2016
DOI: 10.1016/j.bandc.2016.05.006
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Facing competition: Neural mechanisms underlying parallel programming of antisaccades and prosaccades

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Cited by 11 publications
(19 citation statements)
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References 70 publications
(120 reference statements)
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“…It shows strong functional connectivity within the fronto-parietal network in resting state studies (Koval, Hutchison, Lomber, & Everling, 2014) projecting directly and indirectly to SC to mediate top-down resting and excitatory control over SC neurons (Johnston et al, 2014). Others have shown that components of the default mode network including the middle temporal gyrus and the inferior parietal cortex, as well as the parahippocampus, are also involved in active antisaccade generation (Domagalik et al, 2012; Talanow et al, 2016). …”
Section: Discussionmentioning
confidence: 99%
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“…It shows strong functional connectivity within the fronto-parietal network in resting state studies (Koval, Hutchison, Lomber, & Everling, 2014) projecting directly and indirectly to SC to mediate top-down resting and excitatory control over SC neurons (Johnston et al, 2014). Others have shown that components of the default mode network including the middle temporal gyrus and the inferior parietal cortex, as well as the parahippocampus, are also involved in active antisaccade generation (Domagalik et al, 2012; Talanow et al, 2016). …”
Section: Discussionmentioning
confidence: 99%
“…In healthy human participants, antisaccade error rate and the latency of correct antisaccades have been associated with task-related changes in fronto-thalamo-parietal networks during active task performance (Herweg et al, 2014; Jamadar, Johnson, Clough, Egan, & Fielding, 2015; Polli et al, 2005; Talanow et al, 2016). Resting state activity has only recently been related to antisaccade performance in healthy participants (Jamadar, Egan, Calhoun, Johnson, & Fielding, 2016; Marek, Hwang, Foran, Hallquist, & Luna, 2015) revealing associations of antisaccade error rate and response latency with modulations of resting state activity in orbitofrontal and ventrolateral prefrontal cortex as well as medial premotor regions (Cieslik, Seidler, Laird, Fox, & Eickhoff, 2016).…”
Section: Introductionmentioning
confidence: 99%
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“…An increased rate of direction errors in the antisaccade task in schizophrenia is considered to be a marker of response inhibition failure (Clementz, 1998;Hutton & Ettinger, 2006). Concerning the cognitive mechanisms underlying the inhibition of erroneous prosaccades, early approaches assumed sequential processing in successful antisaccade trials, suggesting that the reflex-like prosaccade is first inhibited by processes of goal redefinition, a cancellation signal or an inhibitory signal, before an antisaccade is programmed (Talanow et al, 2016). More recent models, however, emphasize the parallel nature of saccade programming, in line with competition models of inhibitory control (Cutsuridis, Kahramanoglou, Perantonis, Evdokimidis, & Smyrnis, 2005;Talanow et al, 2016).…”
Section: Patients With Schizophreniamentioning
confidence: 99%
“…Concerning the cognitive mechanisms underlying the inhibition of erroneous prosaccades, early approaches assumed sequential processing in successful antisaccade trials, suggesting that the reflex-like prosaccade is first inhibited by processes of goal redefinition, a cancellation signal or an inhibitory signal, before an antisaccade is programmed (Talanow et al, 2016). More recent models, however, emphasize the parallel nature of saccade programming, in line with competition models of inhibitory control (Cutsuridis, Kahramanoglou, Perantonis, Evdokimidis, & Smyrnis, 2005;Talanow et al, 2016). Competition models postulate that coordinates for the exogenously triggered prosaccade and the endogenously initiated antisaccade are programmed immediately after the stimulus is presented, with the stronger or more efficient of the two programs winning the competition.…”
Section: Patients With Schizophreniamentioning
confidence: 99%