Edwin R. Smith

10.2k total citations · 2 hit papers
57 papers, 7.6k citations indexed

About

Edwin R. Smith is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Edwin R. Smith has authored 57 papers receiving a total of 7.6k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 5 papers in Genetics and 5 papers in Plant Science. Recurrent topics in Edwin R. Smith's work include Genomics and Chromatin Dynamics (39 papers), Epigenetics and DNA Methylation (25 papers) and Cancer-related gene regulation (19 papers). Edwin R. Smith is often cited by papers focused on Genomics and Chromatin Dynamics (39 papers), Epigenetics and DNA Methylation (25 papers) and Cancer-related gene regulation (19 papers). Edwin R. Smith collaborates with scholars based in United States, Spain and Canada. Edwin R. Smith's co-authors include Ali Shilatifard, Chengqi Lin, John C. Lucchesi, C. David Allis, Sukesh R. Bhaumik, Jung‐Shin Lee, Fei Chen, Laurence Florens, Michael P. Washburn and Xin Gao and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Edwin R. Smith

57 papers receiving 7.5k citations

Hit Papers

Physical Association and Coordinate Function of the H3 K4... 2005 2026 2012 2019 2005 2007 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
Edwin R. Smith United States 43 6.9k 839 557 555 545 57 7.6k
Gary LeRoy United States 37 5.4k 0.8× 569 0.7× 431 0.8× 395 0.7× 378 0.7× 47 5.9k
Ru Cao United States 23 8.2k 1.2× 1.7k 2.0× 523 0.9× 660 1.2× 1.1k 2.0× 28 9.0k
Sharon Dent United States 49 7.3k 1.1× 745 0.9× 877 1.6× 622 1.1× 607 1.1× 100 8.2k
Alla A. Sigova United States 14 5.6k 0.8× 591 0.7× 382 0.7× 1.2k 2.1× 1.4k 2.5× 20 6.4k
Jens Vilstrup Johansen Denmark 31 4.4k 0.6× 690 0.8× 679 1.2× 174 0.3× 672 1.2× 54 5.6k
Roderick J. O’Sullivan United States 28 5.5k 0.8× 665 0.8× 565 1.0× 762 1.4× 422 0.8× 42 6.5k
Terumi Kohwi-shigematsu United States 42 5.7k 0.8× 1.4k 1.6× 773 1.4× 516 0.9× 527 1.0× 78 7.1k
Arttu Jolma Sweden 19 5.4k 0.8× 823 1.0× 374 0.7× 524 0.9× 669 1.2× 25 6.3k
Frédéric Chédin United States 41 5.5k 0.8× 1.2k 1.5× 424 0.8× 563 1.0× 426 0.8× 58 6.0k
Beverly M. Emerson United States 32 4.6k 0.7× 664 0.8× 915 1.6× 232 0.4× 697 1.3× 44 5.4k

