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

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MR diffusion tensor spectroscopy and imaging

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

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Modulation of Oscillatory Neuronal Synchronization by Selective Visual Attention

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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

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Human Brain: Left-Right Asymmetries in Temporal Speech Region

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Spontaneous neuronal activity distinguishes human dorsal and ventral attention systems

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

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Visual neglect as a disconnection syndrome? A confirmatory case report

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Blindness alters the microstructure of the ventral but not the dorsal visual stream

Reislev, N. L., Kupers, R. C., Siebner, H. R., Ptito, M., & Dyrby, T. B. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1078-8 · Cited by 42

Quantifying Agreement between Anatomical and Functional Interhemispheric Correspondences in the Resting Brain

Jo, H. J., Saad, Z. S., Gotts, S. J., Martin, A. D., & Cox, R. W. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048847 · Cited by 35

White matter integrity disparities between normal-weight and overweight/obese adolescents: an automated fiber quantification tractography study

Carbine, K. A., Duraccio, K. M., Hedges‐Muncy, A., Barnett, K. A., Kirwan, C. B., & Jensen, C. D. (2019) · Brain Imaging and Behavior · doi:10.1007/s11682-019-00036-4 · Cited by 39

Exploring the opinions of the YouTube visitors towards advertisements and its influence on purchase intention among viewers

Sebastian, A. T., Lal, B., Anupama, J., Varghese, J., Tom, A. A., Rajkumar, E., George, A. J., Jeyavel, S., Pandey, V., Wajid, M., et al. (2021) · Cogent Business & Management · doi:10.1080/23311975.2021.1876545 · Cited by 38

Cytoarchitectonic, receptor distribution and functional connectivity analyses of the macaque frontal lobe

Rapan, L., Froudist‐Walsh, S., Niu, M., Xu, T., Zhao, L., Funck, T., Wang, X., Amunts, K., & Palomero‐Gallagher, N. (2023) · eLife · doi:10.7554/elife.82850 · Cited by 39

Higher integrity of the motor and visual pathways in long-term video game players

Zhang, Y., Du, G., Yang, Y., Qin, W., Li, X., & Zhang, Q. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00098 · Cited by 46

Attention and Impulsivity

Nigg, J. T. (2016) · Wiley eBooks · doi:10.1002/9781119125556.devpsy314 · Cited by 41

Fiber pathways connecting cortical areas relevant for spatial orienting and exploration

Suchan, J., Umarova, R. M., Schnell, S., Himmelbach, M., Weiller, C., Karnath, H., & Saur, D. (2013) · Human Brain Mapping · doi:10.1002/hbm.22232 · Cited by 37

The neural basis of improved cognitive performance by threat of shock

Torrisi, S., Robinson, O. J., O’Connell, K., Davis, A., Balderston, N. L., Ernst, M., & Grillon, C. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw088 · Cited by 40

Synchronization of fronto-parietal beta and theta networks as a signature of visual awareness in neglect

Yordanova, J., Kolev, V., Verleger, R., Heide, W., Grumbt, M., & Schürmann, M. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.11.013 · Cited by 35

Evolutionary Specializations of Human Association Cortex

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Structural connectivity in spatial attention network: reconstruction from left hemispatial neglect

Hattori, T., Ito, K., Nakazawa, C., Numasawa, Y., Watanabe, M., Aoki, S., Mizusawa, H., Ishiai, S., & Yokota, T. (2017) · Brain Imaging and Behavior · doi:10.1007/s11682-017-9698-7 · Cited by 35

The asymmetrical effect of leftward and rightward prisms on intact visuospatial cognition

Schintu, S., Patané, I., Caldano, M., et al. (2017) · Cortex · doi:10.1016/j.cortex.2017.09.015 · Cited by 37

The ipsilesional attention bias in right-hemisphere stroke patients as revealed by a realistic visual search task: Neuroanatomical correlates and functional relevance.

