Thomas R. Clandinin

8.1k total citations
85 papers, 4.8k citations indexed

About

Thomas R. Clandinin is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Thomas R. Clandinin has authored 85 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Cellular and Molecular Neuroscience, 38 papers in Molecular Biology and 17 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Thomas R. Clandinin's work include Neurobiology and Insect Physiology Research (66 papers), Retinal Development and Disorders (19 papers) and Animal Behavior and Reproduction (16 papers). Thomas R. Clandinin is often cited by papers focused on Neurobiology and Insect Physiology Research (66 papers), Retinal Development and Disorders (19 papers) and Animal Behavior and Reproduction (16 papers). Thomas R. Clandinin collaborates with scholars based in United States, Canada and Germany. Thomas R. Clandinin's co-authors include S Lawrence Zipursky, Paul W. Sternberg, Damon A. Clark, Marion Silies, Chi‐Hon Lee, Wendy S. Katz, Daryl M. Gohl, Pei-Ling Chen, Tory Herman and Helen H. Yang and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Thomas R. Clandinin

84 papers receiving 4.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas R. Clandinin United States 40 3.1k 2.2k 696 691 688 85 4.8k
Thomas Préat France 41 4.0k 1.3× 1.9k 0.8× 662 1.0× 572 0.8× 1.1k 1.6× 96 6.0k
Benjamin H. White United States 33 3.2k 1.0× 1.6k 0.7× 360 0.5× 352 0.5× 699 1.0× 56 4.4k
J. Douglas Armstrong United Kingdom 39 4.2k 1.4× 2.3k 1.0× 704 1.0× 554 0.8× 1.0k 1.5× 116 6.6k
Ann‐Shyn Chiang Taiwan 36 3.1k 1.0× 1.6k 0.7× 384 0.6× 356 0.5× 836 1.2× 115 5.2k
Paul Garrity United States 39 3.9k 1.3× 1.9k 0.8× 493 0.7× 298 0.4× 765 1.1× 55 6.1k
Leslie C. Griffith United States 45 4.8k 1.5× 2.1k 0.9× 510 0.7× 824 1.2× 803 1.2× 111 6.2k
Erich Buchner Germany 35 4.5k 1.4× 2.5k 1.1× 1.5k 2.1× 436 0.6× 937 1.4× 65 6.2k
Trevor J. Wardill United States 19 3.3k 1.1× 1.6k 0.7× 397 0.6× 1.7k 2.4× 581 0.8× 35 5.4k
Mani Ramaswami United States 41 2.5k 0.8× 3.3k 1.5× 1.2k 1.7× 329 0.5× 355 0.5× 90 5.3k
Roland Strauß Germany 27 2.6k 0.9× 817 0.4× 374 0.5× 364 0.5× 943 1.4× 66 3.5k

Countries citing papers authored by Thomas R. Clandinin

Since Specialization
Citations

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

Fields of papers citing papers by Thomas R. Clandinin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas R. Clandinin. 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 Thomas R. Clandinin. The network helps show where Thomas R. Clandinin may publish in the future.

