Jeffrey Field

8.4k total citations · 1 hit paper
87 papers, 6.7k citations indexed

About

Jeffrey Field is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Jeffrey Field has authored 87 papers receiving a total of 6.7k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Molecular Biology, 22 papers in Cell Biology and 14 papers in Oncology. Recurrent topics in Jeffrey Field's work include Fungal and yeast genetics research (24 papers), Protein Kinase Regulation and GTPase Signaling (22 papers) and Cancer-related Molecular Pathways (12 papers). Jeffrey Field is often cited by papers focused on Fungal and yeast genetics research (24 papers), Protein Kinase Regulation and GTPase Signaling (22 papers) and Cancer-related Molecular Pathways (12 papers). Jeffrey Field collaborates with scholars based in United States, China and Japan. Jeffrey Field's co-authors include Michael Wigler, Daniel Broek, Jun‐ichi Nikawa, Linda Rodgers, Richard A. Lerner, Ian A. Wilson, Yi Tang, J Hurwitz, Anne B. Vojtek and Jeffrey E. Gerst and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Jeffrey Field

85 papers receiving 6.6k citations

Hit Papers

Purification of a RAS-responsive adenylyl cyclase complex... 1988 2026 2000 2013 1988 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jeffrey Field United States 45 4.8k 1.6k 984 631 494 87 6.7k
A.N. Plotnikov United States 39 5.2k 1.1× 1.3k 0.9× 750 0.8× 764 1.2× 385 0.8× 75 6.7k
Tohru Kataoka Japan 48 6.7k 1.4× 1.7k 1.1× 651 0.7× 543 0.9× 362 0.7× 122 8.2k
Judy L. Meinkoth United States 41 4.6k 1.0× 741 0.5× 810 0.8× 779 1.2× 554 1.1× 82 6.5k
Veerle Janssens Belgium 39 5.2k 1.1× 1.3k 0.8× 1.1k 1.1× 446 0.7× 375 0.8× 90 6.9k
Christophé Erneux Belgium 49 5.6k 1.2× 2.1k 1.3× 505 0.5× 333 0.5× 818 1.7× 234 7.4k
Claude Lazure Canada 50 4.0k 0.8× 1.6k 1.0× 1.1k 1.1× 603 1.0× 1.4k 2.8× 163 8.2k
Neil Q. McDonald United Kingdom 47 4.2k 0.9× 1.0k 0.6× 903 0.9× 533 0.8× 1.1k 2.2× 100 6.6k
Chin Ha Chung South Korea 49 5.6k 1.2× 1.3k 0.9× 1.5k 1.6× 921 1.5× 195 0.4× 140 6.7k
Shu Jin Chan United States 45 3.6k 0.7× 1.1k 0.7× 585 0.6× 1.4k 2.3× 800 1.6× 98 6.6k
Guillermo Giménez‐Gallego Spain 40 4.1k 0.8× 1.3k 0.8× 350 0.4× 626 1.0× 635 1.3× 158 5.7k

