The VESPA: A method for the rapid estimation of a visual evoked potential

NeuroImage

Volumn 32, Issue 4, 2006, Pages 1549-1561

  Lalor, Edmund C ^a,b   Pearlmutter, Barak A ^c   Reilly, Richard B ^a,b   McDarby, Gary ^a   Foxe, John J ^b,d  

^a UNIVERSITY COLLEGE DUBLIN   (Ireland)

^b St Vincent's Hospital Ireland   (Ireland)

^c NATIONAL UNIVERSITY OF IRELAND   (Ireland)

^d CITY COLLEGE OF NEW YORK   (United States)

Author keywords

EEG; Experimental design; Magnocellular; Striate cortex; System identification; Visual evoked potential

Indexed keywords

ADULT; ANALYTIC METHOD; ARTICLE; ASSAY; ELECTROENCEPHALOGRAPHY; EVOKED VISUAL RESPONSE; EXPERIMENTAL STUDY; FEMALE; GIANT CELL; HUMAN; HUMAN EXPERIMENT; MALE; NEUROSCIENCE; NORMAL HUMAN; PRIORITY JOURNAL; SIGNAL NOISE RATIO; STIMULUS RESPONSE; STRIATE CORTEX; VISUAL STIMULATION; VISUAL SYSTEM;

ADULT; ALGORITHMS; ELECTROENCEPHALOGRAPHY; EVOKED POTENTIALS, VISUAL; FEMALE; FIXATION, OCULAR; HUMANS; LIGHT; MALE; PATTERN RECOGNITION, VISUAL; PHOTIC STIMULATION; SIGNAL PROCESSING, COMPUTER-ASSISTED; SOFTWARE;

EID: 33748314504     PISSN: 10538119     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroimage.2006.05.054     Document Type: Article

References (31)

