review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1177/1073858408326430 |
P698 | PubMed publication ID | 19516047 |
P50 | author | Nikos K. Logothetis | Q897072 |
Jonas Obleser | Q10307969 | ||
Christopher I Petkov | Q42533242 | ||
P2860 | cites work | The Faculty of Language: What Is It, Who Has It, and How Did It Evolve? | Q22065538 |
Avian brains and a new understanding of vertebrate brain evolution | Q22337223 | ||
Neural correlates of switching from auditory to speech perception | Q28297467 | ||
The cortical organization of speech processing | Q28297888 | ||
Learned birdsong and the neurobiology of human language | Q28757601 | ||
Language within our grasp | Q29614865 | ||
Voice-selective areas in human auditory cortex | Q29619575 | ||
Computational constraints on syntactic processing in a nonhuman primate | Q30011111 | ||
Double dissociation of 'what' and 'where' processing in auditory cortex | Q46647655 | ||
Species-specific calls activate homologs of Broca's and Wernicke's areas in the macaque | Q47194748 | ||
The evolution of the arcuate fasciculus revealed with comparative DTI. | Q47703299 | ||
Harmonic-sensitive neurons in the auditory cortex of the mustache bat | Q48110104 | ||
Broca's region revisited: cytoarchitecture and intersubject variability | Q48140262 | ||
Adaptation to speaker's voice in right anterior temporal lobe | Q48153283 | ||
Robust controlled functional MRI in alert monkeys at high magnetic field: effects of jaw and body movements | Q48164316 | ||
Multiple stages of auditory speech perception reflected in event-related FMRI. | Q48345779 | ||
Parallel processing in the auditory cortex of primates | Q48476038 | ||
Processing of complex sounds in the macaque nonprimary auditory cortex | Q48538316 | ||
Responses to acoustic stimuli of units in the auditory cortex of awake squirrel monkeys | Q48611866 | ||
Vowel sound extraction in anterior superior temporal cortex | Q48700508 | ||
Differential representation of species-specific primate vocalizations in the auditory cortices of marmoset and cat. | Q48718814 | ||
The neurophysiology of functionally meaningful categories: macaque ventrolateral prefrontal cortex plays a critical role in spontaneous categorization of species-specific vocalizations | Q48753479 | ||
Neural substrates of phonemic perception | Q49064873 | ||
Aphasia with predominantly subcortical lesion sites: description of three capsular/putaminal aphasia syndromes | Q49077785 | ||
A voice region in the monkey brain. | Q51964600 | ||
Species-specific calls evoke asymmetric activity in the monkey's temporal poles | Q57532395 | ||
Philosophy and stimulus design for neuroethology of complex-sound processing | Q30333991 | ||
Coding of auditory-stimulus identity in the auditory non-spatial processing stream | Q30435076 | ||
Dual streams of auditory afferents target multiple domains in the primate prefrontal cortex | Q30485291 | ||
Morphology, language and the brain: the decompositional substrate for language comprehension | Q30494104 | ||
The processing and perception of size information in speech sounds | Q30494732 | ||
Functional imaging reveals numerous fields in the monkey auditory cortex | Q30499538 | ||
Toward an evolutionary perspective on conceptual representation: species-specific calls activate visual and affective processing systems in the macaque | Q30499806 | ||
Speech-specific auditory processing: where is it? | Q30541411 | ||
The brain basis of syntactic processes: functional imaging and lesion studies | Q30883447 | ||
Neural representation of vocalizations in the primate ventrolateral prefrontal cortex | Q31112650 | ||
Separate neural subsystems within 'Wernicke's area'. | Q33929467 | ||
Functional specialization in rhesus monkey auditory cortex | Q33942496 | ||
"What" and "where" in the human auditory system | Q33947201 | ||
A new brain region for coordinating speech articulation | Q34063603 | ||
Comparative cytoarchitectonic analysis of the human and the macaque ventrolateral prefrontal cortex and corticocortical connection patterns in the monkey | Q34143565 | ||
The neuroanatomical and functional organization of speech perception | Q34171595 | ||
Positron emission tomographic studies of the cortical anatomy of single-word processing | Q34171829 | ||
The Neural Basis of Language | Q34257504 | ||
Listening to speech activates motor areas involved in speech production | Q34325558 | ||
The auditory behaviour of primates: a neuroethological perspective | Q34461831 | ||
