Structure. Brodmann area 22: posterior superior temporal cortex — the planum temporale and posterior STG belt classically called Wernicke's region, at the auditory-association crown of the dominant hemisphere.
Function. Speech comprehension's waystation: phoneme-to-lexicon conversion and auditory word recognition; its destruction (posterior MCA territory) yields fluent, phonemic-paraphasic speech lacking meaning — Wernicke's aphasia — with intact articulation and grammar-shaped output.
| Instrument | Role | Tier | Credibility | Via | Observed effect |
|---|---|---|---|---|---|
| verb-generation | assessor | secondary | standard-scientific | fMRI | Posterior temporal engagement during lexical retrieval — Wernicke's territory co-activates with frontal produc |
| lexical-decision ↗ | assessor | secondary | standard-scientific | fMRI | Posterior temporal lexical access reads under word/nonword decision. |
| sentence-comprehension | stimulator | primary | standard-scientific | delivery | Comprehending sentences drives Wernicke's territory — the comprehension pole of the lattice. |
| word-listening | assessor | secondary | standard-scientific | fMRI | Posterior temporal word-form processing under passive listening. |
| repetition-priming ↗ | inhibitor | secondary | standard-scientific | delivery | Repetition suppression of posterior-temporal word-form response. |
| verb-generation | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| semantic-decision ↗ | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| semantic-decision ↗ | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| picture-naming | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| picture-naming | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| lexical-decision ↗ | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| phonemic-fluency | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| phonemic-fluency | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| sentence-comprehension | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| rhyming-judgment ↗ | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| rhyming-judgment ↗ | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| word-listening | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| repetition-priming ↗ | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| repetition-priming ↗ | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| word-listening | inhibitor | secondary | standard-scientific | delivery | Repeated spoken words across passive and active listening blocks drove repetition suppression of BOLD in BA41 |
| picture-naming | inhibitor | secondary | standard-scientific | delivery | In fMRI picture naming, items facilitated days earlier by an auditory repetition task showed a repetition-supp |
| semantic-decision ↗ | inhibitor | secondary | standard-scientific | delivery | fMRI associative semantic priming on concrete nouns (related vs unrelated) produced neural suppression in bila |
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| Using perfusion MRI to measure the dynamic changes in neural activation associated with tonic muscular pain. Pain 2010 · 10.1016/j.pain.2009.10.003 |
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| The neural correlates of persuasion: a common network across cultures and media. Journal of cognitive neuroscience 2010 · 10.1162/jocn.2009.21363 |
| Dissociable neural substrates for agentic versus conceptual representations of self. Journal of cognitive neuroscience 2010 · 10.1162/jocn.2009.21368 |
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| Neural correlates of incidental and directed facial emotion processing in adolescents and adults. Social cognitive and affective neuroscience 2009 · 10.1093/scan/nsp029 |
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| The neural correlates of cognitive reappraisal during emotional autobiographical memory recall. Journal of cognitive neuroscience 2013 · 10.1162/jocn_a_00289 |
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| Neurobiological underpinnings of shame and guilt: a pilot fMRI study. Social cognitive and affective neuroscience 2014 · 10.1093/scan/nss114 |
| "The ""vegetarian brain"": chatting with monkeys and pigs?" Brain structure & function 2013 · 10.1007/s00429-012-0455-9 |
| Processing of natural sounds in human auditory cortex: tonotopy, spectral tuning, and relation to voice sensitivity. The Journal of neuroscience : the official journal of the Society for Neuroscience 2012 · 10.1523/JNEUROSCI.1388-12.2012 |
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| Processing of speech and non-speech sounds in the supratemporal plane: Auditory input preference does not predict sensit NeuroImage 2012 · 10.1016/j.neuroimage.2012.10.055 |
