Robert S. Papay

1.3k total citations
42 papers, 1.1k citations indexed

About

Robert S. Papay is a scholar working on Molecular Biology, Rheumatology and Cell Biology. According to data from OpenAlex, Robert S. Papay has authored 42 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 14 papers in Rheumatology and 10 papers in Cell Biology. Recurrent topics in Robert S. Papay's work include Osteoarthritis Treatment and Mechanisms (14 papers), Receptor Mechanisms and Signaling (14 papers) and Proteoglycans and glycosaminoglycans research (10 papers). Robert S. Papay is often cited by papers focused on Osteoarthritis Treatment and Mechanisms (14 papers), Receptor Mechanisms and Signaling (14 papers) and Proteoglycans and glycosaminoglycans research (10 papers). Robert S. Papay collaborates with scholars based in United States, India and United Kingdom. Robert S. Papay's co-authors include Dianne M. Perez, Charles J. Malemud, Beno Michel, John R. Schiltz, Robert J. Gaivin, Dan F. McCune, Ting Shi, Van A. Doze, Boyd R. Rorabaugh and Roland W. Moskowitz and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and The Journal of Comparative Neurology.

In The Last Decade

Robert S. Papay

42 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Robert S. Papay United States	21	348	263	258	174	136	42	1.1k
Starlee Lively Canada	24	507 1.5×	283 1.1×	246 1.0×	115 0.7×	58 0.4×	43	1.6k
Sarina B. Elmariah United States	19	181 0.5×	244 0.9×	314 1.2×	121 0.7×	58 0.4×	42	1.1k
Keiko Kamakura Japan	26	756 2.2×	139 0.5×	572 2.2×	239 1.4×	178 1.3×	67	2.0k
K. Adam Baker Canada	19	444 1.3×	193 0.7×	564 2.2×	125 0.7×	53 0.4×	27	1.4k
Fiona H. Zhou Australia	20	437 1.3×	126 0.5×	325 1.3×	51 0.3×	72 0.5×	39	1.2k
Minoru Hoshimaru Japan	21	790 2.3×	305 1.2×	504 2.0×	156 0.9×	96 0.7×	54	1.8k
Sanja Ivković Serbia	15	1.0k 3.0×	138 0.5×	373 1.4×	57 0.3×	152 1.1×	37	1.6k
Josée Prud’homme Canada	13	490 1.4×	149 0.6×	114 0.4×	267 1.5×	174 1.3×	14	1.1k
Kwok‐Kuen Cheung Hong Kong	20	673 1.9×	127 0.5×	119 0.5×	60 0.3×	102 0.8×	51	1.5k
Nicola Canal Italy	20	361 1.0×	56 0.2×	304 1.2×	69 0.4×	130 1.0×	48	1.3k

Countries citing papers authored by Robert S. Papay

Since Specialization

Citations

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

Fields of papers citing papers by Robert S. Papay

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert S. Papay

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Papay, Robert S. & Dianne M. Perez. (2025). Further In Vitro and Ex Vivo Pharmacological and Kinetic Characterizations of CCF219B: A Positive Allosteric Modulator of the α1A-Adrenergic Receptor. Pharmaceuticals. 18(4). 476–476. 2 indexed citations

Papay, Robert S., Shaun R. Stauffer, & Dianne M. Perez. (2023). A PAM of the α1A-Adrenergic receptor rescues biomarker, long-term potentiation, and cognitive deficits in Alzheimer’s disease mouse models without effects on blood pressure. SHILAP Revista de lepidopterología. 5. 100160–100160. 4 indexed citations

Papay, Robert S., Jonathan D. Macdonald, Shaun R. Stauffer, & Dianne M. Perez. (2022). Characterization of a novel positive allosteric modulator of the α1A-Adrenergic receptor. SHILAP Revista de lepidopterología. 4. 100142–100142. 4 indexed citations

Zhou, Xu, et al.. (2014). Long-term α1B-adrenergic receptor activation shortens lifespan, while α1A-adrenergic receptor stimulation prolongs lifespan in association with decreased cancer incidence. AGE. 36(4). 9675–9675. 20 indexed citations

Papay, Robert S., Ting Shi, Michael T. Piascik, Sathyamangla V. Naga Prasad, & Dianne M. Perez. (2013). α1A-Adrenergic Receptors Regulate Cardiac Hypertrophy In Vivo Through Interleukin-6 Secretion. Molecular Pharmacology. 83(5). 939–948. 13 indexed citations