Machner, B., Könemund, I., von der Gablentz, J., Bays, P. M., & Sprenger, A. (2018) · Neuropsychology · doi:10.1037/neu0000493 · Cited by 38

Posterior Alpha and Gamma Oscillations Index Divergent and Superadditive Effects of Cognitive Interference

Wiesman, A. I., & Wilson, T. W. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz214 · Cited by 38

Prediction of Long-term Cognitive Function After Minor Stroke Using Functional Connectivity

Lopes, R., Bournonville, C., Kuchcinski, G., Dondaine, T., Mendyk, A., Viard, R., Pruvo, J., Hénon, H., Georgakis, M. K., Duering, M., et al. (2021) · Neurology · doi:10.1212/wnl.0000000000011452 · Cited by 37

Sensorimotor, Attentional, and Neuroanatomical Predictors of Upper Limb Motor Deficits and Rehabilitation Outcome after Stroke

D’Imperio, D., Romeo, Z., Maistrello, L., Durgoni, E., Pietà, C. D., Grazia, M. D. F. D., Meneghello, F., Turolla, A., & Zorzi, M. (2021) · Neural Plasticity · doi:10.1155/2021/8845685 · Cited by 37

Lesion symptom mapping of domain-specific cognitive impairments using routine imaging in stroke

Moore, M. J., & Demeyere, N. (2022) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2022.108159 · Cited by 41

Influence of the fragile X mental retardation (FMR1) gene on the brain and working memory in men with normal FMR1 alleles

Wang, J. Y., Hessl, D. R., Iwahashi, C., Cheung, K., Schneider, A., Hagerman, R. J., Hagerman, P. J., & Rivera, S. M. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.09.075 · Cited by 37

Kernel regression estimation of fiber orientation mixtures in diffusion MRI

Cabeen, R. P., Bastin, M. E., & Laidlaw, D. H. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.11.061 · Cited by 37

The right hemisphere is dominant in organization of visual search—A study in stroke patients

Brink, A. F. T., Biesbroek, J. M., Kuijf, H. J., der Stigchel, S. V., Oort, Q., Visser‐Meily, J. M. A., & Nijboer, T. C. W. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.02.004 · Cited by 38

Disruption of the ascending arousal system and cortical attention networks in post-stroke delirium and spatial neglect

Boukrina, O. V., & Barrett, A. M. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.09.024 · Cited by 36

Personalized alpha-tACS targeting left posterior parietal cortex modulates visuo-spatial attention and posterior evoked EEG activity

Radecke, J., Fiene, M., Misselhorn, J., Herrmann, C. S., Engel, A. K., Wolters, C. H., & Schneider, T. R. (2023) · Brain stimulation · doi:10.1016/j.brs.2023.06.013 · Cited by 38

Same task, different strategies: How brain networks can be influenced by memory strategy

Sanfratello, L., Caprihan, A., Stephen, J. M., Knoefel, J. E., Adair, J. C., Qualls, C., Lundy, S. L., & Aine, C. J. (2014) · Human Brain Mapping · doi:10.1002/hbm.22538 · Cited by 42

Predictive value of fractional anisotropy of the arcuate fasciculus for the functional recovery of language after brain tumor resection: A preliminary study

Kinoshita, M., Nakada, M., Okita, H., Hamada, J., & Hayashi, Y. (2013) · Clinical Neurology and Neurosurgery · doi:10.1016/j.clineuro.2013.12.002 · Cited by 36

Flanker interference effects in a line bisection task

Chieffi, S., Iachini, T., Iavarone, A., Messina, G., Viggiano, A., & Monda, M. (2014) · Experimental Brain Research · doi:10.1007/s00221-014-3851-y · Cited by 35

Fgf signaling governs cell fate in the zebrafish pineal complex

Clanton, J. A., Hope, K. D., & Gamse, J. T. (2012) · Development · doi:10.1242/dev.083709 · Cited by 37

Multimodal assessment of hemispheric lateralization for language and its relevance for behavior

Piervincenzi, C., Petrilli, A., Marini, A., Caulo, M., Committeri, G., & Sestieri, C. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.08.018 · Cited by 39

Comparative neuroanatomy: Integrating classic and modern methods to understand association fibers connecting dorsal and ventral visual cortex

