Robert Zaczek

5.8k total citations
91 papers, 3.8k citations indexed

About

Robert Zaczek is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Pharmacology. According to data from OpenAlex, Robert Zaczek has authored 91 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Cellular and Molecular Neuroscience, 39 papers in Molecular Biology and 23 papers in Pharmacology. Recurrent topics in Robert Zaczek's work include Neuroscience and Neuropharmacology Research (50 papers), Cholinesterase and Neurodegenerative Diseases (20 papers) and Stress Responses and Cortisol (18 papers). Robert Zaczek is often cited by papers focused on Neuroscience and Neuropharmacology Research (50 papers), Cholinesterase and Neurodegenerative Diseases (20 papers) and Stress Responses and Cortisol (18 papers). Robert Zaczek collaborates with scholars based in United States, Germany and Poland. Robert Zaczek's co-authors include Joseph T. Coyle, Kerry J. Koller, John W. Ferkany, Paul J. Gilligan, Steven Culp, David W. Robertson, E B De Souza, Robert Schwarcz, J. T. Coyle and Charles F. Albright and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Robert Zaczek

91 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert Zaczek United States 35 2.3k 1.7k 447 407 374 91 3.8k
David W. Schulz United States 28 1.5k 0.6× 1.5k 0.8× 585 1.3× 231 0.6× 426 1.1× 37 2.9k
Richard Bergeron Canada 32 2.2k 1.0× 2.0k 1.2× 463 1.0× 429 1.1× 332 0.9× 65 4.3k
Xavier Langlois Belgium 38 2.3k 1.0× 2.1k 1.2× 292 0.7× 397 1.0× 510 1.4× 104 4.2k
Markus Kessler United States 40 2.7k 1.2× 2.6k 1.5× 247 0.6× 806 2.0× 492 1.3× 79 5.4k
David B. Bylund United States 32 2.4k 1.0× 2.3k 1.3× 366 0.8× 200 0.5× 670 1.8× 89 4.1k
I J Kopin United States 34 2.1k 0.9× 1.1k 0.6× 368 0.8× 383 0.9× 667 1.8× 70 4.2k
Michael F. Mazurek Canada 30 2.0k 0.8× 1.3k 0.8× 199 0.4× 257 0.6× 546 1.5× 56 3.4k
Thomas P. Blackburn United States 30 2.2k 0.9× 1.6k 0.9× 239 0.5× 440 1.1× 320 0.9× 70 3.6k
Naoya Kawashima Japan 20 2.2k 0.9× 1.3k 0.7× 214 0.5× 244 0.6× 531 1.4× 37 3.0k
Matthew P. Galloway United States 35 1.9k 0.8× 1.2k 0.7× 399 0.9× 520 1.3× 362 1.0× 86 3.5k

Countries citing papers authored by Robert Zaczek

Since Specialization
Citations

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

Fields of papers citing papers by Robert Zaczek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert Zaczek. 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 Robert Zaczek. The network helps show where Robert Zaczek may publish in the future.

