Jonathan Chernoff

19.5k total citations · 2 hit papers
207 papers, 15.7k citations indexed

About

Jonathan Chernoff is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Jonathan Chernoff has authored 207 papers receiving a total of 15.7k indexed citations (citations by other indexed papers that have themselves been cited), including 152 papers in Molecular Biology, 59 papers in Cell Biology and 54 papers in Oncology. Recurrent topics in Jonathan Chernoff's work include Protein Kinase Regulation and GTPase Signaling (63 papers), Cancer-related Molecular Pathways (36 papers) and Protein Tyrosine Phosphatases (27 papers). Jonathan Chernoff is often cited by papers focused on Protein Kinase Regulation and GTPase Signaling (63 papers), Cancer-related Molecular Pathways (36 papers) and Protein Tyrosine Phosphatases (27 papers). Jonathan Chernoff collaborates with scholars based in United States, United Kingdom and Russia. Jonathan Chernoff's co-authors include Mary Ann Sells, Zahara M. Jaffer, Maria Radu, Gary Bokoch, Alexander Beeser, Caretha L. Creasy, Ulla G. Knaus, Feng Liu, Luis E. Arias‐Romero and Shubha Bagrodia and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Jonathan Chernoff

204 papers receiving 15.6k citations

Hit Papers

Rho Family GTPases Regulate p38 Mitogen-activated Protein... 1995 2026 2005 2015 1995 1997 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jonathan Chernoff United States 68 11.4k 4.6k 3.4k 2.3k 1.4k 207 15.7k
Andrius Kazlauskas United States 60 9.8k 0.9× 2.2k 0.5× 2.4k 0.7× 2.3k 1.0× 1.1k 0.8× 188 15.1k
Alex Toker United States 73 15.1k 1.3× 3.7k 0.8× 3.1k 0.9× 2.3k 1.0× 1.4k 1.0× 136 20.5k
Christopher J. Marshall United Kingdom 61 15.0k 1.3× 4.8k 1.1× 5.5k 1.6× 1.6k 0.7× 1.4k 1.0× 94 20.2k
Marc Symons United States 54 8.9k 0.8× 4.6k 1.0× 2.3k 0.7× 1.5k 0.6× 1.8k 1.3× 136 12.7k
Yi Zheng United States 83 14.1k 1.2× 6.2k 1.4× 2.8k 0.8× 3.2k 1.4× 1.6k 1.1× 364 21.5k
Daniel D. Billadeau United States 69 7.5k 0.7× 3.2k 0.7× 2.9k 0.9× 4.5k 1.9× 1.2k 0.8× 215 14.4k
Mark R. Philips United States 58 8.2k 0.7× 2.9k 0.6× 1.8k 0.5× 2.0k 0.8× 1.2k 0.9× 129 11.5k
Jürgen Behrens Germany 58 15.5k 1.4× 3.4k 0.7× 3.8k 1.1× 1.0k 0.4× 1.3k 0.9× 113 19.3k
Gregory D. Plowman United States 59 8.6k 0.8× 2.2k 0.5× 5.0k 1.5× 1.6k 0.7× 1.5k 1.1× 98 13.8k
Lewis T. Williams United States 65 15.2k 1.3× 3.5k 0.8× 4.1k 1.2× 4.6k 2.0× 1.5k 1.1× 114 22.0k

Countries citing papers authored by Jonathan Chernoff

Since Specialization
Citations

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

Fields of papers citing papers by Jonathan Chernoff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonathan Chernoff