Countries citing papers authored by Jeffrey Field

Since Specialization
Citations

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

Fields of papers citing papers by Jeffrey Field

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jeffrey Field

This figure shows the co-authorship network connecting the top 25 collaborators of Jeffrey Field. A scholar is included among the top collaborators of Jeffrey Field 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 Jeffrey Field. Jeffrey Field 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.
Xiong, Yao, Simon Berritt, Thomas G. Brooks, et al.. (2019). Targeting MRTF/SRF in CAP2-dependent dilated cardiomyopathy delays disease onset. JCI Insight. 4(6). 17 indexed citations
2.
Lee, Yool, Nicholas F. Lahens, Shirley Zhang, et al.. (2019). G1/S cell cycle regulators mediate effects of circadian dysregulation on tumor growth and provide targets for timed anticancer treatment. PLoS Biology. 17(4). e3000228–e3000228. 89 indexed citations
3.
Liu, Ying, et al.. (2017). Cadmium favors F-actin depolymerization in rat renal mesangial cells by site-specific, disulfide-based dimerization of the CAP1 protein. Archives of Toxicology. 92(3). 1049–1064. 15 indexed citations
4.
Field, Jeffrey, Diana Z. Ye, Fang Liu, et al.. (2015). CAP2 in cardiac conduction, sudden cardiac death and eye development. Scientific Reports. 5(1). 17256–17256. 34 indexed citations
5.
Zhang, Haitao, et al.. (2013). Mammalian Adenylyl Cyclase-associated Protein 1 (CAP1) Regulates Cofilin Function, the Actin Cytoskeleton, and Cell Adhesion. Journal of Biological Chemistry. 288(29). 20966–20977. 74 indexed citations
6.
Ye, Diana Z., Shenghao Jin, Ya Zhuo, & Jeffrey Field. (2011). p21-Activated Kinase 1 (Pak1) Phosphorylates BAD Directly at Serine 111 In Vitro and Indirectly through Raf-1 at Serine 112. PLoS ONE. 6(11). e27637–e27637. 41 indexed citations
7.
Field, Anjalie & Jeffrey Field. (2010). Melamine and cyanuric acid do not interfere with Bradford and Ninhydrin assays for protein determination. Food Chemistry. 121(3). 912–917. 23 indexed citations
8.
Dümmler, Bettina, Kazufumi Ohshiro, Rakesh Kumar, & Jeffrey Field. (2009). Pak protein kinases and their role in cancer. Cancer and Metastasis Reviews. 28(1-2). 51–63. 221 indexed citations
9.
McKenna, Lindsay B., Genfa Zhou, & Jeffrey Field. (2007). Isoform-specific functions of Akt in cell motility. Cellular and Molecular Life Sciences. 64(21). 2723–2725. 11 indexed citations
10.
Zhou, Guo-Lei, et al.. (2006). Opposing Roles for Akt1 and Akt2 in Rac/Pak Signaling and Cell Migration. Journal of Biological Chemistry. 281(47). 36443–36453. 119 indexed citations
11.
Penning, T.M., et al.. (2004). POLYCYCLIC AROMATIC HYDROCARBON O -QUINONES MUTATE p 53 IN HUMAN LUNG ADENOCARCINOMA (A549) CELLS. Polycyclic aromatic compounds. 24(4-5). 583–596. 2 indexed citations
12.
Zhou, Guo-Lei & Jeffrey Field. (2004). Targeting PAK etk…. Cancer Biology & Therapy. 3(1). 102–103. 2 indexed citations
13.
Li, Yiwen, Marco I. González, Judy L. Meinkoth, et al.. (2003). Lysophosphatidic Acid Promotes Survival and Differentiation of Rat Schwann Cells. Journal of Biological Chemistry. 278(11). 9585–9591. 61 indexed citations
14.
Chen, Albert I., Yi Tang, Ya Zhuo, et al.. (2001). Ras activation of PAK protein kinases. Methods in enzymology on CD-ROM/Methods in enzymology. 333. 55–61. 1 indexed citations
15.
Tang, Yi, Honglin Zhou, Albert I. Chen, Randall N. Pittman, & Jeffrey Field. (2000). The Akt Proto-oncogene Links Ras to Pak and Cell Survival Signals. Journal of Biological Chemistry. 275(13). 9106–9109. 198 indexed citations
16.
Freeman, Nancy L., et al.. (1995). An Actin Monomer Binding Activity Localizes to the Carboxyl-terminal Half of the Saccharomyces cerevisiae Cyclase-associated Protein. Journal of Biological Chemistry. 270(10). 5680–5685. 113 indexed citations
17.
Field, Jeffrey, Anne B. Vojtek, Roymarie Ballester, et al.. (1990). Cloning and characterization of CAP, the S. cerevisiae gene encoding the 70 kd adenylyl cyclase-associated protein. Cell. 61(2). 319–327. 212 indexed citations
18.
Field, Jeffrey, Jun‐ichi Nikawa, Daniel Broek, et al.. (1988). Purification of a RAS -Responsive Adenylyl Cyclase Complex from Saccharomyces cerevisiae by Use of an Epitope Addition Method. Molecular and Cellular Biology. 8(5). 2159–2165. 327 indexed citations
19.
Wigler, Michael, Jeffrey Field, Scott Powers, et al.. (1988). Studies of RAS Function in the Yeast Saccharomyces cerevisiae. Cold Spring Harbor Symposia on Quantitative Biology. 53(0). 649–655. 67 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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