Thomas Rosenberg

12.2k total citations · 1 hit paper
205 papers, 7.7k citations indexed

About

Thomas Rosenberg is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Thomas Rosenberg has authored 205 papers receiving a total of 7.7k indexed citations (citations by other indexed papers that have themselves been cited), including 124 papers in Molecular Biology, 59 papers in Ophthalmology and 39 papers in Genetics. Recurrent topics in Thomas Rosenberg's work include Retinal Development and Disorders (69 papers), Retinal Diseases and Treatments (40 papers) and Connexins and lens biology (24 papers). Thomas Rosenberg is often cited by papers focused on Retinal Development and Disorders (69 papers), Retinal Diseases and Treatments (40 papers) and Connexins and lens biology (24 papers). Thomas Rosenberg collaborates with scholars based in Denmark, United States and Germany. Thomas Rosenberg's co-authors include W Wilbrandt, Hans Eiberg, Karen Grønskov, Karen Brøndum‐Nielsen, Birgit Kjer, Marianne Schwartz, Marianne Haim, P Kjer, Lars Hestbjerg Hansen and Ruth Riise and has published in prestigious journals such as Nature Genetics, Annals of Neurology and Scientific Reports.

In The Last Decade

Thomas Rosenberg

200 papers receiving 7.4k citations

Hit Papers

THE CONCEPT OF CARRIER TRANSPORT AND ITS COROLLARIES IN P... 1961 2026 1982 2004 1961 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Rosenberg Denmark 52 5.3k 2.3k 1.8k 1.0k 954 205 7.7k
Josseline Kaplan France 41 6.9k 1.3× 2.6k 1.1× 1.4k 0.8× 773 0.8× 1.0k 1.1× 172 9.0k
Anthony T. Moore United Kingdom 45 5.9k 1.1× 2.3k 1.0× 1.6k 0.9× 895 0.9× 729 0.8× 107 8.0k
Daniel F. Schorderet Switzerland 49 5.7k 1.1× 2.3k 1.0× 1.9k 1.1× 1.7k 1.7× 1.4k 1.5× 253 9.4k
J. Fielding Hejtmancik United States 48 5.6k 1.1× 2.0k 0.9× 2.0k 1.1× 567 0.6× 718 0.8× 191 7.2k
Andreas Gal Germany 57 6.9k 1.3× 2.1k 0.9× 1.8k 1.0× 519 0.5× 1.7k 1.8× 217 11.4k
Eyal Banin Israel 45 4.9k 0.9× 2.4k 1.0× 1.3k 0.7× 1.0k 1.0× 555 0.6× 183 6.4k
Elise Héon Canada 44 5.1k 1.0× 3.9k 1.7× 1.7k 0.9× 1.5k 1.5× 833 0.9× 144 7.3k
Anthony T. Moore United Kingdom 55 8.4k 1.6× 5.7k 2.5× 1.8k 1.0× 1.9k 1.9× 1000 1.0× 266 10.7k
Michael B. Gorin United States 40 3.0k 0.6× 2.5k 1.1× 781 0.4× 1.4k 1.3× 415 0.4× 147 5.5k
Anneke I. den Hollander Netherlands 57 7.8k 1.5× 6.4k 2.8× 1.7k 1.0× 2.7k 2.7× 1.4k 1.5× 230 11.1k

Countries citing papers authored by Thomas Rosenberg

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Rosenberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Rosenberg

