Emiliano Ronzitti

The paper identifies rod bipolar and AII amacrine cells as key to surround responses in OFF retinal ganglion cells through optogenetics and electrophysiology.

This paper introduces VADER1, a red GEVI that enables reliable in vivo two-photon voltage imaging with millisecond resolution and supports dual-color imaging with calcium indicators.

This paper introduces a high-throughput method for in vivo synaptic connectivity mapping using optogenetics and compressive sensing, achieving rapid and accurate identification of synaptic pairs in mice.

This paper introduces FLiT, a method for ultra-fast sequential light targeting to enable precise and scalable control of neuronal networks.

This paper demonstrates a method using a GRIN lens to perform precise 3D optogenetic photostimulation in vivo in mice, enabling deeper tissue penetration and multi-neuron stimulation.

The paper demonstrates that rod bipolar cells provide asymmetric input to direction selective ganglion cells, contributing to their direction selectivity through all-optical manipulation and imaging.

The paper introduces a method for high-resolution multi-cell optogenetic targeting using temporally focused light shaping in Drosophila and zebrafish larvae.

This paper demonstrates sub-millisecond optogenetic activation in mouse visual cortex using parallel holographic illumination, enabling precise control of neuronal activity with millisecond temporal resolution.

This study demonstrates sub-millisecond optogenetic control of neuronal firing using two-photon holographic photoactivation of Chronos, achieving precise and repeated spiking up to 100 Hz.