Damir Sudar
- Genetics top 0.2%
- Molecular Biology top 2%
- Cancer Research top 1%
- Plant Science top 2%
- Pathology and Forensic Medicine top 2%
- Co-authors
- Joe W. GrayOlli KallioniemiAnne KallioniemiDenis RutovitzDan PinkelFred WaldmanSteven M. ClarkRichard Segraves
- Topics
- Genomic variations and chromosomal abnormalities (13 papers)Cell Image Analysis Techniques (11 papers)Gene expression and cancer classification (8 papers)
- Cited by
- GeneticsCancer ResearchBiophysics
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Damir Sudar
32 papers receiving 5.0k citations
Hit Papers
Peers
Comparison fields: 5 of 114
- Genetics 3.2k
- Molecular Biology 2.7k
- Cancer Research 1.3k
- Plant Science 1.1k
- Pathology and Forensic Medicine 711
Countries citing papers authored by Damir Sudar
This map shows the geographic impact of Damir Sudar'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 Damir Sudar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Damir Sudar more than expected).
Fields of papers citing papers by Damir Sudar
This network shows the impact of papers produced by Damir Sudar. 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 Damir Sudar. The network helps show where Damir Sudar may publish in the future.
Co-authorship network of co-authors of Damir Sudar
This figure shows the co-authorship network connecting the top 25 collaborators of Damir Sudar. A scholar is included among the top collaborators of Damir Sudar 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 Damir Sudar. Damir Sudar 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 | 0 | |
| 3 | 9 | |
| 4 | 50 | |
| 5 | 11 | |
| 6 | 96 | |
| 7 | 5 | |
| 8 | 4 | |
| 9 | 100 | |
| 10 | 36 | |
| 11 | High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarraysbreakdown → | 1617 |
| 12 | 2 | |
| 13 | 8 | |
| 14 | 224 | |
| 15 | 62 | |
| 16 | 13 | |
| 17 | 30 | |
| 18 | 17 | |
| 19 | 12 | |
| 20 | 29 |
About Damir Sudar
Damir Sudar is a scholar working on Biophysics, Genetics and Computer Graphics and Computer-Aided Design, having authored 37 papers that have together received 5.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Cell Image Analysis Techniques (11 papers) and Gene expression and cancer classification (8 papers). The work is most often cited by research in Genetics (3.2k citations), Cancer Research (1.3k citations) and Biophysics (243 citations). Damir Sudar has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Joe W. Gray, Olli Kallioniemi, Anne Kallioniemi, Denis Rutovitz, Dan Pinkel, Fred Waldman, Steven M. Clark, Richard Segraves, David Kowbel and Britt‐Marie Ljung. Their work appears in journals such as Science, Proceedings of the National Academy of Sciences and Nature 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.