Theta and delta band activity explain N2 and P3 ERP component activity in a go/no-go task.
- Authors
- Harper, Jeremy; Malone, Stephen M; Bernat, Edward M
- Year
- 2014
- Journal
- Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
- PMID
- 23891195
- DOI
- 10.1016/j.clinph.2013.06.025
- PMCID
- PMC4312493
OBJECTIVES: Recent work indicates that the feedback negativity and P3 components from gambling feedback tasks can be understood as mixtures of functionally distinct processes occurring separately in theta and delta frequency bands. The current study was conducted to assess whether dissociable processes occurring in the theta and delta bands would similarly account for activity underlying N2 and P3 components in a go/no-go task. METHODS: The current study measured EEG signals from 66 participants during a go/no-go task, and a time-frequency principal components analysis decomposition approach was used to extract theta and delta measures from condition averages. RESULTS: Theta and delta measures separately increased in relation to response inhibition, and were uniquely related to the N2 and P3 components, as predicted. CONCLUSIONS: Findings support the view that the theta and delta measures indexed separable processes related to response inhibition, and better indexed the processes underlying N2 and P3 components in this go/no-go task. SIGNIFICANCE: Theta and delta measures may index separable functional processes across other common ERP tasks, and may represent an improved target for research relative to standard time-domain components.
Channel layout of the Neuroscan 128-Channel NSL Quik-Cap. Clusters of channels used for statistical analysis are highlighted. Red: Frontal cluster for theta; blue: central cluster for delta; channels within green oval: fronto-central cluster for N2 and P3 ERPs.
Time-domain and time-frequency (TF) decomposition of stimulus-locked ERPs. All ERPs and TF representations are plotted as the average across corresponding channel clusters (see Figure 1). Row A, waveform plot. Averaged unfiltered stimulus-locked ERP across all trials. TF-representation plot. Averaged unfiltered TF representation of the ERP across all trials. Row B, waveform plots. Averaged ERP activity across all trials, frequency-filtered using a 3rd order Butterworth filter to isolate higher-frequency (1.5 Hz highpass) and lower frequency (1.5 Hz lowpass) activity. TF representation plots. TF representations of the high- and low-frequency data principal component scores across all trials, sorted by percentage variance accounted for post-Varimax rotation. Topographic maps. Scalp topography distributions for the mean of the TF-PCA energy for each TF representation. For the high-frequency data the first PC has a frontal distribution, while the second PC has a mixture of bilateral occipital and frontal distributions. The first two PCs for the low-frequency data share a centro-parietal distribution, while the third PC is mainly frontal.
Time-domain and time-frequency (TF) representations of the no-go minus go differences. All signals and TF-representations are plotted as the average across corresponding channel clusters (see Figure 1). Row A, waveform plot. Averaged unfiltered stimulus-locked ERPs for no-go (red) and go (blue) trials separately. Evident on the no-go trials is the negativity peaking around ~300 ms (no-go N2) and the subsequent positivity (no-go P3). Row B, waveform plots. Average ERPs for no-go and go trials separately, frequency filtered with a 3rd order Butterworth filter to capture the activity in the theta and delta TF-energy PCs (3.25-4.75 and 0.5-1.0 Hz, respectively). These plots depict the increase for no-go activity in both theta and delta frequency bands. TF representation plots. No-go minus go difference representations for the PCs loadings of averaged TF activity. Again, both theta and delta are sensitive to no-go stimuli. Colored topographic maps. Scalp topography for the mean no-go minus go difference of the TF-PCA loadings for theta and delta. Increased no-go theta is maximal at frontal sites, while delta has a more centro-parietal increase for no-go stimuli. Grayscale topographic maps. These topographic maps depict the statistical significance of the no-go minus go Wilcoxon Signed-Ranks test for each channel, where theta showed the most significance for frontal channels and the difference in delta was maximal at central-parietal sites.
No entities extracted from this document yet.
No uploaded files.
