| scholarly article | Q13442814 |
| P50 | author | Nancy Kanwisher | Q6962770 |
| P2093 | author name string | Mona Spiridon | |
| P2860 | cites work | Borders of multiple visual areas in humans revealed by functional magnetic resonance imaging | Q22337051 |
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| Differential sensitivity of human visual cortex to faces, letterstrings, and textures: a functional magnetic resonance imaging study | Q34392270 | ||
| Face-specific processing in the human fusiform gyrus | Q34655516 | ||
| Selective impairment of facial recognition due to a haematoma restricted to the right fusiform and lateral occipital region | Q35463355 | ||
| fMRI of human visual cortex | Q48105271 | ||
| The parahippocampal place area: recognition, navigation, or encoding? | Q48166008 | ||
| Information encoding and the responses of single neurons in the primate temporal visual cortex | Q48235342 | ||
| An area within human ventral cortex sensitive to "building" stimuli: evidence and implications | Q48400465 | ||
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| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1157-1165 | |
| P577 | publication date | 2002-09-01 | |
| P1433 | published in | Neuron | Q3338676 |
| P1476 | title | How distributed is visual category information in human occipito-temporal cortex? An fMRI study. | |
| P478 | volume | 35 |
| Q24634354 | A common, high-dimensional model of the representational space in human ventral temporal cortex |
| Q48354906 | A glimpse into your vision. |
| Q57334804 | A hypothesis about the biological basis of expert intuition |
| Q40624101 | A specialized face-processing model inspired by the organization of monkey face patches explains several face-specific phenomena observed in humans. |
| Q30487391 | A stable topography of selectivity for unfamiliar shape classes in monkey inferior temporal cortex |
| Q34233175 | Age differences in neural distinctiveness revealed by multi-voxel pattern analysis |
| Q38726507 | Ageing differentially affects neural processing of different conflict types-an fMRI study |
| Q51892816 | Are faces special? A case of pure prosopagnosia. |
| Q34530294 | Arguments about the nature of concepts: Symbols, embodiment, and beyond |
| Q57270729 | Brain Reading Using Full Brain Support Vector Machines for Object Recognition: There Is No “Face” Identification Area |
| Q37347997 | Category selectivity in the ventral visual pathway confers robustness to clutter and diverted attention |
| Q51741266 | Coarse-to-fine categorization of visual scenes in scene-selective cortex. |
| Q47299589 | Coding of Object Size and Object Category in Human Visual Cortex |
| Q24276721 | Combinatorial codes in ventral temporal lobe for object recognition: Haxby (2001) revisited: is there a "face" area? |
| Q42629486 | Complementary neural representations for faces and words: a computational exploration |
| Q48420093 | Connectivity-based constraints on category-specificity in the ventral object processing pathway. |
| Q48917579 | Constructing scenes from objects in human occipitotemporal cortex. |
| Q36494362 | Corresponding ECoG and fMRI category-selective signals in human ventral temporal cortex |
| Q33951314 | Culture differences in neural processing of faces and houses in the ventral visual cortex |
| Q28247666 | Decoding mental states from brain activity in humans |
| Q37540384 | Decoding negative affect personality trait from patterns of brain activation to threat stimuli |
| Q34029162 | Decoding patterns of human brain activity |
| Q27500399 | Decoding semantics across fMRI sessions with different stimulus modalities: a practical MVPA study. |
| Q34259785 | Decoding semi-constrained brain activity from FMRI using support vector machines and gaussian processes |
| Q36672010 | Deconstructing visual scenes in cortex: gradients of object and spatial layout information |
| Q49032805 | Defining the face processing network: optimization of the functional localizer in fMRI. |
| Q48427756 | Differential sensitivity to words and shapes in ventral occipito-temporal cortex. |
| Q48338814 | Discrimination training alters object representations in human extrastriate cortex. |
| Q83313503 | Disentangling scene content from spatial boundary: complementary roles for the parahippocampal place area and lateral occipital complex in representing real-world scenes |
| Q48499013 | Dissociable neural patterns of facial identity across changes in viewpoint. |
| Q34029157 | Distributed representations in memory: insights from functional brain imaging |
| Q58707907 | Existence of Initial Dip for BCI: An Illusion or Reality |
| Q34258949 | Expertise increases the functional overlap between face and object perception |
