Elizabeth J. Grayhack

4.2k total citations
43 papers, 3.2k citations indexed

About

Elizabeth J. Grayhack is a scholar working on Molecular Biology, Ecology and Genetics. According to data from OpenAlex, Elizabeth J. Grayhack has authored 43 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 4 papers in Ecology and 4 papers in Genetics. Recurrent topics in Elizabeth J. Grayhack's work include RNA and protein synthesis mechanisms (28 papers), RNA modifications and cancer (23 papers) and RNA Research and Splicing (15 papers). Elizabeth J. Grayhack is often cited by papers focused on RNA and protein synthesis mechanisms (28 papers), RNA modifications and cancer (23 papers) and RNA Research and Splicing (15 papers). Elizabeth J. Grayhack collaborates with scholars based in United States, France and India. Elizabeth J. Grayhack's co-authors include Eric M. Phizicky, Andrei Alexandrov, Stanley Fields, Kimberly Dean, Weifeng Gu, Lakmal Kotelawala, Min‐Hao Kuo, Timothy R. Hughes, Shawna L. Hiley and Stephen McCraith and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Elizabeth J. Grayhack

43 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elizabeth J. Grayhack United States 28 2.9k 330 226 187 187 43 3.2k
Christopher S. Francklyn United States 34 3.3k 1.1× 548 1.7× 98 0.4× 122 0.7× 75 0.4× 68 3.6k
Shaorong Chong United States 22 2.5k 0.9× 376 1.1× 224 1.0× 208 1.1× 119 0.6× 42 2.7k
J. Scott Butler United States 29 2.6k 0.9× 271 0.8× 69 0.3× 92 0.5× 179 1.0× 44 2.8k
Sergey Melnikov United States 20 2.0k 0.7× 219 0.7× 191 0.8× 95 0.5× 116 0.6× 33 2.2k
Tao‐shih Hsieh United States 33 2.9k 1.0× 257 0.8× 549 2.4× 162 0.9× 430 2.3× 68 3.1k
Kozo Tomita Japan 31 1.9k 0.7× 351 1.1× 123 0.5× 255 1.4× 107 0.6× 78 2.3k
Umadas Maitra United States 38 3.4k 1.2× 781 2.4× 231 1.0× 526 2.8× 158 0.8× 102 3.7k
David Kowalski United States 29 2.3k 0.8× 525 1.6× 213 0.9× 193 1.0× 381 2.0× 50 2.5k
Carl Schmitz Australia 4 1.5k 0.5× 169 0.5× 149 0.7× 96 0.5× 88 0.5× 6 2.0k
Yves Méchulam France 38 3.2k 1.1× 764 2.3× 452 2.0× 214 1.1× 54 0.3× 98 3.6k

Countries citing papers authored by Elizabeth J. Grayhack

Since Specialization
Citations

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

Fields of papers citing papers by Elizabeth J. Grayhack

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elizabeth J. Grayhack. 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 Elizabeth J. Grayhack. The network helps show where Elizabeth J. Grayhack may publish in the future.