Takemura, H., Pestilli, F., & Weiner, K. S. (2018) · Neuroscience Research · doi:10.1016/j.neures.2018.10.011 · Cited by 36

Dynamic attentional modulation of vision across space and time after right hemisphere stroke and in ageing

Russell, C., Malhotra, P., Deidda, C., & Husain, M. (2012) · Cortex · doi:10.1016/j.cortex.2012.10.005 · Cited by 35

Concurrent analysis of white matter bundles and grey matter networks in the chimpanzee

Mars, R., O'Muircheartaigh, J., Folloni, D., Li, L.-C., Glasser, M., Jbabdi, S., & Bryant, K. L. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1817-8 · Cited by 29

An overlapping community detection algorithm based on rough clustering of links

Gupta, S., & Kumar, P. (2019) · Data & Knowledge Engineering · doi:10.1016/j.datak.2019.101777 · Cited by 35

Clay art therapy on emotion regulation: Research, theoretical underpinnings, and treatment mechanisms

Nan, J. K.-M., Hinz, L. D., & Lusebrink, V. B. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-817933-8.00009-8 · Cited by 36

Fiber Pathways of Attention Subnetworks Revealed with Tract-Based Spatial Statistics (TBSS) and Probabilistic Tractography

Ge, H., Yin, X., Xu, J., Tang, Y., Han, Y., Xu, W., Pang, Z., Meng, H., & Liu, S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078831 · Cited by 34

Hunting for right and left parietal hot spots using single-pulse TMS: modulation of visuospatial perception during line bisection judgment in the healthy brain

Salatino, A., Poncini, M., George, M. S., & Ricci, R. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.01238 · Cited by 35

Hemispheric modulations of the attentional networks

Spagna, A., Martella, D., Fuentes, L. J., Marotta, A., & Casagrande, M. (2016) · Brain and Cognition · doi:10.1016/j.bandc.2016.07.002 · Cited by 35

Thresholding functional connectomes by means of mixture modeling

Bielczyk, N., Walocha, F., Ebel, P., Haak, K. V., Llera, A., Buitelaar, J. K., Glennon, J. C., & Beckmann, C. F. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.01.003 · Cited by 36

Camera-Based Mirror Visual Feedback: Potential to Improve Motor Preparation in Stroke Patients

Ding, L., Wang, X., Guo, X., Chen, S., Wang, H., Jiang, N., & Jia, J. (2018) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2018.2864990 · Cited by 35

Word learning reveals white matter plasticity in preschool children

Ekerdt, C., Kühn, C., Anwander, A., Bräuer, J., & Friederici, A. D. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02024-7 · Cited by 36

Multiple Network Disconnection in Anosognosia for Hemiplegia

Monai, E., Bernocchi, F., Bisio, M., Bisogno, A. L., Salvalaggio, A., & Corbetta, M. (2020) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2020.00021 · Cited by 33

Fibre-specific laterality of white matter in left and right language dominant people

Verhelst, H., Dhollander, T., Gerrits, R., & Vingerhoets, G. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117812 · Cited by 33

Neural correlates associated with impaired global motion perception in cerebral visual impairment (CVI)

Pamir, Z., Bauer, C. M., Bailin, E. S., Bex, P. J., Somers, D. C., & Merabet, L. B. (2021) · NeuroImage Clinical · doi:10.1016/j.nicl.2021.102821 · Cited by 39

Differential neural network configuration during human path integration

Arnold, A. E. G. F., Burles, F., Bray, S., Levy, R., & Iaria, G. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00263 · Cited by 34

Game theoretical mapping of causal interactions underlying visuo‐spatial attention in the human brain based on stroke lesions

Toba, M. N., Zavaglia, M., Rastelli, F., Valabrègue, R., Pradat-Diehl, P., Valero‐Cabré, A., & Hilgetag, C. C. (2017) · Human Brain Mapping · doi:10.1002/hbm.23601 · Cited by 35

Asymmetry of Hemispheric Network Topology Reveals Dissociable Processes between Functional and Structural Brain Connectome in Community-Living Elders

