| scholarly article | Q13442814 |
| P50 | author | Michael Wibral | Q41047987 |
| P2093 | author name string | Christoph Bledowski | |
| David E J Linden | |||
| David Prvulovic | |||
| Rainer Goebel | |||
| Michael Scherg | |||
| Karsten Hoechstetter | |||
| P2860 | cites work | Control of goal-directed and stimulus-driven attention in the brain | Q27860553 |
| A common network of functional areas for attention and eye movements | Q28288177 | ||
| Localization of the event-related potential novelty response as defined by principal components analysis. | Q30336195 | ||
| The novelty P3: an event-related brain potential (ERP) sign of the brain's evaluation of novelty | Q30655847 | ||
| On the utility of P3 amplitude as a measure of processing capacity | Q33946593 | ||
| P300 as a clinical assay: rationale, evaluation, and findings | Q34057861 | ||
| Correlations and dissociations between BOLD signal and P300 amplitude in an auditory oddball task: a parametric approach to combining fMRI and ERP. | Q34143166 | ||
| Decreased response to novel stimuli after prefrontal lesions in man | Q34250075 | ||
| Contributions of temporal-parietal junction to the human auditory P3. | Q34551181 | ||
| Disruption of attention to novel events after frontal lobe injury in humans | Q35566427 | ||
| Separation and identification of event-related potential components by brain electric source analysis | Q37370990 | ||
| Dissociating the neural mechanisms of visual attention in change detection using functional MRI. | Q38438018 | ||
| The functional neuroanatomy of target detection: an fMRI study of visual and auditory oddball tasks | Q73279324 | ||
| Stimulus characteristics and task category dissociate the anterior and posterior aspects of the novelty P3 | Q73561362 | ||
| Dipolar source modeling of the P300 event-related potential after somatosensory stimulation | Q77359044 | ||
| Attentional systems in target and distractor processing: a combined ERP and fMRI study | Q80193073 | ||
| BESA source coherence: a new method to study cortical oscillatory coupling | Q80589203 | ||
| The functional neuroanatomy of novelty processing: integrating ERP and fMRI results | Q38448935 | ||
| Task-dependent field potentials in human hippocampal formation. | Q38481479 | ||
| Intracerebral potentials to rare target and distractor auditory and visual stimuli. II. Medial, lateral and posterior temporal lobe | Q38575462 | ||
| Intracerebral potentials to rare target and distractor auditory and visual stimuli. I. Superior temporal plane and parietal lobe | Q38575483 | ||
| Stimulus novelty, task relevance and the visual evoked potential in man. | Q39336825 | ||
| Functional magnetic resonance imaging of brain activity in the visual oddball task | Q44209162 | ||
| Contribution of human hippocampal region to novelty detection. | Q45976705 | ||
| The effect of task relevance on the cortical response to changes in visual and auditory stimuli: an event-related fMRI study. | Q46146927 | ||
| Anterior and posterior association cortex contributions to the somatosensory P300. | Q46189569 | ||
| Endogenous potentials after anterior temporal lobectomy | Q46192259 | ||
| P3a from visual stimuli: typicality, task, and topography | Q46456222 | ||
| Effects of choice complexity on different subcomponents of the late positive complex of the event-related potential | Q48170954 | ||
| Quantitative analysis of attention and detection signals during visual search. | Q48226832 | ||
| Combining electrophysiological and hemodynamic measures of the auditory oddball | Q48251805 | ||
| P300 from amnesic patients with bilateral hippocampal lesions | Q48281367 | ||
| Source localization of P300 from oddball, single stimulus, and omitted-stimulus paradigms | Q48311083 | ||
| Generators of the late cognitive potentials in auditory and visual oddball tasks | Q48393816 | ||
| The influence of stimulus deviance and novelty on the P300 and novelty P3. | Q48434266 | ||
| Investigating the generators of the scalp recorded visuo-verbal P300 using cortically constrained source localization. | Q48437331 | ||
| Reproducibility of the hemodynamic response to auditory oddball stimuli: a six-week test-retest study | Q48437339 | ||
| Differential effects of normal aging on sources of standard N1, target N1 and target P300 auditory event-related brain potentials revealed by low resolution electromagnetic tomography (LORETA). | Q48479856 | ||
| Functional imaging of mirror and inverse reading reveals separate coactivated networks for oculomotion and spatial transformations | Q48484155 | ||
| A MEG analysis of the P300 in visual discrimination tasks | Q48528224 | ||
| Functional imaging and localization of electromagnetic brain activity | Q48577728 | ||
