Cited by 280Advanced Neuroimaging Techniques and ApplicationsClassical Anatomy and HistologyNeurobiology of Language and Bilingualism

The DOI matches its Crossref record; 81 of the 81 references it cites were found in a registry or an index.

Analysis of the subcomponents and cortical terminations of the perisylvian superior longitudinal fasciculus: a fiber dissection and DTI tractography study

Martino, Juan, De Witt Hamer, Philip C., Berger, Mitchel S., Lawton, Michael T., Arnold, Christine M., de Lucas, Enrique Marco, Duffau, Hugues·2013·Brain Structure and Function

DOI 10.1007/s00429-012-0386-5

Open this paper in CoChat — free account

Abstract

The anatomy of the perisylvian component of the superior longitudinal fasciculus (SLF) has recently been reviewed by numerous diffusion tensor imaging tractography (DTI) studies. However, little is known about the exact cortical terminations of this tract. The aim of the present work is to isolate the different subcomponents of this tract with fiber dissection and DTI tractography, and to identify the exact cortical connections. Twelve postmortem human hemispheres (6 right and 6 left) were dissected using the cortex-sparing fiber dissection. In addition, three healthy brains were analyzed using DTI-based tractography software. The different components of the perisylvian SLF were isolated and the fibers were followed until the cortical terminations. Three segments of the perisylvian SLF were identified: (1) anterior segment, connecting the supramarginal gyrus and superior temporal gyrus with the precentral gyrus, (2) posterior segment, connecting the posterior portion of the middle temporal gyrus with the angular gyrus, and (3) long segment of the arcuate fasciculus that connects the middle and inferior temporal gyri with the precentral gyrus and posterior portion of the inferior and middle frontal gyri. In the present study, three different components of the perisylvian SLF were identified. For the first time, our dissections revealed that each component was connected to a specific cortical area within the frontal, parietal and temporal lobes. By accurately depicting not only the trajectory but also cortical connections of this bundle, it is possible to develop new insights into the putative functional role of this tract.

Integrity signals

Registry

Crossref · 10.1007/s00429-012-0386-5

Cites

81 of 81 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Working memory: Looking back and looking forward
Baddeley, A. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1201 · Cited by 5,200
Perception of the speech code.
Liberman, A. M., Cooper, F. S., Shankweiler, D. P., & Studdert-Kennedy, M. (1967) · Psychological Review · doi:10.1037/h0020279 · Cited by 3,722
Diffusion tensor imaging: Concepts and applications
Le Bihan, D., Mangin, J., Poupon, C., Clark, C. A., Pappata, S., Molko, N., & Chabriat, H. (2001) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.1076 · Cited by 3,547
The motor theory of speech perception revised
Liberman, A. M., & Mattingly, I. G. (1985) · Cognition · doi:10.1016/0010-0277(85)90021-6 · Cited by 2,970
Large-scale neurocognitive networks and distributed processing for attention, language, and memory
Mesulam, M. (1990) · Annals of Neurology · doi:10.1002/ana.410280502 · Cited by 2,684
Dorsal and ventral streams: a framework for understanding aspects of the functional anatomy of language
Hickok, G., & Poeppel, D. (2004) · Cognition · doi:10.1016/j.cognition.2003.10.011 · Cited by 2,212
Fiber tracking: principles and strategies – a technical review
Mori, S., & van Zijl, P. C. M. (2002) · NMR in Biomedicine · doi:10.1002/nbm.781 · Cited by 2,019
Perisylvian language networks of the human brain
Catani, M., Jones, D. K., & ffytche, D. H. (2005) · Annals of Neurology · doi:10.1002/ana.20319 · Cited by 1,832
A diffusion tensor imaging tractography atlas for virtual in vivo dissections.
CATANI, M., & THIEBAUTDESCHOTTEN, M. (2008) · Cortex · doi:10.1016/j.cortex.2008.05.004 · Cited by 1,642
Virtual in vivo interactive dissection of white matter fasciculi in the human brain
Catani, M., Howard, R. J., Pajevic, S., & Jones, D. K. (2002) · NeuroImage · doi:10.1006/nimg.2002.1136 · Cited by 1,637