| Q46130693 | Face percept formation in human ventral temporal cortex. |
| Q48223453 | Faces and objects in macaque cerebral cortex |
| Q41122001 | Feasibility of BCI Control in a Realistic Smart Home Environment |
| Q37231475 | Frontal and parietal cortical interactions with distributed visual representations during selective attention and action selection. |
| Q36323495 | Frontoparietal activation distinguishes face and space from artifact concepts |
| Q51636840 | Functional analysis of the periphery effect in human building related areas. |
| Q47820499 | Functional magnetic resonance imaging (fMRI) "brain reading": detecting and classifying distributed patterns of fMRI activity in human visual cortex |
| Q47653502 | Functional specialization and convergence in the occipito-temporal cortex supporting haptic and visual identification of human faces and body parts: an fMRI study. |
| Q37231511 | Functional subdomains within human FFA. |
| Q42550029 | Gestural coupling and social cognition: Möbius Syndrome as a case study |
| Q43505871 | High-resolution imaging of the fusiform face area (FFA) using multivariate non-linear classifiers shows diagnosticity for non-face categories |
| Q34554792 | High-resolution imaging reveals highly selective nonface clusters in the fusiform face area. |
| Q34191915 | Imagery and perception share cortical representations of content and location. |
| Q40515537 | Inferior temporal, prefrontal, and hippocampal contributions to visual working memory maintenance and associative memory retrieval. |
| Q46421537 | Insulin affects the neuronal response in the medial temporal lobe in humans |
| Q31142918 | Interpreting fMRI data: maps, modules and dimensions |
| Q37048145 | Intrinsic structure of visual exemplar and category representations in macaque brain |
| Q34692469 | Is region-of-interest overlap comparison a reliable measure of category specificity? |
| Q30474539 | Judging semantic similarity: an event-related fMRI study with auditory word stimuli |
| Q35688773 | Location and spatial profile of category-specific regions in human extrastriate cortex |
| Q33801612 | Low-level image properties of visual objects predict patterns of neural response across category-selective regions of the ventral visual pathway |
| Q27025908 | Low-level properties of natural images predict topographic patterns of neural response in the ventral visual pathway |
| Q30514022 | Mapping brain activation and information during category-specific visual working memory. |
| Q33770021 | Mapping informative clusters in a hierarchical [corrected] framework of FMRI multivariate analysis |
| Q31159439 | Mechanisms of face perception |
| Q33880016 | Multi-voxel pattern analysis of fMRI data predicts clinical symptom severity |
| Q46821611 | Multiple cognitive abilities from a single cortical algorithm |
| Q37628334 | Multiple object properties drive scene-selective regions |
| Q38733681 | Multiple-object Tracking as a Tool for Parametrically Modulating Memory Reactivation |
| Q26994685 | Multivariate cross-classification: applying machine learning techniques to characterize abstraction in neural representations |
| Q33356203 | Multivariate patterns in object-selective cortex dissociate perceptual and physical shape similarity |
| Q48932998 | Multivoxel Object Representations in Adult Human Visual Cortex Are Flexible: An Associative Learning Study. |
| Q35126753 | Neural correlates of categories and concepts |
| Q35622080 | Neural mechanisms for response selection: representation specific or modality independent? |
| Q41245821 | Neural representation of scene boundaries |
| Q30796700 | Neuroimaging weighs in: humans meet macaques in "primate" visual cortex. |
| Q51949037 | Neuropsychological and neuroimaging perspectives on conceptual knowledge: an introduction. |
| Q47595736 | Normal body perception despite the loss of right fusiform gyrus. |
| Q30434142 | On the definition and interpretation of voice selective activation in the temporal cortex. |
| Q44057854 | On the partnership between neural representations of object categories and visual features in the ventral visual pathway. |
| Q37043300 | PRoNTo: pattern recognition for neuroimaging toolbox. |
| Q27303050 | Parametric Coding of the Size and Clutter of Natural Scenes in the Human Brain |
| Q24276725 | Partially distributed representations of objects and faces in ventral temporal cortex |
| Q51948420 | Perceived shape similarity among unfamiliar objects and the organization of the human object vision pathway. |
| Q36263445 | Predicting brain activation patterns associated with individual lexical concepts based on five sensory-motor attributes |
| Q45341273 | Probing principles of large-scale object representation: category preference and location encoding. |
