John P. Capone

2.9k total citations
60 papers, 2.5k citations indexed

About

John P. Capone is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, John P. Capone has authored 60 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 18 papers in Genetics and 17 papers in Epidemiology. Recurrent topics in John P. Capone's work include Peroxisome Proliferator-Activated Receptors (22 papers), Adipose Tissue and Metabolism (16 papers) and Herpesvirus Infections and Treatments (14 papers). John P. Capone is often cited by papers focused on Peroxisome Proliferator-Activated Receptors (22 papers), Adipose Tissue and Metabolism (16 papers) and Herpesvirus Infections and Treatments (14 papers). John P. Capone collaborates with scholars based in Canada, United States and Australia. John P. Capone's co-authors include Richard A. Rachubinski, Kenji Miyata, Sandra L. Marcus, Suresh Subramani, Uttam L. RajBhandary, Stuart L. Marcus, James R. Smiley, Geoff H. Werstuck, Logan W. Donaldson and Shannon E. McCaw and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

John P. Capone

60 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
John P. Capone Canada 28 1.6k 676 580 430 352 60 2.5k
Margarita Hadzopoulou‐Cladaras United States 27 2.0k 1.2× 366 0.5× 528 0.9× 230 0.5× 357 1.0× 41 3.4k
Ulrich Deuschle Germany 26 1.6k 1.0× 315 0.5× 844 1.5× 394 0.9× 198 0.6× 43 2.6k
J Berger United States 20 1.4k 0.9× 329 0.5× 385 0.7× 444 1.0× 159 0.5× 23 2.2k
Naveenan Navaratnam United Kingdom 27 2.0k 1.2× 571 0.8× 210 0.4× 265 0.6× 402 1.1× 43 2.8k
Alex Lipovsky United States 12 1.9k 1.2× 563 0.8× 240 0.4× 362 0.8× 458 1.3× 17 3.0k
Naohito Aoki Japan 26 1.5k 0.9× 253 0.4× 260 0.4× 364 0.8× 505 1.4× 57 2.5k
Sei Yoshida Japan 23 1.1k 0.7× 566 0.8× 333 0.6× 368 0.9× 300 0.9× 41 2.6k
Mario M. Zakin France 31 1.5k 0.9× 171 0.3× 529 0.9× 163 0.4× 283 0.8× 89 2.8k
J A Rodkey United States 23 1.3k 0.8× 188 0.3× 266 0.5× 262 0.6× 292 0.8× 26 2.3k
Hsiu‐Ming Shih Taiwan 28 1.7k 1.1× 279 0.4× 255 0.4× 219 0.5× 621 1.8× 58 2.9k

Countries citing papers authored by John P. Capone

Since Specialization
Citations

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

Fields of papers citing papers by John P. Capone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John P. Capone. 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 John P. Capone. The network helps show where John P. Capone may publish in the future.