Show all 81 references

Research works printed but not linked: 4

Aminoff MJ, Greenberg DA, Simon RP (2005) Clinical neurology. McGraw-Hill, New York
De Renzi E (1989) Agnosia. Recenti Prog Med 80:633–637
Klingler J (1935) Erleichterung der makroskopischen Praeparation des Gehirns durch den Gefrierprozess. Schweiz Arch Neurol Psychiatr 36:247–256
Ludwig E, Klingler J (1956) Atlas Cerebri Humani: Der innere Bau des Gehirns dargestellt auf Grund mackroskopischer Präparate. Brown, Boston

Sorted by citations

Broca and Wernicke are dead, or moving past the classic model of language neurobiology
Tremblay, P., & Dick, A. S. (2016) · Brain and Language · doi:10.1016/j.bandl.2016.08.004 · Cited by 548
Stimulation mapping of white matter tracts to study brain functional connectivity.
Duffau, H. (2015) · Nature Reviews Neurology · doi:10.1038/nrneurol.2015.51 · Cited by 437
The Language Connectome
Dick, A. S., Bernal, B., & Tremblay, P. (2013) · The Neuroscientist · doi:10.1177/1073858413513502 · Cited by 361
Functional Anatomy of the Inferior Longitudinal Fasciculus: From Historical Reports to Current Hypotheses
Herbet, G., Zemmoura, I., & Duffau, H. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00077 · Cited by 296
The huge plastic potential of adult brain and the role of connectomics: new insights provided by serial mappings in glioma surgery
Duffau, H. (2014) · Cortex · doi:10.1016/j.cortex.2013.08.005 · Cited by 331
Revisiting the Functional Anatomy of the Human Brain: Toward a Meta-Networking Theory of Cerebral Functions
Herbet, G., & Duffau, H. (2020) · Physiological Reviews · doi:10.1152/physrev.00033.2019 · Cited by 321
Mapping neuroplastic potential in brain-damaged patients
Herbet, G., Maheu, M., Costi, E., Lafargue, G., & Duffau, H. (2016) · Brain · doi:10.1093/brain/awv394 · Cited by 289
Building connectomes using diffusion MRI: why, how and but
Sotiropoulos, S. N., & Zalesky, A. (2019) · NMR in Biomedicine · doi:10.1002/nbm.3752 · Cited by 290
Subcomponents and connectivity of the superior longitudinal fasciculus in the human brain
Wang, X., Pathak, S., Stefaneanu, L., Yeh, F.-C., Li, S., & Fernandez-Miranda, J. C. (2016) · Brain Structure and Function · doi:10.1007/s00429-015-1028-5 · Cited by 257
On the role of the supramarginal gyrus in phonological processing and verbal working memory: Evidence from rTMS studies
Deschamps, I., Baum, S. R., & Gracco, V. L. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.10.015 · Cited by 228
Mapping critical cortical hubs and white matter pathways by direct electrical stimulation: an original functional atlas of the human brain
Sarubbo, S., Tate, M., De Benedictis, A., Merler, S., Moritz-Gasser, S., Herbet, G., & Duffau, H. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2019.116237 · Cited by 206
Self-citation
Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates
Janelle, F., Iorio-Morin, C., D'amour, S., & Fortin, D. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.794618 · Cited by 189
Inferring a dual-stream model of mentalizing from associative white matter fibres disconnection
Herbet, G., Lafargue, G., Bonnetblanc, F., Moritz‐Gasser, S., de Champfleur, N. M., & Duffau, H. (2014) · Brain · doi:10.1093/brain/awt370 · Cited by 192
Asymmetry, connectivity, and segmentation of the arcuate fascicle in the human brain
Fernandez-Miranda, J. C., Wang, Y., Pathak, S., Stefaneau, L., Verstynen, T., & Yeh, F.-C. F. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0751-7 · Cited by 185
The superior longitudinal fascicle: reconsidering the fronto-parietal neural network based on anatomy and function
