Daniel N. Cox

4.5k total citations · 1 hit paper
65 papers, 3.2k citations indexed

About

Daniel N. Cox is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, Daniel N. Cox has authored 65 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Cellular and Molecular Neuroscience, 25 papers in Molecular Biology and 12 papers in Cell Biology. Recurrent topics in Daniel N. Cox's work include Neurobiology and Insect Physiology Research (30 papers), Cell Image Analysis Techniques (6 papers) and Circadian rhythm and melatonin (6 papers). Daniel N. Cox is often cited by papers focused on Neurobiology and Insect Physiology Research (30 papers), Cell Image Analysis Techniques (6 papers) and Circadian rhythm and melatonin (6 papers). Daniel N. Cox collaborates with scholars based in United States, Germany and United Kingdom. Daniel N. Cox's co-authors include Haifan Lin, Anna Chao, Lisa Chang, Dan Qiao, Nathaniel J. Himmel, Yuh Nung Jan, Akos Szakmary, C. Ryan Campbell, Eswar Prasad R. Iyer and A.E. Senior and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Daniel N. Cox

65 papers receiving 3.2k citations

Hit Papers

A novel class of evolutionarily conserved genes defined b... 1998 2026 2007 2016 1998 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel N. Cox United States 25 2.2k 1.1k 552 436 395 65 3.2k
Robert K. Maeda Switzerland 23 2.5k 1.1× 564 0.5× 650 1.2× 493 1.1× 350 0.9× 36 3.0k
Jaeseob Kim South Korea 16 1.9k 0.9× 321 0.3× 926 1.7× 492 1.1× 496 1.3× 18 2.8k
Bret J. Pearson Canada 29 2.7k 1.2× 757 0.7× 790 1.4× 259 0.6× 276 0.7× 53 3.4k
Tetsuichiro Saito Japan 30 2.4k 1.1× 660 0.6× 1.0k 1.9× 604 1.4× 492 1.2× 62 3.8k
Martha Evans-Holm United States 11 1.7k 0.8× 458 0.4× 807 1.5× 418 1.0× 379 1.0× 11 2.4k
Joseph W. Carlson United States 18 2.8k 1.3× 1.3k 1.2× 1.3k 2.3× 825 1.9× 433 1.1× 25 4.1k
Andrew Bassett United Kingdom 35 3.6k 1.6× 1.1k 1.0× 441 0.8× 733 1.7× 279 0.7× 64 5.0k
Jean‐Stéphane Joly France 27 2.5k 1.1× 244 0.2× 521 0.9× 660 1.5× 570 1.4× 47 3.6k
Tieqiao Wen China 25 1.3k 0.6× 624 0.6× 678 1.2× 285 0.7× 104 0.3× 89 2.4k
Koen J. T. Venken United States 30 3.2k 1.5× 492 0.5× 1.8k 3.3× 904 2.1× 906 2.3× 50 4.8k

Countries citing papers authored by Daniel N. Cox

Since Specialization
Citations

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

Fields of papers citing papers by Daniel N. Cox

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel N. Cox. 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 Daniel N. Cox. The network helps show where Daniel N. Cox may publish in the future.

