
| 20 | 9 |
About Katalin Szakszon
Katalin Szakszon is a scholar working on Genetics, Genetics and Molecular Biology, having authored 29 papers that have together received 276 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (4 papers) and DNA Repair Mechanisms (3 papers). The work is most often cited by research in Clinical Biochemistry (27 citations), Genetics (103 citations) and Molecular Biology (178 citations). Katalin Szakszon has collaborated with scholars based in Hungary, Netherlands and Germany. Frequent co-authors include Éva Oláh, István Balogh, Guntram Borck, Alida C. Knegt, Christian Kubisch, Bruno Dallapiccola, Anikó Újfalusi, Naseebullah Kakar, Carmelo Salpietro and Davor Lessel. Their work appears in journals such as Genes & Development, Journal of Clinical Epidemiology and Journal of Biotechnology.
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.