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A network of occipito-temporal face-sensitive areas besides the right middle fusiform gyrus is necessary for normal face processing
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Location of human face-selective cortex with respect to retinotopic areas
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Prosopagnosia after unilateral right cerebral infarction
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Face perception and within-category discrimination in prosopagnosia
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Prosopagnosia: A defect in visual configural processing
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Neural Darwinism: Selection and reentrant signaling in higher brain function
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fMR-adaptation: a tool for studying the functional properties of human cortical neurons
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A Case of Prosopagnosia Following Moderate Closed Head Injury with Left Hemisphere Focal Lesion
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Prosopagnosia: A Bihemispheric Disorder
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Reaction Time in Brain Disease: Some Reflections
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Recognizing words, pictures, and concepts: A comparison of lexical, object, and reality decisions
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Face recognition and postero-inferior hemispheric lesions
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Becoming a “Greeble” Expert: Exploring Mechanisms for Face Recognition
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Integrated model of visual processing
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The distinct modes of vision offered by feedforward and recurrent processing
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The role of expression and identity in the face-selective responses of neurons in the temporal visual cortex of the monkey
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The Effect of Face Inversion on Activity in Human Neural Systems for Face and Object Perception
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Face processing: Getting by with a little help from its friends
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The functionally defined right occipital and fusiform “face areas” discriminate novel from visually familiar faces
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The functional magnetic resonance imaging hemodynamic response to faces remains stable until the ninth decade
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The distributed human neural system for face perception
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The many faces of configural processing
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A standardized set of 260 pictures: Norms for name agreement, image agreement, familiarity, and visual complexity.
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A cortical representation of the local visual environment
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Multiple processing streams in occipitotemporal visual cortex
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FFA: a flexible fusiform area for subordinate-level visual processing automatized by expertise
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The role of feedback in shaping neural representations in cat visual cortex
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Object-related activity revealed by functional magnetic resonance imaging in human occipital cortex.
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Distributed representation of objects in the human ventral visual pathway
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Functional Imaging Studies of Neuropsychological Patients: Applications and Limitations
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Bodamer's (1947) paper on prosopagnosia
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Parts and Wholes in Face Recognition
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PROSOPAGNOSIA AND AGNOSIA FOR NONCANONICAL VIEWS
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FUNCTIONAL NEUROANATOMY OF FACE AND OBJECT PROCESSING
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A neuromodulatory role for the human amygdala in processing emotional facial expressions
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Distributed Hierarchical Processing in the Primate Cerebral Cortex
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Varieties of Functional Deficits in Prosopagnosia
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A functional MRI study of face recognition in patients with prosopagnosia
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Rapid Automated Algorithm for Aligning and Reslicing PET Images
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Ferrier lecture - Functional architecture of macaque monkey visual cortex
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Representation of visual stimuli in inferior temporal cortex
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The role of the ‘face-cell’ area in the discrimination and recognition of faces by monkeys
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Distributed and Overlapping Representations of Faces and Objects in Ventral Temporal Cortex
inferredcites →https://doi.org/10.1126/science.1598577openalex-snapshot
Sparse Population Coding of Faces in the Inferotemporal Cortex
inferredcites →https://doi.org/10.1136/jnnp.71.2.254openalex-snapshot
Selective impairment of facial recognition due to a haematoma restricted to the right fusiform and lateral occipital region
inferredcites →https://doi.org/10.1146/annurev.ne.13.030190.000513openalex-snapshot
Face Agnosia And The Neural Substrates Of Memory
inferredcites →https://doi.org/10.1146/annurev.neuro.25.112701.142846openalex-snapshot
Beyond Phrenology: What Can Neuroimaging Tell Us About Distributed Circuitry?
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The Fusiform “Face Area” is Part of a Network that Processes Faces at the Individual Level
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Hemispheric Asymmetries for Whole-Based and Part-Based Face Processing in the Human Fusiform Gyrus
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The Representation of Objects in the Human Occipital and Temporal Cortex
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Prosopagnosia as a Deficit in Encoding Curved Surface
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Semantic and Visual Determinants of Face Recognition in a Prosopagnosic Patient
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Can Face Recognition Really be Dissociated from Object Recognition?