Co-authorship network of co-authors of Daniel N. Cox

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel N. Cox. A scholar is included among the top collaborators of Daniel N. Cox 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 Daniel N. Cox. Daniel N. Cox 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.
Patel, Atit A., et al.. (2024). CCT and Cullin1 Regulate the TORC1 Pathway to Promote Dendritic Arborization in Health and Disease. Cells. 13(12). 1029–1029. 1 indexed citations
2.
Sakurai, Akira, et al.. (2023). Cold-Temperature Coding with Bursting and Spiking Based on TRP Channel Dynamics in Drosophila Larva Sensory Neurons. International Journal of Molecular Sciences. 24(19). 14638–14638. 1 indexed citations
3.
4.
Iyer, Eswar Prasad R., et al.. (2023). The Zinc-BED Transcription Factor Bedwarfed Promotes Proportional Dendritic Growth and Branching through Transcriptional and Translational Regulation in Drosophila. International Journal of Molecular Sciences. 24(7). 6344–6344. 1 indexed citations
5.
Taylor, Jack H., James C. Walton, Katharine E. McCann, et al.. (2022). CRISPR-Cas9 editing of the arginine–vasopressin V1a receptor produces paradoxical changes in social behavior in Syrian hamsters. Proceedings of the National Academy of Sciences. 119(19). e2121037119–e2121037119. 20 indexed citations
6.
Patel, Atit A., Akira Sakurai, Nathaniel J. Himmel, & Daniel N. Cox. (2022). Modality specific roles for metabotropic GABAergic signaling and calcium induced calcium release mechanisms in regulating cold nociception. Frontiers in Molecular Neuroscience. 15. 942548–942548. 4 indexed citations
7.
Miller, Cassandra, Bin Dong, Atit A. Patel, et al.. (2021). Rapid subcellular calcium responses and dynamics by calcium sensor G-CatchER+. iScience. 24(3). 102129–102129. 24 indexed citations
8.
Das, Ravi, Sumit Nanda, István Földi, et al.. (2021). Formin 3 directs dendritic architecture via microtubule regulation and is required for somatosensory nociceptive behavior. Development. 148(16). 9 indexed citations
9.
Nanda, Sumit, et al.. (2021). An imaging analysis protocol to trace, quantify, and model multi-signal neuron morphology. STAR Protocols. 2(2). 100567–100567. 5 indexed citations
10.
Himmel, Nathaniel J., et al.. (2020). Phylogenetics Identifies Two Eumetazoan TRPM Clades and an Eighth TRP Family, TRP Soromelastatin (TRPS). Molecular Biology and Evolution. 37(7). 2034–2044. 23 indexed citations
11.
Cox, Daniel N., et al.. (2020). Homeostatic Roles of the Proteostasis Network in Dendrites. Frontiers in Cellular Neuroscience. 14. 264–264. 16 indexed citations
12.
Himmel, Nathaniel J., et al.. (2019). Drosophila menthol sensitivity and the Precambrian origins of transient receptor potential-dependent chemosensation. Philosophical Transactions of the Royal Society B Biological Sciences. 374(1785). 20190369–20190369. 25 indexed citations
13.
Nanda, Sumit, et al.. (2017). Morphological determinants of dendritic arborization neurons in Drosophila larva. Brain Structure and Function. 223(3). 1107–1120. 17 indexed citations
14.
Gokhale, Avanti, Cortnie Hartwig, A. Freeman, et al.. (2016). The Proteome of BLOC-1 Genetic Defects Identifies the Arp2/3 Actin Polymerization Complex to Function Downstream of the Schizophrenia Susceptibility Factor Dysbindin at the Synapse. Journal of Neuroscience. 36(49). 12393–12411. 23 indexed citations
15.
Turner, Heather N., Atit A. Patel, Nathaniel J. Himmel, et al.. (2016). The TRP Channels Pkd2, NompC, and Trpm Act in Cold-Sensing Neurons to Mediate Unique Aversive Behaviors to Noxious Cold in Drosophila. Current Biology. 26(23). 3116–3128. 79 indexed citations
16.
Iyer, Eswar Prasad R., Srividya Chandramouli Iyer, & Daniel N. Cox. (2012). Application of Cell-Specific Isolation to the Study of Dopamine Signaling in Drosophila. Methods in molecular biology. 964. 215–225. 2 indexed citations
17.
Iyer, Srividya Chandramouli, et al.. (2011). Turtle Functions Downstream of Cut in Differentially Regulating Class Specific Dendrite Morphogenesis in Drosophila. PLoS ONE. 6(7). e22611–e22611. 28 indexed citations
18.
Shlobin, Oksana A., Shahzad Ahmad, Eswar Prasad R. Iyer, et al.. (2010). Genomic phenotype of non-cultured pulmonary fibroblasts in idiopathic pulmonary fibrosis. Genomics. 96(3). 134–145. 62 indexed citations
19.
Cox, Daniel N., et al.. (2006). The Role of PIWI and the miRNA Machinery in Drosophila Germline Determination. Current Biology. 16(19). 1884–1894. 212 indexed citations
20.
Cox, Daniel N., et al.. (1998). A novel class of evolutionarily conserved genes defined by piwi are essential for stem cell self-renewal. Genes & Development. 12(23). 3715–3727. 793 indexed citations breakdown →

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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