Shelly Gunn
- Molecular Biology
- Oncology top 10%
- Cancer Research top 10%
- Genetics
- Genetics top 10%
- Co-authors
- Ryan S. RobetoryeAnthony W. TolcherDrew RascoG. MangoldBrianne KaiserAmita PatnaikKyriakos P. PapadopoulosM. Gorre
- Topics
- Genomic variations and chromosomal abnormalities (14 papers)Cancer Genomics and Diagnostics (7 papers)Chronic Lymphocytic Leukemia Research (5 papers)
- Cited by
- GeneticsOncologyCancer Research
- Partner nations
- United StatesNetherlandsFrance
In The Last Decade
Shelly Gunn
27 papers receiving 775 citations
Peers
Comparison fields: 5 of 76
- Molecular Biology 445
- Oncology 298
- Cancer Research 162
- Genetics 154
- Genetics 148
Countries citing papers authored by Shelly Gunn
This map shows the geographic impact of Shelly Gunn'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 Shelly Gunn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shelly Gunn more than expected).
Fields of papers citing papers by Shelly Gunn
This network shows the impact of papers produced by Shelly Gunn. 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 Shelly Gunn. The network helps show where Shelly Gunn may publish in the future.
Co-authorship network of co-authors of Shelly Gunn
This figure shows the co-authorship network connecting the top 25 collaborators of Shelly Gunn. A scholar is included among the top collaborators of Shelly Gunn based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Shelly Gunn. Shelly Gunn is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 26 | |
| 2 | 4 | |
| 3 | Commentary—Redefining HER2-Equivocal Breast Cancers: Lessons Learned from Genomic Pathology | 1 |
| 4 | 9 | |
| 5 | 7 | |
| 6 | 352 | |
| 7 | 0 | |
| 8 | 10 | |
| 9 | 11 | |
| 10 | 4 | |
| 11 | 44 | |
| 12 | 105 | |
| 13 | 18 | |
| 14 | 12 | |
| 15 | 42 | |
| 16 | 2 | |
| 17 | 56 | |
| 18 | 2 | |
| 19 | 15 | |
| 20 | 46 |
About Shelly Gunn
Shelly Gunn is a scholar working on Genetics, Genetics and Cancer Research, having authored 28 papers that have together received 814 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Cancer Genomics and Diagnostics (7 papers) and Chronic Lymphocytic Leukemia Research (5 papers). The work is most often cited by research in Genetics (148 citations), Oncology (298 citations) and Cancer Research (162 citations). Shelly Gunn has collaborated with scholars based in United States, Netherlands and France. Frequent co-authors include Ryan S. Robetorye, Anthony W. Tolcher, Drew Rasco, G. Mangold, Brianne Kaiser, Amita Patnaik, Kyriakos P. Papadopoulos, M. Gorre, Theresa A. Mays and Leslie Smetzer. Their work appears in journals such as Journal of Clinical Oncology, Blood and Cancer 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.