Gene Merutka

2.7k total citations
22 papers, 2.4k citations indexed

About

Gene Merutka is a scholar working on Molecular Biology, Oncology and Spectroscopy. According to data from OpenAlex, Gene Merutka has authored 22 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 7 papers in Oncology and 6 papers in Spectroscopy. Recurrent topics in Gene Merutka's work include Protein Structure and Dynamics (11 papers), Enzyme Structure and Function (6 papers) and Hemoglobin structure and function (4 papers). Gene Merutka is often cited by papers focused on Protein Structure and Dynamics (11 papers), Enzyme Structure and Function (6 papers) and Hemoglobin structure and function (4 papers). Gene Merutka collaborates with scholars based in United States. Gene Merutka's co-authors include Peter E. Wright, H. Jane Dyson, Earle Stellwagen, Jonathan P. Waltho, Richard A. Lerner, Shawn Barney, Stephen R. Petteway, Kelly Guthrie, William Shalongo and John M. Maraganore and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Molecular Biology.

In The Last Decade

Gene Merutka

21 papers receiving 2.4k citations

Peers

Gene Merutka

SPECT

EPIDE

GENET

Mengli Cai United States

Richard Blevins United States

In‐Ja L. Byeon United States

Claudio Vita France

Rasmus H. Fogh United Kingdom

John Ionides United Kingdom

Anne Pajon United Kingdom

David E. Anderson United States

Daniel S. Terry United States

John D. Gross United States

Mengli Cai United States

Gene Merutka

2.0k ×1.0

335 ×0.6

245 ×0.8

SPECT

164 ×0.6

EPIDE

265 ×1.0

GENET

Citations per year, relative to Gene Merutka Gene Merutka (= 1×) peers Mengli Cai

Countries citing papers authored by Gene Merutka

Since Specialization

Citations

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

Fields of papers citing papers by Gene Merutka

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gene Merutka

This figure shows the co-authorship network connecting the top 25 collaborators of Gene Merutka. A scholar is included among the top collaborators of Gene Merutka 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 Gene Merutka. Gene Merutka 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

Scuoppo, Claudio, Karen Mendelson, Lila Ghamsari, et al.. (2025). The C/EBPβ antagonist peptide lucicebtide (ST101) induces macrophage polarization toward a pro-inflammatory phenotype and enhances anti-tumor immune responses. Frontiers in Immunology. 16. 1522699–1522699. 1 indexed citations

Scuoppo, Claudio, Karen Mendelson, Lila Ghamsari, et al.. (2024). Abstract 5332: ST316, a clinical peptide antagonist of beta-catenin, induces anti-tumor immune responses by multiple mechanisms of action. Cancer Research. 84(6_Supplement). 5332–5332.

Scuoppo, Claudio, et al.. (2023). Abstract LB016: Immunotherapeutic potential of ST316, a peptide antagonist of β-catenin. Cancer Research. 83(8_Supplement). LB016–LB016. 2 indexed citations

Ghamsari, Lila, et al.. (2022). Abstract LB045: β-catenin antagonist peptide, ST316, attenuates Wnt-dependent oncogenic activity. Cancer Research. 82(12_Supplement). LB045–LB045. 1 indexed citations

Merutka, Gene, Brian M. Murphy, R. W. Payne, et al.. (2015). Stability of lyophilized teriparatide, PTH(1-34), after reconstitution. European Journal of Pharmaceutics and Biopharmaceutics. 99. 84–93. 11 indexed citations

Dyson, H. Jane, et al.. (1997). Folding propensities of peptide fragments of myoglobin. Protein Science. 6(3). 706–716. 75 indexed citations

Lambert, D.M., Shawn Barney, Anick Lambert, et al.. (1996). Peptides from conserved regions of paramyxovirus fusion (F) proteins are potent inhibitors of viral fusion.. Proceedings of the National Academy of Sciences. 93(5). 2186–2191. 288 indexed citations

Merutka, Gene, H. Jane Dyson, & Peter E. Wright. (1995). ‘Random coil’ 1H chemical shifts obtained as a function of temperature and trifluoroethanol concentration for the peptide series GGXGG. Journal of Biomolecular NMR. 5(1). 14–24. 442 indexed citations

Merutka, Gene, et al.. (1993). Peptide models of protein folding initiation sites. 3. The G-H helical hairpin of myoglobin. Biochemistry. 32(25). 6356–6364. 76 indexed citations

10.

Merutka, Gene, et al.. (1993). Peptide models of protein folding initiation sites. 2. The G-H turn region of myoglobin acts as a helix stop signal. Biochemistry. 32(25). 6348–6355. 63 indexed citations

11.

Merutka, Gene, Dimitrios Morikis, Rafael Brüschweiler, & Peter E. Wright. (1993). NMR evidence for multiple conformations in a highly helical model peptide. Biochemistry. 32(48). 13089–13097. 41 indexed citations

12.

Waltho, Jonathan P., Victoria A. Feher, Gene Merutka, H. Jane Dyson, & Peter E. Wright. (1993). Peptide models of protein folding initiation sites. 1. Secondary structure formation by peptides corresponding to the G- and H-helixes of myoglobin. Biochemistry. 32(25). 6337–6347. 160 indexed citations

13.

Dyson, H. Jane, et al.. (1992). Folding of peptide fragments comprising the complete sequence of proteins. Journal of Molecular Biology. 226(3). 819–835. 156 indexed citations

14.

Dyson, H. Jane, Gene Merutka, Jonathan P. Waltho, Richard A. Lerner, & Peter E. Wright. (1992). Folding of peptide fragments comprising the complete sequence of proteins. Journal of Molecular Biology. 226(3). 795–817. 369 indexed citations

15.

Merutka, Gene, William Shalongo, & Earle Stellwagen. (1991). A model peptide with enhanced helicity. Biochemistry. 30(17). 4245–4248. 81 indexed citations

16.

Merutka, Gene & Earle Stellwagen. (1991). Effect of amino acid ion pairs on peptide helicity. Biochemistry. 30(6). 1591–1594. 84 indexed citations

17.

Merutka, Gene, et al.. (1990). Effect of central-residue replacements on the helical stability of a monomeric peptide. Biochemistry. 29(32). 7511–7515. 108 indexed citations

18.

Merutka, Gene & Earle Stellwagen. (1990). Positional independence and additivity of amino acid replacements on helix stability in monomeric peptides. Biochemistry. 29(4). 894–898. 55 indexed citations

19.

Merutka, Gene & Earle Stellwagen. (1989). Analysis of peptides for helical prediction. Biochemistry. 28(1). 352–357. 33 indexed citations

20.

Maraganore, John M., et al.. (1984). A new class of phospholipases A2 with lysine in place of aspartate 49. Functional consequences for calcium and substrate binding.. Journal of Biological Chemistry. 259(22). 13839–13843. 232 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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