In this knowledge base
| Title | Year | PMID |
|---|---|---|
| A KCNJ6 gene polymorphism modulates theta oscillations during reward processing. | 2017 | 27993610 |
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| A mega-analysis of EEG-based frontal-midline theta neurofeedback reveals learning dynamics, individual variability, and response profiles. | Enriquez-Geppert S et al. | β | 2026 | β |
| Biomarkers for Alzheimer's disease and mild cognitive impairment: Recent advances in task-based EEG. | Tripanpitak K et al. | β | 2026 | β |
| Enhanced visual and auditory inhibitory control in musicians: EEG evidence. | Liu Y et al. | β | 2026 | β |
| Neural mechanisms of response inhibition impairments in patients with perimenopausal insomnia. | Hu D et al. | β | 2026 | β |
| Distinctive Delta and Theta Responses in Deductive and Probabilistic Reasoning. | Sevim EF et al. | β | 2025 | β |
| EEG time-frequency dynamics of early cognitive control development. | Morales S et al. | β | 2025 | β |
| Impact of Transcutaneous Vagus Nerve Stimulation on Event-related Potentials during a Response Inhibition Task. | Li P et al. | β | 2025 | β |
| Impaired response inhibition to negative emotional stimuli in depressed adolescents with non-suicidal self-injury: a neurophysiological perspective. | Zhao L et al. | β | 2025 | β |
| Neural representation of consciously seen and unseen information. | RodrΓguez-San Esteban P et al. | β | 2025 | β |
| Response Inhibition in Children With ADHD: A Time Domain and Time-Frequency Domain Analysis Study. | Zhang Z et al. | β | 2025 | β |
| Short-term recovery sleep attenuates the impairment of response inhibition after total sleep deprivation: Evidence from an event-related potentials study. | Zhang N et al. | β | 2025 | β |
| The N2 During Preschool: Temporal Stability and a Test of Bidirectional Effects With Maternal Emotion Characteristics in a White, European-American Sample. | Akbaryan A et al. | β | 2025 | β |
| Aggressiveness, inhibitory control, and emotional states: A provocation paradigm. | Sebalo I et al. | β | 2024 | β |
| Aperiodic and periodic components of oscillatory brain activity in relation to cognition and symptoms in pediatric ADHD. | Dakwar-Kawar O et al. | β | 2024 | β |
| Cardiac-Sympathetic Contractility and Neural Alpha-Band Power: Cross-Modal Collaboration during Approach-Avoidance Conflict. | Dundon NM et al. | β | 2024 | β |
| Effect of food stimuli presentation on restrained eater's food choice: An ERP study. | Liu Y et al. | β | 2024 | β |
| Emotional arousal pattern (EMAP): A new database for modeling momentary subjective and psychophysiological responding to affective stimuli. | Eisenbarth H et al. | β | 2024 | β |
| Inhibitory control of gait initiation in humans: An electroencephalography study. | Ziri D et al. | β | 2024 | β |
| Integrating EEG biomarkers in the neurocognitive screening of executive functions in substance and behavioral addiction. | Balconi M et al. | β | 2024 | β |
| Interference Control Under the Stroop Task and Brain Oscillatory Activity among Internet Addicts Compared to Non-addicts. | Rostami F et al. | β | 2024 | β |
| Machine learning reveals differential effects of depression and anxiety on reward and punishment processing. | Grabowska A et al. | β | 2024 | β |
| P300 intention recognition based on phase lag index (PLI)-rich-club brain functional network. | Wang Z et al. | β | 2024 | β |
| Shared Psychophysiological Electroencephalographic Features in Maltreated Adolescent Siblings and Twins: A Case Report. | Marcu GM et al. | β | 2024 | β |
| Tactile imagery affects cortical responses to vibrotactile stimulation of the fingertip. | Morozova M et al. | β | 2024 | β |
| The human brain deals with violating general color or depth knowledge in different time courses. | Tang X et al. | β | 2024 | β |
| Theta oscillations within right dorsolateral prefrontal cortex contribute differently to speech versus limb inhibition. | Johari K et al. | β | 2024 | β |
