Non-retinotopic motion induced by a Ternus-Pikler display

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Aversively-motivated associative learning allows animals to avoid harm and thus ensures survival. Aversive learning can be studied by the fear learning paradigm, in which an innocuous sensory stimulus like a tone (conditioned stimulus, CS), acquires a nega ...

The first stage of the Atkinson–Shiffrin model of human memory is a sensory memory (SM). The visual component of the SM was shown to operate within a retinotopic reference frame. However, a retinotopic SM (rSM) is unable to account for vision under natural ...

Visual processing can be seen as the integration and segmentation of features. Objects are composed of contours, integrated into shapes and segmented from other contours. Information also needs to be integrated to solve the ill-posed problems of vision. Fo ...

Information about a moving object is usually poor at each retinotopic location because photoreceptor activation is short, noisy, and affected by shadows, reflections of other objects, and so on. Integration across the motion trajectory may yield a much bet ...

The early visual system is organized retinotopically. However, under ecological viewing conditions, motion perception occurs in non-retinotopic coordinates. Even though many studies revealed the central role of nonretinotopic processes, very little is know ...

In the classic model of vision, processing is local, feedforward and hierarchical. The first stages of the visual system are retinotopic, i.e., neighboring points in the outside world are mapped onto neighboring photoreceptors of the retina and this is pre ...

OBJECTIVE The tremor circuitry has commonly been hypothesized to be driven by one or multiple pacemakers within the cerebello-thalamo-cortical pathway, including the cerebellum, contralateral motor thalamus, and primary motor cortex. However, previous stud ...

The present study describes the ipsilateral and contralateral corticocortical and corticothalamic connectivity of the occipital visual areas 17, 18, 19, and 21 in the ferret using standard anatomical tract-tracing methods. In line with previous studies of ...

Tactile working memory engages a broad network of cortical regions in primates. To assess whether the conclusions drawn from primates apply to rodents, we examined the vibrissal primary somatosensory cortex (vS1) and the prelimbic cortex (PL) in a delayed ...

External stimuli and tasks often elicit negative BOLD responses in various brain regions, and growing experimental evidence supports that these phenomena are functionally meaningful. In this work, the high sensitivity available at 7T was explored to map an ...

Encoding of visual information in the brain is retinotopic: Neighboring points in the visual field are mapped onto neighboring photoreceptors in the retina, and these neighborhood relations are maintained in the early stages of cortical processing. However ...

The spatial organization of mouse frontal cortex is poorly understood. Here, we used voltage-sensitive dye to image electrical activity in the dorsal cortex of awake head-restrained mice. Whisker-deflection evoked the earliest sensory response in a localiz ...

A large portion of the visual cortex is organized retinotopically, but perception is usually non-retinotopic. For example, a reflector on the spoke of a bicycle wheel appears to move on a circular or prolate cycloidal orbit as the bicycle moves forward, wh ...

Classically, stimuli are rendered unconscious by backward masking or binocular rivalry, where it is usually assumed that the mask or the stimulus in the contralateral eye suppress the target. Based, on the Ternus-Pikler display (http://lpsy.epfl.ch/researc ...

The visual representation of the world is often assumed to be retinotopic, and many visual brain areas are indeed organized retinotopically. Visual perception, however, is not based on a reference frame anchored in retinotopic coordinates. For example, whe ...

To cope with the complexity of vision, most models in neuroscience and computer vision are of hierarchical and feedforward nature. Low-level vision, such as edge and motion detection, is explained by basic low-level neural circuits, whose outputs serve as ...

Although visual integration is often thought to be retinotopic, visual features can be integrated across retinotopic locations. For example, when a Vernier is followed by a sequence of flanking lines on either side, a percept of two diverging motion stream ...

Schizophrenia impairs cognitive function as much as perception. For example, patients perceive global motion in random dot kinematograms less strongly, because the integration of the dots into a single Gestalt is complex (e.g., Chen, Nakayama, Levy, Matthy ...

As discovered by the Gestaltists, in particular by Duncker, we often perceive motion to be within a non-retinotopic reference frame. For example, the motion of a reflector on a bicycle appears to be circular, whereas, it traces out a cycloidal path with re ...

Due to the movements of the observer and those of objects in the environment, retinotopic representations are highly unstable during ecological viewing conditions. The phenomenal stability of our perception suggests that retinotopic representations are tra ...

Non-retinotopic motion induced by a Ternus-Pikler display

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Plasticity of sensory representations in the posterior insular cortex during fear learning

Information integration and information storage in retinotopic and non-retinotopic sensory memory

Spatial and temporal integration of visual features

Features integrate along a motion trajectory when object integrity is preserved

Non-retinotopic adaptive center-surround modulation in motion processing

Long-lasting feature integration

Normalization of aberrant pretherapeutic dynamic functional connectivity of extrastriate visual system in patients who underwent thalamotomy with stereotactic radiosurgery for essential tremor: a resting-state functional MRI study

Cortical and thalamic connectivity of occipital visual cortical areas 17, 18, 19, and 21 of the domestic ferret (Mustela putorius furo)

Neuronal Correlates of Tactile Working Memory in Prefrontal and Vibrissal Somatosensory Cortex

Mapping and characterization of positive and negative BOLD responses to visual stimulation in multiple brain regions at 7T

From retinotopic processing to nonretinotopic representation

Parallel pathways from whisker and visual sensory cortices to distinct frontal regions of mouse neocortex

EEG Correlates of Relative Motion Encoding

Retinotopic information is rendered invisible by non-retinotopic processing

Retinotopic encoding of the Ternus-Pikler display reflected in the early visual areas

Putting low-level vision into global context: Why vision cannot be reduced to basic circuits

Mandatory feature integration across retinotopic locations

Local versus global and retinotopic versus non-retinotopic motion processing in schizophrenia

A computational model for reference-frame synthesis with applications to motion perception

Retinotopy of visual masking and non-retinotopic perception during masking