Izabella Klein
About
In The Last Decade
Izabella Klein
20 papers receiving 950 citations
Peers
Comparison fields: 5 of 92
- Oncology 491
- Molecular Biology 426
- Surgery 260
- Pediatrics, Perinatology and Child Health 103
- Physiology 102
Countries citing papers authored by Izabella Klein
This map shows the geographic impact of Izabella Klein'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 Izabella Klein with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Izabella Klein more than expected).
Fields of papers citing papers by Izabella Klein
This network shows the impact of papers produced by Izabella Klein. 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 Izabella Klein. The network helps show where Izabella Klein may publish in the future.
Co-authorship network of co-authors of Izabella Klein
This figure shows the co-authorship network connecting the top 25 collaborators of Izabella Klein. A scholar is included among the top collaborators of Izabella Klein 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 Izabella Klein. Izabella Klein 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 | Familial focal segmental glomerulosclerosis: mutation in inverted formin 2 mimicking Alport syndrome. | 6 |
| 3 | 22 | |
| 4 | 7 | |
| 5 | 78 | |
| 6 | 7 | |
| 7 | 53 | |
| 8 | 14 | |
| 9 | 9 | |
| 10 | 4 | |
| 11 | 85 | |
| 12 | 7 | |
| 13 | Analysis of large structural changes of the factor VIII gene, involving intron 1 and 22, in severe hemophilia A. | 38 |
| 14 | 19 | |
| 15 | 24 | |
| 16 | 43 | |
| 17 | 11 | |
| 18 | 28 | |
| 19 | 464 | |
| 20 | [A new method of molecular testing in the differential diagnosis of hereditary hemochromatosis]. | 4 |
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.