| Transcranial Direct Current Stimulation Decreases P3 Amplitude and Inherent Delta Activity during a Waiting Impulsivity Paradigm: Crossover Study. | Mendes AJ et al. | β | 2024 | β |
| Changing connectivity between premotor and motor cortex changes inter-areal communication in the human brain. | Trajkovic J et al. | β | 2023 | β |
| Development is in the details: Event-related theta oscillations reveal children and adults verify multiplication facts differently. | Wood M et al. | β | 2023 | β |
| Discrimination of auditory verbal hallucination in schizophrenia based on EEG brain networks. | Wang J et al. | β | 2023 | β |
| ERP-aligned delta transcranial alternating current stimulation modulates the P3 amplitude. | Boetzel C et al. | β | 2023 | β |
| Hemispheric asymmetry in the processing of an emotional working memory task. | Abril-Ronderos JP et al. | β | 2023 | β |
| Long-term resting EEG correlates of repetitive mild traumatic brain injury and loss of consciousness: alterations in alpha-beta power. | Franke LM et al. | β | 2023 | β |
| Neural correlates of perceptual texture change during active touch. | Henderson J et al. | β | 2023 | β |
| Resting-state EEG delta and alpha power predict response to cognitive behavioral therapy in depression: a Canadian biomarker integration network for depression study. | Schwartzmann B et al. | β | 2023 | β |
| Social approach and avoidance in language: N400-like ERP negativity indexes congruency and theta rhythms the conflict. | Marrero H et al. | β | 2023 | β |
| Task-Related Reorganization of Cognitive Network in Parkinson's Disease Using Electrophysiology. | Bar-On M et al. | β | 2023 | β |
| The contribution of theta and delta to feedback processing in children with developmental language disorder. | Gul A et al. | β | 2023 | β |
| The Relationship between Formal Music Training and Conflict Control: An ERP Study. | Hao J et al. | β | 2023 | β |
| Alpha and Theta Bands Dynamics Serve Distinct Functions during Perception-Action Integration in Response Inhibition. | Prochnow A et al. | β | 2022 | β |
| A practical introduction to EEG Time-Frequency Principal Components Analysis (TF-PCA). | Buzzell GA et al. | β | 2022 | β |
| A study of longitudinal trends in time-frequency transformations of EEG data during a learning experiment. | Boland J et al. | β | 2022 | β |
| Dynamic networks of P300-related process. | Tao Q et al. | β | 2022 | β |
| Electrophysiological signatures of inhibitory control in children with Tourette syndrome and attention-deficit/hyperactivity disorder. | Morand-Beaulieu S et al. | β | 2022 | β |
| Impaired Inhibitory Control During Walking in Parkinson's Disease Patients: An EEG Study. | Sosnik R et al. | β | 2022 | β |
| Machine Learning Based on Event-Related EEG of Sustained Attention Differentiates Adults with Chronic High-Altitude Exposure from Healthy Controls. | Liu H et al. | β | 2022 | β |
| Multidimensional inhibitory signatures of sentential negation in behavioral variant frontotemporal dementia. | DΓaz-Rivera MN et al. | β | 2022 | β |
| Music training modulates theta brain oscillations associated with response suppression. | Lu J et al. | β | 2022 | β |
| Pre-trial fronto-occipital electrophysiological connectivity affects perception-action integration in response inhibition. | Prochnow A et al. | β | 2022 | β |
| Recommendations and publication guidelines for studies using frequency domain and time-frequency domain analyses of neural time series. | Keil A et al. | β | 2022 | β |
| Resting-state theta activity is linked to information content-specific coding levels during response inhibition. | Pscherer C et al. | β | 2022 | β |
| Sequential gains and losses during gambling feedback: Differential effects in time-frequency delta and theta measures. | Bachman MD et al. | β | 2022 | β |
