Robin Reed

19.5k total citations · 4 hit papers
98 papers, 14.6k citations indexed

About

Robin Reed is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Robin Reed has authored 98 papers receiving a total of 14.6k indexed citations (citations by other indexed papers that have themselves been cited), including 96 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Neurology. Recurrent topics in Robin Reed's work include RNA Research and Splicing (92 papers), RNA and protein synthesis mechanisms (66 papers) and RNA modifications and cancer (55 papers). Robin Reed is often cited by papers focused on RNA Research and Splicing (92 papers), RNA and protein synthesis mechanisms (66 papers) and RNA modifications and cancer (55 papers). Robin Reed collaborates with scholars based in United States, Germany and United Kingdom. Robin Reed's co-authors include Tom Maniatis, Zhaolan Zhou, Ed Hurt, Mingjuan Luo, Or Gozani, Steven P. Gygi, David Staknis, S. Michaud, Anusha P. Dias and Rita Das and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Robin Reed

98 papers receiving 14.3k citations

Hit Papers

An extensive network of coupling among gene expressio... 1987 2026 2000 2013 2002 2002 2002 1987 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
Robin Reed United States 65 13.5k 845 812 809 587 98 14.6k
Maria Carmo‐Fonseca Portugal 60 10.7k 0.8× 1.3k 1.6× 491 0.6× 641 0.8× 726 1.2× 183 12.5k
Lynne E. Maquat United States 73 15.7k 1.2× 1.7k 2.1× 868 1.1× 748 0.9× 756 1.3× 161 18.2k
Javier F. Cáceres United Kingdom 52 11.0k 0.8× 599 0.7× 585 0.7× 481 0.6× 618 1.1× 89 12.2k
Juan Valcárcel Spain 53 10.0k 0.7× 702 0.8× 438 0.5× 392 0.5× 622 1.1× 117 11.1k
Christopher G. Burd United States 48 7.4k 0.5× 596 0.7× 512 0.6× 179 0.2× 538 0.9× 81 9.5k
Michael J. Matunis United States 46 10.3k 0.8× 910 1.1× 498 0.6× 209 0.3× 842 1.4× 94 11.2k
Susan R. Wente United States 53 9.7k 0.7× 725 0.9× 217 0.3× 380 0.5× 370 0.6× 106 11.0k
David L. Bentley United States 62 11.7k 0.9× 1.1k 1.3× 196 0.2× 460 0.6× 1.5k 2.5× 121 13.9k
Kazuko Nishikura United States 59 12.7k 0.9× 713 0.8× 1.3k 1.6× 480 0.6× 1.6k 2.8× 104 14.7k
Christopher W. J. Smith United Kingdom 44 6.9k 0.5× 361 0.4× 805 1.0× 302 0.4× 334 0.6× 93 7.9k

