Christopher Ford

4.3k total citations · 2 hit papers
52 papers, 2.8k citations indexed

About

Christopher Ford is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Christopher Ford has authored 52 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Cellular and Molecular Neuroscience, 35 papers in Molecular Biology and 11 papers in Cognitive Neuroscience. Recurrent topics in Christopher Ford's work include Neuroscience and Neuropharmacology Research (31 papers), Receptor Mechanisms and Signaling (26 papers) and Neurotransmitter Receptor Influence on Behavior (19 papers). Christopher Ford is often cited by papers focused on Neuroscience and Neuropharmacology Research (31 papers), Receptor Mechanisms and Signaling (26 papers) and Neurotransmitter Receptor Influence on Behavior (19 papers). Christopher Ford collaborates with scholars based in United States, Canada and Czechia. Christopher Ford's co-authors include John T. Williams, Gregory P. Mark, Michael R. Bruchas, Stephanie C. Gantz, Paul E. M. Phillips, Edward R. Siuda, Aaron J. Norris, Daniel Y. Hong, Jordan G. McCall and Ream Al‐Hasani and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Christopher Ford

50 papers receiving 2.8k citations

Hit Papers

CRH Engagement of the Loc... 2014 2026 2018 2022 2015 2014 100 200 300 400

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Christopher Ford 1.9k 1.3k 730 276 258 52 2.8k
Yolanda Mateo 2.0k 1.1× 1.2k 0.9× 565 0.8× 184 0.7× 164 0.6× 41 2.6k
Mustapha Riad 2.2k 1.1× 1.2k 0.9× 464 0.6× 232 0.8× 167 0.6× 45 2.8k
Brian A. McCool 2.3k 1.2× 1.2k 0.9× 862 1.2× 387 1.4× 493 1.9× 76 3.4k
Kristen A. Keefe 2.2k 1.1× 1.1k 0.8× 686 0.9× 229 0.8× 340 1.3× 82 3.2k
Jesus Bertran‐Gonzalez 1.7k 0.9× 1.3k 1.0× 699 1.0× 258 0.9× 99 0.4× 29 2.6k
Evgeny A. Budygin 2.7k 1.4× 1.5k 1.1× 1.1k 1.5× 241 0.9× 274 1.1× 74 3.7k
Noboru Hiroi 2.9k 1.5× 2.3k 1.7× 985 1.3× 380 1.4× 258 1.0× 68 4.4k
Rueben A. Gonzales 2.9k 1.5× 1.8k 1.3× 720 1.0× 403 1.5× 223 0.9× 106 3.8k
François Georges 2.6k 1.3× 1.1k 0.8× 1.1k 1.5× 399 1.4× 249 1.0× 50 3.6k
Daniela Di Bella 1.8k 0.9× 1.0k 0.8× 507 0.7× 144 0.5× 206 0.8× 76 3.3k

