Eugene A. Mash

3.3k total citations
126 papers, 2.6k citations indexed

About

Eugene A. Mash is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Eugene A. Mash has authored 126 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Organic Chemistry, 52 papers in Molecular Biology and 19 papers in Spectroscopy. Recurrent topics in Eugene A. Mash's work include Chemical Synthesis and Analysis (26 papers), Asymmetric Synthesis and Catalysis (21 papers) and Synthetic Organic Chemistry Methods (13 papers). Eugene A. Mash is often cited by papers focused on Chemical Synthesis and Analysis (26 papers), Asymmetric Synthesis and Catalysis (21 papers) and Synthetic Organic Chemistry Methods (13 papers). Eugene A. Mash collaborates with scholars based in United States, United Kingdom and Japan. Eugene A. Mash's co-authors include Bhumasamudram Jagadish, Keith A. Nelson, H. Vasken Aposhian, Jay S. Petrick, Robert J. Gillies, Josef Vágner, Victor J. Hruby, Emmanuelle J. Meuillet, Heather L. Handl and Liping Xu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Advanced Materials.

In The Last Decade

Eugene A. Mash

123 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eugene A. Mash United States 30 1.0k 875 313 275 250 126 2.6k
Michael J. Gresser Canada 30 1.9k 1.9× 738 0.8× 242 0.8× 307 1.1× 49 0.2× 61 3.4k
Alain Croisy France 27 737 0.7× 692 0.8× 226 0.7× 330 1.2× 103 0.4× 96 2.4k
Carrie M. Wilmot United States 32 3.1k 3.0× 352 0.4× 240 0.8× 645 2.3× 99 0.4× 93 4.0k
Jeffrey A. Dodge United States 31 1.4k 1.4× 1.1k 1.3× 364 1.2× 116 0.4× 69 0.3× 68 3.4k
Fabrizio Briganti Italy 33 2.5k 2.5× 1.6k 1.8× 246 0.8× 291 1.1× 39 0.2× 113 3.9k
Robert J. Hondal United States 28 2.1k 2.1× 663 0.8× 239 0.8× 181 0.7× 69 0.3× 67 3.6k
Robert F. Anderson New Zealand 36 1.6k 1.6× 997 1.1× 439 1.4× 297 1.1× 104 0.4× 150 3.6k
James G. Muller United States 35 3.1k 3.0× 1.3k 1.5× 1.3k 4.1× 666 2.4× 81 0.3× 63 4.8k
R. Santus France 30 1.1k 1.1× 487 0.6× 86 0.3× 782 2.8× 107 0.4× 127 3.1k
Jóhannes Reynisson New Zealand 33 1.8k 1.8× 1.7k 1.9× 820 2.6× 286 1.0× 49 0.2× 154 3.7k

Countries citing papers authored by Eugene A. Mash

Since Specialization
Citations

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

Fields of papers citing papers by Eugene A. Mash

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eugene A. Mash. 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 Eugene A. Mash. The network helps show where Eugene A. Mash may publish in the future.

