Nathan T. Mortimer

980 total citations
30 papers, 592 citations indexed

About

Nathan T. Mortimer is a scholar working on Immunology, Molecular Biology and Insect Science. According to data from OpenAlex, Nathan T. Mortimer has authored 30 papers receiving a total of 592 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Immunology, 11 papers in Molecular Biology and 11 papers in Insect Science. Recurrent topics in Nathan T. Mortimer's work include Invertebrate Immune Response Mechanisms (13 papers), Insect symbiosis and bacterial influences (9 papers) and Genetics, Aging, and Longevity in Model Organisms (5 papers). Nathan T. Mortimer is often cited by papers focused on Invertebrate Immune Response Mechanisms (13 papers), Insect symbiosis and bacterial influences (9 papers) and Genetics, Aging, and Longevity in Model Organisms (5 papers). Nathan T. Mortimer collaborates with scholars based in United States, Australia and Germany. Nathan T. Mortimer's co-authors include Todd A. Schlenke, Balint Z Kacsoh, Kenneth H. Moberg, James A. Mobley, James Taylor, Jeremy Goecks, Chi-Bin Chien, Arminda Suli, Erin S. Keebaugh and Iain T. Shepherd and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Neuroscience.

In The Last Decade

Nathan T. Mortimer

27 papers receiving 585 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nathan T. Mortimer United States 13 273 232 167 152 99 30 592
Rochele Yamamoto United States 9 225 0.8× 258 1.1× 291 1.7× 174 1.1× 124 1.3× 11 725
Lucie Kučerová Czechia 14 301 1.1× 219 0.9× 187 1.1× 198 1.3× 128 1.3× 31 647
Ingo Zinke Germany 7 243 0.9× 400 1.7× 351 2.1× 310 2.0× 110 1.1× 8 963
Alix J. Rey United Kingdom 6 121 0.4× 417 1.8× 150 0.9× 73 0.5× 154 1.6× 6 660
Shireen-Anne Davies United Kingdom 13 216 0.8× 198 0.9× 429 2.6× 150 1.0× 144 1.5× 18 669
Tomonori Katsuyama Switzerland 12 207 0.8× 341 1.5× 182 1.1× 321 2.1× 59 0.6× 14 683
Aniruddha A. Pandit United Kingdom 7 142 0.5× 188 0.8× 214 1.3× 81 0.5× 139 1.4× 8 421
Deborah K. Hoshizaki United States 14 225 0.8× 393 1.7× 328 2.0× 263 1.7× 134 1.4× 28 905
Enrique Reynaud Mexico 17 166 0.6× 378 1.6× 229 1.4× 57 0.4× 162 1.6× 37 719
Maija Slaidina United States 10 123 0.5× 285 1.2× 409 2.4× 197 1.3× 156 1.6× 12 832

Countries citing papers authored by Nathan T. Mortimer

Since Specialization
Citations

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

Fields of papers citing papers by Nathan T. Mortimer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nathan T. Mortimer