| Slow-Wave EEG Activity Correlates with Impaired Inhibitory Control in Internet Addiction Disorder. | Qi Y et al. | β | 2022 | β |
| To see, not to see or to see poorly: Perceptual quality and guess rate as a function of electroencephalography (EEG) brain activity in an orientation perception task. | Sheldon SS et al. | β | 2022 | β |
| Aiming at ecological validity-Midfrontal theta oscillations in a toy gun shooting task. | Lange L et al. | β | 2021 | β |
| Alteration of Behavioral Inhibitory Control in High-Altitude Immigrants. | Wang J et al. | β | 2021 | β |
| Behavioral and electrocortical effects of transcranial alternating current stimulation during advice-guided decision-making. | Wischnewski M et al. | β | 2021 | β |
| Blind Visualization of Task-Related Networks From Visual Oddball Simultaneous EEG-fMRI Data: Spectral or Spatiospectral Model? | Labounek R et al. | β | 2021 | β |
| Dissociable neural oscillatory mechanisms underlying unconscious priming of externally and intentionally initiated inhibition. | Diao L et al. | β | 2021 | β |
| Electrophysiological biomarkers of behavioral dimensions from cross-species paradigms. | Cavanagh JF et al. | β | 2021 | β |
| Emotional reactivity, suppression of emotions and response inhibition in emotional eaters: A multi-method pilot study. | Wolz I et al. | β | 2021 | β |
| Exploring a sustainable building's impact on occupant mental health and cognitive function in a virtual environment. | Hu M et al. | β | 2021 | β |
| Increasing and decreasing interregional brain coupling increases and decreases oscillatory activity in the human brain. | Sel A et al. | β | 2021 | β |
| Learning something new versus changing your ways: Distinct effects on midfrontal oscillations and cardiac activity for learning and flexible adjustments. | Kaiser J et al. | β | 2021 | β |
| Midfrontal theta as moderator between beta oscillations and precision control. | Watanabe T et al. | β | 2021 | β |
| Midfrontal theta oscillations and conflict monitoring in children and adults. | Chevalier N et al. | β | 2021 | β |
| Persistence of the "Moving Things Are Alive" Heuristic into Adulthood: Evidence from EEG. | Skelling-Desmeules Y et al. | β | 2021 | β |
| Psychopathic traits, inhibition, and positive and negative emotion: Results from an emotional Go/No-Go task. | Fournier LF et al. | β | 2021 | β |
| The influence of monetary reward on proactive and reactive control in adolescent males. | Bowers ME et al. | β | 2021 | β |
| Tool use and function knowledge shape visual object processing. | Foerster FR et al. | β | 2021 | β |
| Acute Aerobic Exercise Ameliorates Cravings and Inhibitory Control in Heroin Addicts: Evidence From Event-Related Potentials and Frequency Bands. | Wang D et al. | β | 2020 | β |
| Acute Alcohol Effects on Response Inhibition Depend on Response Automatization, but not on GABA or Glutamate Levels in the ACC and Striatum. | Bensmann W et al. | β | 2020 | β |
| Comparison of Intentional Inhibition and Reactive Inhibition in Adolescents and Adults: An ERP Study. | Shen Y et al. | β | 2020 | β |
| Delta phase reset predicts conflict-related changes in P3 amplitude and behavior. | Rawls E et al. | β | 2020 | β |
| Electroencephalographic characteristics of word finding during phonological and semantic verbal fluency tasks. | Mousavi N et al. | β | 2020 | β |
| Electroencephalography reveals a selective disruption of cognitive control processes in craving cigarette smokers. | Donohue SE et al. | β | 2020 | β |
| Inter-subject P300 variability relates to the efficiency of brain networks reconfigured from resting- to task-state: Evidence from a simultaneous event-related EEG-fMRI study. | Li F et al. | β | 2020 | β |
| Long-term limb immobilization modulates inhibition-related electrophysiological brain activity. | Bruno V et al. | β | 2020 | β |
| Multi-domain Features of the Non-phase-locked Component of Interest Extracted from ERP Data by Tensor Decomposition. | Zhang G et al. | β | 2020 | β |
