Susanne T. de Bot

1.5k citations
38 papers · 663 indexed · h-index 15
Topics
Genetic Neurodegenerative Diseases (26 papers)Neurological disorders and treatments (13 papers)Hereditary Neurological Disorders (12 papers)

In The Last Decade

Susanne T. de Bot

33 papers receiving 653 citations

Peers

Susanne T. de Bot
Comparison fields: 5 of 63
  • Cellular and Molecular Neuroscience 450
  • Neurology 234
  • Neurology 209
  • Molecular Biology 173
  • Genetics 127
Replace Roberta Anelli with:
Roberta Anelli United States
Takamasa Morimoto Japan
Chiara Pisciotta Italy
Tomohito Kadota Japan
Bart van de Warrenburg Netherlands
Emma J. Quinn United States
V. Fetoni Italy
Roberto Di Fabio Italy
Ajit Kale United States
Judith Thomas Tayra Japan
Susanne T. de Bot relative to Roberta Anelli United States Roberta Anelli's profile →
Citations per field
00.5×3.3×
Roberta Anelli · 1×
Citations per year

Countries citing papers authored by Susanne T. de Bot

Since Specialization
Citations

This map shows the geographic impact of Susanne T. de Bot'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 Susanne T. de Bot with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Susanne T. de Bot more than expected).

Fields of papers citing papers by Susanne T. de Bot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Susanne T. de Bot. 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 Susanne T. de Bot. The network helps show where Susanne T. de Bot may publish in the future.

Co-authorship network of co-authors of Susanne T. de Bot

This figure shows the co-authorship network connecting the top 25 collaborators of Susanne T. de Bot. A scholar is included among the top collaborators of Susanne T. de Bot based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Susanne T. de Bot. Susanne T. de Bot is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
#WorkIndexed citations
1 0
2 5
3 2
4 0
5 2
6 1
7 0
8 1
9 1
10 1
11 3
12 1
13 3
14 43
15 39
16 76
17 29
18 26
19 75
20 37

About Susanne T. de Bot

Susanne T. de Bot is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology, having authored 38 papers that have together received 663 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (26 papers), Neurological disorders and treatments (13 papers) and Hereditary Neurological Disorders (12 papers). The work is most often cited by research in Neurology (234 citations), Cellular and Molecular Neuroscience (450 citations) and Neurology (209 citations). Susanne T. de Bot has collaborated with scholars based in Netherlands, Italy and United Kingdom. Frequent co-authors include Bart P.C. van de Warrenburg, H.P.H. Kremer, Raymund A.C. Roos, Hans Scheffer, Willeke van Roon‐Mom, Sascha Vermeer, Vivian Weerdesteyn, Alexander C. H. Geurts, Erik‐Jan Kamsteeg and Mark de Niet. Their work appears in journals such as Journal of Neuroscience, Brain and Neurology.

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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