The brain differentiates human and non-human grammars: functional localization and structural connectivity | Q34479037 | ||
Association fibre pathways of the brain: parallel observations from diffusion spectrum imaging and autoradiography | Q34575218 | ||
Paul Broca's historic cases: high resolution MR imaging of the brains of Leborgne and Lelong | Q34615252 | ||
Cortical processing of complex sound: a way forward? | Q35718114 | ||
Auditory processing--speech, space and auditory objects | Q36098569 | ||
Sounds do-able: auditory-motor transformations and the posterior temporal plane | Q36282420 | ||
Is neocortex essentially multisensory? | Q36483423 | ||
Role of left inferior prefrontal cortex in retrieval of semantic knowledge: a reevaluation | Q36831984 | ||
Processing of sub-syllabic speech units in the posterior temporal lobe: an fMRI study | Q38415274 | ||
Modulation of neural responses to speech by directing attention to voices or verbal content | Q38428092 | ||
Identification of a pathway for intelligible speech in the left temporal lobe | Q42275641 | ||
Functional mapping of the primate auditory system | Q44288770 | ||
Voxel-based lesion-symptom mapping | Q44755220 | ||
P433 | issue | 5 | |
P304 | page(s) | 419-429 | |
P577 | publication date | 2009-06-10 | |
P1433 | published in | The Neuroscientist | Q7753449 |
P1476 | title | Where are the human speech and voice regions, and do other animals have anything like them? | |
P478 | volume | 15 |
Q38056296 | Beyond the arcuate fasciculus: consensus and controversy in the connectional anatomy of language |
Q21129419 | Birds, primates, and spoken language origins: behavioral phenotypes and neurobiological substrates |
Q28729139 | Communication and the primate brain: insights from neuroimaging studies in humans, chimpanzees and macaques |
Q30618082 | Different forms of effective connectivity in primate frontotemporal pathways |
Q28602077 | Distributed acoustic cues for caller identity in macaque vocalization |
Q30466595 | Dynamics of large-scale cortical interactions at high gamma frequencies during word production: event related causality (ERC) analysis of human electrocorticography (ECoG). |
Q30478107 | Functional properties of human auditory cortical fields. |
Q30476165 | Hierarchical auditory processing directed rostrally along the monkey's supratemporal plane |
Q28648213 | High-field functional magnetic resonance imaging of vocalization processing in marmosets |
Q55318760 | Individual identity and affective valence in marmoset calls: in vivo brain imaging with vocal sound playback. |
Q30422267 | Investigating the neural correlates of voice versus speech-sound directed information in pre-school children |
Q24641994 | Monkey drumming reveals common networks for perceiving vocal and nonvocal communication sounds |
Q47578768 | Obligatory and facultative brain regions for voice-identity recognition |
Q26824564 | On the pursuit of the brain network for proto-syntactic learning in non-human primates: conceptual issues and neurobiological hypotheses |
Q48965365 | Physical and perceptual factors shape the neural mechanisms that integrate audiovisual signals in speech comprehension. |
Q28652143 | Processing of communication sounds: contributions of learning, memory, and experience |
Q48340904 | Processing of natural sounds in human auditory cortex: tonotopy, spectral tuning, and relation to voice sensitivity. |
Q90053052 | Repetition enhancement to voice identities in the dog brain |
Q30454881 | Reward-based learning for virtual neurorobotics through emotional speech processing |
Q30474876 | Segregation of vowels and consonants in human auditory cortex: evidence for distributed hierarchical organization |
Q28596631 | Temporal voice areas exist in autism spectrum disorder but are dysfunctional for voice identity recognition. |
Q26745365 | The Brain from Within |
Q27312437 | The cortical analysis of speech-specific temporal structure revealed by responses to sound quilts |
Q30481871 | The developmental origins of voice processing in the human brain |
Q48876756 | The emergence of cerebral specialization for the human voice over the first months of life |
Q27001532 | The neurobiology of primate vocal communication |
Q27331866 | Topographical functional connectivity patterns exist in the congenitally, prelingually deaf |
Q48644531 | Voice and emotion processing in the human neonatal brain |
Q30465646 | Voice cells in the primate temporal lobe |
Q48827056 | When during development do our brains get tuned to the human voice? |