Kristin Bosse
- Genetics top 10%
- Molecular Biology
- Oncology
- Pediatrics, Perinatology and Child Health
- Pathology and Forensic Medicine
- Co-authors
- Hartmut EngelsPeter ProppingKatrin Elisabeth GielNorbert SchäffelerMartin TeufelStephan ZipfelAlexander HoischenBarbara Wappenschmidt
- Topics
- Genomic variations and chromosomal abnormalities (9 papers)BRCA gene mutations in cancer (7 papers)Chromosomal and Genetic Variations (4 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Kristin Bosse
23 papers receiving 515 citations
Peers
Comparison fields: 5 of 72
- Genetics 312
- Molecular Biology 244
- Oncology 64
- Pediatrics, Perinatology and Child Health 62
- Pathology and Forensic Medicine 57
Countries citing papers authored by Kristin Bosse
This map shows the geographic impact of Kristin Bosse'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 Kristin Bosse with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kristin Bosse more than expected).
Fields of papers citing papers by Kristin Bosse
This network shows the impact of papers produced by Kristin Bosse. 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 Kristin Bosse. The network helps show where Kristin Bosse may publish in the future.
Co-authorship network of co-authors of Kristin Bosse
This figure shows the co-authorship network connecting the top 25 collaborators of Kristin Bosse. A scholar is included among the top collaborators of Kristin Bosse 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 Kristin Bosse. Kristin Bosse is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 74 | |
| 2 | 8 | |
| 3 | 35 | |
| 4 | 17 | |
| 5 | 17 | |
| 6 | 67 | |
| 7 | 5 | |
| 8 | 16 | |
| 9 | 4 | |
| 10 | 73 | |
| 11 | 41 | |
| 12 | 15 | |
| 13 | 7 | |
| 14 | 4 | |
| 15 | 40 | |
| 16 | 5 | |
| 17 | 13 | |
| 18 | 25 | |
| 19 | 17 | |
| 20 | 32 |
About Kristin Bosse
Kristin Bosse is a scholar working on Developmental Biology, Genetics and Dermatology, having authored 24 papers that have together received 526 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), BRCA gene mutations in cancer (7 papers) and Chromosomal and Genetic Variations (4 papers). The work is most often cited by research in Developmental Biology (37 citations), Genetics (312 citations) and Reproductive Medicine (40 citations). Kristin Bosse has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Hartmut Engels, Peter Propping, Katrin Elisabeth Giel, Norbert Schäffeler, Martin Teufel, Stephan Zipfel, Alexander Hoischen, Barbara Wappenschmidt, Regina C. Betz and Ruthild G. Weber. Their work appears in journals such as Journal of Clinical Oncology, Neurology and The American Journal of Human 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.