Cecilie F. Rustad
- Molecular Biology
- Neurology top 10%
- Genetics
- Epidemiology
- Rheumatology top 10%
- Co-authors
- D. Gareth EvansMiriam J. SmithKetil HeimdalNaomi L. BowersAndrew J. WallaceCharlotte von der LippeGuy LeschzinerOlaug K. Rødningen
- Topics
- Genetic Syndromes and Imprinting (3 papers)Neurofibromatosis and Schwannoma Cases (3 papers)Hedgehog Signaling Pathway Studies (2 papers)
- Cited by
- NeurologySensory SystemsGenetics
- Partner nations
- NorwayUnited KingdomUnited States
In The Last Decade
Cecilie F. Rustad
17 papers receiving 485 citations
Peers
Comparison fields: 5 of 65
- Molecular Biology 210
- Neurology 170
- Genetics 116
- Epidemiology 111
- Rheumatology 84
Countries citing papers authored by Cecilie F. Rustad
This map shows the geographic impact of Cecilie F. Rustad'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 Cecilie F. Rustad with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cecilie F. Rustad more than expected).
Fields of papers citing papers by Cecilie F. Rustad
This network shows the impact of papers produced by Cecilie F. Rustad. 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 Cecilie F. Rustad. The network helps show where Cecilie F. Rustad may publish in the future.
Co-authorship network of co-authors of Cecilie F. Rustad
This figure shows the co-authorship network connecting the top 25 collaborators of Cecilie F. Rustad. A scholar is included among the top collaborators of Cecilie F. Rustad 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 Cecilie F. Rustad. Cecilie F. Rustad is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 3 | |
| 2 | 1 | |
| 3 | 0 | |
| 4 | 1 | |
| 5 | 1 | |
| 6 | 5 | |
| 7 | 33 | |
| 8 | 2 | |
| 9 | 53 | |
| 10 | 44 | |
| 11 | 78 | |
| 12 | 21 | |
| 13 | 52 | |
| 14 | 75 | |
| 15 | 33 | |
| 16 | 41 | |
| 17 | 36 | |
| 18 | 12 |
About Cecilie F. Rustad
Cecilie F. Rustad is a scholar working on Genetics, Rheumatology and Genetics, having authored 18 papers that have together received 491 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (3 papers), Neurofibromatosis and Schwannoma Cases (3 papers) and Hedgehog Signaling Pathway Studies (2 papers). The work is most often cited by research in Neurology (170 citations), Sensory Systems (34 citations) and Genetics (72 citations). Cecilie F. Rustad has collaborated with scholars based in Norway, United Kingdom and United States. Frequent co-authors include D. Gareth Evans, Miriam J. Smith, Ketil Heimdal, Naomi L. Bowers, Andrew J. Wallace, Charlotte von der Lippe, Guy Leschziner, Olaug K. Rødningen, Rosalie E. Ferner and Susan Holder. Their work appears in journals such as Neurology, BMJ Open and European 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.