Travis Thomson

2.3k total citations
27 papers, 1.6k citations indexed

About

Travis Thomson is a scholar working on Molecular Biology, Plant Science and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Travis Thomson has authored 27 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Plant Science and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Travis Thomson's work include Chromosomal and Genetic Variations (7 papers), Reproductive Biology and Fertility (5 papers) and CRISPR and Genetic Engineering (5 papers). Travis Thomson is often cited by papers focused on Chromosomal and Genetic Variations (7 papers), Reproductive Biology and Fertility (5 papers) and CRISPR and Genetic Engineering (5 papers). Travis Thomson collaborates with scholars based in United States, Canada and United Kingdom. Travis Thomson's co-authors include Haifan Lin, Paul Lasko, James Ashley, Vivian Budnik, Lee G. Fradkin, Joshua Johnson, Alexey L. Arkov, Zhiping Weng, James B. Yu and Ruth Lehmann and has published in prestigious journals such as Cell, Nature Neuroscience and PLoS ONE.

In The Last Decade

Travis Thomson

25 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Travis Thomson United States 16 1.2k 577 227 198 152 27 1.6k
Lucia Carbone United States 27 1.3k 1.0× 748 1.3× 690 3.0× 213 1.1× 116 0.8× 70 2.0k
John Pham United States 15 1.4k 1.1× 322 0.6× 131 0.6× 505 2.6× 127 0.8× 29 2.1k
Mark Barnett United Kingdom 20 986 0.8× 331 0.6× 433 1.9× 111 0.6× 46 0.3× 32 1.5k
Xinxian Deng United States 21 2.4k 1.9× 504 0.9× 1.1k 5.0× 424 2.1× 131 0.9× 41 2.9k
Gerald M. Pao United States 19 1.5k 1.2× 269 0.5× 469 2.1× 130 0.7× 42 0.3× 29 2.1k
Laurence Ettwiller United States 22 2.0k 1.6× 297 0.5× 479 2.1× 274 1.4× 121 0.8× 49 2.5k
Carolyn M. Price United States 36 2.6k 2.2× 741 1.3× 288 1.3× 78 0.4× 75 0.5× 68 3.5k
Jun Zhong China 20 1.2k 0.9× 196 0.3× 234 1.0× 183 0.9× 57 0.4× 38 1.5k
Elizabeth B. Goodwin United States 20 1.3k 1.0× 98 0.2× 215 0.9× 102 0.5× 147 1.0× 29 1.7k
M. Jordan Rowley United States 22 2.2k 1.8× 1.3k 2.2× 316 1.4× 197 1.0× 89 0.6× 45 2.8k

Countries citing papers authored by Travis Thomson

Since Specialization
Citations

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

Fields of papers citing papers by Travis Thomson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Travis Thomson. 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 Travis Thomson. The network helps show where Travis Thomson may publish in the future.

Co-authorship network of co-authors of Travis Thomson

This figure shows the co-authorship network connecting the top 25 collaborators of Travis Thomson. A scholar is included among the top collaborators of Travis Thomson 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 Travis Thomson. Travis Thomson 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.
Durán‐Laforet, Violeta, Timothy G. Freels, Susanna Molas, et al.. (2025). Suppression of binge alcohol drinking by an inhibitory neuronal ensemble in the mouse medial orbitofrontal cortex. Nature Neuroscience. 28(8). 1741–1752.
2.
Liu, Yumeng, Shuhao Wang, Alfred Simkin, et al.. (2025). Capsid transfer of the retrotransposon Copia controls structural synaptic plasticity in Drosophila. PLoS Biology. 23(2). e3002983–e3002983. 4 indexed citations
3.
Wang, Shuhao, et al.. (2023). Identifying new players in structural synaptic plasticity through dArc1 interrogation. iScience. 26(11). 108048–108048.
5.
Tsuji, Junko, et al.. (2021). Somatic piRNAs and Transposons are Differentially Expressed Coincident with Skeletal Muscle Atrophy and Programmed Cell Death. Frontiers in Genetics. 12. 775369–775369. 7 indexed citations
6.
Ashley, James, et al.. (2018). Retrovirus-like Gag Protein Arc1 Binds RNA and Traffics across Synaptic Boutons. Cell. 172(1-2). 262–274.e11. 312 indexed citations
7.
Li, Yihang, Linda Hassinger, Travis Thomson, et al.. (2016). Lamin Mutations Accelerate Aging via Defective Export of Mitochondrial mRNAs through Nuclear Envelope Budding. Current Biology. 26(15). 2052–2059. 25 indexed citations
8.
Thomson, Travis, Shikui Tu, Sudan N. Loganathan, et al.. (2015). Glycolytic enzymes localize to ribonucleoprotein granules in Drosophila germ cells, bind Tudor and protect from transposable elements. EMBO Reports. 16(3). 379–386. 14 indexed citations
9.
Thomson, Travis, et al.. (2012). Kinematic control and posture optimization of a redundantly actuated quadruped robot. 1895–1900. 26 indexed citations
10.
Yu, James B., Travis Thomson, & Joshua Johnson. (2012). Cross Talk Between Estradiol and mTOR Kinase in the Regulation of Ovarian Granulosa Proliferation. Reproductive Sciences. 19(2). 143–151. 15 indexed citations
11.
Khurana, Jaspreet S., Jie Wang, Jia Xu, et al.. (2011). Adaptation to P Element Transposon Invasion in Drosophila melanogaster. Cell. 147(7). 1551–1563. 175 indexed citations
12.
Yu, James B., et al.. (2011). mTOR Controls Ovarian Follicle Growth by Regulating Granulosa Cell Proliferation. PLoS ONE. 6(7). e21415–e21415. 73 indexed citations
13.
Mclaughlin, Marie, Pasquale Patrizio, Umit A. Kayisli, et al.. (2011). mTOR kinase inhibition results in oocyte loss characterized by empty follicles in human ovarian cortical strips cultured in vitro. Fertility and Sterility. 96(5). 1154–1159.e1. 48 indexed citations
14.
Thomson, Travis, Kathryn Fitzpatrick, & Joshua Johnson. (2010). Intrinsic and extrinsic mechanisms of oocyte loss. Molecular Human Reproduction. 16(12). 916–927. 32 indexed citations
15.
Kirino, Yohei, Anastassios Vourekas, Flávia de Lima Alves, et al.. (2009). Arginine methylation of Aubergine mediates Tudor binding and germ plasm localization. RNA. 16(1). 70–78. 99 indexed citations
16.
Thomson, Travis, et al.. (2008). Isolation of new polar granule components in Drosophila reveals P body and ER associated proteins. Mechanisms of Development. 125(9-10). 865–873. 94 indexed citations
17.
Thomson, Travis & Paul Lasko. (2005). Tudor and its domains: germ cell formation from a Tudor perspective. Cell Research. 15(4). 281–291. 65 indexed citations
18.
Thomson, Travis & Paul Lasko. (2004). Drosophila tudor is essential for polar granule assembly and pole cell specification, but not for posterior patterning. genesis. 40(3). 164–170. 83 indexed citations
19.
Mehta, P., Mohamed Darwish, & Travis Thomson. (1990). Switched-capacitor filters. IEEE Transactions on Power Electronics. 5(3). 331–336. 27 indexed citations
20.
Darwish, M., P. Mehta, & Travis Thomson. (1988). Variable characteristic filters. 424–427. 1 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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