Katharina Steindl
- Molecular Biology
- Genetics top 10%
- Ophthalmology top 5%
- Cell Biology
- Cellular and Molecular Neuroscience
- Co-authors
- Anita RauchPascal JosetHeinrich StichtMarkus ZweierAlessandra BaumerEnzo Maria VingoloAlessandro IannacconeGiovanni Neri
- Topics
- Genomics and Rare Diseases (10 papers)Genomic variations and chromosomal abnormalities (6 papers)Congenital heart defects research (5 papers)
- Partner nations
- SwitzerlandGermanyItaly
In The Last Decade
Katharina Steindl
47 papers receiving 692 citations
Peers
Comparison fields: 5 of 75
- Molecular Biology 411
- Genetics 323
- Ophthalmology 72
- Cell Biology 52
- Cellular and Molecular Neuroscience 49
Countries citing papers authored by Katharina Steindl
This map shows the geographic impact of Katharina Steindl'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 Katharina Steindl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katharina Steindl more than expected).
Fields of papers citing papers by Katharina Steindl
This network shows the impact of papers produced by Katharina Steindl. 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 Katharina Steindl. The network helps show where Katharina Steindl may publish in the future.
Co-authorship network of co-authors of Katharina Steindl
This figure shows the co-authorship network connecting the top 25 collaborators of Katharina Steindl. A scholar is included among the top collaborators of Katharina Steindl 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 Katharina Steindl. Katharina Steindl is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 3 | |
| 2 | 6 | |
| 3 | 10 | |
| 4 | 0 | |
| 5 | 19 | |
| 6 | 11 | |
| 7 | 12 | |
| 8 | 8 | |
| 9 | 2 | |
| 10 | 19 | |
| 11 | Novel Gata6-Mutation in a Boy with Neonatal Diabetes and Diaphragmatic Hernia | 2 |
| 12 | 32 | |
| 13 | 34 | |
| 14 | 26 | |
| 15 | 30 | |
| 16 | 1 | |
| 17 | 39 | |
| 18 | 26 | |
| 19 | 9 | |
| 20 | Effect of azelaic acid on viability, ultrastructure and karyotype of melanoma cells in long-term culture | 2 |
About Katharina Steindl
Katharina Steindl is a scholar working on Genetics, Equine and Applied Microbiology and Biotechnology, having authored 50 papers that have together received 698 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Congenital heart defects research (5 papers). The work is most often cited by research in Genetics (323 citations), Ophthalmology (72 citations) and Molecular Biology (411 citations). Katharina Steindl has collaborated with scholars based in Switzerland, Germany and Italy. Frequent co-authors include Anita Rauch, Pascal Joset, Heinrich Sticht, Markus Zweier, Alessandra Baumer, Enzo Maria Vingolo, Alessandro Iannaccone, Giovanni Neri, Lucia Abela and Barbara Plecko. Their work appears in journals such as PLoS ONE, The American Journal of Human Genetics and Human Molecular Genetics.
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.