1 |
Imagined speech can be decoded from low- and cross-frequency intracranial EEG features
|
|
|
|
In: ISSN: 2041-1723 ; Nature communications, Vol. 13, No 1 (2022) P. 48 (2022)
|
|
BASE
|
|
Show details
|
|
2 |
Imagined speech can be decoded from low- and cross-frequency intracranial EEG features
|
|
|
|
In: Nat Commun (2022)
|
|
BASE
|
|
Show details
|
|
3 |
Selective enhancement of low-gamma activity by tACS improves phonemic processing and reading accuracy in dyslexia
|
|
|
|
In: ISSN: 1544-9173 ; EISSN: 1545-7885 ; PLoS Biology ; https://hal.archives-ouvertes.fr/hal-02958984 ; PLoS Biology, Public Library of Science, 2020, 18 (9), pp.e3000833. ⟨10.1371/journal.pbio.3000833⟩ (2020)
|
|
BASE
|
|
Show details
|
|
4 |
Selective enhancement of low-gamma activity by tACS improves phonemic processing and reading accuracy in dyslexia
|
|
|
|
In: ISSN: 1544-9173 ; PLOS Biology, Vol. 18, No 9 (2020) P. e3000833 (2020)
|
|
BASE
|
|
Show details
|
|
5 |
Prominence of delta oscillatory rhythms in the motor cortex and their relevance for auditory and speech perception
|
|
|
|
In: ISSN: 0149-7634 ; Neuroscience and Biobehavioral Reviews ; https://hal.archives-ouvertes.fr/hal-02007118 ; Neuroscience and Biobehavioral Reviews, Elsevier, 2019, ⟨10.1016/j.neubiorev.2019.09.012⟩ (2019)
|
|
BASE
|
|
Show details
|
|
6 |
The rough sound of salience enhances aversion through neural synchronisation
|
|
|
|
In: ISSN: 2041-1723 ; Nature Communications, Vol. 10, No 1 (2019) P. 3671 (2019)
|
|
BASE
|
|
Show details
|
|
7 |
The rough sound of salience enhances aversion through neural synchronisation
|
|
|
|
BASE
|
|
Show details
|
|
8 |
θ-Band and β-Band Neural Activity Reflects Independent Syllable Tracking and Comprehension of Time-Compressed Speech
|
|
|
|
Abstract:
Recent psychophysics data suggest that speech perception is not limited by the capacity of the auditory system to encode fast acoustic variations through neural γ activity, but rather by the time given to the brain to decode them. Whether the decoding process is bounded by the capacity of θ rhythm to follow syllabic rhythms in speech, or constrained by a more endogenous top-down mechanism, e.g., involving β activity, is unknown. We addressed the dynamics of auditory decoding in speech comprehension by challenging syllable tracking and speech decoding using comprehensible and incomprehensible time-compressed auditory sentences. We recorded EEGs in human participants and found that neural activity in both θ and γ ranges was sensitive to syllabic rate. Phase patterns of slow neural activity consistently followed the syllabic rate (4–14 Hz), even when this rate went beyond the classical θ range (4–8 Hz). The power of θ activity increased linearly with syllabic rate but showed no sensitivity to comprehension. Conversely, the power of β (14–21 Hz) activity was insensitive to the syllabic rate, yet reflected comprehension on a single-trial basis. We found different long-range dynamics for θ and β activity, with β activity building up in time while more contextual information becomes available. This is consistent with the roles of θ and β activity in stimulus-driven versus endogenous mechanisms. These data show that speech comprehension is constrained by concurrent stimulus-driven θ and low-γ activity, and by endogenous β activity, but not primarily by the capacity of θ activity to track the syllabic rhythm. SIGNIFICANCE STATEMENT Speech comprehension partly depends on the ability of the auditory cortex to track syllable boundaries with θ-range neural oscillations. The reason comprehension drops when speech is accelerated could hence be because θ oscillations can no longer follow the syllabic rate. Here, we presented subjects with comprehensible and incomprehensible accelerated speech, and show that neural phase patterns in the θ band consistently reflect the syllabic rate, even when speech becomes too fast to be intelligible. The drop in comprehension, however, is signaled by a significant decrease in the power of low-β oscillations (14–21 Hz). These data suggest that speech comprehension is not limited by the capacity of θ oscillations to adapt to syllabic rate, but by an endogenous decoding process.
|
|
Keyword:
Research Articles
|
|
URL: http://www.ncbi.nlm.nih.gov/pubmed/28729443 https://doi.org/10.1523/JNEUROSCI.2882-16.2017 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6596908/
|
|
BASE
|
|
Hide details
|
|
9 |
Acoustic landmarks drive delta-theta oscillations to enable speech comprehension by facilitating perceptual parsing
|
|
|
|
BASE
|
|
Show details
|
|
10 |
Asymmetric Function of Theta and Gamma Activity in Syllable Processing: An Intra-Cortical Study
|
|
|
|
In: EISSN: 1664-1078 ; Frontiers in Psychology ; https://hal.archives-ouvertes.fr/hal-02088050 ; Frontiers in Psychology, Frontiers, 2012, 3, ⟨10.3389/fpsyg.2012.00248⟩ (2012)
|
|
BASE
|
|
Show details
|
|
11 |
Asymmetric function of theta and gamma activity in syllable processing: an intra-cortical study
|
|
|
|
In: ISSN: 1664-1078 ; Frontiers in Psychology, Vol. 3, No 248 (2012) pp. 1-9 (2012)
|
|
BASE
|
|
Show details
|
|
12 |
Asymmetric Function of Theta and Gamma Activity in Syllable Processing: An Intra-Cortical Study
|
|
|
|
BASE
|
|
Show details
|
|
13 |
Dual Neural Routing of Visual Facilitation in Speech Processing ; Dual Neural Routing of Visual Facilitation in Speech Processing: Visual facilitation of speech processing
|
|
|
|
In: ISSN: 0270-6474 ; EISSN: 1529-2401 ; Journal of Neuroscience ; https://www.hal.inserm.fr/inserm-00429667 ; Journal of Neuroscience, Society for Neuroscience, 2009, 29 (43), pp.13445-13453. ⟨10.1523/JNEUROSCI.3194-09.2009⟩ (2009)
|
|
BASE
|
|
Show details
|
|
14 |
Dual Neural Routing of Visual Facilitation in Speech Processing
|
|
|
|
In: ISSN: 0270-6474 ; EISSN: 1529-2401 ; Journal of Neuroscience ; https://hal.archives-ouvertes.fr/hal-02088005 ; Journal of Neuroscience, Society for Neuroscience, 2009, 29 (43), pp.13445-13453. ⟨10.1523/JNEUROSCI.3194-09.2009⟩ (2009)
|
|
BASE
|
|
Show details
|
|
15 |
Dual Neural Routing of Visual Facilitation in Speech Processing
|
|
|
|
BASE
|
|
Show details
|
|
|
|