Danielle Perrin
Impact in
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
Papers in
-
- Cancer Genomics and Diagnostics 2
- Genetics 3
- Genomic variations and chromosomal abnormalities 2
- Genomics and Rare Diseases 1
- Co-authors
- Stacey L. Gabriel (1 shared paper)Gad A. Getz (1 shared paper)Dennis C. Friedrich (1 shared paper)Trevor J. Pugh (1 shared paper)Danielle Dionne (1 shared paper)Tim J. Fennell (1 shared paper)Chip Stewart (1 shared paper)James C. Meldrim (1 shared paper)
- Journals
- Genome biology (2 papers)Nature Genetics (2 papers)Cancer Discovery (1 paper)Nature Medicine (1 paper)Nucleic Acids Research (1 paper)
- Partner nations
- United StatesItalyCzechia
In The Last Decade
Danielle Perrin
7 papers receiving 1.9k citations
Peers
Comparison fields: 5 of 82
- Cancer Research 489
- Genetics 573
- Molecular Biology 655
- Nephrology 101
- Oncology 168
Countries citing papers authored by Danielle Perrin
This map shows the geographic impact of Danielle Perrin'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 Perrin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Danielle Perrin more than expected).
Fields of papers citing papers by Danielle Perrin
This network shows the impact of papers produced by Danielle Perrin. 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 Perrin. The network helps show where Danielle Perrin may publish in the future.
Co-authors
The 13 scholars most cited alongside Danielle Perrin, 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 | 2014 | 453 | |
| 2 | 2013 | 419 | |
| 3 | 2013 | 389 | |
| 4 | 2016 | 241 | |
| 5 | 2013 | 225 | |
| 6 | 2017 | 144 | |
| 7 | 2010 | 88 |
About Danielle Perrin
Danielle Perrin is a scholar working on Cancer Research, Genetics, Molecular Biology, Nuclear Energy and Engineering and Waste Management and Disposal, having authored 7 papers that have together received 2k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (2 papers), Cancer Genomics and Diagnostics (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Melanoma and MAPK Pathways (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Cancer Research (489 citations), Genetics (573 citations), Molecular Biology (655 citations), Nephrology (101 citations) and Oncology (168 citations). Danielle Perrin has collaborated with scholars based in United States, Italy and Czechia. Frequent co-authors include Stacey L. Gabriel, Gad A. Getz, Dennis C. Friedrich, Trevor J. Pugh, Danielle Dionne, Tim J. Fennell, Chip Stewart, James C. Meldrim, Maura Costello and Lee Lichtenstein. Their work appears in journals such as Genome biology, Nature Genetics, Cancer Discovery, Nature Medicine and Nucleic Acids Research.
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.