Matthew Holderfield
- Molecular Biology top 5%
- Oncology top 5%
- Cell Biology top 5%
- Cancer Research top 10%
- Immunology top 10%
- Co-authors
- Frank McCormickChristopher C.W. HughesMartin McMahonMarian M. DeukerErin M. ConnMartin N. NakatsuRichard C.A. SainsonDarrin D. Stuart
- Topics
- Melanoma and MAPK Pathways (9 papers)Protein Kinase Regulation and GTPase Signaling (8 papers)Angiogenesis and VEGF in Cancer (5 papers)
- Partner nations
- United StatesSwitzerlandFinland
In The Last Decade
Matthew Holderfield
25 papers receiving 2.2k citations
Hit Papers
Peers
Comparison fields: 5 of 107
- Molecular Biology 1.7k
- Oncology 564
- Cell Biology 281
- Cancer Research 266
- Immunology 219
Countries citing papers authored by Matthew Holderfield
This map shows the geographic impact of Matthew Holderfield'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 Matthew Holderfield with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matthew Holderfield more than expected).
Fields of papers citing papers by Matthew Holderfield
This network shows the impact of papers produced by Matthew Holderfield. 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 Matthew Holderfield. The network helps show where Matthew Holderfield may publish in the future.
Co-authorship network of co-authors of Matthew Holderfield
This figure shows the co-authorship network connecting the top 25 collaborators of Matthew Holderfield. A scholar is included among the top collaborators of Matthew Holderfield 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 Matthew Holderfield. Matthew Holderfield is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 1 | |
| 3 | 37 | |
| 4 | 1 | |
| 5 | 94 | |
| 6 | 2 | |
| 7 | 11 | |
| 8 | 32 | |
| 9 | 76 | |
| 10 | 56 | |
| 11 | 155 | |
| 12 | 20 | |
| 13 | 145 | |
| 14 | 90 | |
| 15 | Targeting RAF kinases for cancer therapy: BRAF-mutated melanoma and beyondbreakdown → | 618 |
| 16 | 30 | |
| 17 | 96 | |
| 18 | 274 | |
| 19 | 33 | |
| 20 | 191 |
About Matthew Holderfield
Matthew Holderfield is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Oncology, having authored 25 papers that have together received 2.2k indexed citations. Recurring topics across this work include Melanoma and MAPK Pathways (9 papers), Protein Kinase Regulation and GTPase Signaling (8 papers) and Angiogenesis and VEGF in Cancer (5 papers). The work is most often cited by research in Molecular Biology (1.7k citations), Oncology (564 citations) and Cancer Research (266 citations). Matthew Holderfield has collaborated with scholars based in United States, Switzerland and Finland. Frequent co-authors include Frank McCormick, Christopher C.W. Hughes, Martin McMahon, Marian M. Deuker, Erin M. Conn, Martin N. Nakatsu, Richard C.A. Sainson, Darrin D. Stuart, Tobi Nagel and Douglas A. Johnston. Their work appears in journals such as Cell, Proceedings of the National Academy of Sciences and Nature reviews. Cancer.
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.