Cognitive
Neuroscience Research
Cognitive neuroscience
is the study of human mental functions such as remembering,
attending, decision making, reading and speaking,
problem solving, etc., and the computational processes
and neural mechanisms underlying these functions
in the human brain. The cognitive neuroscience revolution
has led to a significant increase in our understanding
of the workings of the human mind and brain. Our
research in this domain primarily involves investigations
of the neural mechanisms of attention and working
memory, and the changes in these functions with
aging.
The major goal of
the research is to identify the spatiotemporal properties
of neural networks underlying selective and sustained
attention, using both event-related brain potentials (ERPs) and functional magnetic resonance imaging (fMRI). Another focus is to examine how these
networks change with both healthy aging and in persons
at risk for the development of Alzheimers disease (AD).
Using molecular genetic methods, we are also examining
genetic polymorphisms that influence the activity
of neurotransmitters that innervate these brain
networks, both in healthy individuals and in persons at risk for AD.
We are currently using the following cognitive neuroscience
methods in our research:
Event-related brain potentials (ERPs). See also ERP Systems Lab

functional magnetic resonance imaging (fMRI)
Transcranial Doppler Sonography (TCD)
Molecular genetic assays of single nucleotide
polymorphisms
Eye movement analysis

In addition, we are developing
neuroscience methods that can be used to examine
issues of human performance in complex tasks and
environments outside the laboratory.
See Neuroergonomics
Research.
Current Funded
Projects
2006-2007: Principal Investigator, Air Force Research Laboratory (Subcontract, Aptima Inc.) Phase I SBIR, “Quantitative Model of Human Dynamic Attention Allocation,” $29,902.
2004-2007 Principal Investigator, National Institute of Aging Grant R01 AG19653, "Apolipoprotein E, Cognition, and Alzheimer's Disease," $810,563.
Recent
Cognitive Neuroscience Publications
Caggiano, D., Jiang, Y., & Parasuraman, R. (2006). Aging and repetition priming for targets and distracters in a working memory task. Aging, Neuropsychology, and Cognition, 13, 1-22.
Espeseth, T. Greenwood, P. M., Reivang, I., Fjell, A. M., Walvhold, K. B., Westlye, E., Lundervold, A., Rootvelt, H., & Parasuraman, R. (2006). Interactive effects of APOE and CHRNA4 on attention and white matter volume in healthy middle-aged and older adults. Cognitive, Behavioral, and Affective Neuroscience,6(1), 31-43.
Fu, S., Caggiano, D. M., Greenwood, P. M., & Parasuraman, R. (2005a). Event-related potentials reveal dissociable mechanisms for orienting and focusing visuospatial attention. Cognitive Brain Research,23, 341-353.
Fu, S., Greenwood, P. M., & Parasuraman, R. (2005b). Brain mechanisms of involuntary visuospatial attention: An event-related potential study. Human Brain Mapping, 25, 378–390.
Greenwood, P. M., Fossella, J., & Parasuraman, R (2005a). Specificity of the effect of a nicotinic receptor polymorphism on individual differences in visuospatial attention. Journal of Cognitive Neuroscience, 17, 1611-1620.
Greenwood, P., Lambert, C., Sunderland, T., & Parasuraman, R. (2005b). Effects of Apolipoprotein E genotype on spatial attention, working memory, and their interaction in healthy, middle-aged adults: Results from the National Institute of Mental Health’s BIOCARD Study. Neuropsychology, 19, 199-211.
Greenwood, P. M., Sunderland, T., Putnam, K., Levy, J., & Parasuraman, R. (2005c). Scaling of visuospatial attention undergoes differential longitudinal change as a function of APOE genotype prior to old age: Results from the National Institute of Mental Health’s BIOCARD study. Neuropsychology,19, 830-840.
Parasuraman, R., Greenwood, P. M., Kumar, R., & Fossella, J. (2005). Beyond heritability: Neurotransmitter genes differentially modulate visuospatial attention and working memory. Psychological Science, 16(3), 200-207.
Greenwood, P. M., Sunderland, T., Friz, J. L., & Parasuraman, R. (2000). Genetics and visual attention: Selective deficits in healthy adult carriers of the e4 allele of the apolipoprotein E gene. Proceedings of the National Academy of Sciences.97, 11661-11666.
Jiang, Y., Haxby, J. V., Martin, A., Ungerleider, L. G., & Parasuraman, R. (2000). Complementary neural mechanisms for tracking itemsin human working memory. Science, 287, 643-646.
Levy, J., Parasuraman, R, Greenwood, P. G, Dukoff, R., & Sunderland, T. (2000). Acetylcholine affects the spatial distribution of attention: Evidence from Alzheimer’s disease. Neuropsychology, 14, 288-298.
Greenwood, P., & Parasuraman, R. (2004). The scaling of spatial attention in visual search and its modification in healthy aging. Perception and Psychophysics, 66(1), 3-22.
Greenwood, P., & Parasuraman, R. (2003). Normal genetic variation, cognition, and aging. Behavioral and Cognitive Neuroscience Reviews,2, 278-306.
Jiang, Y., Luo, Y., & Parasuraman, R. (2002). Neural correlates of perceptual priming of visual motion. Brain Research Bulletin, 57, 211-219.
Jiang, Y., Luo, Y., & Parasuraman, R. (2002) Two-dimensional visual motion priming is reduced in older adults. Neuropsychology, 16, 140-145.
Parasuraman, R., Greenwood, P., & Sunderland, T. (2002). The apolipoprotein E gene, attention, and brain function. Neuropsychology, 16, 254-274.
Luo, Y., Greenwood, P. M., & Parasuraman, R. (2001). Dynamics of the spatial scale of visual attention revealed by brain event-related potentials. Cognitive Brain Research, 12, 371-381.
Jiang, Y., Haxby, J. V., Martin, A., Ungerleider, L. G., & Parasuraman, R. (2000). Complementary neural mechanisms for tracking itemsin human working memory. Science, 287, 643-646.
Parasuraman, R., Greenwood, P. M., & Alexander, G. E. (2000). Alzheimer’s disease reduces the dynamic range of spatial attention in visual search. Neuropsychologia, 38,1126-1135.
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