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Rosenberg. A scholar is included among the top collaborators of Thomas Rosenberg 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 Thomas Rosenberg. Thomas Rosenberg 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.
Rönnbäck, Cecilia, Cathrine Jespersgaard, Line Kessel, et al.. (2024). A novel GFAP frameshift variant identified in a family with optico-retinal dysplasia and vision impairment. Human Molecular Genetics. 33(24). 2145–2158. 1 indexed citations
3.
Tompson, Stuart W., Kristina N. Whisenhunt, Samuel J. Huang, et al.. (2017). Exome Sequence Analysis of 14 Families With High Myopia. Investigative Ophthalmology & Visual Science. 58(4). 1982–1982. 13 indexed citations
4.
Tompson, Stuart W., et al.. (2016). Whole Exome Sequencing Identifies a Rare Variant Co-segregating with High Myopia. Investigative Ophthalmology & Visual Science. 57(12). 3606–3606. 1 indexed citations
5.
Rendtorff, Nanna Dahl, Lisbeth Tranebjærg, Karen Grønskov, et al.. (2016). Usher syndrome in Denmark: mutation spectrum and some clinical observations. Molecular Genetics & Genomic Medicine. 4(5). 527–539. 20 indexed citations
6.
Rendtorff, Nanna Dahl, Anders Albrechtsen, Mana M. Mehrjouy, et al.. (2015). Partial USH2A deletions contribute to Usher syndrome in Denmark. European Journal of Human Genetics. 23(12). 1646–1651. 8 indexed citations
7.
Baraas, Rigmor C., et al.. (2011). Cone Density And Color Discrimination In Oligocone Trichromacy. Investigative Ophthalmology & Visual Science. 52(14). 3197–3197. 1 indexed citations
8.
Rha, Jungtae, Melissa Wagner-Schuman, Anthony T. Moore, et al.. (2010). Adaptive Optics Imaging of the Cone Mosaic in Oligocone Trichromacy. Investigative Ophthalmology & Visual Science. 51(13). 6296–6296. 1 indexed citations
9.
Bech‐Hansen, N. Torben, Catrina M. Loucks, Chandree L. Beaulieu, et al.. (2010). Mutation Analysis in a Cohort of CSNB Patients: Novel Mutations in TRPM1 Gene. Investigative Ophthalmology & Visual Science. 51(13). 4129–4129. 1 indexed citations
10.
Robitaille, Johane M., et al.. (2009). Phenotypic Variability in Genetically Defined X-linked Congenital Stationary Night Blindness. Investigative Ophthalmology & Visual Science. 50(13). 3721–3721. 2 indexed citations
11.
Grønskov, Karen, et al.. (2006). Bardet–Biedl Syndrome: Does BBS2 Result in A More Serious Phenotype Than BBS1?. Investigative Ophthalmology & Visual Science. 47(13). 4621–4621.
12.
Sjølie, Anne Katrin, et al.. (2003). The prevalence and incidence of visual impairment in people of age 20–59 years in industrialized countries: A review. Ophthalmic Epidemiology. 10(4). 279–291. 15 indexed citations
13.
Sitorus, Rita S., et al.. (2003). Screening of NUB1 in Patients With Leber Congenital Amaurosis. Investigative Ophthalmology & Visual Science. 44(13). 2317–2317. 1 indexed citations
14.
Thiselton, Dawn L., Christiane Alexander, Simon P. Brooks, et al.. (2001). A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect. Human Genetics. 109(5). 498–502. 50 indexed citations
15.
Thiselton, Dawn L., Christiane Alexander, Susan Sklower Brooks, et al.. (2001). OPA1 gene mutations cluster in functional protein domains in ADOA patients and reveal a founder allele in the Danish population.. UCL Discovery (University College London). 1 indexed citations
16.
Tranebjærg, Lisbeth, Thomas Rosenberg, Claes Möller, et al.. (2001). A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation. The American Journal of Human Genetics. 69(1). 228–234. 67 indexed citations
17.
Rosenberg, Thomas, et al.. (1996). The incidence of registered blindness caused by age‐related macular degeneration. Acta Ophthalmologica Scandinavica. 74(4). 399–402. 28 indexed citations
18.
Rosenberg, Thomas, et al.. (1995). Hereditær opticusatrofi. En klinisk-genealogisk status over danske "Leber-slægter". Ugeskrift for Læger. 2707–2711. 1 indexed citations
19.
Eiberg, Hans, Birgit Kjer, P Kjer, & Thomas Rosenberg. (1994). Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis. Human Molecular Genetics. 3(6). 977–980. 115 indexed citations
20.
Rosenberg, Thomas, et al.. (1989). Autosomal dominant congenital cataract Morphology and genetic mapping. Acta Ophthalmologica. 67(2). 151–158. 50 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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