Nakajima, R., Kinoshita, M., Shinohara, H., & Nakada, M. (2019) · Brain Imaging and Behavior · doi:10.1007/s11682-019-00187-4 · Cited by 176
Damage to Broca’s area does not contribute to long-term speech production outcome after stroke
Gajardo-Vidal, A., Lorca-Puls, D. L., team, P., Warner, H., Pshdary, B., Crinion, J. T., Leff, A. P., Hope, T. M. H., Geva, S., Seghier, M. L., et al. (2021) · Brain · doi:10.1093/brain/awaa460 · Cited by 150
Anatomo‐functional study of the temporo‐parieto‐occipital region: dissection, tractographic and brain mapping evidence from a neurosurgical perspective
BENEDICTIS, A. D., Duffau, H., Paradiso, B., Grandi, E., Balbi, S., Granieri, E., Colarusso, E., Chioffi, F., Marras, C. E., & Sarubbo, S. (2014) · Journal of Anatomy · doi:10.1111/joa.12204 · Cited by 167
Fiber tracts of the dorsal language stream in the human brain
Yağmurlu, K., Middlebrooks, E. H., Tanrıöver, N., & Rhoton, A. L. (2015) · Journal of neurosurgery · doi:10.3171/2015.5.jns15455 · Cited by 154
Anatomy and White Matter Connections of the Inferior Temporal Gyrus
Lin, Y., Young, I. M., Conner, A. K., Glenn, C. A., Chakraborty, A. R., Nix, C. E., Bai, M. Y., Dhanaraj, V., Fonseka, R. D., Hormovas, J., et al. (2020) · World Neurosurgery · doi:10.1016/j.wneu.2020.08.058 · Cited by 156
Intraoperative dorsal language network mapping by using single‐pulse electrical stimulation
Yamao, Y., Matsumoto, R., Kunieda, T., Arakawa, Y., Kobayashi, K., Usami, K., Shibata, S., Kikuchi, T., Sawamoto, N., Mikuni, N., et al. (2014) · Human Brain Mapping · doi:10.1002/hbm.22479 · Cited by 150
The Neurobiological Grounding of Persistent Stuttering: from Structure to Function
Neef, N. E., Anwander, A., & Friederici, A. D. (2015) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-015-0579-4 · Cited by 146
New insights into the neural network mediating reading processes provided by cortico‐subcortical electrical mapping
Zemmoura, I., Herbet, G., Moritz‐Gasser, S., & Duffau, H. (2015) · Human Brain Mapping · doi:10.1002/hbm.22766 · Cited by 135
Identifying preoperative language tracts and predicting postoperative functional recovery using HARDI q-ball fiber tractography in patients with gliomas
Caverzasi, E., Hervey‐Jumper, S. L., Jordan, K., Lobach, I. V., Li, J., Panara, V., Racine, C. A., Sankaranarayanan, V., Amirbekian, B., Papinutto, N., et al. (2015) · Journal of neurosurgery · doi:10.3171/2015.6.jns142203 · Cited by 131
Automated white matter fiber tract identification in patients with brain tumors
O’Donnell, L. J., Suter, Y., Rigolo, L., Kahali, P., Zhang, F., Norton, I. H., Albi, A., Olubiyi, O. I., Meola, A., Essayed, W. I., et al. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.11.023 · Cited by 129
Diffuse low-grade glioma: a review on the new molecular classification, natural history and current management strategies
López, P. D. D., Corrales-García, E. M., Martino, J., Aras, E. L., & Dueñas-Polo, M. T. (2017) · Clinical & Translational Oncology · doi:10.1007/s12094-017-1631-4 · Cited by 125
Diffuse low-grade gliomas and neuroplasticity
Duffau, H. (2014) · Diagnostic and Interventional Imaging · doi:10.1016/j.diii.2014.08.001 · Cited by 121
Post mortem mapping of connectional anatomy for the validation of diffusion MRI
Yendiki, A., Aggarwal, M., Axer, M., Howard, A. F. D., van Walsum, A. V. C., & Haber, S. N. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119146 · Cited by 116
Limited plastic potential of the left ventral premotor cortex in speech articulation: evidence From intraoperative awake mapping in glioma patients
