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Preparatory neural networks are impaired in adults with attention-deficit/hyperactivity disorder during the antisaccade task

Schwerdtfeger, R. M. H., Alahyane, N., Brien, D. C., Coe, B. C., Stroman, P. W., & Munoz, D. P. (2012) · NeuroImage Clinical · doi:10.1016/j.nicl.2012.10.006 · Cited by 53 · see citing works

Different involvement of subregions within dorsal premotor and medial frontal cortex for pro- and antisaccades

Cieslik, E. C., Seidler, I., Laird, A. R., Fox, P. T., & Eickhoff, S. B. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.05.012 · Cited by 46 · see citing works

Antisaccade Deficit after Inactivation of the Principal Sulcus in Monkeys

Condy, C., Wattiez, N., Rivaud-Péchoux, S., Tremblay, L., & Gaymard, B. M. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhj140 · Cited by 48 · see citing works

Neural networks related to pro-saccades and anti-saccades revealed by independent component analysis

Domagalik, A., Beldzik, E., Fąfrowicz, M., Ogińska, H., & Marek, T. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.06.006 · Cited by 48 · see citing works

Antisaccade errors reveal cognitive control deficits in Parkinson’s disease with freezing of gait

Walton, C. C., O’Callaghan, C., Hall, J. M., Gilat, M., Mowszowski, L., Naismith, S. L., Burrell, J. R., Shine, J. M., & Lewis, S. J. G. (2015) · Journal of Neurology · doi:10.1007/s00415-015-7910-5 · Cited by 47 · see citing works

Executive Functions Brain System: An Activation Likelihood Estimation Meta-analytic Study

Ardila, A., Bernal, B., & Rosselli, M. (2018) · Archives of Clinical Neuropsychology · doi:10.1093/arclin/acx066 · Cited by 46 · see citing works

Contribution of the central thalamus to the generation of volitional saccades

Tanaka, M., & Kunimatsu, J. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07699.x · Cited by 46 · see citing works

Disconnectivity of the cortical ocular motor control network in autism spectrum disorders

Kenet, T., Orekhova, E. V., Bharadwaj, H., Shetty, N. R., Israeli, E. R., Lee, A. K. C., Agam, Y., Elam, M., Joseph, R. M., Hämäläinen, M., et al. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.010 · Cited by 44 · see citing works

Shared and distinct oculomotor function deficits in schizophrenia and obsessive compulsive disorder

Damilou, A., Apostolakis, S., Thrapsanioti, E., Theleritis, C. G., & Smyrnis, N. (2016) · Psychophysiology · doi:10.1111/psyp.12630 · Cited by 42 · see citing works

Cognition and Eye Movements

White, O. B., & Fielding, J. (2012) · Journal of Neuro-Ophthalmology · doi:10.1097/wno.0b013e3182688230 · Cited by 42 · see citing works

The functional oculomotor network and saccadic cognitive control in healthy elders

Pa, J., Dutt, S., Mirsky, J. B., Heuer, H. W., Keselman, P., Kong, E. L., Trujillo, A. J., Gazzaley, A. H., Kramer, J. H., Seeley, W. W., et al. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.03.051 · Cited by 41 · see citing works

Cortical and cerebellar activation induced by reflexive and voluntary saccades

Schraa‐Tam, C. K. L., van Broekhoven, P. C. A., van der Geest, J. N., Frens, M. A., Smits, M., & van der Lugt, A. (2008) · Experimental Brain Research · doi:10.1007/s00221-008-1569-4 · Cited by 41 · see citing works

Single Neurons in Anterior Cingulate Cortex Signal the Need to Change Action During Performance of a Stop-change Task that Induces Response Competition

Bryden, D. W., Brockett, A. T., Blume, E., Heatley, K. C., Zhao, A., & Roesch, M. R. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy008 · Cited by 38 · see citing works

A meta‐analysis of functional magnetic resonance imaging studies of eye movements and visual word reading

