David Rekosh

6.6k total citations
122 papers, 5.6k citations indexed

About

David Rekosh is a scholar working on Molecular Biology, Virology and Infectious Diseases. According to data from OpenAlex, David Rekosh has authored 122 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 50 papers in Virology and 33 papers in Infectious Diseases. Recurrent topics in David Rekosh's work include HIV Research and Treatment (50 papers), HIV/AIDS drug development and treatment (30 papers) and RNA Research and Splicing (29 papers). David Rekosh is often cited by papers focused on HIV Research and Treatment (50 papers), HIV/AIDS drug development and treatment (30 papers) and RNA Research and Splicing (29 papers). David Rekosh collaborates with scholars based in United States, South Africa and Tanzania. David Rekosh's co-authors include Marie‐Louise Hammarskjöld, Philip T. LoVerde, M L Hammarskjöld, Yeou-Cherng Bor, W. C. Russell, A.J. Robinson, Narasimhachar Srinivasakumar, Alexander J. Smith, Libuse A. Bobek and Marie-Louise Hammarskjöld and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

David Rekosh

121 papers receiving 5.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Rekosh United States 44 3.3k 2.1k 1.2k 971 661 122 5.6k
Jean‐Pierre Lecocq France 34 2.7k 0.8× 952 0.5× 551 0.4× 1.9k 2.0× 439 0.7× 67 5.9k
Margaret Kielian United States 49 2.0k 0.6× 1.2k 0.6× 3.3k 2.6× 652 0.7× 459 0.7× 124 6.8k
William H. Wunner United States 37 1.3k 0.4× 2.5k 1.2× 1.2k 1.0× 945 1.0× 307 0.5× 80 4.9k
Thomas R. Fuerst United States 33 2.5k 0.8× 1.8k 0.9× 2.5k 2.0× 1.5k 1.6× 651 1.0× 74 8.0k
Stefan Höglund Sweden 27 1.5k 0.5× 1.3k 0.6× 1.1k 0.9× 705 0.7× 510 0.8× 67 3.3k
Mette Strand United States 40 1.4k 0.4× 485 0.2× 460 0.4× 798 0.8× 887 1.3× 121 4.7k
Sundararajan Venkatesan United States 37 1.9k 0.6× 2.3k 1.1× 1.3k 1.1× 725 0.7× 667 1.0× 69 4.8k
Manohar R. Furtado United States 34 1.5k 0.4× 2.1k 1.0× 1.8k 1.4× 992 1.0× 405 0.6× 81 4.8k
Edward B. Stephens United States 34 881 0.3× 3.1k 1.5× 1.4k 1.2× 404 0.4× 221 0.3× 117 4.7k
Jason M. Mackenzie Australia 42 1.2k 0.3× 906 0.4× 3.8k 3.1× 569 0.6× 132 0.2× 95 6.5k

Countries citing papers authored by David Rekosh

Since Specialization
Citations

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

Fields of papers citing papers by David Rekosh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Rekosh