Co-authorship network of co-authors of John P. Capone

This figure shows the co-authorship network connecting the top 25 collaborators of John P. Capone. A scholar is included among the top collaborators of John P. Capone 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 John P. Capone. John P. Capone 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.
Stephen, Jancy, et al.. (2012). PPAR ligands decrease human airway smooth muscle cell migration and extracellular matrix synthesis. European Respiratory Journal. 41(2). 425–432. 12 indexed citations
2.
Nair, Parameswaran, et al.. (2008). LXR-induced reverse cholesterol transport in human airway smooth muscle is mediated exclusively by ABCA1. American Journal of Physiology-Lung Cellular and Molecular Physiology. 295(5). L949–L957. 43 indexed citations
3.
Capone, John P., et al.. (2008). Protein kinase C α modulates liver X receptor α transactivation. Journal of Endocrinology. 197(1). 121–130. 27 indexed citations
4.
Capone, John P., et al.. (2006). Host Cell Factor-1 and E2F4 Interact Via Multiple Determinants in Each Protein. Molecular and Cellular Biochemistry. 288(1-2). 79–90. 27 indexed citations
7.
Kassam, Altaf, Christopher J. Winrow, F Fernandez-Rachubinski, John P. Capone, & Richard A. Rachubinski. (2000). The Peroxisome Proliferator Response Element of the Gene Encoding the Peroxisomal β-Oxidation Enzyme Enoyl-CoA Hydratase/3-Hydroxyacyl-CoA Dehydrogenase Is a Target for Constitutive Androstane Receptor β/9-cis-Retinoic Acid Receptor-mediated Transactivation. Journal of Biological Chemistry. 275(6). 4345–4350. 45 indexed citations
8.
Berger, Joel P., John Woods, Nancy S. Hayes, et al.. (2000). A PPARγ mutant serves as a dominant negative inhibitor of PPAR signaling and is localized in the nucleus. Molecular and Cellular Endocrinology. 162(1-2). 57–67. 36 indexed citations
9.
Kassam, Altaf, John P. Capone, & Richard A. Rachubinski. (1999). Orphan Nuclear Hormone Receptor RevErbα Modulates Expression from the Promoter of the Hydratase-dehydrogenase Gene by Inhibiting Peroxisome Proliferator-activated Receptor α-Dependent Transactivation. Journal of Biological Chemistry. 274(32). 22895–22900. 25 indexed citations
10.
Miyata, Kenji, et al.. (1998). Receptor-interacting protein 140 interacts with and inhibits transactivation by, peroxisome proliferator-activated receptor α and liver-X-receptor α. Molecular and Cellular Endocrinology. 146(1-2). 69–76. 61 indexed citations
11.
Kassam, Altaf, John G. Hunter, Richard A. Rachubinski, & John P. Capone. (1998). Subtype- and response element-dependent differences in transactivation by peroxisome proliferator-activated receptors α and γ. Molecular and Cellular Endocrinology. 141(1-2). 153–162. 21 indexed citations
12.
Ulmasov, Barbara, John P. Capone, & William R. Folk. (1997). Regulated expression of plant tRNA genes by the prokaryotic tet and lac repressors. Plant Molecular Biology. 35(4). 417–424. 14 indexed citations
13.
Marcus, Sandra L., Christopher J. Winrow, John P. Capone, & Richard A. Rachubinski. (1996). A p56 Ligand Serves as a Coactivator of an Orphan Nuclear Hormone Receptor. Journal of Biological Chemistry. 271(44). 27197–27200. 34 indexed citations
14.
15.
Winrow, Christopher J., Kenji Miyata, Sandra L. Marcus, et al.. (1995). Calreticulin modulates the in vitro DNA binding but not the in vivo transcriptional activation by peroxisome proliferator-activated receptor/retinoid X receptor heterodimers. Molecular and Cellular Endocrinology. 111(2). 175–179. 14 indexed citations
16.
Miyata, Kenji, Shannon E. McCaw, Sandra L. Marcus, Richard A. Rachubinski, & John P. Capone. (1994). The peroxisome proliferator-activated receptor interacts with the retinoid X receptor in vivo. Gene. 148(2). 327–330. 61 indexed citations
17.
Tapping, Richard I., et al.. (1993). The 5' flanking sequence negatively modulates the in vivo expression and in vitro transcription of a human tRNA gene. Nucleic Acids Research. 21(19). 4476–4482. 14 indexed citations
18.
Capone, John P.. (1989). Screening recombinant baculovirus plaques in situ with antibody probes. PubMed. 6(3). 62–66. 10 indexed citations
19.
Werstuck, Geoff H. & John P. Capone. (1989). Mutational analysis of the herpes simplex virus trans-inducing factor Vmw65. Gene. 75(2). 213–224. 44 indexed citations
20.
Capone, John P.. (1988). Modulation of the Phenotypic Expression of a Human Serine tRNA Gene by 5′-Flanking Sequences. DNA. 7(7). 459–468. 8 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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