J. D. G. Watson

University of Sydney, Sydney, New South Wales, Australia

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Publications (5)27.1 Total impact

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    S.F. Cowell · G.F. Egan · C Code · J Harasty · J.D.G. Watson
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    ABSTRACT: We examined cerebral activation patterns with positron emission tomography (PET) in 12 right-handed normal volunteers while they were completing simple calculation tasks or merely repeating numbers. Using a parametric experimental design, during calculation we found activation in the medial frontal/cingulate gyri, left dorsolateral prefrontal cortex, left anterior insular cortex and right anterior insular cortex/putamen, left lateral parietal cortex, and the medial thalamus. Number repetition engaged bilateral inferior sensorimotor cortex, bilateral temporal areas, and left inferior frontal cortex. These results suggest a functional anatomical network for simple calculation, which includes aspects of attention, auditory, and motor processing and the phonological store and articulatory loop components of working memory; they add some support for a special role of the parietal cortex in calculation tasks.
    NeuroImage 12/2000; 12(5):565-73. DOI:10.1006/nimg.2000.0640 · 6.36 Impact Factor
  • S. F. Cowell · C. Code · J. Harasty · G. F. Egan · J. D. G. Watson
    Nuclear Medicine Communications 05/2000; 21(5). DOI:10.1097/00006231-200005000-00043 · 1.67 Impact Factor
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    ABSTRACT: A moving plaid is a composite pattern produced by superimposing two sinusoidal gratings which differ in orientation and motion direction. The perceived drift direction of a plaid appears to be determined partly by a binocular mechanism, which follows intersection of constraint rules (Burke and Wenderoth, 1993b), and partly by a monocular mechanism, which tracks the dark and bright intersects of the plaid, the contrast envelopes. The first neurones that respond to plaids as patterns rather than component gratings are found in area V5, also known as MT, which is exclusively binocular. Therefore, the psychophysical evidence suggesting that the contrast envelope tracking mechanism is monocular is surprising but has been obtained consistently. We aimed to localize the contrast envelope tracking mechanism by undertaking a positron emission tomography (PET) activation experiment in which the subjects were presented with alternating plaid components during the control scan and with the moving plaid resulting from the superposition of these components as the activation scan. The results showed differential activation in area V3. Recent results from macaque single cell recordings have also demonstrated increased sensitivity to moving plaid stimuli compared to the plaid component gratings in V3 neurones.
    NeuroImage 03/1999; 9(2):227-34. DOI:10.1006/nimg.1998.0398 · 6.36 Impact Factor
  • G. F. Egan · G. J. O'Keefe · C. Sonkilla · J. D. G. Watson · M. Coltheart
    NeuroImage 06/1996; 3(3). DOI:10.1016/S1053-8119(96)80022-X · 6.36 Impact Factor
  • P. Wenderoth · J. D. G. Watson · G. F. Egan · H. J. Tochon-Danguy
    NeuroImage 06/1996; 3(3). DOI:10.1016/S1053-8119(96)80303-X · 6.36 Impact Factor