Matthew S. Crowe

863 total citations · 1 hit paper
8 papers, 691 citations indexed

About

Matthew S. Crowe is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Oncology. According to data from OpenAlex, Matthew S. Crowe has authored 8 papers receiving a total of 691 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Pathology and Forensic Medicine and 3 papers in Oncology. Recurrent topics in Matthew S. Crowe's work include Melanoma and MAPK Pathways (5 papers), Cancer Mechanisms and Therapy (4 papers) and Protein Kinase Regulation and GTPase Signaling (3 papers). Matthew S. Crowe is often cited by papers focused on Melanoma and MAPK Pathways (5 papers), Cancer Mechanisms and Therapy (4 papers) and Protein Kinase Regulation and GTPase Signaling (3 papers). Matthew S. Crowe collaborates with scholars based in United States, United Kingdom and Switzerland. Matthew S. Crowe's co-authors include Christopher M. Counter, Donita C. Brady, Dennis J. Thiele, Michelle L. Turski, A. Chaikuad, G. Aaron Hobbs, Kunhong Xiao, Sharon L. Campbell, Stefan Knapp and Rebekah R. White and has published in prestigious journals such as Nature, Cancer Research and Oncogene.

In The Last Decade

Matthew S. Crowe

8 papers receiving 683 citations

Hit Papers

Copper is required for oncogenic BRAF signalling and tumo... 2014 2026 2018 2022 2014 100 200 300 400
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Copper is required for oncogenic BRAF signalling and tumorigenesis
    2014 487 citations Donita C. Brady, Matthew S. Crowe et al. Nature profile →

Peers

Matthew S. Crowe
Stéphanie Blockhuys Sweden
Nikita Gudekar United States
Mohammad Zulkifli United States
Satish K. Chitneni United States
Věra Richardson Australia
Kuniyuki Katano Japan
Xiumin Di United States
Jourdin R.C. Rouaen Australia
S Clatworthy Australia
Bibbin T. Paul United States
Stéphanie Blockhuys Sweden
Matthew S. Crowe
Citations per year, relative to Matthew S. Crowe Matthew S. Crowe (= 1×) peers Stéphanie Blockhuys

Countries citing papers authored by Matthew S. Crowe

Since Specialization
Citations

This map shows the geographic impact of Matthew S. Crowe'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 S. Crowe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matthew S. Crowe more than expected).

Fields of papers citing papers by Matthew S. Crowe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew S. Crowe. 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 S. Crowe. The network helps show where Matthew S. Crowe may publish in the future.

Co-authorship network of co-authors of Matthew S. Crowe

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew S. Crowe. A scholar is included among the top collaborators of Matthew S. Crowe 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 S. Crowe. Matthew S. Crowe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

8 of 8 papers shown
1.
Crowe, Matthew S., Tatiana Zavorotinskaya, Charles F. Voliva, et al.. (2021). RAF-Mutant Melanomas Differentially Depend on ERK2 Over ERK1 to Support Aberrant MAPK Pathway Activation and Cell Proliferation. Molecular Cancer Research. 19(6). 1063–1075. 3 indexed citations
2.
Brady, Donita C., et al.. (2017). Copper Chelation Inhibits BRAFV600E-Driven Melanomagenesis and Counters Resistance to BRAFV600E and MEK1/2 Inhibitors. Cancer Research. 77(22). 6240–6252. 126 indexed citations
3.
Crowe, Matthew S.. (2015). Biochemical And Tumorigenic Effects Of Redox Modification Of Ras-G12c By Nitric Oxide. Redox Biology. 5. 414–414. 2 indexed citations
4.
Brady, Donita C., Matthew S. Crowe, Michelle L. Turski, et al.. (2014). Copper is required for oncogenic BRAF signalling and tumorigenesis. Nature. 509(7501). 492–496. 487 indexed citations breakdown →
5.
Brady, Donita C., Matthew S. Crowe, Michelle L. Turski, et al.. (2014). Abstract 4427: Copper is required for oncogenic BRAF signaling and tumorigenesis. Cancer Research. 74(19_Supplement). 4427–4427. 2 indexed citations
6.
Brady, Donita C., Matthew S. Crowe, Michelle L. Turski, Dennis J. Thiele, & Christopher M. Counter. (2013). Abstract 4294: Copper is required for oncogenic BRAF signaling and tumorigenesis.. Cancer Research. 73(8_Supplement). 4294–4294. 1 indexed citations
7.
Lampson, Benjamin L., Brooke B. Ancrile, Meghan M. Morrison, et al.. (2012). Targeting eNOS in Pancreatic Cancer. Cancer Research. 72(17). 4472–4482. 56 indexed citations
8.
Kanai, Muneyoshi, Matthew S. Crowe, Yi Zheng, George F. Vande Woude, & Kenji Fukasawa. (2010). RhoA and RhoC are both required for the ROCK II-dependent promotion of centrosome duplication. Oncogene. 29(45). 6040–6050. 14 indexed citations

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.

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