James B. Wiesner

840 total citations
20 papers, 677 citations indexed

About

James B. Wiesner is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Physiology. According to data from OpenAlex, James B. Wiesner has authored 20 papers receiving a total of 677 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Cellular and Molecular Neuroscience, 11 papers in Molecular Biology and 6 papers in Physiology. Recurrent topics in James B. Wiesner's work include Neuroscience and Neuropharmacology Research (7 papers), Neuropeptides and Animal Physiology (7 papers) and Adenosine and Purinergic Signaling (6 papers). James B. Wiesner is often cited by papers focused on Neuroscience and Neuropharmacology Research (7 papers), Neuropeptides and Animal Physiology (7 papers) and Adenosine and Purinergic Signaling (6 papers). James B. Wiesner collaborates with scholars based in United States. James B. Wiesner's co-authors include Robert L. Moss, Bheemarao G. Ugarkar, Mark D. Erion, Robert L. Moss, L. Krulich, James I. Koenig, Steven J. Henriksen, Angelo J. Castellino, Harry E. Gruber and Floyd E. Bloom and has published in prestigious journals such as Brain Research, Endocrinology and Journal of Medicinal Chemistry.

In The Last Decade

James B. Wiesner

20 papers receiving 660 citations

Peers

Countries citing papers authored by James B. Wiesner

Since Specialization

Citations

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

Fields of papers citing papers by James B. Wiesner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James B. Wiesner. 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 B. Wiesner. The network helps show where James B. Wiesner may publish in the future.

