Benjamin Raeder
Impact in
- Cancer Research top 0.2%
- Cancer Genomics and Diagnostics
- Genetics top 0.1%
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Forensic and Genetic Research
- Genomics and Rare Diseases
- Glioma Diagnosis and Treatment
Papers in
-
- Cancer Genomics and Diagnostics 24
- Cancer-related molecular mechanisms research 1
- Genetics 14
- Genomic variations and chromosomal abnormalities 13
- Glioma Diagnosis and Treatment 4
- Co-authors
- Jan O. Korbel (3 shared papers)Sebastian M. Waszak (2 shared papers)Balca R. Mardin (2 shared papers)Adrian M. Stütz (2 shared papers)Alexandros P. Drainas (2 shared papers)Jan Ellenberg (1 shared paper)Joachim Weischenfeldt (1 shared paper)Maia Segura‐Wang (1 shared paper)
- Journals
- Nature Communications (11 papers)Nature (10 papers)Nature Genetics (9 papers)Cancer Cell (2 papers)Nature Biotechnology (2 papers)
- Partner nations
- GermanyCanadaUnited States
In The Last Decade
Benjamin Raeder
41 papers receiving 27.2k citations
Benjamin Raeder's Hit Papers
Peers
Comparison fields: 5 of 168
- Cancer Research 4.9k
- Genetics 9.7k
- Genetics 1.4k
- Molecular Biology 6.8k
- Oncology 1.8k
Countries citing papers authored by Benjamin Raeder
This map shows the geographic impact of Benjamin Raeder'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 Benjamin Raeder with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Benjamin Raeder more than expected).
Fields of papers citing papers by Benjamin Raeder
This network shows the impact of papers produced by Benjamin Raeder. 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 Benjamin Raeder. The network helps show where Benjamin Raeder may publish in the future.
Co-authors
The 25 scholars most cited alongside Benjamin Raeder, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 12887 |
| 2 | The repertoire of mutational signatures in human cancer Hit paper breakdown → | 2020 | 2401 |
| 3 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2169 |
| 4 | An integrated map of structural variation in 2,504 human genomes Hit paper breakdown → | 2015 | 1657 |
| 5 | The evolutionary history of 2,658 cancers Hit paper breakdown → | 2020 | 730 |
| 6 | Dissecting the genomic complexity underlying medulloblastoma Hit paper breakdown → | 2012 | 705 |
| 7 | Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma Hit paper breakdown → | 2013 | 659 |
| 8 | Patterns of somatic structural variation in human cancer genomes Hit paper breakdown → | 2020 | 564 |
| 9 | Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma Hit paper breakdown → | 2014 | 520 |
| 10 | Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing Hit paper breakdown → | 2020 | 489 |
| 11 | Haplotype-resolved diverse human genomes and integrated analysis of structural variation Hit paper breakdown → | 2021 | 438 |
| 12 | Analyses of non-coding somatic drivers in 2,658 cancer whole genomes Hit paper breakdown → | 2020 | 428 |
| 13 | Comprehensive molecular characterization of mitochondrial genomes in human cancers Hit paper breakdown → | 2020 | 319 |
| 14 | Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition Hit paper breakdown → | 2020 | 315 |
| 15 | Genomic basis for RNA alterations in cancer Hit paper breakdown → | 2020 | 310 |
| 16 | 2016 | 304 | |
| 17 | The landscape of viral associations in human cancers Hit paper breakdown → | 2020 | 293 |
| 18 | 2013 | 279 | |
| 19 | 2018 | 219 | |
| 20 | 2015 | 198 |
About Benjamin Raeder
Benjamin Raeder is a scholar working on Cancer Research, Genetics, Genetics, Molecular Biology and Oncology, having authored 42 papers that have together received 27.6k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (24 papers), Genomic variations and chromosomal abnormalities (13 papers), Glioma Diagnosis and Treatment (4 papers), Genomics and Chromatin Dynamics (2 papers), Prostate Cancer Treatment and Research (2 papers), Chromatin Remodeling and Cancer (2 papers), Chromosomal and Genetic Variations (2 papers) and Cancer-related molecular mechanisms research (1 paper). The work is most often cited by research in Cancer Research (4.9k citations), Genetics (9.7k citations), Genetics (1.4k citations), Molecular Biology (6.8k citations) and Oncology (1.8k citations). Benjamin Raeder has collaborated with scholars based in Germany, Canada and United States. Frequent co-authors include Jan O. Korbel, Sebastian M. Waszak, Balca R. Mardin, Adrian M. Stütz, Alexandros P. Drainas, Jan Ellenberg, Joachim Weischenfeldt, Maia Segura‐Wang, Paul A. Northcott and Stefan M. Pfister. Their work appears in journals such as Nature Communications, Nature, Nature Genetics, Cancer Cell and Nature Biotechnology.
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.