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Brian A. Wandell
Researcher at Stanford University
Publications - 350
Citations - 30931
Brian A. Wandell is an academic researcher from Stanford University. The author has contributed to research in topics: Visual cortex & Pixel. The author has an hindex of 83, co-authored 341 publications receiving 28529 citations. Previous affiliations of Brian A. Wandell include PARC & Hewlett-Packard.
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Position sensitivity in the visual word form area
TL;DR: Findings show that position-sensitive information is present in the neural circuitry that conveys visual word form information to language areas, which supports the hypothesis that the VWFA analyzes word forms at an abstract level, far removed from specific stimulus features.
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Trichromatic opponent color classification
TL;DR: Measurements revealed the shapes of the boundaries that separate opponent colors in three-dimensional color space, and the effect of background light on classification was largely explained by separate gain changes in increment and decrement cone signals.
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Cone signal interactions in direction-selective neurons in the middle temporal visual area (MT).
TL;DR: The sensitivity of single MT neurons and the correlation between trial-to-trial variations in single neuron firing and perception are similar for S- and L,M-cone stimuli, further supporting a role for MT in processing chromatic motion.
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The posterior arcuate fasciculus and the vertical occipital fasciculus.
TL;DR: Here, a computational approach is used to create a reproducible method that delineates the pAF and VOF, which are of interest in many different fields and are not an agreed upon anatomical definition.
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White matter consequences of retinal receptor and ganglion cell damage.
Shumpei Ogawa,Shumpei Ogawa,Hiromasa Takemura,Hiromasa Takemura,Hiroshi Horiguchi,Masahiko Terao,Masahiko Terao,Tomoki Haji,Franco Pestilli,Jason D. Yeatman,Hiroshi Tsuneoka,Brian A. Wandell,Yoichiro Masuda,Yoichiro Masuda +13 more
TL;DR: Both photoreceptor layer (CRD) and retinal ganglion cell (LHON) retinal disease causes substantial change in the visual white matter, and diffusion changes measured in the optic tract and the optic radiation differ, suggesting that they are caused by different biological mechanisms.