Thorsten Schmidt
Impact in
-
- Genetic Neurodegenerative Diseases
- Neurology top 1%
- Neurological disorders and treatments
- Amyotrophic Lateral Sclerosis Research
- Parkinson's Disease Mechanisms and Treatments
Papers in
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- Mitochondrial Function and Pathology 20
- Ubiquitin and proteasome pathways 7
- DNA Repair Mechanisms 4
- Nuclear Structure and Function 4
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- Genetic Neurodegenerative Diseases 25
- Co-authors
- Olaf Rieß (20 shared papers)Lüdger Schöls (5 shared papers)Peter Bauer (1 shared paper)Thorsten Schulte (1 shared paper)Tarik Möröy (6 shared papers)Holger Karsunky (6 shared papers)Franco Laccone (4 shared papers)Jana Boy (6 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (2 papers)Human Molecular Genetics (2 papers)Neurobiology of Disease (2 papers)Oncogene (2 papers)Brain (2 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Thorsten Schmidt
70 papers receiving 3.4k citations
Thorsten Schmidt's Hit Papers
Peers
Comparison fields: 5 of 145
- Cellular and Molecular Neuroscience 1.6k
- Neurology 709
- Genetics 289
- Molecular Biology 1.9k
- Neurology 196
Countries citing papers authored by Thorsten Schmidt
This map shows the geographic impact of Thorsten Schmidt'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 Thorsten Schmidt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thorsten Schmidt more than expected).
Fields of papers citing papers by Thorsten Schmidt
This network shows the impact of papers produced by Thorsten Schmidt. 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 Thorsten Schmidt. The network helps show where Thorsten Schmidt may publish in the future.
Co-authors
The 25 scholars most cited alongside Thorsten Schmidt, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 75 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis Hit paper breakdown → | 2004 | 733 |
| 2 | 2002 | 247 | |
| 3 | 1994 | 234 | |
| 4 | 2009 | 190 | |
| 5 | 1998 | 174 | |
| 6 | 2007 | 160 | |
| 7 | 1997 | 135 | |
| 8 | 2002 | 118 | |
| 9 | 2013 | 90 | |
| 10 | 2014 | 85 | |
| 11 | 2009 | 84 | |
| 12 | Zinc finger protein GFI-1 cooperates with myc and pim-1 in T-cell lymphomagenesis by reducing the requirements for IL-2. | 1996 | 82 |
| 13 | 2001 | 80 | |
| 14 | 2002 | 67 | |
| 15 | 1996 | 51 | |
| 16 | 2018 | 49 | |
| 17 | 2009 | 43 | |
| 18 | 2011 | 42 | |
| 19 | 2012 | 42 | |
| 20 | 2009 | 40 |
About Thorsten Schmidt
Thorsten Schmidt is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Genetics and Immunology, having authored 75 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (25 papers), Mitochondrial Function and Pathology (20 papers), Ubiquitin and proteasome pathways (7 papers), Neurological disorders and treatments (5 papers), DNA Repair Mechanisms (4 papers), Nuclear Structure and Function (4 papers), Amyotrophic Lateral Sclerosis Research (3 papers) and Complementary and Alternative Medicine Studies (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.6k citations), Neurology (709 citations), Genetics (289 citations), Molecular Biology (1.9k citations) and Neurology (196 citations). Thorsten Schmidt has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Olaf Rieß, Lüdger Schöls, Peter Bauer, Thorsten Schulte, Tarik Möröy, Holger Karsunky, Franco Laccone, Jana Boy, Karin D. Breunig and Ulrich Dührsen. Their work appears in journals such as Proceedings of the National Academy of Sciences, Human Molecular Genetics, Neurobiology of Disease, Oncogene and Brain.
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.