Mihaela Campan
- Molecular Biology top 5%
- Cancer Research top 5%
- Genetics top 5%
- Oncology top 10%
- Pulmonary and Respiratory Medicine top 10%
- Co-authors
- Peter W. LairdDaniel J. WeisenbergerKimberly D. SiegmundJoanne YoungChristian MarthMartin WidschwendterIan JacobsGilbert Spizzo
- Topics
- Epigenetics and DNA Methylation (22 papers)RNA modifications and cancer (11 papers)Cancer-related gene regulation (7 papers)
- Partner nations
- United StatesAustraliaUnited Kingdom
In The Last Decade
Mihaela Campan
30 papers receiving 2.7k citations
Hit Papers
Peers
Comparison fields: 5 of 108
- Molecular Biology 2.3k
- Cancer Research 604
- Genetics 463
- Oncology 389
- Pulmonary and Respiratory Medicine 298
Countries citing papers authored by Mihaela Campan
This map shows the geographic impact of Mihaela Campan'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 Mihaela Campan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mihaela Campan more than expected).
Fields of papers citing papers by Mihaela Campan
This network shows the impact of papers produced by Mihaela Campan. 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 Mihaela Campan. The network helps show where Mihaela Campan may publish in the future.
Co-authorship network of co-authors of Mihaela Campan
This figure shows the co-authorship network connecting the top 25 collaborators of Mihaela Campan. A scholar is included among the top collaborators of Mihaela Campan 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 Mihaela Campan. Mihaela Campan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 17 | |
| 2 | 87 | |
| 3 | 404 | |
| 4 | 7 | |
| 5 | 84 | |
| 6 | 44 | |
| 7 | 72 | |
| 8 | 56 | |
| 9 | 118 | |
| 10 | 88 | |
| 11 | 99 | |
| 12 | 110 | |
| 13 | 74 | |
| 14 | 142 | |
| 15 | 327 | |
| 16 | CpG Island Methylator Phenotype in Human Colorectal Cancer Is Tightly Associated with BRAF Mutation and Underlies Sporadic Mismatch Repair Deficiency. | 1 |
| 17 | Epigenetic stem cell signature in cancerbreakdown → | 775 |
| 18 | 31 | |
| 19 | 28 | |
| 20 | 111 |
About Mihaela Campan
Mihaela Campan is a scholar working on Cancer Research, Molecular Biology and Neurology, having authored 30 papers that have together received 2.7k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (22 papers), RNA modifications and cancer (11 papers) and Cancer-related gene regulation (7 papers). The work is most often cited by research in Cancer Research (604 citations), Molecular Biology (2.3k citations) and Genetics (463 citations). Mihaela Campan has collaborated with scholars based in United States, Australia and United Kingdom. Frequent co-authors include Peter W. Laird, Daniel J. Weisenberger, Kimberly D. Siegmund, Joanne Young, Christian Marth, Martin Widschwendter, Ian Jacobs, Gilbert Spizzo, Elisabeth Mueller‐Holzner and Daniel Egle. Their work appears in journals such as Nucleic Acids Research, Nature Genetics and Journal of Clinical Oncology.
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.