James F. Kerwin
About
James F. Kerwin is a scholar working on Organic Chemistry, Molecular Biology and Cellular and Molecular Neuroscience.
According to data from OpenAlex, James F. Kerwin has authored 77 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Organic Chemistry, 20 papers in Molecular Biology and 15 papers in Cellular and Molecular Neuroscience. Recurrent topics in James F. Kerwin's work include Nitric Oxide and Endothelin Effects (11 papers), Urinary Bladder and Prostate Research (11 papers) and Hormonal and reproductive studies (10 papers). James F. Kerwin is often cited by papers focused on Nitric Oxide and Endothelin Effects (11 papers), Urinary Bladder and Prostate Research (11 papers) and Hormonal and reproductive studies (10 papers). James F. Kerwin collaborates with scholars based in United States, United Kingdom and France. James F. Kerwin's co-authors include Samuel J. Danishefsky, Paul L. Feldman, Jack R. Lancaster, Michael J. Heller, Ferid Murad, Kunio Ishii, Susumu Kobayashi, Bing Chang, Eric M. Gordon and Marvin J. Miller and has published in prestigious journals such as Science, Journal of the American Chemical Society and Endocrinology.
In The Last Decade
James F. Kerwin
75 papers receiving 2.7k 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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| James F. Kerwin United States | 26 | 1.1k | 997 | 859 | 413 | 359 | 77 | 2.8k | ||
| Paul L. Feldman United States | 25 | 781 0.7× | 831 0.8× | 1.1k 1.2× | 187 0.5× | 452 1.3× | 65 | 3.2k | ||
| Donald J. Wolff United States | 30 | 259 0.2× | 1.7k 1.7× | 905 1.1× | 572 1.4× | 267 0.7× | 50 | 2.8k | ||
| Hidehiko Nakagawa Japan | 40 | 1.2k 1.1× | 2.4k 2.4× | 778 0.9× | 347 0.8× | 680 1.9× | 170 | 4.9k | ||
| Arnold Stern United States | 34 | 254 0.2× | 1.8k 1.8× | 807 0.9× | 246 0.6× | 377 1.1× | 115 | 3.8k | ||
| Thomas A. Dix United States | 30 | 554 0.5× | 1.6k 1.6× | 329 0.4× | 480 1.2× | 190 0.5× | 71 | 3.2k | ||
| Linda J. Roman United States | 36 | 656 0.6× | 1.6k 1.7× | 2.6k 3.0× | 276 0.7× | 664 1.8× | 108 | 4.5k | ||
| Vasanthy Narayanaswami United States | 33 | 290 0.3× | 1.8k 1.8× | 854 1.0× | 271 0.7× | 202 0.6× | 85 | 3.4k | ||
| Boris Schmidt Germany | 35 | 843 0.8× | 1.6k 1.6× | 1.0k 1.2× | 550 1.3× | 83 0.2× | 136 | 3.9k | ||
| Detcho A. Stoyanovsky United States | 31 | 322 0.3× | 2.0k 2.0× | 777 0.9× | 165 0.4× | 441 1.2× | 75 | 3.4k | ||
| Wolfgang Nastainczyk Germany | 36 | 272 0.2× | 2.5k 2.5× | 382 0.4× | 706 1.7× | 327 0.9× | 81 | 4.0k |
Countries citing papers authored by James F. Kerwin
Since
Specialization
Citations
This map shows the geographic impact of James F. Kerwin'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 James F. Kerwin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James F. Kerwin more than expected).
Fields of papers citing papers by James F. Kerwin
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by James F. Kerwin. 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 James F. Kerwin. The network helps show where James F. Kerwin may publish in the future.
Co-authorship network of co-authors of James F. Kerwin
This figure shows the co-authorship network connecting the top 25 collaborators of James F. Kerwin. A scholar is included among the top collaborators of James F. Kerwin 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 James F. Kerwin. James F. Kerwin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Witte, David G., Michael E. Brune, Ivan Milicic, et al.. (2002). Modeling of Relationships between Pharmacokinetics and Blockade of Agonist-Induced Elevation of Intraurethral Pressure and Mean Arterial Pressure in Conscious Dogs Treated with α1-Adrenoceptor Antagonists. Journal of Pharmacology and Experimental Therapeutics. 300(2). 495–504.
2.
Hancock, Arthur A., Steven A. Buckner, Michael E. Brune, et al.. (2002). Preclinical Pharmacology of Fiduxosin, a Novel α1-Adrenoceptor Antagonist with Uroselective Properties. Journal of Pharmacology and Experimental Therapeutics. 300(2). 478–486.
3.
Meyer, Michael D., Robert J. Altenbach, Fatima Z. Basha, et al.. (2001). Structure−Activity Studies for a Novel Series of Bicyclic Substituted Hexahydrobenz[e]isoindole α1A Adrenoceptor Antagonists as Potential Agents for the Symptomatic Treatment of Benign Prostatic Hyperplasia. Journal of Medicinal Chemistry. 44(12). 1971–1985.