Zhou, W., & Hua Shu, A. (2017) · Brain and Behavior · doi:10.1002/brb3.683 · Cited by 38 · see citing works

Dorsolateral prefrontal cortex hyperactivity during inhibitory control in children with ADHD in the antisaccade task

Fernández-Ruíz, J., Schwerdtfeger, R. M. H., Alahyane, N., Brien, D. C., Coe, B. C., & Munoz, D. P. (2019) · Brain Imaging and Behavior · doi:10.1007/s11682-019-00196-3 · Cited by 38 · see citing works

Different neuronal pathways support the generation of general and specific mental images

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Attentional control deficits in social anxiety: Investigating inhibition and shifting functions using a mixed antisaccade paradigm

Liang, C. (2018) · Journal of Behavior Therapy and Experimental Psychiatry · doi:10.1016/j.jbtep.2018.03.004 · Cited by 32 · see citing works

Hyperfrontality in patients with schizophrenia during saccade and antisaccade tasks: A study with fMRI

Motoshita, M., Matsuura, M., Ohkubo, T., Ohkubo, H., Kanaka, N., Matsushima, E., Taira, M., Kojima, T., & Matsuda, T. (2009) · Psychiatry and Clinical Neurosciences · doi:10.1111/j.1440-1819.2009.01941.x · Cited by 31 · see citing works

Cerebellar Contributions to the Processing of Saccadic Errors

van Broekhoven, P. C. A., Schraa‐Tam, C. K. L., van der Lugt, A., Smits, M., Frens, M. A., & van der Geest, J. N. (2009) · The Cerebellum · doi:10.1007/s12311-009-0116-6 · Cited by 31 · see citing works

Differing effects of prosaccades and antisaccades on postural stability

Legrand, A., Doré-Mazars, K., Lazarreschi, J., Lemoine, C., Olivier, I., Barra, J., & Bucci, M. P. (2013) · Experimental Brain Research · doi:10.1007/s00221-013-3519-z · Cited by 30 · see citing works

Frequency- and State-Dependent Network Effects of Electrical Stimulation Targeting the Ventral Tegmental Area in Macaques

Murris, S. R., Arsenault, J. T., & Vanduffel, W. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa007 · Cited by 30 · see citing works

Cortical sources of ERP in prosaccade and antisaccade eye movements using realistic source models

Richards, J. E. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00027 · Cited by 30 · see citing works

Distributed representations of the "preparatory set" in the frontal oculomotor system: a TMS study

Nagel, M., Sprenger, A., Lencer, R., Kömpf, D., Siebner, H. R., & Heide, W. (2008) · BMC Neuroscience · doi:10.1186/1471-2202-9-89 · Cited by 29 · see citing works

Repelling the young and attracting the old: Examining age-related differences in saccade trajectory deviations.

Campbell, K. L., Al-Aidroos, N., Pratt, J., & Hasher, L. (2009) · Psychology and Aging · doi:10.1037/a0014106 · Cited by 28 · see citing works

Age-related deficits in voluntary control over saccadic eye movements: consideration of electrical brain stimulation as a therapeutic strategy

Chen, P. L., & Machado, L. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.02.010 · Cited by 27 · see citing works

Saccadic eye movements: what do they tell us about aging cognition?

Noiret, N., Vigneron, B., Diogo, M., Vandel, P., & Laurent, É. (2016) · Aging Neuropsychology and Cognition · doi:10.1080/13825585.2016.1237613 · Cited by 27 · see citing works

Transcranial Direct Current Stimulation of the Frontal Eye Fields during Pro- and Antisaccade Tasks

Ryota Kanai, C., Muggleton, N. G., & Walsh, V. (2012) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2012.00045 · Cited by 27 · see citing works

Neural correlates of individual differences in fixation duration during natural reading

Henderson, J. M., Choi, W., Luke, S. G., & Schmidt, J. (2017) · Quarterly Journal of Experimental Psychology · doi:10.1080/17470218.2017.1329322 · Cited by 26 · see citing works