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| Dopamine precursor depletion impairs timing in healthy volunteers by attenuating activity in putamen and supplementary The Journal of neuroscience : the official journal of the Society for Neuroscience 2012 · 10.1523/JNEUROSCI.1258-12.2012 |
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| Mental images across the adult lifespan: a behavioural and fMRI investigation of motor execution and motor imagery. Experimental brain research 2013 · 10.1007/s00221-012-3331-1 |
| Jazz drummers recruit language-specific areas for the processing of rhythmic structure. Cerebral cortex (New York, N.Y. : 1991) 2014 · 10.1093/cercor/bhs367 |
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| Neuroimaging to detect cortical projection of vestibular response to caloric stimulation in young and older adults using NeuroImage 2013 · 10.1016/j.neuroimage.2013.02.061 |
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| The neural bases of the multiplication problem-size effect across countries. Frontiers in human neuroscience 2013 · 10.3389/fnhum.2013.00189 |
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| Convergent Findings of Altered Functional and Structural Brain Connectivity in Individuals with High Functioning Autism: PloS one 2013 · 10.1371/journal.pone.0067329 |
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| Capturing the musical brain with Lasso: Dynamic decoding of musical features from fMRI data. NeuroImage 2013 · 10.1016/j.neuroimage.2013.11.017 |
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| Brain basis of communicative actions in language PMID 26505303 |
| A human brain atlas derived via n-cut parcellation of resting-state and task-based fMRI data PMID 26523655 |
| Identifying environmental sounds: a multimodal mapping study PMID 26539096 |
| Differential Neural Processing during Motor Imagery of Daily Activities in Chronic Low Back Pain Patients PMID 26569602 |
| NEREC, an effective brain mapping protocol for combined language and long-term memory functions PMID 26575255 |
| Emotional susceptibility trait modulates insula responses and functional connectivity in flavor processing PMID 26594159 |
| Less efficient and costly processes of frontal cortex in childhood chronic fatigue syndrome PMID 26594619 |
| Prefrontal cortex connectivity dysfunction in performing the Fist–Edge–Palm task in patients with first-episode schizoph PMID 26594623 |
| Autistic fluid intelligence: Increased reliance on visual functional connectivity with diminished modulation of coupling PMID 26594629 |
| Conflict monitoring in speech processing: An fMRI study of error detection in speech production and perception PMID 26608243 |
| Individual differences in the attentional blink: Evidence from the amplitude of low-frequency fluctuations in non-blinke PMID 26610651 |
| Past experience shapes ongoing neural patterns for language PMID 26624517 |
| Neural Patterns of the Implicit Association Test PMID 26635570 |
| Executive attention control and emotional responding in attention-deficit/hyperactivity disorder — A functional MRI stud PMID 26640766 |
| Evidence for a Caregiving Instinct: Rapid Differentiation of Infant from Adult Vocalizations Using Magnetoencephalograph PMID 26656998 |
| How does language distance between L1 and L2 affect the L2 brain network? An fMRI study of Korean–Chinese–English trilin PMID 26673115 |
| Neural correlates of state-based decision-making in younger and older adults PMID 26690805 |
| Theory of Mind and the Whole Brain Functional Connectivity: Behavioral and Neural Evidences with the Amsterdam Resting S PMID 26696924 |
| Increases in the right dorsolateral prefrontal cortex and decreases the rostral prefrontal cortex activation after-8 wee PMID 26720411 |
| Rhythm makes the world go round: An MEG-TMS study on the role of right TPJ theta oscillations in embodied perspective ta PMID 26722994 |
| How the brain attunes to sentence processing: Relating behavior, structure, and function PMID 26777477 |
| Brain responses in humans reveal ideal observer-like sensitivity to complex acoustic patterns PMID 26787854 |
| Abnormal functional connectivity density in first-episode, drug-naive adult patients with major depressive disorder PMID 26826535 |
| Neural responses to a modified Stroop paradigm in patients with complex chronic musculoskeletal pain compared to matched PMID 26833066 |
| Violence-related content in video game may lead to functional connectivity changes in brain networks as revealed by fMRI PMID 26855192 |