| Q30883061 | Processing faces and facial expressions |
| Q41817810 | Reading the mind's eye: decoding category information during mental imagery |
| Q33759502 | Reduced neural selectivity increases fMRI adaptation with age during face discrimination. |
| Q33552316 | Relating Population-Code Representations between Man, Monkey, and Computational Models |
| Q37020134 | Representational similarity analysis - connecting the branches of systems neuroscience |
| Q33280883 | Rethinking cortical organization: moving away from discrete areas arranged in hierarchies |
| Q36610235 | Role of the amygdala in processing visual social stimuli |
| Q25237892 | Selective response to letter categorization within the left fusiform gyrus |
| Q34338793 | Selectivity for the human body in the fusiform gyrus |
| Q34469967 | Separate face and body selectivity on the fusiform gyrus. |
| Q27302351 | Similarity-Based Fusion of MEG and fMRI Reveals Spatio-Temporal Dynamics in Human Cortex During Visual Object Recognition |
| Q35170398 | Sparse estimation automatically selects voxels relevant for the decoding of fMRI activity patterns |
| Q28281995 | Sparsely-distributed organization of face and limb activations in human ventral temporal cortex |
| Q36129384 | Spatiotemporal activity estimation for multivoxel pattern analysis with rapid event-related designs |
| Q48624069 | Sub-exemplar shape tuning in human face-related areas. |
| Q26859158 | Survey of encoding and decoding of visual stimulus via FMRI: an image analysis perspective |
| Q50588656 | Task alters category representations in prefrontal but not high-level visual cortex. |
| Q27318325 | The Invariance Hypothesis Implies Domain-Specific Regions in Visual Cortex |
| Q36672575 | The Representation of Object-Directed Action and Function Knowledge in the Human Brain |
| Q36655225 | The advantage of brief fMRI acquisition runs for multi-voxel pattern detection across runs. |
| Q57719283 | The brain of the beholder: honouring individual representational idiosyncrasies |
| Q30991427 | The chronoarchitecture of the cerebral cortex |
| Q36670031 | The distribution of category and location information across object-selective regions in human visual cortex |
| Q30500074 | The emergence of the social brain network: evidence from typical and atypical development |
| Q34084322 | The functional architecture of the ventral temporal cortex and its role in categorization |
| Q28255809 | The fusiform face area subserves face perception, not generic within-category identification |
| Q36659880 | The fusiform face area: a cortical region specialized for the perception of faces |
| Q42832709 | The importance of visual features in generic vs. specialized object recognition: a computational study |
| Q33605958 | The neural bases of spatial frequency processing during scene perception |
| Q30793095 | The neural basis of object perception. |
| Q37578405 | The neural basis of temporal individuation and its capacity limits in the human brain. |
| Q43708355 | The neural basis of visual word form processing: a multivariate investigation. |
| Q41872236 | The neural representation of Arabic digits in visual cortex. |
| Q35867448 | The physiology of perception in human temporal lobe is specialized for contextual novelty |
| Q48872328 | The role of sensorimotor learning in the perception of letter-like forms: tracking the causes of neural specialization for letters. |
| Q34183868 | The role of the fusiform face area in social cognition: implications for the pathobiology of autism |
| Q33819785 | The role of the occipital face area in the cortical face perception network |
| Q31134162 | Theoretical, statistical, and practical perspectives on pattern-based classification approaches to the analysis of functional neuroimaging data |
| Q34691536 | Too real for comfort? Uncanny responses to computer generated faces. |
| Q34116608 | Top-down engagement modulates the neural expressions of visual expertise. |
| Q36305942 | Training conquers multitasking costs by dividing task representations in the frontoparietal-subcortical system |
| Q34407348 | Unique semantic space in the brain of each beholder predicts perceived similarity |
| Q48368632 | Viewpoint-specific scene representations in human parahippocampal cortex |
| Q90354642 | Visual experiences during letter production contribute to the development of the neural systems supporting letter perception |
| Q34307486 | Visual object understanding |
| Q46178614 | What evidence supports special processing for faces? A cautionary tale for fMRI interpretation |
| Q48913925 | Within-subject reproducibility of category-specific visual activation with functional MRI. |
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