Radka Stoeva
About
In The Last Decade
Radka Stoeva
7 papers receiving 183 citations
Peers
Comparison fields: 5 of 46
- Genetics 126
- Molecular Biology 89
- Reproductive Medicine 47
- Plant Science 31
- Pediatrics, Perinatology and Child Health 30
Countries citing papers authored by Radka Stoeva
This map shows the geographic impact of Radka Stoeva'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 Radka Stoeva with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Radka Stoeva more than expected).
Fields of papers citing papers by Radka Stoeva
This network shows the impact of papers produced by Radka Stoeva. 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 Radka Stoeva. The network helps show where Radka Stoeva may publish in the future.
Co-authorship network of co-authors of Radka Stoeva
This figure shows the co-authorship network connecting the top 25 collaborators of Radka Stoeva. A scholar is included among the top collaborators of Radka Stoeva 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 Radka Stoeva. Radka Stoeva is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 0 | |
| 3 | 1 | |
| 4 | 21 | |
| 5 | Three cases of two unrelated families with a microduplication 22q11.2: developmental skull defects and phenotype variability | 74 |
| 6 | A novel SOX9 nonsense mutation, q401x, in a case of campomelic dysplasia with XY sex reversal. | 6 |
| 7 | 92 | |
| 8 | Clinical and molecular-cytogenetic studies of cryptic chromosome aberrations in individuals with idiopathic mental retardation and multiple congenital malformations. | 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.