This figure shows the co-authorship network connecting the top 25 collaborators of Nathan T. Mortimer. A scholar is included among the top collaborators of Nathan T. Mortimer 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 Nathan T. Mortimer. Nathan T. Mortimer 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.
Mortimer, Nathan T. & Todd A. Schlenke. (2025). Multifaceted Defenses Against Parasitoid Wasps in Diptera. Annual Review of Genetics. 59(1). 369–394.
2.
Mortimer, Nathan T., et al.. (2025). Rethinking parasitoid venoms: beyond immune suppression. Trends in Parasitology. 41(8). 607–609.
3.
Zhao, Cheng, Lauren Troy, Joe Van Buskirk, et al.. (2025). Geographic variability of interstitial lung disease diagnoses and impact of air pollution on disease outcomes. Respiratory Medicine. 239. 107996–107996.
4.
Schlenke, Todd A., et al.. (2024). Host JAK-STAT activity is a target of parasitoid wasp virulence strategies. PLoS Pathogens. 20(7). e1012349–e1012349. 2 indexed citations
5.
Barbee, Scott A., et al.. (2021). Drosophila p38 MAPK interacts with BAG‐3/starvin to regulate age‐dependent protein homeostasis. Aging Cell. 20(11). e13481–e13481. 4 indexed citations
6.
Mortimer, Nathan T., Balint Z Kacsoh, Susanna E. Brantley, et al.. (2021). Extracellular matrix protein N-glycosylation mediates immune self-tolerance inDrosophila melanogaster. Proceedings of the National Academy of Sciences. 118(39). 13 indexed citations
7.
Mortimer, Nathan T., et al.. (2021). Immune Cell Production Is Targeted by Parasitoid Wasp Virulence in a Drosophila–Parasitoid Wasp Interaction. Pathogens. 10(1). 49–49. 4 indexed citations
8.
Barbee, Scott A., et al.. (2020). Evolutionarily conserved transcription factors drive the oxidative stress response in Drosophila. Journal of Experimental Biology. 223(Pt 14). 5 indexed citations
9.
Sargent, Luke, Yating Liu, Wilson Leung, et al.. (2020). G-OnRamp: Generating genome browsers to facilitate undergraduate-driven collaborative genome annotation. PLoS Computational Biology. 16(6). e1007863–e1007863. 3 indexed citations
10.
Mortimer, Nathan T., et al.. (2020). Connecting the dots: avian eggshell pigmentation, female condition and paternal provisioning effort. Biological Journal of the Linnean Society. 130(1). 114–127. 8 indexed citations
11.
Wagner, Nicole, et al.. (2019). Bioinformatic analysis suggests potential mechanisms underlying parasitoid venom evolution and function. Genomics. 112(2). 1096–1104. 12 indexed citations
12.
Mortimer, Nathan T., et al.. (2015). Drosophila Shep and C. elegans SUP-26 are RNA-binding proteins that play diverse roles in nervous system development. Development Genes and Evolution. 225(6). 319–330. 8 indexed citations
13.
Kacsoh, Balint Z, et al.. (2013). Fruit Flies Medicate Offspring After Seeing Parasites. Science. 339(6122). 947–950. 136 indexed citations
14.
Goecks, Jeremy, et al.. (2013). Integrative Approach Reveals Composition of Endoparasitoid Wasp Venoms. PLoS ONE. 8(5). e64125–e64125. 76 indexed citations
15.
Mortimer, Nathan T. & Kenneth H. Moberg. (2013). The Archipelago Ubiquitin Ligase Subunit Acts in Target Tissue to Restrict Tracheal Terminal Cell Branching and Hypoxic-Induced Gene Expression. PLoS Genetics. 9(2). e1003314–e1003314. 8 indexed citations
16.
Mortimer, Nathan T.. (2013). Parasitoid wasp virulence. Fly. 7(4). 242–248. 16 indexed citations
17.
Mortimer, Nathan T., Balint Z Kacsoh, Erin S. Keebaugh, & Todd A. Schlenke. (2012). Mgat1-dependent N-glycosylation of Membrane Components Primes Drosophila melanogaster Blood Cells for the Cellular Encapsulation Response. PLoS Pathogens. 8(7). e1002819–e1002819. 39 indexed citations
18.
Mortimer, Nathan T. & Kenneth H. Moberg. (2009). Regulation of Drosophila embryonic tracheogenesis by dVHL and hypoxia. Developmental Biology. 329(2). 294–305. 23 indexed citations
19.
Mortimer, Nathan T. & Kenneth H. Moberg. (2007). The Drosophila F-box protein Archipelago controls levels of the Trachealess transcription factor in the embryonic tracheal system. Developmental Biology. 312(2). 560–571. 20 indexed citations
20.
Suli, Arminda, Nathan T. Mortimer, Iain T. Shepherd, & Chi-Bin Chien. (2006). Netrin/DCC Signaling Controls Contralateral Dendrites of Octavolateralis Efferent Neurons. Journal of Neuroscience. 26(51). 13328–13337. 44 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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