Peter Ledochowitsch

The paper presents a database of spiking activity in the mouse visual system during an image change detection task, revealing task-specific coding patterns across brain regions.

The paper analyzes neuronal variability across brain states to understand how factors like internal dynamics, behavior, and stimuli influence sensory processing over time.

The paper analyzes saccade-responsive neurons in visual cortex, finding their distribution varies by cell type, area, and layer, but they do not show distinct visual response properties.

The paper identifies diverse functional neuron types in the visual cortex that process novel and familiar stimuli in mice.

This study investigates the localization and origins of sensory-evoked ECoG signals, finding they originate primarily from infragranular layers of a single cortical column in rats.

DeepInterpolation improves signal-to-noise ratio in neuroscience data without sacrificing resolution, enhancing detection of neuronal activity across multiple modalities.

This study compares neuronal responses in visual cortex using electrophysiology and two-photon imaging in awake mice, finding differences in responsiveness and selectivity and exploring data transformations to reconcile them.

The paper characterizes the relationship between spiking activity and fluorescence signals in GCaMP6-expressing neurons, finding GCaMP6s has better single-spike detection than GCaMP6f.

The paper presents a dataset and analysis of spiking activity across multiple mouse visual areas, revealing that functional connectivity mirrors anatomical hierarchy.

The paper examines how visual experience affects activity dynamics and stimulus coding in excitatory and VIP inhibitory cells in mouse visual cortex during a change detection task.

The paper presents a large-scale dataset of neural activity in the mouse visual cortex and shows that responses to different stimuli are largely independent, suggesting multi-layer hierarchical computation.

This study calibrates two-photon calcium imaging to recover action potentials in mice, finding that fluorescence changes are inconsistent for small spike numbers and vary by mouse line.

This paper demonstrates the feasibility of two-photon frequency division multiplexing (2P-FDM) for recording calcium signals in brain tissue, showing a significant reduction in cross-talk and improved signal quality.