James G. Davis

5.5k total citations
52 papers, 3.0k citations indexed

About

James G. Davis is a scholar working on Molecular Biology, Oncology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, James G. Davis has authored 52 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 11 papers in Oncology and 10 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in James G. Davis's work include HER2/EGFR in Cancer Research (8 papers), Monoclonal and Polyclonal Antibodies Research (6 papers) and Marine animal studies overview (4 papers). James G. Davis is often cited by papers focused on HER2/EGFR in Cancer Research (8 papers), Monoclonal and Polyclonal Antibodies Research (6 papers) and Marine animal studies overview (4 papers). James G. Davis collaborates with scholars based in United States, China and Canada. James G. Davis's co-authors include Mark I. Greene, Chester A. Mathis, Brian J. Lopresti, Steven T. DeKosky, Daniel Kaufer, Larry S. Ivanco, Joseph A. Baur, Nicolaas I. Bohnen, Robert Y. Moore and Kunio Dobashi and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

James G. Davis

52 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James G. Davis United States 28 1.0k 608 586 574 423 52 3.0k
Jeffrey M. Gidday United States 38 2.1k 2.0× 783 1.3× 162 0.3× 701 1.2× 957 2.3× 89 5.8k
Mario Passalacqua Italy 34 1.5k 1.5× 172 0.3× 260 0.4× 485 0.8× 511 1.2× 124 3.1k
Kazuaki Yoshikawa Japan 43 3.6k 3.5× 172 0.3× 414 0.7× 963 1.7× 1.2k 2.7× 142 5.7k
Yunjuan Sun United States 31 3.2k 3.1× 537 0.9× 276 0.5× 911 1.6× 2.3k 5.4× 55 7.4k
Shigetoshi Yano Japan 35 1.5k 1.5× 1.5k 2.5× 232 0.4× 368 0.6× 1.1k 2.6× 137 4.9k
Maria K. Lehtinen United States 30 2.5k 2.4× 313 0.5× 191 0.3× 387 0.7× 1.2k 2.8× 63 4.5k
Sebastiano Cavallaro Italy 39 2.2k 2.2× 915 1.5× 253 0.4× 486 0.8× 1.7k 3.9× 186 4.5k
Yuichi Makino Japan 33 2.9k 2.9× 250 0.4× 596 1.0× 797 1.4× 788 1.9× 82 5.6k
Laura Korhonen Sweden 41 2.3k 2.3× 505 0.8× 135 0.2× 719 1.3× 1.3k 3.0× 110 5.0k
Ana Martín-Villalba Germany 37 3.2k 3.1× 449 0.7× 518 0.9× 519 0.9× 1.3k 3.0× 69 5.7k

Countries citing papers authored by James G. Davis

Since Specialization
Citations

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

Fields of papers citing papers by James G. Davis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James G. Davis. 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 James G. Davis. The network helps show where James G. Davis may publish in the future.