| Two bilateral sources of the late AEP as identified by a spatio-temporal dipole model | Q48586673 | ||
| Combined event-related fMRI and EEG evidence for temporal-parietal cortex activation during target detection | Q48618125 | ||
| Dipole source analysis of P300 component of the auditory evoked potential: a methodological advance? | Q48705961 | ||
| P300 in patients with unilateral temporal lobectomies: the effects of reduced stimulus quality | Q48721967 | ||
| Infrequent events transiently activate human prefrontal and parietal cortex as measured by functional MRI. | Q48786473 | ||
| Sequence-sensitive subcomponents of P300: topographical analyses and dipole source localization | Q48813326 | ||
| Generators for human P300 elicited by somatosensory stimuli using multiple dipole source analysis | Q48877973 | ||
| Multiple dipole analysis of visual event-related potentials during oddball paradigm with silent counting | Q48918274 | ||
| Dipole-modeling of the visual evoked P300. | Q48970641 | ||
| Rapid prefrontal-hippocampal habituation to novel events. | Q52000072 | ||
| Multiple equivalent current dipole source localization of visual event-related potentials during oddball paradigm with motor response. | Q52027285 | ||
| Developmental evidence for modality-dependent P300 generators: a normative study. | Q52244354 | ||
| Electric source localization of the auditory P300 agrees with magnetic source localization | Q56895500 | ||
| Integration of fMRI and simultaneous EEG: towards a comprehensive understanding of localization and time-course of brain activity in target detection | Q58444374 | ||
| Evoked dipole source potentials of the human auditory cortex | Q68970928 | ||
| Auditory and visual P300s in temporal lobectomy patients: evidence for modality-dependent generators | Q69454113 | ||
| The P300 to novel and target events: a spatiotemporal dipole model analysis | Q71351256 | ||
| Intracerebral potentials to rare target and distractor auditory and visual stimuli. III. Frontal cortex | Q71690211 | ||
| Reduction of P3b in patients with temporo-parietal lesions | Q72447929 | ||
| The hippocampal formation as a source of the slow endogenous potentials | Q72692075 | ||
| New concepts of brain source imaging and localization | Q73130473 | ||
| P433 | issue | 42 | |
| P921 | main subject | functional magnetic resonance imaging | Q903809 |
| P304 | page(s) | 9353-9360 | |
| P577 | publication date | 2004-10-01 | |
| P1433 | published in | Journal of Neuroscience | Q1709864 |
| P1476 | title | Localizing P300 generators in visual target and distractor processing: a combined event-related potential and functional magnetic resonance imaging study | |
| P478 | volume | 24 |
| Q64059691 | "Hit the missing stimulus". A simultaneous EEG-fMRI study to localize the generators of endogenous ERPs in an omitted target paradigm |
| Q33639084 | A Comparative Study of Average, Linked Mastoid, and REST References for ERP Components Acquired during fMRI. |
| Q33770043 | A New Generation of Brain-Computer Interfaces Driven by Discovery of Latent EEG-fMRI Linkages Using Tensor Decomposition. |
| Q30446741 | A modified oddball paradigm for investigation of neural correlates of attention: a simultaneous ERP-fMRI study. |
| Q33856165 | A tactile P300 brain-computer interface |
| Q60306420 | Aberrant timing and oddball detection in Schizophrenia: findings from a signed differential mapping meta-analysis |
| Q46808350 | Acute and subchronic effects of amitriptyline on processing capacity in neuropathic pain patients using visual event-related potentials: preliminary findings |
| Q36332996 | Age-Related Inter-Region EEG Coupling Changes During the Control of Bottom-Up and Top-Down Attention |
| Q33874949 | Age-related frontoparietal changes during the control of bottom-up and top-down attention: an ERP study |
| Q59808082 | Aging of stimulus-driven and goal-directed attentional processes in young immigrants with long-term high altitude exposure in Tibet: An ERP study |
| Q37186475 | Altered prefrontal function with aging: insights into age-associated performance decline. |
| Q37040377 | Anger management: age differences in emotional modulation of visual processing. |
| Q34157628 | Assessing the spatiotemporal evolution of neuronal activation with single-trial event-related potentials and functional MRI. |
| Q80479899 | At your own peril: an ERP study of voluntary task set selection processes in the medial frontal cortex |
| Q46092771 | Attention in essential tremor: evidence from event-related potentials |
| Q89172112 | Attentional responses on an auditory oddball predict false memory susceptibility |
| Q61813297 | Brain Vital Signs: Expanding From the Auditory to Visual Modality |
| Q36879977 | Brain potentials distinguish new and studied objects during working memory |
