Thomas Rosenberg
- Ophthalmology top 0.2%
- Retinal Diseases and Treatments 40
- Sensory Systems top 1%
- Molecular Biology top 1%
- Retinal Development and Disorders 69
- Connexins and lens biology 24
- Mitochondrial Function and Pathology 19
- RNA regulation and disease 16
- Genetics top 1%
- Cell Biology top 1%
- melanin and skin pigmentation 16
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- Ophthalmology and Visual Impairment Studies 19
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- Retinopathy of Prematurity Studies 16
- Co-authors
- W WilbrandtHans EibergKaren GrønskovKaren Brøndum‐NielsenBirgit KjerMarianne SchwartzMarianne HaimP Kjer
- Journals
- Investigative Ophthalmology & Visual Science (29 papers)Acta Ophthalmologica (19 papers)Human Mutation (11 papers)
- Partner nations
- DenmarkUnited StatesGermany
In The Last Decade
Thomas Rosenberg
200 papers receiving 7.4k citations
Hit Papers
Peers
Comparison fields: 5 of 150
- Ophthalmology 2.3k
- Sensory Systems 409
- Molecular Biology 5.3k
- Genetics 1.8k
- Cell Biology 954
Countries citing papers authored by Thomas Rosenberg
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
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
The 25 scholars most cited alongside Thomas Rosenberg, 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 | 2024 | 3 | |
| 2 | 2024 | 1 | |
| 3 | 2017 | 13 | |
| 4 | Whole Exome Sequencing Identifies a Rare Variant Co-segregating with High Myopia | 2016 | 1 |
| 5 | 2015 | 8 | |
| 6 | Outcome of cataract surgery in patients with Retinitis Pigmentosa | 2012 | 2 |
| 7 | A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases. | 2011 | 50 |
| 8 | Cone Density And Color Discrimination In Oligocone Trichromacy | 2011 | 1 |
| 9 | Mutation Analysis in a Cohort of CSNB Patients: Novel Mutations in TRPM1 Gene | 2010 | 1 |
| 10 | Adaptive Optics Imaging of the Cone Mosaic in Oligocone Trichromacy | 2010 | 1 |
| 11 | Phenotypic Variability in Genetically Defined X-linked Congenital Stationary Night Blindness | 2009 | 2 |
| 12 | N965S is a common ABCA4 variant in Stargardt-related retinopathies in the Danish population. | 2007 | 52 |
| 13 | Variation of Phenotype in Patients With Compound Heterozygous Mutations of RetGC1 Depending on the Affected Domains | 2006 | 2 |
| 14 | Bardet–Biedl Syndrome: Does BBS2 Result in A More Serious Phenotype Than BBS1? | 2006 | 0 |
| 15 | Screening of NUB1 in Patients With Leber Congenital Amaurosis | 2003 | 1 |
| 16 | 2003 | 15 | |
| 17 | A comprehensive survey of spectrum of mutations in the OPA1 gene in patients with optic atrophy | 2002 | 1 |
| 18 | OPA1 gene mutations cluster in functional protein domains in ADOA patients and reveal a founder allele in the Danish population. | 2001 | 1 |
| 19 | 1996 | 28 | |
| 20 | Hereditær opticusatrofi. En klinisk-genealogisk status over danske "Leber-slægter" | 1995 | 1 |
About Thomas Rosenberg
Thomas Rosenberg is a scholar working on Ophthalmology, Sensory Systems and Molecular Biology, having authored 205 papers that have together received 7.7k indexed citations. Recurring topics across this work include Retinal Development and Disorders (69 papers), Retinal Diseases and Treatments (40 papers), Connexins and lens biology (24 papers), Ophthalmology and Visual Impairment Studies (19 papers), Mitochondrial Function and Pathology (19 papers), RNA regulation and disease (16 papers), melanin and skin pigmentation (16 papers) and Retinopathy of Prematurity Studies (16 papers). The work is most often cited by research in Ophthalmology (2.3k citations), Sensory Systems (409 citations) and Molecular Biology (5.3k citations). Thomas Rosenberg has collaborated with scholars based in Denmark, United States and Germany. Frequent 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. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Acta Ophthalmologica, Human Mutation, European Journal of Human Genetics and Human Genetics.
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.