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Electrophysiological Studies of Face Perception in Humans
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Face-Specific Processing in the Human Fusiform Gyrus
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Revisiting snodgrass and Vanderwart's object database: Color and texture improve object recognition
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Intact recognition of facial expression, gender, and age in patients with impaired recognition of face identity
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Lesions of the fusiform face area impair perception of facial configuration in prosopagnosia
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The Fusiform Face Area: A Module in Human Extrastriate Cortex Specialized for Face Perception
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Temporal Cortex Activation in Humans Viewing Eye and Mouth Movements
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Visual Object ProcessingAuthor's Note: The preparation of this chapter was supported in part by the National Science Foundation (Grant Nos. 0745820 and 1059088) and a Google Gift to S.E.P. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the…
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Alterations in whole-brain white matter fiber networks in individuals with autism spectrum disorder after social skills training
inferred← citeshttps://doi.org/10.1016/j.brainresrev.2009.05.006openalex-snapshot
Dorsal–ventral integration in object recognition
inferred← citeshttps://doi.org/10.1016/j.brs.2016.04.003openalex-snapshot
Investigating the Causal Role of rOFA in Holistic Detection of Mooney Faces and Objects: An fMRI-guided TMS Study
inferred← citeshttps://doi.org/10.1016/j.bspc.2020.102368openalex-snapshot
Exploration of face-perceptual ability by EEG induced deep learning algorithm
inferred← citeshttps://doi.org/10.1016/j.clinph.2017.02.009openalex-snapshot
Visual stimuli modulate frontal oscillatory rhythms in a cortically blind patient: Evidence for top-down visual processing
inferred← citeshttps://doi.org/10.1016/j.clinph.2019.06.229openalex-snapshot
Electrophysiological evidence of altered facial expressions recognition in Alzheimer’s disease: A comprehensive ERP study
inferred← citeshttps://doi.org/10.1016/j.cognition.2014.11.037openalex-snapshot
Face inversion and acquired prosopagnosia reduce the size of the perceptual field of view
inferred← citeshttps://doi.org/10.1016/j.cognition.2026.106445openalex-snapshot
Evidence for top-down constraints and form-based prediction in 4–5 year-olds' lexical processing
inferred← citeshttps://doi.org/10.1016/j.cortex.2008.04.003openalex-snapshot
Disconnection in prosopagnosia and face processing
inferred← citeshttps://doi.org/10.1016/j.cortex.2009.04.003openalex-snapshot
The inversion effect in visual word form processing
inferred← citeshttps://doi.org/10.1016/j.cortex.2009.06.001openalex-snapshot
Impaired processing of relative distances between features and of the eye region in acquired prosopagnosia—Two sides of the same holistic coin?
inferred← citeshttps://doi.org/10.1016/j.cortex.2009.07.004openalex-snapshot
Acquired prosopagnosia abolishes the face inversion effect
inferred← citeshttps://doi.org/10.1016/j.cortex.2010.04.009openalex-snapshot
A new selective developmental deficit: Impaired object recognition with normal face recognition
inferred← citeshttps://doi.org/10.1016/j.cortex.2010.07.009openalex-snapshot
When the brain remembers, but the patient doesn’t: Converging fMRI and EEG evidence for covert recognition in a case of prosopagnosia
inferred← citeshttps://doi.org/10.1016/j.cortex.2011.06.006openalex-snapshot
Reduced early visual emotion discrimination as an index of diminished emotion processing in Parkinson’s disease? – Evidence from event-related brain potentials
