Mathias P. Mertes

2.3k total citations
110 papers, 1.8k citations indexed

About

Mathias P. Mertes is a scholar working on Organic Chemistry, Molecular Biology and Oncology. According to data from OpenAlex, Mathias P. Mertes has authored 110 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Organic Chemistry, 55 papers in Molecular Biology and 15 papers in Oncology. Recurrent topics in Mathias P. Mertes's work include Biochemical and Molecular Research (26 papers), Synthesis and Characterization of Heterocyclic Compounds (18 papers) and DNA and Nucleic Acid Chemistry (14 papers). Mathias P. Mertes is often cited by papers focused on Biochemical and Molecular Research (26 papers), Synthesis and Characterization of Heterocyclic Compounds (18 papers) and DNA and Nucleic Acid Chemistry (14 papers). Mathias P. Mertes collaborates with scholars based in United States, Belgium and Poland. Mathias P. Mertes's co-authors include Kristin Bowman Mertes, Mir Wais Hosseini, Erik De Clercq, J.‐M. Lehn, Jean‐Marie Lehn, Linda Maggiora, Paul F. Torrence, David Shugar, Christopher F. Bigge and Paulos Yohannes and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and Accounts of Chemical Research.

In The Last Decade

Mathias P. Mertes

99 papers receiving 1.6k citations

Peers

Mathias P. Mertes
Arthur D. Broom United States
Haoyun An United States
L. Todaro United States
Larry W. McLaughlin United States
Mark L. McLaughlin United States
Kevin Parris United States
Arthur D. Broom United States
Mathias P. Mertes
Citations per year, relative to Mathias P. Mertes Mathias P. Mertes (= 1×) peers Arthur D. Broom

Countries citing papers authored by Mathias P. Mertes

Since Specialization
Citations

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

Fields of papers citing papers by Mathias P. Mertes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mathias P. Mertes. 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 Mathias P. Mertes. The network helps show where Mathias P. Mertes may publish in the future.

Co-authorship network of co-authors of Mathias P. Mertes

This figure shows the co-authorship network connecting the top 25 collaborators of Mathias P. Mertes. A scholar is included among the top collaborators of Mathias P. Mertes 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 Mathias P. Mertes. Mathias P. Mertes 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.
Wang, Binghe, Fusao Takusagawa, Mathias P. Mertes, & Kristin Bowman‐James. (1993). Structure of the product from a novel cyclization reaction involving a C(6)-substituted uridine analog. Acta Crystallographica Section C Crystal Structure Communications. 49(9). 1568–1571. 2 indexed citations
2.
Chang, George, et al.. (1988). Linear free energy relationship studies of enzyme active site binding: thymidylate synthase. Journal of Medicinal Chemistry. 31(6). 1141–1147. 4 indexed citations
3.
Decedue, Charles J., et al.. (1987). Inactivation of thymidylate synthase at an alternate high-affinity binding site. Journal of Medicinal Chemistry. 30(10). 1705–1706.
4.
Mertes, Mathias P., et al.. (1987). Selective addition of methanol to 1,2-epoxy-1-vinylcyclopentane. The Journal of Organic Chemistry. 52(13). 2950–2953. 5 indexed citations
5.
Yohannes, Paulos, et al.. (1987). Specificity, catalysis, and regulation: effects of metal ions on polyammonium macrocycle catalyzed dephosphorylation of ATP. Inorganic Chemistry. 26(11). 1751–1755. 34 indexed citations
6.
Maggiora, Linda, et al.. (1984). Palladium(II)-catalyzed olefin-coupling reactions of kainic acid: effects of substitution on the isopropenyl group on receptor binding. Journal of Medicinal Chemistry. 27(1). 52–56. 17 indexed citations
7.
Mertes, Mathias P., et al.. (1983). Synthesis and conformational aspects of cis- and trans-3-carbomethoxy-6-oxabicyclo[3.1.0]hexane. The Journal of Organic Chemistry. 48(20). 3594–3597. 6 indexed citations
8.
Clercq, Erik De, Jan Balzarini, Paul F. Torrence, et al.. (1981). Thymidylate Synthetase as Target Enzyme for the Inhibitory Activity of 5-Substituted 2'-Deoxyuridines on Mouse Leukemia L1210 Cell Growth. Molecular Pharmacology. 19(2). 321–330. 124 indexed citations
9.
Bigge, Christopher F., et al.. (1980). Palladium-catalyzed coupling reactions of uracil nucleosides and nucleotides. Journal of the American Chemical Society. 102(6). 2033–2038. 48 indexed citations
10.
Clercq, Erik De, J Descamps, Charles L. Schmidt, & Mathias P. Mertes. (1979). Antiviral activity of 5-methylthiomethyl-2′deoxyuridine and other 5-substituted 2′-deoxyuridines. Biochemical Pharmacology. 28(22). 3249–3254. 20 indexed citations
11.
Bigge, Christopher F., et al.. (1979). Synthesis of 5-styryl derivatives of uracil nucleosides and nucleotides.. Tetrahedron Letters. 20(19). 1653–1656. 7 indexed citations
12.
Henderson, James D., Curtis R. Partington, & Mathias P. Mertes. (1979). Synthesis and pH effects on the hydrolysis of 5'-adenosyl phenylalaninate. The Journal of Organic Chemistry. 44(6). 1003–1006. 3 indexed citations
13.
Mertes, Mathias P., et al.. (1978). 5-Nitro-2′-deoxyuridine 5′-monophosphate is a potent irreversible inhibitor of Lactobacillus caesi thymidylate synthetase. Biochemical and Biophysical Research Communications. 84(4). 1054–1059. 9 indexed citations
14.
Mertes, Mathias P., et al.. (1976). ChemInform Abstract: 5‐IODOACETAMIDOMETHYL‐2′‐DEOXYURIDINE 5′‐PHOSPHATE. A SELECTIVE INHIBITOR OF MAMMALIAN THYMIDYLATE SYNTHETASES. Chemischer Informationsdienst. 7(44). 2 indexed citations
15.
Mertes, Mathias P. & M. T. SHIPCHANDLER. (1971). Charge-spatial models. 2. Cis and trans-3- and -4-carboxycyclohexyl phosphates and the carboxylate esters as analogs of 2'-deoxyuridine 5'-phosphate. Journal of Medicinal Chemistry. 14(3). 257–258.
16.
Mertes, Mathias P. & Lin Ai. (1970). Cofactor inhibition of thymidylate synthetase. Tetrahydrofolic acid analogs. Journal of Medicinal Chemistry. 13(1). 77–82. 12 indexed citations
17.
Mertes, Mathias P., et al.. (1969). .omega.-Dithiolanyl amino acids. Journal of Medicinal Chemistry. 12(2). 342–343.
18.
Mertes, Mathias P., et al.. (1968). Bisquaternary ammonium indolines and perhydroindoles in ganglionic blockade. Journal of Medicinal Chemistry. 11(1). 106–111. 8 indexed citations
19.
Mertes, Mathias P. & J. Smrt. (1968). Nucleic acid components and their analogues. CXV. Synthesis of N4-hydroxy-6-azacytidine 5'-phosphate and 5'-diphosphate. Collection of Czechoslovak Chemical Communications. 33(10). 3304–3312. 1 indexed citations
20.
Mertes, Mathias P.. (1966). Experimentation in Instruction: Pharmaceutical Analysis. American Journal of Pharmaceutical Education. 30(5). 746–749.

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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