1. Alexander K., Rajagopalan A., Seiple W., Zemon V., and Fishman G. Contrast response properties of magnocellular and parvocellular pathways in retinitis pigmentosa assessed by the visual evoked potential. Invest. Ophthalmol. Visual Sci. 46 8 (2005) 2967-2973
2. Buracas G., and Boynton G. Efficient design of event-related fMRI experiments using M-sequences. NeuroImage 16 3 (2002) 801-813
3. Cobb W., and Dawson G. The latency and form in man of the occipital potentials evoked by bright flashes. J. Physiol. 152 (1960) 108-121
4. Coppola R. A system transfer function for visual evoked potentials. In: Lehmann D., and Callaway E. (Eds). Human Evoked Potentials: Applications and Problems, NATO III: Human Factors vol. 9 (1979), Plenum Press 69-82
5. Delorme A., and Makeig S. EEGLAB: an open source toolbox for analysis of single-trial EEG dynamics including independent component analysis. J. Neurosci. Methods 134 1 (2004) 9-21
6. Doniger G., Foxe J., Schroeder C.E., anMurray M., Higgins B., and Javitt D. Visual perceptual learning in human object recognition areas: a repetition priming study using high-density electrical mapping. NeuroImage 13 2 (2001) 305-313
7. Fotiou F., Fountoulakis K., Iacovides A., and Kaprinis G. Pattern-reversed visual evoked potentials in subtypes of major depression. Psychiatry Res. 118 3 (2003) 259-271
8. Foxe J., and Simpson G. Flow of activation from v1 to frontal cortex in humans: a framework for defining 'early' visual processing. Exp. Brain Res. 142 1 (2002) 139-150
9. Foxe J., Murray M., and Javitt D. Fillingin in schizophrenia: a high-density electrical mapping and source-analysis investigation of illusory contour processing. Cereb. Cortex 15 (2005) 1914-1927
10. Gomez-Gonzalez C., Clark V., Fan S., Luck S., and Hillyard S. Sources of attention-sensitive visual event-related potentials. Brain Topogr. 7 1 (1994) 41-51
11. Gruber T., Müller M.M., Keil A., and Elbert T. Selective visual-spatial attention alters induced gamma band responses in the human EEG. Clin. Neurophysiol. 110 12 (1999) 2074-2085
12. Halliday A., McDonald W., and Mushin J. Delayed visual evoked response in optic neuritis. Lancet 6 1 (1972) 982-985
13. Hubel D., and Wiesel T. Receptive fields of single neurones in the cat's striate cortex. J. Physiol. 148 (1959) 574-591
14. Kelly S.P., Lalor E.C., Reilly R.B., and Foxe J.J. Visual spatial attention tracking using high-density SSVEP data for independent brain-computer communication. IEEE Trans. Neu. Syst. Rehab. 13 2 (2005) 172-178
15. Kemner C., Verbaten M., Cuperus J., Camfferman G., and Van Engeland H. Visual and somatosensory event-related brain potentials in autistic children and three different control groups. Electroencephalogr. Clin. Neurophysiol. 92 3 (1994) 225-237
16. Kupersmith M., Siegel I., Carr R.J.R., Flamm E., and Shakin E. Visual evoked potentials in chiasmal gliomas in four adults. Arch. Neurol. 38 6 (1981) 362-365
17. Malpeli J., Lee D., and Baker F. Laminar and retinotopic organization of the macaque lateral geniculate nucleus: magnocellular and parvocellular magnification functions. J. Comp. Neurol. 375 3 (1996) 363-377
18. Markey, H.K. and Antheil, G. (1942). Secret communication system. US Patent 2,292,387.
19. Marmarelis P.Z., and Marmarelis V.Z. Analysis of Physiological Systems: The White Noise Approach (1978), Plenum Press
20. Matthews W., Small D., Small M., and Pountney E. Pattern reversal evoked visual potential in the diagnosis of multiple sclerosis. J. Neurol., Neurosurg. Psychiatry 40 10 (1977) 1009-1014
21. Maunsell J., Ghose G., Assad J., McAdams C., Boudreau C., and Noerager B. Visual response latencies of magnocellular and parvocellular lgn neurons in macaque monkeys. Vis. Neurosci. 16 (1999) 1-14
22. Müller M.M., and Hillyard S.A. Concurrent recording of steady-state and transient event-related potentials as indices of visual-spatial selective attention. Clin. Neurophysiol. 111 (2000) 1544-1552
23. Müller M.M., Gruber T., and Keil A. Modulation of induced gamma band activity in the human EEG by attention and visual information processing. Int. J. Psychophysiol. 38 3 (2000) 283-299
24. Müller M.M., Malinowski P., Gruber T., and Hillyard S.A. Sustained division of the attentional spotlight. Nature 424 7 (2003) 309-312
25. Murray M., Foxe D., Javitt D., and Foxe J. Setting boundaries: brain dynamics of modal and amodal illusory shape completion in humans. J. Neurosci. 24 31 (2004) 6898-6903
26. Regan D. Human Brain Electrophysiology: Evoked Potentials and Evoked Magnetic Fields in Science and Medicine (1989), Elsevier
27. Schroeder C., Mehta A., and Givre S. A spatiotemporal profile of visual system activation revealed by current source density analysis in the awake macaque. Cerebral. Cortex 8 7 (1998) 575-592
28. Shibata T., Shimoyama I., Ito T., Abla D., Iwasa H., Koseki K., Yamaouchi N., Sato T., and Nakajima Y. Attention changes the peak latency of the visual gamma-band oscillation of the EEG. NeuroReport 10 6 (1999) 167-170
29. Tyler C. Analysis of visual modulation sensitivity: II. Peripheral retina and the role of photoreceptor dimensions. J. Opt. Soc. Am. 2 (1985) 393-398
30. Vaughan Jr. H., and Hull R. Functional relation between stimulus intensity and photically evoked cerebral responses in man. Nature 206 985 (1965) 720-722
31. Yamaguchi S., Tsuchiya H., and Kobayashi S. Electrophysiologic correlates of visuospatial attention shift. EEG and Clinical Neurophysiology 94 6 (1995) 450-461