Co-authorship network of co-authors of James G. Davis

This figure shows the co-authorship network connecting the top 25 collaborators of James G. Davis. A scholar is included among the top collaborators of James G. Davis 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 James G. Davis. James G. Davis 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.
Doke, Tomohito, Sarmistha Mukherjee, Dhanunjay Mukhi, et al.. (2023). NAD+ precursor supplementation prevents mtRNA/RIG-I-dependent inflammation during kidney injury. Nature Metabolism. 5(3). 414–430. 62 indexed citations
2.
Frederick, David W., Emanuele Loro, Ling Liu, et al.. (2016). Loss of NAD Homeostasis Leads to Progressive and Reversible Degeneration of Skeletal Muscle. Cell Metabolism. 24(2). 269–282. 273 indexed citations
3.
Davis, James G., et al.. (2016). Diagnosis of neonatal neuroblastoma with postmortem magnetic resonance imaging. Radiology Case Reports. 12(1). 191–195. 3 indexed citations
4.
Zhang, Jing, Yan Zhu, Guanxia Zhan, et al.. (2014). Extended Wakefulness: Compromised Metabolics in and Degeneration of Locus Ceruleus Neurons. Journal of Neuroscience. 34(12). 4418–4431. 117 indexed citations
5.
Naidoo, Nirinjini, James G. Davis, Jingxu Zhu, et al.. (2013). Aging and sleep deprivation induce the unfolded protein response in the pancreas: implications for metabolism. Aging Cell. 13(1). 131–141. 48 indexed citations
6.
Lamming, Dudley W., Lan Ye, Pekka Katajisto, et al.. (2012). Rapamycin-Induced Insulin Resistance Is Mediated by mTORC2 Loss and Uncoupled from Longevity. Science. 335(6076). 1638–1643. 52 indexed citations
7.
Davis, James G., X. Steven Wan, Jeffrey H. Ware, & Ann R. Kennedy. (2010). Dietary Supplements Reduce the Cataractogenic Potential of Proton and HZE-Particle Radiation in Mice. Radiation Research. 173(3). 353–361. 30 indexed citations
8.
Kennedy, Ann R., James G. Davis, William W. Carlton, & Jeffrey H. Ware. (2008). Effects of Dietary Antioxidant Supplementation on the Development of Malignant Lymphoma and Other Neoplastic Lesions in Mice Exposed to Proton or Iron-Ion Radiation. Radiation Research. 169(6). 615–625. 43 indexed citations
9.
Wambi, Chris, Jenine K. Sanzari, X. Steven Wan, et al.. (2008). Dietary Antioxidants Protect Hematopoietic Cells and Improve Animal Survival after Total-Body Irradiation. Radiation Research. 169(4). 384–396. 69 indexed citations
10.
Bohnen, Nicolaas I., Daniel Kaufer, Larry S. Ivanco, et al.. (2003). Cortical Cholinergic Function Is More Severely Affected in Parkinsonian Dementia Than in Alzheimer Disease. Archives of Neurology. 60(12). 1745–1745. 428 indexed citations
11.
Neep, David J., Denise Gay, Huizhen Zhao, et al.. (2002). Characterization of Mouse tGolgin-1 (Golgin-245/ trans -Golgi p230/256 kD Golgin) and Its Upregulation during Oligodendrocyte Development. DNA and Cell Biology. 21(7). 505–517. 6 indexed citations
12.
Murayama, Emi, Yasuaki Takagi, Tsuyoshi Ohira, et al.. (2002). Fish otolith contains a unique structural protein, otolin‐1. European Journal of Biochemistry. 269(2). 688–696. 113 indexed citations
13.
Matsunaga, Tatsuo, James G. Davis, & Mark I. Greene. (2001). Adult Rat Otic Placode-Derived Neurons and Sensory Epithelium Express All Four erbB Receptors: A Role in Regulating Vestibular Ganglion Neuron Viability. DNA and Cell Biology. 20(6). 307–319. 4 indexed citations
14.
Park, Byeong‐Woo, Donald M. O’Rourke, Qiang Wang, et al.. (1999). Induction of the Tat-binding protein 1 gene accompanies the disabling of oncogenic erbB receptor tyrosine kinases. Proceedings of the National Academy of Sciences. 96(11). 6434–6438. 16 indexed citations
15.
O’Rourke, Donald M., James G. Davis, Chuan-Jin Wu, et al.. (1998). Inhibition of a naturally occurring EGFR oncoprotein by the p185neu ectodomain: implications for subdomain contributions to receptor assembly. Oncogene. 16(9). 1197–1207. 47 indexed citations
16.
Zhang, Hongtao, Xin Zhang, Huizhen Zhao, et al.. (1997). Relationship of p215BRCA1 to tyrosine kinase signaling pathways and the cell cycle in normal and transformed cells. Oncogene. 14(24). 2863–2869. 20 indexed citations
17.
Ichimiya, Shingo, et al.. (1996). Cloning of m-ehk2 from the Murine Inner Ear, an eph Family Receptor Tyrosine Kinase Expressed in the Developing and Adult Cochlea. DNA and Cell Biology. 15(10). 817–825. 22 indexed citations
18.
Karbe, H., Andrew Kertesz, James G. Davis, et al.. (1994). Quantification of functional deficit in Alzheimer's disease using a computer-assisted mapping program for99mTc-HMPAO SPECT. Neuroradiology. 36(1). 1–6. 43 indexed citations
19.
Davis, James G., et al.. (1991). Isolation and characterization of a neu protein-specific activating factor from human ATL-2 cell conditioned medium. Biochemical and Biophysical Research Communications. 179(3). 1536–1542. 15 indexed citations
20.
Kokai, Yasuo, Jeffrey N. Myers, Takuro Wada, et al.. (1989). Synergistic interaction of p185c-neu and the EGF receptor leads to transformation of rodent fibroblasts. Cell. 58(2). 287–292. 281 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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