Arthur E. Jacobson

2.3k total citations
82 papers, 1.9k citations indexed

About

Arthur E. Jacobson is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Organic Chemistry. According to data from OpenAlex, Arthur E. Jacobson has authored 82 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 51 papers in Cellular and Molecular Neuroscience and 20 papers in Organic Chemistry. Recurrent topics in Arthur E. Jacobson's work include Receptor Mechanisms and Signaling (37 papers), Pharmacological Receptor Mechanisms and Effects (36 papers) and Neuropeptides and Animal Physiology (31 papers). Arthur E. Jacobson is often cited by papers focused on Receptor Mechanisms and Signaling (37 papers), Pharmacological Receptor Mechanisms and Effects (36 papers) and Neuropeptides and Animal Physiology (31 papers). Arthur E. Jacobson collaborates with scholars based in United States, United Kingdom and Japan. Arthur E. Jacobson's co-authors include Kenner C. Rice, Richard B. Rothman, Kenner C. Rice, Victor Bykov, Brian R. de Costa, J. Edwin Blalock, Brian R. DeCosta, Daniel J.J. Carr, Wayne D. Bowen and Linda S. Brady and has published in prestigious journals such as Brain Research, FEBS Letters and Journal of Medicinal Chemistry.

In The Last Decade

Arthur E. Jacobson

82 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arthur E. Jacobson United States 24 1.3k 1.2k 325 200 102 82 1.9k
Charles H. Mitch United States 25 1.0k 0.8× 1.1k 0.9× 251 0.8× 184 0.9× 172 1.7× 61 1.7k
Philip F. VonVoigtlander United States 23 1.5k 1.1× 1.4k 1.1× 389 1.2× 485 2.4× 100 1.0× 60 2.3k
Hyacinth C. Akunne United States 24 1.0k 0.8× 925 0.7× 248 0.8× 107 0.5× 84 0.8× 49 1.5k
W. Soudijn Netherlands 29 899 0.7× 1.2k 1.0× 379 1.2× 239 1.2× 166 1.6× 98 2.4k
Cécile Béguin United States 19 880 0.7× 793 0.6× 240 0.7× 182 0.9× 125 1.2× 23 1.4k
I. van Wijngaarden Netherlands 24 730 0.6× 856 0.7× 377 1.2× 173 0.9× 151 1.5× 55 1.8k
P. S. Portoghese United States 24 1.6k 1.2× 1.4k 1.1× 222 0.7× 375 1.9× 115 1.1× 57 2.0k
L. Pichat France 16 1.3k 1.0× 1.1k 0.9× 379 1.2× 115 0.6× 139 1.4× 99 2.0k
Sarah Grimwood United States 28 1.0k 0.8× 1.1k 0.9× 401 1.2× 147 0.7× 194 1.9× 52 2.0k
P. F. VON VOIGTLANDER United States 15 1.3k 1.0× 890 0.7× 152 0.5× 294 1.5× 142 1.4× 41 1.9k

Countries citing papers authored by Arthur E. Jacobson

Since Specialization
Citations

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

Fields of papers citing papers by Arthur E. Jacobson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Arthur E. Jacobson. 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 Arthur E. Jacobson. The network helps show where Arthur E. Jacobson may publish in the future.

