about
Insect stereopsis demonstrated using a 3D insect cinema.Balance and coordination after viewing stereoscopic 3D televisionThe contrast sensitivity function of the praying mantis Sphodromantis lineola.Invisible noise obscures visible signal in insect motion detectionVertical binocular disparity is encoded implicitly within a model neuronal population tuned to horizontal disparity and orientation.A simple model accounts for the response of disparity-tuned V1 neurons to anticorrelated images.Understanding the cortical specialization for horizontal disparity.Stereoacuity with Frisby and revised FD2 stereo tests.The place of human psychophysics in modern neuroscience.Effects of age on a real-world What-Where-When memory task.Early computational processing in binocular vision and depth perception.A Single Mechanism Can Account for Human Perception of Depth in Mixed Correlation Random Dot Stereograms.Sensors for impossible stimuli may solve the stereo correspondence problem.The Stereoscopic Anisotropy Develops During Childhood.The binocular advantage in visuomotor tasks involving tools.Small or far away? Size and distance perception in the praying mantis.A quantitative explanation of responses to disparity-defined edges in macaque V2.Neurons in Striate Cortex Signal Disparity in Half-Matched Random-Dot Stereograms.Viewing 3D TV over two months produces no discernible effects on balance, coordination or eyesight.Stereo vision and strabismusStereopsis in animals: evolution, function and mechanisms.Unravelling the illusion of flicker fusion.Avoiding monocular artifacts in clinical stereotests presented on column-interleaved digital stereoscopic displays.Overestimation of stereo thresholds by the TNO stereotest is not due to global stereopsis.The optomotor response of the praying mantis is driven predominantly by the central visual field.Reduced visual surround suppression in schizophrenia shown by measuring contrast detection thresholdsStereo correspondence is optimized for large viewing distances.A specialization for vertical disparity discontinuities.Testing the horizontal-vertical stereo anisotropy with the critical-band masking paradigm.A Bayesian model of stereopsis depth and motion direction discrimination.Visual perception: one world from two eyes.The relative weight of shape and non-rigid motion cues in object perception: a model of the parameters underlying dynamic object discrimination.Thresholds for sine-wave corrugations defined by binocular disparity in random dot stereograms: Factor analysis of individual differences reveals two stereoscopic mechanisms tuned for spatial frequency.Two common psychophysical measures of surround suppression reflect independent neuronal mechanisms.Moderate acute alcohol intoxication has minimal effect on surround suppression measured with a motion direction discrimination task.Blindness to background: an inbuilt bias for visual objects.Does depth perception require vertical-disparity detectors?Conjunctions between motion and disparity are encoded with the same spatial resolution as disparity alone.Stereo vision requires an explicit encoding of vertical disparity.All Pulfrich-like illusions can be explained without joint encoding of motion and disparity.
P50
Q27302975-5B74B80D-967A-4319-BB39-5C043DD9289BQ27335722-B29F0003-B2CA-401C-BE47-482F7B1F51FDQ30658584-F57C037A-BF68-486E-BBF9-5971F13FCC34Q30855751-D99D3339-8A62-46B8-9183-EDE2A9240687Q30981771-0C735504-7705-4792-997A-00C215729715Q34189844-FF67AEA4-6FEE-4AEB-80C7-A50D58CB5F87Q34406794-0280E28F-E6F5-4FE8-9513-F4CFAF4DC848Q35070704-6BD53B99-53B8-4F1B-99E7-C69CE9E85F78Q35177010-471AC1C0-B37B-485F-A0D3-D67D4A3BFC17Q35618357-BBEECBBB-2F05-4383-973B-58D72EFBCFC1Q35911887-6F5EC1BD-CCDE-4D2B-9AEF-2530B81D7BE4Q36022760-99F378E0-CD0A-4616-A96D-CC2FDF2061DBQ36137276-BE38D9DD-A12E-4091-9DDC-52600CD3EAE9Q36677010-BC58F7A6-CA8A-4D2E-9D1D-A5D0B006C298Q36915189-7EC41855-F8AB-4E9E-9382-4C73BC714941Q36991196-886BBAE4-F76B-46E5-A75C-A35F0E167FBFQ37131756-52D508A7-C29F-4F38-8F18-350D4495E067Q37198430-F4764FE8-DD8C-4E8D-91A8-84CA9C10367EQ37300217-9D7C7363-CAA0-4D55-AB63-6672216D6D0AQ38283153-CA7B8235-E12E-4F9F-BEA3-CB6D5A8CFC8AQ38654931-934FD72B-6DE4-4D86-8980-EC5538CB189FQ39114114-574788E6-40CF-442F-9A7C-49773708C527Q40420735-38A50F60-CA26-46D3-A6B6-DFDDCE2D79D8Q41052927-8E2CDF78-CE1D-4D74-9CFD-49E03E361375Q41853407-7A916B49-3042-4689-84DE-79F5945888BBQ42029797-3F8AAF5B-AE8E-4845-B8EC-453D4AAF3DF7Q42855575-B00313F8-3070-454E-BFAF-157C24170082Q43106125-2B90C497-8970-4D44-A8C5-013200DC36E9Q43699009-98D8FF22-D47C-483C-BCDC-1C11E4F8BF2BQ43929643-37185A29-8089-447C-B49F-9806EBF2E3D0Q46932109-A75C3BBB-960A-4DD5-BEBE-5E346C06CD76Q47320951-12108EC6-53D2-47DC-9FFA-66053117A577Q47444893-B302C18C-7B7F-4E46-8E7D-7233417255F2Q48074129-02D5C6CA-136A-4390-9274-DDF19A5B2B49Q48135612-123BE46F-93B8-480E-8AFE-04ADDF9D67E2Q48206577-F8D97F7C-F353-485E-8A01-FA3F33E63D4FQ48316401-EC3344CB-4E53-4029-8826-515F4592AACAQ48340847-F088D1D4-42E9-4816-8D95-C6C66DC6A346Q48458100-DB76D58B-4DCB-4BF8-8E08-621286B0D7ACQ48670839-83D627C1-AAD6-4C3D-8779-310D9FC7289B
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Jenny Read
@ast
Jenny Read
@en
Jenny Read
@es
Jenny Read
@nl
type
label
Jenny Read
@ast
Jenny Read
@en
Jenny Read
@es
Jenny Read
@nl
prefLabel
Jenny Read
@ast
Jenny Read
@en
Jenny Read
@es
Jenny Read
@nl
P106
P1153
15136816000
P31
P496
0000-0002-9029-5185