Kristina Narfström
About
In The Last Decade
Kristina Narfström
113 papers receiving 2.9k citations
Peers
Comparison fields: 5 of 115
- Molecular Biology 2.2k
- Ophthalmology 1.1k
- Cellular and Molecular Neuroscience 819
- Genetics 599
- Radiology, Nuclear Medicine and Imaging 337
Countries citing papers authored by Kristina Narfström
This map shows the geographic impact of Kristina Narfström'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 Kristina Narfström with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kristina Narfström more than expected).
Fields of papers citing papers by Kristina Narfström
This network shows the impact of papers produced by Kristina Narfström. 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 Kristina Narfström. The network helps show where Kristina Narfström may publish in the future.
Co-authorship network of co-authors of Kristina Narfström
This figure shows the co-authorship network connecting the top 25 collaborators of Kristina Narfström. A scholar is included among the top collaborators of Kristina Narfström 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 Kristina Narfström. Kristina Narfström is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 26 | |
| 2 | 33 | |
| 3 | 17 | |
| 4 | CrxRdy Cat: An Excellent Large Animal Model For Severe Dominant Retinopathies Associated With CRX Mutations Based On Its Functional And Structural Characterization | 1 |
| 5 | 107 | |
| 6 | Development of Müller-Like Cells After Subretinal Transplantation of Feline Red Fluorescent Retinal Progenitors in Abyssinian Cat Hereditary Retinal Degeneration | 1 |
| 7 | Evaluation of Intravitreal cis-Retinoid Replacement Therapy in a Canine Model of Leber’s Congenital Amaurosis | 2 |
| 8 | Assessment of Retinal Function in Normal Cats and in Cats Affected with the CEP290 Mutation Using Scotopic and Photopic ERG Light Intensity Series | 1 |
| 9 | 25 | |
| 10 | An Optimized Adeno-Associated Virus (AAV) for Treatment of Leber Congenital Amaurosis (LCA-RPE65) | 1 |
| 11 | 17 | |
| 12 | Functional and Structural Assessment of Retinal Sheet Allograft Transplantation in Feline Hereditary Retinal Degeneration | 10 |
| 13 | 10 | |
| 14 | 10 | |
| 15 | Enrofloxacin and the Feline Retina | 1 |
| 16 | A BLIND TRIAL VERIFICATION AND RULES FOR USE OF AN OPTIMIZED EQUATION, COMBINING SELECTED ERG SCORES, TO EFFICIENTLY DETECT RECESSIVE ROD CONE DEGENERATION IN ABYSSINIAN CATS. | 2 |
| 17 | The Systemic and Ocular Immune Response After Recombinant Adeno-Associated Virus Gene Transfer of RPE65 in 6 Dogs Affected With the RPE65 Null Mutation | 1 |
| 18 | Electroretinographic Monitoring of Gene Therapy Treated RPE65 Null Mutation Dog, a Model for Human Leber's Congenital Amaurosis | 1 |
| 19 | Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect. | 178 |
| 20 | 15 |
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.