Matthew Volgraf

2.7k total citations
19 papers, 1.7k citations indexed

About

Matthew Volgraf is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Materials Chemistry. According to data from OpenAlex, Matthew Volgraf has authored 19 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Cellular and Molecular Neuroscience, 9 papers in Molecular Biology and 4 papers in Materials Chemistry. Recurrent topics in Matthew Volgraf's work include Photoreceptor and optogenetics research (8 papers), Retinal Development and Disorders (4 papers) and Photochromic and Fluorescence Chemistry (4 papers). Matthew Volgraf is often cited by papers focused on Photoreceptor and optogenetics research (8 papers), Retinal Development and Disorders (4 papers) and Photochromic and Fluorescence Chemistry (4 papers). Matthew Volgraf collaborates with scholars based in United States, Japan and Germany. Matthew Volgraf's co-authors include Dirk Trauner, Ehud Y. Isacoff, Pau Gorostiza, Rika Numano, Richard Krämer, Stephanie Szobota, Matthew R. Banghart, Jian Payandeh, Ethan K. Scott and Doris L. Fortin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Neuron.

In The Last Decade

Matthew Volgraf

19 papers receiving 1.7k citations

Peers

Matthew Volgraf

CMN

Andreas Reiner Germany

Matthew R. Banghart United States

Joshua Levitz United States

James A. Frank Germany

Johannes Broichhagen Germany

Stephanie Szobota United States

Cyril Goudet France

Alexandre Mourot France

George Papageorgiou United Kingdom

Katharine Borges United States

Andreas Reiner Germany

Matthew Volgraf

1.1k ×1.0

CMN

951 ×1.1

630 ×0.9

147 ×0.6

130 ×1.0

Citations per year, relative to Matthew Volgraf Matthew Volgraf (= 1×) peers Andreas Reiner

Countries citing papers authored by Matthew Volgraf

Since Specialization

Citations

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

Fields of papers citing papers by Matthew Volgraf

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew Volgraf

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

All Works

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19 of 19 papers shown

Kschonsak, Marc, Christine C. Jao, Christopher P. Arthur, et al.. (2023). Cryo-EM reveals an unprecedented binding site for NaV1.7 inhibitors enabling rational design of potent hybrid inhibitors. eLife. 12. 17 indexed citations

Villemure, Elisia, Jack A. Terrett, Robin Larouche‐Gauthier, et al.. (2021). A Retrospective Look at the Impact of Binding Site Environment on the Optimization of TRPA1 Antagonists. ACS Medicinal Chemistry Letters. 12(8). 1230–1237. 10 indexed citations

Payandeh, Jian & Matthew Volgraf. (2021). Ligand binding at the protein–lipid interface: strategic considerations for drug design. Nature Reviews Drug Discovery. 20(9). 710–722. 76 indexed citations

Chernov-Rogan, Tania, Eleonora Gianti, Chang Liu, et al.. (2019). TRPA1 modulation by piperidine carboxamides suggests an evolutionarily conserved binding site and gating mechanism. Proceedings of the National Academy of Sciences. 116(51). 26008–26019. 18 indexed citations

Wang, Tzu-Ming, Brandon M. Brown, Lunbin Deng, et al.. (2017). A novel NMDA receptor positive allosteric modulator that acts via the transmembrane domain. Neuropharmacology. 121. 204–218. 32 indexed citations

Wang, Xiaojing, Aleksandr Kolesnikov, Suzanne Tay, et al.. (2017). Discovery of 5-Azaindazole (GNE-955) as a Potent Pan-Pim Inhibitor with Optimized Bioavailability. Journal of Medicinal Chemistry. 60(10). 4458–4473. 19 indexed citations

Hackos, David H., Patrick J. Lupardus, Teddy Grand, et al.. (2016). Positive Allosteric Modulators of GluN2A-Containing NMDARs with Distinct Modes of Action and Impacts on Circuit Function. Neuron. 89(5). 983–999. 139 indexed citations

Volgraf, Matthew, Lina Chan, Malcolm P. Huestis, et al.. (2014). Synthesis, characterization, and PK/PD studies of a series of spirocyclic pyranochromene BACE1 inhibitors. Bioorganic & Medicinal Chemistry Letters. 24(11). 2477–2480. 9 indexed citations

Huestis, Malcolm P., Wendy Liu, Matthew Volgraf, et al.. (2013). Diethylaminosulfur trifluoride-mediated intramolecular cyclization of 2-hydroxycycloalkylureas to fused bicyclic aminooxazoline compounds and evaluation of their biochemical activity against β-secretase-1 (BACE-1). Tetrahedron Letters. 54(43). 5802–5807. 3 indexed citations

10.

Lumb, Jean‐Philip, et al.. (2012). Total Synthesis of Exiguamines A and B Inspired by Catecholamine Chemistry. Chemistry - A European Journal. 18(16). 4999–5005. 33 indexed citations

11.

Numano, Rika, Pau Gorostiza, Matthew Volgraf, et al.. (2010). Nanosculpting reversed wavelength sensitivity into a photoswitchable iGluR. Neuroscience Research. 68. e112–e112. 1 indexed citations

12.

Numano, Rika, Stephanie Szobota, Albert Y. Lau, et al.. (2009). Nanosculpting reversed wavelength sensitivity into a photoswitchable iGluR. Proceedings of the National Academy of Sciences. 106(16). 6814–6819. 74 indexed citations

13.

Volgraf, Matthew, Jean‐Philip Lumb, Harry C. Brastianos, et al.. (2008). Biomimetic synthesis of the IDO inhibitors exiguamine A and B. Nature Chemical Biology. 4(9). 535–537. 55 indexed citations

14.

Gorostiza, Pau, Matthew Volgraf, Rika Numano, et al.. (2007). Mechanisms of photoswitch conjugation and light activation of an ionotropic glutamate receptor. Proceedings of the National Academy of Sciences. 104(26). 10865–10870. 149 indexed citations

15.

Szobota, Stephanie, Pau Gorostiza, Filippo Del Bene, et al.. (2007). Remote Control of Neuronal Activity with a Light-Gated Glutamate Receptor. Neuron. 54(4). 535–545. 262 indexed citations

16.

Wang, Sheng, Stephanie Szobota, Yuan Wang, et al.. (2007). All Optical Interface for Parallel, Remote, and Spatiotemporal Control of Neuronal Activity. Nano Letters. 7(12). 3859–3863. 55 indexed citations

17.

Volgraf, Matthew, et al.. (2006). Reversibly Caged Glutamate: A Photochromic Agonist of Ionotropic Glutamate Receptors. Journal of the American Chemical Society. 129(2). 260–261. 141 indexed citations

18.

Banghart, Matthew R., Matthew Volgraf, & Dirk Trauner. (2006). Engineering Light-Gated Ion Channels. Biochemistry. 45(51). 15129–15141. 127 indexed citations

19.

Volgraf, Matthew, Pau Gorostiza, Rika Numano, et al.. (2005). Allosteric control of an ionotropic glutamate receptor with an optical switch. Nature Chemical Biology. 2(1). 47–52. 486 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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