Alexander Spauschus
About
In The Last Decade
Alexander Spauschus
16 papers receiving 972 citations
Peers
Comparison fields: 5 of 68
- Molecular Biology 753
- Cellular and Molecular Neuroscience 649
- Cardiology and Cardiovascular Medicine 247
- Psychiatry and Mental health 166
- Neurology 143
Countries citing papers authored by Alexander Spauschus
This map shows the geographic impact of Alexander Spauschus'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 Alexander Spauschus with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexander Spauschus more than expected).
Fields of papers citing papers by Alexander Spauschus
This network shows the impact of papers produced by Alexander Spauschus. 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 Alexander Spauschus. The network helps show where Alexander Spauschus may publish in the future.
Co-authorship network of co-authors of Alexander Spauschus
This figure shows the co-authorship network connecting the top 25 collaborators of Alexander Spauschus. A scholar is included among the top collaborators of Alexander Spauschus 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 Alexander Spauschus. Alexander Spauschus is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 5 | |
| 2 | A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy (vol 122, pg 817, 1999) | 0 |
| 3 | 18 | |
| 4 | 51 | |
| 5 | 291 | |
| 6 | 19 | |
| 7 | Functional analysis of compound heterozygosity in hyperekplexia mutations of the human glycine receptor alpha 1 subunit. | 1 |
| 8 | 36 | |
| 9 | 196 | |
| 10 | 20 | |
| 11 | 57 | |
| 12 | 29 | |
| 13 | 17 | |
| 14 | 63 | |
| 15 | 29 | |
| 16 | 76 | |
| 17 | 83 |
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.