Günther Rudolph

2.8k total citations
64 papers, 1.1k citations indexed

About

Günther Rudolph is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Günther Rudolph has authored 64 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 35 papers in Ophthalmology and 10 papers in Genetics. Recurrent topics in Günther Rudolph's work include Retinal Development and Disorders (25 papers), Retinal Diseases and Treatments (17 papers) and Glaucoma and retinal disorders (12 papers). Günther Rudolph is often cited by papers focused on Retinal Development and Disorders (25 papers), Retinal Diseases and Treatments (17 papers) and Glaucoma and retinal disorders (12 papers). Günther Rudolph collaborates with scholars based in Germany, United Kingdom and United States. Günther Rudolph's co-authors include Christos Haritoglou, Bernhard H. F. Weber, Ulrich Kellner, Susanne Kohl, Bernd Wissinger, Franziska Krämer, Eberhart Zrenner, Thomas Berninger, Antje Bernd and Anselm Kampik and has published in prestigious journals such as The Lancet, Neurology and Scientific Reports.

In The Last Decade

Günther Rudolph

61 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Günther Rudolph Germany 19 809 646 204 187 124 64 1.1k
Philipp Herrmann Germany 20 752 0.9× 912 1.4× 160 0.8× 407 2.2× 108 0.9× 72 1.3k
Joseph C. Giacalone United States 19 1.3k 1.6× 433 0.7× 463 2.3× 180 1.0× 88 0.7× 37 1.7k
T. Michael Nork United States 23 1.0k 1.3× 1.2k 1.9× 135 0.7× 552 3.0× 84 0.7× 89 1.8k
Muhammad Imran Khan Netherlands 20 663 0.8× 496 0.8× 242 1.2× 151 0.8× 90 0.7× 66 1.0k
Fiona Blanco‐Kelly Spain 23 1.3k 1.6× 517 0.8× 358 1.8× 137 0.7× 121 1.0× 70 1.6k
Gezhi Xu China 21 773 1.0× 962 1.5× 83 0.4× 535 2.9× 106 0.9× 112 1.6k
Frank C. Schlichtenbrede Germany 20 720 0.9× 910 1.4× 265 1.3× 618 3.3× 36 0.3× 50 1.5k
Caroline Thaung United Kingdom 13 319 0.4× 232 0.4× 134 0.7× 137 0.7× 57 0.5× 57 619
J. R. Samples United States 18 516 0.6× 1.1k 1.7× 267 1.3× 410 2.2× 214 1.7× 28 1.7k
David Bessant United Kingdom 14 292 0.4× 345 0.5× 99 0.5× 279 1.5× 52 0.4× 21 639

Countries citing papers authored by Günther Rudolph

Since Specialization
Citations

This map shows the geographic impact of Günther Rudolph'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 Günther Rudolph with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Günther Rudolph more than expected).

Fields of papers citing papers by Günther Rudolph

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Günther Rudolph. 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 Günther Rudolph. The network helps show where Günther Rudolph may publish in the future.

Co-authorship network of co-authors of Günther Rudolph

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

All Works

20 of 20 papers shown
1.
Priglinger, Claudia, Maximilian Gerhardt, Günther Rudolph, Siegfried Priglinger, & Stylianos Michalakis. (2023). Gentherapie in der Augenheilkunde. Die Ophthalmologie. 120(8). 867–882.
2.
Gerhardt, Maximilian, Claudia Priglinger, Günther Rudolph, et al.. (2022). Gene Therapy with Voretigene Neparvovec Improves Vision and Partially Restores Electrophysiological Function in Pre-School Children with Leber Congenital Amaurosis. Biomedicines. 11(1). 103–103. 21 indexed citations
3.
Michalakis, Stylianos, et al.. (2022). RPE65-assoziierte Netzhautdystrophie: Gentherapie kann das Sehen verbessern. MMW - Fortschritte der Medizin. 164(S4). 40–41. 1 indexed citations
4.
Štingl, Katarína, Anja K. Mayer, Lejla Mulahasanovic, et al.. (2017). CDHR1 mutations in retinal dystrophies. Scientific Reports. 7(1). 6992–6992. 34 indexed citations
5.
Nentwich, Michael, et al.. (2015). Genotyp-Phänotyp-Korrelation bei Patienten mit PRPH2-Mutationen. Klinische Monatsblätter für Augenheilkunde. 232(3). 266–274. 4 indexed citations
6.
Nentwich, Martin M., et al.. (2015). Artificial Iris Implantation in a 9-Year-Old Boy. European Journal of Ophthalmology. 25(6). e109–e111. 1 indexed citations
7.
Zobor, Ditta, Franco Stanzial, Ulrich Kellner, et al.. (2014). Retinal structure and function in Achromatopsia: the CNGA3 phenotype. 55(13). 346–346. 1 indexed citations
8.
Kampik, Anselm, et al.. (2010). Ablatio retinae bei Kindern und Jugendlichen: Ätiologie und Risikofaktoren. Der Ophthalmologe. 107(2). 165–174. 1 indexed citations
9.
Kampik, Anselm, et al.. (2009). Ablatio retinae bei Kindern und Jugendlichen. Der Ophthalmologe. 107(2). 165–174. 4 indexed citations
10.
Kitiratschky, Veronique, Antje Bernd, Eberhart Zrenner, et al.. (2008). ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies. European Journal of Human Genetics. 16(7). 812–819. 49 indexed citations
11.
Fisher, Sheila, Andrea Rivera, Lars G. Fritsche, et al.. (2007). Case-control genetic association study of fibulin-6 (FBLN6orHMCN1) variants in age-related macular degeneration (AMD). Human Mutation. 28(4). 406–413. 25 indexed citations
12.
Kampik, Anselm, et al.. (2004). Zentrale Pigmentepitheldefekte bei einer 33-jhrigen Patientin: Eine 33-jhrige Patientin mit neurologischer Symptomatik, zentralen Pigmentepitheldefekten und eingeschrnkter Blickhebung. Der Ophthalmologe. 101(8). 1 indexed citations
13.
Rudolph, Günther, et al.. (2004). Klinische und genetische Befunde unter besonderer Betrachtung kornealer Ver�nderungen bei Lowe-Syndrom. Der Ophthalmologe. 101(6). 595–9. 1 indexed citations
14.
Neubauer, Aljoscha S., et al.. (2004). The Multifocal Pattern Electroretinogram in Chloroquine Retinopathy. Ophthalmic Research. 36(2). 106–113. 5 indexed citations
15.
Wolf, Armin, et al.. (2004). Zentrale Pigmentepitheldefekte bei einer 33-j�hrigen Patientin. Der Ophthalmologe. 101(8). 841–2. 1 indexed citations
16.
Klopp, Norman, Elise Héon, Gail Billingsley, et al.. (2003). Further Genetic Heterogeneity for Autosomal Dominant Human Sutural Cataracts. Ophthalmic Research. 35(2). 71–77. 12 indexed citations
17.
18.
Sauer, Christian, Karen L. White, Ulrich Kellner, et al.. (2001). EFEMP1 is not associated with sporadic early onset drusen. Ophthalmic Genetics. 22(1). 27–34. 7 indexed citations
19.
Schworm, Hermann Dieter & Günther Rudolph. (2000). Comitant strabismus. Current Opinion in Ophthalmology. 11(5). 310–317. 3 indexed citations
20.
Mansergh, Fiona C., Paul F. Kenna, Günther Rudolph, et al.. (1995). Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.. Journal of Medical Genetics. 32(11). 855–858. 7 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.

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