A lateralized brain network for visuospatial attention

Control of goal-directed and stimulus-driven attention in the brain

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Orienting of Attention

Posner, M. I. (1980) · Quarterly Journal of Experimental Psychology · doi:10.1080/00335558008248231 · Cited by 9,670

MR diffusion tensor spectroscopy and imaging

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Three-dimensional tracking of axonal projections in the brain by magnetic resonance imaging

Mori, S., Crain, B. J., Chacko, V. P., & van Zijl, P. C. M. (1999) · Annals of Neurology · doi:10.1002/1531-8249(199902)45:2 · Cited by 3,513

Modulation of Oscillatory Neuronal Synchronization by Selective Visual Attention

Fries, P., Reynolds, J. H., Rorie, A. E., & Desimone, R. (2001) · Science · doi:10.1126/science.1055465 · Cited by 2,786

A cortical network for directed attention and unilateral neglect

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Top-Down Versus Bottom-Up Control of Attention in the Prefrontal and Posterior Parietal Cortices

Buschman, T. J., & Miller, E. K. (2007) · Science · doi:10.1126/science.1138071 · Cited by 2,380

Human Brain: Left-Right Asymmetries in Temporal Speech Region

Geschwind, N., & Levitsky, W. (1968) · Science · doi:10.1126/science.161.3837.186 · Cited by 2,248

Spontaneous neuronal activity distinguishes human dorsal and ventral attention systems

Fox, M. D., Corbetta, M., Snyder, A. Z., Vincent, J. L., & Raichle, M. E. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604187103 · Cited by 2,101

Pseudoneglect: a review and meta-analysis of performance factors in line bisection tasks

Jewell, G., & McCourt, M. E. (2000) · Neuropsychologia · doi:10.1016/s0028-3932(99)00045-7 · Cited by 1,187

The role of left fronto-parietal tracts in hand selection: Evidence from neurosurgery

Howells, H., Puglisi, G., Leonetti, A., Viganò, L., Fornia, L., Simone, L., Forkel, S. J., Rossi, M., Riva, M., Cerri, G., et al. (2020) · Cortex · doi:10.1016/j.cortex.2020.03.018 · Cited by 19

Development of white matter tracts between and within the dorsal and ventral streams

Vinci‐Booher, S., Caron, B. A., Bullock, D. N., James, K. H., & Pestilli, F. (2022) · Brain Structure and Function · doi:10.1007/s00429-021-02414-5 · Cited by 21

Hemifield asymmetries differentiate VSTM for single- and multiple-feature objects

Sheremata, S., & Shomstein, S. (2014) · Attention Perception & Psychophysics · doi:10.3758/s13414-014-0689-0 · Cited by 19

Disentangling subgroups of participants recruiting shared as well as different brain regions for the execution of the verb generation task: A data-driven fMRI study

Cerliani, L., Thomas, R. M., Aquino, D., Contarino, V. E., & Bizzi, A. (2016) · Cortex · doi:10.1016/j.cortex.2016.11.017 · Cited by 18

Long association tracts of the human white matter: an analysis of 18 hemisphere dissections and in vivo HARDI-CSD tractography

Goryaynov, S. A., Kondrashov, A. V., Goldberg, M., Batalov, A. I., Sufianov, R. A., Zakharova, N. E., Pronin, I., Golbin, D. A., Zhukov, V. Y., Dobrovol’skiy, G. F., et al. (2017) · Burdenko s Journal of Neurosurgery · doi:10.17116/neiro201780713-25 · Cited by 19

Investigation of superior longitudinal fasciculus fiber complexity in recent onset psychosis

Szeszko, P. R., Tan, E. T., Uluğ, A. M., Kingsley, P. B., Gallego, J. A., Rhindress, K., Malhotra, A. K., Robinson, D. G., & Marinelli, L. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.10.019 · Cited by 19

Functional connectivity during smooth pursuit eye movements

Schröder, R., Kasparbauer, A., Meyhöfer, I., Steffens, M., Trautner, P., & Ettinger, U. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00317.2020 · Cited by 20

Voxelwise structural disconnection mapping: Methodological validation and recommendations