| Q50879094 | Brain signatures of perceiving a smile: Time course and source localization. |
| Q36721856 | Capturing dynamic patterns of task-based functional connectivity with EEG. |
| Q30468476 | Causality in the association between P300 and alpha event-related desynchronization |
| Q64062853 | Challenges of P300 Modulation Using Transcranial Alternating Current Stimulation (tACS) |
| Q35998463 | Changes in P3b Latency and Amplitude Reflect Expertise Acquisition in a Football Visuomotor Learning Task |
| Q92503560 | Closed-loop digital meditation improves sustained attention in young adults |
| Q48235953 | Cognitive function, P3a/P3b brain potentials, and cortical thickness in aging |
| Q40939917 | Cognitive outcome and gamma noise power unrelated to neuregulin 1 and 3 variation in schizophrenia. |
| Q99371663 | Cognitive task-related functional connectivity alterations in temporal lobe epilepsy |
| Q33646988 | Coherent Activity in Bilateral Parieto-Occipital Cortices during P300-BCI Operation |
| Q27303961 | Comparison of auditory and visual oddball fMRI in schizophrenia |
| Q93014542 | Comparison of cognitive auditory event related potentials and executive functions in adolescent athletes and non-athletes - A cross sectional study |
| Q30404373 | Concurrent brain responses to separate auditory and visual targets |
| Q48122950 | Cross-modal attention capture by affective stimuli: evidence from event-related potentials |
| Q60801854 | Decreased entropy modulation of EEG response to novelty and relevance in schizophrenia during a P300 task |
| Q45906557 | Decreased spectral entropy modulation in patients with schizophrenia during a P300 task. |
| Q113504985 | Deep neural networks constrained by neural mass models improve electrophysiological source imaging of spatiotemporal brain dynamics |
| Q50317785 | Deficits of entropy modulation in schizophrenia are predicted by functional connectivity strength in the theta band and structural clustering. |
| Q89888868 | Deficits of entropy modulation of the EEG: A biomarker for altered function in schizophrenia and bipolar disorder? |
| Q30407504 | Development of behavioral parameters and ERPs in a novel-target visual detection paradigm in children, adolescents and young adults. |
| Q60919442 | Different Contexts in the Oddball Paradigm Induce Distinct Brain Networks in Generating the P300 |
| Q28654684 | Differential activation of human core, non-core and auditory-related cortex during speech categorization tasks as revealed by intracranial recordings |
| Q41887024 | Differential roles of the dorsal prefrontal and posterior parietal cortices in visual search: a TMS study |
| Q35000744 | Dipole source analysis of auditory P300 response in depressive and anxiety disorders |
| Q34873309 | Direction and magnitude of nicotine effects on the fMRI BOLD response are related to nicotine effects on behavioral performance |
| Q33744871 | Dynamic Responses in Brain Networks to Social Feedback: A Dual EEG Acquisition Study in Adolescent Couples |
| Q52647973 | EEG Correlates of Preparatory Orienting, Contextual Updating, and Inhibition of Sensory Processing in Left Spatial Neglect. |
| Q36060773 | EEG correlates of Fitts's law during preparation for action. |
| Q55483350 | Effect of task difficulty on blood-oxygen-level-dependent signal: A functional magnetic resonance imaging study in a motion discrimination task. |
| Q36088217 | Effect of the Green/Blue Flicker Matrix for P300-Based Brain-Computer Interface: An EEG-fMRI Study |
| Q33904930 | Effective connectivity analysis of fMRI and MEG data collected under identical paradigms |
| Q36698473 | Electrophysiological Correlates of Refreshing: Event-related Potentials Associated with Directing Reflective Attention to Face, Scene, or Word Representations |
| Q36476962 | Electrophysiological correlates of fearful and sad distraction on target processing in adolescents with attention deficit-hyperactivity symptoms and affective disorders |
| Q30474887 | Electrophysiological evidence for impaired attentional engagement with phonologically acceptable misspellings in developmental dyslexia |
| Q48937005 | Elevated midline-parietal gamma band noise power in schizophrenia but not in bipolar patients. |
| Q57989564 | Emerging Neurotechnologies for Lie-Detection: Promises and Perils |
| Q52657206 | Event-Related Potentials during a Gambling Task in Young Adults with Attention-Deficit/Hyperactivity Disorder. |
| Q33667617 | Evidence for a Priori Existence of Attentional Bias Subgroups in Emotional Processing of Aversive Stimuli |
| Q51603329 | Exploring the detection of associatively novel events using fMRI. |
| Q48532032 | Fast optical imaging of frontal cortex during active and passive oddball tasks. |
| Q48416867 | Frontoparietal activity with minimal decision and control. |
