Arie Struyk

1.8k total citations
28 papers, 1.1k citations indexed

About

Arie Struyk is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Arie Struyk has authored 28 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, 10 papers in Cellular and Molecular Neuroscience and 9 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Arie Struyk's work include Ion channel regulation and function (11 papers), Cardiac electrophysiology and arrhythmias (8 papers) and Neuroscience and Neural Engineering (6 papers). Arie Struyk is often cited by papers focused on Ion channel regulation and function (11 papers), Cardiac electrophysiology and arrhythmias (8 papers) and Neuroscience and Neural Engineering (6 papers). Arie Struyk collaborates with scholars based in United States, Belgium and Japan. Arie Struyk's co-authors include Stephen C. Cannon, James L. Salzer, Yu Fu, Orlando D. Gil, George Zanazzi, Fenfen Wu, Wentao Mi, Kylie A. Scoggan, Dennis E. Bulman and Vladislav S. Markin and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Neuroscience and Brain.

In The Last Decade

Arie Struyk

28 papers receiving 1.0k citations

Peers

Arie Struyk

CMN

CCM

PHYSI

Romina Combi Italy

Hsiang‐Yu Yang Taiwan

Jack Tseng United States

Eugene Wyatt United States

Jared Kushner United States

Peter C. Meighan United States

Najate Benamer France

Michelle Apperson United States

Michael Tanowitz United States

P. J. Marangos United States

Romina Combi Italy

Arie Struyk

496 ×0.7

375 ×0.9

CMN

65 ×0.2

CCM

155 ×1.4

97 ×1.0

PHYSI

Citations per year, relative to Arie Struyk Arie Struyk (= 1×) peers Romina Combi

Countries citing papers authored by Arie Struyk

Since Specialization

Citations

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

Fields of papers citing papers by Arie Struyk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arie Struyk

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

All Works

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20 of 20 papers shown

Alexopoulou, Zoi, et al.. (2022). Neurodegenerative Diseases: The Value of Early Predictive End Points. Clinical Pharmacology & Therapeutics. 111(4). 835–839. 8 indexed citations

García, David Vállez, Talakad G. Lohith, Eric D. Hostetler, et al.. (2021). A dual-time-window protocol to reduce acquisition time of dynamic tau PET imaging using [18F]MK-6240. EJNMMI Research. 11(1). 49–49. 11 indexed citations

Hendrix, James A., Angela Britton, Bradley T. Christian, et al.. (2021). Longitudinal investigation for enhancing Down Syndrome Research (LIFE‐DSR) Study: Tau PET and CSF sub‐studies. Alzheimer s & Dementia. 17(S4). 2 indexed citations

Ballard, Jeanine, Joshua D. Vardigan, Fuqiang Zhao, et al.. (2021). Translational Pharmacokinetic–Pharmacodynamic Modeling of NaV1.7 Inhibitor MK-2075 to Inform Human Efficacious Dose. Frontiers in Pharmacology. 12. 786078–786078. 5 indexed citations

Koole, Michel, Talakad G. Lohith, John L. Valentine, et al.. (2019). Preclinical Safety Evaluation and Human Dosimetry of [18F]MK-6240, a Novel PET Tracer for Imaging Neurofibrillary Tangles. Molecular Imaging and Biology. 22(1). 173–180. 20 indexed citations

Struyk, Arie, Cynthia Gargano, S. Aubrey Stoch, et al.. (2016). Pharmacodynamic effects of suvorexant and zolpidem on EEG during sleep in healthy subjects. European Neuropsychopharmacology. 26(10). 1649–1656. 19 indexed citations

Gotter, Anthony L., Mark S. Forman, C. Meacham Harrell, et al.. (2016). Orexin 2 Receptor Antagonism is Sufficient to Promote NREM and REM Sleep from Mouse to Man. Scientific Reports. 6(1). 27147–27147. 67 indexed citations

Wu, Fenfen, Wentao Mi, Yu Fu, Arie Struyk, & Stephen C. Cannon. (2016). Mice with an Na_V1.4 sodium channel null allele have latent myasthenia, without susceptibility to periodic paralysis. Brain. 139(6). 1688–1699. 17 indexed citations

Wu, Fenfen, Wentao Mi, Erick O. Hernández‐Ochoa, et al.. (2012). A calcium channel mutant mouse model of hypokalemic periodic paralysis. Journal of Clinical Investigation. 122(12). 4580–4591. 80 indexed citations

10.

Wu, Fenfen, Wentao Mi, Dennis K. Burns, et al.. (2011). A sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis. Journal of Clinical Investigation. 121(10). 4082–4094. 59 indexed citations

11.

Kudryashova, Elena, Arie Struyk, Ekaterina Mokhonova, Stephen C. Cannon, & Melissa J. Spencer. (2011). The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype. Human Molecular Genetics. 20(20). 3925–3932. 35 indexed citations

12.

Struyk, Arie, et al.. (2010). Arginine Mutations in the S4 VSD of NaV1.4 Associated with Hypokalemic Periodic Paralysis, But Not with Paramyotonia, Create a Gating Pore Conductance. Biophysical Journal. 98(3). 111a–111a. 1 indexed citations

13.

Fu, Yu, Arie Struyk, Vladislav S. Markin, & Stephen C. Cannon. (2010). Gating behaviour of sodium currents in adult mouse muscle recorded with an improved two‐electrode voltage clamp. The Journal of Physiology. 589(3). 525–546. 21 indexed citations

14.

Struyk, Arie, et al.. (2008). Gating Pore Currents in DIIS4 Mutations of NaV1.4 Associated with Periodic Paralysis: Saturation of Ion Flux and Implications for Disease Pathogenesis. The Journal of General Physiology. 132(4). 447–464. 58 indexed citations

15.

Struyk, Arie & Stephen C. Cannon. (2007). Paradoxical depolarization of BA ²⁺ ‐ treated muscle exposed to low extracellular K ⁺ : Insights into resting potential abnormalities in hypokalemic paralysis. Muscle & Nerve. 37(3). 326–337. 59 indexed citations

16.

Struyk, Arie & Stephen C. Cannon. (2007). A Na+ Channel Mutation Linked to Hypokalemic Periodic Paralysis Exposes a Proton-selective Gating Pore. The Journal of General Physiology. 130(1). 11–20. 131 indexed citations

17.

Struyk, Arie & Stephen C. Cannon. (2002). Slow Inactivation Does Not Block the Aqueous Accessibility to the Outer Pore of Voltage-gated Na Channels. The Journal of General Physiology. 120(4). 509–516. 30 indexed citations

18.

Gil, Orlando D., George Zanazzi, Arie Struyk, & James L. Salzer. (1998). Neurotrimin Mediates Bifunctional Effects on Neurite Outgrowth via Homophilic and Heterophilic Interactions. Journal of Neuroscience. 18(22). 9312–9325. 92 indexed citations

19.

Salzer, James L., et al.. (1990). Structure and Function of the Myelin‐Associated Glycoproteins^a. Annals of the New York Academy of Sciences. 605(1). 302–312. 35 indexed citations

20.

Knowlton, Robert G., Eric J. Weaver, Arie Struyk, et al.. (1989). Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen gene.. PubMed. 45(5). 681–8. 92 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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