Structure. Brodmann area 37: the occipitotemporal (fusiform/posterior parahippocampal) transition cortex at the ventral stream's temporal terminus.
Function. The visual word form area lives at its left lateral-fusiform edge (letter-string expertise), alongside colour and object/face transitions; its damage produces alexia without agraphia and visual object anomia.
| Instrument | Role | Tier | Credibility | Via | Observed effect |
|---|---|---|---|---|---|
| facial-emotion | stimulator | primary | highly-credible | delivery | The fusiform face area drives structural face encoding. |
| face-identity | stimulator | primary | highly-credible | delivery | The fusiform face area — Kanwisher's canonical FFA paradigm: faces drive fusiform more than any matched catego |
| oddball ↗ | stimulator | secondary | standard-scientific | delivery | Novel vs familiar scenes and faces in this fMRI study drove a main effect of novelty in bilateral fusiform, in |
| reward-prediction ↗ | stimulator | secondary | standard-scientific | delivery | Delivered gambling pictures vs neutral pictures drove higher occipitotemporal activation in problem gamblers v |
| reward-prediction ↗ | assessor | secondary | standard-scientific | fMRI | Social and monetary incentive-delay fMRI: correct-feedback > baseline ANOVA showed main-effect activation incl |
| nback ↗ | assessor | secondary | standard-scientific | fMRI | Working-memory binding fMRI: delay-period maintenance in a 3-item delayed-match-to-sample task (6-s retention |
| emotional-stroop ↗ | assessor | secondary | standard-scientific | fMRI | Affective Stroop fMRI (positive/neutral/negative images under varying cognitive load): left fusiform gyri show |
| face-identity | assessor | secondary | standard-scientific | fMRI | Masked and long-lag face-priming fMRI: face-vs-scramble localizers identified the left FFA in 15/16 participan |
| face-identity | inhibitor | secondary | standard-scientific | delivery | Canonical repetition suppression under masking: briefly flashed identical face primes (masked, unseen) reduced |
| oddball ↗ | inhibitor | secondary | standard-scientific | delivery | Same novelty paradigm: 115 images were pre-familiarized before scanning; familiar (repeated) stimuli elicited |
| lexical-decision ↗ | stimulator | secondary | standard-scientific | delivery | Decoded profile of left fusiform is dominated by task-evoking word-processing terms (words 0.012, reading 0.01 |
| rhyming-judgment ↗ | assessor | secondary | standard-scientific | fMRI | During fMRI rhyme judgment on spoken words overlaid with tones, selective attention to speech left the left mi |
| repetition-priming ↗ | inhibitor | secondary | standard-scientific | delivery | In fMRI masked face priming (forward mask, 50 ms subliminal prime, backward mask, then fame judgment on the ta |
| face-identity | inhibitor | secondary | standard-scientific | fMRI | Left mid-fusiform suppression under masked face priming generalized across view changes (within- vs cross-view |
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| Attentional control in anterior cingulate cortex based on probabilistic cueing. Journal of cognitive neuroscience 2011 · 10.1162/jocn.2010.21435 |
| Does sleep promote false memories? Journal of cognitive neuroscience 2011 · 10.1162/jocn.2010.21448 |
| Brain activation during the perception of distorted body images in eating disorders. Psychiatry research 2010 · 10.1016/j.pscychresns.2009.09.001 |
| Action selection: a race model for selected and non-selected actions distinguishes the contribution of premotor and pref NeuroImage 2010 · 10.1016/j.neuroimage.2010.02.045 |
| Conflict and inhibition differentially affect the N200/P300 complex in a combined go/nogo and stop-signal task. NeuroImage 2010 · 10.1016/j.neuroimage.2010.02.043 |
| Neural correlates of recognition memory for emotional faces and scenes. Social cognitive and affective neuroscience 2011 · 10.1093/scan/nsq003 |
| Comparison of the disparity between Talairach and MNI coordinates in functional neuroimaging data: validation of the Lan NeuroImage 2010 · 10.1016/j.neuroimage.2010.02.048 |
| Dissociating linguistic and task-related activity in the left inferior frontal gyrus. Journal of cognitive neuroscience 2011 · 10.1162/jocn.2010.21450 |
| Audiovisual functional magnetic resonance imaging adaptation reveals multisensory integration effects in object-related The Journal of neuroscience : the official journal of the Society for Neuroscience 2010 · 10.1523/JNEUROSCI.5074-09.2010 |
