Stereopsis and magnocellular sensitivity in schizophrenia

References

• Breitmeyer BG, Ganz L. Implications of sustained and transient channels for theories of visual pattern masking, saccadic suppression, and information processing. Psychol Rev 1976; 83: 1–36
   PubMed Web of Science ®Google Scholar
• Butler PD, Javitt DC. Early-stage visual processing deficits in schizophrenia. Curr Opin Psychiatry 2005; 18: 151–157
   PubMed Web of Science ®Google Scholar
• Butler PD, Schechter I, Zemon V, et al. Dysfunction of early-stage visual processing in schizophrenia. Am J Psychiatry 2001; 158: 1126–1133
   PubMed Web of Science ®Google Scholar
• Butler PD, Zemon V, Schechter I, et al. Early-stage visual processing and cortical amplification deficits in schizophrenia. Arch Gen Psychiatry 2005; 62: 495–504
   PubMed Web of Science ®Google Scholar
• Butler PD, Martinez A, Foxe J, et al. Subcortical visual dysfunction in schizophrenia drives secondary cortical impairments. Brain 2007; 130: 417–430
   PubMed Web of Science ®Google Scholar
• Cadenhead KS, Geyer MA, Butler RW, Perry W, Sprock J, Braff DL. Information processing deficits of schizophrenia patients: relationship to clinical ratings, gender and medication status. Schizophr Res 1997; 28: 51–62
   PubMed Web of Science ®Google Scholar
• Ferster D. A comparison of binocular depth mechanisms in areas 17 and 18 of the cat visual cortex. J Physiol (London) 1981; 311: 623–655
   Google Scholar
• De Yoe EA, Van Essen DC. Concurrent processing streams in monkey visual cortex. Trends Neurosc 1988; 11: 219–226
   PubMed Web of Science ®Google Scholar
• Green MF, Nuechterlein KH, Mintz J. Backward masking in schizophrenia and mania, II: specifying the visual channels. Arch Gen Psychiatry 1994; 51: 945–951
   PubMed Web of Science ®Google Scholar
• Green MF, Nuechterlein KH, Breitmeyer B, Tsuang J, Mintz J. Forward and backward visual masking in schizophrenia: influence of age. Psychol Med 2003; 33: 887–895
   PubMed Web of Science ®Google Scholar
• Hendry SH, Reid RC. The koniocellular pathway in primate vision. Annu Rev Neurosci 2000; 23: 127–153
   PubMed Web of Science ®Google Scholar
• Kingdom FA, Simmons DR, Rainville S. On the apparent collapse of stereopsis in random-dot-stereograms at isoluminance. Vis Res 1999; 39: 2127–2141
   PubMed Web of Science ®Google Scholar
• Keri S, Antal A, Szekeres G, Benedek G, Janka Z. Spatiotemporal visual processing in schizophrenia. J Neuropsychiatr Clin Neurosci 2002; 14: 190–196
   PubMed Web of Science ®Google Scholar
• Keri S, Kelemen O, Benedek G, Janka Z. Vernier threshold in patients with schizophrenia and their unaffected siblings. Neuropsychology 2004; 18: 537–542
   PubMed Web of Science ®Google Scholar
• Livingstone MS, Hubel DH. Psychophysical evidence for separate channels for the perception of form, color, movement and depth. J Neurosci 1987; 7: 3416–3468
   PubMed Web of Science ®Google Scholar
• Livingstone MS, Hubel DH. Segregation of form, color, movement, and depth: Anatomy, physiology, and perception. Science 1988; 240: 740–749
   PubMed Web of Science ®Google Scholar
• Martin KAC. Parallel pathways converge. Curr Biol 1992; 2: 555–557
   PubMedGoogle Scholar
• McClure RK. The visual backward masking deficit in schizophrenia. Prog Neuro-Psychopharmacol Biol Psychiatry 2001; 25: 301–311