Co-authorship network of co-authors of Elizabeth J. Grayhack

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth J. Grayhack. A scholar is included among the top collaborators of Elizabeth J. Grayhack 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 Elizabeth J. Grayhack. Elizabeth J. Grayhack 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.
2.
3.
Grayhack, Elizabeth J., et al.. (2017). Synonymous Codons: Choose Wisely for Expression. Trends in Genetics. 33(4). 283–297. 142 indexed citations
4.
Dean, Kimberly, et al.. (2016). RNA-ID, a Powerful Tool for Identifying and Characterizing Regulatory Sequences. Methods in enzymology on CD-ROM/Methods in enzymology. 572. 237–253. 2 indexed citations
5.
Quivey, Robert G., Elizabeth J. Grayhack, Roberta C. Faustoferri, et al.. (2015). Functional profiling in Streptococcus mutans: construction and examination of a genomic collection of gene deletion mutants. Molecular Oral Microbiology. 30(6). 474–495. 36 indexed citations
6.
Grayhack, Elizabeth J., et al.. (2015). Asc1, homolog of human RACK1, prevents frameshifting in yeast by ribosomes stalled at CGA codon repeats. RNA. 21(5). 935–945. 56 indexed citations
7.
Grant, Thomas D., Edward H. Snell, Joseph R. Luft, et al.. (2011). Structural conservation of an ancient tRNA sensor in eukaryotic glutaminyl-tRNA synthetase. Nucleic Acids Research. 40(8). 3723–3731. 14 indexed citations
8.
Dean, Kimberly, et al.. (2010). Control of translation efficiency in yeast by codon–anticodon interactions. RNA. 16(12). 2516–2528. 123 indexed citations
9.
Jackman, Jane E., Elizabeth J. Grayhack, & Eric M. Phizicky. (2008). The use of Saccharomyces cerevisiae proteomic libraries to identify RNA-modifying proteins. Methods in molecular biology. 488. 383–393. 2 indexed citations
10.
Kotelawala, Lakmal, Elizabeth J. Grayhack, & Eric M. Phizicky. (2007). Identification of yeast tRNA Um44 2′-O-methyltransferase (Trm44) and demonstration of a Trm44 role in sustaining levels of specific tRNASer species. RNA. 14(1). 158–169. 69 indexed citations
11.
Jackman, Jane E., Lakmal Kotelawala, Elizabeth J. Grayhack, & Eric M. Phizicky. (2007). Identification and Characterization of Modification Enzymes by Biochemical Analysis of the Proteome. Methods in enzymology on CD-ROM/Methods in enzymology. 425. 139–152. 3 indexed citations
12.
Crary, Sharon M., et al.. (2007). The 2′-O-methyltransferase responsible for modification of yeast tRNA at position 4. RNA. 13(3). 404–413. 40 indexed citations
13.
Alexandrov, Andrei, Weifeng Gu, Shawna L. Hiley, et al.. (2006). Rapid tRNA Decay Can Result from Lack of Nonessential Modifications. Molecular Cell. 21(1). 87–96. 397 indexed citations
14.
Phizicky, Eric M. & Elizabeth J. Grayhack. (2006). Proteome-Scale Analysis of Biochemical Activity. Critical Reviews in Biochemistry and Molecular Biology. 41(5). 315–327. 11 indexed citations
15.
Yang, Chunxing, et al.. (2005). Pseudouridylation of yeast U2 snRNA is catalyzed by either an RNA‐guided or RNA‐independent mechanism. The EMBO Journal. 24(13). 2403–2413. 63 indexed citations
16.
Martzen, Mark R., Stephen McCraith, Sherry L. Spinelli, et al.. (2002). Biochemical genomics approach to map activities to genes activities to gene. Methods in enzymology on CD-ROM/Methods in enzymology. 350. 546–559. 28 indexed citations
17.
Grayhack, Elizabeth J. & Eric M. Phizicky. (2001). Genomic analysis of biochemical function. Current Opinion in Chemical Biology. 5(1). 34–39. 14 indexed citations
18.
Kuo, Min‐Hao & Elizabeth J. Grayhack. (1994). A library of yeast genomic MCM1 binding sites contains genes involved in cell cycle control, cell wall and membrane structure, and metabolism.. Molecular and Cellular Biology. 14(1). 348–359. 31 indexed citations
19.
Grayhack, Elizabeth J.. (1992). The Yeast a1 and MCM1 Proteins Bind a Single Strand of Their Duplex DNA Recognition Site. Molecular and Cellular Biology. 12(8). 3573–3582. 2 indexed citations
20.
Grayhack, Elizabeth J., Xiuyi A. Yang, Lester F. Lau, & Jason Roberts. (1985). Phage lambda gene Q antiterminator recognizes RNA polymerase near the promoter and accelerates it through a pause site. Cell. 42(1). 259–269. 138 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Christopher S. Francklyn Breakdown of academic impact, for papers by Shaorong Chong Breakdown of academic impact, for papers by J. Scott Butler Breakdown of academic impact, for papers by Sergey Melnikov Breakdown of academic impact, for papers by Tao‐shih Hsieh Breakdown of academic impact, for papers by Kozo Tomita Breakdown of academic impact, for papers by Umadas Maitra Breakdown of academic impact, for papers by David Kowalski Breakdown of academic impact, for papers by Carl Schmitz Breakdown of academic impact, for papers by Yves Méchulam
Rankless by CCL
2026