inferred← citeshttps://doi.org/10.1016/j.cortex.2012.09.010openalex-snapshot
Structural connectivity in a single case of progressive prosopagnosia: The role of the right inferior longitudinal fasciculus
inferred← citeshttps://doi.org/10.1016/j.cortex.2013.07.011openalex-snapshot
People-selectivity, audiovisual integration and heteromodality in the superior temporal sulcus
inferred← citeshttps://doi.org/10.1016/j.cortex.2013.11.011openalex-snapshot
When a loved one feels unfamiliar: A case study on the neural basis of Capgras delusion
inferred← citeshttps://doi.org/10.1016/j.cortex.2014.02.024openalex-snapshot
Rapid, high-frequency, and theta-coupled gamma oscillations in the inferior occipital gyrus during face processing
inferred← citeshttps://doi.org/10.1016/j.cortex.2014.11.015openalex-snapshot
Reconstructing dynamic mental models of facial expressions in prosopagnosia reveals distinct representations for identity and expression
inferred← citeshttps://doi.org/10.1016/j.cortex.2014.12.020openalex-snapshot
The neural basis of perceiving person interactions
inferred← citeshttps://doi.org/10.1016/j.cortex.2015.01.025openalex-snapshot
Category search speeds up face-selective fMRI responses in a non-hierarchical cortical face network
inferred← citeshttps://doi.org/10.1016/j.cortex.2015.05.026openalex-snapshot
Beyond the core face-processing network: Intracerebral stimulation of a face-selective area in the right anterior fusiform gyrus elicits transient prosopagnosia
inferred← citeshttps://doi.org/10.1016/j.cortex.2016.04.024openalex-snapshot
Seeing the eyes in acquired prosopagnosia
inferred← citeshttps://doi.org/10.1016/j.cortex.2016.08.008openalex-snapshot
Contributions of feature shapes and surface cues to the recognition and neural representation of facial identity
inferred← citeshttps://doi.org/10.1016/j.cortex.2016.10.001openalex-snapshot
Individual differences in structural and functional connectivity predict speed of emotion discrimination
inferred← citeshttps://doi.org/10.1016/j.cortex.2018.03.011openalex-snapshot
Influence of task instructions and stimuli on the neural network of face processing: An ALE meta-analysis
inferred← citeshttps://doi.org/10.1016/j.cortex.2018.11.008openalex-snapshot
The cortical face network of the prosopagnosic patient PS with fast periodic stimulation in fMRI
inferred← citeshttps://doi.org/10.1016/j.cortex.2020.03.033openalex-snapshot
Dissociable pathways for moving and static face perception begin in early visual cortex: Evidence from an acquired prosopagnosic
inferred← citeshttps://doi.org/10.1016/j.cortex.2021.01.021openalex-snapshot
Category-selective deficits are the exception and not the rule: Evidence from a case-series of 64 patients with ventral occipito-temporal cortex damage
inferred← citeshttps://doi.org/10.1016/j.cortex.2022.04.010openalex-snapshot
Probing the attentional modulation of unconscious processing under interocular suppression in a spatial cueing paradigm
inferred← citeshttps://doi.org/10.1016/j.cub.2007.07.063openalex-snapshot
TMS Evidence for the Involvement of the Right Occipital Face Area in Early Face Processing
inferred← citeshttps://doi.org/10.1016/j.cub.2007.08.008openalex-snapshot
Face Perception: Broken into Parts
inferred← citeshttps://doi.org/10.1016/j.cub.2009.01.007openalex-snapshot
Triple Dissociation of Faces, Bodies, and Objects in Extrastriate Cortex
inferred← citeshttps://doi.org/10.1016/j.cub.2009.04.060openalex-snapshot
Functional MRI Reveals Compromised Neural Integrity of the Face Processing Network in Congenital Prosopagnosia
inferred← citeshttps://doi.org/10.1016/j.cub.2020.07.067openalex-snapshot
Face-Specific Perceptual Distortions Reveal A View- and Orientation-Independent Face Template
inferred← citeshttps://doi.org/10.1016/j.dcn.2017.11.010openalex-snapshot
Development of face recognition: Dynamic causal modelling of MEG data
inferred← citeshttps://doi.org/10.1016/j.dr.2018.12.001openalex-snapshot
