Greg D. Field

The paper introduces a computational framework to design stimuli that selectively manipulate specific retinal ganglion cell types with minimal impact on others.

The paper uses encoding manifolds to analyze how mouse visual cortical areas represent natural scenes and static gratings, revealing layer-specific and cell-type-specific response patterns.

This paper introduces a high-throughput method for studying retinal ganglion cell projections, physiology, and morphology across species without relying on genetically modified animals.

The paper decomposes retinal ganglion cell electrical images to infer cell types and functional properties using a novel optimization-based algorithm.

The paper identifies functional diversity in primate retinal ganglion cells (RGCs) through multi-electrode recordings, revealing non-classical receptive field structures and specialized roles beyond spatial filtering.

This paper develops a deep learning model of the retina with photoreceptor adaptation mechanisms, improving prediction of primate and rat retinal ganglion cell responses to dynamic stimuli.

This study compares how retinal and V1 neural populations encode visual features, finding discrete encoding in retina and continuous in V1, with CNNs resembling retinal encoding.

This study shows that gene therapy for retinitis pigmentosa is most effective when administered before 50% rod loss, as later treatment fails to restore normal retinal function.

The paper introduces a scalable variational inference method for estimating low-rank spatio-temporal receptive fields in neural data, showing improved performance over existing estimators.

This paper introduces a 1-photon light-sheet microscopy system for high-throughput, high-resolution functional analysis of retinal neurons.

The paper shows that cones and their retinal pathways remain functional in advanced retinal degeneration, even as cones lose their outer-segment structures.

The paper introduces DART.2, a method for cell-specific drug delivery, demonstrating robust bidirectional editing of neurotransmission in mice.

The paper examines how light adaptation affects the spatiotemporal receptive field structures of retinal ganglion cell types in rats, finding that their relative organization is largely preserved.

This study shows that cone-mediated signaling remains robust in retinal ganglion cells despite rod photoreceptor degeneration, suggesting gene therapies may still effectively preserve vision.

This study shows that local synaptic inhibition in the cerebellar granule cell layer sparsens sensory responses and enables pattern separation, crucial for sensorimotor learning in mice.

The paper uses efficient coding theory to show how retinal mosaics and cell types emerge with varying channel capacity and noise levels.

The paper shows that rod photoreceptors use coordinated, multivesicular release to efficiently transmit single photon responses under low-light conditions.

The paper uses efficient coding theory to determine the optimal spatial arrangement of ON and OFF receptive fields in the retina based on noise and stimulus statistics.

The paper shows that ignoring correlated noise in retinal ganglion cells leads to poor decoding performance under moonlight conditions.

The paper studies how populations of direction-selective retinal ganglion cells encode and decode global motion, finding that larger populations achieve high temporal precision despite sparse and broadly tuned responses.

This study shows that Thrombospondin-1 promotes circuit-specific synapse formation in direction-selective retinal ganglion cells via β1-integrin.

This study shows that activating rod input in a retinal degeneration model restores synaptic structure, circuitry, and visual signaling in adult mice.

The paper investigates how GABAergic inhibition affects the sensitivity, receptive field size, and response polarity of direction-selective ganglion cells under low light conditions.

This study examines the temporal resolution of primate rod photoreceptor responses to single photons and identifies key noise sources limiting their ability to encode photon arrival timing.

The paper examines ON and OFF retinal ganglion cell pathways in rats, finding pathway-specific asymmetries in receptive field properties.

The paper shows that starburst amacrine cells use homotypic contacts to initiate formation of a dendritic scaffold in the retina, which is critical for direction-selective circuitry.