Szabolcs Kéri

Prof. Szabolcs Kéri

Department of Cognitive Sciences, Budapest University of Technology and Economics, 1111 Budapest, Hungary
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Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 2018 in Progress in Neuro-Psychopharmacology and Biological Psychiatry
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Journal Article
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HLHua Li
Hua Li
ASAadi P. Sagar
Aadi P. Sagar
Szabolcs KériSzabolcs Kéri
Szabolcs Kéri

1 September 2009 in Psychological Science
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Journal Article
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Szabolcs KériSzabolcs Kéri
Szabolcs Kéri

1 September 2003 in Brain Research Reviews
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Journal Article
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Szabolcs KériSzabolcs Kéri
Szabolcs Kéri

1 December 2018 in Journal of Affective Disorders
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Journal Article
Closed access
HLHua Li
Hua Li
ASAadi P. Sagar
Aadi P. Sagar
Szabolcs KériSzabolcs Kéri
Szabolcs Kéri

29 June 2005 in Psychological Medicine
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Journal Article
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Szabolcs KériSzabolcs Kéri
Szabolcs Kéri
IKImre Kiss
Imre Kiss
OKOguz Kelemen
Oguz Kelemen
GBGyörgy Benedek
György Benedek
ZJZoltán Janka
Zoltán Janka
Background. Schizophrenia is associated with impaired visual information processing. The aim of this study was to investigate the relationship between anomalous perceptual experiences, positive and negative symptoms, perceptual organization, rapid categorization of natural images and magnocellular (M) and parvocellular (P) visual pathway functioning.Method. Thirty-five unmedicated patients with schizophrenia and 20 matched healthy control volunteers participated. Anomalous perceptual experiences were assessed with the Bonn Scale for the Assessment Basic Symptoms (BSABS). General intellectual functions were evaluated with the revised version of the Wechsler Adult Intelligence Scale. The 1–9 version of the Continuous Performance Test (CPT) was used to investigate sustained attention. The following psychophysical tests were used: detection of Gabor patches with collinear and orthogonal flankers (perceptual organization), categorization of briefly presented natural scenes (rapid visual processing), low-contrast and frequency-doubling vernier threshold (M pathway functioning), isoluminant colour vernier threshold and high spatial frequency discrimination (P pathway functioning).Results. The patients with schizophrenia were impaired on test of perceptual organization, rapid visual processing and M pathway functioning. There was a significant correlation between BSABS scores, negative symptoms, perceptual organization, rapid visual processing and M pathway functioning. Positive symptoms, IQ, CPT and P pathway measures did not correlate with these parameters. The best predictor of the BSABS score was the perceptual organization deficit.Conclusions. These results raise the possibility that multiple facets of visual information processing deficits can be explained by M pathway dysfunctions in schizophrenia, resulting in impaired attentional modulation of perceptual organization and of natural image categorization.

1 January 2004 in Neuropsychology
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Journal Article
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Szabolcs KériSzabolcs Kéri
Szabolcs Kéri
OKOguz Kelemen
Oguz Kelemen
GBGyörgy Benedek
György Benedek
ZJZoltán Janka
Zoltán Janka
The aim of this study was to investigate magnocellular (M) and parvocellular (P) visual functions in nonmedicated patients with schizophrenia and in their unaffected siblings. Possible abnormalities in cortical integration of retinal receptive fields also were addressed. Twenty-two nonmedicated patients with schizophrenia, their unaffected siblings, and 20 age- and IQ-matched healthy control subjects received 4 vernier acuity tasks (blue-on-yellow, frequency-doubling, achromatic low and high contrast conditions) in which they were asked to detect the spatial alignment of dots and gratings. Results revealed that the patients with schizophrenia and their unaffected siblings showed selective dysfunctions in the frequency-doubling and achromatic low contrast conditions, which were devoted to investigate M pathways. In the isoluminant blue-on-yellow and high contrast achromatic conditions, there were no significant differences between the experimental groups. These results suggest that the deficit of M pathway is an endophenotype of schizophrenia.