| Multivariate Pattern Analysis Techniques for Electroencephalography Data to Study Flanker Interference Effects. | LΓ³pez-GarcΓa D et al. | β | 2020 | β |
| Neural dynamics of executive function in cognitively able kindergarteners with autism spectrum disorders as predictors of concurrent academic achievement. | Kim SH et al. | β | 2020 | β |
| Objective Extraction of Evoked Event-Related Oscillation from Time-Frequency Representation of Event-Related Potentials. | Zhang G et al. | β | 2020 | β |
| Pre-trial theta band activity in the ventromedial prefrontal cortex correlates with inhibition-related theta band activity in the right inferior frontal cortex. | AdelhΓΆfer N et al. | β | 2020 | β |
| Response inhibition alterations in migraine: evidence from event-related potentials and evoked oscillations. | Chen G et al. | β | 2020 | β |
| Resting theta activity is associated with specific coding levels in event-related theta activity during conflict monitoring. | Pscherer C et al. | β | 2020 | β |
| Adolescent cognitive control, theta oscillations, and social observation. | Buzzell GA et al. | β | 2019 | β |
| Anodal tDCS affects neuromodulatory effects of the norepinephrine system on superior frontal theta activity during response inhibition. | AdelhΓΆfer N et al. | β | 2019 | β |
| Beneficial effects of acute high-intensity exercise on electrophysiological indices of attention processes in young adult men. | Du Rietz E et al. | β | 2019 | β |
| Body representations as indexed by oscillatory EEG activities in the context of tactile novelty processing. | Shen G et al. | β | 2019 | β |
| Brain Electrical Activity Associated With Visual Attention and Reactive Motor Inhibition in Patients With Fibromyalgia. | GonzΓ‘lez-Villar AJ et al. | β | 2019 | β |
| Brain Inhibitory Mechanisms Are Involved in the Processing of Sentential Negation, Regardless of Its Content. Evidence From EEG Theta and Beta Rhythms. | BeltrΓ‘n D et al. | β | 2019 | β |
| EEG-ERP dynamics in a visual Continuous Performance Test. | Karamacoska D et al. | β | 2019 | β |
| Immediate versus delayed control demands elicit distinct mechanisms for instantiating proactive control. | Janowich JR et al. | β | 2019 | β |
| Left-Hemispheric Asymmetry for Object-Based Attention: an ERP Study. | Orlandi A et al. | β | 2019 | β |
| Long-term impact of prenatal exposure to chemotherapy on executive functioning: An ERP study. | Blommaert J et al. | β | 2019 | β |
| Midfrontal neural dynamics distinguish between general control and inhibition-specific processes in the stopping of motor actions. | Kaiser J et al. | β | 2019 | β |
| Multivariate pattern analysis techniques for electroencephalography data to study interference effects | LΓ³pez-GarcΓa D et al. | β | 2019 | β |
| Neither wrong nor right: Theta and delta power increase during performance monitoring under conditions of uncertainty. | Sandre A et al. | β | 2019 | β |
| Neural Evidence of Superior Memory: How to Capture Brain Activities of Encoding Processes Underlying Superior Memory. | Yoon JS et al. | β | 2019 | β |
| On the interrelation of 1/<i>f</i> neural noise and norepinephrine system activity during motor response inhibition. | Pertermann M et al. | β | 2019 | β |
| On the relevance of EEG resting theta activity for the neurophysiological dynamics underlying motor inhibitory control. | Pscherer C et al. | β | 2019 | β |
| Single-trial EEG dissociates motivation and conflict processes during decision-making under risk. | Pornpattananangkul N et al. | β | 2019 | β |
| The Modulation of Neural Noise Underlies the Effectiveness of Methylphenidate Treatment in Attention-Deficit/Hyperactivity Disorder. | Pertermann M et al. | β | 2019 | β |
| The Presynaptic Regulation of Dopamine and Norepinephrine Synthesis Has Dissociable Effects on Different Kinds of Cognitive Conflicts. | Bensmann W et al. | β | 2019 | β |
