Kristen Rasmussen
- Genetics
- Molecular Biology
- Surgery
- Pathology and Forensic Medicine
- Pediatrics, Perinatology and Child Health
- Co-authors
- Elizabeth McPhersonPhilip F. GiampietroKara ReynoldsChristina ZaleskiCatherine A. McCartyRobert D. BlankStuart SchwartzDavid T. Miller
- Topics
- Genomics and Rare Diseases (3 papers)Genomic variations and chromosomal abnormalities (3 papers)RNA modifications and cancer (2 papers)
- Partner nations
- United StatesUnited KingdomMalaysia
In The Last Decade
Kristen Rasmussen
9 papers receiving 261 citations
Peers
Comparison fields: 5 of 53
- Genetics 163
- Molecular Biology 114
- Surgery 38
- Pathology and Forensic Medicine 33
- Pediatrics, Perinatology and Child Health 33
Countries citing papers authored by Kristen Rasmussen
This map shows the geographic impact of Kristen Rasmussen'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 Kristen Rasmussen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kristen Rasmussen more than expected).
Fields of papers citing papers by Kristen Rasmussen
This network shows the impact of papers produced by Kristen Rasmussen. 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 Kristen Rasmussen. The network helps show where Kristen Rasmussen may publish in the future.
Co-authorship network of co-authors of Kristen Rasmussen
This figure shows the co-authorship network connecting the top 25 collaborators of Kristen Rasmussen. A scholar is included among the top collaborators of Kristen Rasmussen 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 Kristen Rasmussen. Kristen Rasmussen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 32 | |
| 2 | 46 | |
| 3 | 21 | |
| 4 | 10 | |
| 5 | 36 | |
| 6 | 0 | |
| 7 | 54 | |
| 8 | 44 | |
| 9 | 3 | |
| 10 | 17 |
About Kristen Rasmussen
Kristen Rasmussen is a scholar working on Genetics, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 10 papers that have together received 263 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Genetics (163 citations), Pathology and Forensic Medicine (33 citations) and Pediatrics, Perinatology and Child Health (33 citations). Kristen Rasmussen has collaborated with scholars based in United States, United Kingdom and Malaysia. Frequent co-authors include Elizabeth McPherson, Philip F. Giampietro, Kara Reynolds, Christina Zaleski, Catherine A. McCarty, Robert D. Blank, Stuart Schwartz, David T. Miller, Jane L. Schuette and Darrel Waggoner. Their work appears in journals such as Cancer Research, Journal of Bone and Mineral Research and Genetics in Medicine.
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.