Gavin MacBeath

11.6k total citations · 4 hit papers
83 papers, 8.0k citations indexed

About

Gavin MacBeath is a scholar working on Molecular Biology, Oncology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Gavin MacBeath has authored 83 papers receiving a total of 8.0k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 32 papers in Oncology and 25 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Gavin MacBeath's work include Monoclonal and Polyclonal Antibodies Research (25 papers), HER2/EGFR in Cancer Research (24 papers) and Advanced Biosensing Techniques and Applications (24 papers). Gavin MacBeath is often cited by papers focused on Monoclonal and Polyclonal Antibodies Research (25 papers), HER2/EGFR in Cancer Research (24 papers) and Advanced Biosensing Techniques and Applications (24 papers). Gavin MacBeath collaborates with scholars based in United States, Germany and Canada. Gavin MacBeath's co-authors include Stuart L. Schreiber, Andrew Gordus, Peter K. Sorger, Jordan A. Krall, Richard B. Jones, Donald Hilvert, Taranjit S. Gujral, Angela N. Koehler, Mark Sevecka and Peter Kast and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Gavin MacBeath

81 papers receiving 7.8k citations

Hit Papers

Printing Proteins as Microarrays for High-Throughput Func... 2000 2026 2008 2017 2000 2002 2005 2012 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Gavin MacBeath United States 34 6.2k 2.0k 1.7k 978 683 83 8.0k
Rebecca L. Rich United States 44 5.1k 0.8× 1.2k 0.6× 950 0.5× 843 0.9× 251 0.4× 71 7.8k
David G. Myszka United States 62 9.1k 1.5× 2.9k 1.4× 1.7k 1.0× 938 1.0× 430 0.6× 133 13.2k
Robert Karlsson Sweden 31 4.2k 0.7× 2.3k 1.1× 1.1k 0.7× 325 0.3× 273 0.4× 65 6.1k
Juri G. Gelovani United States 59 5.1k 0.8× 2.3k 1.1× 2.2k 1.3× 2.3k 2.3× 286 0.4× 247 11.3k
Emanuel F. Petricoin United States 51 6.7k 1.1× 1.4k 0.7× 945 0.5× 1.5k 1.5× 2.3k 3.3× 195 9.5k
Virginia Espina United States 49 5.0k 0.8× 1.2k 0.6× 871 0.5× 1.3k 1.3× 1.5k 2.2× 152 7.3k
Julia Wulfkuhle United States 36 4.1k 0.7× 918 0.4× 778 0.4× 1.2k 1.2× 1.2k 1.8× 81 5.8k
Philippe I. H. Bastiaens Germany 56 8.5k 1.4× 746 0.4× 808 0.5× 1.3k 1.4× 316 0.5× 138 11.3k
Jason W. Chin United Kingdom 73 15.5k 2.5× 2.4k 1.2× 511 0.3× 1.6k 1.6× 428 0.6× 156 18.2k
Derek N. Woolfson United Kingdom 65 10.1k 1.6× 746 0.4× 741 0.4× 376 0.4× 619 0.9× 214 13.3k

Countries citing papers authored by Gavin MacBeath

Since Specialization
Citations

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

Fields of papers citing papers by Gavin MacBeath

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gavin MacBeath. 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 Gavin MacBeath. The network helps show where Gavin MacBeath may publish in the future.

