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| Q34984088 | Absent event-related potential (ERP) word repetition effects in mild Alzheimer's disease |
| Q48485478 | Age and novelty: event-related brain potentials and autonomic activity |
| Q30479690 | Age-related changes in early novelty processing as measured by ERPs |
| Q42019791 | Age-related changes in electrophysiological and neuropsychological indices of working memory, attention control, and cognitive flexibility |
| Q51974104 | Age-related changes in executive function: an event-related potential (ERP) investigation of task-switching. |
| Q33559770 | An ERP analysis of recognition and categorization decisions in a prototype-distortion task |
| Q38412075 | An ERP study of second language learning after childhood: effects of proficiency |
| Q33194631 | Anatomy of an error: ERP and fMRI. |
| Q38485753 | Are depictive gestures like pictures? commonalities and differences in semantic processing |
| Q92749647 | Assessing the information content of ERP signals in schizophrenia using multivariate decoding methods |
| Q48634428 | Attending points in time and space. |
| Q51956365 | Brain potential correlates of face recognition: geometric distortions and the N250r brain response to stimulus repetitions. |
| Q33492763 | Brain potentials of conflict and error-likelihood following errorful and errorless learning in obsessive-compulsive disorder |
| Q46777063 | Contextual priming in grapheme-color synesthetes and yoked controls: 400 msec in the life of a synesthete |
| Q35570819 | Cortical regions recruited for complex active-learning strategies and action planning exhibit rapid reactivation during memory retrieval |
| Q35800510 | Delineating the neural signatures of tracking spatial position and working memory during attentive tracking |
| Q33679320 | Dissociation of the electrophysiological correlates of familiarity strength and item repetition |
| Q34233230 | Does compensatory neural activity survive old-old age? |
| Q88225288 | ENHANCING IMPLICIT LEARNING WITH POSTHYPNOTIC SUGGESTION: An ERP Study |
| Q34324687 | ERP abnormalities elicited by word repetition in fragile X-associated tremor/ataxia syndrome (FXTAS) and amnestic MCI. |
| Q30499468 | ERP evidence for different strategies in the processing of case markers in native speakers and non-native learners |
| Q55031270 | Effect of pattern awareness on the behavioral and neurophysiological correlates of visual statistical learning. |
| Q37360094 | Effects of multiple study-test repetition on the neural correlates of recognition memory: ERPs dissociate remembering and knowing |
| Q51866982 | Effects of temporal trial-by-trial cuing on early and late stages of auditory processing: evidence from event-related potentials. |
| Q35685961 | Electrophysiological correlates associated with contributions of perceptual and conceptual fluency to familiarity |
| Q48805351 | Electrophysiological correlates of exemplar-specific processes in implicit and explicit memory. |
| Q48535576 | Electrophysiological evidence for endogenous control of attention in switching between languages in overt picture naming |
| Q38425987 | Electrophysiological evidence for serial sentence processing: a comparison between non-preferred and ungrammatical continuations |
| Q45371559 | Electrophysiological indices of abnormal error-processing in adolescents with attention deficit hyperactivity disorder (ADHD). |
| Q37227132 | Event-related potential signatures of relational memory |
| Q51966630 | Event-related potentials associated with masked priming of test cues reveal multiple potential contributions to recognition memory. |
| Q35994917 | Event-related potentials elicited by errors during the stop-signal task. II: human effector-specific error responses |
| Q38389546 | FN400 and LPC memory effects for concrete and abstract words |
| Q30469157 | FN400 potentials are functionally identical to N400 potentials and reflect semantic processing during recognition testing |
| Q37330934 | Familiarity and conceptual priming engage distinct cortical networks. |
| Q90303805 | Fast periodic visual stimulation to study tool-selective processing in the human brain |
| Q28255091 | From orthography to phonetics: ERP measures of grapheme-to-phoneme conversion mechanisms in reading |
| Q33246165 | Gender differences in hemispheric asymmetry for face processing |
| Q30375137 | Graded expectations: Predictive processing and the adjustment of expectations during spoken language comprehension. |
| Q37352104 | Grammatical markers switch roles and elicit different electrophysiological responses under shallow and deep semantic requirements |
| Q36026977 | Homologous mechanisms of visuospatial working memory maintenance in macaque and human: properties and sources |
| Q33325736 | Internal and external information in error processing |
| Q36240065 | Investigating the age-related "anterior shift" in the scalp distribution of the P3b component using principal component analysis |
| Q34789668 | Mechanisms underlying age- and performance-related differences in working memory |
| Q35035554 | Modality Switching in a Property Verification Task: An ERP Study of What Happens When Candles Flicker after High Heels Click |
| Q48177580 | Monitoring in language perception: Electrophysiological and hemodynamic responses to spelling violations |
| Q48479023 | Neural correlates of conflict processing |
| Q51937006 | Neural correlates of retrieval orientation: effects of study-test similarity. |
| Q41837420 | Neural processing of fearful and happy facial expressions during emotion-relevant and emotion-irrelevant tasks: A fixation-to-feature approach |
| Q35760237 | Neurophysiological Evidence of Compensatory Brain Mechanisms in Early-Stage Multiple Sclerosis. |
| Q36157819 | Old-new ERP effects and remote memories: the late parietal effect is absent as recollection fails whereas the early mid-frontal effect persists as familiarity is retained |
| Q48500080 | Orienting attention to points in time improves stimulus processing both within and across modalities |
| Q51855003 | Planning of visually guided reach-to-grasp movements: inference from reaction time and contingent negative variation (CNV). |
| Q34251499 | Recording infant ERP data for cognitive research |
| Q38416213 | Repetition-priming modulates category-related effects on event-related potentials: further evidence for multiple cortical semantic systems |
| Q36898890 | Sensorimotor semantics on the spot: brain activity dissociates between conceptual categories within 150 ms. |
| Q42328107 | Separating content-specific retrieval from post-retrieval processing |
| Q45901322 | Study-test congruency affects encoding-related brain activity for some but not all stimulus materials. |
| Q90623191 | Studying brain activity during word-by-word interactions using wireless EEG |
| Q30581514 | Switch-related and general preparation processes in task-switching: evidence from multivariate pattern classification of EEG data. |
| Q35940087 | The FN400 indexes familiarity-based recognition of faces |
| Q48344459 | The N1 effect of temporal attention is independent of sound location and intensity: implications for possible mechanisms of temporal attention |
| Q37310066 | The beat goes on: rhythmic modulation of cortical potentials by imagined tapping. |
| Q50694467 | The electrophysiological correlate of contour integration is similar for color and luminance mechanisms. |
| Q35660822 | The influence of language proficiency on lexical semantic processing in native and late learners of English |
| Q47897702 | The neural fate of neutral information in emotion-enhanced memory. |
| Q30499730 | The neural organization of semantic memory: Electrophysiological activity suggests feature-based segregation |
| Q50783543 | Thirty-site P300 scalp distribution, amplitude variance across sites, and amplitude in detection of deceptive concealment of multiple guilty items. |
| Q48356969 | Time course of brain activity during change blindness and change awareness: performance is predicted by neural events before change onset |
| Q34417102 | Time to go our separate ways: opposite effects of study duration on priming and recognition reveal distinct neural substrates |
| Q24645237 | Updating P300: an integrative theory of P3a and P3b |
| Q34089103 | Voluntary control over prestimulus activity related to encoding. |
| Q27332159 | Words and melody are intertwined in perception of sung words: EEG and behavioral evidence |
| Q30500382 | Words and pictures: an electrophysiological investigation of domain specific processing in native Chinese and English speakers |