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Modulation of BOLD response in motion sensitive lateral temporal cortex by real and fictive motion sentences
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In: http://crl.ucsd.edu/newsletter/Publications/Saygin_McCulluogh_Emmorey_JCN_2010.pdf (2010)
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What is involved and what is necessary for complex linguistic and nonlinguistic auditory processing: Evidence from functional magnetic resonance imaging and lesion data
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In: http://eprints.ucl.ac.uk/3670/1/3670.pdf (2007)
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Grammaticality Judgment under Non-Optimal Processing Conditions: Deficits induced in normal participants resemble those observed in aphasic patients
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In: http://crl.ucsd.edu/~saygin/papers/tjudgedegabs.pdf (2003)
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Voxel-based lesion-symptom mapping.
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In: https://crl.ucsd.edu/%7Esaygin/papers/vlsm_nn03.pdf (2003)
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Pragmatics in Human-Computer Conversations
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In: http://crl.ucsd.edu/~saygin/papers/saygin-jop.pdf (2002)
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Processing figurative language in a multi-lingual task: Translation, transfer and metaphor
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In: http://crl.ucsd.edu/~saygin/papers/corplingpaper.pdf (2001)
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Turing Test: 50 years later
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In: http://www.cs.bilkent.edu.tr/~ilyas/PDF/minds2000.pdf (1999)
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Neural Resources for Processing Language and Environmental Sounds: Evidence from aphasia
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In: http://crl.ucsd.edu/~saygin/papers/Saygin03Brain.pdf
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RUNNING TITLE: LANGUAGE AND THE BRAIN Language and the Brain
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In: http://www.alphalab.psyc.bbk.ac.uk/Publications/LizFestscriftChaptLangBrain.pdf
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| 10 |
FORUM LANGUAGE IN AN EMBODIED BRAIN: THE ROLE OF ANIMAL MODELS
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In: http://crl.ucsd.edu/~saygin/papers/cortexforum04.pdf
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Abstract:
hich language is built also exists in non-human animals. For instance, certain lower-level perceptual mechanisms critical for speech comprehension (and previously thought to be speech-specific) are found not only in primates, but in other mammals and in some birds. As an example, categorical perception of the voice onset times (VOT) that distinguish different phonemes (like `ta' and `da') has been documented in such animals as chinchillas and Japanese quail; electrophysiological studies in macaque primary auditory cortex reveal that this phenomenon may be constrained by the basic physiological response to acoustic transients (Steinschneider et al., 1995). On a more macroscopic level, structural asymmetry in Broca's area (roughly Brodmann's areas 44/45) and the planum temporale -- also cited as evidence for language specialization in humans -- has been found in great apes (Cantalupo and Hopkins, 2001; Gannon et al., 1998). Antero- and retrograde tracing of pathways in macaque linking a
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URL: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.3.4038
http://crl.ucsd.edu/~saygin/papers/cortexforum04.pdf
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