| Abnormal spontaneous brain activity in type 2 diabetes with and without microangiopathy revealed by regional homogeneity PMID 26860674 |
| Language comprehension and brain function in individuals with an optimal outcome from autism PMID 26862477 |
| Reliability of Task-Based fMRI for Preoperative Planning: A Test-Retest Study in Brain Tumor Patients and Healthy Contro PMID 26894279 |
| Brain correlates of phonological recoding of visual symbols PMID 26902821 |
| Altered effective connectivity of posterior thalamus in migraine with cutaneous allodynia: a resting-state fMRI study wi PMID 26922333 |
| Differences in the central-nervous processing of olfactory stimuli according to their hedonic and arousal characteristic PMID 26968764 |
| Higher body mass index in older adults is associated with lower gray matter volume: implications for memory performance PMID 26973099 |
| Cough Is Dangerous: Neural Correlates of Implicit Body Symptoms Associations PMID 26973558 |
| Massive cortical reorganization in sighted Braille readers PMID 26976813 |
| Primary somatosensory contribution to action observation brain activity—combining fMRI and cTBS PMID 26979966 |
| Testosterone reduces functional connectivity during the ‘Reading the Mind in the Eyes’ Test PMID 26994483 |
| Functional brain substrate of quality of life in patients with schizophrenia: A brain SPECT multidimensional analysis PMID 27000309 |
| Sex-specific neural circuits of emotion regulation in the centromedial amygdala PMID 27004933 |
| Surface-Based Morphometry of Cortical Thickness and Surface Area Associated with Heschl's Gyri Duplications in 430 Healt PMID 27014013 |
| Higher Language Ability is Related to Angular Gyrus Activation Increase During Semantic Processing, Independent of Sente PMID 27014040 |
| Neural correlates for perception of companion animal photographs PMID 27020140 |
| Mindful attention to breath regulates emotions via increased amygdala–prefrontal cortex connectivity PMID 27033686 |
| Neuronal interactions in areas of spatial attention reflect avoidance of disgust, but orienting to danger PMID 27039145 |
| Functional Magnetic Resonance Imaging Study of Brain Activity Associated With Pitch Adaptation During Phonation in Healt PMID 27049447 |
| Does Older Adults’ Cognitive Function Disrupt the Malleability of Their Attitudes toward Outgroup Members?: An fMRI Inve PMID 27074046 |
| Functional Correlates of childhood maltreatment and symptom severity during affective theory of mind tasks in chronic de PMID 27107154 |
| Auditory motion in the sighted and blind: Early visual deprivation triggers a large-scale imbalance between auditory and PMID 27107468 |
| Athlete or athletic? Limited differential brain activation in person descriptions using nouns or adjectives PMID 27172859 |
| Resting state functional connectivity of the hippocampus along the anterior–posterior axis and its association with glut PMID 27182810 |
| Anhedonia and general distress show dissociable ventromedial prefrontal cortex connectivity in major depressive disorder PMID 27187232 |
| Task and Resting-State fMRI Reveal Altered Salience Responses to Positive Stimuli in Patients with Major Depressive Diso PMID 27192082 |
| The Human Brainnetome Atlas: A New Brain Atlas Based on Connectional Architecture PMID 27230218 |
| Variable activation in striatal subregions across components of a social influence task in young adult cannabis users PMID 27257518 |
| Neural activity during self-referential working memory and the underlying role of the amygdala in social anxiety disorde PMID 27260987 |
| Amplitude of low frequency fluctuations during resting state predicts social well-being PMID 27263835 |
| Does the sound of a barking dog activate its corresponding visual form? An fMRI investigation of modality-specific seman PMID 27289210 |
| Behavioural and neuroimaging changes after naming therapy for semantic variant primary progressive aphasia PMID 27297727 |
| Neural Processing of Familiar and Unfamiliar Children’s Faces: Effects of Experienced Love Withdrawal, but No Effects of PMID 27303279 |
| Understanding the internal states of others by listening to action verbs PMID 27312746 |
| Brain Activation during Memory Encoding in Type 2 Diabetes Mellitus: A Discordant Twin Pair Study PMID 27314047 |
| Effects of aging on task- and stimulus-related cerebral attention networks PMID 27318136 |
| Neural Correlates of Auditory Figure-Ground Segregation Based on Temporal Coherence PMID 27325682 |
| Temporal dynamics of brain activation during 40 minutes of pleasant touch PMID 27338514 |
| Prediction and unconscious attention operate synergistically to facilitate stimulus processing: An fMRI study PMID 27351781 |
