Marion Neuillé
About
In The Last Decade
Marion Neuillé
12 papers receiving 275 citations
Peers
Comparison fields: 5 of 38
- Molecular Biology 244
- Cellular and Molecular Neuroscience 131
- Ophthalmology 81
- Genetics 28
- Endocrinology, Diabetes and Metabolism 26
Countries citing papers authored by Marion Neuillé
This map shows the geographic impact of Marion Neuillé'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 Marion Neuillé with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marion Neuillé more than expected).
Fields of papers citing papers by Marion Neuillé
This network shows the impact of papers produced by Marion Neuillé. 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 Marion Neuillé. The network helps show where Marion Neuillé may publish in the future.
Co-authorship network of co-authors of Marion Neuillé
This figure shows the co-authorship network connecting the top 25 collaborators of Marion Neuillé. A scholar is included among the top collaborators of Marion Neuillé 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 Marion Neuillé. Marion Neuillé is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 13 | |
| 2 | 5 | |
| 3 | 20 | |
| 4 | 12 | |
| 5 | Novel mutations in SLC24A1 leading to congenital stationary night blindness (CSNB) | 1 |
| 6 | 41 | |
| 7 | LRIT3 is essential to localize TRPM1 to the dendritic tips of ON-bipolar cells and may play a role in cone synapse formation | 1 |
| 8 | 42 | |
| 9 | 39 | |
| 10 | 45 | |
| 11 | Whole exome sequencing identifies mutations in LRIT3 as a cause for autosomal recessive complete congenital stationary night blindness | 2 |
| 12 | 55 |
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.