Sonja Hutter
Impact in
- Genetics top 0.5%
- Glioma Diagnosis and Treatment
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 8
- Glioma Diagnosis and Treatment 7
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- Neurofibromatosis and Schwannoma Cases 4
- Co-authors
- Fredrik J. Swartling (5 shared papers)Holger Weishaupt (4 shared papers)Sara Bolin (2 shared papers)David Jones (4 shared papers)Anders Sundström (3 shared papers)Stefan M. Pfister (3 shared papers)Hildegard Kehrer‐Sawatzki (3 shared papers)Rosario Michael Piro (2 shared papers)
- Journals
- Nature Communications (2 papers)Nature (2 papers)Cancer Cell (1 paper)Human Genetics (1 paper)Nature Genetics (1 paper)
- Partner nations
- GermanySwedenUnited States
In The Last Decade
Sonja Hutter
16 papers receiving 2.9k citations
Sonja Hutter's Hit Papers
Peers
Comparison fields: 5 of 90
- Genetics 1.3k
- Cancer Research 577
- Neurology 550
- Molecular Biology 1.8k
- Developmental Neuroscience 55
Countries citing papers authored by Sonja Hutter
This map shows the geographic impact of Sonja Hutter'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 Sonja Hutter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sonja Hutter more than expected).
Fields of papers citing papers by Sonja Hutter
This network shows the impact of papers produced by Sonja Hutter. 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 Sonja Hutter. The network helps show where Sonja Hutter may publish in the future.
Co-authors
The 25 scholars most cited alongside Sonja Hutter, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Dissecting the genomic complexity underlying medulloblastoma Hit paper breakdown → | 2012 | 702 |
| 2 | Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma Hit paper breakdown → | 2013 | 657 |
| 3 | Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition Hit paper breakdown → | 2014 | 617 |
| 4 | Epigenomic alterations define lethal CIMP-positive ependymomas of infancy Hit paper breakdown → | 2014 | 485 |
| 5 | 2018 | 220 | |
| 6 | 2016 | 66 | |
| 7 | 2019 | 48 | |
| 8 | 2014 | 38 | |
| 9 | 2017 | 27 | |
| 10 | 2021 | 26 | |
| 11 | 2016 | 26 | |
| 12 | 2016 | 25 | |
| 13 | 2022 | 20 | |
| 14 | 2023 | 18 | |
| 15 | 2023 | 14 | |
| 16 | 2015 | 1 |
About Sonja Hutter
Sonja Hutter is a scholar working on Genetics, Neurology, Cancer Research, Molecular Biology and Rheumatology, having authored 16 papers that have together received 3.0k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (7 papers), Chromatin Remodeling and Cancer (5 papers), Hedgehog Signaling Pathway Studies (4 papers), Neurofibromatosis and Schwannoma Cases (4 papers), Meningioma and schwannoma management (2 papers), Bone Tumor Diagnosis and Treatments (2 papers), Protein Degradation and Inhibitors (2 papers) and Epigenetics and DNA Methylation (2 papers). The work is most often cited by research in Genetics (1.3k citations), Cancer Research (577 citations), Neurology (550 citations), Molecular Biology (1.8k citations) and Developmental Neuroscience (55 citations). Sonja Hutter has collaborated with scholars based in Germany, Sweden and United States. Frequent co-authors include Fredrik J. Swartling, Holger Weishaupt, Sara Bolin, David Jones, Anders Sundström, Stefan M. Pfister, Hildegard Kehrer‐Sawatzki, Rosario Michael Piro, Said Chosro Farschtschi and Victor Felix Mautner. Their work appears in journals such as Nature Communications, Nature, Cancer Cell, Human Genetics and Nature 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.