van Geemen, K., Herbet, G., Moritz‐Gasser, S., & Duffau, H. (2014) · Human Brain Mapping · doi:10.1002/hbm.22275 · Cited by 115
Self-citation
Functional maps of direct electrical stimulation-induced speech arrest and anomia: a multicentre retrospective study
Lu, J., Zhao, Z., Zhang, J., Wu, B., Zhu, Y., Chang, E. F., Wu, J., Duffau, H., & Berger, M. S. (2021) · Brain · doi:10.1093/brain/awab125 · Cited by 114
Anatomy and White Matter Connections of the Superior Frontal Gyrus
Briggs, R. G., Khan, A. W., Chakraborty, A. R., Abraham, C. J., Anderson, C. D., Karas, P. J., Bonney, P. A., Palejwala, A. H., Conner, A. K., OʼDonoghue, D. L., et al. (2019) · Clinical Anatomy · doi:10.1002/ca.23523 · Cited by 115
Anatomy and White Matter Connections of the Middle Frontal Gyrus
Briggs, R. G., Lin, Y., Dadario, N. B., Kim, S. J., Young, I. M., Bai, M. Y., Dhanaraj, V., Fonseka, R. D., Hormovas, J., Tanglay, O., et al. (2021) · World Neurosurgery · doi:10.1016/j.wneu.2021.03.045 · Cited by 112
A Neurosurgical Functional Dissection of the Middle Precentral Gyrus during Speech Production
Silva, A. B., Liu, J. R., Zhao, L., Levy, D. F., Scott, T. L., & Chang, E. F. (2022) · The Journal of Neuroscience · doi:10.1523/jneurosci.1614-22.2022 · Cited by 111
Proposal of an optimized strategy for intraoperative testing of speech and language during awake mapping
Mandonnet, E., Sarubbo, S., & Duffau, H. (2016) · Neurosurgical Review · doi:10.1007/s10143-016-0723-x · Cited by 115
Anatomy and white matter connections of the inferior frontal gyrus
Briggs, R. G., Chakraborty, A. R., Anderson, C. D., Abraham, C. J., Palejwala, A. H., Conner, A. K., Pelargos, P. E., OʼDonoghue, D. L., Glenn, C. A., & Sughrue, M. E. (2019) · Clinical Anatomy · doi:10.1002/ca.23349 · Cited by 113
Tractography methods and findings in brain tumors and traumatic brain injury
Yeh, F.-C. F., Andrei Irimia, A., Bastos, D. C. D. A., & Golby, A. J. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118651 · Cited by 110
Converging evidence for a cortico-subcortical network mediating lexical retrieval.
Herbet, G., Moritz-Gasser, S., Boiseau, M., Duvaux, S., Cochereau, J., & Duffau, H. (2016) · Brain : a journal of neurology · doi:10.1093/brain/aww220 · Cited by 99
Anatomy and white-matter connections of the precuneus
Tanglay, O., Young, I. M., Dadario, N. B., Briggs, R. G., Fonseka, R. D., Dhanaraj, V., Hormovas, J., Lin, Y., & Sughrue, M. E. (2021) · Brain Imaging and Behavior · doi:10.1007/s11682-021-00529-1 · Cited by 101
Neural pathways subserving face-based mentalizing
Yordanova, Y. N., Duffau, H., & Herbet, G. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1388-0 · Cited by 102
New insights in the homotopic and heterotopic connectivity of the frontal portion of the human corpus callosum revealed by microdissection and diffusion tractography
De Benedictis, A., Petit, L., Descoteaux, M., Marras, C. E., Barbareschi, M., Corsini, F., Dallabona, M., Chioffi, F., & Sarubbo, S. (2016) · Human Brain Mapping · doi:10.1002/hbm.23339 · Cited by 97
On the Neuroanatomy and Functional Role of the Inferior Parietal Lobule and Intraparietal Sulcus
Binkofski, F., Klann, J., & Caspers, S. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-407794-2.00004-3 · Cited by 100
The Dangers of Magnetic Resonance Imaging Diffusion Tensor Tractography in Brain Surgery
Duffau, H. (2013) · World Neurosurgery · doi:10.1016/j.wneu.2013.01.116 · Cited by 95
Interfering with the neural activity of mirror-related frontal areas impairs mentalistic inferences
Herbet, G., Lafargue, G., Moritz‐Gasser, S., Bonnetblanc, F., & Duffau, H. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0777-x · Cited by 97