Co-authorship network of co-authors of James B. Wiesner

This figure shows the co-authorship network connecting the top 25 collaborators of James B. Wiesner. A scholar is included among the top collaborators of James B. Wiesner 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 B. Wiesner. James B. Wiesner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Adenosine Kinase Inhibitors. 5. Synthesis, Enzyme Inhibition, and Analgesic Activity of Diaryl-erythro-furanosyltubercidin Analogues 2005 ·Journal of Medicinal Chemistry ·Serge H. Boyer, Bheemarao G. Ugarkar, (unknown), (unknown), Michael C. Matelich, (unknown), Jorge Gomez‐Galeno, Rohan Mendonca, Megumi Tsuchiya, Atsushi Nagahisa, (unknown), James B. Wiesner, Mark D. Erion	32
2	Adenosine Kinase Inhibitors. 6. Synthesis, Water Solubility, and Antinociceptive Activity of 5-Phenyl-7-(5-deoxy-β-d-ribofuranosyl)pyrrolo[2,3-d]pyrimidines Substituted at C4 with Glycinamides and Related Compounds 2005 ·Journal of Medicinal Chemistry ·Brett C. Bookser, Bheemarao G. Ugarkar, Michael C. Matelich, Robert H. Lemus, Matthew Allan, Megumi Tsuchiya, (unknown), Atsushi Nagahisa, James B. Wiesner, Mark D. Erion	50
3	Adenosine Kinase Inhibitors. 2. Synthesis, Enzyme Inhibition, and Antiseizure Activity of Diaryltubercidin Analogues 2000 ·Journal of Medicinal Chemistry ·Bheemarao G. Ugarkar, Angelo J. Castellino, (unknown), (unknown), James B. Wiesner, (unknown), Mark D. Erion	47
4	Adenosine Kinase Inhibitors. 1. Synthesis, Enzyme Inhibition, and Antiseizure Activity of 5-Iodotubercidin Analogues 2000 ·Journal of Medicinal Chemistry ·Bheemarao G. Ugarkar, (unknown), (unknown), (unknown), (unknown), James B. Wiesner, Mark D. Erion	95
5	Adenosine Kinase Inhibitors as a Novel Approach to Anticonvulsant Therapy 1999 ·Journal of Pharmacology and Experimental Therapeutics ·James B. Wiesner, Bheemarao G. Ugarkar, Angelo J. Castellino, J. Barankiewicz, (unknown), Harry E. Gruber, Alan C. Foster, Mark D. Erion	79
6	P.6.063 Lorazepam for stupor and mutism: A double-blind placebo-controlled cross-over study 1997 ·European Neuropsychopharmacology ·(unknown), Christoph Klawe, Margarete Müller, James B. Wiesner, Otto Benkert	2
7	Design, Synthesis and Anticonvulsant Activity of the Potent Adenosine Kinase Inhibitor GP3269 1997 ·Nucleosides and Nucleotides ·Mark D. Erion, Bheemarao G. Ugarkar, (unknown), Angelo J. Castellino, James M. Fujitaki, Ross Dixon, James R. Appleman, James B. Wiesner	18
8	Regulation of Endogenous Adenosine Levels in the CNS: Potential for Therapy in Stroke, Epilepsy and Pain 1995 ·Advances in experimental medicine and biology ·Alan C. Foster, Leonard P. Miller, James B. Wiesner	4
9	Adenosinergic Modulation of Homocysteine‐Induced Seizures in Mice 1990 ·Epilepsia ·Paul J. Marangos, Tyler J. Loftus, James B. Wiesner, T. E. Lowe, E. Rossi, (unknown), Harry E. Gruber	64
10	Long-term potentiation of evoked and spontaneous neuronal activity in the grafted hippocampus 1989 ·Experimental Brain Research ·(unknown), James B. Wiesner, S.J. Henriksen, Fred H. Gage	21
11	Opioids in the Hippocampus: Progress Obtained From In Vivo Electrophysiological Analyses 1988 ·PsycEXTRA Dataset ·S.J. Henriksen, James B. Wiesner, Guy Chouvet	9
12	Ethanol enhances recurrent inhibition in the dentate gyrus of the hippocampus 1987 ·Neuroscience Letters ·James B. Wiesner, Steven J. Henriksen, Floyd E. Bloom	17
13	Enkephalin enhances responsiveness to perforant path input while decreasing spontaneous activity in the dentate gyrus 1987 ·Neuroscience Letters ·James B. Wiesner, Steven J. Henriksen	17
14	Effect of β-endorphin on sociosexual proclivity in a choice paradigm 1986 ·Pharmacology Biochemistry and Behavior ·James B. Wiesner, Carol A. Dudley, Robert L. Moss	6
15	Suppression of Receptive and Proceptive Behavior in Ovariectomized, Estrogen-Progesterone-Primed Rats by Intraventricular Beta-Endorphin: Studies of Behavioral Specificity 1986 ·Neuroendocrinology ·James B. Wiesner, Robert L. Moss	37
16	Behavioural specificity of β-endorphin suppression of sexual behavior: differential receptor antagonism 1986 ·Pharmacology Biochemistry and Behavior ·James B. Wiesner, Robert L. Moss	26
17	Opioid enhancement of perforant path transmission: effect of an enkephalin analog on inhibition and facilitation in the dentate gyrus 1986 ·Brain Research ·James B. Wiesner, Steven J. Henriksen, Floyd E. Bloom	16
18	POSSIBLE DELTA RECEPTOR MEDIATION OF THE EFFECT OF,β-ENDORPHIN ON LUTE IN IZ ING HORMONE (LH) RELEASE, BUT NOT ON PROLACTIN (PRL) RELEASE, IN THE OVARIECTOMI ZED RAT¹ 1985 ·Endocrinology ·James B. Wiesner, James I. Koenig, L. Krulich, Robert L. Moss	25
19	Beta-endorphin suppression of lordosis behavior in female rats; Lack of effect of peripherally-administered naloxone 1984 ·Life Sciences ·James B. Wiesner, Robert L. Moss	41
20	Site of action for β-endorphin-induced changes in plasma luteinizing hormone and prolactin in the ovariectomized rat 1984 ·Life Sciences ·James B. Wiesner, James I. Koenig, L. Krulich, Robert L. Moss	71

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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