Impaired Neurocognitive Performance and Mortality in HIV: Assessing the Prognostic Value of the HIV-Dementia Scale

Banerjee, N., McIntosh, R. C., & Ironson, G. H. (2019) · AIDS and Behavior · doi:10.1007/s10461-019-02423-w · Cited by 25 · see citing works

Inhibitory saccadic dysfunction is associated with cerebellar injury in multiple sclerosis

Kolbe, S., Kilpatrick, T. J., Mitchell, P. J., White, O. B., Egan, G. F., & Fielding, J. (2013) · Human Brain Mapping · doi:10.1002/hbm.22329 · Cited by 25 · see citing works

Developmental changes in oculomotor control and working-memory efficiency

Eenshuistra, R. M., Ridderinkhof, K. R., Weidema, M. A., & van der Molen, M. W. (2006) · Acta Psychologica · doi:10.1016/j.actpsy.2006.09.012 · Cited by 25 · see citing works

Distinct Neural Correlates for Volitional Generation and Inhibition of Saccades

Reuter, B., Kaufmann, C., Bender, J., Pinkpank, T., & Kathmann, N. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21235 · Cited by 23 · see citing works

Deficit of inhibition motor control in untreated patients with schizophrenia: Further support from visually guided saccade paradigms

Krebs, M., Bourdel, M., Ramdane-Cherif, Z., Bouhours, P., Löo, H., Poirier, M. F., & Amado, I. (2010) · Psychiatry Research · doi:10.1016/j.psychres.2009.07.008 · Cited by 22 · see citing works

Spatio-temporal Brain Dynamics Underlying Saccade Execution, Suppression, and Error-related Feedback

Herdman, A. T., & Ryan, J. D. (2007) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2007.19.3.420 · Cited by 22 · see citing works

Conflict Resolution as Near-Threshold Decision-Making: A Spiking Neural Circuit Model with Two-Stage Competition for Antisaccadic Task

Lo, C., & Wang, X. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005081 · Cited by 20 · see citing works

Inconvenient correlation – RT–BOLD relationship for homogeneous and fast reactions

Domagalik, A., Beldzik, E., Ogińska, H., Marek, T., & Fąfrowicz, M. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.08.012 · Cited by 20 · see citing works

Modulation of cognitive control levels via manipulation of saccade trial-type probability assessed with event-related BOLD fMRI

Pierce, J. E., & McDowell, J. E. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00776.2015 · Cited by 20 · see citing works

Oculomotor and Inhibitory Control in Dyslexia

Wilcockson, T. D. W., Mardanbegi, D., Sawyer, P., Gellersen, H. W., Xia, B., & Crawford, T. J. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00066 · Cited by 18 · see citing works

Investigating inhibitory control in children with epilepsy: An fMRI study

Triplett, R. L., Velanova, K., Luna, B., Padmanabhan, A., Gaillard, W. D., & Asato, M. R. (2014) · Epilepsia · doi:10.1111/epi.12768 · Cited by 17 · see citing works

Attentional capture in schizophrenia: Failure to resist interference from motion signals

Ducato, M. G., Michael, G. A., Thomas, P., Despretz, P., Monestès, J., Loas, G., & Boucart, M. (2008) · Cognitive Neuropsychiatry · doi:10.1080/13546800701706530 · Cited by 17 · see citing works

Task-demands and audio-visual stimulus configurations modulate neural activity in the human thalamus

Bonath, B., Tyll, S., Budinger, E., Krauel, K., Hopf, J., & Noesselt, T. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.10.018 · Cited by 15 · see citing works

Brain activation related to retrosaccades in saccade experiments

Raemaekers, M. A. H., Vink, M., van den Heuvel, M. P., Kahn, R. S., & Ramsey, N. F. (2005) · Neuroreport · doi:10.1097/00001756-200507130-00003 · Cited by 14 · see citing works

Pilot study of response inhibition and error processing in the posterior medial prefrontal cortex in healthy youth

