Michaela Thoenes
Impact in
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- Hearing, Cochlea, Tinnitus, Genetics
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- Genetics and Neurodevelopmental Disorders
Papers in
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- Peroxisome Proliferator-Activated Receptors 1
- DNA Repair Mechanisms 1
- Genetics 2
- Forensic and Genetic Research 1
- Genetics and Neurodevelopmental Disorders 1
- Co-authors
- Hanno J. Bolz (4 shared papers)Daniel Swan (3 shared papers)Peter Nürnberg (5 shared papers)Ghada M. H. Abdel‐Salam (1 shared paper)Hanan H. Afifi (1 shared paper)Friederike Körber (1 shared paper)Gudrun Nürnberg (5 shared papers)Raoul Heller (4 shared papers)
In The Last Decade
Michaela Thoenes
9 papers receiving 229 citations
Peers
Comparison fields: 5 of 47
- Sensory Systems 24
- Genetics 85
- Cellular and Molecular Neuroscience 43
- Rheumatology 29
- Molecular Biology 116
Countries citing papers authored by Michaela Thoenes
This map shows the geographic impact of Michaela Thoenes'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 Michaela Thoenes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michaela Thoenes more than expected).
Fields of papers citing papers by Michaela Thoenes
This network shows the impact of papers produced by Michaela Thoenes. 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 Michaela Thoenes. The network helps show where Michaela Thoenes may publish in the future.
Co-authors
The 25 scholars most cited alongside Michaela Thoenes, 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 | 2014 | 68 | |
| 2 | 2015 | 46 | |
| 3 | 2015 | 32 | |
| 4 | 2017 | 28 | |
| 5 | 2013 | 28 | |
| 6 | 2017 | 15 | |
| 7 | Identification of a novel LCA5 mutation in a Pakistani family with Leber congenital amaurosis and cataracts. | 2011 | 8 |
| 8 | 2018 | 3 | |
| 9 | 2021 | 2 |
About Michaela Thoenes
Michaela Thoenes is a scholar working on Molecular Biology, Genetics, Immunology, Surgery and Pathology and Forensic Medicine, having authored 9 papers that have together received 230 indexed citations. Recurring topics across this work include interferon and immune responses (2 papers), Peroxisome Proliferator-Activated Receptors (1 paper), Orthopedic Surgery and Rehabilitation (1 paper), DNA Repair Mechanisms (1 paper), Forensic and Genetic Research (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Immunodeficiency and Autoimmune Disorders (1 paper) and Microtubule and mitosis dynamics (1 paper). The work is most often cited by research in Sensory Systems (24 citations), Genetics (85 citations), Cellular and Molecular Neuroscience (43 citations), Rheumatology (29 citations) and Molecular Biology (116 citations). Michaela Thoenes has collaborated with scholars based in Germany, Egypt and Poland. Frequent co-authors include Hanno J. Bolz, Daniel Swan, Peter Nürnberg, Ghada M. H. Abdel‐Salam, Hanan H. Afifi, Friederike Körber, Gudrun Nürnberg, Raoul Heller, Maha S. Zaki and Inga Ebermann. Their work appears in journals such as Orphanet Journal of Rare Diseases, European Journal of Human Genetics, Frontiers in Genetics, Human Molecular Genetics and Human Mutation.
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.