Sun, Y., Li, J., Suckling, J., & Feng, L. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00361 · Cited by 36

Dissociation between line bisection and mental-number-line bisection in healthy adults

Rotondaro, F., Merola, S., Aiello, M., et al. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2015.07.016 · Cited by 34

Development of Right-hemispheric Dominance of Inferior Parietal Lobule in Proprioceptive Illusion Task

Naito, E., Morita, T., Saito, D. N., Ban, M., Shimada, K., Okamoto, Y., Kosaka, H., Okazawa, H., & Asada, M. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx223 · Cited by 33

Long‐range connectomics

Jbabdi, S., & Behrens, T. E. J. (2013) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12271 · Cited by 31

Cingulate neglect in humans: Disruption of contralesional reward learning in right brain damage

Lecce, F., Rotondaro, F., Bonnı̀, S., Carlesimo, G. A., de Schotten, M. T., Tomaiuolo, F., & Doricchi, F. (2014) · Cortex · doi:10.1016/j.cortex.2014.08.008 · Cited by 33

Adult developmental trajectories of pseudoneglect in the tactile, visual and auditory modalities and the influence of starting position and stimulus length

Brooks, J. L., Darling, S., Malvaso, C., & Sala, S. D. (2016) · Brain and Cognition · doi:10.1016/j.bandc.2015.12.001 · Cited by 32

The Superoanterior Fasciculus (SAF): A Novel White Matter Pathway in the Human Brain?

Dávid, S., Heemskerk, A. M., Corrivetti, F., de Schotten, M. T., Sarubbo, S., Corsini, F., BENEDICTIS, A. D., Petit, L., Viergever, M. A., Jones, D. K., et al. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2019.00024 · Cited by 32

Microstructural degeneration and cerebrovascular risk burden underlying executive dysfunction after stroke

Veldsman, M., Werden, E., Egorova, N., Khlif, M. S., & Brodtmann, A. G. (2020) · Scientific Reports · doi:10.1038/s41598-020-75074-w · Cited by 33

Superior longitudinal fasciculus (SLF) I and II: an anatomical and functional review

VERGANI, F., Ghimire, P., RAJASHEKHAR, D., et al. (2022) · Journal of Neurosurgical Sciences · doi:10.23736/s0390-5616.21.05327-3 · Cited by 33

Language learning and brain reorganization in a 3.5-year-old child with left perinatal stroke revealed using structural and functional connectivity

Clément, F., Ripollés, P., Bosch, L., Garcı́a-Alix, A., Muchart, J., Sierpowska, J., Fons, C., Solé, J., Rebollo, M., Gaitán, H., et al. (2016) · Cortex · doi:10.1016/j.cortex.2016.01.010 · Cited by 33

The White Matter Microintegrity Alterations of Neocortical and Limbic Association Fibers in Major Depressive Disorder and Panic Disorder

Lai, C., & Wu, Y. (2016) · Medicine · doi:10.1097/md.0000000000002982 · Cited by 33

A matter of hand: Causal links between hand dominance, structural organization of fronto-parietal attention networks, and variability in behavioural responses to transcranial magnetic stimulation

Cazzoli, D., & Chechlacz, M. (2016) · Cortex · doi:10.1016/j.cortex.2016.06.015 · Cited by 33

Prism adaptation changes resting-state functional connectivity in the dorsal stream of visual attention networks in healthy adults: A fMRI study

Tsujimoto, K., Mizuno, K., Nishida, D., Tahara, M., Yamada, E., Shindo, S., Kasuga, S., & Liu, M. (2018) · Cortex · doi:10.1016/j.cortex.2018.10.018 · Cited by 34

Impaired Activation of Visual Attention Network for Motion Salience Is Accompanied by Reduced Functional Connectivity between Frontal Eye Fields and Visual Cortex in Strabismic Amblyopia

Wang, H., Crewther, S. G., Liang, M., Laycock, R., Yu, T., Alexander, B., Crewther, D. P., Wang, J., & Yin, Z. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00195 · Cited by 33

Connectivity of Frontoparietal Regions Reveals Executive Attention and Consciousness Interactions

