Henry L. Levin

5.6k total citations · 1 hit paper
69 papers, 3.5k citations indexed

About

Henry L. Levin is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Henry L. Levin has authored 69 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Molecular Biology, 54 papers in Plant Science and 6 papers in Genetics. Recurrent topics in Henry L. Levin's work include Chromosomal and Genetic Variations (50 papers), Fungal and yeast genetics research (26 papers) and CRISPR and Genetic Engineering (25 papers). Henry L. Levin is often cited by papers focused on Chromosomal and Genetic Variations (50 papers), Fungal and yeast genetics research (26 papers) and CRISPR and Genetic Engineering (25 papers). Henry L. Levin collaborates with scholars based in United States, United Kingdom and Cameroon. Henry L. Levin's co-authors include John V. Moran, Jef D. Boeke, Daniel C. Weaver, Hirotaka Ebina, Guillaume Bourque, Cédric Feschotte, Dixie L. Mager, Mary Gehring, Vera Gorbunova and Todd S. Macfarlan and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Henry L. Levin

68 papers receiving 3.4k citations

Hit Papers

Ten things you should know about transposable elements 2018 2026 2020 2023 2018 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
Henry L. Levin United States 30 2.7k 2.2k 440 181 180 69 3.5k
Michaël Imbeault Switzerland 22 1.8k 0.7× 1.0k 0.5× 412 0.9× 259 1.4× 120 0.7× 23 2.4k
Marcelo Valle de Sousa Brazil 31 1.3k 0.5× 567 0.3× 696 1.6× 187 1.0× 490 2.7× 145 3.0k
Paul D. Friesen United States 38 3.2k 1.2× 687 0.3× 515 1.2× 57 0.3× 218 1.2× 66 3.9k
Jade K. Forwood Australia 30 2.1k 0.8× 492 0.2× 631 1.4× 197 1.1× 436 2.4× 153 3.6k
Ian A. Hope United Kingdom 28 3.2k 1.2× 444 0.2× 700 1.6× 55 0.3× 160 0.9× 57 4.4k
Frank Schwach United Kingdom 21 2.0k 0.7× 2.0k 0.9× 108 0.2× 88 0.5× 276 1.5× 27 3.8k
N. Kyle Tanner France 19 2.5k 0.9× 286 0.1× 294 0.7× 86 0.5× 163 0.9× 36 2.9k
Crisanto Gutiérrez Spain 48 5.1k 1.9× 5.4k 2.5× 580 1.3× 35 0.2× 91 0.5× 159 7.3k
Charlotta Funaya Germany 19 1.3k 0.5× 620 0.3× 153 0.3× 67 0.4× 230 1.3× 32 1.9k
Steven G. Sedgwick United Kingdom 30 3.2k 1.2× 525 0.2× 829 1.9× 39 0.2× 153 0.8× 63 3.8k

Countries citing papers authored by Henry L. Levin

Since Specialization
Citations

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

Fields of papers citing papers by Henry L. Levin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Henry L. Levin. 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 Henry L. Levin. The network helps show where Henry L. Levin may publish in the future.