Wawrzyniak, M., Stockert, A., Klingbeil, J., et al. (2022) · NeuroImage Clinical · doi:10.1016/j.nicl.2022.103132 · Cited by 18

Glioma lateralization: Focus on the anatomical localization and the distribution of molecular alterations (Review)

Çini, N., Pennisi, M., Genç, S., Spandidos, D. A., Falzone, L., Mitsias, P., Tsatsakis, A., & Taghizadehghalehjoughi, A. (2024) · Oncology Report · doi:10.3892/or.2024.8798 · Cited by 17

Botallo's error, or the quandaries of the universality assumption

Bartolomeo, P., Malkinson, T. S., & Vito, S. D. (2016) · Cortex · doi:10.1016/j.cortex.2016.09.026 · Cited by 18

No Interaction between tDCS Current Strength and Baseline Performance: A Conceptual Replication

Learmonth, G., Felisatti, F., Siriwardena, N., Checketts, M., Benwell, C., Märker, G., Thut, G., & Harvey, M. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00664 · Cited by 23

Interhemispheric Asymmetry of Network Connecting Between Frontal and Temporoparietal Cortices: A Corticocortical-Evoked Potential Study

Kanno, A., Enatsu, R., Ookawa, S., et al. (2018) · World Neurosurgery · doi:10.1016/j.wneu.2018.08.137 · Cited by 18

Influence of reward learning on visual attention and eye movements in a naturalistic environment: A virtual reality study

Bourgeois, A., Badier, E., Baron, N., Carruzzo, F., & Vuilleumier, P. O. (2018) · PLoS ONE · doi:10.1371/journal.pone.0207990 · Cited by 20

Spatial organization of occipital white matter tracts in the common marmoset

Kaneko, T., Takemura, H., Pestilli, F., Silva, A. C., Ye, F. Q., & Leopold, D. A. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02060-3 · Cited by 18

Hemisphere-specific Parietal Contributions to the Interplay between Working Memory and Attention

Kiyonaga, A., Powers, J., Chiu, Y., & Egner, T. (2021) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01740 · Cited by 20

Right and left neglect are not anatomically homologous: A voxel-lesion symptom mapping study

Moore, M. J., Gillebert, C. R., & Demeyere, N. (2021) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2021.108024 · Cited by 20

Distinct roles of the intraparietal sulcus and temporoparietal junction in attentional capture from distractor features: An individual differences approach

Painter, D. R., Dux, P. E., & Mattingley, J. B. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2015.02.029 · Cited by 18

Fronto-parietal organization for response times in inhibition of return: The FORTIOR model

Malkinson, T. S., & Bartolomeo, P. (2017) · Cortex · doi:10.1016/j.cortex.2017.11.005 · Cited by 18

A Practical Approach to Imaging of the Supplementary Motor Area and Its Subcortical Connections

de la Peña, M. J., Robles, S. G., de Vega, V. M., et al. (2020) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-020-01070-2 · Cited by 17

TBSS and probabilistic tractography reveal white matter connections for attention to object features

Mayer, K. M., & Vuong, Q. C. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0631-6 · Cited by 17

Alpha oscillations and the control of voluntary saccadic behavior

Hamm, J. P., Sabatinelli, D., & Clementz, B. A. (2012) · Experimental Brain Research · doi:10.1007/s00221-012-3167-8 · Cited by 17

The causal role of the left parietal lobe in facilitation and inhibition of return

Martín‐Arévalo, E., Lupiáñez, J., Narganes-Pineda, C., Marino, G., COLÁS-BLANCO, I., & Chica, A. B. (2019) · Cortex · doi:10.1016/j.cortex.2019.04.025 · Cited by 17

Network-based Responses to the Psychomotor Vigilance Task during Lapses in Adolescents after Short and Extended Sleep

DiFrancesco, M. W., Dyk, T. R. V., Altaye, M., Drummond, S. P. A., & Beebe, D. W. (2019) · Scientific Reports · doi:10.1038/s41598-019-50180-6 · Cited by 17

Estimating the Heritability of Developmental Change in Neural Connectivity, and Its Association With Changing Symptoms of Attention-Deficit/Hyperactivity Disorder

Sudre, G. P., Bouyssi-Kobar, M., Norman, L. J., Sharp, W. S., Choudhury, S., & Shaw, P. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.06.007 · Cited by 18

