On the public citation graph

Electrical fields induced inside the rat brain with skin, skull, and dural placements of the current injection electrode

https://doi.org/10.1371/journal.pone.0203727
0 signed · 76 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/archneurpsyc.1950.02310190108008openalex-snapshot
THE CURRENT PATH IN ELECTRIC CONVULSION SHOCK
inferredcites →https://doi.org/10.1016/0014-4886(62)90056-0openalex-snapshot
Influence of transcortical d-c currents on cortical neuronal activity
inferredcites →https://doi.org/10.1016/j.bbi.2017.04.008openalex-snapshot
Safety parameter considerations of anodal transcranial Direct Current Stimulation in rats
inferredcites →https://doi.org/10.1016/j.brs.2009.03.005openalex-snapshot
Gyri-precise head model of transcranial direct current stimulation: Improved spatial focality using a ring electrode versus conventional rectangular pad
inferredcites →https://doi.org/10.1016/j.brs.2009.03.007openalex-snapshot
Role of cortical cell type and morphology in subthreshold and suprathreshold uniform electric field stimulation in vitro
inferredcites →https://doi.org/10.1016/j.brs.2016.06.004openalex-snapshot
Safety of Transcranial Direct Current Stimulation: Evidence Based Update 2016
inferredcites →https://doi.org/10.1016/j.brs.2017.02.007openalex-snapshot
Safety and tolerability of transcranial direct current stimulation to stroke patients – A phase I current escalation study
inferredcites →https://doi.org/10.1016/j.clinph.2006.04.009openalex-snapshot
Modeling the current distribution during transcranial direct current stimulation
inferredcites →https://doi.org/10.1016/j.clinph.2009.01.022openalex-snapshot
Safety limits of cathodal transcranial direct current stimulation in rats
inferredcites →https://doi.org/10.1016/j.clinph.2009.03.023openalex-snapshot
What does the ratio of injected current to electrode area tell us about current density in the brain during tDCS?
inferredcites →https://doi.org/10.1016/j.clinph.2010.04.033openalex-snapshot
Electrode-distance dependent after-effects of transcranial direct and random noise stimulation with extracephalic reference electrodes
inferredcites →https://doi.org/10.1016/j.clinph.2010.05.020openalex-snapshot
Electrode montages for tDCS and weak transcranial electrical stimulation: Role of “return” electrode’s position and size
inferredcites →https://doi.org/10.1016/j.clinph.2015.11.012openalex-snapshot
A technical guide to tDCS, and related non-invasive brain stimulation tools
inferredcites →https://doi.org/10.1016/j.clinph.2016.08.016openalex-snapshot
Animal models of transcranial direct current stimulation: Methods and mechanisms
inferredcites →https://doi.org/10.1016/j.clinph.2017.06.001openalex-snapshot
Low intensity transcranial electric stimulation: Safety, ethical, legal regulatory and application guidelines
inferredcites →https://doi.org/10.1016/j.neuroimage.2015.01.033openalex-snapshot
Determinants of the electric field during transcranial direct current stimulation
inferredcites →https://doi.org/10.1016/j.nlm.2011.06.018openalex-snapshot
Cumulative benefits of frontal transcranial direct current stimulation on visuospatial working memory training and skill learning in rats
inferredcites →https://doi.org/10.1016/s1388-2457(02)00437-6openalex-snapshot
Brain polarization in humans: a reappraisal of an old tool for prolonged non-invasive modulation of brain excitability
inferredcites →https://doi.org/10.1038/s41467-018-02928-3openalex-snapshot
Direct effects of transcranial electric stimulation on brain circuits in rats and humans
inferredcites →https://doi.org/10.1038/srep31236openalex-snapshot
Spatiotemporal structure of intracranial electric fields induced by transcranial electric stimulation in humans and nonhuman primates
inferredcites →https://doi.org/10.1073/pnas.42.9.687openalex-snapshot
MEASUREMENT OF IMPOSED VOLTAGE GRADIENT ADEQUATE TO MODULATE NEURONAL FIRING
inferredcites →https://doi.org/10.1088/1741-2560/5/1/006openalex-snapshot
Incorporation of the electrode–electrolyte interface into finite-element models of metal microelectrodes
inferredcites →https://doi.org/10.1088/1741-2560/5/2/007openalex-snapshot
Transcranial current stimulation focality using disc and ring electrode configurations: FEM analysis
inferredcites →https://doi.org/10.1088/1741-2560/8/6/066017openalex-snapshot
A finite element analysis of the effect of electrode area and inter-electrode distance on the spatial distribution of the current density in tDCS
inferredcites →https://doi.org/10.1109/ner.2011.5910483openalex-snapshot
Finite element simulation of transcranial current stimulation in realistic rat head model
inferredcites →https://doi.org/10.1109/tbme.1982.324910openalex-snapshot
Analysis and Control of the Current Distribution under Circular Dispersive Electrodes
inferredcites →https://doi.org/10.1109/tbme.2014.2322774openalex-snapshot
Comparison of Cephalic and Extracephalic Montages for Transcranial Direct Current Stimulation—A Numerical Study
inferredcites →https://doi.org/10.1109/tnsre.2012.2200046openalex-snapshot
Transcranial Current Brain Stimulation (tCS): Models and Technologies
inferredcites →https://doi.org/10.1111/j.1460-9568.2005.04233.xopenalex-snapshot
How does transcranial DC stimulation of the primary motor cortex alter regional neuronal activity in the human brain?