Co-authorship network of co-authors of Arthur E. Jacobson

This figure shows the co-authorship network connecting the top 25 collaborators of Arthur E. Jacobson. A scholar is included among the top collaborators of Arthur E. Jacobson 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 Arthur E. Jacobson. Arthur E. Jacobson 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.
Torres, Oscar B., Agnieszka Sulima, Arthur E. Jacobson, et al.. (2018). A rapid solution-based method for determining the affinity of heroin hapten-induced antibodies to heroin, its metabolites, and other opioids. Analytical and Bioanalytical Chemistry. 410(16). 3885–3903. 10 indexed citations
2.
Kim, In Jong, Christina M. Dersch, Richard B. Rothman, Arthur E. Jacobson, & Kenner C. Rice. (2004). A critical structural determinant of opioid receptor interaction with phenolic 5-phenylmorphans. Bioorganic & Medicinal Chemistry. 12(16). 4543–4550. 15 indexed citations
3.
Hsin, Ling‐Wei, Xinrong Tian, Elizabeth Webster, et al.. (2002). CRHR1 Receptor binding and lipophilicity of pyrrolopyrimidines, potential nonpeptide corticotropin-releasing hormone type 1 receptor antagonists. Bioorganic & Medicinal Chemistry. 10(1). 175–183. 32 indexed citations
4.
Ullrich, Thomas, et al.. (2001). Derivatives of 17-(2-methylallyl)-substituted noroxymorphone: variation of the delta address and its effects on affinity and selectivity for the delta opioid receptor. Bioorganic & Medicinal Chemistry Letters. 11(21). 2883–2885. 7 indexed citations
5.
Bowen, Wayne D., et al.. (1995). Ibogaine and its congeners are σ2 receptor-selective ligands with moderate affinity. European Journal of Pharmacology. 279(1). R1–R3. 75 indexed citations
6.
Lipovac, M. N., Berislav V. Zloković, Arthur E. Jacobson, et al.. (1993). Metaphit‐Induced Audiogenic Seizures in Mice: II. Studies on N‐Methyl‐d‐Aspartic Acid, GABA, and Sodium Channel Receptors and on the Disposition of Metaphit in the Brain. Epilepsia. 34(2). 211–219. 16 indexed citations
7.
Reith, Maarten E.A., et al.. (1992). Evidence for mutually exclusive binding of cocaine, BTCP, GBR 12935, and dopamine to the dopamine transporter. European Journal of Pharmacology Molecular Pharmacology. 227(4). 417–425. 63 indexed citations
8.
Rothman, Richard B., Joseph B. Long, Victor Bykov, et al.. (1991). Upregulation of the opioid receptor complex by the chronic administration of morphine: A biochemical marker related to the development of tolerance and dependence. Peptides. 12(1). 151–160. 54 indexed citations
9.
Xu, H. Y., et al.. (1991). Preliminary ligand binding data for subtypes of the delta opioid receptor in rat brain membranes. Life Sciences. 49(18). PL141–PL146. 25 indexed citations
10.
Carr, Daniel J.J., Brian R. DeCosta, Arthur E. Jacobson, Kenner C. Rice, & J. Edwin Blalock. (1991). Enantioselective kappa opioid binding sites on the macrophage cell line, P388d1. Life Sciences. 49(1). 45–51. 24 indexed citations
11.
Rothman, Richard B., Victor Bykov, Brian R. de Costa, et al.. (1990). Interaction of endogenous opioid peptides and other drugs with four kappa opioid binding sites in guinea pig brain. Peptides. 11(2). 311–331. 130 indexed citations
12.
Thurkauf, Andrew, Mariena V. Mattson, Charles P. France, et al.. (1990). Synthesis, phencyclidine-like pharmacology, and antiischemic potential of meta-substituted 1-(1-phenylcyclohexyl)-1,2,3,6-tetrahydropyridines. Journal of Medicinal Chemistry. 33(8). 2211–2215. 4 indexed citations
13.
Rothman, Richard B., Arthur E. Jacobson, Mariena V. Mattson, et al.. (1989). Probes for narcotic receptor mediated phenomena. 15. (3S,4S)-(+)-trans-3-Methylfentanyl isothiocyanate, a potent site-directed acylating agent for the .delta.-opioid receptors in vitro. Journal of Medicinal Chemistry. 32(6). 1392–1398. 20 indexed citations
14.
Lipovac, M. N., Ábel Lajtha, Berislav V. Zloković, et al.. (1989). Metaphit, an isothiocyanate analog of PCP, induces audiogenic seizures in mice. European Journal of Pharmacology. 165(1). 155–159. 23 indexed citations
15.
Zimányi, I, Arthur E. Jacobson, Kenner C. Rice, Ábel Lajtha, & Maarten E. A. Reith. (1989). Long‐term blockade of the dopamine uptake complex by metaphit, an isothiocyanate derivative of phencyclidine. Synapse. 3(3). 239–245. 10 indexed citations
16.
May, Everette L. & Arthur E. Jacobson. (1989). The Committee on Problems of Drug Dependence: A legacy of the National Academy of Sciences. A historical account. Drug and Alcohol Dependence. 23(3). 183–218. 20 indexed citations
17.
Carr, Daniel J.J., et al.. (1988). Evidence for a δ-class opioid receptor on cells of the immune system. Cellular Immunology. 116(1). 44–51. 80 indexed citations
18.
Bowen, Wayne D., et al.. (1988). Differential coupling of mu-competitive and mu-noncompetitive delta opiate receptors to guanine nucleotide binding proteins in rat brain membranes. Biochemical Pharmacology. 37(3). 467–472. 7 indexed citations
19.
Tocqué, Bruno, et al.. (1987). The μ-opioid receptor in the 7315c tumor cell. European Journal of Pharmacology. 143(1). 127–130. 9 indexed citations
20.
Koek, Wouter, J H Woods, Arthur E. Jacobson, & K.C. Rice. (1987). Phencyclidine (PCP)-like discriminative stimulus effects of metaphit and of 2-amino-5-phosphonovalerate in pigeons: generality across different training doses of PCP. Psychopharmacology. 93(4). 437–42. 20 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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