Figen Celep
About
In The Last Decade
Figen Celep
17 papers receiving 171 citations
Peers
Comparison fields: 5 of 45
- Genetics 80
- Pediatrics, Perinatology and Child Health 72
- Molecular Biology 47
- Surgery 35
- Public Health, Environmental and Occupational Health 27
Countries citing papers authored by Figen Celep
This map shows the geographic impact of Figen Celep'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 Figen Celep with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Figen Celep more than expected).
Fields of papers citing papers by Figen Celep
This network shows the impact of papers produced by Figen Celep. 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 Figen Celep. The network helps show where Figen Celep may publish in the future.
Co-authorship network of co-authors of Figen Celep
This figure shows the co-authorship network connecting the top 25 collaborators of Figen Celep. A scholar is included among the top collaborators of Figen Celep 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 Figen Celep. Figen Celep is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 10 | |
| 2 | 12 | |
| 3 | Ring chromosome 18 in a child with febrile seizures. | 2 |
| 4 | 1 | |
| 5 | Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance. | 3 |
| 6 | 23 | |
| 7 | Chromosomal abnormalities in 457 Turkish patients with MCA/MR. | 4 |
| 8 | 38 | |
| 9 | 10 | |
| 10 | Secondary glioblastoma multiforme with a new translocation t(3;3)(q21;q26) following treatment of acute lymphoblastic leukemia. | 6 |
| 11 | 6 | |
| 12 | Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies. | 2 |
| 13 | Fuhrmann syndrome associated with cortical dysplasia. | 3 |
| 14 | Frequency of cardiovascular and gastrointestinal malformations, leukemia and hypothyroidism in children with Down syndrome in Trabzon, Turkey. | 9 |
| 15 | 8 | |
| 16 | 40 | |
| 17 | A case of VATER association associated with 9qh+. | 17 |
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.