Serdar Ceylaner
About
In The Last Decade
Serdar Ceylaner
205 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 100
- Molecular Biology 683
- Genetics 502
- Surgery 242
- Pediatrics, Perinatology and Child Health 194
- Clinical Biochemistry 144
Countries citing papers authored by Serdar Ceylaner
This map shows the geographic impact of Serdar Ceylaner'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 Serdar Ceylaner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Serdar Ceylaner more than expected).
Fields of papers citing papers by Serdar Ceylaner
This network shows the impact of papers produced by Serdar Ceylaner. 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 Serdar Ceylaner. The network helps show where Serdar Ceylaner may publish in the future.
Co-authorship network of co-authors of Serdar Ceylaner
This figure shows the co-authorship network connecting the top 25 collaborators of Serdar Ceylaner. A scholar is included among the top collaborators of Serdar Ceylaner 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 Serdar Ceylaner. Serdar Ceylaner 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 | 1 | |
| 3 | 1 | |
| 4 | 5 | |
| 5 | 1 | |
| 6 | 8 | |
| 7 | 18 | |
| 8 | 1 | |
| 9 | 11 | |
| 10 | 0 | |
| 11 | 7 | |
| 12 | 5 | |
| 13 | 5 | |
| 14 | 0 | |
| 15 | 0 | |
| 16 | 6 | |
| 17 | 18 | |
| 18 | Pyridoxine-dependent epilepsy in two Turkish patients in Turkey and review of the literature. | 5 |
| 19 | A Feingold syndrome case with previously undescribed features and a new mutation. | 1 |
| 20 | Multiple Pterygium Syndrome: A Case Report, Comparison with Fetal Akinesia Sequence and Pterygium Syndrome | 1 |
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.