Miler T. Lee

3.6k total citations · 3 hit papers
22 papers, 2.3k citations indexed

About

Miler T. Lee is a scholar working on Molecular Biology, Cancer Research and Cellular and Molecular Neuroscience. According to data from OpenAlex, Miler T. Lee has authored 22 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 6 papers in Cancer Research and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Miler T. Lee's work include RNA Research and Splicing (12 papers), RNA modifications and cancer (5 papers) and RNA and protein synthesis mechanisms (5 papers). Miler T. Lee is often cited by papers focused on RNA Research and Splicing (12 papers), RNA modifications and cancer (5 papers) and RNA and protein synthesis mechanisms (5 papers). Miler T. Lee collaborates with scholars based in United States, Russia and Germany. Miler T. Lee's co-authors include Antonio J. Giráldez, Ariel Bazzini, Ashley R. Bonneau, Elizabeth Fleming, Carter M. Takacs, Charles E. Vejnar, Romain Christiano, Tobias C. Walther, Nikolaus Rajewsky and Sebastian D. Mackowiak and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Miler T. Lee

22 papers receiving 2.3k citations

Hit Papers

Ribosome Profiling Shows That miR-430 Reduces Translation... 2012 2026 2016 2021 2012 2014 2014 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Miler T. Lee United States 13 2.0k 688 232 172 160 22 2.3k
Ariel Paulson United States 19 1.1k 0.6× 278 0.4× 196 0.8× 90 0.5× 121 0.8× 28 1.5k
Laurence Ettwiller United States 22 2.0k 1.0× 274 0.4× 479 2.1× 121 0.7× 297 1.9× 49 2.5k
Oliver H. Tam United States 13 2.4k 1.2× 895 1.3× 270 1.2× 115 0.7× 740 4.6× 20 2.7k
Manuela Weier Switzerland 8 1.3k 0.6× 443 0.6× 535 2.3× 113 0.7× 298 1.9× 9 1.8k
Yavuz Ariyürek Netherlands 25 1.8k 0.9× 346 0.5× 530 2.3× 51 0.3× 380 2.4× 40 2.5k
Craig A. Smibert Canada 32 2.5k 1.2× 228 0.3× 470 2.0× 127 0.7× 210 1.3× 45 3.1k
Kazuhiro R. Nitta Japan 13 2.8k 1.4× 226 0.3× 504 2.2× 36 0.2× 302 1.9× 30 3.1k
Alexander Mazo United States 33 3.2k 1.6× 278 0.4× 488 2.1× 94 0.5× 560 3.5× 62 3.6k
Naoya Kenmochi Japan 23 1.8k 0.9× 220 0.3× 224 1.0× 31 0.2× 159 1.0× 55 2.2k
Robert Hock Germany 23 2.0k 1.0× 209 0.3× 315 1.4× 65 0.4× 254 1.6× 31 2.4k