Countries citing papers authored by Robin Reed

Since Specialization
Citations

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

Fields of papers citing papers by Robin Reed

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robin Reed

This figure shows the co-authorship network connecting the top 25 collaborators of Robin Reed. A scholar is included among the top collaborators of Robin Reed 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 Robin Reed. Robin Reed 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.
Yu, Yong & Robin Reed. (2015). FUS functions in coupling transcription to splicing by mediating an interaction between RNAP II and U1 snRNP. Proceedings of the National Academy of Sciences. 112(28). 8608–8613. 85 indexed citations
2.
Shi, Min, H. Zhang, Lantian Wang, et al.. (2015). Premature termination codons are recognized in the nucleus in a reading-frame-dependent manner. Cell Discovery. 1(1). 34 indexed citations
3.
Lei, Haixin, Anusha P. Dias, & Robin Reed. (2011). Export and stability of naturally intronless mRNAs require specific coding region sequences and the TREX mRNA export complex. Proceedings of the National Academy of Sciences. 108(44). 17985–17990. 79 indexed citations
4.
Folco, Eric G., et al.. (2011). The anti-tumor drug E7107 reveals an essential role for SF3b in remodeling U2 snRNP to expose the branch point-binding region. Genes & Development. 25(5). 440–444. 129 indexed citations
5.
Yu, Yong, Rita Das, Eric G. Folco, & Robin Reed. (2010). A model in vitro system for co-transcriptional splicing. Nucleic Acids Research. 38(21). 7570–7578. 13 indexed citations
6.
Valencia, Patricia, Anusha P. Dias, & Robin Reed. (2008). Splicing promotes rapid and efficient mRNA export in mammalian cells. Proceedings of the National Academy of Sciences. 105(9). 3386–3391. 193 indexed citations
7.
Hims, Matthew M., El Chérif Ibrahim, Maire Leyne, et al.. (2007). Therapeutic potential and mechanism of kinetin as a treatment for the human splicing disease familial dysautonomia. Journal of Molecular Medicine. 85(2). 149–161. 48 indexed citations
8.
Reed, Robin & Hong Cheng. (2005). TREX, SR proteins and export of mRNA. Current Opinion in Cell Biology. 17(3). 269–273. 164 indexed citations
9.
Rodríguez‐Navarro, Susana, Tamás Fischer, Mingjuan Luo, et al.. (2004). Sus1, a Functional Component of the SAGA Histone Acetylase Complex and the Nuclear Pore-Associated mRNA Export Machinery. Cell. 116(1). 75–86. 293 indexed citations
10.
Reed, Robin. (2003). Coupling transcription, splicing and mRNA export. Current Opinion in Cell Biology. 15(3). 326–331. 202 indexed citations
11.
Chua, Katrin F. & Robin Reed. (2001). An Upstream AG Determines Whether a Downstream AG Is Selected during Catalytic Step II of Splicing. Molecular and Cellular Biology. 21(5). 1509–1514. 76 indexed citations
12.
Luo, Mingjuan, et al.. (2001). Pre-mRNA splicing and mRNA export linked by direct interactions between UAP56 and Aly. Nature. 413(6856). 644–647. 327 indexed citations
13.
Will, Cindy L., Claudia Schneider, Robin Reed, & Reinhard Lührmann. (1999). Identification of Both Shared and Distinct Proteins in the Major and Minor Spliceosomes. Science. 284(5422). 2003–2005. 109 indexed citations
14.
Chua, Katrin F. & Robin Reed. (1999). Human step II splicing factor hSlu7 functions in restructuring the spliceosome between the catalytic steps of splicing. Genes & Development. 13(7). 841–850. 47 indexed citations
15.
Luo, Mingjuan & Robin Reed. (1999). Splicing is required for rapid and efficient mRNA export in metazoans. Proceedings of the National Academy of Sciences. 96(26). 14937–14942. 314 indexed citations
16.
Bedford, Mark T., et al.. (1998). WW domain-mediated interactions reveal a spliceosome-associated protein that binds a third class of proline-rich motif: The proline glycine and methionine-rich motif. Proceedings of the National Academy of Sciences. 95(18). 10602–10607. 137 indexed citations
17.
Berglund, J. Andrew, Katrin F. Chua, Nadja Abovich, Robin Reed, & Michael Rosbash. (1997). The Splicing Factor BBP Interacts Specifically with the Pre-mRNA Branchpoint Sequence UACUAAC. Cell. 89(5). 781–787. 282 indexed citations
18.
Chiara, María‐Dolores & Robin Reed. (1995). A two-step mechanism for 5' and 3' splice-site pairing. Nature. 375(6531). 510–513. 84 indexed citations
19.
Staknis, David & Robin Reed. (1994). Direct Interactions between Pre-mRNA and Six U2 Small Nuclear Ribonucleoproteins during Spliceosome Assembly. Molecular and Cellular Biology. 14(5). 2994–3005. 45 indexed citations
20.
Wong, Sze Chuen Cesar, et al.. (1987). A new mutation in IVS-1 of the human beta globin gene causing beta thalassemia due to abnormal splicing. Blood. 70(1). 147–151. 58 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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