E Apfelstedt-Sylla

1.7k total citations
19 papers, 1.3k citations indexed

About

E Apfelstedt-Sylla is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ophthalmology. According to data from OpenAlex, E Apfelstedt-Sylla has authored 19 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Ophthalmology. Recurrent topics in E Apfelstedt-Sylla's work include Retinal Development and Disorders (15 papers), Photoreceptor and optogenetics research (6 papers) and Retinal Diseases and Treatments (6 papers). E Apfelstedt-Sylla is often cited by papers focused on Retinal Development and Disorders (15 papers), Photoreceptor and optogenetics research (6 papers) and Retinal Diseases and Treatments (6 papers). E Apfelstedt-Sylla collaborates with scholars based in Germany, United States and Poland. E Apfelstedt-Sylla's co-authors include Eberhart Zrenner, Mathias W. Seeliger, Samuel G. Jacobson, Susanne Kohl, Bernd Wissinger, Birgit Lorenz, Ulf Kretschmann, Ian Giddings, Klaus Rüther and Bernhard H. F. Weber and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and American Journal of Ophthalmology.

In The Last Decade

E Apfelstedt-Sylla

19 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
E Apfelstedt-Sylla Germany 15 1.2k 698 360 194 173 19 1.3k
Naheed W. Khan United States 23 1.4k 1.2× 706 1.0× 483 1.3× 181 0.9× 197 1.1× 43 1.6k
C.F. Inglehearn United Kingdom 19 1.2k 1.0× 410 0.6× 363 1.0× 216 1.1× 142 0.8× 34 1.3k
Rosa Riveiro-Álvarez Spain 24 1.2k 1.1× 640 0.9× 166 0.5× 160 0.8× 160 0.9× 53 1.5k
Gesine B. Jaissle Germany 23 1.1k 0.9× 1.2k 1.7× 386 1.1× 203 1.0× 688 4.0× 40 2.0k
Thaddeus P. Dryja United States 10 1.4k 1.2× 563 0.8× 578 1.6× 166 0.9× 112 0.6× 11 1.5k
Silke Feil Switzerland 19 1.3k 1.1× 375 0.5× 427 1.2× 256 1.3× 97 0.6× 33 1.4k
Sylvain Hanein France 20 1.3k 1.1× 535 0.8× 305 0.8× 195 1.0× 119 0.7× 45 1.6k
Markus N. Preising Germany 25 1.5k 1.3× 1.2k 1.8× 210 0.6× 264 1.4× 383 2.2× 77 1.8k
Dominique Ducroq France 17 1.2k 1.0× 756 1.1× 182 0.5× 161 0.8× 181 1.0× 20 1.3k
Carol Davenport United States 6 1.2k 1.0× 230 0.3× 630 1.8× 228 1.2× 70 0.4× 7 1.3k