This figure shows the co-authorship network connecting the top 25 collaborators of Jonathan Chernoff. A scholar is included among the top collaborators of Jonathan Chernoff 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 Jonathan Chernoff. Jonathan Chernoff 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.
Chow, Hoi Yee, et al.. (2024). Synergistic effect of PAK and Hippo pathway inhibitor combination in NF2-deficient Schwannoma. PLoS ONE. 19(7). e0305121–e0305121. 3 indexed citations
2.
Somanath, Payaningal R., et al.. (2023). Targeting P21-Activated Kinase-1 for Metastatic Prostate Cancer. Cancers. 15(8). 2236–2236. 8 indexed citations
3.
Chernoff, Jonathan, et al.. (2023). RHOA drivers take alternate routes in gastric cancer. Science Signaling. 16(816). eadk9171–eadk9171. 2 indexed citations
4.
Risteski, Patrik, Yang Yang, Huan Chen, et al.. (2023). The TRIM69-MST2 signaling axis regulates centrosome dynamics and chromosome segregation. Nucleic Acids Research. 51(19). 10568–10589. 7 indexed citations
5.
Villamar‐Cruz, Olga, Marco A. Loza-Mejía, Genaro Patiño‐López, et al.. (2023). A PTP1B-Cdk3 Signaling Axis Promotes Cell Cycle Progression of Human Glioblastoma Cells through an Rb-E2F Dependent Pathway. Molecular and Cellular Biology. 43(12). 631–649. 1 indexed citations
6.
Kurimchak, Alison, Valerie L. Sodi, Nishi Srivastava, et al.. (2020). Functional proteomics interrogation of the kinome identifies MRCKA as a therapeutic target in high-grade serous ovarian carcinoma. Science Signaling. 13(619). 19 indexed citations
7.
Uribe‐Alvarez, Cristina, et al.. (2020). Targeting effector pathways in RAC1 P29S -driven malignant melanoma. Small GTPases. 12(4). 273–281. 12 indexed citations
8.
Kurimchak, Alison, et al.. (2019). Intrinsic Resistance to MEK Inhibition through BET Protein–Mediated Kinome Reprogramming in NF1-Deficient Ovarian Cancer. Molecular Cancer Research. 17(8). 1721–1734. 25 indexed citations
9.
Semenova, Galina, Yin‐Ming Kuo, Andrew J. Andrews, et al.. (2017). An Essential Role for the Tumor-Suppressor Merlin in Regulating Fatty Acid Synthesis. Cancer Research. 77(18). 5026–5038. 20 indexed citations
10.
Reddy, Pavankumar N.G., Maria Radu, Ke Xu, et al.. (2016). p21-activated kinase 2 regulates HSPC cytoskeleton, migration, and homing via CDC42 activation and interaction with β-Pix. Blood. 127(16). 1967–1975. 24 indexed citations
11.
Singh, Nikhlesh K., Sivareddy Kotla, James Traylor, et al.. (2015). Disruption of p21-activated kinase 1 gene diminishes atherosclerosis in apolipoprotein E-deficient mice. Nature Communications. 6(1). 7450–7450. 23 indexed citations
12.
Arias‐Romero, Luis E., et al.. (2013). Pak1 Kinase Links ErbB2 to β-Catenin in Transformation of Breast Epithelial Cells. Cancer Research. 73(12). 3671–3682. 64 indexed citations
13.
Chow, Hoi Yee, Adrian M. Jubb, Zahara M. Jaffer, et al.. (2012). p21-Activated Kinase 1 Is Required for Efficient Tumor Formation and Progression in a Ras-Mediated Skin Cancer Model. Cancer Research. 72(22). 5966–5975. 101 indexed citations
14.
Menges, Craig W., Eleonora Sementino, Jacqueline Talarchek, et al.. (2012). Group I p21-Activated Kinases (PAKs) Promote Tumor Cell Proliferation and Survival through the AKT1 and Raf–MAPK Pathways. Molecular Cancer Research. 10(9). 1178–1188. 40 indexed citations
15.
Delorme-Walker, Violaine, Jeffrey R. Peterson, Jonathan Chernoff, et al.. (2011). Pak1 regulates focal adhesion strength, myosin IIA distribution, and actin dynamics to optimize cell migration. The Journal of Cell Biology. 193(7). 1289–1303. 80 indexed citations
16.
Arias‐Romero, Luis E., Sayanti Saha, Olga Villamar‐Cruz, et al.. (2009). Activation of Src by Protein Tyrosine Phosphatase 1B Is Required for ErbB2 Transformation of Human Breast Epithelial Cells. Cancer Research. 69(11). 4582–4588. 76 indexed citations
17.
Cotteret, Sophie & Jonathan Chernoff. (2005). Pak GITs to Aurora-A. Developmental Cell. 9(5). 573–574. 12 indexed citations
18.
Reynolds, Lucinda F., et al.. (2004). Vav1 Transduces T Cell Receptor Signals to the Activation of the Ras/ERK Pathway via LAT, Sos, and RasGRP1. Journal of Biological Chemistry. 279(18). 18239–18246. 80 indexed citations
19.
Dadke, Shrikrishna & Jonathan Chernoff. (2003). Protein-Tyrosine Phosphatase 1B as a Potential Drug Target for Obesity. PubMed. 3(4). 299–304. 24 indexed citations
20.
Ottilie, Sabine, Peter J. Miller, Douglas I. Johnson, et al.. (1995). Fission yeast pak1+ encodes a protein kinase that interacts with Cdc42p and is involved in the control of cell polarity and mating.. The EMBO Journal. 14(23). 5908–5919. 132 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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