| Emotional complexity and the neural representation of emotion in motion. Social cognitive and affective neuroscience 2011 · 10.1093/scan/nsq021 |
| Beyond the memory mechanism: person-selective and nonselective processes in recognition of personally familiar faces. Journal of cognitive neuroscience 2011 · 10.1162/jocn.2010.21469 |
| Overrecruitment in the aging brain as a function of task demands: evidence for a compensatory view. Journal of cognitive neuroscience 2011 · 10.1162/jocn.2010.21490 |
| Hippocampal activation during retrieval of spatial context from episodic and semantic memory. Behavioural brain research 2010 · 10.1016/j.bbr.2010.04.010 |
| Dissociable neural responses to hands and non-hand body parts in human left extrastriate visual cortex. Journal of neurophysiology 2010 · 10.1152/jn.00215.2010 |
| How instructions modify perception: an fMRI study investigating brain areas involved in attributing human agency. NeuroImage 2010 · 10.1016/j.neuroimage.2010.04.025 |
| Increased neural activation during picture encoding and retrieval in 60-year-olds compared to 20-year-olds. Neuropsychologia 2010 · 10.1016/j.neuropsychologia.2010.04.011 |
| New method for fMRI investigations of language: defining ROIs functionally in individual subjects. Journal of neurophysiology 2010 · 10.1152/jn.00032.2010 |
| Neural correlates and effective connectivity of subjective colors during the Benham's top illusion: a functional MRI stu Cerebral cortex (New York, N.Y. : 1991) 2011 · 10.1093/cercor/bhq066 |
| Automatic top-down processing explains common left occipito-temporal responses to visual words and objects. Cerebral cortex (New York, N.Y. : 1991) 2011 · 10.1093/cercor/bhq063 |
| Dissociating the neural correlates of intra-item and inter-item working-memory binding. PloS one 2010 · 10.1371/journal.pone.0010214 |
| The literate brain: the relationship between spelling and reading. Journal of cognitive neuroscience 2011 · 10.1162/jocn.2010.21507 |
| Nicotine replacement in abstinent smokers improves cognitive withdrawal symptoms with modulation of resting brain netwo NeuroImage 2010 · 10.1016/j.neuroimage.2010.04.251 |
| Neural mechanisms of repetition priming of familiar and globally unfamiliar visual objects. Brain research 2010 · 10.1016/j.brainres.2010.04.071 |
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| Prior auditory information shapes visual category-selectivity in ventral occipito-temporal cortex. NeuroImage 2010 · 10.1016/j.neuroimage.2010.05.002 |
| Neural competition for conscious representation across time: an fMRI study. PloS one 2010 · 10.1371/journal.pone.0010556 |
| Lateral prefrontal cortex subregions make dissociable contributions during fluid reasoning. Cerebral cortex (New York, N.Y. : 1991) 2011 · 10.1093/cercor/bhq085 |
| Decreased regional homogeneity in insula and cerebellum: a resting-state fMRI study in patients with major depression an Psychiatry research 2010 · 10.1016/j.pscychresns.2010.03.004 |
| Failing compensatory mechanisms during working memory in older apolipoprotein E-epsilon4 healthy adults. Brain imaging and behavior 2010 · 10.1007/s11682-010-9097-9 |
| Gender differences in brain activation during encoding and recognition of male and female faces. Brain imaging and behavior 2010 · 10.1007/s11682-009-9085-0 |
| Disturbed functional connectivity of cortical activation during semantic discrimination in patients with schizophrenia a Brain imaging and behavior 2010 · 10.1007/s11682-010-9090-3 |
| Which way was I going? Contextual retrieval supports the disambiguation of well learned overlapping navigational routes. The Journal of neuroscience : the official journal of the Society for Neuroscience 2010 · 10.1523/JNEUROSCI.6021-09.2010 |
| Taking perspective into account in a communicative task. NeuroImage 2010 · 10.1016/j.neuroimage.2010.05.056 |
| Brain responses to facial expressions of pain: emotional or motor mirroring? NeuroImage 2010 · 10.1016/j.neuroimage.2010.05.037 |
| The effect of arousal on the emotional memory network depends on valence. NeuroImage 2010 · 10.1016/j.neuroimage.2010.06.015 |
| The neural correlates of highly iconic structures and topographic discourse in French Sign Language as observed in six h Brain and language 2010 · 10.1016/j.bandl.2010.05.003 |
| Visuohaptic convergence in a corticocerebellar network. The European journal of neuroscience 2010 · 10.1111/j.1460-9568.2010.07208.x |
| The effect of acute citalopram on face emotion processing in remitted depression: a pharmacoMRI study. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2011 · 10.1016/j.euroneuro.2010.06.008 |