Microstructural white matter connectivity underlying the attentional networks system

Luna, F. G., Lupiáñez, J., & Martín‐Arévalo, E. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.113079 · Cited by 17

Visual Information Routes in the Posterior Dorsal and Ventral Face Network Studied with Intracranial Neurophysiology and White Matter Tract Endpoints

Babo-Rebelo, M., Puce, A., Bullock, D. N., Hugueville, L., Pestilli, F., Adam, C., Lehongre, K., Lambrecq, V., Dinkelacker, V., & George, N. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab212 · Cited by 18

It Is Not Just in the Genes

Manns, M. (2021) · Symmetry · doi:10.3390/sym13101815 · Cited by 16

Cognitive and functional deficits are associated with white matter abnormalities in two independent cohorts of patients with schizophrenia

Yamada, S., Takahashi, S., Malchow, B., Papazova, I., Stoecklein, S., Ertl-Wagner, B. B., Papazov, B., Kumpf, U., Wobrock, T., Keller-Varady, K., et al. (2021) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-021-01363-8 · Cited by 17

Cortical EEG components that reflect inverse effectiveness during visuotactile integration processing

Kanayama, N., Kimura, K., & Hiraki, K. (2014) · Brain Research · doi:10.1016/j.brainres.2014.12.017 · Cited by 17

Selective TMS-induced modulation of functional connectivity correlates with changes in behavior

Balan, P. F., Gerits, A., Mantini, D., & Vanduffel, W. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.01.076 · Cited by 17

The Brain’s Asymmetric Frequency Tuning: Asymmetric Behavior Originates from Asymmetric Perception

Felisatti, A., Aagten‐Murphy, D., Laubrock, J., Shaki, S., & Fischer, M. H. (2020) · Symmetry · doi:10.3390/sym12122083 · Cited by 23

The effect of cognitive load on horizontal and vertical spatial asymmetries

Ciricugno, A., Bartlett, M. L., Gwinn, O. S., Carragher, D. J., & Nicholls, M. E. R. (2021) · Laterality Asymmetries of Body Brain and Cognition · doi:10.1080/1357650x.2021.1920972 · Cited by 16

Hierarchical psychophysiological pathways subtend perceptual asymmetries in Neglect

Gregorio, F. D., Petrone, V., Casanova, E., Lullini, G., Romei, V., Piperno, R., & Porta, F. L. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.119942 · Cited by 18

Comprehensive voxel-wise, tract-based, and network lesion mapping reveals unique architectures of right and left visuospatial neglect

Moore, M. J., Hearne, L. J., Demeyere, N., & Mattingley, J. B. (2023) · Brain Structure and Function · doi:10.1007/s00429-023-02702-2 · Cited by 17

Altered anterior‐posterior connectivity through the arcuate fasciculus in temporal lobe epilepsy

Takaya, S., Liu, H., Greve, D. N., Tanaka, N., Leveroni, C. L., Cole, A. J., & Stufflebeam, S. M. (2016) · Human Brain Mapping · doi:10.1002/hbm.23319 · Cited by 16

Delineating function and connectivity of optokinetic hubs in the cerebellum and the brainstem

Ruehl, R. M., Hinkel, C., Bauermann, T., & zu Eulenburg, P. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1461-8 · Cited by 16

Functional reorganization during the recovery of contralesional target selection deficits after prefrontal cortex lesions in macaque monkeys

Adam, R., Johnston, K., Menon, R. S., & Everling, S. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116339 · Cited by 17

Game theoretical mapping of white matter contributions to visuospatial attention in stroke patients with hemineglect

Toba, M. N., Zavaglia, M., Malherbe, C., Moreau, T., Rastelli, F., Kaglik, A., Valabrègue, R., Pradat-Diehl, P., Hilgetag, C. C., & Valero‐Cabré, A. (2020) · Human Brain Mapping · doi:10.1002/hbm.24987 · Cited by 17

A comparison of lesion mapping analyses based on CT versus MR imaging in stroke

Moore, M. J., Jenkinson, M., Griffanti, L., et al. (2023) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2023.108564 · Cited by 16