Countries citing papers authored by Miler T. Lee

Since Specialization
Citations

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

Fields of papers citing papers by Miler T. Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miler T. Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Miler T. Lee. A scholar is included among the top collaborators of Miler T. Lee 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 Miler T. Lee. Miler T. Lee 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.
Miller, Jennifer, et al.. (2025). H3K4me2 distinguishes a distinct class of enhancers during the maternal-to-zygotic transition. PLoS Biology. 23(7). e3003239–e3003239. 1 indexed citations
2.
Nicotra, Matthew L., et al.. (2023). Parallels and contrasts between the cnidarian and bilaterian maternal-to-zygotic transition are revealed in Hydractinia embryos. PLoS Genetics. 19(7). e1010845–e1010845. 1 indexed citations
3.
Carlson, Anne E., et al.. (2023). Hybridization led to a rewired pluripotency network in the allotetraploid Xenopus laevis. eLife. 12. 5 indexed citations
4.
Lee, Miler T., et al.. (2021). RNA degradation is required for the germ-cell to maternal transition in Drosophila. Current Biology. 31(14). 2984–2994.e7. 18 indexed citations
5.
Carlson, Anne E., et al.. (2020). Optimized design of antisense oligomers for targeted rRNA depletion. Nucleic Acids Research. 49(1). e5–e5. 11 indexed citations
6.
Sanders, Steven M., Katherine M. Buckley, Daniel J. Bain, et al.. (2020). Zinc protection of fertilized eggs is an ancient feature of sexual reproduction in animals. PLoS Biology. 18(7). e3000811–e3000811. 11 indexed citations
7.
Lederer, Alex R., Marcie H. Warner, Travis N. Mavrich, et al.. (2019). The Paf1 Complex Broadly Impacts the Transcriptome of Saccharomyces cerevisiae. Genetics. 212(3). 711–728. 12 indexed citations
8.
Vejnar, Charles E., Carter M. Takacs, Valeria Yartseva, et al.. (2019). Genome wide analysis of 3′ UTR sequence elements and proteins regulating mRNA stability during maternal-to-zygotic transition in zebrafish. Genome Research. 29(7). 1100–1114. 48 indexed citations
9.
Lee, Miler T., et al.. (2018). The TMEM16A channel mediates the fast polyspermy block in Xenopus laevis. The Journal of General Physiology. 150(9). 1249–1259. 26 indexed citations
10.
Lee, Miler T., et al.. (2018). PLC and IP3-evoked Ca2+ release initiate the fast block to polyspermy inXenopus laeviseggs. The Journal of General Physiology. 150(9). 1239–1248. 9 indexed citations
11.
Yartseva, Valeria, Carter M. Takacs, Charles E. Vejnar, Miler T. Lee, & Antonio J. Giráldez. (2016). RESA identifies mRNA-regulatory sequences at high resolution. Nature Methods. 14(2). 201–207. 29 indexed citations
12.
Lee, Miler T., Ashley R. Bonneau, & Antonio J. Giráldez. (2014). Zygotic Genome Activation During the Maternal-to-Zygotic Transition. Annual Review of Cell and Developmental Biology. 30(1). 581–613. 443 indexed citations breakdown →
13.
Bazzini, Ariel, Timothy G. Johnstone, Romain Christiano, et al.. (2014). Identification of small ORFs in vertebrates using ribosome footprinting and evolutionary conservation. The EMBO Journal. 33(9). 981–993. 493 indexed citations breakdown →
14.
Francis, Chantal, Miler T. Lee, Mugdha Khaladkar, et al.. (2014). Divergence of RNA localization between rat and mouse neurons reveals the potential for rapid brain evolution. BMC Genomics. 15(1). 883–883. 20 indexed citations
15.
Lee, Miler T., Ashley R. Bonneau, Carter M. Takacs, et al.. (2013). Nanog, Pou5f1 and SoxB1 activate zygotic gene expression during the maternal-to-zygotic transition. Nature. 503(7476). 360–364. 362 indexed citations
16.
Khaladkar, Mugdha, Peter T. Buckley, Miler T. Lee, et al.. (2013). Subcellular RNA Sequencing Reveals Broad Presence of Cytoplasmic Intron-Sequence Retaining Transcripts in Mouse and Rat Neurons. PLoS ONE. 8(10). e76194–e76194. 31 indexed citations
17.
Bazzini, Ariel, Miler T. Lee, & Antonio J. Giráldez. (2012). Ribosome Profiling Shows That miR-430 Reduces Translation Before Causing mRNA Decay in Zebrafish. Science. 336(6078). 233–237. 560 indexed citations breakdown →
18.
Buckley, Peter T., Miler T. Lee, Jai‐Yoon Sul, et al.. (2011). Cytoplasmic Intron Sequence-Retaining Transcripts Can Be Dendritically Targeted via ID Element Retrotransposons. Neuron. 69(5). 877–884. 113 indexed citations
19.
Lee, Miler T. & Junhyong Kim. (2008). Self Containment, a Property of Modular RNA Structures, Distinguishes microRNAs. PLoS Computational Biology. 4(8). e1000150–e1000150. 12 indexed citations
20.
Lee, Miler T., et al.. (2008). Computational Sensing and in vitro Classification of GMOs and Biomolecular Events. OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information). 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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