Keith G. Phillips

1.2k total citations
23 papers, 784 citations indexed

About

Keith G. Phillips is a scholar working on Cellular and Molecular Neuroscience, Cognitive Neuroscience and Physiology. According to data from OpenAlex, Keith G. Phillips has authored 23 papers receiving a total of 784 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cellular and Molecular Neuroscience, 14 papers in Cognitive Neuroscience and 5 papers in Physiology. Recurrent topics in Keith G. Phillips's work include Neuroscience and Neuropharmacology Research (13 papers), Neural dynamics and brain function (10 papers) and Memory and Neural Mechanisms (7 papers). Keith G. Phillips is often cited by papers focused on Neuroscience and Neuropharmacology Research (13 papers), Neural dynamics and brain function (10 papers) and Memory and Neural Mechanisms (7 papers). Keith G. Phillips collaborates with scholars based in United Kingdom, United States and Belgium. Keith G. Phillips's co-authors include Gary Gilmour, Hugh Marston, Enrique Jambrina, Johanna Jackson, Jennifer Li, Fiona M. Menzies, Kevin Fox, Neil R. Hardingham, Mark D. Tricklebank and Keith A. Wafford and has published in prestigious journals such as Neuron, Journal of Neuroscience and Nature Neuroscience.

In The Last Decade

Keith G. Phillips

23 papers receiving 771 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Keith G. Phillips United Kingdom 15 436 384 233 196 99 23 784
Lori A. Newman United States 12 460 1.1× 369 1.0× 221 0.9× 133 0.7× 138 1.4× 17 815
Olivia A. Shipton United Kingdom 8 495 1.1× 320 0.8× 184 0.8× 269 1.4× 129 1.3× 8 831
Tim S. Heistek Netherlands 16 548 1.3× 372 1.0× 234 1.0× 174 0.9× 169 1.7× 27 917
Ksenia V. Kastanenka United States 15 285 0.7× 223 0.6× 273 1.2× 316 1.6× 137 1.4× 25 790
François Gastambide United Kingdom 16 511 1.2× 281 0.7× 340 1.5× 83 0.4× 64 0.6× 21 863
Sjoukje D. Kuipers Norway 9 438 1.0× 167 0.4× 249 1.1× 117 0.6× 98 1.0× 12 803
Jaime G. Maldonado‐Avilés United States 9 485 1.1× 236 0.6× 328 1.4× 100 0.5× 83 0.8× 10 1.0k
Samuel W. Centanni United States 18 602 1.4× 357 0.9× 248 1.1× 86 0.4× 58 0.6× 30 932
Linda Palmer United States 10 446 1.0× 238 0.6× 202 0.9× 103 0.5× 65 0.7× 21 693
Camilla L. Patti Brazil 17 384 0.9× 386 1.0× 171 0.7× 161 0.8× 87 0.9× 32 896