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| Decrements in hippocampal activity with item repetition during continuous recognition: an fMRI study. Journal of cognitive neuroscience 2011 · 10.1162/jocn.2010.21535 |
| Comparing segmentation by time and by motion in visual search: an FMRI investigation. Journal of cognitive neuroscience 2011 · 10.1162/jocn.2010.21531 |
| Investigation of acupoint specificity by functional connectivity analysis based on graph theory. Neuroscience letters 2010 · 10.1016/j.neulet.2010.06.091 |
| Brain responses differ to faces of mothers and fathers. Brain and cognition 2010 · 10.1016/j.bandc.2010.06.003 |
| Enhanced resting-state connectivity of amygdala in the immediate aftermath of acute psychological stress. NeuroImage 2010 · 10.1016/j.neuroimage.2010.05.070 |
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| Developmental differences in medial temporal lobe function during memory encoding. The Journal of neuroscience : the official journal of the Society for Neuroscience 2010 · 10.1523/JNEUROSCI.3500-09.2010 |
| Neural precursors of delayed insight. Journal of cognitive neuroscience 2011 · 10.1162/jocn.2010.21550 |
| Multiple mechanisms of consciousness: the neural correlates of emotional awareness. The Journal of neuroscience : the official journal of the Society for Neuroscience 2010 · 10.1523/JNEUROSCI.6434-09.2010 |
| Cerebral hyporesponsiveness and cognitive impairment 10 years after chemotherapy for breast cancer. Human brain mapping 2011 · 10.1002/hbm.21102 |
| Active and passive touch differentially activate somatosensory cortex in texture perception. Human brain mapping 2011 · 10.1002/hbm.21091 |
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| Neural sensitivity to social rejection is associated with inflammatory responses to social stress. Proceedings of the National Academy of Sciences of the United States of America 2010 · 10.1073/pnas.1009164107 |
| Two distinct neural networks support the mapping of meaning to a novel word. Human brain mapping 2011 · 10.1002/hbm.21093 |
| Persistent posterior and transient anterior medial temporal lobe activity during navigation. NeuroImage 2010 · 10.1016/j.neuroimage.2010.05.074 |
| Decreased prefrontal cortex activity in mild traumatic brain injury during performance of an auditory oddball task. Brain imaging and behavior 2010 · 10.1007/s11682-010-9102-3 |
| Superior parietal lobule dysfunction in a homogeneous group of dyslexic children with a visual attention span disorder. Brain and language 2011 · 10.1016/j.bandl.2010.06.005 |
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| Differential activity for animals and manipulable objects in the anterior temporal lobes. Journal of cognitive neuroscience 2011 · 10.1162/jocn.2010.21567 |
| The neural network sustaining the crossmodal processing of human gender from faces and voices: an fMRI study. NeuroImage 2011 · 10.1016/j.neuroimage.2010.08.073 |
| Distinct neural systems involved in agency and animacy detection. Journal of cognitive neuroscience 2011 · 10.1162/jocn.2010.21574 |
| fMRI memory assessment in healthy subjects: a new approach to view lateralization data at an individual level. Brain imaging and behavior 2011 · 10.1007/s11682-010-9106-z |
| Emotion processing in the aging brain is modulated by semantic elaboration. Neuropsychologia 2011 · 10.1016/S1053-8119(03)00169-1 |
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| Distinct neural correlates for two types of inhibition in bilinguals: response inhibition versus interference suppressio Brain and cognition 2010 · 10.1016/j.bandc.2010.09.004 |
| Methylphenidate enhances brain activation and deactivation responses to visual attention and working memory tasks in hea NeuroImage 2011 · 10.1016/j.neuroimage.2010.10.060 |
| Prediction of subsequent recognition performance using brain activity in the medial temporal lobe. NeuroImage 2011 · 10.1016/j.neuroimage.2010.10.066 |
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| The neural basis of visual dominance in the context of audio-visual object processing. NeuroImage 2011 · 10.1016/j.neuroimage.2010.11.051 |
| A new paradigm (Westphal-Paradigm) to study the neural correlates of panic disorder with agoraphobia. European archives of psychiatry and clinical neuroscience 2011 · 10.1007/s00406-010-0167-1 |
| Neural correlates of learning to attend. Frontiers in human neuroscience 2010 · 10.3389/fnhum.2010.00216 |
