Bernhard H. F. Weber

27.8k total citations · 3 hit papers
396 papers, 15.2k citations indexed

About

Bernhard H. F. Weber is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Bernhard H. F. Weber has authored 396 papers receiving a total of 15.2k indexed citations (citations by other indexed papers that have themselves been cited), including 236 papers in Molecular Biology, 148 papers in Ophthalmology and 79 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Bernhard H. F. Weber's work include Retinal Development and Disorders (147 papers), Retinal Diseases and Treatments (136 papers) and Retinal Imaging and Analysis (50 papers). Bernhard H. F. Weber is often cited by papers focused on Retinal Development and Disorders (147 papers), Retinal Diseases and Treatments (136 papers) and Retinal Imaging and Analysis (50 papers). Bernhard H. F. Weber collaborates with scholars based in Germany, United States and Canada. Bernhard H. F. Weber's co-authors include Heidi Stöhr, David Depew, Lars G. Fritsche, Claudia N. Keilhauer, Felix Graßmann, Karen L. White, Robert S. Molday, Andrea Rivera, Ute Felbor and Ulrich Kellner and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Bernhard H. F. Weber

382 papers receiving 14.7k citations

Hit Papers

Hypothetical LOC387715 is a second major susceptibility g... 1994 2026 2004 2015 2005 1994 2018 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bernhard H. F. Weber Germany 62 9.1k 6.8k 3.9k 1.8k 1.7k 396 15.2k
Alan C. Bird United Kingdom 85 11.0k 1.2× 18.0k 2.7× 10.2k 2.7× 1.2k 0.7× 1.6k 1.0× 354 24.8k
Alan F. Wright United Kingdom 58 6.9k 0.8× 3.0k 0.4× 1.7k 0.5× 3.6k 1.9× 1.0k 0.6× 227 11.9k
William W. Hauswirth United States 84 21.0k 2.3× 6.9k 1.0× 2.2k 0.6× 7.2k 3.9× 5.3k 3.2× 409 24.9k
Val C. Sheffield United States 91 17.1k 1.9× 6.6k 1.0× 2.5k 0.7× 10.4k 5.7× 1.6k 1.0× 312 27.6k
Edwin M. Stone United States 100 22.3k 2.5× 14.4k 2.1× 5.6k 1.4× 6.7k 3.7× 3.3k 2.0× 548 32.8k
Thaddeus P. Dryja United States 72 15.2k 1.7× 7.5k 1.1× 1.8k 0.5× 3.2k 1.7× 4.0k 2.4× 180 20.7k
David A. Mackey Australia 59 5.8k 0.6× 8.5k 1.3× 5.3k 1.4× 1.6k 0.9× 395 0.2× 443 15.1k
Alex W. Hewitt Australia 50 3.4k 0.4× 4.2k 0.6× 3.0k 0.8× 964 0.5× 347 0.2× 328 8.7k
Jeremy Nathans United States 90 21.9k 2.4× 3.0k 0.4× 1.2k 0.3× 2.7k 1.5× 8.9k 5.4× 202 27.3k
Peter Humphries Ireland 42 4.6k 0.5× 1.7k 0.3× 559 0.1× 731 0.4× 1.8k 1.1× 177 6.3k

Countries citing papers authored by Bernhard H. F. Weber

Since Specialization
Citations

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

Fields of papers citing papers by Bernhard H. F. Weber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bernhard H. F. Weber. 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 Bernhard H. F. Weber. The network helps show where Bernhard H. F. Weber may publish in the future.

