Sharleen Zhou

6.7k total citations · 1 hit paper
37 papers, 5.5k citations indexed

About

Sharleen Zhou is a scholar working on Molecular Biology, Immunology and Epidemiology. According to data from OpenAlex, Sharleen Zhou has authored 37 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 6 papers in Immunology and 4 papers in Epidemiology. Recurrent topics in Sharleen Zhou's work include Genomics and Chromatin Dynamics (17 papers), RNA Research and Splicing (10 papers) and DNA Repair Mechanisms (5 papers). Sharleen Zhou is often cited by papers focused on Genomics and Chromatin Dynamics (17 papers), RNA Research and Splicing (10 papers) and DNA Repair Mechanisms (5 papers). Sharleen Zhou collaborates with scholars based in United States, Poland and Russia. Sharleen Zhou's co-authors include Robert Tjian, David S. King, Qiang Zhou, Kunxin Luo, Shannon L. Stroschein, David Julius, Weidong Wang, Yutong Xue, Anders M. Näär and Wei Wang and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Sharleen Zhou

37 papers receiving 5.4k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A heteromeric Texas coral snake toxin targets acid-sensing ion channels to produce pain

2011 267 citations Christopher J. Bohlen, Sharleen Zhou et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sharleen Zhou United States	31	4.5k	842	543	398	392	37	5.5k
Michael R. Lerner United States	23	2.8k 0.6×	621 0.7×	211 0.4×	608 1.5×	248 0.6×	43	4.6k
Matilda Katan United Kingdom	45	4.0k 0.9×	569 0.7×	347 0.6×	705 1.8×	1.5k 3.8×	102	5.8k
Martin C. Schmidt United States	36	3.8k 0.8×	852 1.0×	288 0.5×	256 0.6×	373 1.0×	80	4.7k
Parry Guilford New Zealand	42	4.5k 1.0×	1.1k 1.3×	1.2k 2.2×	265 0.7×	629 1.6×	95	7.8k
Grace Gill United States	36	5.6k 1.2×	1.2k 1.4×	1.0k 1.9×	686 1.7×	506 1.3×	53	6.6k
Yoshikazu Nakamura Japan	45	4.4k 1.0×	1.4k 1.7×	421 0.8×	411 1.0×	694 1.8×	166	6.3k
Ora A. Weisz United States	39	2.9k 0.6×	458 0.5×	154 0.3×	417 1.0×	1.7k 4.5×	108	4.7k
Michael W. Pennington United States	45	4.2k 0.9×	972 1.2×	316 0.6×	939 2.4×	119 0.3×	117	6.1k
Holger Kramer United Kingdom	35	2.6k 0.6×	395 0.5×	494 0.9×	364 0.9×	337 0.9×	82	4.0k
Zheng Li China	36	2.0k 0.4×	652 0.8×	194 0.4×	190 0.5×	195 0.5×	185	3.5k

Countries citing papers authored by Sharleen Zhou

Since Specialization

Citations

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

Fields of papers citing papers by Sharleen Zhou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sharleen Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Sharleen Zhou. A scholar is included among the top collaborators of Sharleen Zhou 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 Sharleen Zhou. Sharleen Zhou is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Huo, Yanwu, Ki Hyun Nam, Fang Ding, et al.. (2014). Structures of CRISPR Cas3 offer mechanistic insights into Cascade-activated DNA unwinding and degradation. Nature Structural & Molecular Biology. 21(9). 771–777. 141 indexed citations

Brandman, Onn, Jacob Stewart-Ornstein, Daisy Y.L. Wong, et al.. (2012). A Ribosome-Bound Quality Control Complex Triggers Degradation of Nascent Peptides and Signals Translation Stress. Cell. 151(5). 1042–1054. 485 indexed citations

Li, Feng, Jeremy Herrera, Sharleen Zhou, Dmitri Maslov, & Larry Simpson. (2011). Trypanosome REH1 is an RNA helicase involved with the 3′–5′ polarity of multiple gRNA-guided uridine insertion/deletion RNA editing. Proceedings of the National Academy of Sciences. 108(9). 3542–3547. 44 indexed citations

Bohlen, Christopher J., Avi Priel, Sharleen Zhou, et al.. (2010). A Bivalent Tarantula Toxin Activates the Capsaicin Receptor, TRPV1, by Targeting the Outer Pore Domain. Cell. 141(5). 834–845. 254 indexed citations

