Inga Ebermann
Impact in
- Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
- Neurology top 5%
- Vestibular and auditory disorders
Papers in
-
- Hearing, Cochlea, Tinnitus, Genetics 12
-
- Retinal Development and Disorders 3
- Connexins and lens biology 2
- DNA Repair Mechanisms 1
- Co-authors
- Hanno J. Bolz (17 shared papers)Gudrun Nürnberg (9 shared papers)Peter Nürnberg (9 shared papers)Peter Charbel Issa (3 shared papers)Hendrik P. N. Scholl (3 shared papers)Claudia Dafinger (4 shared papers)Robert K. Koenekoop (5 shared papers)Elvir Bećirović (2 shared papers)
- Journals
- European Journal of Human Genetics (3 papers)Journal of Clinical Investigation (3 papers)Human Mutation (2 papers)Orphanet Journal of Rare Diseases (2 papers)The Journal of Cell Biology (1 paper)
- Partner nations
- GermanyCanadaUnited States
In The Last Decade
Inga Ebermann
19 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 69
- Sensory Systems 456
- Neurology 134
- Molecular Biology 753
- Otorhinolaryngology 43
- Ophthalmology 83
Countries citing papers authored by Inga Ebermann
This map shows the geographic impact of Inga Ebermann'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 Inga Ebermann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Inga Ebermann more than expected).
Fields of papers citing papers by Inga Ebermann
This network shows the impact of papers produced by Inga Ebermann. 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 Inga Ebermann. The network helps show where Inga Ebermann may publish in the future.
Co-authors
The 25 scholars most cited alongside Inga Ebermann, 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 | 2010 | 188 | |
| 2 | 2006 | 187 | |
| 3 | 2011 | 151 | |
| 4 | 2012 | 129 | |
| 5 | 2007 | 76 | |
| 6 | 2012 | 63 | |
| 7 | 2009 | 54 | |
| 8 | 2015 | 48 | |
| 9 | 2007 | 39 | |
| 10 | 2009 | 33 | |
| 11 | 2008 | 30 | |
| 12 | 2013 | 30 | |
| 13 | 2008 | 29 | |
| 14 | Protocadherin-21 (PCDH21), a candidate gene for human retinal dystrophies. | 2005 | 19 |
| 15 | Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse origin. | 2010 | 14 |
| 16 | Two truncating USH3A mutations, including one novel, in a German family with Usher syndrome. | 2007 | 12 |
| 17 | 2009 | 11 | |
| 18 | 2011 | 11 | |
| 19 | 2008 | 7 |
About Inga Ebermann
Inga Ebermann is a scholar working on Sensory Systems, Molecular Biology, Neurology, Genetics and Immunology, having authored 19 papers that have together received 1.1k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (12 papers), Retinal Development and Disorders (3 papers), Neutrophil, Myeloperoxidase and Oxidative Mechanisms (2 papers), Connexins and lens biology (2 papers), Vestibular and auditory disorders (2 papers), Fetal and Pediatric Neurological Disorders (1 paper), DNA Repair Mechanisms (1 paper) and Metabolism and Genetic Disorders (1 paper). The work is most often cited by research in Sensory Systems (456 citations), Neurology (134 citations), Molecular Biology (753 citations), Otorhinolaryngology (43 citations) and Ophthalmology (83 citations). Inga Ebermann has collaborated with scholars based in Germany, Canada and United States. Frequent co-authors include Hanno J. Bolz, Gudrun Nürnberg, Peter Nürnberg, Peter Charbel Issa, Hendrik P. N. Scholl, Claudia Dafinger, Robert K. Koenekoop, Elvir Bećirović, Irma López and Elena Aller. Their work appears in journals such as European Journal of Human Genetics, Journal of Clinical Investigation, Human Mutation, Orphanet Journal of Rare Diseases and The Journal of Cell Biology.
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.