Motor versus body awareness: Voxel-based lesion analysis in anosognosia for hemiplegia and somatoparaphrenia following right hemisphere stroke
Moro, V., Pernigo, S., Manos Tsakiris, A., Avesani, R., Edelstyn, N. M. J., Jenkinson, P. M., & Fotopoulou, A. (2016) · Cortex · doi:10.1016/j.cortex.2016.07.001 · Cited by 98
Inferior Parietal Lobule Contributions to Visual Word Recognition
Sliwinska, M. W., James, A., & Devlin, J. T. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00721 · Cited by 90
A probabilistic map of negative motor areas of the upper limb and face: a brain stimulation study
Rech, F., Herbet, G., Gaudeau, Y., Wantz-Mézières, S., Moureau, J.-M., Moritz‐Gasser, S., & Duffau, H. (2019) · Brain · doi:10.1093/brain/awz021 · Cited by 91
Three-Dimensional Topographic Fiber Tract Anatomy of the Cerebrum
Yağmurlu, K., Vlasak, A. L., & Rhoton, A. L. (2015) · Operative Neurosurgery · doi:10.1227/neu.0000000000000704 · Cited by 90
Structural and functional integration between dorsal and ventral language streams as revealed by blunt dissection and direct electrical stimulation
Sarubbo, S., BENEDICTIS, A. D., Merler, S., Mandonnet, E., Barbareschi, M., Dallabona, M., Chioffi, F., & Duffau, H. (2016) · Human Brain Mapping · doi:10.1002/hbm.23281 · Cited by 89
Subcortical anatomy of the lateral association fascicles of the brain: A review
Martino, J., & De Lucas, E. M. (2014) · Clinical Anatomy · doi:10.1002/ca.22321 · Cited by 89
A taxonomy of the brain’s white matter: twenty-one major tracts for the 21st century
Bullock, D. N., Hayday, E., Grier, M. D., Tang, W., Pestilli, F., & Heilbronner, S. R. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab500 · Cited by 99
Decoding the superior parietal lobule connections of the superior longitudinal fasciculus/arcuate fasciculus in the human brain
Kamali, A., Sair, H. I., Radmanesh, A., & Hasan, K. M. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.07.035 · Cited by 88
A Connectomic Atlas of the Human Cerebrum—Chapter 1: Introduction, Methods, and Significance
Baker, C. M., Burks, J. D., Briggs, R. G., Conner, A. K., Glenn, C. A., Sali, G., McCoy, T. M., Battiste, J. D., OʼDonoghue, D. L., & Sughrue, M. E. (2018) · Operative Neurosurgery · doi:10.1093/ons/opy253 · Cited by 84
Tracing short connections of the temporo-parieto-occipital region in the human brain using diffusion spectrum imaging and fiber dissection
Wu, Y., Sun, D., Wang, Y., Wang, Y., & Wang, Y. (2016) · Brain Research · doi:10.1016/j.brainres.2016.05.046 · Cited by 85
A contemporary framework of language processing in the human brain in the context of preoperative and intraoperative language mapping
Middlebrooks, E. H., Yağmurlu, K., Szaflarski, J. P., Rahman, M., & Bozkurt, B. (2016) · Neuroradiology · doi:10.1007/s00234-016-1772-0 · Cited by 87
Neuropsychological evidence for the crucial role of the right arcuate fasciculus in the face-based mentalizing network: A disconnection analysis
Nakajima, R., Yordanova, Y. N., Duffau, H., & Herbet, G. (2018) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2018.01.024 · Cited by 84
Diffusion MRI tractography for neurosurgery: The basics, current state, technical reliability and challenges
Yang, J. Y.-M., Yeh, C.-H., Poupon, C., & Calamante, F. (2021) · Physics in Medicine & Biology · doi:10.1088/1361-6560/ac0d90 · Cited by 80
How Klingler’s dissection permits exploration of brain structural connectivity? An electron microscopy study of human white matter
Zemmoura, I., Blanchard, E., Raynal, P. I., Rousselot‐Denis, C., Destrieux, C., & Velut, S. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1050-7 · Cited by 81
