Mary F. Malley
About
Mary F. Malley is a scholar working on Organic Chemistry, Molecular Biology and Oncology.
According to data from OpenAlex, Mary F. Malley has authored 64 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Organic Chemistry, 25 papers in Molecular Biology and 10 papers in Oncology. Recurrent topics in Mary F. Malley's work include Radiopharmaceutical Chemistry and Applications (6 papers), Synthesis and Biological Evaluation (6 papers) and Synthesis of heterocyclic compounds (6 papers). Mary F. Malley is often cited by papers focused on Radiopharmaceutical Chemistry and Applications (6 papers), Synthesis and Biological Evaluation (6 papers) and Synthesis of heterocyclic compounds (6 papers). Mary F. Malley collaborates with scholars based in United States, Malaysia and Sweden. Mary F. Malley's co-authors include Jack Z. Gougoutas, George C. Rovnyak, Karnail S. Atwal, S. David Kimball, Anders Hedberg, Suzanne Moreland, Joseph E. Schwartz, Michael F. Tweedle, Krishan Kumar and Lynn C. Francesconi and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Molecular Biology and Analytical Chemistry.
In The Last Decade
Mary F. Malley
63 papers receiving 3.3k citations
Hit Papers
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late) cites · hero ref
| Name | h | Career | Trend | Papers | Cites | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| Mary F. Malley United States | 29 | 2.1k | 740 | 657 | 432 | 417 | 64 | 3.6k | ||
| Jack Z. Gougoutas United States | 30 | 2.7k 1.2× | 876 1.2× | 707 1.1× | 376 0.9× | 524 1.3× | 109 | 4.3k | ||
| L. Todaro United States | 29 | 1.2k 0.6× | 788 1.1× | 512 0.8× | 180 0.4× | 422 1.0× | 74 | 2.2k | ||
| R. Curtis Haltiwanger United States | 33 | 2.7k 1.3× | 824 1.1× | 520 0.8× | 132 0.3× | 1.3k 3.0× | 177 | 4.4k | ||
| Giuseppe Ermondi Italy | 30 | 703 0.3× | 1.3k 1.8× | 777 1.2× | 327 0.8× | 239 0.6× | 114 | 3.0k | ||
| Jean Bernadou France | 30 | 1.1k 0.5× | 1.5k 2.0× | 1.0k 1.6× | 104 0.2× | 821 2.0× | 105 | 3.2k | ||
| Grety Rihs Switzerland | 32 | 2.2k 1.0× | 873 1.2× | 502 0.8× | 50 0.1× | 689 1.7× | 148 | 3.5k | ||
| J. V. Silverton United States | 27 | 1.2k 0.5× | 1.1k 1.4× | 629 1.0× | 77 0.2× | 541 1.3× | 123 | 2.8k | ||
| Alessandro Dondoni Italy | 37 | 5.3k 2.5× | 2.6k 3.5× | 468 0.7× | 351 0.8× | 521 1.2× | 113 | 6.1k | ||
| John T. Welch United States | 33 | 3.8k 1.8× | 1.6k 2.2× | 306 0.5× | 52 0.1× | 755 1.8× | 149 | 5.7k | ||
| Frank M. Boeckler Germany | 30 | 1.2k 0.6× | 1.8k 2.5× | 530 0.8× | 94 0.2× | 395 0.9× | 75 | 3.6k |
Countries citing papers authored by Mary F. Malley
Since
Specialization
Citations
This map shows the geographic impact of Mary F. Malley'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 Mary F. Malley with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mary F. Malley more than expected).
Fields of papers citing papers by Mary F. Malley
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Mary F. Malley. 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 Mary F. Malley. The network helps show where Mary F. Malley may publish in the future.
Co-authorship network of co-authors of Mary F. Malley
This figure shows the co-authorship network connecting the top 25 collaborators of Mary F. Malley. A scholar is included among the top collaborators of Mary F. Malley 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 Mary F. Malley. Mary F. Malley is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Sheppeck, James E., John L. Gilmore, Hai-yun Xiao, et al.. (2013). Discovery of potent and selective nonsteroidal indazolyl amide glucocorticoid receptor agonists. Bioorganic & Medicinal Chemistry Letters. 23(19). 5442–5447.
2.
Liu, Chunjian, James C. Lin, Christoph Gesenberg, et al.. (2013). Synthesis and evaluation of carbamoylmethylene linked prodrugs of BMS-582949, a clinical p38α inhibitor. Bioorganic & Medicinal Chemistry Letters. 23(10). 3028–3033.
3.
Sitkoff, Doree, Ning Lee, Bruce A. Ellsworth, et al.. (2010). Cannabinoid CB1 receptor ligand binding and function examined through mutagenesis studies of F200 and S383. European Journal of Pharmacology. 651(1-3). 9–17.
4.
Das, Jagabandhu, S. David Kimball, Steven E. Hall, et al.. (2002). Molecular design and structure–Activity relationships leading to the potent, selective, and orally active thrombin active site inhibitor BMS-189664. Bioorganic & Medicinal Chemistry Letters. 12(1). 45–49.
5.
Macor, John E., et al.. (2000). Studies towards understanding the mechanism of the unusual rearrangement of certain 5-propargyloxyindoles. Tetrahedron Letters. 41(19). 3541–3545.