Countries citing papers authored by Christopher Ford

Since Specialization
Citations

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

Fields of papers citing papers by Christopher Ford

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher Ford

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher Ford. A scholar is included among the top collaborators of Christopher Ford 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 Ford. Christopher Ford 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.
Kim, Yoon Seok, Lief E. Fenno, Charu Ramakrishnan, et al.. (2025). Salience Signaling and Stimulus Scaling of Ventral Tegmental Area Glutamate Neuron Subtypes. Journal of Neuroscience. 45(27). e1073242025–e1073242025.
3.
Rajgor, Dipen, Sara E. Gookin, Mark L. Dell’Acqua, et al.. (2024). miRNA-mediated control of gephyrin synthesis drives sustained inhibitory synaptic plasticity. EMBO Reports. 25(11). 5141–5168. 2 indexed citations
4.
Ford, Christopher, et al.. (2024). Reduced striatal M4-cholinergic signaling following dopamine loss contributes to parkinsonian and l -DOPA–induced dyskinetic behaviors. Science Advances. 10(47). eadp6301–eadp6301. 7 indexed citations
5.
Rodriguez‐Contreras, Dayana, Joseph J. Lebowitz, Lev M. Fedorov, et al.. (2022). Gait Abnormalities and Aberrant D2 Receptor Expression and Signaling in Mice Carrying the Human Pathogenic Mutation DRD2. Molecular Pharmacology. 103(3). 188–198. 3 indexed citations
6.
Ford, Christopher, et al.. (2022). Divergent properties and independent regulation of striatal dopamine and GABA co-transmission. Cell Reports. 39(7). 110823–110823. 22 indexed citations
7.
Cai, Yuan, et al.. (2021). Loss of nigral excitation of cholinergic interneurons contributes to parkinsonian motor impairments. Neuron. 109(7). 1137–1149.e5. 37 indexed citations
8.
Giannotti, Giuseppe, Jasper A. Heinsbroek, James E. Orfila, et al.. (2021). Extinction blunts paraventricular thalamic contributions to heroin relapse. Cell Reports. 36(8). 109605–109605. 17 indexed citations
9.
Liu, Qi, Martin Schneider, Michael J. Grybko, et al.. (2019). A Photoactivatable Botulinum Neurotoxin for Inducible Control of Neurotransmission. Neuron. 101(5). 863–875.e6. 36 indexed citations
10.
Barcomb, Kelsey, et al.. (2019). Cholinergic Transmission at Muscarinic Synapses in the Striatum Is Driven Equally by Cortical and Thalamic Inputs. Cell Reports. 28(4). 1003–1014.e3. 26 indexed citations
11.
Gulati, Sahil, Hui Jin, Ikuo Masuho, et al.. (2018). Targeting G protein-coupled receptor signaling at the G protein level with a selective nanobody inhibitor. Nature Communications. 9(1). 1996–1996. 68 indexed citations
12.
Donthamsetti, Prashant, Steven G. Grinnell, Amy Hauck Newman, et al.. (2018). Regional Heterogeneity of D2-Receptor Signaling in the Dorsal Striatum and Nucleus Accumbens. Neuron. 98(3). 575–587.e4. 49 indexed citations
13.
McCall, Jordan G., Ream Al‐Hasani, Edward R. Siuda, et al.. (2015). CRH Engagement of the Locus Coeruleus Noradrenergic System Mediates Stress-Induced Anxiety. Neuron. 87(3). 605–620. 445 indexed citations breakdown →
14.
Bender, Kevin J., Christopher Ford, & Laurence O. Trussell. (2010). Dopaminergic Modulation of Axon Initial Segment Calcium Channels Regulates Action Potential Initiation. Neuron. 68(3). 500–511. 89 indexed citations
15.
Ford, Christopher, Paul E. M. Phillips, & John T. Williams. (2009). The Time Course of Dopamine Transmission in the Ventral Tegmental Area. Journal of Neuroscience. 29(42). 13344–13352. 64 indexed citations
16.
Beckstead, Michael J., Stephanie C. Gantz, Christopher Ford, et al.. (2009). CRF Enhancement of GIRK Channel-Mediated Transmission in Dopamine Neurons. Neuropsychopharmacology. 34(8). 1926–1935. 54 indexed citations
17.
Ford, Christopher, Kenneth Wong, Van B. Lu, E Chaves, & Peter A. Smith. (2008). Differential Neurotrophic Regulation of Sodium and Calcium Channels in an Adult Sympathetic Neuron. Journal of Neurophysiology. 99(3). 1319–1332. 10 indexed citations
18.
Ford, Christopher & John T. Williams. (2008). Mesoprefrontal Dopamine Neurons Distinguish Themselves. Neuron. 57(5). 631–632. 4 indexed citations
19.
Ford, Christopher, Michael J. Beckstead, & John T. Williams. (2006). Kappa Opioid Inhibition of Somatodendritic Dopamine Inhibitory Postsynaptic Currents. Journal of Neurophysiology. 97(1). 883–891. 64 indexed citations
20.
Filtz, Theresa M., et al.. (1994). Mechanisms of up-regulation of D2L dopamine receptors by agonists and antagonists in transfected HEK-293 cells.. Journal of Pharmacology and Experimental Therapeutics. 271(3). 1574–1582. 31 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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