inferredcites →https://doi.org/10.1111/j.1469-7793.2000.t01-1-00633.xopenalex-snapshot
Excitability changes induced in the human motor cortex by weak transcranial direct current stimulation
inferredcites →https://doi.org/10.1111/j.1600-0447.1944.tb04586.xopenalex-snapshot
ON ELECTRIC CONVULSIVE THERAPY
inferredcites →https://doi.org/10.1113/jphysiol.1964.sp007425openalex-snapshot
The action of brief polarizing currents on the cerebral cortex of the rat (1) during current flow and (2) in the production of long‐lasting after‐effects
inferredcites →https://doi.org/10.1113/jphysiol.1986.sp015963openalex-snapshot
Modulation by applied electric fields of Purkinje and stellate cell activity in the isolated turtle cerebellum.
inferredcites →https://doi.org/10.1113/jphysiol.1988.sp017232openalex-snapshot
Effects of electric fields on transmembrane potential and excitability of turtle cerebellar Purkinje cells in vitro.
inferredcites →https://doi.org/10.1113/jphysiol.2003.055772openalex-snapshot
Effects of uniform extracellular DC electric fields on excitability in rat hippocampal slices in vitro
inferredcites →https://doi.org/10.1149/1.2424003openalex-snapshot
Resistance for Flow of Current to a Disk
inferredcites →https://doi.org/10.1152/jn.01312.2006openalex-snapshot
Shaping the Effects of Transcranial Direct Current Stimulation of the Human Motor Cortex
inferredcites →https://doi.org/10.1523/jneurosci.5252-09.2010openalex-snapshot
Transcranial Electric Stimulation Entrains Cortical Neuronal Populations in Rats
inferredcites →https://doi.org/10.3389/fnsys.2013.00006openalex-snapshot
Transcranial direct-current stimulation increases extracellular dopamine levels in the rat striatum
inferredcites →https://doi.org/10.7554/elife.18834openalex-snapshot
Measurements and models of electric fields in the in vivo human brain during transcranial electric stimulation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4168479openalex-extracted
Intensity-Dependent Gamma Electrical Stimulation Regulates Microglial Activation, Reduces Beta-Amyloid Load, and Facilitates Memory in a Mouse Model of Alzheimer's Disease
inferred← citeshttps://doi.org/10.1002/admt.202101514openalex-snapshot
Coagulation Bath‐Assisted 3D Printing of PEDOT:PSS with High Resolution and Strong Substrate Adhesion for Bioelectronic Devices
inferred← citeshttps://doi.org/10.1007/s12311-024-01756-0openalex-snapshot
Cerebellar Transcranial AC Stimulation Produces a Frequency-Dependent Bimodal Cerebellar Output Pattern
inferred← citeshttps://doi.org/10.1016/j.brs.2020.08.017openalex-snapshot
Entrainment of cerebellar purkinje cells with directional AC electric fields in anesthetized rats
inferred← citeshttps://doi.org/10.1016/j.brs.2024.04.007openalex-snapshot
Transcranial electric stimulation modulates firing rate at clinically relevant intensities
inferred← citeshttps://doi.org/10.1016/j.cortex.2025.05.006openalex-snapshot
Sparks fade with distance: The effect of electric field distribution on global motion perception using different tES techniques
inferred← citeshttps://doi.org/10.1016/j.jiec.2025.06.033openalex-snapshot
Infusion and iontophoresis for directional delivery of compounds to the brain
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2022.109761openalex-snapshot
A microfluidic perspective on conventional in vitro transcranial direct current stimulation methods
inferred← citeshttps://doi.org/10.1016/j.jtbi.2022.111093openalex-snapshot
Simulation of the electrical stimulation of the rat brain using sleep frequencies: A finite element modeling approach
inferred← citeshttps://doi.org/10.1016/j.neulet.2020.135492openalex-snapshot
Cortical direct current stimulation improves signal transmission between the motor cortices of rats
inferred← citeshttps://doi.org/10.1038/s41467-021-22468-7openalex-snapshot
Toward integrative approaches to study the causal role of neural oscillations via transcranial electrical stimulation
inferred← citeshttps://doi.org/10.1039/d3lc00492aopenalex-snapshot
Brain stimulation-on-a-chip: a neuromodulation platform for brain slices
inferred← citeshttps://doi.org/10.1088/1741-2552/ad9ad1openalex-snapshot
Transsynaptic modulation of cerebellar nuclear cells: theta AC-burst stimulation
inferred← citeshttps://doi.org/10.1088/1741-2552/ae44cfopenalex-snapshot
Measuring transcranial magnetic stimulation-induced electric fields in anatomically and conductively accurate rat head phantoms
inferred← citeshttps://doi.org/10.1101/2023.04.13.536696openalex-snapshot
On-chip brain slice stimulation: precise control of electric fields and tissue orientation
inferred← citeshttps://doi.org/10.1109/embc.2019.8856830openalex-snapshot
Modulation of Multiunit Spike Activity by Transcranial AC Stimulation (tACS) in the Rat Cerebellar Cortex
inferred← citeshttps://doi.org/10.1109/embc58623.2025.11254703openalex-snapshot
Electrophysiological Interference for Deep Brain Modulation*
inferred← citeshttps://doi.org/10.1109/map.2026.3655613openalex-snapshot
Advances in Computational Electromagnetics for Enhanced Noninvasive Brain Stimulation: E-field dosimetry, uncertainty quantification, optimization, and neural response modeling.