| Increased fMRI signal with age in familial Alzheimer's disease mutation carriers. Neurobiology of aging 2012 · 10.1093/cercor/bhq158 |
| Limitation of physical performance in a muscle fatiguing handgrip exercise is mediated by thalamo-insular activity. Human brain mapping 2011 · 10.1002/hbm.21177 |
| Finding your voice: a singing lesson from functional imaging. Human brain mapping 2011 · 10.1002/hbm.21173 |
| Striatal responses to negative monetary outcomes differ between temperamentally inhibited and non-inhibited adolescents. Neuropsychologia 2011 · 10.1016/j.neuropsychologia.2010.12.015 |
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| Patterns of brain reorganization subsequent to left fusiform damage: fMRI evidence from visual processing of words and p NeuroImage 2011 · 10.1016/j.neuroimage.2010.12.024 |
| Opposing patterns of neural priming in same-exemplar vs. different-exemplar repetition predict subsequent memory. NeuroImage 2011 · 10.1016/j.neuroimage.2010.12.034 |
| How does your own knowledge influence the perception of another person's action in the human brain? Social cognitive and affective neuroscience 2012 · 10.1093/scan/nsq102 |
| Grounding emotion in situated conceptualization. Neuropsychologia 2011 · 10.1016/j.neuropsychologia.2010.12.032 |
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| Face processing changes in normal aging revealed by fMRI adaptation. Journal of cognitive neuroscience 2011 · 10.1162/jocn_a_00026 |
| Is morality unified? Evidence that distinct neural systems underlie moral judgments of harm, dishonesty, and disgust. Journal of cognitive neuroscience 2011 · 10.1162/jocn_a_00017 |
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| Separating brain processing of pain from that of stimulus intensity. Human brain mapping 2012 · 10.1002/hbm.21256 |
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| Neural dissociation of number from letter recognition and its relationship to parietal numerical processing. Journal of cognitive neuroscience 2012 · 10.1162/jocn_a_00085 |
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| Neural changes associated to procedural learning and automatization process in Developmental Coordination Disorder and/o PMID 27546352 |
| Brain Activity in Response to Trauma-specific, Negative, and Neutral Stimuli. A fMRI Study of Recent Road Traffic Accide PMID 27547195 |
| The Role of the Subgenual Anterior Cingulate Cortex and Amygdala in Environmental Sensitivity to Infant Crying PMID 27560361 |
| Mapping the Multiple Graded Contributions of the Anterior Temporal Lobe Representational Hub to Abstract and Social Conc PMID 27600844 |
| Four Functionally Distinct Regions in the Left Supramarginal Gyrus Support Word Processing PMID 27600852 |
| Age-related differences in brain activity during implicit and explicit processing of fearful facial expressions PMID 27614138 |
| Functional alterations of fronto-limbic circuit and default mode network systems in first-episode, drug-naïve patients w PMID 27639862 |
| Charting the effects of TMS with fMRI: Modulation of cortical recruitment within the distributed network supporting sema PMID 27650816 |
| The retrieval of perceptual memory details depends on right hippocampal integrity and activation PMID 27665526 |
| Detection of central circuits implicated in the formation of novel pain memories PMID 27695361 |
| The brain‐derived neurotrophic factor Val66Met polymorphism affects encoding of object locations during active navigatio PMID 27717213 |
| Learning and retrieving holistic and componential visual-verbal associations in reading and object naming PMID 27720949 |
| Influence of Temporal Expectations on Response Priming by Subliminal Faces PMID 27764124 |
| Snap Your Fingers! An ERP/sLORETA Study Investigating Implicit Processing of Self- vs. Other-Related Movement Sounds Usi PMID 27777557 |
| Self-similarity and recursion as default modes in human cognition PMID 27780529 |
| Attentional Networks in Adolescents with High-functioning Autism: An fMRI Investigation PMID 27843514 |
| Age-related alterations in functional connectivity patterns during working memory encoding of emotional items PMID 27865969 |
| Testing the Limits of Skill Transfer for Scrabble Experts in Behavior and Brain PMID 27881960 |
| Recapitulation of emotional source context during memory retrieval PMID 27923474 |
| Distinct Neural Substrates for Maintaining Locations and Spatial Relations in Working Memory PMID 27932963 |
| Age-related differences in resolving semantic and phonological competition during receptive language tasks PMID 27984068 |
