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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Moving beyond belief: A narrative review of potential biomarkers for transcutaneous vagus nerve stimulation
Andreas M. Burger, Martina D’Agostini, Bart Verkuil, et al.
Psychophysiology (2020) Vol. 57, Iss. 6
Open Access | Times Cited: 108

Showing 1-25 of 108 citing articles:

International Consensus Based Review and Recommendations for Minimum Reporting Standards in Research on Transcutaneous Vagus Nerve Stimulation (Version 2020)
Adam D. Farmer, Adam Strzelczyk, Alessandra Finisguerra, et al.
Frontiers in Human Neuroscience (2021) Vol. 14
Open Access | Times Cited: 242
Does transcutaneous auricular vagus nerve stimulation affect vagally mediated heart rate variability? A living and interactive Bayesian meta‐analysis
Vinzent Wolf, Anne Kühnel, Vanessa Teckentrup, et al.
Psychophysiology (2021) Vol. 58, Iss. 11
Open Access | Times Cited: 70
Transcutaneous cervical vagus nerve stimulation improves sensory performance in humans: a randomized controlled crossover pilot study
Michael Jigo, Jason B. Carmel, Qi Wang, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 12
Transcutaneous Auricular Vagus Nerve Stimulation Does Not Accelerate Fear Extinction: A Randomized, Sham‐Controlled Study
Martina D’Agostini, Lucas Vanden Bossche, Andreas M. Burger, et al.
Psychophysiology (2025) Vol. 62, Iss. 1
Closed Access | Times Cited: 1
Stimulate to Remember? The Effects of Short Burst of Transcutaneous Vagus Nerve Stimulation (taVNS) on Memory Performance and Pupil Dilation
Mareike Ludwig, Matthew J. Betts, Dorothea Hämmerer
Psychophysiology (2025) Vol. 62, Iss. 1
Open Access | Times Cited: 1
Three Hundred Hertz Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) Impacts Pupil Size Non‐Linearly as a Function of Intensity
Ian Phillips, Michael Johns, Nick B. Pandža, et al.
Psychophysiology (2025) Vol. 62, Iss. 2
Open Access | Times Cited: 1
Neuro-cardiac coupling predicts transcutaneous auricular vagus nerve stimulation effects
Marius Keute, Kathrin Machetanz, Levan Berelidze, et al.
Brain stimulation (2021) Vol. 14, Iss. 2, pp. 209-216
Open Access | Times Cited: 48
Mental health during the COVID-19 pandemic and beyond: The importance of the vagus nerve for biopsychosocial resilience
Josefien Dedoncker, M. Vanderhasselt, Cristina Ottaviani, et al.
Neuroscience & Biobehavioral Reviews (2021) Vol. 125, pp. 1-10
Open Access | Times Cited: 44
Auricular Vagus Neuromodulation—A Systematic Review on Quality of Evidence and Clinical Effects
Nishant Verma, Jonah Mudge, Maïsha Kasole, et al.
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 41
Effects of transcutaneous auricular vagus nerve stimulation on reversal learning, tonic pupil size, salivary alpha‐amylase, and cortisol
Martina D’Agostini, Andreas M. Burger, Mathijs Franssen, et al.
Psychophysiology (2021) Vol. 58, Iss. 10
Open Access | Times Cited: 41
Short bursts of transcutaneous auricular vagus nerve stimulation enhance evoked pupil dilation as a function of stimulation parameters
Martina D’Agostini, Andreas M. Burger, Mathijs Franssen, et al.
Cortex (2022) Vol. 159, pp. 233-253
Open Access | Times Cited: 36
Evidence for a modulating effect of transcutaneous auricular vagus nerve stimulation (taVNS) on salivary alpha-amylase as indirect noradrenergic marker: A pooled mega-analysis
Manon Giraudier, Carlos Ventura‐Bort, Andreas M. Burger, et al.
Brain stimulation (2022) Vol. 15, Iss. 6, pp. 1378-1388
Open Access | Times Cited: 33
No evidence for a modulating effect of continuous transcutaneous auricular vagus nerve stimulation on markers of noradrenergic activity
Martina D’Agostini, Andreas M. Burger, Gustavo Villca Ponce, et al.