   PubMed Web of Science ®Google Scholar
• Merigan WH, Maunsell JHR. How parallel are the primate visual pathways?. Annu Rev Neurosci 1993; 16: 369–402
   PubMed Web of Science ®Google Scholar
• Nassi JJ, Lyon DC, Callaway EM. The parvocellular LGN provides a robust disynaptic input to the visual motion area MT. Neuron 2006; 50: 319–327
   PubMed Web of Science ®Google Scholar
• O'Donnell BF, Bismark A, Hetrick WP, Bodkins M, Vohs JL, Shekhar A. Early stage vision in schizophrenia and schizotypal personality disorder. Schizophr Res 2006; 86: 89–98
   PubMed Web of Science ®Google Scholar
• Ohzawa I, Freeman RD. The binocular organization of simple cells in the cat's visual cortex. J Neurophysiol 1986a; 56: 221–242
   PubMed Web of Science ®Google Scholar
• Ohzawa I, Freeman RD. The binocular organization of complex cells in the cat's visual cortex. J Neurophysiol 1986b; 56: 243–259
   PubMedGoogle Scholar
• Ohzawa I, DeAngelis GC, Freeman RD. Stereoscopic depth discrimination in the visual cortex: neurons ideally suited as disparity detectors. Science 1990; 249: 1037–1041
   PubMed Web of Science ®Google Scholar
• Poggio GF, Fischer B. Binocular interaction and depth sensitivity in striate and prestriate cortex of behaving rhesus monkey. J Neurophysiol 1977; 40: 1392–1405
   PubMed Web of Science ®Google Scholar
• Rassovsky Y, Green MF, Nuechterlein KH, Breitmeyer B, Mintz J. Paracontrast and metacontrast in schizophrenia: clarifying the mechanism for visual masking deficits. Schizophr Res 2004; 71: 485–492
   PubMed Web of Science ®Google Scholar
• Rund BR. Backward-masking performance in chronic and nonchronic schizophrenics, affectively disturbed patients, and normal control subjects. J Abnorm Psychol 1993; 102: 74–81
   PubMed Web of Science ®Google Scholar
• Scharff LV, Geisler WS. Stereopsis at isoluminance in the absence of chromatic aberrations. J Opt Soc Am A 1992; 9: 868–876
   PubMedGoogle Scholar
• Schechter I, Butler PD, Silipo G, Zemon V, Javitt DC. Magnocellular and parvocellular contributions to backward masking dysfunction in schizophrenia. Schizophr Res 2003; 64: 91–101
   PubMed Web of Science ®Google Scholar
• Schechter I, Butler PD, Zemon VM, et al. Impairments in generation of early-stage transient visual evoked potentials to magno- and parvocellular-selective stimuli in schizophrenia. Clin Neurophysiol 2005; 116: 2204–2215
   PubMed Web of Science ®Google Scholar
• Schechter I, Butler PD, Jalbrzikowski M, Pasternak R, Saperstein AM, Javitt DC. A new dimension of sensory dysfunction: stereopsis deficits in schizophrenia. Biol Psychiatry 2006; 60: 1282–1284
   PubMed Web of Science ®Google Scholar
• Schiller PH, Logothetis NK. The color-opponent and broad-band channels of the primate visual system. Trend Neurosci 1990; 13: 392–398
   PubMed Web of Science ®Google Scholar
• Schiller PH, Logothetis NK., Charles ER. Functions of the colour-opponent and broad-band channels of the visual system. Nature 1990a; 343: 68–70
   PubMed Web of Science ®Google Scholar
• Schiller PH, Logothetis NK, Charles ER. Role of the color-opponent and broad-band channels in vision. Vis Neurosci 1990b; 5: 321–46
   PubMed Web of Science ®Google Scholar
• Schiller PH, Slocum WM, Weiner VS. How the parallel channels of the retina contribute to depth processing. Eur J Neurosci 2007; 26: 1307–1321
   PubMedGoogle Scholar
