Charles T. Anderson

2.0k total citations
33 papers, 1.5k citations indexed

About

Charles T. Anderson is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Charles T. Anderson has authored 33 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Cellular and Molecular Neuroscience, 15 papers in Molecular Biology and 15 papers in Cognitive Neuroscience. Recurrent topics in Charles T. Anderson's work include Neuroscience and Neuropharmacology Research (14 papers), Hearing, Cochlea, Tinnitus, Genetics (11 papers) and Neural dynamics and brain function (8 papers). Charles T. Anderson is often cited by papers focused on Neuroscience and Neuropharmacology Research (14 papers), Hearing, Cochlea, Tinnitus, Genetics (11 papers) and Neural dynamics and brain function (8 papers). Charles T. Anderson collaborates with scholars based in United States, China and France. Charles T. Anderson's co-authors include Thanos Tzounopoulos, Gordon M. Shepherd, Patrick L. Sheets, Taro Kiritani, Jing Zheng, Stephen J. Lippard, Peter Dallos, Mary Ann Cheatham, Soma Sengupta and Jian Zuo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Neuron.

In The Last Decade

Charles T. Anderson

31 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Charles T. Anderson United States	20	550	506	438	437	299	33	1.5k
Dennis G. Drescher United States	27	217 0.4×	425 0.8×	869 2.0×	877 2.0×	316 1.1×	78	2.0k
Karin E. Borgmann‐Winter United States	17	227 0.4×	540 1.1×	556 1.3×	379 0.9×	263 0.9×	29	1.5k
J. Mark Kinzie United States	11	249 0.5×	1.3k 2.6×	1.0k 2.3×	396 0.9×	170 0.6×	19	1.9k
Thomas P. Segerson United States	22	197 0.4×	1.3k 2.7×	722 1.6×	331 0.8×	226 0.8×	25	2.7k
Marian J. Drescher United States	21	148 0.3×	280 0.6×	539 1.2×	625 1.4×	215 0.7×	54	1.2k
Michael R. Martin United States	20	226 0.4×	645 1.3×	390 0.9×	300 0.7×	91 0.3×	49	1.2k
Vincent Breton‐Provencher United States	14	461 0.8×	465 0.9×	251 0.6×	228 0.5×	39 0.1×	17	1.1k
Megumi Kaneko Japan	23	649 1.2×	1.2k 2.5×	727 1.7×	112 0.3×	55 0.2×	55	2.2k
Francisco J. Alvarez‐Leefmans United States	24	123 0.2×	993 2.0×	1.2k 2.8×	151 0.3×	117 0.4×	38	1.9k
Nicholas A. Bock Canada	25	584 1.1×	233 0.5×	364 0.8×	29 0.1×	93 0.3×	49	1.7k

Countries citing papers authored by Charles T. Anderson

Since Specialization

Citations

This map shows the geographic impact of Charles T. Anderson'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 Charles T. Anderson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Charles T. Anderson more than expected).

Fields of papers citing papers by Charles T. Anderson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charles T. Anderson. 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 Charles T. Anderson. The network helps show where Charles T. Anderson may publish in the future.

Co-authorship network of co-authors of Charles T. Anderson

This figure shows the co-authorship network connecting the top 25 collaborators of Charles T. Anderson. A scholar is included among the top collaborators of Charles T. Anderson 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 Charles T. Anderson. Charles T. Anderson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Webb, Bradley A., et al.. (2025). The Astrocytic Zinc Transporter ZIP12 Is a Synaptic Protein That Contributes to Synaptic Zinc Levels in the Mouse Auditory Cortex. Journal of Neuroscience. 45(13). e2067242025–e2067242025.

Hruska, Martin, et al.. (2024). Trans-synaptic Association of Vesicular Zinc Transporter 3 and Shank3 Supports Synapse-Specific Dendritic Spine Structure and Function in the Mouse Auditory Cortex. Journal of Neuroscience. 44(28). e0619242024–e0619242024. 6 indexed citations

Anderson, Charles T., et al.. (2024). Cell-type-specific enhancement of deviance detection by synaptic zinc in the mouse auditory cortex. Proceedings of the National Academy of Sciences. 121(40). e2405615121–e2405615121. 3 indexed citations

Guan, Tongju, Neil Billington, Sanford L. Boye, et al.. (2024). TUBB4B is essential for the cytoskeletal architecture of cochlear supporting cells and motile cilia development. Communications Biology. 7(1). 1146–1146. 1 indexed citations

