Robert A. Reenan

8.4k total citations
60 papers, 5.0k citations indexed

About

Robert A. Reenan is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Insect Science. According to data from OpenAlex, Robert A. Reenan has authored 60 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Insect Science. Recurrent topics in Robert A. Reenan's work include RNA regulation and disease (36 papers), RNA Research and Splicing (31 papers) and CRISPR and Genetic Engineering (20 papers). Robert A. Reenan is often cited by papers focused on RNA regulation and disease (36 papers), RNA Research and Splicing (31 papers) and CRISPR and Genetic Engineering (20 papers). Robert A. Reenan collaborates with scholars based in United States, United Kingdom and Russia. Robert A. Reenan's co-authors include Richard D. Kolodner, Yiannis A. Savva, Michael J. Palladino, Leila E. Rieder, Liam P. Keegan, Mary A. O’Connell, Barry Ganetzky, James E.C. Jepson, Cynthia Staber and Stephen L. Helfand and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Robert A. Reenan

60 papers receiving 4.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert A. Reenan United States 34 4.1k 607 591 458 383 60 5.0k
Jing-Ruey Joanna Yeh United States 28 4.8k 1.2× 318 0.5× 351 0.6× 457 1.0× 1.1k 2.8× 48 5.9k
David A. Wassarman United States 30 3.0k 0.7× 120 0.2× 549 0.9× 225 0.5× 343 0.9× 68 3.9k
Andrew Bassett United Kingdom 35 3.6k 0.9× 369 0.6× 441 0.7× 1.1k 2.4× 733 1.9× 64 5.0k
Ronald Ellis United States 29 3.5k 0.9× 176 0.3× 468 0.8× 449 1.0× 648 1.7× 49 6.1k
Lizabeth A. Perkins United States 28 2.8k 0.7× 187 0.3× 907 1.5× 334 0.7× 714 1.9× 37 4.0k
Jacques Montagne France 22 1.7k 0.4× 354 0.6× 898 1.5× 163 0.4× 380 1.0× 42 2.9k
Juan R. Riesgo‐Escovar Mexico 24 1.5k 0.4× 346 0.6× 867 1.5× 166 0.4× 245 0.6× 48 2.5k
Peter L. Jones United States 34 2.6k 0.6× 124 0.2× 203 0.3× 195 0.4× 763 2.0× 64 3.6k
Peder Zipperlen Switzerland 8 4.5k 1.1× 209 0.3× 371 0.6× 576 1.3× 744 1.9× 10 6.4k
Ryusuke Niwa Japan 37 2.0k 0.5× 1.3k 2.2× 2.3k 3.9× 316 0.7× 1.0k 2.6× 87 4.7k

Countries citing papers authored by Robert A. Reenan

Since Specialization
Citations

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

Fields of papers citing papers by Robert A. Reenan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert A. Reenan. 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 Robert A. Reenan. The network helps show where Robert A. Reenan may publish in the future.