inferred← citeshttps://doi.org/10.1109/tnsre.2022.3179537openalex-snapshot
Designing and Pilot Testing a Novel Transcranial Temporal Interference Stimulation Device for Neuromodulation
inferred← citeshttps://doi.org/10.1186/s12984-024-01451-5openalex-snapshot
Pilot study of using transcranial temporal interfering theta-burst stimulation for modulating motor excitability in rat
inferred← citeshttps://doi.org/10.1186/s13195-020-00656-9openalex-snapshot
Intracranial alternating current stimulation facilitates neurogenesis in a mouse model of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1186/s13578-023-01085-5openalex-snapshot
Intensity-dependent gamma electrical stimulation regulates microglial activation, reduces beta-amyloid load, and facilitates memory in a mouse model of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1013471openalex-snapshot
EFMouse: A toolbox to model stimulation-induced electric fields in the mouse brain
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2157515/v1openalex-snapshot
Intensity-dependent gamma electrical stimulation regulates microglial activation, reduces beta-amyloid load, and facilitates memory in a mouse model of Alzheimer’s disease
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2157515/v2openalex-snapshot
Intensity-dependent gamma electrical stimulation regulates microglial activation, reduces beta-amyloid load, and facilitates memory in a mouse model of Alzheimer’s disease
inferred← citeshttps://doi.org/10.3389/fnana.2023.1128193openalex-snapshot
Comparing the effects of transcranial alternating current and temporal interference (tTIS) electric stimulation through whole-brain mapping of c-Fos immunoreactivity
inferred← citeshttps://doi.org/10.3389/fncir.2021.693073openalex-snapshot
Cortical Electrical Stimulation Ameliorates Traumatic Brain Injury-Induced Sensorimotor and Cognitive Deficits in Rats
inferred← citeshttps://doi.org/10.3389/fnhum.2021.652393openalex-snapshot
Improving the Effect of Transcranial Alternating Current Stimulation (tACS): A Systematic Review
inferred← citeshttps://doi.org/10.3389/fnsys.2023.1173738openalex-snapshot
Modulation of cerebellar cortical, cerebellar nuclear and vestibular nuclear activity using alternating electric currents
inferred← citeshttps://doi.org/10.3390/biomedicines10081965openalex-snapshot
Short-Term Cortical Electrical Stimulation during the Acute Stage of Traumatic Brain Injury Improves Functional Recovery
inferred← citeshttps://doi.org/10.56766/ntms.1419119openalex-snapshot
A Newly Defined Electromagnetic Dural Armor Functioned as a Brain Protecting Cerebrosphere: A Preliminary Theoretical Analysis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26944500openalex-snapshot
Additional file 1 of Pilot study of using transcranial temporal interfering theta-burst stimulation for modulating motor excitability in rat
inferred← citeshttps://doi.org/10.7554/elife.100941openalex-snapshot
Somatodendritic orientation determines tDCS-induced neuromodulation of Purkinje cell activity in awake mice
inferred← citeshttps://doi.org/10.7554/elife.100941.1openalex-snapshot
Somatodendritic orientation determines tDCS-induced neuromodulation of Purkinje cell activity in awake mice
inferred← citeshttps://doi.org/10.7554/elife.100941.2openalex-snapshot
Somatodendritic orientation determines tDCS-induced neuromodulation of Purkinje cell activity in awake mice
inferred← citeshttps://doi.org/10.7554/elife.100941.3openalex-snapshot
Somatodendritic orientation determines tDCS-induced neuromodulation of Purkinje cell activity in awake mice
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.