Dance and music training have different effects on white matter diffusivity in sensorimotor pathways
Giacosa, C., Karpati, F. J., Foster, N. E. V., Penhune, V. B., & Hyde, K. L. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.04.048 · Cited by 88
Stem-, Spraak- en Taalpathologie
(2019) · Stem- Spraak- en Taalpathologie · doi:10.21827/5ce671ea62a92 · Cited by 80
Past Makes Future: Role of pFC in Prediction
Fuster, J. M., & Bressler, S. L. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00746 · Cited by 83
Structural white matter asymmetries in relation to functional asymmetries during speech perception and production
Ocklenburg, S., Hugdahl, K., & Westerhausen, R. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.07.076 · Cited by 81
White matter connections of the inferior parietal lobule: A study of surgical anatomy
Burks, J. D., Boettcher, L. B., Conner, A. K., Glenn, C. A., Bonney, P. A., Baker, C. M., Briggs, R. G., Pittman, N. A., OʼDonoghue, D. L., Wu, D. H., et al. (2017) · Brain and Behavior · doi:10.1002/brb3.640 · Cited by 79
Chronic spatial working memory deficit associated with the superior longitudinal fasciculus: a study using voxel-based lesion-symptom mapping and intraoperative direct stimulation in right prefrontal glioma surgery
Kinoshita, M., Nakajima, R., Shinohara, H., Miyashita, K., Tanaka, S., Okita, H., Nakada, M., & Hayashi, Y. (2016) · Journal of neurosurgery · doi:10.3171/2015.10.jns1591 · Cited by 76
Awake mapping for low-grade gliomas involving the left sagittal stratum: anatomofunctional and surgical considerations
Chan‐Seng, E., Moritz‐Gasser, S., & Duffau, H. (2014) · Journal of neurosurgery · doi:10.3171/2014.1.jns132015 · Cited by 71
Associative white matter connecting the dorsal and ventral posterior human cortex
Bullock, D. N., Takemura, H., Caiafa, C. F., Kitchell, L. M., McPherson, B., Caron, B. A., & Pestilli, F. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01907-8 · Cited by 72
Brain connectomics applied to oncological neuroscience: from a traditional surgical strategy focusing on glioma topography to a meta-network approach
Duffau, H. (2021) · Acta Neurochirurgica · doi:10.1007/s00701-021-04752-z · Cited by 69
Self-citation
Controversy over the temporal cortical terminations of the left arcuate fasciculus: a reappraisal
Giampiccolo, D., & Duffau, H. (2022) · Brain · doi:10.1093/brain/awac057 · Cited by 73
Photogrammetry of the Human Brain: A Novel Method for Three-Dimensional Quantitative Exploration of the Structural Connectivity in Neurosurgery and Neurosciences
BENEDICTIS, A. D., Nocerino, E., Menna, F., Fabio Remondino, A., Barbareschi, M., Rozzanigo, U., Corsini, F., Olivetti, E., Marras, C. E., Chioffi, F., et al. (2018) · World Neurosurgery · doi:10.1016/j.wneu.2018.04.036 · Cited by 64
The anatomo-functional connectivity of word repetition: insights provided by awake brain tumor surgery
Moritz‐Gasser, S., & Duffau, H. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00405 · Cited by 64
Different neural substrates for executive functions in youths with ADHD: a diffusion spectrum imaging tractography study
Chiang, H.-L., Chen, Y.-J., Shang, C.-Y., Tseng, W.-Y. I., & Gau, S. S.-F. (2016) · Psychological Medicine · doi:10.1017/s0033291715002767 · Cited by 62
A narrative review of the anatomy and function of the white matter tracts in language production and comprehension
Shekari, E., & Nozari, N. (2023) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2023.1139292 · Cited by 73