| Q33906488 | Functional fractionation of the stimulus-driven attention network. |
| Q30486072 | Hemispheric differences in hemodynamics elicited by auditory oddball stimuli |
| Q35681232 | Impaired Early Attentional Processes in Parkinson's Disease: A High-Resolution Event-Related Potentials Study |
| Q38971128 | Impaired auditory-to-motor entrainment in Parkinson's disease |
| Q36005051 | Impaired target detection in schizophrenia and the ventral attentional network: Findings from a joint event-related potential-functional MRI analysis |
| Q64102582 | Increased Neural Activity in Hazardous Drinkers During High Workload in a Visual Working Memory Task: A Preliminary Assessment Through Event-Related Potentials |
| Q30489024 | Increased brain activation during the processing of spatially invalidly cued targets |
| Q83061355 | Involvement of the subthalamic nucleus and globus pallidus internus in attention |
| Q42597485 | Large-scale brain networks account for sustained and transient activity during target detection |
| Q47382551 | Mechanisms for attentional modulation by threatening emotions of fear, anger, and disgust |
| Q51922208 | Mental chronometry of working memory retrieval: a combined functional magnetic resonance imaging and event-related potentials approach. |
| Q21563595 | Mental training affects distribution of limited brain resources |
| Q60920699 | Mimicking Schizophrenia: Reducing P300b by Minimally Fragmenting Healthy Participants' Selves Using Immersive Virtual Reality Embodiment |
| Q57176442 | Mindfulness-based training with transcranial direct current stimulation modulates neuronal resource allocation in working memory: A randomized pilot study with a nonequivalent control group |
| Q33975747 | Modulation of the cortical processing of novel and target stimuli by drugs affecting glutamate and GABA neurotransmission |
| Q30475698 | Multi-set canonical correlation analysis for the fusion of concurrent single trial ERP and functional MRI. |
| Q30353804 | Musical experts recruit action-related neural structures in harmonic anomaly detection: evidence for embodied cognition in expertise |
| Q28109670 | Neural Correlates of Attention to Human-Made Sounds: An ERP Study |
| Q58754479 | Neural Correlates of Conscious Motion Perception |
| Q41462922 | Neural Signatures of Rational and Heuristic Choice Strategies: A Single Trial ERP Analysis |
| Q27333105 | Neural correlates of auditory perceptual awareness under informational masking |
| Q90471904 | Neural dynamics of grip and goal integration during the processing of others' actions with objects: An ERP study |
| Q37359175 | Neural generators of ERPs linked with Necker cube reversals |
| Q43908407 | Neural markers of automatic and controlled attention during immediate and delayed action |
| Q91962988 | Neural signatures of reward and sensory error feedback processing in motor learning |
| Q37471945 | Neural signatures of stimulus features in visual working memory--a spatiotemporal approach. |
| Q35122602 | Neuroanatomical distinctions within the semantic system during sentence comprehension: evidence from functional magnetic resonance imaging |
| Q30488646 | Neurophysiological endophenotypes across bipolar and schizophrenia psychosis |
| Q37153318 | No Effect of Anodal Transcranial Direct Current Stimulation Over the Motor Cortex on Response-Related ERPs during a Conflict Task. |
| Q37244218 | One-year developmental stability and covariance among oddball, novelty, go/no-go, and flanker event-related potentials in adolescence: A monozygotic twin study |
| Q36944158 | Opposite neural signatures of motion-induced blindness in human dorsal and ventral visual cortex |
| Q44447818 | P300 deficits in adults with attention deficit hyperactivity disorder: a meta-analysis. |
| Q30417341 | P300 event-related potential as an indicator of inattentional deafness? |
| Q35928748 | Posttraumatic stress disorder is associated with limited executive resources in a working memory task |
| Q35096525 | Progressive reduction of visual P300 amplitude in patients with first-episode schizophrenia: an ERP study |
| Q48889295 | Pupil diameter covaries with BOLD activity in human locus coeruleus |
| Q37426687 | Re-evaluating the role of TPJ in attentional control: contextual updating? |
| Q92141067 | Reduced influence of perceptual context in schizophrenia: behavioral and neurophysiological evidence |
| Q88251666 | Relations between structural and EEG-based graph metrics in healthy controls and schizophrenia patients |
| Q90471935 | Resting-state EEG activity predicts frontoparietal network reconfiguration and improved attentional performance |
| Q37509924 | Robust single trial identification of conscious percepts triggered by sensory events of variable saliency. |