Representational pseudoneglect in line bisection

Darling, S., Logie, R. H., & Sala, S. D. (2012) · Psychonomic Bulletin & Review · doi:10.3758/s13423-012-0285-z · Cited by 16

Dissociations between spatial-attentional processes within parietal cortex: insights from hybrid spatial cueing and change detection paradigms

Vandenberghe, R. R., & Gillebert, C. R. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00366 · Cited by 18

Reaction Time in a Visual 4-Choice Reaction Time Task: ERP Effects of Motor Preparation and Hemispheric Involvement

Antonova, I., van Swam, C., Hubl, D., Dierks, T., Griškova-Bulanova, I., & Koenig, T. W. (2016) · Brain Topography · doi:10.1007/s10548-016-0473-7 · Cited by 34

An investigation of the mechanisms underlying the effects of viewing distance and stimulus length on attentional asymmetries during line bisection

Nicholls, M. E. R., Beckman, E., & Churches, O. F. (2016) · Attention Perception & Psychophysics · doi:10.3758/s13414-016-1122-7 · Cited by 16

Relating individual differences in white matter pathways to children’s arithmetic fluency: a spherical deconvolution study

Polspoel, B., Vandermosten, M., & Smedt, B. D. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1770-6 · Cited by 16

Improvement of phonemic fluency following leftward prism adaptation

Turriziani, P., Chiaramonte, G., Mangano, G. R., Bonaventura, R. E., Smirni, D., & Oliveri, M. (2021) · Scientific Reports · doi:10.1038/s41598-021-86625-0 · Cited by 16

White matter microstructure and verbal fluency

Egorova, N., Chen, L., Khlif, M. S., & Brodtmann, A. G. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02579-7 · Cited by 15

Ecdysone signaling determines lateral polarity and remodels neurites to form Drosophila’s left-right brain asymmetry

Sakamura, S., Hsu, F.-Y., Tsujita, A., Abubaker, M. B., Chiang, A., & Matsuno, K. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112337 · Cited by 14

Why Are Most Humans Right-Handed? The Modified Fighting Hypothesis

Larsson, M. L., Schepman, A., & Rodway, P. (2023) · Symmetry · doi:10.3390/sym15040940 · Cited by 17

Improved prediction of glioma‐related aphasia by diffusion MRI metrics, machine learning, and automated fiber bundle segmentation

Shams, B., Reisch, K., Vajkoczy, P., Lippert, C., Picht, T., & Fekonja, L. S. (2023) · Human Brain Mapping · doi:10.1002/hbm.26393 · Cited by 15

Hesitant avoidance while walking: an error of social behavior generated by mutual interaction

Honma, M., Koyama, S., & Kawamura, M. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01013 · Cited by 16

Asymmetries in spatial perception are more prevalent under explicit than implicit attention

Noël, B., van der Kamp, J., Weigelt, M., et al. (2015) · Consciousness and Cognition · doi:10.1016/j.concog.2015.03.001 · Cited by 15

Distributed performance of white matter properties in chess players: A DWI study using automated fiber quantification

Zhou, S., Jin, L., He, J., Zeng, Q., Wu, Y., Cao, Z., & Feng, Y. (2018) · Brain Research · doi:10.1016/j.brainres.2018.07.003 · Cited by 15

Typical visual unfamiliar face individuation in left and right mesial temporal epilepsy

Volfart, A., Jonas, J., Maillard, L. G., Busigny, T., Rossion, B., & Brissart, H. (2020) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2020.107583 · Cited by 15

Revisiting Persistent Neuronal Activity During Covert Spatial Attention

Amengual, J. L., & Hamed, S. B. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.679796 · Cited by 17

The role of transcranial magnetic stimulation in understanding attention-related networks in single subjects

Yeager, B. E., Dougher, C. C., Cook, R. H., & Medaglia, J. D. (2021) · Current Research in Neurobiology · doi:10.1016/j.crneur.2021.100017 · Cited by 17

Establishing the functional relevancy of white matter connections in the visual system and beyond

Grotheer, M., Kubota, E. C., & Kalanit Grill-spector, A. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02423-4 · Cited by 15

The Differential Effects of Acute Right- vs. Left-Sided Vestibular Deafferentation on Spatial Cognition in Unilateral Labyrinthectomized Mice