Subcortical surgical anatomy of the lateral frontal region: human white matter dissection and correlations with functional insights provided by intraoperative direct brain stimulation
BENEDICTIS, A. D., Sarubbo, S., & Duffau, H. (2012) · Journal of neurosurgery · doi:10.3171/2012.7.jns12628 · Cited by 61
Anatomical variability of the arcuate fasciculus: a systematical review
Bernard, F., Zemmoura, I., Ter Minassian, A., Lemée, J.-M., & Menei, P. (2019) · Surgical and Radiologic Anatomy · doi:10.1007/s00276-019-02244-5 · Cited by 55
Musical expertise is related to altered functional connectivity during audiovisual integration
Paraskevopoulos, E., Kraneburg, A., Herholz, S. C., Bamidis, P. D., & Pantev, C. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510662112 · Cited by 56
Parcellation‐based tractographic modeling of the dorsal attention network
Allan, P. G., Briggs, R. G., Conner, A. K., O’Neal, C. M., Bonney, P. A., Maxwell, B. D., Baker, C. M., Burks, J. D., Sali, G., Glenn, C. A., et al. (2019) · Brain and Behavior · doi:10.1002/brb3.1365 · Cited by 59
Diffusion Tensor Imaging Is a Research and Educational Tool, but Not Yet a Clinical Tool
Duffau, H. (2013) · World Neurosurgery · doi:10.1016/j.wneu.2013.08.054 · Cited by 57
FIBRASCAN: A novel method for 3D white matter tract reconstruction in MR space from cadaveric dissection
Zemmoura, I., Serres, B., Andersson, F., Barantin, L., Tauber, C., Filipiak, I., Cottier, J.-P., Venturini, G., & Destrieux, C. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.09.016 · Cited by 56
Microarchitecture and connectivity of the parietal lobe
Caspers, S., & Zilles, K. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63622-5.00003-6 · Cited by 59
Middle Frontal Gyrus and Area 55b: Perioperative Mapping and Language Outcomes
Hazem, S., Awan, M., Lavrador, J., Patel, S., Wren, H., Lucena, O., Semedo, C., Irzan, H., Melbourne, A., Ourselin, S., et al. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.646075 · Cited by 49
Structure, asymmetry, and connectivity of the human temporo-parietal aslant and vertical occipital fasciculi
Panesar, S. S., Alves-Belo, J. T., Yeh, F.-C. F., & Fernandez-Miranda, J. C. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1812-0 · Cited by 56
Mind-Reading Ability and Structural Connectivity Changes in Aging
Cabinio, M., Rossetto, F., Blasi, V., Savazzi, F. A., Castelli, I., Massaro, D., Valle, A., Nemni, R., Clerici, M., Marchetti, A., et al. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01808 · Cited by 59
A Connectomic Atlas of the Human Cerebrum—Chapter 10: Tractographic Description of the Superior Longitudinal Fasciculus
Conner, A. K., Briggs, R. G., Rahimi, M., Sali, G., Baker, C. M., Burks, J. D., Glenn, C. A., Battiste, J. D., & Sughrue, M. E. (2018) · Operative Neurosurgery · doi:10.1093/ons/opy264 · Cited by 53
Foix-Chavany-Marie syndrome caused by a disconnection between the right pars opercularis of the inferior frontal gyrus and the supplementary motor area
Martino, J., de Lucas, E. M., Ibáñez-Plágaro, F. J., Valle-Folgueral, J. M., & Vázquez-Barquero, A. (2012) · Journal of neurosurgery · doi:10.3171/2012.7.jns12404 · Cited by 53
The Unique Fiber Anatomy of Middle Temporal Gyrus Default Mode Connectivity
Briggs, R. G., Tanglay, O., Dadario, N. B., Young, I. M., Fonseka, R. D., Hormovas, J., Dhanaraj, V., Lin, Y., Kim, S. J., Bouvette, C. A., et al. (2021) · Operative Neurosurgery · doi:10.1093/ons/opab109 · Cited by 52
Awake brain mapping of cortex and subcortical pathways in brain tumor surgery.
Freyschlag, C. F., & Duffau, H. (2014) · PubMed · Cited by 49
A Review of Cortical and Subcortical Stimulation Mapping for Language