Countries citing papers authored by E Apfelstedt-Sylla

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of E Apfelstedt-Sylla

This figure shows the co-authorship network connecting the top 25 collaborators of E Apfelstedt-Sylla. A scholar is included among the top collaborators of E Apfelstedt-Sylla 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 E Apfelstedt-Sylla. E Apfelstedt-Sylla is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Scholl, Hendrik P. N., H Langrová, Bernhard H. F. Weber, Eberhart Zrenner, & E Apfelstedt-Sylla. (2001). Clinical electrophysiology of two rod pathways: normative values and clinical application. Graefe s Archive for Clinical and Experimental Ophthalmology. 239(2). 71–80. 18 indexed citations
2.
Broghammer, Martina, Eberhart Zrenner, E Apfelstedt-Sylla, et al.. (2001). Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders. International Journal of Molecular Medicine. 8(1). 53–8. 1 indexed citations
3.
Seeliger, Mathias W., Eberhart Zrenner, E Apfelstedt-Sylla, & Gesine B. Jaissle. (2001). Identification of Usher syndrome subtypes by ERG implicit time.. PubMed. 42(12). 3066–71. 28 indexed citations
4.
Sadowski, Bettina, et al.. (2001). Tamoxifen Side Effects, Age-Related Macular Degeneration (AMD) or Cancer Associated Retinopathy (CAR)?. European Journal of Ophthalmology. 11(3). 309–312. 8 indexed citations
5.
Thompson, Debra A., P Gyürüs, Eve L. Bingham, et al.. (2000). Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.. PubMed. 41(13). 4293–9. 214 indexed citations
6.
Rivera, Andrea, Karen L. White, Heidi Stöhr, et al.. (2000). A Comprehensive Survey of Sequence Variation in the ABCA4 (ABCR) Gene in Stargardt Disease and Age-Related Macular Degeneration. The American Journal of Human Genetics. 67(4). 800–813. 277 indexed citations
7.
Kohl, Susanne, Ian Giddings, Herbert Jägle, et al.. (1998). Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel. Nature Genetics. 19(3). 257–259. 262 indexed citations
8.
Seeliger, Mathias W., Ulf Kretschmann, E Apfelstedt-Sylla, Klaus Rüther, & Eberhart Zrenner. (1998). Multifocal electroretinography in retinitis pigmentosa. American Journal of Ophthalmology. 125(2). 214–226. 80 indexed citations
9.
Seeliger, Mathias W., Ulf Kretschmann, E Apfelstedt-Sylla, & Eberhart Zrenner. (1998). Implicit time topography of multifocal electroretinograms.. PubMed. 39(5). 718–23. 55 indexed citations
10.
Kohl, Susanne, Ian Giddings, Dorothea Besch, et al.. (1998). The Role of the Peripherin/<i>RDS</i> Gene in Retinal Dystrophies. Cells Tissues Organs. 162(2-3). 75–84. 54 indexed citations
11.
Kretschmann, Ulf, Mathias W. Seeliger, Klaus Rüether, et al.. (1998). Multifocal electroretinography in patients with Stargardt's macular dystrophy. British Journal of Ophthalmology. 82(3). 267–275. 68 indexed citations
12.
Kohl, Susanne, E Apfelstedt-Sylla, Ulrich Kellner, et al.. (1997). RDS/peripherin gene mutations are frequent causes of central retinal dystrophies.. Journal of Medical Genetics. 34(8). 620–626. 54 indexed citations
13.
Felbor, Ute, Heidi Stöhr, Thomas Amann, et al.. (1996). A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy.. Journal of Medical Genetics. 33(3). 233–236. 28 indexed citations
14.
Rüther, Klaus, et al.. (1995). [Social ophthalmologic aspects of retinitis pigmentosa].. PubMed. 92(5). 704–7. 6 indexed citations
15.
16.
Apfelstedt-Sylla, E, M Horn, Klaus Rüther, et al.. (1993). Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsin.. British Journal of Ophthalmology. 77(8). 495–501. 26 indexed citations
17.
Rüether, Klaus, E Apfelstedt-Sylla, & Eberhart Zrenner. (1993). Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type.. PubMed. 2(6). 429–35. 24 indexed citations
18.
Rüther, Klaus, et al.. (1992). [Retinitis pigmentosa. Clinical findings, results of molecular genetic techniques and research perspectives].. PubMed. 89(1). 5–21. 3 indexed citations
19.
Apfelstedt-Sylla, E, et al.. (1992). Diffuse loss of rod function in autosomal dominant retinitis pigmentosa with pro-347-leu mutation of rhodopsin.. PubMed. 1(5). 319–27. 28 indexed citations

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Naheed W. Khan Breakdown of academic impact, for papers by C.F. Inglehearn Breakdown of academic impact, for papers by Rosa Riveiro-Álvarez Breakdown of academic impact, for papers by Gesine B. Jaissle Breakdown of academic impact, for papers by Thaddeus P. Dryja Breakdown of academic impact, for papers by Silke Feil Breakdown of academic impact, for papers by Sylvain Hanein Breakdown of academic impact, for papers by Markus N. Preising Breakdown of academic impact, for papers by Dominique Ducroq Breakdown of academic impact, for papers by Carol Davenport
Rankless by CCL
2026