T. Grimm
Impact in
- Ophthalmology top 5%
- Retinal Diseases and Treatments
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- Genetic Neurodegenerative Diseases
Papers in
-
- Retinal Development and Disorders 2
- Ion Transport and Channel Regulation 1
- Ion channel regulation and function 1
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- Genetic Neurodegenerative Diseases 3
- Co-authors
- P.S. Harper (1 shared paper)Manuela C. Koch (2 shared papers)Bernhard H. F. Weber (2 shared papers)Karen L. White (1 shared paper)Heidi Stöhr (1 shared paper)Birgit Lorenz (1 shared paper)Bernhard Jurklies (1 shared paper)Hendrik P. N. Scholl (1 shared paper)
- Journals
- Muscle & Nerve (1 paper)British Journal of Ophthalmology (1 paper)Experimental and Clinical Endocrinology & Diabetes (1 paper)The American Journal of Human Genetics (1 paper)Klinische Pädiatrie (1 paper)
- Partner nations
- GermanyFranceUnited Kingdom
In The Last Decade
T. Grimm
8 papers receiving 474 citations
Peers
Comparison fields: 5 of 60
- Ophthalmology 127
- Cellular and Molecular Neuroscience 122
- Molecular Biology 320
- Neurology 45
- Radiology, Nuclear Medicine and Imaging 47
Countries citing papers authored by T. Grimm
This map shows the geographic impact of T. Grimm'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 T. Grimm with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Grimm more than expected).
Fields of papers citing papers by T. Grimm
This network shows the impact of papers produced by T. Grimm. 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 T. Grimm. The network helps show where T. Grimm may publish in the future.
Co-authors
The 25 scholars most cited alongside T. Grimm, 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 | 2000 | 278 | |
| 2 | Genetic risks for children of women with myotonic dystrophy. | 1991 | 114 |
| 3 | 2016 | 53 | |
| 4 | 2007 | 15 | |
| 5 | 2002 | 15 | |
| 6 | 1996 | 8 | |
| 7 | Mutations in severe hemophilia A: distribution within the factor VIII gene, origin and influence on inhibitor development. | 1997 | 5 |
| 8 | 1995 | 2 | |
| 9 | 2008 | 0 |
About T. Grimm
T. Grimm is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Social Psychology and Cardiology and Cardiovascular Medicine, having authored 9 papers that have together received 490 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (3 papers), Retinal Development and Disorders (2 papers), Retinal Diseases and Treatments (1 paper), Ion Transport and Channel Regulation (1 paper), Hemophilia Treatment and Research (1 paper), Ion channel regulation and function (1 paper), Metabolism and Genetic Disorders (1 paper) and Immunodeficiency and Autoimmune Disorders (1 paper). The work is most often cited by research in Ophthalmology (127 citations), Cellular and Molecular Neuroscience (122 citations), Molecular Biology (320 citations), Neurology (45 citations) and Radiology, Nuclear Medicine and Imaging (47 citations). T. Grimm has collaborated with scholars based in Germany, France and United Kingdom. Frequent co-authors include P.S. Harper, Manuela C. Koch, Bernhard H. F. Weber, Karen L. White, Heidi Stöhr, Birgit Lorenz, Bernhard Jurklies, Hendrik P. N. Scholl, Andrea Rivera and E Apfelstedt-Sylla. Their work appears in journals such as Muscle & Nerve, British Journal of Ophthalmology, Experimental and Clinical Endocrinology & Diabetes, The American Journal of Human Genetics and Klinische Pädiatrie.
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.