Gerald Gish

9.8k total citations · 2 hit papers
77 papers, 7.8k citations indexed

About

Gerald Gish is a scholar working on Molecular Biology, Oncology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Gerald Gish has authored 77 papers receiving a total of 7.8k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Molecular Biology, 18 papers in Oncology and 13 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Gerald Gish's work include Protein Kinase Regulation and GTPase Signaling (19 papers), Monoclonal and Polyclonal Antibodies Research (13 papers) and Ubiquitin and proteasome pathways (10 papers). Gerald Gish is often cited by papers focused on Protein Kinase Regulation and GTPase Signaling (19 papers), Monoclonal and Polyclonal Antibodies Research (13 papers) and Ubiquitin and proteasome pathways (10 papers). Gerald Gish collaborates with scholars based in Canada, United States and Sweden. Gerald Gish's co-authors include Tony Pawson, Frauke Alves, Wolfgang F. Vogel, Fritz Eckstein, Robert J. Ingham, Zhou Songyang, Piers Nash, Peter van der Geer, Sandra E. Wiley and Mark Henkemeyer and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Gerald Gish

77 papers receiving 7.7k citations

Hit Papers

SH2 and SH3 domains: From structure to function 1992 2026 2003 2014 1992 1997 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
Gerald Gish Canada 42 5.4k 1.5k 1.4k 1.2k 928 77 7.8k
Peter van der Geer United States 38 5.5k 1.0× 1.9k 1.2× 1.5k 1.1× 1.3k 1.1× 1.7k 1.8× 62 8.3k
Michael F. Moran Canada 44 5.5k 1.0× 1.2k 0.8× 1.5k 1.1× 816 0.7× 521 0.6× 120 7.3k
Victor A. Fried United States 33 6.3k 1.2× 2.2k 1.4× 1.4k 1.0× 956 0.8× 498 0.5× 53 8.3k
Anthony I. Magee United Kingdom 52 7.4k 1.4× 2.7k 1.8× 1.2k 0.9× 1.4k 1.2× 432 0.5× 144 10.3k
László Buday Hungary 36 4.3k 0.8× 1.1k 0.7× 1.4k 1.0× 936 0.8× 519 0.6× 93 6.0k
Xosé R. Bustelo Spain 57 7.0k 1.3× 1.9k 1.3× 2.0k 1.5× 2.8k 2.4× 1.2k 1.3× 172 11.1k
Ivan Gout United Kingdom 52 9.7k 1.8× 2.8k 1.8× 1.7k 1.2× 2.3k 2.0× 660 0.7× 157 12.8k
Michael Fry United Kingdom 46 8.7k 1.6× 2.2k 1.5× 1.3k 0.9× 1.0k 0.9× 400 0.4× 99 10.8k
Nicholas F. Totty United Kingdom 43 7.9k 1.5× 2.6k 1.7× 1.9k 1.4× 1.8k 1.5× 474 0.5× 66 11.3k
Michel Streuli United States 45 5.5k 1.0× 1.3k 0.8× 1.2k 0.9× 3.2k 2.7× 549 0.6× 60 8.1k

