E Apfelstedt-Sylla
- Ophthalmology top 0.5%
- Retinal Diseases and Treatments 6
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- Photoreceptor and optogenetics research 6
- Neuroscience and Neural Engineering 2
- Neuroscience and Neuropharmacology Research 2
- Molecular Biology top 10%
- Retinal Development and Disorders 15
- Retinoids in leukemia and cellular processes 2
- Cell Biology top 10%
- Sensory Systems top 10%
- Hearing, Cochlea, Tinnitus, Genetics 1
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- Retinopathy of Prematurity Studies 2
- Co-authors
- Eberhart ZrennerMathias W. SeeligerSamuel G. JacobsonBernd WissingerSusanne KohlBirgit LorenzUlf KretschmannIan Giddings
- Journals
- Nature Genetics (1 paper)The American Journal of Human Genetics (1 paper)American Journal of Ophthalmology (1 paper)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
E Apfelstedt-Sylla
19 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 63
- Ophthalmology 698
- Cellular and Molecular Neuroscience 360
- Molecular Biology 1.2k
- Cell Biology 194
- Sensory Systems 38
Countries citing papers authored by E Apfelstedt-Sylla
This map shows the geographic impact of E Apfelstedt-Sylla'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 E Apfelstedt-Sylla with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E Apfelstedt-Sylla more than expected).
Fields of papers citing papers by E Apfelstedt-Sylla
This network shows the impact of papers produced by E Apfelstedt-Sylla. 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 E Apfelstedt-Sylla. The network helps show where E Apfelstedt-Sylla may publish in the future.
Co-authorship network
The 25 scholars most cited alongside E Apfelstedt-Sylla, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 1 | |
| 2 | 2001 | 18 | |
| 3 | Identification of Usher syndrome subtypes by ERG implicit time. | 2001 | 28 |
| 4 | 2001 | 8 | |
| 5 | Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration. | 2000 | 214 |
| 6 | 2000 | 277 | |
| 7 | 1998 | 80 | |
| 8 | 1998 | 262 | |
| 9 | Implicit time topography of multifocal electroretinograms. | 1998 | 55 |
| 10 | 1998 | 54 | |
| 11 | 1998 | 68 | |
| 12 | 1997 | 54 | |
| 13 | 1996 | 28 | |
| 14 | [Social ophthalmologic aspects of retinitis pigmentosa]. | 1995 | 6 |
| 15 | 1995 | 57 | |
| 16 | 1993 | 26 | |
| 17 | Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type. | 1993 | 24 |
| 18 | [Retinitis pigmentosa. Clinical findings, results of molecular genetic techniques and research perspectives]. | 1992 | 3 |
| 19 | Diffuse loss of rod function in autosomal dominant retinitis pigmentosa with pro-347-leu mutation of rhodopsin. | 1992 | 28 |
About E Apfelstedt-Sylla
E Apfelstedt-Sylla is a scholar working on Ophthalmology, Cellular and Molecular Neuroscience and Molecular Biology, having authored 19 papers that have together received 1.3k indexed citations. Recurring topics across this work include Retinal Development and Disorders (15 papers), Photoreceptor and optogenetics research (6 papers), Retinal Diseases and Treatments (6 papers), Neuroscience and Neural Engineering (2 papers), Retinoids in leukemia and cellular processes (2 papers), Neuroscience and Neuropharmacology Research (2 papers), Retinopathy of Prematurity Studies (2 papers) and Hearing, Cochlea, Tinnitus, Genetics (1 paper). The work is most often cited by research in Ophthalmology (698 citations), Cellular and Molecular Neuroscience (360 citations) and Molecular Biology (1.2k citations). E Apfelstedt-Sylla has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Eberhart Zrenner, Mathias W. Seeliger, Samuel G. Jacobson, Bernd Wissinger, Susanne Kohl, Birgit Lorenz, Ulf Kretschmann, Ian Giddings, Klaus Rüther and Bernhard H. F. Weber. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics and American Journal of Ophthalmology.
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.