Ola Sandgren
Impact in
- Ophthalmology top 0.5%
- Retinal Diseases and Treatments
- Glaucoma and retinal disorders
- Molecular Biology top 5%
- Retinal Development and Disorders
- Amyloidosis: Diagnosis, Treatment, Outcomes
Papers in
-
- Retinal Development and Disorders 23
- Amyloidosis: Diagnosis, Treatment, Outcomes 18
-
- Retinal Diseases and Treatments 11
- Glaucoma and retinal disorders 4
- Co-authors
- Gösta Holmgren (13 shared papers)Marie Burstedt (16 shared papers)Irina Golovleva (17 shared papers)Sten Andréasson (4 shared papers)Kristina Forsman‐Semb (4 shared papers)Claes Wadelius (4 shared papers)Ulf Drugge (3 shared papers)Konstantin Petrukhin (2 shared papers)
- Journals
- Acta Ophthalmologica (5 papers)Amyloid (4 papers)European Journal of Human Genetics (3 papers)Ophthalmic Genetics (3 papers)Advances in experimental medicine and biology (3 papers)
- Partner nations
- SwedenUnited StatesJapan
In The Last Decade
Ola Sandgren
49 papers receiving 2.0k citations
Ola Sandgren's Hit Papers
Peers
Comparison fields: 5 of 75
- Ophthalmology 696
- Molecular Biology 1.8k
- Cell Biology 345
- Cellular and Molecular Neuroscience 325
- Genetics 259
Countries citing papers authored by Ola Sandgren
This map shows the geographic impact of Ola Sandgren'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 Ola Sandgren with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ola Sandgren more than expected).
Fields of papers citing papers by Ola Sandgren
This network shows the impact of papers produced by Ola Sandgren. 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 Ola Sandgren. The network helps show where Ola Sandgren may publish in the future.
Co-authors
The 25 scholars most cited alongside Ola Sandgren, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 49 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Identification of the gene responsible for Best macular dystrophy Hit paper breakdown → | 1998 | 541 |
| 2 | 1993 | 120 | |
| 3 | Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26. | 1999 | 104 |
| 4 | 1995 | 87 | |
| 5 | 1999 | 84 | |
| 6 | 1995 | 62 | |
| 7 | 1996 | 61 | |
| 8 | Ocular phenotype of bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene. | 2001 | 59 |
| 9 | 2003 | 57 | |
| 10 | 1995 | 57 | |
| 11 | 2008 | 48 | |
| 12 | 2007 | 48 | |
| 13 | 1988 | 44 | |
| 14 | 2015 | 41 | |
| 15 | 1998 | 39 | |
| 16 | 1991 | 38 | |
| 17 | 1992 | 38 | |
| 18 | 2005 | 30 | |
| 19 | 2008 | 26 | |
| 20 | 1990 | 25 |
About Ola Sandgren
Ola Sandgren is a scholar working on Molecular Biology, Ophthalmology, Cell Biology, Genetics and Physiology, having authored 49 papers that have together received 2.0k indexed citations. Recurring topics across this work include Retinal Development and Disorders (23 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (18 papers), Retinal Diseases and Treatments (11 papers), Dermatological and Skeletal Disorders (9 papers), Alzheimer's disease research and treatments (7 papers), Cellular transport and secretion (5 papers), Glaucoma and retinal disorders (4 papers) and Trace Elements in Health (4 papers). The work is most often cited by research in Ophthalmology (696 citations), Molecular Biology (1.8k citations), Cell Biology (345 citations), Cellular and Molecular Neuroscience (325 citations) and Genetics (259 citations). Ola Sandgren has collaborated with scholars based in Sweden, United States and Japan. Frequent co-authors include Gösta Holmgren, Marie Burstedt, Irina Golovleva, Sten Andréasson, Kristina Forsman‐Semb, Claes Wadelius, Ulf Drugge, Konstantin Petrukhin, Benjamin Bakall and Kristina Forsman. Their work appears in journals such as Acta Ophthalmologica, Amyloid, European Journal of Human Genetics, Ophthalmic Genetics and Advances in experimental medicine and biology.
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.