Marc J. C. Scanio

1.5k total citations
13 papers, 638 citations indexed

About

Marc J. C. Scanio is a scholar working on Organic Chemistry, Molecular Biology and Physiology. According to data from OpenAlex, Marc J. C. Scanio has authored 13 papers receiving a total of 638 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Organic Chemistry, 6 papers in Molecular Biology and 4 papers in Physiology. Recurrent topics in Marc J. C. Scanio's work include Cyclopropane Reaction Mechanisms (5 papers), Ion channel regulation and function (4 papers) and Pain Mechanisms and Treatments (4 papers). Marc J. C. Scanio is often cited by papers focused on Cyclopropane Reaction Mechanisms (5 papers), Ion channel regulation and function (4 papers) and Pain Mechanisms and Treatments (4 papers). Marc J. C. Scanio collaborates with scholars based in United States, United Kingdom and Denmark. Marc J. C. Scanio's co-authors include Paul A. Wender, Gabriel G. Gamber, Michael E. Kort, Michael F. Jarvis, Alaric J. Dyckman, Craig O. Husfeld, Lei Zhang, Robert D. Hubbard, Robert Sun and Travis J. Williams and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Journal of Medicinal Chemistry.

In The Last Decade

Marc J. C. Scanio

13 papers receiving 627 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marc J. C. Scanio United States	11	451	161	112	59	45	13	638
John V. Mulcahy United States	8	258 0.6×	191 1.2×	65 0.6×	46 0.8×	33 0.7×	12	430
Kethireddy V.V. Ananthalakshmi Kuwait	13	183 0.4×	147 0.9×	56 0.5×	122 2.1×	13 0.3×	21	463
David K.H. Lee United States	11	173 0.4×	176 1.1×	116 1.0×	156 2.6×	24 0.5×	19	439
Clare London United States	9	114 0.3×	185 1.1×	73 0.7×	105 1.8×	11 0.2×	12	300
Andrew M. Griffin United States	12	124 0.3×	211 1.3×	35 0.3×	104 1.8×	25 0.6×	21	424
Motonori Miyakawa Japan	12	102 0.2×	213 1.3×	31 0.3×	84 1.4×	20 0.4×	13	416
Francesca Fabrizi Italy	6	112 0.2×	217 1.3×	116 1.0×	47 0.8×	9 0.2×	8	378
Dieter Riddall United Kingdom	11	137 0.3×	172 1.1×	51 0.5×	132 2.2×	6 0.1×	14	418
John R. Boot United Kingdom	13	99 0.2×	214 1.3×	56 0.5×	127 2.2×	11 0.2×	26	458

Countries citing papers authored by Marc J. C. Scanio

Since Specialization

Citations

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

Fields of papers citing papers by Marc J. C. Scanio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marc J. C. Scanio. 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 Marc J. C. Scanio. The network helps show where Marc J. C. Scanio may publish in the future.

Co-authorship network of co-authors of Marc J. C. Scanio

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

All Works

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13 of 13 papers shown

1.

Zhang, Di, Rama Thimmapaya, Xu‐Feng Zhang, et al.. (2011). KCNQ2/3 openers show differential selectivity and site of action across multiple KCNQ channels. Journal of Neuroscience Methods. 200(1). 54–62. 9 indexed citations

2.

Scanio, Marc J. C., Lei Shi, William H. Bunnelle, et al.. (2011). Structure–Activity Studies of Diazabicyclo[3.3.0]octane-Substituted Pyrazines and Pyridines as Potent α4β2 Nicotinic Acetylcholine Receptor Ligands. Journal of Medicinal Chemistry. 54(21). 7678–7692. 6 indexed citations

3.

Scanio, Marc J. C., Lei Shi, Irene Drizin, et al.. (2010). Discovery and biological evaluation of potent, selective, orally bioavailable, pyrazine-based blockers of the Nav1.8 sodium channel with efficacy in a model of neuropathic pain. Bioorganic & Medicinal Chemistry. 18(22). 7816–7825. 27 indexed citations

4.

Matulenko, Mark A., Marc J. C. Scanio, & Michael E. Kort. (2009). Voltage-Gated Sodium Channel Blockers for the Treatment of Chronic Pain. Current Topics in Medicinal Chemistry. 9(4). 362–376. 24 indexed citations

5.

Bunnelle, William H., Karin Tietje, Jennifer M. Frost, et al.. (2009). Octahydropyrrolo[3,4-c]pyrrole: A Diamine Scaffold for Construction of Either α4β2 or α7-Selective Nicotinic Acetylcholine Receptor (nAChR) Ligands. Substitutions that Switch Subtype Selectivity. Journal of Medicinal Chemistry. 52(14). 4126–4141. 21 indexed citations

6.

Joshi, S. K., Prisca Honoré, Gricelda Hernandez, et al.. (2008). Additive Antinociceptive Effects of the Selective Nav1.8 Blocker A-803467 and Selective TRPV1 Antagonists in Rat Inflammatory and Neuropathic Pain Models. Journal of Pain. 10(3). 306–315. 40 indexed citations

7.

McGaraughty, Steve, Katharine L. Chu, Marc J. C. Scanio, et al.. (2007). A Selective Nav1.8 Sodium Channel Blocker, A-803467 [5-(4-Chlorophenyl-N-(3,5-dimethoxyphenyl)furan-2-carboxamide], Attenuates Spinal Neuronal Activity in Neuropathic Rats. Journal of Pharmacology and Experimental Therapeutics. 324(3). 1204–1211. 69 indexed citations

8.

Wender, Paul A., F. Christopher Bi, Gabriel G. Gamber, et al.. (2002). Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads. Pure and Applied Chemistry. 74(1). 25–31. 117 indexed citations

9.

Wender, Paul A., et al.. (2002). Transition Metal-Catalyzed Hetero-[5 + 2] Cycloadditions of Cyclopropyl Imines and Alkynes: Dihydroazepines from Simple, Readily Available Starting Materials. Journal of the American Chemical Society. 124(51). 15154–15155. 148 indexed citations

10.

Wender, Paul A., Gabriel G. Gamber, & Marc J. C. Scanio. (2001). Serial [5+2]/[4+2] Cycloadditions: Facile, Preparative, Multi‐Component Syntheses of Polycyclic Compounds from Simple, Readily Available Starting Materials. Angewandte Chemie International Edition. 40(20). 3895–3897. 51 indexed citations

11.

Wender, Paul A., Gabriel G. Gamber, & Marc J. C. Scanio. (2001). Serial [5+2]/[4+2] Cycloadditions: Facile, Preparative, Multi-Component Syntheses of Polycyclic Compounds from Simple, Readily Available Starting Materials This research was supported by grant CHE-9800445 from the National Science Foundation. The Stanford Graduate Fellowship (M.J.C.S. and G.G.G.) is gratefully acknowledged.. PubMed. 40(20). 3895–3897. 48 indexed citations

12.

Wender, Paul A., Gabriel G. Gamber, & Marc J. C. Scanio. (2001). Serial [5+2]/[4+2] Cycloadditions: Facile, Preparative, Multi-Component Syntheses of Polycyclic Compounds from Simple, Readily Available Starting Materials. Angewandte Chemie. 113(20). 4013–4015. 13 indexed citations

13.

Wender, Paul A., Alaric J. Dyckman, Craig O. Husfeld, & Marc J. C. Scanio. (2000). A New and Practical Five-Carbon Component for Metal-Catalyzed [5 + 2] Cycloadditions: Preparative Scale Syntheses of Substituted Cycloheptenones. Organic Letters. 2(11). 1609–1611. 65 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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