4.
Meyer, Michael D., Robert J. Altenbach, Fatima Z. Basha, et al.. (2000). Structure−Activity Studies for a Novel Series of Tricyclic Substituted Hexahydrobenz[e]isoindole α1A Adrenoceptor Antagonists as Potential Agents for the Symptomatic Treatment of Benign Prostatic Hyperplasia (BPH). Journal of Medicinal Chemistry. 43(8). 1586–1603.
5.
Gordon, Eric M. & James F. Kerwin. (1998). Combinatorial chemistry and molecular diversity in drug discovery. Wiley eBooks.
6.
Hancock, Arthur A., Michael E. Brune, David G. Witte, et al.. (1998). Actions of A-131701, a Novel, Selective Antagonist for Alpha-1A Compared with Alpha-1B Adrenoceptors on Intraurethral and Blood Pressure Responses in Conscious Dogs and a Pharmacodynamic Assessment of in Vivo Prostatic Selectivity. Journal of Pharmacology and Experimental Therapeutics. 285(2). 628–642.
7.
Witte, David G., et al.. (1997). Relationships between Pharmacokinetics and Blockade of Agonist-Induced Prostatic Intraurethral Pressure and Mean Arterial Pressure in the Conscious Dog After Single and Repeated Daily Oral Administration of Terazosin. Journal of Pharmacology and Experimental Therapeutics. 282(2). 891–898.
8.
Hancock, Arthur A., C R Vitt, Sheila M. Knepper, et al.. (1996). Pharmacologic characterization of CHIR 2279, an N-substituted glycine peptoid with high-affinity binding for alpha 1-adrenoceptors.. Journal of Pharmacology and Experimental Therapeutics. 277(2). 885–899.
9.
Brune, Michael E., et al.. (1996). Effects of Selective and Nonselective Alpha-1 -Adrenoceptor Antagonists on Intraurethral and Arterial Pressures in Intact Conscious Dogs. Pharmacology. 53(6). 356–368.
10.
MacKichan, Joanna K., Lene Thomsen, James F. Kerwin, Jean‐Paul Latgé, & Anne Beauvais. (1995). Unsaturated fatty acids are the active molecules of a glucan-synthase-inhibitory fraction isolated from entomophthoralean protoplasts. Microbiology. 141(10). 2757–2762.
11.
Kerwin, James F. & Michael J. Heller. (1994). The arginine‐nitric oxide pathway: A target for new drugs. Medicinal Research Reviews. 14(1). 23–74.
12.
Raszkiewicz, J L, Donald G. Linville, James F. Kerwin, Frank L. Wagenaar, & Stephen P. Arnerić. (1992). Nitric oxide synthase is critical in mediating basal forebrain regulation of cortical cerebral circulation. Journal of Neuroscience Research. 33(1). 129–135.
13.
Ishii, Kunio, James F. Kerwin, & Ferid Murad. (1990). Nω-Nitro-L -arginine: a potent inhibitor of the L -arginine-dependent soluble guanylate cyclase activation pathway in LLC-PK1 cells. Canadian Journal of Physiology and Pharmacology. 68(6). 749–751.
14.
Murad, Ferid, Kazuo Ishii, Ulrich Förstermann, et al.. (1990). EDRF is an intracellular second messenger and autacoid to regulate cyclic GMP synthesis in many cells.. PubMed. 24. 441–8.
15.
Kerwin, James F., Alex M. Nadzan, Hana Kopecka, et al.. (1989). Hybrid cholecystokinin (CCK) antagonists: new implications in the design and modification of CCK antagonists. Journal of Medicinal Chemistry. 32(4). 739–742.
16.
Danishefsky, Samuel J., Susumu Kobayashi, & James F. Kerwin. (1982). Cram rule selectivity in the Lewis acid catalyzed cyclocondensation of chiral aldehydes. A convenient route to chiral systems of biological interest. The Journal of Organic Chemistry. 47(10). 1981–1983.
17.
Mattingly, Phillip G., James F. Kerwin, & Marvin J. Miller. (1979). A facile synthesis of substituted N-hydroxy-2-azetidinones. A biogenetic type .beta.-lactam synthesis. Journal of the American Chemical Society. 101(14). 3983–3985.
18.
Saunders, Harry L., et al.. (1962). Some Effects of 3:5:3′-Triiodothyropropionic Acid, Methyl Ether in the Rat. Endocrinology. 70(3). 365–374.
19.
Kerwin, James F., et al.. (1961). The Synthesis of Some Potential Hypoglycemic Agents1. The Journal of Organic Chemistry. 26(5). 1551–1553.
20.
Kerwin, James F., et al.. (1951). Adrenergic Blocking Agents. III. N-(Aryloxyisopropyl)-β-haloethylamines1. Journal of the American Chemical Society. 73(9). 4162–4168.
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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