Nguyen, T. T., Nam, G., Kang, J., Han, G. C., Kim, J., Dieterich, M., & Oh, S. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.789487 · Cited by 15

Brain disconnectome mapping derived from white matter lesions and serum neurofilament light levels in multiple sclerosis: A longitudinal multicenter study

Rise, H. H., Brune, S., Chien, C., Berge, T., Bos, S. D., Andorrà, M., Valdeolivas, I. P., Beyer, M. K., Sowa, P., Scheel, M., et al. (2022) · NeuroImage Clinical · doi:10.1016/j.nicl.2022.103099 · Cited by 15

Hemispheric asymmetry in the hierarchical perception of music and speech.

Rosenthal, M. (2016) · Psychological Bulletin · doi:10.1037/bul0000076 · Cited by 15

Barratt Impulsivity in Healthy Adults Is Associated with Higher Gray Matter Concentration in the Parietal Occipital Cortex that Represents Peripheral Visual Field

Ide, J. S., Tung, H. C., Yang, C.-T., Tseng, Y., & Li, C. R. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00222 · Cited by 15

Different patterns of confabulation in left visuo-spatial neglect

Barba, G. D., Brazzarola, M., Barbera, C., Marangoni, S., Causin, F., Bartolomeo, P., & de Schotten, M. T. (2018) · Experimental Brain Research · doi:10.1007/s00221-018-5281-8 · Cited by 15

White matter pathways for prosodic structure building: A case study

Sammler, D., Cunitz, K., Gierhan, S. M. E., Anwander, A., Adermann, J., Meixensberger, J., & Friederici, A. D. (2018) · Brain and Language · doi:10.1016/j.bandl.2018.05.001 · Cited by 16

Mapping visuospatial attention: the greyscales task in combination with repetitive navigated transcranial magnetic stimulation

Giglhuber, K., Maurer, S., Zimmer, C., Meyer, B., & Krieg, S. M. (2018) · BMC Neuroscience · doi:10.1186/s12868-018-0440-1 · Cited by 15

Regions of white matter abnormalities in the arcuate fasciculus in veterans with anger and aggression problems

Dávid, S., Heesink, L., Geuze, E., Gladwin, T. E., van Honk, J., Kleber, R. J., & Leemans, A. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-02016-2 · Cited by 17

A toggle switch of visual awareness?

Le, A., Stojanoski, B. B., Khan, S., et al. (2014) · Cortex · doi:10.1016/j.cortex.2014.09.015 · Cited by 15

The cost of attentional reorienting on conscious visual perception: an MEG study

Spagna, A., Bayle, D. J., Romeo, Z., Malkinson, T. S., Liu, J., Yahia‐Cherif, L., Chica, A. B., & Bartolomeo, P. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac192 · Cited by 15

Using neuroimaging genomics to investigate the evolution of human brain structure

Alagöz, G., Molz, B., Eising, E., Schijven, D., Francks, C., Stein, J. L., & Fisher, S. E. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2200638119 · Cited by 15

Adaptive compensation of arcuate fasciculus lateralization in developmental dyslexia

Zhao, J., Zhao, Y., Song, Z., et al. (2022) · Cortex · doi:10.1016/j.cortex.2023.05.017 · Cited by 14

A map of white matter tracts in a lesser ape, the lar gibbon

Bryant, K. L., Manger, P., Bertelsen, M. F., Khrapitchev, A., Sallet, J., Benn, R. A., & Mars, R. (2023) · Brain Structure and Function · doi:10.1007/s00429-023-02709-9 · Cited by 8

Dysfunction of the magnocellular subdivision of the visual thalamus in developmental dyslexia

Müller-Axt, C., Kauffmann, L., Eichner, C., & von Kriegstein, K. (2024) · Brain · doi:10.1093/brain/awae235 · Cited by 14

Effector-dependent neglect and splenial disconnection: a spherical deconvolution tractography study

Lunven, M., de Schotten, M. T., Glize, B., Migliaccio, R., Jacquin‐Courtois, S., Cotton, F., Bartolomeo, P., & Gilles Rode, A. (2014) · Experimental Brain Research · doi:10.1007/s00221-014-4051-5 · Cited by 14