Co-authorship network of co-authors of Robert Zaczek

This figure shows the co-authorship network connecting the top 25 collaborators of Robert Zaczek. A scholar is included among the top collaborators of Robert Zaczek 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 Robert Zaczek. Robert Zaczek 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.
Myers, Scott J., Lawrence J. Wilson, Yesim A. Tahirovic, et al.. (2021). A Glutamate N-Methyl-d-Aspartate (NMDA) Receptor Subunit 2B–Selective Inhibitor of NMDA Receptor Function with Enhanced Potency at Acidic pH and Oral Bioavailability for Clinical Use. Journal of Pharmacology and Experimental Therapeutics. 379(1). 41–52. 10 indexed citations
2.
Li, Yu-Wen, Matthew A. Seager, Karen Heman, et al.. (2015). Biochemical and behavioral effects of PDE10A inhibitors: Relationship to target site occupancy. Neuropharmacology. 102. 121–135. 15 indexed citations
3.
Lodge, Nicholas J., Frederick T. Chin, Douglas D. Dischino, et al.. (2014). Synthesis and evaluation of candidate PET radioligands for corticotropin-releasing factor type-1 receptors. Nuclear Medicine and Biology. 41(6). 524–535. 14 indexed citations
4.
Dzierba, Carolyn D., Thais M. Sielecki, Argyrios G. Arvanitis, et al.. (2012). Synthesis and structure–activity relationships of pyrido[3,2-b]pyrazin-3(4H)-ones and pteridin-7(8H)-ones as corticotropin-releasing factor-1 receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 22(15). 4986–4989. 5 indexed citations
5.
Yang, Michael G., J. SCOTT WELLS, Brian M. Cochran, et al.. (2007). Design and synthesis of benzoazepinone-derived cyclic malonamides and aminoamides as potent γ-secretase inhibitors. Bioorganic & Medicinal Chemistry Letters. 17(14). 3910–3915. 12 indexed citations
6.
Goldstein, Margi E., Yang Cao, Jeremy H. Toyn, et al.. (2007). Ex Vivo Occupancy of γ-Secretase Inhibitors Correlates with Brain β-Amyloid Peptide Reduction in Tg2576 Mice. Journal of Pharmacology and Experimental Therapeutics. 323(1). 102–108. 8 indexed citations
7.
Iben, Lawrence G., Richard E. Olson, Sukhanya Jayachandra, et al.. (2007). Signal Peptide Peptidase and γ-Secretase Share Equivalent Inhibitor Binding Pharmacology. Journal of Biological Chemistry. 282(51). 36829–36836. 19 indexed citations
8.
Dzierba, Carolyn D., Amy Takvorian, Maria Rafalski, et al.. (2004). Synthesis, Structure−Activity Relationships, and in Vivo Properties of 3,4-Dihydro-1H-pyrido[2,3-b]pyrazin-2-ones as Corticotropin-Releasing Factor-1 Receptor Antagonists. Journal of Medicinal Chemistry. 47(23). 5783–5790. 11 indexed citations
9.
Arvanitis, Argyrios G., Richard G. Wilde, Gary A. Cain, et al.. (2003). Imidazo[4,5-b]pyridines as corticotropin releasing factor receptor ligands. Bioorganic & Medicinal Chemistry Letters. 13(1). 125–128. 11 indexed citations
10.
Arvanitis, Argyrios G., Richard G. Wilde, Lawrence W. Fitzgerald, et al.. (2003). Imidazo[4,5-c]pyridines as corticotropin releasing factor receptor ligands. Bioorganic & Medicinal Chemistry Letters. 13(1). 129–131. 7 indexed citations
11.
Szewczyk, Grzegorz, Dariusz Szukiewicz, Robert Zaczek, & D. Maślińska. (2000). Mast cells in the mouse mammary gland--correlation with the development of lactiferous structures.. PubMed. 48(1-2). 13–7. 7 indexed citations
12.
Beck, James P., et al.. (1999). Purin-8-ones as corticotropin-releasing hormone (CRH-R1) receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 9(7). 967–972. 26 indexed citations
13.
Beck, James P., et al.. (1999). Thiazolo[4,5-d]pyrimidine thiones and -ones as corticotropin-releasing hormone (CRH-R1) receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 9(8). 1185–1188. 24 indexed citations
15.
Zaczek, Robert, Steven Culp, Harry Goldberg, David J. McCann, & E B De Souza. (1991). Interactions of [3H]amphetamine with rat brain synaptosomes. I. Saturable sequestration.. Journal of Pharmacology and Experimental Therapeutics. 257(2). 820–829. 34 indexed citations
16.
Zaczek, Robert, Giuseppe Battaglia, Steven Culp, et al.. (1990). Effects of repeated fenfluramine administration on indices of monoamine function in rat brain: pharmacokinetic, dose response, regional specificity and time course data.. Journal of Pharmacology and Experimental Therapeutics. 253(1). 104–112. 101 indexed citations
17.
Zaczek, Robert, et al.. (1984). Kainic acid: insights from a neurotoxin into the pathophysiology of Huntington's disease.. PubMed. 5(6). 617–24. 17 indexed citations
18.
Ferkany, John W., et al.. (1984). Glutamate-containing dipeptides enhance specific binding at glutamate receptors and inhibit specific binding at kainate receptors in rat brain. Neuroscience Letters. 44(3). 281–286. 10 indexed citations
19.
Zaczek, Robert, et al.. (1983). Failure of folic acid derivatives to mimic the actions of kainic acid in brain in vitro or in vivo.. PubMed. 4(5). 573–9. 11 indexed citations
20.
Zaczek, Robert, et al.. (1981). Neuronal receptor sites for kainic acid: correlations with neurotoxicity.. PubMed. 27. 337–46. 21 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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