Christopher Davis

795 total citations
23 papers, 545 citations indexed

About

Christopher Davis is a scholar working on Cognitive Neuroscience, Molecular Biology and Pharmacology. According to data from OpenAlex, Christopher Davis has authored 23 papers receiving a total of 545 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Cognitive Neuroscience, 5 papers in Molecular Biology and 4 papers in Pharmacology. Recurrent topics in Christopher Davis's work include Motor Control and Adaptation (5 papers), Visual perception and processing mechanisms (4 papers) and Fungal Biology and Applications (3 papers). Christopher Davis is often cited by papers focused on Motor Control and Adaptation (5 papers), Visual perception and processing mechanisms (4 papers) and Fungal Biology and Applications (3 papers). Christopher Davis collaborates with scholars based in United States, Canada and Netherlands. Christopher Davis's co-authors include William L. Roberts, Nicholas P. Money, J.P. Ravishankar, Paul Brickett, Jeanette N. McClintick, Jeffrey A. Willy, Michael E. Fusakio, Tracy G. Anthony, Lakshmi Reddy Palam and T. Baird and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Annals of the New York Academy of Sciences.

In The Last Decade

Christopher Davis

23 papers receiving 532 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher Davis United States 13 148 142 81 73 71 23 545
Norman Maclean United Kingdom 10 305 2.1× 34 0.2× 79 1.0× 31 0.4× 15 0.2× 20 654
Tomonari Awaya Japan 17 691 4.7× 80 0.6× 44 0.5× 42 0.6× 21 0.3× 55 1.1k
Brian T. Faddis United States 15 376 2.5× 44 0.3× 8 0.1× 92 1.3× 13 0.2× 31 1.0k
Christer Nilsson Sweden 16 277 1.9× 67 0.5× 23 0.3× 35 0.5× 354 5.0× 31 1.1k
Yuanyuan Xie China 16 285 1.9× 37 0.3× 15 0.2× 45 0.6× 6 0.1× 41 773
Ridha Mrad Tunisia 17 601 4.1× 116 0.8× 20 0.2× 53 0.7× 11 0.2× 89 1.0k
Megumi Suzuki Japan 14 351 2.4× 78 0.5× 116 1.4× 13 0.2× 6 0.1× 43 627
Frans Stafleu Netherlands 10 150 1.0× 16 0.1× 31 0.4× 9 0.1× 14 0.2× 24 644
Yuko Taniguchi Japan 16 264 1.8× 162 1.1× 7 0.1× 29 0.4× 23 0.3× 33 1.3k
Scott M. Paul United States 17 331 2.2× 8 0.1× 152 1.9× 29 0.4× 19 0.3× 35 983

Countries citing papers authored by Christopher Davis

Since Specialization
Citations

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

Fields of papers citing papers by Christopher Davis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher Davis

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher Davis. A scholar is included among the top collaborators of Christopher 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 Christopher Davis. Christopher 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.
Sait, Sameer Farouk, Kwan Ho Tang, Steven P. Angus, et al.. (2024). Hydroxychloroquine prevents resistance and potentiates the antitumor effect of SHP2 inhibition in NF1-associated malignant peripheral nerve sheath tumors. Proceedings of the National Academy of Sciences. 122(1). e2407745121–e2407745121. 2 indexed citations
2.
Stieglitz, Elliot, Alex G. Lee, Steven P. Angus, et al.. (2024). Efficacy of the Allosteric MEK Inhibitor Trametinib in Relapsed and Refractory Juvenile Myelomonocytic Leukemia: a Report from the Children’s Oncology Group. Cancer Discovery. 14(9). 1590–1598. 4 indexed citations
3.
Stieglitz, Elliot, Alex Lee, Steven P. Angus, et al.. (2023). Efficacy of the Allosteric MEK Inhibitor Trametinib in Relapsed and Refractory Juvenile Myelomonocytic Leukemia: A Report from the Children's Oncology Group. Blood. 142(Supplement 1). 74–74. 2 indexed citations
4.
Baird, T., Lakshmi Reddy Palam, Michael E. Fusakio, et al.. (2014). Selective mRNA translation during eIF2 phosphorylation induces expression of IBTKα. Molecular Biology of the Cell. 25(10). 1686–1697. 93 indexed citations
5.
Sorror, Mohamed L., Paul J. Martin, Rainer Storb, et al.. (2014). Pretransplant comorbidities predict severity of acute graft-versus-host disease and subsequent mortality. Blood. 124(2). 287–295. 73 indexed citations
6.
Gambaro, Karen, Colleen Crane, Suzanna L. Arcand, et al.. (2013). Small cell ovarian carcinoma: genomic stability and responsiveness to therapeutics. Orphanet Journal of Rare Diseases. 8(1). 33–33. 29 indexed citations
7.
Chinen, Javier, et al.. (2012). Presentation of atopic disease in a large cohort of pediatric liver transplant recipients. Pediatric Transplantation. 16(4). 379–384. 34 indexed citations
8.
Fletcher, Horace, et al.. (2010). Commonly used botanicals and vitamins and their impact on blood pressure and blood loss in surgical gynaecology patients. Journal of Obstetrics and Gynaecology. 30(3). 272–276. 2 indexed citations
9.
Money, Nicholas P., Christopher Davis, & J.P. Ravishankar. (2004). Biomechanical evidence for convergent evolution of the invasive growth process among fungi and oomycete water molds. Fungal Genetics and Biology. 41(9). 872–876. 45 indexed citations
10.
Ravishankar, J.P., et al.. (2001). Mechanics of Solid Tissue Invasion by the Mammalian Pathogen Pythium insidiosum. Fungal Genetics and Biology. 34(3). 167–175. 42 indexed citations
11.
Davis, Christopher, et al.. (1999). Evaporative cooling of mushrooms. Mycologia. 91(2). 351–352. 13 indexed citations
12.
Johns, Scott, Christopher Davis, & Nicholas P. Money. (1999). Pulses in turgor pressure and water potential: resolving the mechanics of hyphal growth. Microbiological Research. 154(3). 225–231. 23 indexed citations
13.
Davis, Christopher, et al.. (1999). Evaporative Cooling of Mushrooms. Mycologia. 91(2). 351–351. 7 indexed citations
14.
Brickett, Paul, et al.. (1980). Dual on-line computers for research in cognitive psychophysiology. Behavior Research Methods. 12(2). 248–250. 2 indexed citations
15.
Davis, Christopher, et al.. (1977). A Weight Illusion Produced by Lifting Movements. Perceptual and Motor Skills. 44(1). 299–305. 9 indexed citations
16.
Davis, Christopher & Paul Brickett. (1977). The role of preparatory muscular tension in the size-weight illusion. Perception & Psychophysics. 22(3). 262–264. 18 indexed citations
17.
Davis, Christopher & William L. Roberts. (1976). Lifting movements in the size-weight illusion. Perception & Psychophysics. 20(1). 33–36. 78 indexed citations
18.
Davis, Christopher. (1974). The role of effective lever length in the perception of lifted weights. Perception & Psychophysics. 16(1). 67–69. 8 indexed citations
19.
Davis, Christopher. (1973). Mechanical advantage in the size-weight illusion. Perception & Psychophysics. 13(2). 238–240. 17 indexed citations
20.
Davis, Christopher & Randal D. Beaton. (1968). Facilitation and adaptation of the human quadriceps stretch reflex produced by auditory stimulation.. Journal of Comparative and Physiological Psychology. 66(2). 483–487. 16 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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