Magali Loyer
About
In The Last Decade
Magali Loyer
13 papers receiving 360 citations
Peers
Comparison fields: 5 of 50
- Molecular Biology 310
- Ophthalmology 169
- Genetics 86
- Cellular and Molecular Neuroscience 51
- Cell Biology 48
Countries citing papers authored by Magali Loyer
This map shows the geographic impact of Magali Loyer'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 Magali Loyer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Magali Loyer more than expected).
Fields of papers citing papers by Magali Loyer
This network shows the impact of papers produced by Magali Loyer. 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 Magali Loyer. The network helps show where Magali Loyer may publish in the future.
Co-authorship network of co-authors of Magali Loyer
This figure shows the co-authorship network connecting the top 25 collaborators of Magali Loyer. A scholar is included among the top collaborators of Magali Loyer 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 Magali Loyer. Magali Loyer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 21 | |
| 2 | 17 | |
| 3 | Functional analyses of mutant recessive GUCY2D alleles identified in Leber congenital amaurosis patients: protein domain comparisons and dominant negative effects. | 36 |
| 4 | A three base pair deletion encoding the amino acid (lysine-270) in the alpha-cone transducin gene. | 3 |
| 5 | 64 | |
| 6 | 21 | |
| 7 | 30 | |
| 8 | 91 | |
| 9 | Novel mutations and DNA-based screening in non-Jewish carriers of Tay-Sachs disease. | 15 |
| 10 | Pigment epithelium derived factor as a candidate gene for Leber's congenital amaurosis | 1 |
| 11 | 7 | |
| 12 | 23 | |
| 13 | Mutations participating in interallelic complementation in propionic acidemia. | 38 |
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.