Danielle Schüler
Impact in
- Genetics top 0.5%
- Glioma Diagnosis and Treatment
- Cancer Research top 5%
- MicroRNA in disease regulation
- Cancer, Hypoxia, and Metabolism
- Cancer Genomics and Diagnostics
Papers in
- Genetics 3
- Glioma Diagnosis and Treatment 3
- Genomic variations and chromosomal abnormalities 1
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- Prenatal Screening and Diagnostics 1
- Co-authors
- Paul Kleihues (3 shared papers)Hiroko Ohgaki (3 shared papers)Urs M. Lütolf (3 shared papers)Yasuhiro Yonekawa (3 shared papers)M. Gazi Yaşargil (3 shared papers)Nicole Probst‐Hensch (2 shared papers)Sonja Horstmann (2 shared papers)T Nishikawa (1 shared paper)
- Journals
- Lung Cancer (1 paper)Cancer Research (1 paper)Human Heredity (1 paper)Journal of neurosurgery (1 paper)Acta Neuropathologica (1 paper)
- Partner nations
- United StatesFranceSwitzerland
In The Last Decade
Danielle Schüler
5 papers receiving 1.4k citations
Danielle Schüler's Hit Papers
Peers
Comparison fields: 5 of 76
- Genetics 887
- Cancer Research 394
- Neurology 148
- Molecular Biology 512
- Oncology 175
Countries citing papers authored by Danielle Schüler
This map shows the geographic impact of Danielle Schüler'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 Danielle Schüler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Danielle Schüler more than expected).
Fields of papers citing papers by Danielle Schüler
This network shows the impact of papers produced by Danielle Schüler. 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 Danielle Schüler. The network helps show where Danielle Schüler may publish in the future.
Co-authors
The 18 scholars most cited alongside Danielle Schüler, 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 | Genetic Pathways to Glioblastoma Hit paper breakdown → | 2004 | 992 |
| 2 | 2004 | 247 | |
| 3 | 2003 | 185 | |
| 4 | 1977 | 8 | |
| 5 | 1994 | 2 |
About Danielle Schüler
Danielle Schüler is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Oncology, Epidemiology and Genetics, having authored 5 papers that have together received 1.4k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (3 papers), Neurogenesis and neuroplasticity mechanisms (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Cancer Genomics and Diagnostics (1 paper), Meningioma and schwannoma management (1 paper), Prenatal Screening and Diagnostics (1 paper) and Cancer-related Molecular Pathways (1 paper). The work is most often cited by research in Genetics (887 citations), Cancer Research (394 citations), Neurology (148 citations), Molecular Biology (512 citations) and Oncology (175 citations). Danielle Schüler has collaborated with scholars based in United States, France and Switzerland. Frequent co-authors include Paul Kleihues, Hiroko Ohgaki, Urs M. Lütolf, Yasuhiro Yonekawa, M. Gazi Yaşargil, Nicole Probst‐Hensch, Sonja Horstmann, T Nishikawa, Paulo César Maiorka and Paola Pisani. Their work appears in journals such as Lung Cancer, Cancer Research, Human Heredity, Journal of neurosurgery and Acta Neuropathologica.
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.