Andrew T. Ishida

1.6k total citations
47 papers, 1.4k citations indexed

About

Andrew T. Ishida is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Andrew T. Ishida has authored 47 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Cellular and Molecular Neuroscience, 43 papers in Molecular Biology and 4 papers in Cognitive Neuroscience. Recurrent topics in Andrew T. Ishida's work include Neuroscience and Neuropharmacology Research (35 papers), Retinal Development and Disorders (31 papers) and Photoreceptor and optogenetics research (21 papers). Andrew T. Ishida is often cited by papers focused on Neuroscience and Neuropharmacology Research (35 papers), Retinal Development and Disorders (31 papers) and Photoreceptor and optogenetics research (21 papers). Andrew T. Ishida collaborates with scholars based in United States, Japan and Switzerland. Andrew T. Ishida's co-authors include William K. Stell, David O. Lightfoot, Jacques Neyton, Gordon Fain, Gloria J. Partida, Yuki Hayashida, Makoto Tachibana, A Kaneko, Toshihide Tabata and Vytautas P. Bindokas and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Neuroscience.

In The Last Decade

Andrew T. Ishida

46 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew T. Ishida United States 21 1.2k 1.2k 141 69 61 47 1.4k
Zhuo-Hua Pan United States 19 928 0.8× 1.0k 0.9× 151 1.1× 51 0.7× 112 1.8× 21 1.5k
Roberta G. Pourcho United States 30 1.8k 1.5× 1.8k 1.5× 151 1.1× 133 1.9× 73 1.2× 48 2.1k
Eric M. Lasater United States 23 1.4k 1.2× 1.3k 1.1× 167 1.2× 76 1.1× 73 1.2× 44 1.6k
G. Falk United Kingdom 23 1.3k 1.1× 1.4k 1.2× 251 1.8× 61 0.9× 54 0.9× 50 1.9k
S. M. Wu United States 17 825 0.7× 797 0.7× 191 1.4× 48 0.7× 22 0.4× 33 978
J. E. Dowling United States 12 836 0.7× 753 0.6× 204 1.4× 105 1.5× 31 0.5× 14 1.1k
Yoshiki Ueda Japan 10 497 0.4× 509 0.4× 69 0.5× 35 0.5× 40 0.7× 13 709
JE Dowling United States 10 606 0.5× 599 0.5× 90 0.6× 52 0.8× 55 0.9× 13 728
Heinz W�ssle Germany 9 1.1k 0.9× 918 0.8× 48 0.3× 126 1.8× 46 0.8× 10 1.2k
Ramon F. Dacheux United States 29 2.3k 1.9× 2.3k 1.9× 461 3.3× 109 1.6× 87 1.4× 46 2.7k

Countries citing papers authored by Andrew T. Ishida

Since Specialization
Citations

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

Fields of papers citing papers by Andrew T. Ishida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew T. Ishida

