Amithys Rahimian
Impact in
- Genetics top 5%
- Glioma Diagnosis and Treatment
-
- MicroRNA in disease regulation
- Cancer, Hypoxia, and Metabolism
- Cancer Genomics and Diagnostics
Papers in
- Genetics 7
- Glioma Diagnosis and Treatment 7
-
- Angiogenesis and VEGF in Cancer 2
- Chromatin Remodeling and Cancer 2
- Epigenetics and DNA Methylation 1
- Co-authors
- Marc Sanson (9 shared papers)Karima Mokhtari (8 shared papers)Marianne Labussière (8 shared papers)Anna Luisa Di Stefano (4 shared papers)Khê Hoang‐Xuan (5 shared papers)Ahmed Idbaïh (4 shared papers)Vincent Gleize (2 shared papers)Stephanie Mangesius (2 shared papers)
- Journals
- Journal of Neuro-Oncology (2 papers)The Oncologist (1 paper)Scientific Reports (1 paper)Acta Neuropathologica (1 paper)British Journal of Cancer (1 paper)
- Partner nations
- FranceItalyUnited Kingdom
In The Last Decade
Amithys Rahimian
10 papers receiving 392 citations
Peers
Comparison fields: 5 of 50
- Genetics 225
- Cancer Research 88
- Molecular Biology 148
- Physiology 46
- Oncology 45
Countries citing papers authored by Amithys Rahimian
This map shows the geographic impact of Amithys Rahimian'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 Amithys Rahimian with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amithys Rahimian more than expected).
Fields of papers citing papers by Amithys Rahimian
This network shows the impact of papers produced by Amithys Rahimian. 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 Amithys Rahimian. The network helps show where Amithys Rahimian may publish in the future.
Co-authors
The 25 scholars most cited alongside Amithys Rahimian, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 146 | |
| 2 | 2015 | 65 | |
| 3 | 2018 | 41 | |
| 4 | 2015 | 34 | |
| 5 | 2014 | 30 | |
| 6 | 2016 | 30 | |
| 7 | 2015 | 23 | |
| 8 | 2015 | 16 | |
| 9 | 2016 | 7 | |
| 10 | 2014 | 1 |
About Amithys Rahimian
Amithys Rahimian is a scholar working on Genetics, Molecular Biology, Cancer Research, Pulmonary and Respiratory Medicine and Physiology, having authored 10 papers that have together received 393 indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (7 papers), Angiogenesis and VEGF in Cancer (2 papers), Ferroptosis and cancer prognosis (2 papers), Cancer, Hypoxia, and Metabolism (2 papers), Chromatin Remodeling and Cancer (2 papers), MicroRNA in disease regulation (1 paper), Epigenetics and DNA Methylation (1 paper) and Telomeres, Telomerase, and Senescence (1 paper). The work is most often cited by research in Genetics (225 citations), Cancer Research (88 citations), Molecular Biology (148 citations), Physiology (46 citations) and Oncology (45 citations). Amithys Rahimian has collaborated with scholars based in France, Italy and United Kingdom. Frequent co-authors include Marc Sanson, Karima Mokhtari, Marianne Labussière, Anna Luisa Di Stefano, Khê Hoang‐Xuan, Ahmed Idbaïh, Vincent Gleize, Stephanie Mangesius, Richard S. Houlston and Marine Giry. Their work appears in journals such as Journal of Neuro-Oncology, The Oncologist, Scientific Reports, Acta Neuropathologica and British Journal of Cancer.
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.