Co-authorship network of co-authors of Gavin MacBeath

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

All Works

20 of 20 papers shown
1.
Malki, Monzr M. Al, Alla Keyzner, Hyung C. Suh, et al.. (2024). A phase 1 trial of TSC-100 and TSC-101, engineered T cell therapies that target minor histocompatibility antigens to eliminate residual disease after hematopoietic cell transplantation.. Journal of Clinical Oncology. 42(16_suppl). TPS2678–TPS2678. 1 indexed citations
2.
Thomas, Sajeve, Brian S. Henick, Rom S. Leidner, et al.. (2024). Initial data from a phase 1, first-in-human clinical trial for T-Plex, a multiplexed, enhanced T cell receptor-engineered T cell therapy (TCR-T) for solid tumors.. Journal of Clinical Oncology. 42(16_suppl). 2542–2542.
3.
Ferretti, Andrew, Tomasz Kula, Yifan Wang, et al.. (2020). Unbiased Screens Show CD8+ T Cells of COVID-19 Patients Recognize Shared Epitopes in SARS-CoV-2 that Largely Reside outside the Spike Protein. Immunity. 53(5). 1095–1107.e3. 182 indexed citations
4.
Sabnis, Gauri, Bambang S. Adiwijaya, Gabriela Garcia, et al.. (2015). Seribantumab, an Anti-ERBB3 Antibody, Delays the Onset of Resistance and Restores Sensitivity to Letrozole in an Estrogen Receptor–Positive Breast Cancer Model. Molecular Cancer Therapeutics. 14(11). 2642–2652. 19 indexed citations
5.
Yarar, Defne, Johanna Lahdenranta, William Kubasek, Ulrik B. Nielsen, & Gavin MacBeath. (2015). Heregulin–ErbB3-Driven Tumor Growth Persists in PI3 Kinase Mutant Cancer Cells. Molecular Cancer Therapeutics. 14(9). 2072–2080. 4 indexed citations
6.
Qian, Guoqing, Ning Jiang, Dongsheng Wang, et al.. (2015). Heregulin and HER3 are prognostic biomarkers in oropharyngeal squamous cell carcinoma. Cancer. 121(20). 3600–3611. 33 indexed citations
7.
Jiang, Ning, Dongsheng Wang, Zhongliang Hu, et al.. (2014). Combination of Anti-HER3 Antibody MM-121/SAR256212 and Cetuximab Inhibits Tumor Growth in Preclinical Models of Head and Neck Squamous Cell Carcinoma. Molecular Cancer Therapeutics. 13(7). 1826–1836. 50 indexed citations
8.
Gujral, Taranjit S., Marina Chan, Leonid Peshkin, et al.. (2014). A Noncanonical Frizzled2 Pathway Regulates Epithelial-Mesenchymal Transition and Metastasis. Cell. 159(4). 844–856. 271 indexed citations
9.
Allen, John E., Brian C. Russo, Soo Young Lee, et al.. (2014). Systematic Analysis of Bacterial Effector-Postsynaptic Density 95/Disc Large/Zonula Occludens-1 (PDZ) Domain Interactions Demonstrates Shigella OspE Protein Promotes Protein Kinase C Activation via PDLIM Proteins. Journal of Biological Chemistry. 289(43). 30101–30113. 14 indexed citations
10.
Onsum, Matthew, Elena Geretti, Violette Paragas, et al.. (2013). Single-Cell Quantitative HER2 Measurement Identifies Heterogeneity and Distinct Subgroups within Traditionally Defined HER2-Positive Patients. American Journal Of Pathology. 183(5). 1446–1460. 72 indexed citations
11.
Kaushansky, Alexis, et al.. (2013). Phosphotyrosine Signaling Proteins that Drive Oncogenesis Tend to be Highly Interconnected. Molecular & Cellular Proteomics. 12(5). 1204–1213. 28 indexed citations
12.
Gujral, Taranjit S., et al.. (2013). Family-wide Investigation of PDZ Domain-Mediated Protein-Protein Interactions Implicates β-Catenin in Maintaining the Integrity of Tight Junctions. Chemistry & Biology. 20(6). 816–827. 27 indexed citations
13.
MacBeath, Gavin, et al.. (2012). Cross-talk between Receptor Tyrosine Kinase and Tumor Necrosis Factor-α Signaling Networks Regulates Apoptosis but not Proliferation. Molecular & Cellular Proteomics. 11(6). M111.013292–M111.013292. 19 indexed citations
14.
Gujral, Taranjit S., Robert L. Karp, David W. Chan, et al.. (2012). Profiling phospho-signaling networks in breast cancer using reverse-phase protein arrays. Oncogene. 32(29). 3470–3476. 62 indexed citations
15.
Krall, Jordan A., et al.. (2011). High- and Low-Affinity Epidermal Growth Factor Receptor-Ligand Interactions Activate Distinct Signaling Pathways. PLoS ONE. 6(1). e15945–e15945. 83 indexed citations
16.
Shalek, Alex K., Jacob T. Robinson, Ethan S. Karp, et al.. (2010). Vertical silicon nanowires as a universal platform for delivering biomolecules into living cells. Proceedings of the National Academy of Sciences. 107(5). 1870–1875. 466 indexed citations
17.
Kaushansky, Alexis, et al.. (2008). A quantitative study of the recruitment potential of all intracellulartyrosine residues on EGFR, FGFR1 and IGF1R. Molecular BioSystems. 4(6). 643–653. 44 indexed citations
18.
Kaushansky, Alexis, Andrew Gordus, Bogdan Budnik, et al.. (2008). System-wide Investigation of ErbB4 Reveals 19 Sites of Tyr Phosphorylation that Are Unusually Selective in Their Recruitment Properties. Chemistry & Biology. 15(8). 808–817. 64 indexed citations
19.
Jones, Richard B., Andrew Gordus, Jordan A. Krall, & Gavin MacBeath. (2005). A quantitative protein interaction network for the ErbB receptors using protein microarrays. Nature. 439(7073). 168–174. 569 indexed citations breakdown →
20.
Nielsen, Ulrik B., et al.. (2003). Profiling receptor tyrosine kinase activation by using Ab microarrays. Proceedings of the National Academy of Sciences. 100(16). 9330–9335. 179 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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