Co-authorship network of co-authors of Bernhard H. F. Weber

This figure shows the co-authorship network connecting the top 25 collaborators of Bernhard H. F. Weber. A scholar is included among the top collaborators of Bernhard H. F. Weber 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 Bernhard H. F. Weber. Bernhard H. F. Weber 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.
Stöhr, Heidi & Bernhard H. F. Weber. (2025). Genetics and diagnostics of inherited retinal diseases in the era of whole genome sequencing. Medizinische Genetik. 37(1). 3–10. 1 indexed citations
2.
Kiel, Christina, Heidi Stöhr, Georg Spital, et al.. (2024). 18-Years of single-centre DNA testing in over 7000 index cases with inherited retinal dystrophies and optic neuropathies. Scientific Reports. 14(1). 25529–25529. 2 indexed citations
3.
Khan, Mubeen, Ketan Mishra, Laura Whelan, et al.. (2023). Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability. Human Genetics and Genomics Advances. 4(4). 100237–100237. 7 indexed citations
4.
Zimmermann, Martina E., Mathias Gorski, Felix Günther, et al.. (2023). Genetic Risk Score Analysis Supports a Joint View of Two Classification Systems for Age-Related Macular Degeneration. Investigative Ophthalmology & Visual Science. 64(12). 31–31. 2 indexed citations
5.
6.
Brandl, Caroline, Martina E. Zimmermann, Felix Günther, et al.. (2018). On the impact of different approaches to classify age-related macular degeneration: Results from the German AugUR study. Scientific Reports. 8(1). 8675–8675. 34 indexed citations
7.
Kellner, Ulrich, et al.. (2016). Wide-field MultiColor Spectral Imaging and Wide-field Spectral Domain Optical Coherence Tomography Imaging in Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 57(12). 146–146. 2 indexed citations
8.
Kellner, Ulrich, et al.. (2015). Inherited Retinal or Optic Nerve Disorders – Five Steps to Diagnosis (Originaltitel: Erbliche Netzhaut- und Sehbahnerkrankungen – 5 Schritte zur Diagnose). University of Regensburg Publication Server (University of Regensburg). 1 indexed citations
9.
Stellzig‐Eisenhauer, Angelika, Eva L. Decker, Philipp Meyer‐Marcotty, et al.. (2013). [Primary failure of eruption (PFE). Clinical and molecular genetics analysis] Article in French. University of Regensburg Publication Server (University of Regensburg). 2 indexed citations
10.
Weber, Bernhard H. F. & Thomas Langmann. (2013). Retinal degeneration : methods and protocols. Humana Press eBooks. 6 indexed citations
11.
Langmann, Thomas, Christoph Moehle, Marcus Karlstetter, & Bernhard H. F. Weber. (2013). Loss of MicroRNA-124 and MicroRNA-126 expression regulates inflammatory microglial activation in inherited retinal degeneration. Investigative Ophthalmology & Visual Science. 54(15). 4517–4517. 1 indexed citations
12.
Kellner, Ulrich, et al.. (2012). Hereditäre Netzhautdystrophien. Klinische Monatsblätter für Augenheilkunde. 229(2). 171–196. 3 indexed citations
13.
Hibbard, Michael, et al.. (2011). Toward One Oregon: Rural-Urban Interdependence and the Evolution of a State. 9 indexed citations
14.
Weinberger, A, Christine Skerka, Peter F. Zipfel, et al.. (2006). Intravitreal Levels of Human Complement Factor H (CFH). Investigative Ophthalmology & Visual Science. 47(13). 5240–5240. 1 indexed citations
15.
Mooy, Cornelia M., L. Ingeborgh van den Born, Seerp Baarsma, et al.. (2002). Hereditary X-Linked Juvenile Retinoschisis: A Review of the Role of Müller Cells. Archives of Ophthalmology. 120(7). 979–979. 48 indexed citations
16.
Weber, Bernhard H. F., Heinrich Schrewe, Laurie L. Molday, et al.. (2002). Inactivation of the murine X-linked juvenile retinoschisis gene, Rs1h, suggests a role of retinoschisin in retinal cell layer organisation and synaptic structure. University of Birmingham Research Portal (University of Birmingham). 181 indexed citations
17.
Weber, Bernhard H. F. & David Depew. (2001). Developmental Systems, Darwinian Evolution,and the Unity of Science. Nordic Journal of Psychiatry. 68(1). 53–9. 18 indexed citations
18.
Stöhr, Heidi, et al.. (2000). EST mining of the UniGene dataset to identify retina-specific genes. Cytogenetic and Genome Research. 91(1-4). 267–277. 21 indexed citations
19.
Collins, Colin C., Gordon B. Hutchinson, David Kowbel, et al.. (1992). The human β-subunit of rod photoreceptor cGMP phosphodiesterase: Complete retinal cDNA sequence and evidence for expression in brain. Genomics. 13(3). 698–704. 26 indexed citations
20.
Mosandl, Armin, Klaus Rettinger, Bernhard H. F. Weber, & Dominic Henn. (1990). Investigations on the enantiomer distribution of 2-methylbutanoic acid in fruits and other foodstuffs by multidimensional gas chromatography (MDGC).. Deutsche Lebensmittel-Rundschau. 86(12). 375–379. 14 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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