6.
Malley, Mary F., et al.. (1996). Crystallographic determination of the structures of human α‐thrombin complexed with BMS‐186282 and BMS‐189090. Protein Science. 5(2). 221–228.
7.
Kimball, S. David, John T. Hunt, Joel C. Barrish, et al.. (1993). 1-benzazepin-2-one calcium channel blockers—VI. Receptor-binding model and possible relationship to desmethoxyverapamil.. Bioorganic & Medicinal Chemistry. 1(4). 285–307.
8.
Barrish, Joel C., Steven H. Spergel, Suzanne Moreland, et al.. (1993). Conformationally constrained calcium channel blockers: Novel mimics of 1-benzazepin-2-ones. Bioorganic & Medicinal Chemistry. 1(4). 309–325.
9.
Meanwell, Nicholas A., J. Romine, Michael Rosenfeld, et al.. (1993). Nonprostanoid prostacyclin mimetics. 5. Structure-activity relationships associated with [3-[4-(4,5-diphenyl-2-oxazolyl)-5-oxazolyl]phenoxy]acetic acid. Journal of Medicinal Chemistry. 36(24). 3884–3903.
10.
Rovnyak, George C., Karnail S. Atwal, Anders Hedberg, et al.. (1992). Dihydropyrimidine calcium channel blockers. 4. Basic 3-substituted-4-aryl-1,4-dihydropyrimidine-5-carboxylic acid esters. Potent antihypertensive agents. Journal of Medicinal Chemistry. 35(17). 3254–3263.
11.
Rovnyak, George C., S. David Kimball, David Floyd, et al.. (1991). ChemInform Abstract: Dihydropyrimidine Calcium Channel Blockers. Part 2. 3‐Substituted 4‐ Aryl‐1,4‐dihydro‐6‐methyl‐5‐pyrimidinecarboxylic Acid Esters as Potent Mimics of Dihydropyridines.. ChemInform. 22(8).
12.
Jurisson, Silvia S., Lynn C. Francesconi, Karen E. Linder, et al.. (1991). Syntheses, characterization, and reactivity of manganese and rhenium dioxime complexes. X-ray crystal structure of MnII(CDO)(CDOH)2(BPh(OCH3))2, an unusual pseudoclathrochelate complex, and ReIIICl(CDO)(CDOH)2BPh. Inorganic Chemistry. 30(8). 1820–1827.
13.
Rovnyak, George C., Niels H. Andersen, Jack Z. Gougoutas, et al.. (1991). Active conformation of 1,4-dihydropyridine calcium entry blockers. Effect of size of 2-aryl substituent on rotameric equilibria and receptor binding. Journal of Medicinal Chemistry. 34(8). 2521–2524.
14.
Bisacchi, Gregory S., Christopher Cianci, Junius M. Clark, et al.. (1991). Synthesis and antiviral activity of enantiomeric forms of cyclobutyl nucleoside analogs. Journal of Medicinal Chemistry. 34(4). 1415–1421.
15.
Atwal, Karnail S., George C. Rovnyak, Joseph E. Schwartz, et al.. (1990). Dihydropyrimidine calcium channel blockers: 2-heterosubstituted 4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines. Journal of Medicinal Chemistry. 33(5). 1510–1515.
16.
Atwal, Karnail S., George C. Rovnyak, S. David Kimball, et al.. (1990). Dihydropyrimidine calcium channel blockers. II. 3-Substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines. Journal of Medicinal Chemistry. 33(9). 2629–2635.
17.
Linder, Karen E., et al.. (1989). A re‐assessment of the oxidation state of Tc(DMG)3(μ‐OH)SnCl3: Evidence for Tc(III). Journal of Labelled Compounds and Radiopharmaceuticals. 26(1-12). 266–268.
18.
Rovnyak, George C., Niels H. Andersen, Jack Z. Gougoutas, et al.. (1988). Studies directed toward ascertaining the active conformation of 1,4-dihydropyridine calcium entry blockers. Journal of Medicinal Chemistry. 31(5). 936–944.
19.
Thottathil, John K., et al.. (1986). A meso specific reaction. Tetrahedron Letters. 27(14). 1533–1536.
20.
Tymiak, Adrienne A., Catherine A. Culver, Mary F. Malley, & Jack Z. Gougoutas. (1986). ChemInform Abstract: Structure of Obafluorin (I): An Antibacterial β‐Lactone from Pseudomonas fluorescens.. Chemischer Informationsdienst. 17(25).
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.
Explore authors with similar magnitude of impact
Breakdown of academic impact, for papers by Jack Z. Gougoutas Breakdown of academic impact, for papers by L. Todaro Breakdown of academic impact, for papers by R. Curtis Haltiwanger Breakdown of academic impact, for papers by Giuseppe Ermondi Breakdown of academic impact, for papers by Jean Bernadou Breakdown of academic impact, for papers by Grety Rihs Breakdown of academic impact, for papers by J. V. Silverton Breakdown of academic impact, for papers by Alessandro Dondoni Breakdown of academic impact, for papers by John T. Welch Breakdown of academic impact, for papers by Frank M. Boeckler