Countries citing papers authored by Keith G. Phillips

Since Specialization
Citations

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

Fields of papers citing papers by Keith G. Phillips

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Keith G. Phillips

This figure shows the co-authorship network connecting the top 25 collaborators of Keith G. Phillips. A scholar is included among the top collaborators of Keith G. Phillips 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 Keith G. Phillips. Keith G. Phillips 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.
Pia, H. W., Zahra Nochi, Alexander Gramm Kristensen, et al.. (2023). The test–retest reliability of large and small fiber nerve excitability testing with threshold tracking. Clinical Neurophysiology Practice. 8. 71–78. 2 indexed citations
2.
Niel, Johannes, Petra Bloms‐Funke, Ombretta Caspani, et al.. (2022). Pharmacological Probes to Validate Biomarkers for Analgesic Drug Development. International Journal of Molecular Sciences. 23(15). 8295–8295. 1 indexed citations
3.
Papanikolaou, Amalia, et al.. (2022). Plasticity in visual cortex is disrupted in a mouse model of tauopathy. Communications Biology. 5(1). 77–77. 17 indexed citations
4.
Papanikolaou, Amalia, et al.. (2022). Altered low-frequency brain rhythms precede changes in gamma power during tauopathy. iScience. 25(10). 105232–105232. 4 indexed citations
5.
Pietro, Giuseppe Di, Giulia Di Stefano, Caterina Leone, et al.. (2021). The N13 spinal component of somatosensory evoked potentials is modulated by heterotopic noxious conditioning stimulation suggesting an involvement of spinal wide dynamic range neurons. Neurophysiologie Clinique. 51(6). 517–523. 9 indexed citations
6.
Witton, Jonathan, et al.. (2020). Impaired speed encoding and grid cell periodicity in a mouse model of tauopathy. eLife. 9. 17 indexed citations
7.
Jackson, Johanna, Enrique Jambrina, Jennifer Li, et al.. (2019). Targeting the Synapse in Alzheimer’s Disease. Frontiers in Neuroscience. 13. 735–735. 162 indexed citations
8.
Danjou, Philippe, Pilar Garcés, Emma J. Wams, et al.. (2018). Electrophysiological assessment methodology of sensory processing dysfunction in schizophrenia and dementia of the Alzheimer type. Neuroscience & Biobehavioral Reviews. 97. 70–84. 17 indexed citations
9.
Huxter, John R., Stuart A Bowyer, J. Ryan Butler, et al.. (2017). TaiNi: Maximizing research output whilst improving animals’ welfare in neurophysiology experiments. Scientific Reports. 7(1). 8086–8086. 16 indexed citations
10.
Baker, Keeley L., Michael W. Conway, Gary Gilmour, et al.. (2017). Coordinated Acetylcholine Release in Prefrontal Cortex and Hippocampus Is Associated with Arousal and Reward on Distinct Timescales. Cell Reports. 18(4). 905–917. 116 indexed citations
11.
Meftah, S., Tracey K. Murray, Peter J. Craig, et al.. (2017). Tracking progressive pathological and functional decline in the rTg4510 mouse model of tauopathy. Alzheimer s Research & Therapy. 9(1). 77–77. 40 indexed citations
12.
Murray, Tracey K., Mark Ward, Marc Goodfellow, et al.. (2016). Electrical and Network Neuronal Properties Are Preferentially Disrupted in Dorsal, But Not Ventral, Medial Entorhinal Cortex in a Mouse Model of Tauopathy. Journal of Neuroscience. 36(2). 312–324. 47 indexed citations
13.
Esclassan, Frédéric, et al.. (2014). Phenotypic characterization of nonsocial behavioral impairment in neurexin 1α knockout rats.. Behavioral Neuroscience. 129(1). 74–85. 45 indexed citations
14.
Phillips, Keith G., Ullrich Bartsch, Dale M. Edgar, et al.. (2012). Decoupling of Sleep-Dependent Cortical and Hippocampal Interactions in a Neurodevelopmental Model of Schizophrenia. Neuron. 76(3). 526–533. 102 indexed citations
15.
Chen, Ying, Lisa M. Broad, Keith G. Phillips, & Ruud Zwart. (2011). Partial agonists for α4β2 nicotinic receptors stimulate dopaminergic neuron firing with relatively enhanced maximal effects. British Journal of Pharmacology. 165(4). 1006–1016. 6 indexed citations
16.
Filippi, Giovanna De, Adrian J. Mogg, Keith G. Phillips, et al.. (2010). The subtype-selective nicotinic acetylcholine receptor positive allosteric potentiator 2087101 differentially facilitates neurotransmission in the brain. European Journal of Pharmacology. 643(2-3). 218–224. 9 indexed citations
17.
Wright, Nicholas F., Stanislaw Glazewski, Neil R. Hardingham, et al.. (2008). Laminar analysis of the role of GluR1 in experience-dependent and synaptic depression in barrel cortex. Nature Neuroscience. 11(10). 1140–1142. 22 indexed citations
18.
Phillips, Keith G., Neil R. Hardingham, & Kevin Fox. (2008). Postsynaptic Action Potentials Are Required for Nitric-Oxide-Dependent Long-Term Potentiation in CA1 Neurons of Adult GluR1 Knock-Out and Wild-Type Mice. Journal of Neuroscience. 28(52). 14031–14041. 41 indexed citations
19.
Chen, Ying, et al.. (2005). GABAB receptor modulators potentiate baclofen‐induced depression of dopamine neuron activity in the rat ventral tegmental area. British Journal of Pharmacology. 144(7). 926–932. 34 indexed citations
20.
Chen, Ying, Keith G. Phillips, Giovanni Benedetti, et al.. (2003). The nicotinic α4β2 receptor selective agonist, TC-2559, increases dopamine neuronal activity in the ventral tegmental area of rat midbrain slices. Neuropharmacology. 45(3). 334–344. 37 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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