Martín-Signes, M., Paz‐Alonso, P. M., & Chica, A. B. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy332 · Cited by 32

Cognitive Training in Young Patients With Traumatic Brain Injury: A Fixel-Based Analysis

Verhelst, H., Giraldo, D. L., Linden, C. V., Vingerhoets, G., Jeurissen, B., & Caeyenberghs, K. (2019) · Neurorehabilitation and neural repair · doi:10.1177/1545968319868720 · Cited by 32

Subdividing the superior longitudinal fasciculus using local quantitative MRI

Schurr, R., Zelman, A., & Mezer, A. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116439 · Cited by 32

From competition to cooperation: Visual neglect across the hemispheres

Bartolomeo, P. (2021) · Revue Neurologique · doi:10.1016/j.neurol.2021.07.015 · Cited by 32

Causal involvement of the left angular gyrus in higher functions as revealed by transcranial magnetic stimulation: a systematic review

Wagner, J., & Rusconi, E. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02576-w · Cited by 32

Different Cortical Mechanisms for Spatial vs. Feature-Based Attentional Selection in Visual Working Memory

Heuer, A., Schubö, A., & Crawford, J. D. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00415 · Cited by 29

Multivariate Analysis of Structural and Functional Neuroimaging Can Inform Psychiatric Differential Diagnosis

Stoyanov, D., Kandilarova, S., Aryutova, K., Paunova, R., Todeva-Radneva, A., Latypova, A., & Kherif, F. (2020) · Diagnostics · doi:10.3390/diagnostics11010019 · Cited by 28

Hodology of the superior longitudinal system of the human brain: a historical perspective, the current controversies, and a proposal

Vavassori, L., Sarubbo, S., & Petit, L. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02265-0 · Cited by 27

Mapping lesion, structural disconnection, and functional disconnection to symptoms in semantic aphasia

Souter, N. E., Wang, X., Thompson, H. E., Krieger‐Redwood, K., Halai, A. D., Ralph, M. A. L., de Schotten, M. T., & Jefferies, E. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02526-6 · Cited by 34

Leftward attentional bias in a simulated driving task

Benedetto, S., Pedrotti, M., Brémond, R., & Baccino, T. (2013) · Transportation Research Part F Traffic Psychology and Behaviour · doi:10.1016/j.trf.2013.07.006 · Cited by 32

Dysconnectivity of the Agency Network in Schizophrenia: A Functional Magnetic Resonance Imaging Study

Koreki, A., Maeda, T., Okimura, T., Terasawa, Y., Kikuchi, T., Umeda, S., Nishikata, S., Yagihashi, T., Kasahara, M., Nagai, C., et al. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00171 · Cited by 31

Microstructure of the superior longitudinal fasciculus predicts stimulation-induced interference with on-line motor control

Rodríguez‐Herreros, B., Amengual, J. L., Gurtubay-Antolín, A., Richter, L., Jauer, P., Erdmann, C., Schweikard, A., López‐Moliner, J., Rodríguez‐Fornells, A., & Münte, T. F. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.06.070 · Cited by 32

Right hemisphere dominance directly predicts both baseline V1 cortical excitability and the degree of top-down modulation exerted over low-level brain structures

Arshad, Q., Siddiqui, S., Ramachandran, S., et al. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.10.045 · Cited by 30

Network Dynamics of Attention During a Naturalistic Behavioral Paradigm

Weber, R., Alicea, B., Huskey, R., & Mathiak, K. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00182 · Cited by 31

Anatomy of nerve fiber bundles at micrometer-resolution in the vervet monkey visual system

Takemura, H., Palomero‐Gallagher, N., Axer, M., Gräßel, D., Jorgensen, M. J., Woods, R. P., & Zilles, K. (2020) · eLife · doi:10.7554/elife.55444 · Cited by 30

Fronto-parietal networks underlie the interaction between executive control and conscious perception: Evidence from TMS and DWI

Martín-Signes, M., Cano-Melle, C., & Chica, A. B. (2020) · Cortex · doi:10.1016/j.cortex.2020.09.027 · Cited by 30