Shi, Ting, Robert S. Papay, & Dianne M. Perez. (2012). α_1A-Adrenergic receptor differentially regulates STAT3 phosphorylation through PKCϵ and PKCδ in myocytes. Journal of Receptors and Signal Transduction. 32(2). 76–86. 7 indexed citations

Doze, Van A., Robert S. Papay, Manveen K. Gupta, et al.. (2011). Long-Term α1A-Adrenergic Receptor Stimulation Improves Synaptic Plasticity, Cognitive Function, Mood, and Longevity. Molecular Pharmacology. 80(4). 747–758. 65 indexed citations

Gupta, Manveen K., Robert S. Papay, Chris Jurgens, et al.. (2009). α1-Adrenergic Receptors Regulate Neurogenesis and Gliogenesis. Molecular Pharmacology. 76(2). 314–326. 36 indexed citations

Shi, Ting, Zhong-Hui Duan, Robert S. Papay, et al.. (2006). Novel α1-Adrenergic Receptor Signaling Pathways: Secreted Factors and Interactions with the Extracellular Matrix. Molecular Pharmacology. 70(1). 129–142. 15 indexed citations

10.

Papay, Robert S., Robert J. Gaivin, Archana Jha, et al.. (2006). Localization of the mouse α1A-adrenergic receptor (AR) in the brain: α1AAR is expressed in neurons, GABAergic interneurons, and NG2 oligodendrocyte progenitors. The Journal of Comparative Neurology. 497(2). 209–222. 88 indexed citations

11.

Rorabaugh, Boyd R., et al.. (2005). Both α- and α-adrenergic receptors crosstalk to downregulate β-ARs in mouse heart: coupling to differential PTX-sensitive pathways. Journal of Molecular and Cellular Cardiology. 39(5). 777–784. 20 indexed citations

12.

Papay, Robert S., Robert J. Gaivin, Dan F. McCune, et al.. (2004). Mouse α_1B‐adrenergic receptor is expressed in neurons and NG2 oligodendrocytes. The Journal of Comparative Neurology. 478(1). 1–10. 44 indexed citations

13.

Gonzalez‐Cabrera, Pedro J., Robert J. Gaivin, June Yun, et al.. (2003). Genetic Profiling of α1-Adrenergic Receptor Subtypes by Oligonucleotide Microarrays: Coupling to Interleukin-6 Secretion but Differences in STAT3 Phosphorylation and gp-130. Molecular Pharmacology. 63(5). 1104–1116. 36 indexed citations

14.

Papay, Robert S., Michael J. Zuscik, Sean Ross, et al.. (2002). Mice expressing the α_1B‐adrenergic receptor induces a synucleinopathy with excessive tyrosine nitration but decreased phosphorylation. Journal of Neurochemistry. 83(3). 623–634. 34 indexed citations

15.

Averbook, Bruce J., JoAnn C. L. Schuh, Robert S. Papay, & Charles R. Maliszewski. (2002). Antitumor Effects of Flt3 Ligand in Transplanted Murine Tumor Models. Journal of Immunotherapy. 25(1). 27–35. 14 indexed citations

16.

Malemud, Charles J., Robert S. Papay, & Thomas M. Hering. (1996). FORSKOLIN STIMULATES AGGRECAN GENE EXPRESSION IN CULTURED BOVINE CHONDROCYTES. American Journal of Therapeutics. 3(2). 120–128. 3 indexed citations

17.

Malemud, Charles J., Robert S. Papay, Thomas M. Hering, et al.. (1995). Phenotypic modulation of newly synthesized proteoglycans in human cartilage and chondrocytes. Osteoarthritis and Cartilage. 3(4). 227–238. 17 indexed citations

18.

Yoo, Jung U., Robert S. Papay, & Charles J. Malemud. (1992). Suppression of Proteoglycan Synthesis in Chondrocyte Cultures Derived from Canine Intervertebral Disc. Spine. 17(2). 221–224. 14 indexed citations

19.

Malemud, Charles J. & Robert S. Papay. (1992). Synthesis of low buoyant density proteoglycans by human chondrocytes in culture. Matrix. 12(6). 427–438. 1 indexed citations

20.

Malemud, Charles J., Robert S. Papay, Paul Hasler, & Gary M. Kammer. (1990). cAMP-dependent protein kinase in chondrocyte cultures: Holoenzyme activation, phosphorylation of cellular proteins, effects of NSAIDs and possible role in proteoglycan synthesis. Seminars in Arthritis and Rheumatism. 19(4). 10–15. 2 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.

Explore authors with similar magnitude of impact