| Resting State Functional Connectivity MRI among Spectral MEG Current Sources in Children on the Autism Spectrum PMID 27375419 |
| Effects of Body Mass Index and Body Fat Percent on Default Mode, Executive Control, and Salience Network Structure and F PMID 27378831 |
| Neural activation during imitation with or without performance feedback: An fMRI study PMID 27422729 |
| Exploring the anatomical encoding of voice with a mathematical model of the vocal system PMID 27436593 |
| Exploring the Neural Representation of Novel Words Learned through Enactment in a Word Recognition Task PMID 27445918 |
| The translocator protein gene is associated with symptom severity and cerebral pain processing in fibromyalgia PMID 27448744 |
| Behavioral and neuroimaging responses induced by mental imagery of threatening scenarios PMID 27452804 |
| Dissociable relations between amygdala subregional networks and psychopathy trait dimensions in conduct‐disordered juven PMID 27453465 |
| Increased Amplitude of Thalamocortical Low-Frequency Oscillations in Patients with Migraine PMID 27466345 |
| Down but not out in posterior cingulate cortex: Deactivation yet functional coupling with prefrontal cortex during deman PMID 27485753 |
| Impact of language on functional connectivity for audiovisual speech integration PMID 27510407 |
| Altered Vision-Related Resting-State Activity in Pituitary Adenoma Patients with Visual Damage PMID 27512990 |
| Degree connectivity in body dysmorphic disorder and relationships with obsessive and compulsive symptoms PMID 27514293 |
| Brain networks of temporal preparation: A multiple regression analysis of neuropsychological data PMID 27521744 |
| Whispering - The hidden side of auditory communication PMID 27530550 |
| Effect of Mild Thyrotoxicosis on Performance and Brain Activations in a Working Memory Task PMID 27536945 |
| Neural networks for harmonic structure in music perception and action PMID 27542722 |
| Neural changes associated to procedural learning and automatization process in Developmental Coordination Disorder and/o PMID 27546352 |
| The Role of the Subgenual Anterior Cingulate Cortex and Amygdala in Environmental Sensitivity to Infant Crying PMID 27560361 |
| Dough, tough, cough, rough: A “fast” fMRI localizer of component processes in reading PMID 27592331 |
| Mapping the Multiple Graded Contributions of the Anterior Temporal Lobe Representational Hub to Abstract and Social Conc PMID 27600844 |
| Age-related differences in brain activity during implicit and explicit processing of fearful facial expressions PMID 27614138 |
| Parametric modulation of reward sequences during a reversal task in ACC and VMPFC but not amygdala and striatum PMID 27622399 |
| Differential Involvement of the Anterior Temporal Lobes in Famous People Semantics PMID 27625630 |
| 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 |
| Prior Consumption of a Fat Meal in Healthy Adults Modulates the Brain’s Response to Fat123 PMID 27655761 |
| Neurofeedback training effects on inhibitory brain activation in ADHD: A matter of learning? PMID 27659116 |
| When the brain takes ‘BOLD’ steps: Real-time fMRI neurofeedback can further enhance the ability to gradually self-regula PMID 27659118 |
| The impact of aging on the neural networks involved in gaze and emotional processing PMID 27716474 |
| The network substrate of confabulatory tendencies in Alzheimer's disease PMID 27720424 |
| The role of the left inferior parietal lobule in second language learning: An intensive language training fMRI study PMID 27725166 |
| Central Pain Processing in Early-Stage Parkinson's Disease: A Laser Pain fMRI Study PMID 27776130 |
| Mentalizing in schizophrenia: A multivariate functional MRI study PMID 27793657 |
| Development of the Intrinsic Language Network in Preschool Children from Ages 3 to 5 Years PMID 27812160 |
| Neural substrates of sublexical processing for spelling PMID 27838547 |
| Intranasal Oxytocin Enhances Connectivity in the Neural Circuitry Supporting Social Motivation and Social Perception in PMID 27845765 |
| Temporal reliability of ultra-high field resting-state MRI for single-subject sensorimotor and language mapping PMID 27864079 |
| Olanzapine modulation of long- and short-range functional connectivity in the resting brain in a sample of patients with PMID 27887859 |
| Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia PMID 27913157 |
| Dance and music share gray matter structural correlates PMID 27923638 |
| Neural correlates of the affective properties of spontaneous and volitional laughter types PMID 27940151 |
| Disentangling meaning in the brain: Left temporal involvement in agreement processing PMID 27984788 |