Co-authorship network of co-authors of Robert A. Reenan

This figure shows the co-authorship network connecting the top 25 collaborators of Robert A. Reenan. A scholar is included among the top collaborators of Robert A. Reenan 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 Robert A. Reenan. Robert A. Reenan 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.
Held, Aaron, et al.. (2019). Circuit Dysfunction in SOD1-ALS Model First Detected in Sensory Feedback Prior to Motor Neuron Degeneration Is Alleviated by BMP Signaling. Journal of Neuroscience. 39(12). 2347–2364. 29 indexed citations
2.
Kumar, Anita, et al.. (2018). Give me a SINE: how Selective Inhibitors of Nuclear Export modulate autophagy and aging. Molecular & Cellular Oncology. 5(5). e1502511–e1502511. 6 indexed citations
3.
Johnson, Joseph R., et al.. (2018). Nuclear Export Inhibition Enhances HLH-30/TFEB Activity, Autophagy, and Lifespan. Cell Reports. 23(7). 1915–1921. 69 indexed citations
4.
Wu, Zhijin, Joshua Amaya, Aaron Held, et al.. (2018). Meta-analysis of Genetic Modifiers Reveals Candidate Dysregulated Pathways in Amyotrophic Lateral Sclerosis. Neuroscience. 396. A3–A20. 16 indexed citations
5.
Savva, Yiannis A., et al.. (2017). Predicting RNA hyper-editing with a novel tool when unambiguous alignment is impossible. BMC Genomics. 18(1). 522–522. 1 indexed citations
6.
Savva, Yiannis A., et al.. (2012). Auto-regulatory RNA editing fine-tunes mRNA re-coding and complex behaviour in Drosophila. Nature Communications. 3(1). 790–790. 49 indexed citations
7.
Jepson, James E.C., et al.. (2011). Visualizing adenosine-to-inosine RNA editing in the Drosophila nervous system. Nature Methods. 9(2). 189–194. 20 indexed citations
8.
Pittendrigh, Barry R., May R. Berenbaum, Manfredo J. Seufferheld, et al.. (2011). Simplify, simplify. Communicative & Integrative Biology. 4(2). 188–191. 5 indexed citations
9.
Jepson, James E.C., et al.. (2011). Modulation of dADAR-dependent RNA editing by the Drosophila fragile X mental retardation protein. Nature Neuroscience. 14(12). 1517–1524. 67 indexed citations
10.
Jepson, James E.C., et al.. (2010). Engineered Alterations in RNA Editing Modulate Complex Behavior in Drosophila. Journal of Biological Chemistry. 286(10). 8325–8337. 60 indexed citations
11.
Jepson, James E.C. & Robert A. Reenan. (2010). Unraveling pleiotropic functions of A-To-I RNA editing in Drosophila. Fly. 4(2). 154–158. 6 indexed citations
12.
Reenan, Robert A. & Blanka Rogina. (2008). Acquired temperature‐sensitive paralysis as a biomarker of declining neuronal function in aging Drosophila. Aging Cell. 7(2). 179–186. 9 indexed citations
13.
Reenan, Robert A., et al.. (2007). Comparative Genomic and Bioinformatic Approaches for the Identification of New Adenosine‐to‐Inosine Substrates. Methods in enzymology on CD-ROM/Methods in enzymology. 424. 245–264. 3 indexed citations
14.
Reenan, Robert A.. (2005). Molecular determinants and guided evolution of species-specific RNA editing. Nature. 434(7031). 409–413. 97 indexed citations
15.
Keegan, Liam P., James Brindle, Angela Gallo, et al.. (2005). Tuning of RNA editing by ADAR is required in Drosophila. The EMBO Journal. 24(12). 2183–2193. 77 indexed citations
16.
Parisky, Katherine M., et al.. (2004). Identification of alternative splicing regulators by RNA interference in Drosophila. Proceedings of the National Academy of Sciences. 101(45). 15974–15979. 245 indexed citations
17.
Hoopengardner, Barry, et al.. (2003). Nervous System Targets of RNA Editing Identified by Comparative Genomics. Science. 301(5634). 832–836. 313 indexed citations
18.
Reenan, Robert A., Christopher J. Hanrahan, & Barry Ganetzky. (2000). The mlenapts RNA Helicase Mutation in Drosophila Results in a Splicing Catastrophe of the para Na + Channel Transcript in a Region of RNA Editing. Neuron. 25(1). 139–149. 154 indexed citations
19.
Palladino, Michael J., Liam P. Keegan, Mary A. O’Connell, & Robert A. Reenan. (2000). A-to-I Pre-mRNA Editing in Drosophila Is Primarily Involved in Adult Nervous System Function and Integrity. Cell. 102(4). 437–449. 314 indexed citations
20.
Alani, Eric, Robert A. Reenan, & Richard D. Kolodner. (1994). Interaction between mismatch repair and genetic recombination in Saccharomyces cerevisiae.. Genetics. 137(1). 19–39. 205 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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