Zhao, Shengyu, Mikhail Drobizhev, Charles T. Anderson, et al.. (2023). A genetically encoded far-red fluorescent indicator for imaging synaptically released Zn ²⁺. Science Advances. 9(9). eadd2058–eadd2058. 18 indexed citations

Xiong, Shanshan, et al.. (2018). Fine Control of Sound Frequency Tuning and Frequency Discrimination Acuity by Synaptic Zinc Signaling in Mouse Auditory Cortex. Journal of Neuroscience. 39(5). 854–865. 24 indexed citations

Moutal, Aubin, Jami L. Saloman, Karen A. Hartnett, et al.. (2017). Targeting a Potassium Channel/Syntaxin Interaction Ameliorates Cell Death in Ischemic Stroke. Journal of Neuroscience. 37(23). 5648–5658. 26 indexed citations

Anderson, Charles T., et al.. (2017). Cell-specific gain modulation by synaptically released zinc in cortical circuits of audition. eLife. 6. 37 indexed citations

Perez‐Rosello, Tamara, et al.. (2015). Tonic zinc inhibits spontaneous firing in dorsal cochlear nucleus principal neurons by enhancing glycinergic neurotransmission. DSpace@MIT (Massachusetts Institute of Technology). 1 indexed citations

10.

Middleton, Jason W., Charles T. Anderson, Katharine Borges, et al.. (2015). Cell-Specific Activity-Dependent Fractionation of Layer 2/3→5B Excitatory Signaling in Mouse Auditory Cortex. Journal of Neuroscience. 35(7). 3112–3123. 32 indexed citations

11.

Kalappa, Bopanna I., Charles T. Anderson, Jacob M. Goldberg, Stephen J. Lippard, & Thanos Tzounopoulos. (2015). AMPA receptor inhibition by synaptically released zinc. Proceedings of the National Academy of Sciences. 112(51). 15749–15754. 93 indexed citations

12.

Perez‐Rosello, Tamara, et al.. (2015). Tonic zinc inhibits spontaneous firing in dorsal cochlear nucleus principal neurons by enhancing glycinergic neurotransmission. Neurobiology of Disease. 81. 14–19. 27 indexed citations

13.

Srivastava, Deepak P., Kevin M. Woolfrey, Kelly A. Jones, et al.. (2012). An Autism-Associated Variant of Epac2 Reveals a Role for Ras/Epac2 Signaling in Controlling Basal Dendrite Maintenance in Mice. PLoS Biology. 10(6). e1001350–e1001350. 66 indexed citations

14.

Qiu, Shenfeng, Charles T. Anderson, Pat Levitt, & Gordon M. Shepherd. (2011). Circuit-Specific Intracortical Hyperconnectivity in Mice with Deletion of the Autism-Associated Met Receptor Tyrosine Kinase. Journal of Neuroscience. 31(15). 5855–5864. 93 indexed citations

15.

Homma, Kazuaki, Katharine K. Miller, Charles T. Anderson, et al.. (2010). Interaction between CFTR and prestin (SLC26A5). Biochimica et Biophysica Acta (BBA) - Biomembranes. 1798(6). 1029–1040. 41 indexed citations

16.

Cheatham, Mary Ann, et al.. (2009). A Chimera Analysis ofPrestinKnock-Out Mice. Journal of Neuroscience. 29(38). 12000–12008. 11 indexed citations

17.

Dallos, Peter, Xudong Wu, Mary Ann Cheatham, et al.. (2008). Prestin-Based Outer Hair Cell Motility Is Necessary for Mammalian Cochlear Amplification. Neuron. 58(3). 333–339. 279 indexed citations

18.

Cheatham, Mary Ann, Jing Zheng, Guo Guang Du, et al.. (2007). Evaluation of an Independent Prestin Mouse Model Derived from the 129S1 Strain. Audiology and Neurotology. 12(6). 378–390. 24 indexed citations

19.

Zheng, Jing, Guo Guang Du, Charles T. Anderson, et al.. (2006). Analysis of the Oligomeric Structure of the Motor Protein Prestin. Journal of Biological Chemistry. 281(29). 19916–19924. 81 indexed citations

20.

Guzmán-Flores, C, et al.. (1963). PYRAMIDAL INFLUENCES UPON POTENTIALS EVOKED IN SENSORY NUCLEI.. PubMed. 21. 65–75. 7 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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