Specific maternal brain responses to their own child’s face: An fMRI meta-analysis
inferred← citeshttps://doi.org/10.1016/j.euroneuro.2012.06.003openalex-snapshot
Acute pharmacologically induced shifts in serotonin availability abolish emotion-selective responses to negative face emotions in distinct brain networks
inferred← citeshttps://doi.org/10.1016/j.exer.2018.09.013openalex-snapshot
Early monocular enucleation selectively disrupts neural development of face perception in the occipital face area
inferred← citeshttps://doi.org/10.1016/j.ijpsycho.2007.04.003openalex-snapshot
Interplay between familiarity and orientation in face processing: An ERP study
inferred← citeshttps://doi.org/10.1016/j.ijpsycho.2007.04.005openalex-snapshot
Visual verbal working memory processing may be interfered by previously seen faces
inferred← citeshttps://doi.org/10.1016/j.ijpsycho.2010.08.007openalex-snapshot
Processing of visual stimuli in borderline personality disorder: A combined behavioural and magnetoencephalographic study
inferred← citeshttps://doi.org/10.1016/j.ijpsycho.2011.12.004openalex-snapshot
Trait anxiety and involuntary processing of facial emotions
inferred← citeshttps://doi.org/10.1016/j.infbeh.2014.08.008openalex-snapshot
Maternal cradling bias and early communicative interactions: Implications for early identification of children at risk
inferred← citeshttps://doi.org/10.1016/j.jad.2013.10.016openalex-snapshot
The neural representation of emotionally neutral faces and places in patients with panic disorder with agoraphobia
inferred← citeshttps://doi.org/10.1016/j.jns.2016.11.080openalex-snapshot
Apomorphine pump in advanced Parkinson's disease: Effects on motor and nonmotor symptoms with brain metabolism correlations
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2024.12.016openalex-snapshot
The characteristics of event-related potentials in generalized anxiety disorder: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2026.03.021openalex-snapshot
Associations between childhood trauma and amygdala- and insula-centered resting-state functional connectivity in alcohol use disorder
inferred← citeshttps://doi.org/10.1016/j.metip.2026.100241openalex-snapshot
Quantifying individual recognition sensitivity to static and dynamic facial expressions
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2009.02.004openalex-snapshot
Neural bases of eye and gaze processing: The core of social cognition
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2009.05.008openalex-snapshot
Neuropsychological mechanisms of visual face and body perception
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2014.10.022openalex-snapshot
Person recognition and the brain: Merging evidence from patients and healthy individuals
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2024.105535openalex-snapshot
The anterior fusiform gyrus: The ghost in the cortical face machine
inferred← citeshttps://doi.org/10.1016/j.neulet.2008.12.039openalex-snapshot
A distributed neural system for top-down face processing
inferred← citeshttps://doi.org/10.1016/j.neulet.2019.134344openalex-snapshot
Effects of individuation and categorization on face representations in the visual cortex
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2017.05.018openalex-snapshot
Neural changes related to motion processing in healthy aging
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2004.03.025openalex-snapshot
Activation of the fusiform gyrus when individuals with autism spectrum disorder view faces
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2004.12.018openalex-snapshot
Self-face recognition activates a frontoparietal “mirror” network in the right hemisphere: an event-related fMRI study
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2005.07.041openalex-snapshot
Face, eye and object early processing: What is the face specificity?
