Kristin Mrasek
- Genetics top 1%
- Molecular Biology top 10%
- Plant Science top 2%
- Pediatrics, Perinatology and Child Health top 2%
- Cancer Research
- Co-authors
- Thomas LiehrAnja WeiseHeike StarkeNadezda KosyakovaAnita HellerVladimir A. TrifonovUwe ClaussenU. Claussen
- Topics
- Genomic variations and chromosomal abnormalities (66 papers)Chromosomal and Genetic Variations (51 papers)Prenatal Screening and Diagnostics (27 papers)
- Partner nations
- GermanyRussiaUnited States
In The Last Decade
Kristin Mrasek
84 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 76
- Genetics 1.3k
- Molecular Biology 891
- Plant Science 842
- Pediatrics, Perinatology and Child Health 500
- Cancer Research 115
Countries citing papers authored by Kristin Mrasek
This map shows the geographic impact of Kristin Mrasek'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 Mrasek with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kristin Mrasek more than expected).
Fields of papers citing papers by Kristin Mrasek
This network shows the impact of papers produced by Kristin Mrasek. 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 Mrasek. The network helps show where Kristin Mrasek may publish in the future.
Co-authorship network of co-authors of Kristin Mrasek
This figure shows the co-authorship network connecting the top 25 collaborators of Kristin Mrasek. A scholar is included among the top collaborators of Kristin Mrasek 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 Mrasek. Kristin Mrasek is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 6 | |
| 2 | 7 | |
| 3 | 4 | |
| 4 | 6 | |
| 5 | 9 | |
| 6 | 13 | |
| 7 | 7 | |
| 8 | 14 | |
| 9 | 30 | |
| 10 | 3 | |
| 11 | Partial monosomy 4q and partial trisomy 13q: phenotype and molecular mapping of the breakpoints | 1 |
| 12 | 3 | |
| 13 | 20 | |
| 14 | 11 | |
| 15 | 11 | |
| 16 | 21 | |
| 17 | 17 | |
| 18 | 34 | |
| 19 | 32 | |
| 20 | 41 |
About Kristin Mrasek
Kristin Mrasek is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science, having authored 86 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (66 papers), Chromosomal and Genetic Variations (51 papers) and Prenatal Screening and Diagnostics (27 papers). The work is most often cited by research in Genetics (1.3k citations), Pediatrics, Perinatology and Child Health (500 citations) and Plant Science (842 citations). Kristin Mrasek has collaborated with scholars based in Germany, Russia and United States. Frequent co-authors include Thomas Liehr, Anja Weise, Heike Starke, Nadezda Kosyakova, Anita Heller, Vladimir A. Trifonov, Uwe Claussen, U. Claussen, Н. Б. Рубцов and Samarth Bhatt. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and Oncogene.
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.