Fitzgerald, K. D., Zbrozek, C. D., Welsh, R. C., Britton, J. C., Liberzon, I., & Taylor, S. F. (2008) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2008.01906.x · Cited by 12 · see citing works

Evaluation of rigid registration methods for whole head imaging in diffuse optical tomography

Wu, X., Eggebrecht, A. T., Ferradal, S. L., Culver, J. P., & Dehghani, H. (2015) · Neurophotonics · doi:10.1117/1.nph.2.3.035002 · Cited by 11 · see citing works

Schnelle Augenbewegungen und visuelle Fixation bei Kindern mit ADHS

Folta-Schoofs, K., & Mähler, C. (2010) · Kindheit und Entwicklung · doi:10.1026/0942-5403/a000037 · Cited by 11 · see citing works

Nystagmus using video-oculography in psychiatric patients

Kiyomizu, K., Matsuda, K., Torihara, K., Nakayama, M., Komaki, S., Tono, T., Ishida, Y., Yoshida, K., & Kimitsuki, T. (2008) · European Archives of Oto-Rhino-Laryngology · doi:10.1007/s00405-008-0848-9 · Cited by 10 · see citing works

Thalamic roles in eye movements

Tanaka, M., & Kunimatsu, J. (2011) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780199539789.013.0013 · Cited by 10 · see citing works

Interference between oculomotor and postural tasks in 7–8-year-old children and adults

Legrand, A., Doré-Mazars, K., Lemoine, C., Nougier, V., & Olivier, I. (2016) · Experimental Brain Research · doi:10.1007/s00221-016-4565-0 · Cited by 10 · see citing works

An effective screening model for subjective cognitive decline in community-dwelling older adults based on gait analysis and eye tracking

Hao, C., Zhang, X., An, J., Bao, W., Yang, F., Chen, J., Hou, S., Wang, Z., Du, S., Zhao, Y., et al. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1444375 · Cited by 9 · see citing works

Clinical testing of mild traumatic brain injury using computerised eye-tracking tests

Cade, A. E., & Turnbull, P. (2022) · Clinical and Experimental Optometry · doi:10.1080/08164622.2021.2018915 · Cited by 9 · see citing works

Functional Neuroanatomy of the Human Accommodation Response to an “E” Target Varying from -3 to -6 Diopters

Lv, X., Chen, Y., Tan, W., Yu, Y., Zou, H., Shao, Y. R., Zan, S., Tao, J., & Miao, W. (2020) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2020.00029 · Cited by 9 · see citing works

Human Variability of fMRI Brain Activation in Response to Oculomotor Stimuli

Della-Justina, H. M., Pastorello, B., Santos-Pontelli, T. E. G., Pontes‐Neto, O. M., dos Santos, A. C., Baffa, O., Colafêmina, J. F., Leite, J. P., & de Araújo, D. B. (2007) · Brain Topography · doi:10.1007/s10548-007-0037-y · Cited by 9 · see citing works

Neural correlates of antisaccade deficits in schizophrenia, an fMRI study

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Saccadic and smooth pursuit eye movement abnormalities in first episode schizophrenia

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Distinct Neural Correlates for Volitional Generation and Inhibition of Saccades

Reuter, B., Kaufmann, C., Bender, J., Pinkpank, T., & Kathmann, N. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21235 · Cited by 23 · see citing works

Quantitative meta-analysis of fMRI and PET studies reveals consistent activation in fronto-striatal-parietal regions and cerebellum during antisaccades and prosaccades

Jamadar, S. D., Fielding, J., & Egan, G. F. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00749 · Cited by 127 · see citing works

Hyperfrontality in patients with schizophrenia during saccade and antisaccade tasks: A study with fMRI

Motoshita, M., Matsuura, M., Ohkubo, T., Ohkubo, H., Kanaka, N., Matsushima, E., Taira, M., Kojima, T., & Matsuda, T. (2009) · Psychiatry and Clinical Neurosciences · doi:10.1111/j.1440-1819.2009.01941.x · Cited by 31 · see citing works