Countries citing papers authored by Gerald Gish

Since Specialization
Citations

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

Fields of papers citing papers by Gerald Gish

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gerald Gish

This figure shows the co-authorship network connecting the top 25 collaborators of Gerald Gish. A scholar is included among the top collaborators of Gerald Gish 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 Gerald Gish. Gerald Gish 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.
Malik, Ahmad, Dzana Dervovic, Ricky Tsai, et al.. (2023). The NOTCH-RIPK4-IRF6-ELOVL4 Axis Suppresses Squamous Cell Carcinoma. Cancers. 15(3). 737–737. 14 indexed citations
2.
Orlicky, Stephen, Jonah Beenstock, Derek F. Ceccarelli, et al.. (2021). Bipartite binding of the N terminus of Skp2 to cyclin A. Structure. 29(9). 975–988.e5. 7 indexed citations
3.
Dubé, Alexandre K., David Bradley, François Chartier, et al.. (2021). Protein context shapes the specificity of SH3 domain-mediated interactions in vivo. Nature Communications. 12(1). 1597–1597. 39 indexed citations
4.
Daou, Salima, Manisha Talukdar, Jinle Tang, et al.. (2020). A phenolic small molecule inhibitor of RNase L prevents cell death from ADAR1 deficiency. Proceedings of the National Academy of Sciences. 117(40). 24802–24812. 21 indexed citations
5.
Zhao, Dorothy Yanling, Gerald Gish, Ulrich Braunschweig, et al.. (2015). SMN and symmetric arginine dimethylation of RNA polymerase II C-terminal domain control termination. Nature. 529(7584). 48–53. 183 indexed citations
6.
Matskova, Liudmila, Gerald Gish, Maria Fernanda de Paula Werner, et al.. (2014). SYK interaction with ITGβ4 suppressed by Epstein-Barr virus LMP2A modulates migration and invasion of nasopharyngeal carcinoma cells. Oncogene. 34(34). 4491–4499. 20 indexed citations
7.
Guettler, Sebastian, José LaRose, Evangelia Petsalaki, et al.. (2012). Structural Basis and Sequence Rules for Substrate Recognition by Tankyrase Explain the Basis for Cherubism Disease. Cell. 148(1-2). 376–376. 4 indexed citations
8.
Filippakopoulos, P., Michael Kofler, Oliver Hantschel, et al.. (2008). Structural Coupling of SH2-Kinase Domains Links Fes and Abl Substrate Recognition and Kinase Activation. Cell. 134(5). 793–803. 156 indexed citations
9.
Bakal, Chris, Dina Finan, José LaRose, et al.. (2005). The Rho GTP exchange factor Lfc promotes spindle assembly in early mitosis. Proceedings of the National Academy of Sciences. 102(27). 9529–9534. 50 indexed citations
10.
Kitching, A. Richard, Michael Wong, Angelika M. Burger, et al.. (2003). The RING-H2 protein RNF11 is differentially expressed in breast tumours and interacts with HECT-type E3 ligases. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1639(2). 104–112. 44 indexed citations
11.
Kunath, Tilo, Gerald Gish, Heiko Lickert, et al.. (2003). Transgenic RNA interference in ES cell–derived embryos recapitulates a genetic null phenotype. Nature Biotechnology. 21(5). 559–561. 211 indexed citations
12.
Gruenheid, Samantha, Rebekah DeVinney, Friedhelm Bladt, et al.. (2001). Enteropathogenic E. coli Tir binds Nck to initiate actin pedestal formation in host cells. Nature Cell Biology. 3(9). 856–859. 295 indexed citations
13.
Lorenzo, M. J. Varas, Gerald Gish, Carol Houghton, et al.. (1997). RET alternate splicing influences the interaction of activated RET with the SH2 and PTB domains of Shc, and the SH2 domain of Grb2. Oncogene. 14(7). 763–771. 107 indexed citations
14.
Geer, Peter van der, Sandra E. Wiley, Gerald Gish, & Tony Pawson. (1996). The Shc adaptor protein is highly phosphorylated at conserved, twin tyrosine residues (Y239/240) that mediate protein–protein interactions. Current Biology. 6(11). 1435–1444. 202 indexed citations
15.
Li, Shuncheng, Ka‐Man Venus Lai, Gerald Gish, et al.. (1996). Characterization of the Phosphotyrosine-binding Domain of the Drosophila Shc Protein. Journal of Biological Chemistry. 271(50). 31855–31862. 14 indexed citations
16.
Lai, Ka‐Man Venus, Jean Paul Olivier, Gerald Gish, et al.. (1995). A Drosophila shc Gene Product Is Implicated in Signaling by the DER Receptor Tyrosine Kinase. Molecular and Cellular Biology. 15(9). 4810–4818. 51 indexed citations
17.
Raabe, Thomas, Jean Paul Olivier, Barry J. Dickson, et al.. (1995). Biochemical and genetic analysis of the Drk SH2/SH3 adaptor protein of Drosophila.. The EMBO Journal. 14(11). 2509–2518. 61 indexed citations
18.
Geer, Peter van der, Sandra E. Wiley, Jean Paul Olivier, et al.. (1995). A conserved amino-terminal Shc domain binds to phosphotyrosine motifs in activated receptors and phosphopeptides. Current Biology. 5(4). 404–412. 161 indexed citations
19.
Marengère, Luc E. M., Zhou Songyang, Gerald Gish, et al.. (1994). SH2 domain specificity and activity modified by a single residue. Nature. 369(6480). 502–505. 152 indexed citations
20.
Pawson, Tony & Gerald Gish. (1992). SH2 and SH3 domains: From structure to function. Cell. 71(3). 359–362. 873 indexed citations breakdown →

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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