Iris Selander
Impact in
- Cancer Research top 0.2%
- Cancer Genomics and Diagnostics
- Oncology top 1%
- Pancreatic and Hepatic Oncology Research
Papers in
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- Cancer Genomics and Diagnostics 16
-
- Genetic factors in colorectal cancer 9
- Co-authors
- Laurent Briollais (1 shared paper)Shamini Selvarajah (1 shared paper)Spring Holter (1 shared paper)Ayelet Borgida (1 shared paper)Gloria M. Petersen (1 shared paper)Ashton Anthony Connor (1 shared paper)Jordan P. Lerner‐Ellis (1 shared paper)Robert C. Grant (1 shared paper)
- Journals
- Nature Communications (11 papers)Nature (6 papers)Nature Genetics (5 papers)Nature Biotechnology (1 paper)JAMA Oncology (1 paper)
- Partner nations
- CanadaUnited StatesGermany
In The Last Decade
Iris Selander
27 papers receiving 9.5k citations
Iris Selander's Hit Papers
Peers
Comparison fields: 5 of 147
- Cancer Research 4.4k
- Oncology 2.2k
- Molecular Biology 5.1k
- Pathology and Forensic Medicine 1.1k
- Genetics 1.4k
Countries citing papers authored by Iris Selander
This map shows the geographic impact of Iris Selander'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 Iris Selander with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Iris Selander more than expected).
Fields of papers citing papers by Iris Selander
This network shows the impact of papers produced by Iris Selander. 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 Iris Selander. The network helps show where Iris Selander may publish in the future.
Co-authors
The 9 scholars most cited alongside Iris Selander, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The repertoire of mutational signatures in human cancer Hit paper breakdown → | 2020 | 2339 |
| 2 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2109 |
| 3 | The evolutionary history of 2,658 cancers Hit paper breakdown → | 2020 | 705 |
| 4 | Patterns of somatic structural variation in human cancer genomes Hit paper breakdown → | 2020 | 550 |
| 5 | Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing Hit paper breakdown → | 2020 | 476 |
| 6 | Analyses of non-coding somatic drivers in 2,658 cancer whole genomes Hit paper breakdown → | 2020 | 419 |
| 7 | 2020 | 317 | |
| 8 | Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition Hit paper breakdown → | 2020 | 309 |
| 9 | 2020 | 301 | |
| 10 | 2020 | 293 | |
| 11 | 2014 | 253 | |
| 12 | 2016 | 217 | |
| 13 | 2020 | 184 | |
| 14 | 2020 | 160 | |
| 15 | 2020 | 159 | |
| 16 | 2020 | 152 | |
| 17 | 2020 | 104 | |
| 18 | 2020 | 92 | |
| 19 | 2020 | 83 | |
| 20 | 2020 | 77 |
About Iris Selander
Iris Selander is a scholar working on Cancer Research, Pathology and Forensic Medicine, Molecular Biology, Genetics and Oncology, having authored 27 papers that have together received 9.6k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (16 papers), Genetic factors in colorectal cancer (9 papers), Genomics and Chromatin Dynamics (4 papers), RNA modifications and cancer (4 papers), RNA Research and Splicing (4 papers), Genomics and Phylogenetic Studies (3 papers), Genomics and Rare Diseases (3 papers) and Pancreatic and Hepatic Oncology Research (3 papers). The work is most often cited by research in Cancer Research (4.4k citations), Oncology (2.2k citations), Molecular Biology (5.1k citations), Pathology and Forensic Medicine (1.1k citations) and Genetics (1.4k citations). Iris Selander has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include Laurent Briollais, Shamini Selvarajah, Spring Holter, Ayelet Borgida, Gloria M. Petersen, Ashton Anthony Connor, Jordan P. Lerner‐Ellis, Robert C. Grant and Steven Gallinger. Their work appears in journals such as Nature Communications, Nature, Nature Genetics, Nature Biotechnology and JAMA Oncology.
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.