Sigrun Fuchs
- Co-authors
- Serdar CeylanerBernd RöslerRainer KoenigDieter KotzotUrsula G. FrosterJürgen KohlhaseDavid ChitayatRainer König
- Topics
- Genetic Syndromes and Imprinting (2 papers)Genetic and Kidney Cyst Diseases (2 papers)Pharmacological Effects and Assays (2 papers)
- Partner nations
- GermanyTürkiyeUnited States
In The Last Decade
Sigrun Fuchs
14 papers receiving 307 citations
Peers
Comparison fields: 5 of 53
- Molecular Biology 204
- Genetics 186
- Pediatrics, Perinatology and Child Health 61
- Rheumatology 19
- Surgery 17
Countries citing papers authored by Sigrun Fuchs
This map shows the geographic impact of Sigrun Fuchs'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 Sigrun Fuchs with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sigrun Fuchs more than expected).
Fields of papers citing papers by Sigrun Fuchs
This network shows the impact of papers produced by Sigrun Fuchs. 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 Sigrun Fuchs. The network helps show where Sigrun Fuchs may publish in the future.
Co-authorship network of co-authors of Sigrun Fuchs
This figure shows the co-authorship network connecting the top 25 collaborators of Sigrun Fuchs. A scholar is included among the top collaborators of Sigrun Fuchs 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 Sigrun Fuchs. Sigrun Fuchs is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 3 | |
| 2 | 3 | |
| 3 | 0 | |
| 4 | 79 | |
| 5 | 1 | |
| 6 | 97 | |
| 7 | 16 | |
| 8 | 20 | |
| 9 | 7 | |
| 10 | 19 | |
| 11 | 2 | |
| 12 | 21 | |
| 13 | [Psychiatric manifestations in Wilson's disease]. | 11 |
| 14 | 23 | |
| 15 | 13 |
About Sigrun Fuchs
Sigrun Fuchs is a scholar working on Equine, Developmental Biology and Genetics, having authored 15 papers that have together received 315 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (2 papers), Genetic and Kidney Cyst Diseases (2 papers) and Pharmacological Effects and Assays (2 papers). The work is most often cited by research in Genetics (186 citations), Developmental Biology (12 citations) and Pediatrics, Perinatology and Child Health (61 citations). Sigrun Fuchs has collaborated with scholars based in Germany, Türkiye and United States. Frequent co-authors include Serdar Ceylaner, Bernd Rösler, Rainer Koenig, Dieter Kotzot, Ursula G. Froster, Jürgen Kohlhase, David Chitayat, Rainer König, Tara Montgomery and Ulrich Langenbeck. Their work appears in journals such as Human Mutation, European Journal of Human Genetics and American Journal of Medical Genetics.
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.