Tobias Staudigl

The paper shows that coordinated gaze shifts during memory retrieval are temporally linked to image memory reactivation, indicating that actions structure memory reactivation and predict retrieval success.

This study shows that breathing phase during sleep influences memory reactivation by aligning it with slow oscillation-spindle cycles, enhancing associative memory.

This study uses MEG to track ripple-like activity during human sleep, showing its association with memory consolidation and reactivation.

The paper identifies a 19-45 Hz thalamic oscillation specific to REM sleep and wakefulness, distinguishing conscious states in humans.

This study shows respiration influences neural dynamics during memory retrieval, with key brain signals linked to memory performance being synchronized with the respiratory cycle.

This study examines how respiratory rhythms influence aperiodic brain activity during the wake-sleep cycle in humans, finding phase shifts and reduced variability in respiration-brain coupling during sleep transitions.

The paper shows saccade-based grid-like codes in the entorhinal cortex during scene image study, linked to recognition memory performance.

This study links alpha/beta oscillations to oculomotor dynamics rather than memory performance, showing that eye movements drive alpha/beta power changes.

This study shows that spindle-locked ripples in human NREM sleep are critical for memory reactivation, supporting their role in memory consolidation.

This study identifies electrophysiological signatures of veridical head direction in humans using EEG and intracranial recordings, revealing a posterior central signature and medial temporal lobe involvement.

This study shows that imperceptible 65Hz sensory stimulation enhances episodic memory recall by entraining endogenous 32.5Hz oscillations, while perceptible 32.5Hz and 43.3Hz stimulation do not have the same effect.

The paper shows that gaze variability and alpha/beta oscillation amplitude modulations in visual cortex predict memory performance and are functionally linked during visual information encoding.

This study shows respiration modulates sleep oscillations and memory reactivation in humans by enhancing slow oscillations, spindles, and their coupling during inhalation peaks.

This study uses intrathalamic recordings to show that different thalamic nuclei coordinate neocortical oscillations during NREM sleep in humans, with distinct timing relationships between thalamic and cortical slow oscillations and spindles.

The paper investigates how saccades coordinate with neural circuits and hippocampal patterns to support memory formation during visual exploration.

The paper shows that thalamocortical interactions predict human visual perception, with mediodorsal thalamic activity mediating prefrontal cortex contributions to perceptual performance.

This study shows that endogenous memory reactivation during sleep is linked to slow oscillation spindle complexes and predicts memory consolidation in humans.

The paper shows that alpha/beta power decreases during encoding predict similar decreases during retrieval in episodic memory tasks.

The paper investigates saccadic modulation of neural activity in the human anterior thalamus during visual active sensing, finding phase concentration and suppression of high-frequency activity.

The paper shows that subcortical structures like the globus pallidus and thalamus influence interhemispheric modulation of alpha power during reward-related attention tasks.

The paper investigates how memory performance is influenced by the match or mismatch between encoding and retrieval modalities using MEG and a computational model.

The paper shows that memory reactivation patterns reoccur during NREM sleep at a 1 Hz slow oscillatory rhythm, coordinated by theta oscillations.

This paper decodes stimulus modality from single-trial MEG high frequency activity across subjects using beamformer source reconstruction and random forest classification, achieving 66.44% accuracy.

The paper shows that saccades are phase-locked to visual alpha oscillations in occipital and medial temporal lobe regions, enhancing memory encoding of visual scenes.