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew T. Ishida. A scholar is included among the top collaborators of Andrew T. Ishida 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 Andrew T. Ishida. Andrew T. Ishida 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.
Ogata, Genki, et al.. (2022). Calcium/calmodulin-dependent protein kinase II associates with the K+ channel isoform Kv4.3 in adult rat optic nerve. Frontiers in Neuroanatomy. 16. 958986–958986.
2.
Ogata, Genki, et al.. (2020). Extraretinal Spike Normalization in Retinal Ganglion Cell Axons. eNeuro. 7(2). ENEURO.0504–19.2020. 2 indexed citations
3.
Partida, Gloria J., et al.. (2018). Autophosphorylated CaMKII Facilitates Spike Propagation in Rat Optic Nerve. Journal of Neuroscience. 38(37). 8087–8105. 4 indexed citations
4.
Stradleigh, Tyler W. & Andrew T. Ishida. (2015). Fixation strategies for retinal immunohistochemistry. Progress in Retinal and Eye Research. 48. 181–202. 23 indexed citations
5.
Ogata, Genki, Tyler W. Stradleigh, Gloria J. Partida, & Andrew T. Ishida. (2012). Dopamine and full‐field illumination activate D1 and D2‐D5‐type receptors in adult rat retinal ganglion cells. The Journal of Comparative Neurology. 520(17). 4032–4049. 30 indexed citations
6.
Partida, Gloria J., et al.. (2008). HCN4-like immunoreactivity in rat retinal ganglion cells. Visual Neuroscience. 25(1). 95–102. 9 indexed citations
7.
Ishida, Andrew T., et al.. (2007). Ih Without Kir in Adult Rat Retinal Ganglion Cells. Journal of Neurophysiology. 97(5). 3790–3799. 33 indexed citations
8.
Witkovsky, Paul, William K. Stell, & Andrew T. Ishida. (2006). Circuits and Properties of Signal Transmission in the Retina. Journal of Neurophysiology. 96(2). 509–511. 3 indexed citations
9.
Hayashida, Yuki, Gloria J. Partida, & Andrew T. Ishida. (2004). Dissociation of retinal ganglion cells without enzymes. Journal of Neuroscience Methods. 137(1). 25–35. 12 indexed citations
10.
İnceoğlu, Bora, Yuki Hayashida, József Langó, Andrew T. Ishida, & Bruce D. Hammock. (2002). A single charged surface residue modifies the activity of ikitoxin, a beta‐type Na+ channel toxin from Parabuthus transvaalicus. European Journal of Biochemistry. 269(22). 5369–5376. 23 indexed citations
11.
Chiba, Chikafumi, et al.. (2000). Functional differentiation of ganglion cells from multipotent progenitor cells in sliced retina of adult goldfish. The Journal of Comparative Neurology. 419(3). 297–305. 6 indexed citations
12.
Sakaguchi, Hironobu, et al.. (2000). Voltage-gated Na+ channel EOIII-segment-like immunoreactivity in fish retinal ganglion cells. Visual Neuroscience. 17(4). 647–655. 2 indexed citations
13.
Hidaka, Shigekazu & Andrew T. Ishida. (1998). Voltage-gated Na + current availability after step- and spike-shaped conditioning depolarizations of retinal ganglion cells. Pflügers Archiv - European Journal of Physiology. 436(4). 497–508. 33 indexed citations
14.
Tabata, Toshihide, Baldomero M. Olivera, & Andrew T. Ishida. (1996). ω-Conotoxin-MVIID Blocks an ω-Conotoxin-GVIA-sensitive, High-threshold Ca2+ Current in Fish Retinal Ganglion Cells. Neuropharmacology. 35(5). 633–636. 4 indexed citations
15.
Bindokas, Vytautas P. & Andrew T. Ishida. (1996). Conotoxin-sensitive and conotoxin-resistant Ca2+ currents in fish retinal ganglion cells. Journal of Neurobiology. 29(4). 429–444. 16 indexed citations
16.
Ishida, Andrew T.. (1995). Ion channel components of retinal ganglion cells. Progress in Retinal and Eye Research. 15(1). 261–280. 37 indexed citations
17.
Ishida, Andrew T.. (1992). Chapter 2 The physiology of GABAA receptors in retinal neurons. Progress in brain research. 90. 29–45. 20 indexed citations
18.
Ishida, Andrew T., et al.. (1991). Cold inhibits neurite outgrowth from single retinal ganglion cells isolated from adult goldfish. Experimental Eye Research. 52(2). 175–191. 12 indexed citations
19.
Ishida, Andrew T.. (1991). Regenerative sodium and calcium currents in goldfish retinal ganglion cell somata. Vision Research. 31(3). 477–485. 18 indexed citations
20.
Ishida, Andrew T., et al.. (1991). Synchronous neurite branchings in single goldfish retinal ganglion cells. Visual Neuroscience. 6(5). 537–549. 2 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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