Thorsten Schmidt

5.4k citations
75 papers · 3.5k · 1 hit paper · h-index 29

Impact in

Papers in

Thorsten Schmidt

70 papers receiving 3.4k citations

Thorsten Schmidt's Hit Papers

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis 2004 · 733 citations
7330+7+14Years since publication200400600

Peers

Thorsten Schmidt
Comparison fields: 5 of 145
  • Cellular and Molecular Neuroscience 1.6k
  • Neurology 709
  • Genetics 289
  • Molecular Biology 1.9k
  • Neurology 196
Replace Avraham Shaag with:
Avraham Shaag Israel
Brett A. Johnson United States
Hubert Hondermarck France
Steven L. Carroll United States
Simon Edvardson Israel
Steven A. Reeves United States
Montserrat Camps Switzerland
Kyung‐Min Noh United States
Muxin Gu United Kingdom
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Thorsten Schmidt relative to Avraham Shaag Israel Avraham Shaag's profile →
Citations per field
00.5×2.6×
Avraham Shaag · 1×
Citations per year

Countries citing papers authored by Thorsten Schmidt

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Thorsten Schmidt Line = papers co-authored together Thorsten Schmidt links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

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 →
2004733
2 2002247
3 1994234
4 2009190
5 1998174
6 2007160
7 1997135
8 2002118
9 201390
10 201485
11 200984
12
Zinc finger protein GFI-1 cooperates with myc and pim-1 in T-cell lymphomagenesis by reducing the requirements for IL-2.
199682
13 200180
14 200267
15 199651
16 201849
17 200943
18 201142
19 201242
20 200940

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.

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