| Q28730890 | Role of basal ganglia circuits in resisting interference by distracters: a swLORETA study |
| Q33976542 | Role of frontal and parietal cortices in the control of bottom-up and top-down attention in humans |
| Q30465170 | Sequential temporo-fronto-temporal activation during monitoring of the auditory environment for temporal patterns |
| Q24278596 | Simultaneous EEG-fMRI reveals a temporal cascade of task-related and default-mode activations during a simple target detection task |
| Q24276753 | Simultaneous EEG-fMRI reveals temporal evolution of coupling between supramodal cortical attention networks and the brainstem |
| Q30480289 | Single-trial discrimination for integrating simultaneous EEG and fMRI: identifying cortical areas contributing to trial-to-trial variability in the auditory oddball task |
| Q30826616 | Somato-motor inhibitory processing in humans: evidence from neurophysiology and neuroimaging |
| Q36310408 | Source analysis of P3a and P3b components to investigate interaction of depression and anxiety in attentional systems. |
| Q33831042 | Spatial attention effects of disgusted and fearful faces |
| Q46614467 | Spatial distribution and cognitive correlates of gamma noise power in schizophrenia. |
| Q36813851 | Stimulus sequence context differentially modulates inhibition-related theta and delta band activity in a go/no-go task |
| Q35158984 | Structural integrity of the prefrontal cortex modulates electrocortical sensitivity to reward. |
| Q58699586 | Successful Encoding during Natural Reading Is Associated with Fixation-Related Potentials and Large-Scale Network Deactivation |
| Q90224465 | Target-related parietal P3 and medial frontal theta index the genetic risk for problematic substance use |
| Q30500196 | Temporal dynamics of selective attention and conflict resolution during cross-dimensional Go-NoGo decisions |
| Q30845694 | The Role of Associative Cortices and Hippocampus during Movement Perturbations |
| Q30490351 | The effects of HIV on P300 are moderated by familial risk for substance dependence: implications for a theory of brain reserve |
| Q36381095 | The fixation and saccade P3. |
| Q36887537 | The neural basis of visual body perception. |
| Q92058186 | The reduced left hippocampal volume related to the delayed P300 latency in amnestic mild cognitive impairment |
| Q51575296 | The relationship between reaction time and response variability and somatosensory No-go potentials. |
| Q89983411 | The response relevance of visual stimuli modulates the P3 component and the underlying sensorimotor network |
| Q30488103 | The timing of feedback to early visual cortex in the perception of long-range apparent motion |
| Q48330366 | Theta- and delta-band EEG network dynamics during a novelty oddball task |
| Q30498166 | Time course of electromagnetic activity associated with detection of rare events. |
| Q30828674 | Timing and sequence of brain activity in top-down control of visual-spatial attention |
| Q64086695 | To integrate or not to integrate: Temporal dynamics of hierarchical Bayesian causal inference |
| Q55331724 | Top-Down Disconnectivity in Schizophrenia During P300 Tasks. |
| Q48111848 | Topography of activation deficits in schizophrenia during P300 task related to cognition and structural connectivity. |
| Q34863548 | Towards intelligent environments: an augmented reality-brain-machine interface operated with a see-through head-mount display |
| Q92892265 | Transcranial Alternating Current Stimulation (tACS) as a Tool to Modulate P300 Amplitude in Attention Deficit Hyperactivity Disorder (ADHD): Preliminary Findings |
| Q30373274 | Transient Distraction and Attentional Control during a Sustained Selective Attention Task. |
| Q50069287 | Transient and sustained incentive effects on electrophysiological indices of cognitive control in younger and older adults |
| Q48169437 | Tuned by experience: How orientation probability modulates early perceptual processing |
| Q45216754 | Two P300 generators in the hippocampal formation. |
| Q24645237 | Updating P300: an integrative theory of P3a and P3b |
| Q34005750 | Updating of context in working memory: an event-related potential study |
| Q51613333 | Variation at NRG1 genotype related to modulation of small-world properties of the functional cortical network. |
| Q30536336 | Visual event-related potentials as markers of hyperarousal in Gulf War illness: evidence against a stress-related etiology |
| Q37068093 | Visual motion event related potentials distinguish aging and Alzheimer's disease |
| Q55453357 | Visual target modulation of functional connectivity networks revealed by self-organizing group ICA |
| Q36959150 | Working memory load for faces modulates P300, N170, and N250r |
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