Individual differences in children’s global motion sensitivity correlate with TBSS-based measures of the superior longitudinal fasciculus

Braddick, O., Atkinson, J., Akshoomoff, N. A., Newman, E. R., Curley, L. B., Gonzalez, M. R., Brown, T. T., Dale, A. M., & Jernigan, T. L. (2016) · Vision Research · doi:10.1016/j.visres.2016.09.013 · Cited by 31

Diffusion-weighted imaging evidence of altered white matter development from late childhood to early adulthood in Autism Spectrum Disorder

Karahanoğlu, F. I., Baran, B., Nguyen, Q. T. H., Meskaldji, D. E., Yendiki, A., Vangel, M. G., Santangelo, S. L., & Manoach, D. S. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.06.002 · Cited by 32

To the Other Side of the Neglected Brain

Koch, G., Veniero, D., & Caltagirone, C. (2012) · The Neuroscientist · doi:10.1177/1073858412447874 · Cited by 29

Age dependency and lateralization in the three branches of the human superior longitudinal fasciculus

Amemiya, K., Naito, E., & Takemura, H. (2021) · Cortex · doi:10.1016/j.cortex.2021.02.027 · Cited by 32

Mapping brain-wide excitatory projectome of primate prefrontal cortex at submicron resolution and comparison with diffusion tractography

Yan, M., Yu, W., Lv, Q., Lv, Q., Bo, T., Chen, X., Liu, Y., Zhan, Y., Yan, S., Shen, X., et al. (2022) · eLife · doi:10.7554/elife.72534 · Cited by 30

Structural asymmetry of cortical visual areas is related to ocular dominance

Jensen, B. H., Hougaard, A., Amin, F. M., et al. (2015) · Neuroreport · doi:10.1097/wnr.0000000000000470 · Cited by 29

Emotional processing and its impact on unilateral neglect and extinction

Domínguez‐Borràs, J., Saj̈, A., Armony, J. L., & Vuilleumier, P. O. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.03.003 · Cited by 33

Critical Neural Networks in Awake Surgery for Gliomas

Kinoshita, M., Miyashita, K., Tsutsui, T., Furuta, T., & Nakada, M. (2016) · Neurologia medico-chirurgica · doi:10.2176/nmc.ra.2016-0069 · Cited by 29

Reduced fine motor competence in children with ADHD is associated with atypical microstructural organization within the superior longitudinal fasciculus

Hyde, C. E., Sciberras, E., Efron, D., Fuelscher, I. T., & Silk, T. J. (2020) · Brain Imaging and Behavior · doi:10.1007/s11682-020-00280-z · Cited by 29

Word inversion sensitivity as a marker of visual word form area lateralization: An application of a novel multivariate measure of laterality

Carlos, B. J., Hirshorn, E. A., Durisko, C., Fiez, J. A., & Coutanche, M. N. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.02.044 · Cited by 29

Disconnection somewhere down the line: Multivariate lesion-symptom mapping of the line bisection error

Wiesen, D., Karnath, H., & Sperber, C. (2020) · Cortex · doi:10.1016/j.cortex.2020.09.012 · Cited by 27

Age-Related Differences in White Matter: Understanding Tensor-Based Results Using Fixel-Based Analysis.

Kelley, S., Plass, J., Bender, A. R., & Polk, T. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab056 · Cited by 30

Anatomy and White Matter Connections of the Superior Parietal Lobule

Lin, Y., Dadario, N. B., Hormovas, J., Young, I. M., Briggs, R. G., Mackenzie, A., Palejwala, A. H., Fonseka, R. D., Kim, S. J., Tanglay, O., et al. (2021) · Operative Neurosurgery · doi:10.1093/ons/opab174 · Cited by 28

Contribution of the medial eye field network to the voluntary deployment of visuospatial attention

Herbet, G., & Duffau, H. (2022) · Nature Communications · doi:10.1038/s41467-022-28030-3 · Cited by 28

Segregated circuits for phonemic and semantic fluency: A novel patient-tailored disconnection study