| Modulation of ventral striatal activity by cognitive effort PMID 27989778 |
| Whole-brain functional connectivity during acquisition of novel grammar: Distinct functional networks depend on language PMID 27993693 |
| Shared orthographic neuronal representations for spelling and reading PMID 28011250 |
| Increase of posterior connectivity in aging within the Ventral Attention Network: A functional connectivity analysis usi PMID 28012826 |
| Effects of Intensity of Facial Expressions on Amygdalar Activation Independently of Valence PMID 28066216 |
| A Reduction in Delay Discounting by Using Episodic Future Imagination and the Association with Episodic Memory Capacity PMID 28105009 |
| Preliminary fMRI findings concerning the influence of 5‐HTPon food selection PMID 28127513 |
| How white and black bodies are perceived depends on what emotion is expressed PMID 28128279 |
| Activation of writing-specific brain regions when reading Chinese as a second language. Effects of training modality and PMID 28131811 |
| Effortful control and resting state networks: A longitudinal EEG study PMID 28153691 |
| Disrupted Causal Connectivity Anchored in the Posterior Cingulate Cortex in Amnestic Mild Cognitive Impairment PMID 28167926 |
| Cross-modal representation of spoken and written word meaning in left pars triangularis PMID 28213115 |
| Multimodal representations of person identity individuated with fMRI PMID 28242496 |
| fMRI study of graduated emotional charge for detection of covert activity using passive listening to narratives PMID 28245989 |
| Neural foundations of overt and covert actions PMID 28323166 |
| Imagining the future: The core episodic simulation network dissociates as a function of timecourse and the amount of sim PMID 28324695 |
| Neurological evidence for the role of construal level in future-directed thought PMID 28338716 |
| Functional Brain Activation in Response to a Clinical Vestibular Test Correlates with Balance PMID 28344549 |
| Neurocultural evidence that ideal affect match promotes giving PMID 28379542 |
| You talkin’ to me?Communicative talker gaze activates left-lateralized superior temporal cortex during perception of deg PMID 28400328 |
| Development of sensitivity versus specificity for print in the visual word form area PMID 28411527 |
| Mapping Dorsal and Ventral Caudate in Older Adults: Method and Validation PMID 28420985 |
| 15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia PMID 28440815 |
| Visual integration enhances associative memory equally for young and older adults without reducing hippocampal encoding PMID 28456521 |
| Recovery of orthographic processing after stroke: A longitudinal fMRI study PMID 28463704 |
| Using short-range and long-range functional connectivity to identify schizophrenia with a family-based case-control desi PMID 28463748 |
| The neural correlates of theory of mind and their role during empathy and the game of chess: A functional magnetic reson PMID 28495332 |
| Patterns of response to scrambled scenes reveal the importance of visual properties in the organization of scene-selecti PMID 28499144 |
| Brain activation of semantic category-based grouping in multiple identity tracking task PMID 28505166 |
| Trait Rumination Influences Neural Correlates of the Anticipation but Not the Consumption Phase of Reward Processing PMID 28539875 |
| Right Lateral Cerebellum Represents Linguistic Predictability PMID 28546307 |
| Body mass is positively associated with neural response to sweet taste, but not alcohol, among drinkers PMID 28549645 |
| Parallel Regulation of Memory and Emotion Supports the Suppression of Intrusive Memories PMID 28559378 |
| Kinematics in the brain: unmasking motor control strategies? PMID 28573311 |
| Specific brain activation patterns associated with two neuromuscular electrical stimulation protocols PMID 28577338 |
| Primary angle-closure glaucomas disturb regional spontaneous brain activity in the visual pathway: an fMRI study PMID 28579788 |
| Effect of verbal task complexity in a working memory paradigm in patients with type 1 diabetes. A fMRI study PMID 28582399 |
| Modes of Effective Connectivity within Cortical Pathways Are Distinguished for Different Categories of Visual Context: A PMID 28588458 |
| Brain activity related to working memory for temporal order and object information PMID 28602963 |
| Prenatal manganese exposure and intrinsic functional connectivity of emotional brain areas in children PMID 28610744 |
| Plastic reorganization of neural systems for perception of others in the congenitally blind PMID 28669909 |
