M. Catherine Johnson

855 total citations
20 papers, 617 citations indexed

About

M. Catherine Johnson is a scholar working on Molecular Biology, Organic Chemistry and Oncology. According to data from OpenAlex, M. Catherine Johnson has authored 20 papers receiving a total of 617 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Organic Chemistry and 4 papers in Oncology. Recurrent topics in M. Catherine Johnson's work include Peptidase Inhibition and Analysis (4 papers), Synthesis and Reactions of Organic Compounds (3 papers) and Phenothiazines and Benzothiazines Synthesis and Activities (3 papers). M. Catherine Johnson is often cited by papers focused on Peptidase Inhibition and Analysis (4 papers), Synthesis and Reactions of Organic Compounds (3 papers) and Phenothiazines and Benzothiazines Synthesis and Activities (3 papers). M. Catherine Johnson collaborates with scholars based in United States and United Kingdom. M. Catherine Johnson's co-authors include Robert V. Hoffman, S.E. Greasley, Rose Ann Ferre, Liming Dong, Chuangxing Guo, Joseph Marakovits, Xinjun Hou, Brion W. Murray, Eleanor Dagostino and James Thomson and has published in prestigious journals such as Journal of Medicinal Chemistry, The Journal of Organic Chemistry and Tetrahedron Letters.

In The Last Decade

M. Catherine Johnson

19 papers receiving 595 citations

Peers

M. Catherine Johnson
Thomas E. Barta United States
Gunnar J. Hanson United States
Helen Browne United Kingdom
Jonathan L. Doty United States
E. Thoreau France
Gary D. Probst United States
John W. Rice United States
Amy F. Barabasz United States
Hachemi Kadri United Kingdom
Masaichi Warizaya Japan
Thomas E. Barta United States
M. Catherine Johnson
Citations per year, relative to M. Catherine Johnson M. Catherine Johnson (= 1×) peers Thomas E. Barta

Countries citing papers authored by M. Catherine Johnson

Since Specialization
Citations

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

Fields of papers citing papers by M. Catherine Johnson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Catherine Johnson. 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 M. Catherine Johnson. The network helps show where M. Catherine Johnson may publish in the future.

Co-authorship network of co-authors of M. Catherine Johnson

This figure shows the co-authorship network connecting the top 25 collaborators of M. Catherine Johnson. A scholar is included among the top collaborators of M. Catherine Johnson 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 M. Catherine Johnson. M. Catherine Johnson 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.
2.
Guo, Chuangxing, Xinjun Hou, Liming Dong, et al.. (2014). Structure-based design of novel human Pin1 inhibitors (III): Optimizing affinity beyond the phosphate recognition pocket. Bioorganic & Medicinal Chemistry Letters. 24(17). 4187–4191. 38 indexed citations
3.
Chekler, Eugene L. Piatnitski, M. Catherine Johnson, James T. Anderson, et al.. (2014). 1-(2-Hydroxy-2-methyl-3-phenoxypropanoyl)indoline-4-carbonitrile Derivatives as Potent and Tissue Selective Androgen Receptor Modulators. Journal of Medicinal Chemistry. 57(6). 2462–2471. 13 indexed citations
4.
Johnson, M. Catherine, Qiyue Hu, Laura Lingardo, et al.. (2011). Novel isoquinolone PDK1 inhibitors discovered through fragment-based lead discovery. Journal of Computer-Aided Molecular Design. 25(7). 689–698. 15 indexed citations
5.
Zapf, Christoph W., Jonathan D. Bloom, Zhong Li, et al.. (2011). Discovery of a stable macrocyclic o-aminobenzamide Hsp90 inhibitor which significantly decreases tumor volume in a mouse xenograft model. Bioorganic & Medicinal Chemistry Letters. 21(15). 4602–4607. 24 indexed citations
6.
Cole, Derek C., Andrea Olland, Jaison Jacob, et al.. (2010). Identification and Characterization of Acidic Mammalian Chitinase Inhibitors. Journal of Medicinal Chemistry. 53(16). 6122–6128. 30 indexed citations
7.
Dong, Liming, Joseph Marakovits, Xinjun Hou, et al.. (2010). Structure-based design of novel human Pin1 inhibitors (II). Bioorganic & Medicinal Chemistry Letters. 20(7). 2210–2214. 70 indexed citations
8.
Guo, Chuangxing, Xinjun Hou, Liming Dong, et al.. (2009). Structure-based design of novel human Pin1 inhibitors (I). Bioorganic & Medicinal Chemistry Letters. 19(19). 5613–5616. 91 indexed citations
9.
Kung, Pei‐Pei, Lee Funk, Jerry Meng, et al.. (2008). Dihydroxylphenyl amides as inhibitors of the Hsp90 molecular chaperone. Bioorganic & Medicinal Chemistry Letters. 18(23). 6273–6278. 38 indexed citations
10.
Gopalsamy, Ariamala, Mengxiao Shi, Jennifer M. Golas, et al.. (2008). Discovery of Benzisoxazoles as Potent Inhibitors of Chaperone Heat Shock Protein 90. Journal of Medicinal Chemistry. 51(3). 373–375. 75 indexed citations
11.
Zehnder, Luke R., Jerry Meng, Donald J. Skalitzky, et al.. (2005). Design, synthesis, and biological evaluation of novel human 5′-deoxy-5′-methylthioadenosine phosphorylase (MTAP) substrates. Bioorganic & Medicinal Chemistry Letters. 15(11). 2829–2833. 14 indexed citations
12.
Hoffman, Robert V., et al.. (2002). Synthesis of 2-Oxazolone-4-carboxylates from 3-Nosyloxy- and 3-Bromo-2-ketoesters. The Journal of Organic Chemistry. 67(4). 1102–1108. 25 indexed citations
13.
Johnson, M. Catherine, et al.. (1999). Preparation of 1-substituted-3,3-dinitroazetidines. Journal of Energetic Materials. 17(2-3). 233–252. 30 indexed citations
14.
Johnson, M. Catherine, et al.. (1998). Preparation of β-Fluoro-α-ketoesters from α-Ketoesters and Their Conversion to (Z)-β-Fluoro-α-aminoacrylate Derivatives. The Journal of Organic Chemistry. 63(18). 6409–6413. 10 indexed citations
15.
Hoffman, Robert V., et al.. (1998). Synthesis of 4-carboethoxy-4-oxazolin-2-ones from 3-nosyloxy-2-ketoesters. Tetrahedron Letters. 39(11). 1283–1286. 6 indexed citations
16.
Hoffman, Robert V., et al.. (1997). Synthesis and Reactions of 3-(Nosyloxy)-2-keto Esters. The Journal of Organic Chemistry. 62(8). 2458–2465. 13 indexed citations
17.
18.
Johnson, M. Catherine, et al.. (1977). The Smiles Rearrangement of 2-Aryloxy-2-methylpropanamides. Synthesis ofN-Aryl-2-hydroxy-2-methylpropanamides. Synthesis. 1977(1). 31–33. 14 indexed citations
19.
Johnson, M. Catherine, et al.. (1977). A Smiles Rearrangement Involving Non-Activated Aromatic Systems; the Facile Conversion of Phenols to Anilines. Synthesis. 1977(1). 33–34. 30 indexed citations
20.
Atkinson, John D. & M. Catherine Johnson. (1968). Syntheses of some highly substituted pyridines, 2,7-naphthyridines and 1H-pyrimido[4,5,6-i,j][2,7]naphthyridines. Journal of the Chemical Society C Organic. 1252–1252. 3 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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