| 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 |
| Functional Dysconnection of the Inferior Frontal Gyrus in Young People With Bipolar Disorder or at Genetic High Risk PMID 28031150 |
| Ipsilateral Putamen and Insula Activation by Both Left and Right GB34 Acupuncture Stimulation: An fMRI Study on Healthy PMID 28053642 |
| Predicting the Multisensory Consequences of One’s Own Action: BOLD Suppression in Auditory and Visual Cortices PMID 28060861 |
| Internal and external attention and the default mode network PMID 28110087 |
| Changes in functional organization and white matter integrity in the connectome in Parkinson's disease PMID 28116232 |
| Increase in brain activation due to sub-tasks during driving: fMRI study using new MR-compatible driving simulator PMID 28126038 |
| How white and black bodies are perceived depends on what emotion is expressed PMID 28128279 |
| Long-Term Experience of Chinese Calligraphic Handwriting Is Associated with Better Executive Functions and Stronger Rest PMID 28129407 |
| Activation of writing-specific brain regions when reading Chinese as a second language. Effects of training modality and PMID 28131811 |
| Theta and high-beta networks for feedback processing: a simultaneous EEG–fMRI study in healthy male subjects PMID 28140398 |
| Isolating response inhibition in the brain: Parietal versus frontal contribution PMID 28142026 |
| Practice and Learning: Spatiotemporal Differences in Thalamo-Cortical-Cerebellar Networks Engagement across Learning Pha PMID 28167919 |
| The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functio PMID 28213119 |
| Neural correlates of graphic cigarette warning labels predict smoking cessation relapse PMID 28236714 |
| Multimodal representations of person identity individuated with fMRI PMID 28242496 |
| “Decoding versus comprehension”: Brain responses underlying reading comprehension in children with autism PMID 28242518 |
| fMRI study of graduated emotional charge for detection of covert activity using passive listening to narratives PMID 28245989 |
| Sensory over-responsivity and social cognition in ASD: Effects of aversive sensory stimuli and attentional modulation on PMID 28284787 |
| Brain MRI data in Chinese dyslexic children performing an auditory rhyming judgment task PMID 28289697 |
| Social-cognitive brain function and connectivity during visual perspective-taking in autism and schizophrenia PMID 28291690 |
| Neural foundations of overt and covert actions PMID 28323166 |
| Real‐time fMRIneurofeedback in adolescents with attention deficit hyperactivity disorder PMID 28342214 |
| Not in one metric: Neuroticism modulates different resting state metrics within distinctive brain regions PMID 28342970 |
| Functional Brain Activation in Response to a Clinical Vestibular Test Correlates with Balance PMID 28344549 |
| Combination of volume and perfusion parameters reveals different types of grey matter changes in schizophrenia PMID 28348393 |
| Brain activity associated with selective attention, divided attention and distraction PMID 28363436 |
| Don’t worry, be happy - Neural correlates of the influence of musically induced mood on self-evaluation PMID 28392302 |
| The effect of constraining eye-contact during dynamic emotional face perception—an fMRI study PMID 28402536 |
| Family history and APOE4 risk for Alzheimer's disease impact the neural correlates of episodic memory by early midlife PMID 28413778 |
| The Neural Basis of Speech Perception through Lipreading and Manual Cues: Evidence from Deaf Native Users of Cued Speech PMID 28424636 |
| How does first language (L1) influence second language (L2) reading in the brain? Evidence from Korean-English and Chine PMID 28437658 |
| Using short-range and long-range functional connectivity to identify schizophrenia with a family-based case-control desi PMID 28463748 |
| Brain activation upon ideal-body media exposure and peer feedback in late adolescent girls PMID 28474292 |
| Functional connectivity in incarcerated male adolescents with psychopathic traits PMID 28521281 |
| Independent contributions of fMRI familiarity and novelty effects to recognition memory and their stability across the a PMID 28528847 |
| A Comparative Study of Average, Linked Mastoid, and REST References for ERP Components Acquired during fMRI PMID 28529472 |
| Dissociating Effects of Scrambling and Topicalization within the Left Frontal and Temporal Language Areas: An fMRI Study PMID 28536551 |
| Depression in patients with SAPHO syndrome and its relationship with brain activity and connectivity PMID 28545486 |