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2005.12.011openalex-snapshot
The fusiform face area is tuned for curvilinear patterns with more high-contrasted elements in the upper part
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2006.05.037openalex-snapshot
Faces are represented holistically in the human occipito-temporal cortex
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2006.07.045openalex-snapshot
Developmental differences in the neural bases of the face inversion effect show progressive tuning of face-selective regions to the upright orientation
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2006.09.051openalex-snapshot
Understanding the functional neuroanatomy of acquired prosopagnosia
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2007.02.047openalex-snapshot
When thoughts become action: An fMRI paradigm to study volitional brain activity in non-communicative brain injured patients
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2007.05.030openalex-snapshot
From a face to its category via a few information processing states in the brain
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2007.10.040openalex-snapshot
Let’s face it: It’s a cortical network
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2007.10.047openalex-snapshot
Constraining the cortical face network by neuroimaging studies of acquired prosopagnosia
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2007.11.012openalex-snapshot
The roles of “face” and “non-face” areas during individual face perception: Evidence by fMRI adaptation in a brain-damaged prosopagnosic patient
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2008.06.042openalex-snapshot
Position-specific and position-invariant face aftereffects reflect the adaptation of different cortical areas
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2008.09.011openalex-snapshot
The correlates of subjective perception of identity and expression in the face network: An fMRI adaptation study
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2008.12.041openalex-snapshot
Forward and backward connections in the brain: A DCM study of functional asymmetries
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2009.01.062openalex-snapshot
Selecting forward models for MEG source-reconstruction using model-evidence
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2009.10.092openalex-snapshot
Avoiding non-independence in fMRI data analysis: Leave one subject out
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2009.12.093openalex-snapshot
Unattended emotional faces elicit early lateralized amygdala–frontal and fusiform activations
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2009.12.106openalex-snapshot
Discovering structure in the space of fMRI selectivity profiles
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2010.03.044openalex-snapshot
Decomposing the neural mechanisms of visual search through model-based analysis of fMRI: Top-down excitation, active ignoring and the use of saliency by the right TPJ
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2010.04.262openalex-snapshot
Sparsely-distributed organization of face and limb activations in human ventral temporal cortex
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2010.06.029openalex-snapshot
Why is the N170 enhanced for inverted faces? An ERP competition experiment
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2011.05.004openalex-snapshot
Stereotype-based modulation of person perception
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2011.07.018openalex-snapshot
Temporal dynamics of face selection mechanism in the context of similar and dissimilar faces: ERP evidence for biased competition within the ventral occipito-temporal cortex using ICA
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2012.02.038openalex-snapshot
Stimulus repetition probability effects on repetition suppression are position invariant for faces
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2012.08.021openalex-snapshot
The changing landscape of functional brain networks for face processing in typical development
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2012.11.060openalex-snapshot
Differential face-network adaptation in children, adolescents and adults
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2013.02.068openalex-snapshot
FMRI analysis of contrast polarity in face-selective cortex in humans and monkeys
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2013.06.083openalex-snapshot
Fusing concurrent EEG–fMRI with dynamic causal modeling: Application to effective connectivity during face perception
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2014.06.017openalex-snapshot
Intracerebral electrical stimulation of a face-selective area in the right inferior occipital cortex impairs individual face discrimination
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2014.07.006openalex-snapshot
Surface-based mixed effects multilevel analysis of grouped human electrocorticography
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2014.08.011openalex-snapshot
Face processing regions are sensitive to distinct aspects of temporal sequence in facial dynamics
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2016.01.041openalex-snapshot
Modelling the perceptual similarity of facial expressions from image statistics and neural responses
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2017.01.043openalex-snapshot
Causal evidence of the involvement of the right occipital face area in face-identity acquisition
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2017.06.018openalex-snapshot
Frontal temporal and parietal systems synchronize within and across brains during live eye-to-eye contact
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2017.07.061openalex-snapshot
Discrimination of a medial functional module within the temporal lobe using an effective connectivity model: A CCEP study
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2017.08.074openalex-snapshot
Intracranial Markers of Conscious Face Perception in Humans
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2017.12.023openalex-snapshot
The neural network for face recognition: Insights from an fMRI study on developmental prosopagnosia
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2018.09.027openalex-snapshot
A face is more than just the eyes, nose, and mouth: fMRI evidence that face-selective cortex represents external features
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2019.04.058openalex-snapshot
Perceiving animacy purely from visual motion cues involves intraparietal sulcus
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2019.116229openalex-snapshot
Patterns of individual differences in fiber tract integrity of the face processing brain network support neurofunctional models
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2020.116754openalex-snapshot
The ‘Narcissus Effect’: Top-down alpha-beta band modulation of face-related brain areas during self-face processing
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2020.117669openalex-snapshot
White matter fascicles and cortical microstructure predict reading-related responses in human ventral temporal cortex
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2022.118932openalex-snapshot
Intracerebral electrical stimulation of the right anterior fusiform gyrus impairs human face identity recognition
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2022.119310openalex-snapshot
Neural processing of poems and songs is based on melodic properties
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