• Schwartz BD, McGinn T, Winstead DK. Disordered spatiotemporal processing in schizophrenics. Biol Psychiatry 1987; 22: 688–698
   PubMed Web of Science ®Google Scholar
• Selemon LD, Begovic A. Stereologic analysis of the lateral geniculate nucleus of the thalamus in normal and schizophrenic subjects. Psychiatry Res 2007; 151: 1–10
   PubMed Web of Science ®Google Scholar
• Shipp S, Zeki S. Segregation of pathways leading from area V2 to areas V4 and V5 of macaque monkey visual cortex. Nature 1985; 315: 322–324
   PubMed Web of Science ®Google Scholar
• Simmons DR, Kingdom FA. Contrast thresholds for stereoscopic depth identification with isoluminant and isochromatic stimuli. Vis Res 1994; 34: 2971–2982
   PubMed Web of Science ®Google Scholar
• Simmons DR, Kingdom FA. Differences between stereopsis with isoluminant and isochromatic stimuli. J Opt Soc Am A 1995; 12: 2094–2104
   Google Scholar
• Sincich LC, Park KF, Wohlgemuth MJ, Horton JC. Bypassing V1: a direct geniculate input to area MT. Nat Neurosci 2004; 7: 1123–1128
   PubMed Web of Science ®Google Scholar
• Skottun BC. The magnocellular deficit theory of dyslexia: the evidence from contrast sensitivity. Vision Res 2000; 40: 111–127
   PubMed Web of Science ®Google Scholar
• Skottun BC. On the use of metacontrast to assess magnocellular function in dyslexic readers. Percept Psychophys 2001; 63: 1271–1274
   PubMed Web of Science ®Google Scholar
• Skottun BC, Skoyles JR. Is coherent motion an appropriate test for magnocellular sensitivity?. Brain Cogn 2006; 61: 172–180
   PubMed Web of Science ®Google Scholar
• Skottun BC, Skoyles JR. Metacontrast, target recovery, and the magno- and parvocellular systems: a perspective. Vis Neurosci 2007a; 24: 177–181
   PubMed Web of Science ®Google Scholar
• Skottun BC, Skoyles J. A few remarks on assessing magnocellular sensitivity in Schizophrenic patients. Brain 2007b; 130: e 83
   Google Scholar
• Skottun BC, Skoyles JR. Some remarks on the use of visually evoked potentials to measure magnocellular activity. Clin Neurophysiol 2007c; 118: 1903–1905
   PubMedGoogle Scholar
• Skottun BC, Skoyles JR. Contrast sensitivity and magnocellular functioning in schizophrenia. Vision Res 2007d; 47: 2923–2933
   PubMed Web of Science ®Google Scholar
• Slaghuis WL. Contrast sensitivity for stationary and drifting spatial frequency gratings in positive- and negative-symptom schizophrenia. J Abnorm Psychol 1998; 107: 49–62
   PubMed Web of Science ®Google Scholar
• Slaghuis WL. Spatio-temporal luminance contrast sensitivity and visual backward masking in schizophrenia. Exp Brain Res 2004; 156: 196–211
   PubMed Web of Science ®Google Scholar
• Slaghuis WL, Bishop AM. Luminance flicker sensitivity in positive- and negative-symptom schizophrenia. Exp Brain Res 2001; 138: 88–99
   PubMedGoogle Scholar
• Slaghuis WL, Thompson AK. The effect of peripheral visual motion on focal contrast sensitivity in positive- and negative-symptom schizophrenia. Neuropsychologia 2003; 41: 968–980
   PubMed Web of Science ®Google Scholar
• Uhlhaas PJ, Mishara AL. Perceptual anomalies in schizophrenia: integrating phenomenology and cognitive neuroscience. Schizophr Bull 2007; 33: 142–156
   PubMed Web of Science ®Google Scholar
• Zeki SM. Colour coding in rhesus monkey prestriate cortex. Brain Res 1973; 53: 422–427
   PubMed Web of Science ®Google Scholar