Impaired illness awareness in schizophrenia and posterior corpus callosal white matter tract integrity

Gerretsen, P., Rajji, T. K., Shah, P., Shahab, S., Sanches, M., Graff‐Guerrero, A., Menon, M., Pollock, B. G., Mamo, D. C., Mulsant, B. H., et al. (2019) · Schizophrenia · doi:10.1038/s41537-019-0076-x · Cited by 15

Neural Connectivity Changes Facilitated by Familiar Auditory Sensory Training in Disordered Consciousness: A TBI Pilot Study

Pape, T., Livengood, S. L., Kletzel, S., Blabas, B., Guernon, A., Bhaumik, D. K., Bhaumik, R., Mallinson, T., Weaver, J., Higgins, J. P., et al. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.01027 · Cited by 17

A Cortical Parcellation Based Analysis of Ventral Premotor Area Connectivity

Sheets, J. R., Briggs, R. G., Dadario, N. B., Young, I. M., Bai, M. Y., Poologaindran, A., Baker, C. M., Conner, A. K., & Sughrue, M. E. (2021) · Neurological Research · doi:10.1080/01616412.2021.1902702 · Cited by 14

Multisensory deficits in dyslexia may result from a locus coeruleus attentional network dysfunction

Kershner, J. R. (2021) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2021.108023 · Cited by 16

The interactive functional biases of manual, language and attention systems

Serrien, D. J., & O’Regan, L. (2022) · Cognitive Research Principles and Implications · doi:10.1186/s41235-022-00365-x · Cited by 17

Structural hemispheric asymmetries

Ocklenburg, S., & Güntürkün, O. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-99737-9.00001-x · Cited by 15

Arrhythmic activity in the left frontal eye field facilitates conscious visual perception in humans

Chanes, L., Quentin, R., Vernet, M., & Valero‐Cabré, A. (2015) · Cortex · doi:10.1016/j.cortex.2015.05.016 · Cited by 16

Effects of Parkinson’s disease on optic flow perception for heading direction during navigation

Lin, C.-C., WAGENAAR, R. C., Young, D. E., et al. (2014) · Experimental Brain Research · doi:10.1007/s00221-014-3853-9 · Cited by 14

The frequency and severity of extinction after stroke affecting different vascular territories

Chechlacz, M., Rotshtein, P., Demeyere, N., Bickerton, W., & Humphreys, G. W. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.12.016 · Cited by 14

Anatomical connectivity changes in bipolar disorder and schizophrenia investigated using whole-brain tract-based spatial statistics and machine learning approaches

Sütçübaşı, B., Metin, S. Z., Erguzel, T. T., Metin, B., Taş, C., Arıkan, M. K., & Tarhan, N. (2019) · Neural Computing and Applications · doi:10.1007/s00521-018-03992-y · Cited by 14

Phone messages affect the detection of approaching pedestrians in healthy young and older adults immersed in a virtual community environment

Silva, W. S., McFadyen, B. J., Kehayia, E., Azevedo, N., Fung, J., & Lamontagne, A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0217062 · Cited by 14

Individual Variability in Performance Reflects Selectivity of the Multiple Demand Network among Children and Adults

Schettini, E., Hiersche, K. J., & Saygin, Z. M. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1460-22.2023 · Cited by 14

Deployment of spatial attention without moving the eyes is boosted by oculomotor adaptation

Habchi, O., Rey, E., Mathieu, R., et al. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00426 · Cited by 13

The role of the right posterior parietal cortex in prism adaptation and its aftereffects

Terruzzi, S., Crivelli, D., Pisoni, A., Mattavelli, G. C., Lauro, L. J. R., Bolognini, N., & Vallar, G. (2020) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2020.107672 · Cited by 13

The Role of White Matter Disconnection in the Symptoms Relating to the Anarchic Hand Syndrome: A Single Case Study

Pacella, V., Ricciardi, G. K., Bonadiman, S., et al. (2021) · Brain Sciences · doi:10.3390/brainsci11050632 · Cited by 13

Asymmetry of Interhemispheric Connectivity during Rapid Movements of Right and Left Hands: A TMS-EEG Study

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