| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/HBM.23348 |
| P698 | PubMed publication ID | 27585292 |
| P50 | author | Justin M. Ales | Q59563892 |
| Bruno Rossion | Q87875867 | ||
| P2093 | author name string | Francesco Gentile | |
| P2860 | cites work | Microgenesis of Face Perception | Q57482673 |
| Spatio-temporal localization of the face inversion effect: an event-related potentials study | Q58419529 | ||
| The Face-Inversion Effect as a Deficit in the Encoding of Configural Information: Direct Evidence | Q61050742 | ||
| Spatial frequency bandwidth used in the recognition of facial images | Q73628587 | ||
| Integrated model of visual processing | Q77110173 | ||
| Let's face it: it's a cortical network | Q80155952 | ||
| Constraining the cortical face network by neuroimaging studies of acquired prosopagnosia | Q80216152 | ||
| Differential selectivity for dynamic versus static information in face-selective cortical regions | Q83806314 | ||
| Looking at upside-down faces | Q22337287 | ||
| Thresholding of statistical maps in functional neuroimaging using the false discovery rate | Q28208414 | ||
| The fusiform face area: a module in human extrastriate cortex specialized for face perception | Q28238243 | ||
| The fusiform face area is not sufficient for face recognition: evidence from a patient with dense prosopagnosia and no occipital face area | Q28269273 | ||
| Sparsely-distributed organization of face and limb activations in human ventral temporal cortex | Q28281995 | ||
| Functional neuroanatomy of face and object processing. A positron emission tomography study | Q28297846 | ||
| Searching for faces in scrambled scenes | Q29041508 | ||
| The face-detection effect: configuration enhances detection | Q29304482 | ||
| The Neural Basis of the Behavioral Face-Inversion Effect | Q29392882 | ||
| The distributed human neural system for face perception | Q29619352 | ||
| Visual neurones responsive to faces in the monkey temporal cortex | Q30053858 | ||
| Neural representations of faces and limbs neighbor in human high-level visual cortex: evidence for a new organization principle. | Q30531087 | ||
| Tracking cognitive processes with functional MRI mental chronometry | Q30793109 | ||
| Temporal cortex activation in humans viewing eye and mouth movements. | Q32108829 | ||
| A preference for contralateral stimuli in human object- and face-selective cortex. | Q33288967 | ||
| An image-dependent representation of familiar and unfamiliar faces in the human ventral stream. | Q33731359 | ||
| Larger neural responses produce BOLD signals that begin earlier in time. | Q33745360 | ||
| Perceptual expectation evokes category-selective cortical activity | Q33780912 | ||
| Low-level image properties of visual objects predict patterns of neural response across category-selective regions of the ventral visual pathway | Q33801612 | ||
| The effect of face inversion on activity in human neural systems for face and object perception | Q33852652 | ||
| Electrophysiological studies of human face perception. I: Potentials generated in occipitotemporal cortex by face and non-face stimuli | Q33871353 | ||
| The neuropsychology of face perception: beyond simple dissociations and functional selectivity | Q33887789 | ||
| The fusiform "face area" is part of a network that processes faces at the individual level | Q33912730 | ||
| Neural tuning for face wholes and parts in human fusiform gyrus revealed by FMRI adaptation | Q33995440 | ||
| Electrophysiological Studies of Face Perception in Humans | Q34081017 | ||
| Defining face perception areas in the human brain: a large-scale factorial fMRI face localizer analysis | Q34254072 | ||
| Selectivity for the human body in the fusiform gyrus | Q34338793 | ||
| The reverse hierarchy theory of visual perceptual learning | Q34353362 | ||
| Face-Specific Resting Functional Connectivity between the Fusiform Gyrus and Posterior Superior Temporal Sulcus | Q34371174 | ||
| Lower-level stimulus features strongly influence responses in the fusiform face area | Q34398828 | ||
| Separate face and body selectivity on the fusiform gyrus. | Q34469967 | ||
| From coarse to fine? Spatial and temporal dynamics of cortical face processing | Q34488126 | ||
| Holistic face categorization in higher order visual areas of the normal and prosopagnosic brain: toward a non-hierarchical view of face perception | Q34514367 | ||
| Explicating the face perception network with white matter connectivity | Q34695566 | ||
| Perceptual shape sensitivity to upright and inverted faces is reflected in neuronal adaptation | Q35564114 | ||
| An objective method for measuring face detection thresholds using the sweep steady-state visual evoked response | Q35867078 | ||
| Neural microgenesis of personally familiar face recognition | Q36055557 | ||
| Faciotopy-A face-feature map with face-like topology in the human occipital face area | Q36276706 | ||
| Role of fusiform and anterior temporal cortical areas in facial recognition | Q36319543 | ||
| The fusiform face area: a cortical region specialized for the perception of faces | Q36659880 | ||
| The distribution of category and location information across object-selective regions in human visual cortex | Q36670031 | ||
| Different neural mechanisms within occipitotemporal cortex underlie repetition suppression across same and different-size faces | Q36736915 | ||
| Relating retinotopic and object-selective responses in human lateral occipital cortex. | Q36805065 | ||
| Time course of visual perception: coarse-to-fine processing and beyond | Q36988767 | ||
| An anterior temporal face patch in human cortex, predicted by macaque maps | Q37076948 | ||
| A face-selective ventral occipito-temporal map of the human brain with intracerebral potentials | Q37102432 | ||
| Neural representations of faces and body parts in macaque and human cortex: a comparative FMRI study. | Q37190501 | ||
| Disconnection in prosopagnosia and face processing. | Q37206039 | ||
| The improbable simplicity of the fusiform face area | Q38000451 | ||
| Understanding face perception by means of human electrophysiology | Q38202334 | ||
