Joseph V. Gray

1.6k total citations
21 papers, 1.4k citations indexed

About

Joseph V. Gray is a scholar working on Molecular Biology, Cell Biology and Materials Chemistry. According to data from OpenAlex, Joseph V. Gray has authored 21 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 5 papers in Cell Biology and 4 papers in Materials Chemistry. Recurrent topics in Joseph V. Gray's work include Fungal and yeast genetics research (12 papers), Enzyme Structure and Function (4 papers) and Endoplasmic Reticulum Stress and Disease (3 papers). Joseph V. Gray is often cited by papers focused on Fungal and yeast genetics research (12 papers), Enzyme Structure and Function (4 papers) and Endoplasmic Reticulum Stress and Disease (3 papers). Joseph V. Gray collaborates with scholars based in United Kingdom, United States and Canada. Joseph V. Gray's co-authors include Gregory A. Petsko, Dagmar Ringe, Richard A. Singer, Gerald C. Johnston, Margaret Werner‐Washburne, Sue Ann Krause, Jeremy R. Knowles, Eleanor W. Trotter, Yuh Min Chook and William N. Lipscomb and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Joseph V. Gray

21 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joseph V. Gray United Kingdom 13 1.2k 277 218 148 102 21 1.4k
Peter Sheffield United States 12 975 0.8× 293 1.1× 68 0.3× 182 1.2× 40 0.4× 28 1.3k
Andrew W. Truman United States 22 1.6k 1.3× 312 1.1× 167 0.8× 192 1.3× 90 0.9× 55 1.7k
Monique Bolotin‐Fukuhara France 32 2.2k 1.8× 172 0.6× 208 1.0× 65 0.4× 48 0.5× 81 2.4k
Reinhard Dechant Switzerland 17 1.1k 0.9× 298 1.1× 126 0.6× 47 0.3× 84 0.8× 27 1.4k
Mikael Molin Sweden 18 906 0.8× 132 0.5× 136 0.6× 47 0.3× 183 1.8× 32 1.1k
Claes Andréasson Sweden 25 1.4k 1.2× 518 1.9× 101 0.5× 105 0.7× 112 1.1× 40 1.5k
Olivier Deloche Switzerland 14 1.3k 1.1× 390 1.4× 171 0.8× 49 0.3× 120 1.2× 15 1.5k
Alexander DeLuna Mexico 21 1.4k 1.2× 87 0.3× 331 1.5× 74 0.5× 102 1.0× 42 1.7k
Dmitry A. Knorre Russia 19 996 0.8× 110 0.4× 133 0.6× 27 0.2× 88 0.9× 67 1.3k
Lyra Chang United States 16 1.4k 1.2× 339 1.2× 52 0.2× 199 1.3× 55 0.5× 20 1.7k

Countries citing papers authored by Joseph V. Gray

Since Specialization
Citations

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

Fields of papers citing papers by Joseph V. Gray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joseph V. Gray. 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 Joseph V. Gray. The network helps show where Joseph V. Gray may publish in the future.

Co-authorship network of co-authors of Joseph V. Gray

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph V. Gray. A scholar is included among the top collaborators of Joseph V. Gray 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 Joseph V. Gray. Joseph V. Gray 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.
Duan, Chengjie, Arnaud Baslé, Joseph V. Gray, et al.. (2020). Ascertaining the biochemical function of an essential pectin methylesterase in the gut microbe Bacteroides thetaiotaomicron. Journal of Biological Chemistry. 295(52). 18625–18637. 9 indexed citations
2.
Burgess, Karl, et al.. (2014). Recovery from Rapamycin. Journal of Biological Chemistry. 289(38). 26554–26565. 9 indexed citations
3.
Coward, Kevin & Joseph V. Gray. (2014). Audit of Practical Work Undertaken by Undergraduate Bioscience Students Across the UK Higher Education Sector. ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam). 2 indexed citations
4.
Krause, Sue Ann, et al.. (2012). Functional specialization of the yeast Rho1 GTP exchange factors. Journal of Cell Science. 125(Pt 11). 2721–31. 24 indexed citations
5.
Gray, Joseph V. & Sue Ann Krause. (2009). Chapter 3 Synthetic Genetic Interactions. Advances in genetics. 66. 61–84. 2 indexed citations
6.
Krause, Sue Ann & Joseph V. Gray. (2009). The functional relationships underlying a synthetic genetic network. Communicative & Integrative Biology. 2(1). 4–6. 3 indexed citations
7.
Krause, Sue Ann, Hong Xu, & Joseph V. Gray. (2008). The Synthetic Genetic Network around PKC1 Identifies Novel Modulators and Components of Protein Kinase C Signaling in Saccharomyces cerevisiae. Eukaryotic Cell. 7(11). 1880–1887. 18 indexed citations
8.
Gray, Joseph V. & Sue Ann Krause. (2007). Identifying in vivo pathways using genome-wide genetic networks. Biochemical Society Transactions. 35(6). 1538–1541. 2 indexed citations
9.
Gray, Joseph V., Gregory A. Petsko, Gerald C. Johnston, et al.. (2004). “Sleeping Beauty”: Quiescence inSaccharomyces cerevisiae. Microbiology and Molecular Biology Reviews. 68(2). 187–206. 468 indexed citations
10.
Rayner, Tim F., Joseph V. Gray, & Jeremy Thorner. (2002). Direct and Novel Regulation of cAMP-dependent Protein Kinase by Mck1p, a Yeast Glycogen Synthase Kinase-3. Journal of Biological Chemistry. 277(19). 16814–16822. 21 indexed citations
11.
Krause, Sue Ann & Joseph V. Gray. (2002). The Protein Kinase C Pathway Is Required for Viability in Quiescence in Saccharomyces cerevisiae. Current Biology. 12(7). 588–593. 68 indexed citations
12.
Trotter, Eleanor W., et al.. (2002). Misfolded Proteins Are Competent to Mediate a Subset of the Responses to Heat Shock in Saccharomyces cerevisiae. Journal of Biological Chemistry. 277(47). 44817–44825. 137 indexed citations
13.
Trotter, Eleanor W., et al.. (2001). Protein misfolding and temperature up-shift cause G 1 arrest via a common mechanism dependent on heat shock factor in Saccharomyces cerevisiae. Proceedings of the National Academy of Sciences. 98(13). 7313–7318. 89 indexed citations
14.
15.
Gray, Joseph V. & Keith Johnson. (1997). Waiting for frataxin. Nature Genetics. 16(4). 323–325. 4 indexed citations
16.
Walker, Brian, Joseph V. Gray, Qiming J. Wang, et al.. (1995). Carboxyfluorescein and biotin neuromedin C analogues: Synthesis and applications. Peptides. 16(2). 255–261. 3 indexed citations
17.
Chook, Yuh Min, Joseph V. Gray, Hengming Ke, & William N. Lipscomb. (1994). The Monofunctional Chorismate Mutase from Bacillus subtilis. Journal of Molecular Biology. 240(5). 476–500. 158 indexed citations
18.
Gray, Joseph V. & Jeremy R. Knowles. (1994). Monofunctional Chorismate Mutase from Bacillus subtilis: FTIR Studies and the Mechanism of Action of the Enzyme. Biochemistry. 33(33). 9953–9959. 26 indexed citations
19.
Gray, Joseph V., Béatrice Golinelli‐Pimpaneau, & Jeremy R. Knowles. (1990). Monofunctional chorismate mutase from Bacillus subtilis: purification of the protein, molecular cloning of the gene, and overexpression of the gene product in Escherichia coli. Biochemistry. 29(2). 376–383. 35 indexed citations
20.

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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