Rando Allikmets
About
In The Last Decade
Rando Allikmets
211 papers receiving 14.6k citations
Hit Papers
Peers
Comparison fields: 5 of 142
- Molecular Biology 9.1k
- Ophthalmology 6.3k
- Oncology 2.6k
- Radiology, Nuclear Medicine and Imaging 2.3k
- Immunology 2.0k
Countries citing papers authored by Rando Allikmets
This map shows the geographic impact of Rando Allikmets'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 Rando Allikmets with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rando Allikmets more than expected).
Fields of papers citing papers by Rando Allikmets
This network shows the impact of papers produced by Rando Allikmets. 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 Rando Allikmets. The network helps show where Rando Allikmets may publish in the future.
Co-authorship network of co-authors of Rando Allikmets
This figure shows the co-authorship network connecting the top 25 collaborators of Rando Allikmets. A scholar is included among the top collaborators of Rando Allikmets 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 Rando Allikmets. Rando Allikmets is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 6 | |
| 2 | 9 | |
| 3 | 1 | |
| 4 | 22 | |
| 5 | Rare variants in the phosphoglycerate dehydrogenase (PHGDH) gene in MacTel patients lead to decreased enzymatic activity | 1 |
| 6 | In silico functional meta-analysis of 5,962 ABCA4 variants in 3,928 Stargardt disease and cone-rod dystrophy cases | 1 |
| 7 | 39 | |
| 8 | Genome-Wide Association Study of Advanced Age-Related Macular Degeneration Identifies a New Susceptibility Locus in the Lipid Metabolism Pathway, Hepatic Lipase (LIPC) | 1 |
| 9 | Peripapillary Atrophy in Stargardt Disease | 6 |
| 10 | Autofluorescence Metrics in Stargardt Disease | 1 |
| 11 | The Phenotypes of Patients and Heterozygous Carriers With RDH12 Mutations Are Different From Those With RPE65 Mutations | 1 |
| 12 | Linkage and mutation analysis to identify the gene associated with macular degeneration segregating in a cynomolgus monkey (Macaca fascicularis) pedigree. | 1 |
| 13 | 26 | |
| 14 | Isolation and characterization of a novel RPE fluorophore:An all–trans–retinal dimer. | 4 |
| 15 | MULTIALLELIC INHERITANCE AND/OR MODIFIER ALLELES IN LEBER CONGENITAL AMAUROSIS: ANALYSIS WITH THE LCA DISEASE CHIP | 2 |
| 16 | Phenotype-Genotype Correlation in Patients With the Goldmann-Favre Syndrome | 1 |
| 17 | Evaluation of Laminin Genes (LAMC1, LAMC2 and LAMB3) in Patients with Age-related Maculopathy | 1 |
| 18 | New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease. | 69 |
| 19 | 313 | |
| 20 | 188 |
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.