Co-authorship network of co-authors of Eugene A. Mash

This figure shows the co-authorship network connecting the top 25 collaborators of Eugene A. Mash. A scholar is included among the top collaborators of Eugene A. Mash 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 Eugene A. Mash. Eugene A. Mash 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.
Sierra‐Álvarez, Reyes, et al.. (2020). Covalent bonding of aromatic amine daughter products of 2,4-dinitroanisole (DNAN) with model quinone compounds representing humus via nucleophilic addition. Environmental Pollution. 268(Pt B). 115862–115862. 12 indexed citations
2.
Sierra‐Álvarez, Reyes, et al.. (2019). Coupling reactions between reduced intermediates of insensitive munitions compound analog 4-nitroanisole. Chemosphere. 222. 789–796. 7 indexed citations
3.
Sierra‐Álvarez, Reyes, et al.. (2017). Evidence of anaerobic coupling reactions between reduced intermediates of 4-nitroanisole. Chemosphere. 195. 372–380. 12 indexed citations
4.
Morales, Mark, et al.. (2013). Substrate-Dependent Ligand Inhibition of the Human Organic Cation Transporter OCT2. Journal of Pharmacology and Experimental Therapeutics. 346(2). 300–310. 84 indexed citations
5.
Martinez, Gary V., N. Suryakiran, Parastou Foroutan, et al.. (2013). Demonstration of a sucrose-derived contrast agent for magnetic resonance imaging of the GI tract. Bioorganic & Medicinal Chemistry Letters. 23(7). 2061–2064. 3 indexed citations
6.
Jagadish, Bhumasamudram, et al.. (2012). Tumor Xenograft Response to Redox-Active Therapies Assessed by Magnetic Resonance Imaging Using a Thiol-Bearing DOTA Complex of Gadolinium. Translational Oncology. 5(3). 190–199. 8 indexed citations
7.
Song, Zuohe, Lei Du‐Cuny, Li Zhou, et al.. (2011). Development of sulfonamide AKT PH domain inhibitors. Bioorganic & Medicinal Chemistry. 19(6). 2046–2054. 26 indexed citations
8.
Xu, Liping, et al.. (2011). A sucrose-derived scaffold for multimerization of bioactive peptides. Bioorganic & Medicinal Chemistry. 19(21). 6474–6482. 8 indexed citations
9.
Jagadish, Bhumasamudram, et al.. (2010). On the synthesis of 1,4,7-tris(tert-butoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane. Tetrahedron Letters. 52(17). 2058–2061. 33 indexed citations
10.
Xu, Liping, Josef Vágner, Bhumasamudram Jagadish, et al.. (2010). Synthesis and characterization of a Eu-DTPA-PEGO-MSH(4) derivative for evaluation of binding of multivalent molecules to melanocortin receptors. Bioorganic & Medicinal Chemistry Letters. 20(8). 2489–2492. 8 indexed citations
11.
Xu, Liping, Josef Vágner, J.S. Josan, et al.. (2009). Enhanced targeting with heterobivalent ligands. Molecular Cancer Therapeutics. 8(8). 2356–2365. 46 indexed citations
12.
Song, Zuohe, Lei Du‐Cuny, Li Zhou, et al.. (2009). In vitro and In vivo Activity of Novel Small-Molecule Inhibitors Targeting the Pleckstrin Homology Domain of Protein Kinase B/AKT. Cancer Research. 69(12). 5073–5081. 48 indexed citations
13.
Du‐Cuny, Lei, Zuohe Song, Garth Powis, et al.. (2009). Computational modeling of novel inhibitors targeting the Akt pleckstrin homology domain. Bioorganic & Medicinal Chemistry. 17(19). 6983–6992. 30 indexed citations
14.
Vágner, Josef, Liping Xu, Heather L. Handl, et al.. (2008). Heterobivalent Ligands Crosslink Multiple Cell‐Surface Receptors: The Human Melanocortin‐4 and δ‐Opioid Receptors. Angewandte Chemie International Edition. 47(9). 1685–1688. 62 indexed citations
15.
Jagadish, Bhumasamudram, M.D. Carducci, Alice Dawson, Gary S. Nichol, & Eugene A. Mash. (2008). (S,S)-4′′-Cyano-7,7′′-dimethoxy-3′,6′-dioxodispiro[indane-2,2′-piperazine-5′,2′′-indane]-4-carboxamide methanol solvate: interrupting the amide-to-amide hydrogen-bonded tape. Acta Crystallographica Section C Crystal Structure Communications. 64(8). o431–o433. 1 indexed citations
16.
Akare, Sandeep, et al.. (2006). Deoxycholic Acid Induces Intracellular Signaling through Membrane Perturbations. Journal of Biological Chemistry. 281(21). 14948–14960. 113 indexed citations
17.
Handl, Heather L., Josef Vágner, Haiyong Han, et al.. (2004). Hitting multiple targets with multimeric ligands. Expert Opinion on Therapeutic Targets. 8(6). 565–586. 93 indexed citations
18.
Bednarczyk, Dallas, et al.. (2000). NBD-TMA: a novel fluorescent substrate of the peritubular organic cation transporter of renal proximal tubules. Pflügers Archiv - European Journal of Physiology. 440(1). 184–192. 35 indexed citations
19.
Li, Yushun, Dean E. Carter, & Eugene A. Mash. (1998). Synthesis of The Mono-Cysteine Disulfide ofMeso-2,3-Dimercaptosuccinic Acid. Synthetic Communications. 28(11). 2057–2062. 1 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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