Zigiotto, L., Vavassori, L., Annicchiarico, L., Corsini, F., Avesani, P., Rozzanigo, U., Sarubbo, S., & Papagno, C. (2022) · NeuroImage: Clinical · doi:10.1016/j.nicl.2022.103149 · Cited by 25

Behavioural asymmetries on the greyscales task: The influence of native reading direction

Friedrich, T. E., & Elias, L. J. (2014) · Culture and Brain · doi:10.1007/s40167-014-0019-3 · Cited by 28

Tract-based analysis of white matter integrity in psychotic and nonpsychotic bipolar disorder

Ji, A. B., Godwin, D., Rutlin, J. R., Kandala, S., Shimony, J. S., & Mamah, D. T. (2016) · Journal of Affective Disorders · doi:10.1016/j.jad.2016.11.038 · Cited by 29

White matter microstructure of attentional networks predicts attention and consciousness functional interactions

Chica, A. B., de Schotten, M. T., Bartolomeo, P., & Paz‐Alonso, P. M. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1511-2 · Cited by 27

Neuroimaging in the Diagnosis of Chronic Traumatic Encephalopathy: A Systematic Review

Sparks, P., Lawrence, T. P., & Hinze, S. (2017) · Clinical Journal of Sport Medicine · doi:10.1097/jsm.0000000000000541 · Cited by 32

Inappropriate rightward saccades after right hemisphere damage: Oculomotor analysis and anatomical correlates

Bourgeois, A., Chica, A. B., Migliaccio, R., Bayle, D. J., Duret, C., Pradat-Diehl, P., Lunven, M., Pouget, P., & Bartolomeo, P. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2015.04.013 · Cited by 27

Asymmetrical white matter networks for attending to global versus local features

Chechlacz, M., Mantini, D., Gillebert, C. R., & Humphreys, G. W. (2015) · Cortex · doi:10.1016/j.cortex.2015.01.022 · Cited by 28

Object and space perception – Is it a matter of hemisphere?

Schintu, S., Hadj‐Bouziane, F., Monte, O. D., Knutson, K. M., Pardini, M., Wassermann, E. M., Grafman, J. H., & Krüeger, F. (2014) · Cortex · doi:10.1016/j.cortex.2014.04.009 · Cited by 30

Prismatic Adaptation Modulates Oscillatory EEG Correlates of Motor Preparation but Not Visual Attention in Healthy Participants

Bracco, M., Veniero, D., Oliveri, M., & Thut, G. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1422-17.2017 · Cited by 26

The role of the parietal cortex in sensorimotor transformations and action coding

Binkofski, F., & Buccino, G. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63622-5.00024-3 · Cited by 26

Structural white and gray matter differences in a large sample of patients with Posttraumatic Stress Disorder and a healthy and trauma-exposed control group: Diffusion tensor imaging and region-based morphometry

Siehl, S., Wicking, M., Pohlack, S. T., Winkelmann, T., Zidda, F., Steiger-White, F., King, J. A., Burgess, N., Flor, H., & Nees, F. (2020) · NeuroImage Clinical · doi:10.1016/j.nicl.2020.102424 · Cited by 29

Human emotion and cerebral lateralization : a study of depression as an expression of right hemisphere activity

Handel, M. (1984) · University Microfilms International eBooks

Cerebral Lateralization of Global-Local Processing in Left- and Right-Handed People

Goodarzi, M. A., Taghavi, M. R., & Zoughi, M. R. (2005) · Perceptual and Motor Skills · doi:10.2466/pms.100.3.734-742 · Cited by 4

Dominance of the right hemisphere for visually guided actions

Weiller, C., Siebner, H. R., Klöppel, S., et al. (2005) · Aktuelle Neurologie · doi:10.1055/s-2005-919574

Emotions and the Right Side of the Brain

Tommasi, L. (2020) · Laterality Asymmetries of Body Brain and Cognition · doi:10.1080/1357650x.2020.1842435 · Cited by 7

Lateralization for orientation in split-brain monkeys

Hamilton, C. R. (1983) · Behavioural Brain Research · doi:10.1016/0166-4328(83)90044-x · Cited by 62