| Anger Weakens Behavioral Inhibition Selectively in Contact Athletes. | Xia X et al. | β | 2018 | β |
| Anxiety and feedback processing in a gambling task: Contributions of time-frequency theta and delta. | Ellis JS et al. | β | 2018 | β |
| Decreased occipital alpha oscillation in children who stutter during a visual Go/Nogo task. | Piispala J et al. | β | 2018 | β |
| Different Contexts in the Oddball Paradigm Induce Distinct Brain Networks in Generating the P300. | Li F et al. | β | 2018 | β |
| Effects of reward context on feedback processing as indexed by time-frequency analysis. | Watts ATM et al. | β | 2018 | β |
| Evidence for a neural dual-process account for adverse effects of cognitive control. | Zink N et al. | β | 2018 | β |
| Impact of alcohol use on EEG dynamics of response inhibition: a cotwin control analysis. | Harper J et al. | β | 2018 | β |
| Independent contributions of theta and delta time-frequency activity to the visual oddball P3b. | Bachman MD et al. | β | 2018 | β |
| Machine learning provides novel neurophysiological features that predict performance to inhibit automated responses. | Vahid A et al. | β | 2018 | β |
| Pain Expressions and Inhibitory Control in Patients With Fibromyalgia: Behavioral and Neural Correlates. | Pidal-Miranda M et al. | β | 2018 | β |
| Predictions through evidence accumulation over time. | Darriba Γ et al. | β | 2018 | β |
| Sentential negation modulates inhibition in a stop-signal task. Evidence from behavioral and ERP data. | BeltrΓ‘n D et al. | β | 2018 | β |
| Utilizing time-frequency amplitude and phase synchrony measure to assess feedback processing in a gambling task. | Watts ATM et al. | β | 2018 | β |
| A brief historical perspective on the advent of brain oscillations in the biological and psychological disciplines. | KarakaΕ S et al. | β | 2017 | β |
| A KCNJ6 gene polymorphism modulates theta oscillations during reward processing. | Kamarajan C et al. | β | 2017 | β |
| Appetitive and aversive motivation in dysphoria: A time-domain and time-frequency study of response inhibition. | Messerotti Benvenuti S et al. | β | 2017 | β |
| Binge drinking affects brain oscillations linked to motor inhibition and execution. | LΓ³pez-Caneda E et al. | β | 2017 | β |
| Brain electrical activity signatures during performance of the Multisource Interference Task. | GonzΓ‘lez-Villar AJ et al. | β | 2017 | β |
| Defining the Neural Substrate of the Adult Outcome of Childhood ADHD: A Multimodal Neuroimaging Study of Response Inhibition. | Szekely E et al. | β | 2017 | β |
| Demands on response inhibition processes determine modulations of theta band activity in superior frontal areas and correlations with pupillometry - Implications for the norepinephrine system during inhibitory control. | Dippel G et al. | β | 2017 | β |
| Effects on P3 of spreading targets and response prompts apart. | Verleger R et al. | β | 2017 | β |
| Expectancy effects in feedback processing are explained primarily by time-frequency delta not theta. | Watts ATM et al. | β | 2017 | β |
| Performance on emotional tasks engaging cognitive control depends on emotional intelligence abilities: an ERP study. | MegΓas A et al. | β | 2017 | β |
| Proactive Control: Neural Oscillatory Correlates of Conflict Anticipation and Response Slowing. | Chang A et al. | β | 2017 | β |
| The relationship between ERP components and EEG spatial complexity in a visual Go/Nogo task. | Jia H et al. | β | 2017 | β |
| Theta- and delta-band EEG network dynamics during a novelty oddball task. | Harper J et al. | β | 2017 | β |
| The two faces of avoidance: Time-frequency correlates of motivational disposition in blood phobia. | Mennella R et al. | β | 2017 | β |
| Time-frequency phase-synchrony approaches with ERPs. | Aviyente S et al. | β | 2017 | β |
| Web addiction in the brain: Cortical oscillations, autonomic activity, and behavioral measures. | Balconi M et al. | β | 2017 | β |