| From Thirst to Satiety: The Anterior Mid-Cingulate Cortex and Right Posterior Insula Indicate Dynamic Changes in Incenti PMID 28553214 |
| Human cortical activity evoked by contextual processing in attentional orienting PMID 28592863 |
| Attempts at memory control induce dysfunctional brain activation profiles in Generalized Anxiety Disorder: An explorator PMID 28599173 |
| Neural mechanisms underlying sound-induced visual motion perception: An fMRI study PMID 28600968 |
| Neural activity during attentional conflict predicts reduction in tinnitus perception following rTMS PMID 28629874 |
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| Avoidant Responses to Interpersonal Provocation Are Associated with Increased Amygdala and Decreased Mentalizing Network PMID 28660251 |
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| Effective Connectivity between Ventral Occipito-Temporal and Ventral Inferior Frontal Cortex during Lexico-Semantic Proc PMID 28690506 |
| Examining distinct working memory processes in children and adolescents using fMRI: Results and validation of a modified PMID 28704424 |
| Functional magnetic resonance imaging response as an early biomarker of cognitive decline in elderly patients with metab PMID 28711765 |
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| Language for action: Motor resonance during the processing of human and robotic voices PMID 28829994 |
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*Temporal lobe · Mai atlas of record · 1312 studies · 165 papers on disk*
This is Wernicke's territory — the posterior superior temporal crown where speech becomes meaning. Its planum temporale is among the most asymmetric structures in the human brain, and its destruction produces the most poignant syndrome in neurology: fluent, effortless, grammar-shaped speech that means nothing.
Brodmann area 22: posterior superior temporal cortex — the planum temporale and posterior STG belt classically called Wernicke's region, at the auditory-association crown of the dominant hemisphere.
*— {'source': 'Gazzaniga, Ivry & Mangun', 'work': 'Cognitive Neuroscience: The Biology of the Mind, 4th ed., W. W. Norton', 'kind': 'textbook', 'locator': 'ch. 11, Language'}*
Speech comprehension's waystation: phoneme-to-lexicon conversion and auditory word recognition; its destruction (posterior MCA territory) yields fluent, phonemic-paraphasic speech lacking meaning — Wernicke's aphasia — with intact articulation and grammar-shaped output.
The functional record: phoneme-to-lexicon conversion and auditory word recognition. The decoded profile is the linguistic one — auditory, speech, language, reading, words — and the coactivation map is a language network in miniature: planum temporale (1,468 shared studies), superior temporal sulcus (1,385), middle temporal (1,173), the auditory core+belt (920). The graded matrix carries the language family: sentence-comprehension as stimulator, verb-generation and lexical-decision as assessors.
*— {'source': 'Gazzaniga, Ivry & Mangun', 'work': 'Cognitive Neuroscience: The Biology of the Mind, 4th ed., W. W. Norton', 'kind': 'textbook', 'locator': 'ch. 11, Language'}*
Read the map as the arcuate territory's receiving end: whatever the frontal production regions articulate, this crown first comprehends — the coactivation gradient runs from the planum through the temporal belt exactly as the classic model draws it.
Co-activation partners of record: Planum temporale:1468, Superior temporal sulcus:1385, Middle temporal gyrus:1173, BA 41/42 - auditory core+belt:920, Superior temporal gyrus:903, Transverse temporal gyrus:816, Inferior frontal gyrus, opercular part:761, Inferior frontal gyrus, triangular part:604.
Posterior MCA territory damage: Wernicke's aphasia — fluent phonemic paraphasia lacking meaning, with the patient's own incomprehension absent (unlike Broca's). The 1999 auditory-system study in its evidence grounds the sensory side: the region sits at the top of the ascending auditory hierarchy.
10.1093/cercor/9.1.3510.1093/cercor/9.1.6510.1016/S0896-6273(00)80759-X10.1016/S0926-6410(99)00012-91312 studies total touch this region in the Neurosynth corpus of record; the full literature lives beside this dossier.
Candidate levers (Neurosynth-decoded terms — auditory(perception), speech(method-other), language(language), temporal(method-other), reading(language), sounds(method-other), superior temporal(method-other), words(method-other) …) are the foundation for the thousands of instruments to come; they are ungraded by law.
Planum temporale:1468, Superior temporal sulcus:1385, Middle temporal gyrus:1173, BA 41/42 - auditory core+belt:920 — each name is a dossier stop in this explorer.