Countries citing papers authored by Edwin R. Smith

Since Specialization
Citations

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

Fields of papers citing papers by Edwin R. Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edwin R. Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Edwin R. Smith. A scholar is included among the top collaborators of Edwin R. Smith 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 Edwin R. Smith. Edwin R. Smith 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.
Cao, Kaixiang, Patrick A. Ozark, Juan Wang, et al.. (2020). DOT1L-controlled cell-fate determination and transcription elongation are independent of H3K79 methylation. Proceedings of the National Academy of Sciences. 117(44). 27365–27373. 42 indexed citations
2.
Rickels, Ryan, Marta Iwanaszko, Patrick A. Ozark, et al.. (2020). A small UTX stabilization domain of Trr is conserved within mammalian MLL3-4/COMPASS and is sufficient to rescue loss of viability in null animals. Genes & Development. 34(21-22). 1493–1502. 18 indexed citations
3.
Aoi, Yuki, Edwin R. Smith, Avani P. Shah, et al.. (2020). NELF Regulates a Promoter-Proximal Step Distinct from RNA Pol II Pause-Release. Molecular Cell. 78(2). 261–274.e5. 112 indexed citations
4.
Cao, Kaixiang, Clayton K. Collings, Marc A. Morgan, et al.. (2018). An Mll4/COMPASS-Lsd1 epigenetic axis governs enhancer function and pluripotency transition in embryonic stem cells. Science Advances. 4(1). eaap8747–eaap8747. 48 indexed citations
5.
Chen, Fei, Edwin R. Smith, & Ali Shilatifard. (2018). Born to run: control of transcription elongation by RNA polymerase II. Nature Reviews Molecular Cell Biology. 19(7). 464–478. 286 indexed citations
6.
Liang, Kaiwei, Andrew Volk, Jeffrey S. Haug, et al.. (2017). Therapeutic Targeting of MLL Degradation Pathways in MLL-Rearranged Leukemia. Cell. 168(1-2). 59–72.e13. 89 indexed citations
7.
Rickels, Ryan, Hans-Martin Herz, Christie C. Sze, et al.. (2017). Histone H3K4 monomethylation catalyzed by Trr and mammalian COMPASS-like proteins at enhancers is dispensable for development and viability. Nature Genetics. 49(11). 1647–1653. 143 indexed citations
8.
Kumar, Bony De, Mark E. Parrish, Brian D. Slaughter, et al.. (2015). Analysis of dynamic changes in retinoid-induced transcription and epigenetic profiles of murine Hox clusters in ES cells. Genome Research. 25(8). 1229–1243. 49 indexed citations
9.
Luo, Zhuojuan, Xin Gao, Chengqi Lin, et al.. (2015). Zic2 Is an Enhancer-Binding Factor Required for Embryonic Stem Cell Specification. Molecular Cell. 57(4). 685–694. 80 indexed citations
10.
Smith, Edwin R. & Ali Shilatifard. (2014). Enhancer biology and enhanceropathies. Nature Structural & Molecular Biology. 21(3). 210–219. 220 indexed citations
11.
Thornton, Janet L., Gerwin Westfield, Yoh-hei Takahashi, et al.. (2014). Context dependency of Set1/COMPASS-mediated histone H3 Lys4 trimethylation. Genes & Development. 28(2). 115–120. 42 indexed citations
12.
Hu, Deqing, Edwin R. Smith, Alexander S. Garruss, et al.. (2013). The Little Elongation Complex Functions at Initiation and Elongation Phases of snRNA Gene Transcription. Molecular Cell. 51(4). 493–505. 53 indexed citations
13.
Smith, Edwin R. & Ali Shilatifard. (2013). Transcriptional elongation checkpoint control in development and disease. Genes & Development. 27(10). 1079–1088. 52 indexed citations
14.
Hu, Deqing, Alexander S. Garruss, Xin Gao, et al.. (2013). The Mll2 branch of the COMPASS family regulates bivalent promoters in mouse embryonic stem cells. Nature Structural & Molecular Biology. 20(9). 1093–1097. 142 indexed citations
15.
Lin, Chengqi, Alexander S. Garrett, Bony De Kumar, et al.. (2011). Dynamic transcriptional events in embryonic stem cells mediated by the super elongation complex (SEC). Genes & Development. 25(14). 1486–1498. 149 indexed citations
16.
Smith, Edwin R., Chengqi Lin, & Ali Shilatifard. (2011). The super elongation complex (SEC) and MLL in development and disease. Genes & Development. 25(7). 661–672. 256 indexed citations
17.
Smith, Edwin R. & Ali Shilatifard. (2010). The Chromatin Signaling Pathway: Diverse Mechanisms of Recruitment of Histone-Modifying Enzymes and Varied Biological Outcomes. Molecular Cell. 40(5). 689–701. 181 indexed citations
18.
Morra, Rosa, Edwin R. Smith, Ruth Yokoyama, & John C. Lucchesi. (2007). The MLE Subunit of the Drosophila MSL Complex Uses Its ATPase Activity for Dosage Compensation and Its Helicase Activity for Targeting. Molecular and Cellular Biology. 28(3). 958–966. 33 indexed citations
20.
Taylor, Thomas H., et al.. (1994). Linear IgA disease autoantigen is a 120 KD Anchoring filament protein. Journal of Investigative Dermatology. 103(3). 442. 3 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026