| Attentional gain and processing capacity limits predict the propensity to neglect unexpected visual stimuli. | Papera M et al. | β | 2016 | β |
| Brain and behavioral inhibitory control of kindergartners facing negative emotions. | Farbiash T et al. | β | 2016 | β |
| Concurrent information affects response inhibition processes via the modulation of theta oscillations in cognitive control networks. | Chmielewski WX et al. | β | 2016 | β |
| Contextually sensitive power changes across multiple frequency bands underpin cognitive control. | Cooper PS et al. | β | 2016 | β |
| Deficit in rewarding mechanisms and prefrontal left/right cortical effect in vulnerability for internet addiction. | Balconi M et al. | β | 2016 | β |
| Gender-related Differences in Inhibitory Control and Sustained Attention among Adolescents with Prenatal Cocaine Exposure. | Banz BC et al. | β | 2016 | β |
| Is P3 a strategic or a tactical component? Relationships of P3 sub-components to response times in oddball tasks with go, no-go and choice responses. | Verleger R et al. | β | 2016 | β |
| Multiple Language Use Influences Oculomotor Task Performance: Neurophysiological Evidence of a Shared Substrate between Language and Motor Control. | Heidlmayr K et al. | β | 2016 | β |
| Neural correlates of multimodal metaphor comprehension: Evidence from event-related potentials and time-frequency decompositions. | Ma Q et al. | β | 2016 | β |
| Neuroimaging measures of error-processing: Extracting reliable signals from event-related potentials and functional magnetic resonance imaging. | Steele VR et al. | β | 2016 | β |
| Response mode-dependent differences in neurofunctional networks during response inhibition: an EEG-beamforming study. | Dippel G et al. | β | 2016 | β |
| Review of evoked and event-related delta responses in the human brain. | GΓΌntekin B et al. | β | 2016 | β |
| Sentential Negation Might Share Neurophysiological Mechanisms with Action Inhibition. Evidence from Frontal Theta Rhythm. | de Vega M et al. | β | 2016 | β |
| Single Trial EEG Patterns for the Prediction of Individual Differences in Fluid Intelligence. | Qazi EU et al. | β | 2016 | β |
| Stimulus sequence context differentially modulates inhibition-related theta and delta band activity in a go/no-go task. | Harper J et al. | β | 2016 | β |
| When the brain simulates stopping: Neural activity recorded during real and imagined stop-signal tasks. | GonzΓ‘lez-Villar AJ et al. | β | 2016 | β |
| Anterior cingulate activity to monetary loss and basal ganglia activity to monetary gain uniquely contribute to the feedback negativity. | Foti D et al. | β | 2015 | β |
| Complementary roles of cortical oscillations in automatic and controlled processing during rapid serial tasks. | Isabella S et al. | β | 2015 | β |
| Deficient Event-Related Theta Oscillations in Individuals at Risk for Alcoholism: A Study of Reward Processing and Impulsivity Features. | Kamarajan C et al. | β | 2015 | β |
| Feature extraction and classification for EEG signals using wavelet transform and machine learning techniques. | Amin HU et al. | β | 2015 | β |
| Neurofeedback and its possible relevance for the treatment of Tourette syndrome. | Farkas A et al. | β | 2015 | β |
| Time-frequency theta and delta measures index separable components of feedback processing in a gambling task. | Bernat EM et al. | β | 2015 | β |
| Time-frequency analysis of the event-related potentials associated with the Stroop test. | Ergen M et al. | β | 2014 | β |
| When holding your horses meets the deer in the headlights: time-frequency characteristics of global and selective stopping under conditions of proactive and reactive control. | Lavallee CF et al. | β | 2014 | β |
| Midfrontal conflict-related theta-band power reflects neural oscillations that predict behavior. | Cohen MX et al. | β | 2013 | β |
| Reduced negative affect response in female psychopaths. | Eisenbarth H et al. | β | 2013 | β |