Co-authorship network of co-authors of Thomas R. Clandinin

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas R. Clandinin. A scholar is included among the top collaborators of Thomas R. Clandinin 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 Thomas R. Clandinin. Thomas R. Clandinin 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.
Druckmann, Shaul, et al.. (2024). A recurrent neural circuit in Drosophila temporally sharpens visual inputs. Current Biology. 35(2). 333–346.e6. 1 indexed citations
2.
Mano, Omer, et al.. (2023). Long-timescale anti-directional rotation in Drosophila optomotor behavior. eLife. 12. 3 indexed citations
3.
4.
Turner, Maxwell H., Kevin Mann, & Thomas R. Clandinin. (2021). The connectome predicts resting-state functional connectivity across the Drosophila brain. Current Biology. 31(11). 2386–2394.e3. 17 indexed citations
5.
Tsai, Jessica W., et al.. (2019). Transcriptional Feedback Links Lipid Synthesis to Synaptic Vesicle Pools in Drosophila Photoreceptors. Neuron. 101(4). 721–737.e4. 19 indexed citations
6.
Barnhart, Erin L., et al.. (2018). Sequential Nonlinear Filtering of Local Motion Cues by Global Motion Circuits. Neuron. 100(1). 229–243.e3. 12 indexed citations
7.
Wang, Irving E., Sylvain W. Lapan, M. Lucila Scimone, Thomas R. Clandinin, & Peter W. Reddien. (2016). Hedgehog signaling regulates gene expression in planarian glia. eLife. 5. 58 indexed citations
8.
Leong, Jonathan C. S., et al.. (2016). Direction Selectivity in Drosophila Emerges from Preferred-Direction Enhancement and Null-Direction Suppression. Journal of Neuroscience. 36(31). 8078–8092. 61 indexed citations
9.
Gao, Xiaojing, Olena Riabinina, Jun Li, et al.. (2015). A transcriptional reporter of intracellular Ca2+ in Drosophila. Nature Neuroscience. 18(6). 917–925. 64 indexed citations
10.
Fisher, Yvette E., et al.. (2015). A Class of Visual Neurons with Wide-Field Properties Is Required for Local Motion Detection. Current Biology. 25(24). 3178–3189. 39 indexed citations
11.
Clark, Damon A., James E. Fitzgerald, Justin M. Ales, et al.. (2014). Flies and humans share a motion estimation strategy that exploits natural scene statistics. Nature Neuroscience. 17(2). 296–303. 67 indexed citations
12.
Wernet, Mathias F., Martha Klovstad, & Thomas R. Clandinin. (2014). A Drosophila Toolkit for the Visualization and Quantification of Viral Replication Launched from Transgenic Genomes. PLoS ONE. 9(11). e112092–e112092. 2 indexed citations
13.
Freifeld, Limor, Damon A. Clark, Mark J. Schnitzer, Mark Horowitz, & Thomas R. Clandinin. (2013). GABAergic Lateral Interactions Tune the Early Stages of Visual Processing in Drosophila. Neuron. 78(6). 1075–1089. 59 indexed citations
14.
Prakash, Saurabh, Catherine Dubreuil, Aurnab Ghose, et al.. (2009). Complex interactions amongst N-cadherin, DLAR, and Liprin-α regulate Drosophila photoreceptor axon targeting. Developmental Biology. 336(1). 10–19. 35 indexed citations
15.
Mast, Joshua D., Katharine M. Tomalty, Hannes Vogel, & Thomas R. Clandinin. (2008). Reactive oxygen species act remotely to cause synapse loss in a Drosophila model of developmental mitochondrial encephalopathy. Journal of Cell Science. 121(15). 1 indexed citations
16.
Clandinin, Thomas R.. (2005). Surprising Twists to Exocyst Function. Neuron. 46(2). 164–166. 10 indexed citations
17.
Choe, Kwang‐Min & Thomas R. Clandinin. (2005). Thinking about Visual Behavior; Learning about Photoreceptor Function. Current topics in developmental biology. 69. 187–213. 18 indexed citations
18.
Clandinin, Thomas R., et al.. (2001). Drosophila LAR Regulates R1-R6 and R7 Target Specificity in the Visual System. Neuron. 32(2). 237–248. 124 indexed citations
19.
Salecker, Iris, Thomas R. Clandinin, & S Lawrence Zipursky. (1998). Hedgehog and Spitz. Cell. 95(5). 587–590. 11 indexed citations
20.
Clandinin, Thomas R., Wendy S. Katz, & Paul W. Sternberg. (1997). Caenorhabditis elegansHOM-C Genes Regulate the Response of Vulval Precursor Cells to Inductive Signal. Developmental Biology. 182(1). 150–161. 86 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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