Park, Chiwook, et al.. (2007). Energetics-based Protein Profiling on a Proteomic Scale: Identification of Proteins Resistant to Proteolysis. Journal of Molecular Biology. 368(5). 1426–1437. 67 indexed citations

Ball, Alexander R., John A. Schmiesing, Jong-Soo Kim, et al.. (2006). Condensin I Interacts with the PARP-1-XRCC1 Complex and Functions in DNA Single-Strand Break Repair. Molecular Cell. 21(6). 837–848. 122 indexed citations

Pan, Deng, Shannon L. Stroschein, Xueliang Zhu, et al.. (2005). The Integral Inner Nuclear Membrane Protein MAN1 Physically Interacts with the R-Smad Proteins to Repress Signaling by the Transforming Growth Factor-β Superfamily of Cytokines. Journal of Biological Chemistry. 280(16). 15992–16001. 145 indexed citations

Yang, Fajun, et al.. (2004). The activator-recruited cofactor/Mediator coactivator subunit ARC92 is a functionally important target of the VP16 transcriptional activator. Proceedings of the National Academy of Sciences. 101(8). 2339–2344. 103 indexed citations

Yin, Jinhu, Lisa B. Haney, Scott F. Walk, et al.. (2004). Nuclear localization of the DOCK180/ELMO complex. Archives of Biochemistry and Biophysics. 429(1). 23–29. 20 indexed citations

10.

Beall, Eileen L., J. Robert Manak, Sharleen Zhou, et al.. (2002). Role for a Drosophila Myb-containing protein complex in site-specific DNA replication. Nature. 420(6917). 833–837. 184 indexed citations

11.

Hochheimer, Andreas, et al.. (2002). TRF2 associates with DREF and directs promoter-selective gene expression in Drosophila. Nature. 420(6914). 439–445. 174 indexed citations

12.

Gregson, Heather C., et al.. (2001). A Potential Role for Human Cohesin in Mitotic Spindle Aster Assembly. Journal of Biological Chemistry. 276(50). 47575–47582. 65 indexed citations

13.

O’Keeffe, Bridget, Yick W. Fong, Dan Chen, Sharleen Zhou, & Qiang Zhou. (2000). Requirement for a Kinase-specific Chaperone Pathway in the Production of a Cdk9/Cyclin T1 Heterodimer Responsible for P-TEFb-mediated Tat Stimulation of HIV-1 Transcription. Journal of Biological Chemistry. 275(1). 279–287. 153 indexed citations

14.

Ryu, Soojin, Sharleen Zhou, Andreas G. Ladurner, & Robert Tjian. (1999). The transcriptional cofactor complex CRSP is required for activity of the enhancer-binding protein Sp1. Nature. 397(6718). 446–450. 292 indexed citations

15.

Näär, Anders M., et al.. (1999). Composite co-activator ARC mediates chromatin-directed transcriptional activation. Nature. 398(6730). 828–832. 364 indexed citations

16.

Schmiesing, John A., Alexander R. Ball, Heather C. Gregson, et al.. (1998). Identification of two distinct human SMC protein complexes involved in mitotic chromosome dynamics. Proceedings of the National Academy of Sciences. 95(22). 12906–12911. 92 indexed citations

17.

Poon, David, et al.. (1997). Cloning and Characterization of an Essential Saccharomyces cerevisiae Gene, TAF40, Which Encodes yTAFII40, an RNA Polymerase II-specific TATA-binding Protein-associated Factor. Journal of Biological Chemistry. 272(14). 9436–9442. 26 indexed citations

18.

Wang, Xia, et al.. (1997). Drosophila TFIIE: Purification, cloning, and functional reconstitution. Proceedings of the National Academy of Sciences. 94(2). 433–438. 6 indexed citations

19.

Dikstein, Rivka, Sharleen Zhou, & Robert Tjian. (1996). Human TAFII105 Is a Cell Type–Specific TFIID Subunit Related to hTAFII130. Cell. 87(1). 137–146. 146 indexed citations

20.

Wilson, Linda K., Bret M. Benton, Sharleen Zhou, Jeremy Thorner, & Greg S. Martin. (1995). The Yeast Immunophilin Fpr3 Is a Physiological Substrate of the Tyrosine-specific Phosphoprotein Phosphatase Ptp1. Journal of Biological Chemistry. 270(42). 25185–25193. 20 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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