This figure shows the co-authorship network connecting the top 25 collaborators of David Rekosh. A scholar is included among the top collaborators of David Rekosh 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 David Rekosh. David Rekosh 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.
Jackson, Patrick, et al.. (2023). Rev–Rev Response Element Activity Selection Bias at the Human Immunodeficiency Virus Transmission Bottleneck. Open Forum Infectious Diseases. 10(10). ofad486–ofad486. 1 indexed citations
2.
Rekosh, David, et al.. (2022). HIV-1 Rev-RRE functional activity in primary isolates is highly dependent on minimal context-dependent changes in Rev. Scientific Reports. 12(1). 18416–18416. 5 indexed citations
3.
Jackson, Patrick, et al.. (2020). Sequence and Functional Variation in the HIV-1 Rev Regulatory Axis. Current HIV Research. 18(2). 85–98. 8 indexed citations
4.
Grabski, David F., Aakrosh Ratan, Laurie R. Gray, et al.. (2020). Human endogenous retrovirus-K mRNA expression and genomic alignment data in hepatoblastoma. SHILAP Revista de lepidopterología. 31. 105895–105895. 4 indexed citations
5.
Jackson, Patrick, Laurie R. Gray, Kathryn Anastos, et al.. (2019). Evolution of the HIV-1 Rev Response Element during Natural Infection Reveals Nucleotide Changes That Correlate with Altered Structure and Increased Activity over Time. Journal of Virology. 93(11). 13 indexed citations
6.
Jackson, Patrick, et al.. (2019). A novel retroviral vector system to analyze expression from mRNA with retained introns using fluorescent proteins and flow cytometry. Scientific Reports. 9(1). 6467–6467. 6 indexed citations
7.
Jackson, Patrick, et al.. (2017). High level of HIV-1 drug resistance mutations in patients with unsuppressed viral loads in rural northern South Africa. AIDS Research and Therapy. 14(1). 36–36. 29 indexed citations
8.
Jackson, Patrick, Denis M. Tebit, David Rekosh, & Marie‐Louise Hammarskjöld. (2016). Rev–RRE Functional Activity Differs Substantially Among Primary HIV-1 Isolates. AIDS Research and Human Retroviruses. 32(9). 923–934. 25 indexed citations
9.
Wang, Baomin, David Rekosh, & Marie‐Louise Hammarskjöld. (2015). Evolutionary conservation of a molecular machinery for export and expression of mRNAs with retained introns. RNA. 21(3). 426–437. 12 indexed citations
10.
Bor, Yeou-Cherng, et al.. (2011). The Tpr protein regulates export of mRNAs with retained introns that traffic through the Nxf1 pathway. RNA. 17(7). 1344–1356. 71 indexed citations
11.
Chang, Hua, et al.. (2011). Single-Nucleotide Changes in the HIV Rev-Response Element Mediate Resistance to Compounds That Inhibit Rev Function. Journal of Virology. 85(8). 3940–3949. 16 indexed citations
12.
Bessong, Pascal, M. Jeffrey Mphahlele, Isaac Choge, et al.. (2006). Resistance Mutational Analysis of HIV Type 1 Subtype C among Rural South African Drug-Naive Patients Prior to Large-Scale Availability of Antiretrovirals. AIDS Research and Human Retroviruses. 22(12). 1306–1312. 29 indexed citations
13.
Olivieri, Kevin C., Aprille L. Matthews, Mark David, et al.. (2006). The envelope gene is a cytopathic determinant of CCR5 tropic HIV-1. Virology. 358(1). 23–38. 22 indexed citations
14.
Giordano, Vincenzo, Dong‐Yan Jin, David Rekosh, & Kuan-Teh Jeang. (2000). Intravirion Targeting of a Functional Anti-Human Immunodeficiency Virus Ribozyme Directed to pol. Virology. 267(2). 174–184. 12 indexed citations
15.
Dundr, Miroslav, U. Thomas Meier, Nancy J. Lewis, et al.. (1997). A class of nonribosomal nucleolar components is located in chromosome periphery and in nucleolus-derived foci during anaphase and telophase. Chromosoma. 105(7-8). 407–417. 74 indexed citations
16.
Keulen, Harry van, et al.. (1991). Characterization of a 54-nucleotide gap region in the 28S rRNA gene of Schistosoma mansoni. Molecular and Biochemical Parasitology. 45(2). 205–214. 24 indexed citations
17.
Spotila, Loretta D., Hirohisa Hirai, David Rekosh, & Philip T. LoVerde. (1989). A retroposon-like short repetitive DNA element in the genome of the human blood fluke, Schistosoma mansoni. Chromosoma. 97(6). 421–428. 48 indexed citations
18.
LoVerde, Philip T., David Rekosh, & Libuse A. Bobek. (1989). Developmentally regulated gene expression in Schistosoma. Experimental Parasitology. 68(1). 116–120. 11 indexed citations
19.
Rekosh, David, et al.. (1989). Schistosoma mansoni: Identification and characterization of schistosomula polypeptides. Experimental Parasitology. 69(2). 249–262. 7 indexed citations
20.
Spotila, Loretta D., et al.. (1987). A cloned DNA probe identifies the sex of Schistosoma mansoni cercariae. Molecular and Biochemical Parasitology. 26(1-2). 17–20. 25 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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