Robert O. Duncan
University of California, San Diego
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Featured researches published by Robert O. Duncan.
Neuron | 2003
Robert O. Duncan; Geoffrey M. Boynton
We measured linear cortical magnification factors in V1 with fMRI, and we measured visual acuity (Vernier and grating) in the same observers. The cortical representation of both Vernier and grating acuity thresholds in V1 was found to be roughly constant across all eccentricities. We also found a within-observer correlation between cortical magnification and Vernier acuity, further supporting claims that Vernier acuity is limited by cortical magnification in V1.
Progress in Retinal and Eye Research | 2007
Robert O. Duncan; Pamela A. Sample; Robert N. Weinreb; Christopher Bowd; Linda M. Zangwill
Primary open angle glaucoma (POAG) is a progressive optic neuropathy characterized by retinal ganglion cell loss. Experimental primate glaucoma indicates neuronal degeneration of the lateral geniculate nucleus (LGN) and activity changes in the visual cortex (V1). Neuronal degeneration has also been shown in a post-mortem human study of the optic nerve, LGN and visual cortex. Functional magnetic resonance imaging (fMRI), a non-invasive means of inferring function-specific neuronal activity, provides an opportunity to evaluate glaucomatous changes in neuronal activity throughout the visual pathway in vivo. The purpose of this study is to demonstrate that the relationship between visual field loss in human POAG and the functional organization of V1 can be measured using novel fMRI analysis methods. Visual field defects were measured using standard automated perimetry (SAP). A retinotopic map of visual space was obtained for V1, and the retinotopy data was fit with a template. The template was used to project regions within the visual field onto a flattened representation of V1. Viewing through the glaucomatous vs. fellow eye was compared by alternately presenting each eye with a scotoma-mapping stimulus. The resulting blood oxygen level dependent (BOLD) fMRI response was compared to interocular differences in thresholds for corresponding regions of the visual field. The spatial pattern of activity observed in the flattened representation agreed with the pattern of visual field loss. Furthermore, the amplitude of the BOLD response was correlated on a pointwise basis with the difference in sensitivity thresholds between the glaucomatous and fellow eyes (r = 0.53, p < 0.0001). The BOLD signal in human V1 is altered for POAG patients in a manner consistent with the loss of visual function. FMRI of visual brain areas is a potential means for quantifying glaucomatous changes in neuronal activity. This should enhance our understanding of glaucoma, and could lead to new diagnostic techniques and therapies.
Vision Research | 2012
Robert O. Duncan; Pamela A. Sample; Christopher Bowd; Robert N. Weinreb; Linda M. Zangwill
PURPOSE Altered metabolic activity has been identified as a potential contributing factor to the neurodegeneration associated with primary open angle glaucoma (POAG). Consequently, we sought to determine whether there is a relationship between the loss of visual function in human glaucoma and resting blood perfusion within primary visual cortex (V1). METHODS Arterial spin labeling (ASL) functional magnetic resonance imaging (fMRI) was conducted in 10 participants with POAG. Resting cerebral blood flow (CBF) was measured from dorsal and ventral V1. Behavioral measurements of visual function were obtained using standard automated perimetry (SAP), short-wavelength automated perimetry (SWAP), and frequency-doubling technology perimetry (FDT). Measurements of CBF were compared to differences in visual function for the superior and inferior hemifield. RESULTS Differences in CBF between ventral and dorsal V1 were correlated with differences in visual function for the superior versus inferior visual field. A statistical bootstrapping analysis indicated that the observed correlations between fMRI responses and measurements of visual function for SAP (r=0.49), SWAP (r=0.63), and FDT (r=0.43) were statistically significant (all p<0.05). CONCLUSIONS Resting blood perfusion in human V1 is correlated with the loss of visual function in POAG. Altered CBF may be a contributing factor to glaucomatous optic neuropathy, or it may be an indication of post-retinal glaucomatous neurodegeneration caused by damage to the retinal ganglion cells.
Human Brain Mapping | 2008
Kun Lu; Joanna E. Perthen; Robert O. Duncan; Linda M. Zangwill; Thomas T. Liu
To date, functional magnetic resonance imaging (fMRI) studies of the lateral geniculate nucleus (LGN) have primarily focused on measures of the blood oxygenation level dependent (BOLD) signal. Arterial spin labeling (ASL) is an MRI method that can provide direct measures of functional cerebral blood flow (CBF) changes. Because CBF is a well‐defined physiological quantity that contributes to BOLD contrast, CBF measures can be used to improve the quantitative interpretation of fMRI studies. However, due in part to the low intrinsic signal‐to‐noise ratio of the ASL method, measures of functional CBF changes in the LGN are challenging and have not previously been reported. In this study, we demonstrate the feasibility of using ASL fMRI to measure the CBF response of the LGN to visual stimulation on a 3 T MRI system. The use of background suppression and physiological noise reduction techniques allowed reliable detection of LGN activation in all five subjects studied. The measured percent CBF response during activation ranged from 40 to 100%, assuming no interaction between the left and right LGN. Hum Brain Mapp 2008.
international conference on interactive digital storytelling | 2017
Colette Daiute; Robert O. Duncan
This poster presents cross-disciplinary theory to identify inter-dependent processes of digital and human systems involved in Interactive Digital Narrative (IDN). Extending previous research on IDN design affordances and Human Development (HD) capacities, the project explores theory with a method for understanding reciprocal person-program synergies. The poster defines this program-person synergy as “interactive imagining” and sketches a research approach for studying such shared processing. This illustrative research method involves the think-aloud protocol method adapted to foster IDN designer-player dialogue around problematic, surprising or otherwise interesting IDN episodes, indicated in previous pilot gameplay. The poster outlines a think-aloud study to examine the nature and impact of interactive imagining among student designer-players in an interdisciplinary college setting. The goal of this inquiry is to expand the definition of IDN as an inter-subjective process including the meta-reflections of designer and player, thereby advancing IDN theory and practice.
The Journal of Neuroscience | 2000
Robert O. Duncan; Thomas D. Albright; Gene R. Stoner
Cerebral Cortex | 2007
Robert O. Duncan; Geoffrey M. Boynton
Investigative Ophthalmology & Visual Science | 2007
Robert O. Duncan; Pamela A. Sample; Robert N. Weinreb; Christopher Bowd; Linda M. Zangwill
Journal of Vision | 2010
Robert O. Duncan; Geoffrey M. Boynton
Journal of Vision | 2002
Geoffrey M. Boynton; Robert O. Duncan