Co-authorship network of co-authors of Henry L. Levin

This figure shows the co-authorship network connecting the top 25 collaborators of Henry L. Levin. A scholar is included among the top collaborators of Henry L. Levin 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 Henry L. Levin. Henry L. Levin 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.
Levin, Henry L., et al.. (2025). The 5′ truncation of retrotransposon L1: a process of genome integrity. Genetics. 231(4).
2.
Arkhipova, Irina R., Kathleen H. Burns, Katherine B. Chiappinelli, et al.. (2023). Meeting report: transposable elements at the crossroads of evolution, health and disease 2023. Mobile DNA. 14(1). 19–19. 1 indexed citations
3.
Ahn, Hyo Won, Lindsay M. Payer, Tongguang Wang, et al.. (2022). Retrotransposon insertions associated with risk of neurologic and psychiatric diseases. EMBO Reports. 24(1). e55197–e55197. 3 indexed citations
4.
Li, Feng, Caroline Esnault, Yabin Guo, et al.. (2022). Identification of an integrase-independent pathway of retrotransposition. Science Advances. 8(26). eabm9390–eabm9390. 6 indexed citations
5.
Jeffares, Daniel, Christoph Sadée, Maria Rodríguez‐López, et al.. (2019). Fitness Landscape of the Fission Yeast Genome. Molecular Biology and Evolution. 36(8). 1612–1623. 9 indexed citations
6.
Esnault, Caroline, Michael Lee, C. Ham, & Henry L. Levin. (2018). Transposable element insertions in fission yeast drive adaptation to environmental stress. Genome Research. 29(1). 85–95. 31 indexed citations
7.
Kumar, Sudhir, et al.. (2018). High-Frequency Lithium Acetate Transformation of Schizosaccharomyces pombe. Methods in molecular biology. 1721. 167–177. 14 indexed citations
8.
Kumar, Sudhir, et al.. (2018). Duplication and Transformation of the Schizosaccharomyces pombe Collection of Deletion Strains. Methods in molecular biology. 1721. 197–215. 2 indexed citations
9.
Abrams, John, Irina R. Arkhipova, Marlene Belfort, et al.. (2018). Meeting report: mobile genetic elements and genome plasticity 2018. Mobile DNA. 9(1). 21–21. 1 indexed citations
10.
Kumar, Sudhir, et al.. (2017). Host factors that promote retrotransposon integration are similar in distantly related eukaryotes. PLoS Genetics. 13(12). e1006775–e1006775. 6 indexed citations
11.
Singh, Parmit K., Matthew Plumb, Andrea L. Ferris, et al.. (2015). LEDGF/p75 interacts with mRNA splicing factors and targets HIV-1 integration to highly spliced genes. Genes & Development. 29(21). 2287–2297. 83 indexed citations
12.
Tanaka, Atsunari, Hideki Tanizawa, Sira Sriswasdi, et al.. (2012). Epigenetic Regulation of Condensin-Mediated Genome Organization during the Cell Cycle and upon DNA Damage through Histone H3 Lysine 56 Acetylation. Molecular Cell. 48(4). 532–546. 65 indexed citations
13.
Levin, Henry L. & John V. Moran. (2011). Dynamic interactions between transposable elements and their hosts. Nature Reviews Genetics. 12(9). 615–627. 416 indexed citations
14.
Guo, Yabin & Henry L. Levin. (2009). High-throughput sequencing of retrotransposon integration provides a saturated profile of target activity in Schizosaccharomyces pombe. Genome Research. 20(2). 239–248. 53 indexed citations
15.
Ebina, Hirotaka, et al.. (2008). The GP(Y/F) Domain of TF1 Integrase Multimerizes when Present in a Fragment, and Substitutions in This Domain Reduce Enzymatic Activity of the Full-length Protein. Journal of Biological Chemistry. 283(23). 15965–15974. 6 indexed citations
16.
Ebina, Hirotaka & Henry L. Levin. (2007). Stress Management: How Cells Take Control of Their Transposons. Molecular Cell. 27(2). 180–181. 16 indexed citations
17.
Levin, Henry L., et al.. (2000). Nuclear Import of the Retrotransposon Tf1 Is Governed by a Nuclear Localization Signal That Possesses a Unique Requirement for the FXFG Nuclear Pore Factor Nup124p. Molecular and Cellular Biology. 20(20). 7798–7812. 39 indexed citations
18.
Levin, Henry L., et al.. (1998). Schizosaccharomyces pombe Retrotransposon Tf2 Mobilizes Primarily through Homologous cDNA Recombination. Molecular and Cellular Biology. 18(11). 6839–6852. 30 indexed citations
19.
Levin, Henry L.. (1997). It's Prime Time for Reverse Transcriptase. Cell. 88(1). 5–8. 36 indexed citations
20.
Lin, Jennifer & Henry L. Levin. (1997). A complex structure in the mRNA of Tf1 is recognized and cleaved to generate the primer of reverse transcription.. Genes & Development. 11(2). 270–285. 38 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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