Serge Fitoussi
About
In The Last Decade
Serge Fitoussi
15 papers receiving 397 citations
Peers
Comparison fields: 5 of 74
- Molecular Biology 173
- Surgery 61
- Ophthalmology 52
- Genetics 52
- Cardiology and Cardiovascular Medicine 47
Countries citing papers authored by Serge Fitoussi
This map shows the geographic impact of Serge Fitoussi'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 Serge Fitoussi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Serge Fitoussi more than expected).
Fields of papers citing papers by Serge Fitoussi
This network shows the impact of papers produced by Serge Fitoussi. 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 Serge Fitoussi. The network helps show where Serge Fitoussi may publish in the future.
Co-authorship network of co-authors of Serge Fitoussi
This figure shows the co-authorship network connecting the top 25 collaborators of Serge Fitoussi. A scholar is included among the top collaborators of Serge Fitoussi 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 Serge Fitoussi. Serge Fitoussi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 82 | |
| 2 | 69 | |
| 3 | 1 | |
| 4 | 1 | |
| 5 | Preliminary safety and tolerability results of intravitreal administration of GS010, a recombinant adeno-associated viral vector serotype 2 (rAAV2/2) containing human wildtype mitochondrial NADH dehydrogenase 4 (ND4) gene in patients with Leber Hereditary Optic Neuropathy (LHON) due to the G11778A ND4 mitochondrial DNA mutation | 1 |
| 6 | 21 | |
| 7 | 11 | |
| 8 | 23 | |
| 9 | 13 | |
| 10 | 21 | |
| 11 | 31 | |
| 12 | 15 | |
| 13 | 73 | |
| 14 | 35 | |
| 15 | 19 |
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.