| The Difference of Neural Networks between Bimanual Antiphase and In-Phase Upper Limb Movements: A Preliminary Functional PMID 28701822 |
| Functional Connectivity Differences in the Insular Sub-regions in Migraine without Aura: A Resting-State Functional Magn PMID 28701932 |
| Reading network in dyslexia: Similar, yet different PMID 28715717 |
| Neuroimaging Correlates of Post-Stroke Aphasia Rehabilitation in a Pilot Randomized Trial of Constraint-Induced Aphasia PMID 28719572 |
| Illuminating the conceptual structure of the space of moral violations with searchlight representational similarity anal PMID 28743459 |
| Failure in Cognitive Suppression of Negative Affect in Adolescents with Generalized Anxiety Disorder PMID 28747683 |
| Neural differences underlying face processing in veterans with TBI and co-occurring TBI and PTSD PMID 28753471 |
| Neural Response to Biological Motion in Healthy Adults Varies as a Function of Autistic-Like Traits PMID 28769743 |
| d-Cycloserine facilitates extinction learning and enhances extinction-related brain activation PMID 28807795 |
| Functional Connectivity of the Corpus Callosum in Epilepsy Patients with Secondarily Generalized Seizures PMID 28912749 |
| Investigating the Neural Correlates of Emotion–Cognition Interaction Using an Affective Stroop Task PMID 28919871 |
*Temporal lobe · Mai atlas of record · 1131 studies · 182 papers on disk*
The fusiform gyrus is the ventral stream's temporal terminus — occipitotemporal transition cortex (area 37) where the brain's visual expertise lives: the visual word form area at its left lateral edge, colour, objects and faces along its length.
Brodmann area 37: the occipitotemporal (fusiform/posterior parahippocampal) transition cortex at the ventral stream's temporal terminus.
*— {'source': 'Gazzaniga, Ivry & Mangun', 'work': 'Cognitive Neuroscience: The Biology of the Mind, 4th ed., W. W. Norton', 'kind': 'textbook', 'locator': 'ch. 6, Object Recognition'}*
The visual word form area lives at its left lateral-fusiform edge (letter-string expertise), alongside colour and object/face transitions; its damage produces alexia without agraphia and visual object anomia.
The functional record: the visual word form area lives at the left lateral-fusiform edge (letter-string expertise), alongside colour and object/face transitions; its damage produces alexia without agraphia — you can write words you can no longer read. The decoded profile is face, reading, words, objects. The graded matrix carries two highly-credible stimulators: facial-emotion and face-identity — Kanwisher's FFA paradigm paradigm-adjacent, the fusiform's face expertise recorded.
*— {'source': 'Gazzaniga, Ivry & Mangun', 'work': 'Cognitive Neuroscience: The Biology of the Mind, 4th ed., W. W. Norton', 'kind': 'textbook', 'locator': 'ch. 11, Language'}*
Collateral sulcus (711 shared studies), entorhinal cortex (519), inferior occipital gyrus (519), amygdala (500), parahippocampal gyrus (477) — the ventral stream's temporal end, wired to the memory system beside it.
Co-activation partners of record: Collateral sulcus:711, Entorhinal cortex:519, Inferior occipital gyrus:519, Amygdala:500, Parahippocampal gyrus:477, Amygdala:460, Middle temporal gyrus:443, Hippocampal fissure:443.
Alexia without agraphia and visual object agnosia — the record's dissociations, where writing survives reading's loss. The face-expertise literature completes the picture: prosopagnosia's seat is this region's right-hemisphere twin.
The adjacency harvest gave this dossier its breadth: fusiform papers live inside the occipitotemporal, face, word and memory literatures at once — a transition cortex cited from every side. Its left-hemisphere word-form specialization (the VWFA) versus the right's face expertise is the textbook hemispheric division, and both live in this one gyrus.
10.1016/S0896-6273(00)80456-010.1073/pnas.95.21.1265710.1073/pnas.96.4.166910.1016/S0028-3932(98)00107-910.1093/brain/122.11.21591131 studies total touch this region in the Neurosynth corpus of record; the full literature lives beside this dossier.
Candidate levers (Neurosynth-decoded terms — face(perception), reading(language), semantic(method-other), words(method-other), fusiform(anatomy-reference), objects(perception), object(perception), visual(method-other) …) are the foundation for the thousands of instruments to come; they are ungraded by law.
Collateral sulcus:711, Entorhinal cortex:519, Inferior occipital gyrus:519, Amygdala:500 — each name is a dossier stop in this explorer.