Psychophysiology (2022) Vol. 59, Iss. 4
Open Access | Times Cited: 30
Phasic, Event-Related Transcutaneous Auricular Vagus Nerve Stimulation Modifies Behavioral, Pupillary, and Low-Frequency Oscillatory Power Responses
Christian Wienke, Marcus Grueschow, Aiden Haghikia, et al.
Journal of Neuroscience (2023) Vol. 43, Iss. 36, pp. 6306-6319
Open Access | Times Cited: 22
Short-term transcutaneous vagus nerve stimulation increases pupil size but does not affect EEG alpha power: A replication of Sharon et al. (2021, Journal of Neuroscience)
Beth Lloyd, Franz Wurm, Roy de Kleijn, et al.
Brain stimulation (2023) Vol. 16, Iss. 4, pp. 1001-1008
Open Access | Times Cited: 20
Auricular Transcutaneous Vagus Nerve Stimulation Specifically Enhances Working Memory Gate Closing Mechanism: A System Neurophysiological Study
Anyla Konjusha, Shijing Yu, Moritz Mückschel, et al.
Journal of Neuroscience (2023) Vol. 43, Iss. 25, pp. 4709-4724
Open Access | Times Cited: 17
Transcutaneous Auricular Vagus Nerve Stimulation to Improve Emotional State
Ainara Aranberri Ruiz
Biomedicines (2024) Vol. 12, Iss. 2, pp. 407-407
Open Access | Times Cited: 6
Impaired Phasic Discharge of Locus Coeruleus Neurons Based on Persistent High Tonic Discharge—A New Hypothesis With Potential Implications for Neurodegenerative Diseases
Kathrin Janitzky
Frontiers in Neurology (2020) Vol. 11
Open Access | Times Cited: 44
The Vagal Autonomic Pathway of COVID-19 at the Crossroad of Alzheimer’s Disease and Aging: A Review of Knowledge
Claire-Marie Rangon, Slavica Krantic, Emmanuel Moyse, et al.
Journal of Alzheimer s Disease Reports (2020) Vol. 4, Iss. 1, pp. 537-551
Open Access | Times Cited: 40
Transcutaneous vagus nerve stimulation (tVNS) in stroke: the evidence, challenges and future directions
Sheharyar Baig, Marharyta Kamarova, Ali Ali, et al.
Autonomic Neuroscience (2021) Vol. 237, pp. 102909-102909
Open Access | Times Cited: 39
Transcutaneous auricular vagus nerve stimulators: a review of past, present, and future devices
Lei Wang, Yu Wang, Yifei Wang, et al.
Expert Review of Medical Devices (2021) Vol. 19, Iss. 1, pp. 43-61
Closed Access | Times Cited: 37
State-of-the-art imaging of neuromodulatory subcortical systems in aging and Alzheimer’s disease: Challenges and opportunities
Nina Engels, Elouise A. Koops, Prokopis C. Prokopiou, et al.
Neuroscience & Biobehavioral Reviews (2022) Vol. 144, pp. 104998-104998
Open Access | Times Cited: 25
Transcutaneous Vagus Nerve Stimulation Modulates EEG Microstates and Delta Activity in Healthy Subjects
Lorenzo Ricci, Pierpaolo Croce, Jacopo Lanzone, et al.
Brain Sciences (2020) Vol. 10, Iss. 10, pp. 668-668
Open Access | Times Cited: 36
Current challenges in reliably targeting the noradrenergic locus coeruleus using transcutaneous auricular vagus nerve stimulation (taVNS)
Mareike Ludwig, Christian Wienke, Matthew J. Betts, et al.
Autonomic Neuroscience (2021) Vol. 236, pp. 102900-102900
Closed Access | Times Cited: 31
The effects of transcutaneous auricular vagal nerve stimulation on pupil size
Fioravante Capone, Francesco Motolese, Antonio Di Zazzo, et al.
Clinical Neurophysiology (2021) Vol. 132, Iss. 8, pp. 1859-1865
Closed Access | Times Cited: 28
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