Heidrun Holland
- Co-authors
- Wolfgang KruppRonald KoschnyPeter AhnertManfred BauerJürgen MeixensbergerUrsula G. FrosterE. Sander ConnollyWilliam J. Mack
- Topics
- Glioma Diagnosis and Treatment (9 papers)Genomic variations and chromosomal abnormalities (7 papers)Cancer Genomics and Diagnostics (6 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Heidrun Holland
43 papers receiving 836 citations
Peers
Comparison fields: 5 of 95
- Molecular Biology 304
- Surgery 226
- Epidemiology 160
- Immunology 135
- Genetics 117
Countries citing papers authored by Heidrun Holland
This map shows the geographic impact of Heidrun Holland'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 Heidrun Holland with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heidrun Holland more than expected).
Fields of papers citing papers by Heidrun Holland
This network shows the impact of papers produced by Heidrun Holland. 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 Heidrun Holland. The network helps show where Heidrun Holland may publish in the future.
Co-authorship network of co-authors of Heidrun Holland
This figure shows the co-authorship network connecting the top 25 collaborators of Heidrun Holland. A scholar is included among the top collaborators of Heidrun Holland 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 Heidrun Holland. Heidrun Holland 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 | 4 | |
| 3 | 19 | |
| 4 | 8 | |
| 5 | 7 | |
| 6 | 30 | |
| 7 | 15 | |
| 8 | 1 | |
| 9 | 19 | |
| 10 | 5 | |
| 11 | 4 | |
| 12 | 17 | |
| 13 | 7 | |
| 14 | 10 | |
| 15 | 4 | |
| 16 | 4 | |
| 17 | 37 | |
| 18 | 20 | |
| 19 | 7 | |
| 20 | 1 |
About Heidrun Holland
Heidrun Holland is a scholar working on Genetics, Cancer Research and Immunology, having authored 44 papers that have together received 872 indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Cancer Genomics and Diagnostics (6 papers). The work is most often cited by research in Neurology (108 citations), Genetics (117 citations) and Neurology (103 citations). Heidrun Holland has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Wolfgang Krupp, Ronald Koschny, Peter Ahnert, Manfred Bauer, Jürgen Meixensberger, Ursula G. Froster, E. Sander Connolly, William J. Mack, Andrew F. Ducruet and Sergei A. Sosunov. Their work appears in journals such as PLoS ONE, Circulation Research and Clinical Cancer Research.
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.