| Neural systems underlying the recognition of familiar and newly learned faces. | Q38446964 | ||
| Quantifying interindividual variability and asymmetry of face-selective regions: a probabilistic functional atlas | Q39029122 | ||
| A Revised Neural Framework for Face Processing | Q39322850 | ||
| On the computational architecture of the neocortex. II. The role of cortico-cortical loops | Q41113085 | ||
| Faces in the cloud: Fourier power spectrum biases ultrarapid face detection. | Q42695320 | ||
| Temporal frequency tuning of cortical face-sensitive areas for individual face perception | Q43451801 | ||
| Separate parts of occipito-temporal white matter fibers are associated with recognition of faces and places | Q44500722 | ||
| Variation of BOLD hemodynamic responses across subjects and brain regions and their effects on statistical analyses. | Q46821723 | ||
| Beyond the core face-processing network: Intracerebral stimulation of a face-selective area in the right anterior fusiform gyrus elicits transient prosopagnosia | Q48094530 | ||
| Activation of the right inferior frontal cortex during assessment of facial emotion | Q48115340 | ||
| External facial features modify the representation of internal facial features in the fusiform face area | Q48229941 | ||
| A network of occipito-temporal face-sensitive areas besides the right middle fusiform gyrus is necessary for normal face processing | Q48247751 | ||
| Category search speeds up face-selective fMRI responses in a non-hierarchical cortical face network | Q48266810 | ||
| Understanding the functional neuroanatomy of acquired prosopagnosia | Q48271602 | ||
| Separable effects of inversion and contrast-reversal on face detection thresholds and response functions: a sweep VEP study | Q48285883 | ||
| Effective connectivity within the distributed cortical network for face perception | Q48327032 | ||
| The variability of human, BOLD hemodynamic responses. | Q48352823 | ||
| The influence of stimulus orientation on the vertex positive scalp potential evoked by faces | Q48380397 | ||
| Evidence accumulation in cell populations responsive to faces: an account of generalisation of recognition without mental transformations. | Q48396559 | ||
| A steady-state visual evoked potential approach to individual face perception: effect of inversion, contrast-reversal and temporal dynamics | Q48400515 | ||
| What is "special" about face perception? | Q48415031 | ||
| Detecting fearful and neutral faces: BOLD latency differences in amygdala-hippocampal junction. | Q48429151 | ||
| Faces are represented holistically in the human occipito-temporal cortex | Q48462074 | ||
| Selectivity for low-level features of objects in the human ventral stream. | Q48472618 | ||
| Anatomical correlates of the functional organization in the human occipitotemporal cortex | Q48517014 | ||
| How the brain learns to see objects and faces in an impoverished context | Q48615361 | ||
| Intracerebral electrical stimulation of a face-selective area in the right inferior occipital cortex impairs individual face discrimination | Q48711806 | ||
| Recovery from adaptation to facial identity is larger for upright than inverted faces in the human occipito-temporal cortex | Q48726605 | ||
| Category-selective patterns of neural response in the ventral visual pathway in the absence of categorical information. | Q48778784 | ||
| Effects of attention and emotion on face processing in the human brain: an event-related fMRI study | Q48827317 | ||
| White-matter connectivity between face-responsive regions in the human brain | Q48916066 | ||
| Resting-state neural activity across face-selective cortical regions is behaviorally relevant. | Q49052546 | ||
| Face categorization in visual scenes may start in a higher order area of the right fusiform gyrus: evidence from dynamic visual stimulation in neuroimaging | Q49082564 | ||
| Extensive visual training in adulthood significantly reduces the face inversion effect. | Q50782913 | ||
| The robustness of perception. | Q50961216 | ||
| Measuring structural-functional correspondence: spatial variability of specialised brain regions after macro-anatomical alignment. | Q51536406 | ||
| Robust sensitivity to facial identity in the right human occipito-temporal cortex as revealed by steady-state visual-evoked potentials. | Q51888026 | ||
| Face detection in normal and prosopagnosic individuals. | Q51937594 | ||
| Is it an animal? Is it a human face? Fast processing in upright and inverted natural scenes. | Q51947348 | ||
| Patches with links: a unified system for processing faces in the macaque temporal lobe. | Q51955592 | ||
| The representation of parts and wholes in face-selective cortex. | Q51966992 | ||
| Face detection: mapping human performance. | Q52004866 | ||
| Cerebral lateralisation at different stages of facial processing. | Q52257492 | ||
| On second glance: still no high-level pop-out effect for faces. | Q52566040 | ||
| Picture-plane inversion leads to qualitative changes of face perception. | Q52586218 | ||
| Reduced structural connectivity in ventral visual cortex in congenital prosopagnosia. | Q52590484 | ||
| Fast saccades toward faces: face detection in just 100 ms. | Q53067705 | ||
| The face-detection effect | Q55982829 | ||
| P433 | issue | 1 | |
| P1104 | number of pages | 20 | |
| P304 | page(s) | 120-139 | |
| P577 | publication date | 2016-09-01 | |
| P1433 | published in | Human Brain Mapping | Q5936947 |
| P1476 | title | Being BOLD: The neural dynamics of face perception | |
| P478 | volume | 38 |
| Q48112645 | Approaching the Ground Truth: Revealing the Functional Organization of Human Multisensory STC Using Ultra-High Field fMRI. |
| Q89405710 | Temporal multivariate pattern analysis (tMVPA): A single trial approach exploring the temporal dynamics of the BOLD signal |
| Q92624045 | The bottom-up and top-down processing of faces in the human occipitotemporal cortex |
| Q93025208 | The inferior occipital gyrus is a major cortical source of the face-evoked N170: Evidence from simultaneous scalp and intracerebral human recordings |
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