Young, J. S., Lee, A. T., & Chang, E. F. (2020) · Neurosurgery · doi:10.1093/neuros/nyaa436 · Cited by 52
Anatomy and White Matter Connections of the Parahippocampal Gyrus
Lin, Y., Dhanaraj, V., Mackenzie, A., Young, I. M., Tanglay, O., Briggs, R. G., Chakraborty, A. R., Hormovas, J., Fonseka, R. D., Kim, S. J., et al. (2021) · World Neurosurgery · doi:10.1016/j.wneu.2020.12.136 · Cited by 50
Mapping the human middle longitudinal fasciculus through a focused anatomo-imaging study: shifting the paradigm of its segmentation and connectivity pattern
Kalyvas, A., Koutsarnakis, C., Komaitis, S., Karavasilis, E., Christidi, F., Skandalakis, G. P., Liouta, E., Papakonstantinou, O., Kelekis, N., Duffau, H., et al. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01987-6 · Cited by 48
Multi-region hemispheric specialization differentiates human from nonhuman primate brain function
Wey, H., Phillips, K. A., McKay, D. R., Laird, A. R., Kochunov, P., Davis, M. D., Glahn, D. C., Duong, T. Q., & Fox, P. T. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0620-9 · Cited by 46
Awake surgery between art and science. Part II: language and cognitive mapping.
Talacchi, A., Santini, B., Casartelli, M., Monti, A., Capasso, R., & Miceli, G. (2013) · Europe PMC (PubMed Central) · doi:10.11138/fneur/2013.28.3.223 · Cited by 48
Electrical stimulation of the dorsolateral prefrontal cortex impairs semantic cognition
Herbet, G., Moritz‐Gasser, S., & Duffau, H. (2018) · Neurology · doi:10.1212/wnl.0000000000005174 · Cited by 48
Three-Dimensional Modeling and Augmented and Virtual Reality Simulations of the White Matter Anatomy of the Cerebrum
Gurses, M. E., Güngör, A., Gökalp, E., Hanalıoğlu, Ş., Okumus, S. Y. K., Tatar, İ., Berker, M., Cohen‐Gadol, A., & Türe, U. (2022) · Operative Neurosurgery · doi:10.1227/ons.0000000000000361 · Cited by 44
White matter properties differ in 6-year old Readers and Pre-readers
Travis, K. E., Adams, J. N., Kovachy, V. N., Ben‐Shachar, M., & Feldman, H. M. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1302-1 · Cited by 47
Developmental trajectory of the prefrontal cortex: a systematic review of diffusion tensor imaging studies
Sousa, S. S., Amaro, E., Crego, A., Gonçalves, Ó. F., & Sampaio, A. (2017) · Brain Imaging and Behavior · doi:10.1007/s11682-017-9761-4 · Cited by 46
Disentangling the relation between left temporoparietal white matter and reading: A spherical deconvolution tractography study
Vanderauwera, J., Vandermosten, M., Dell’Acqua, F., Wouters, J. M., & Ghesquière, P. (2015) · Human Brain Mapping · doi:10.1002/hbm.22848 · Cited by 45
Characterisation of white matter asymmetries in the healthy human brain using diffusion MRI fixel-based analysis
Arun, A. H., Connelly, A., Smith, R., & Calamante, F. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117505 · Cited by 44
Superficial white matter bundle atlas based on hierarchical fiber clustering over probabilistic tractography data
Román, C., Hernández, C., Figueroa, M. E., Houenou, J., Poupon, C., Mangin, J., & Guevara, P. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119550 · Cited by 44
White Matter Diffusion of Major Fiber Tracts Implicated in Autism Spectrum Disorder
Libero, L. E., Burge, W. K., Deshpande, H., Pestilli, F., & Kana, R. K. (2016) · Brain Connectivity · doi:10.1089/brain.2016.0442 · Cited by 43
The prenatal brain readiness for speech processing: A review on foetal development of auditory and primordial language networks
Ghio, M., Cara, C., & Tettamanti, M. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.07.009 · Cited by 42
Altered brain structures in the dorsal and ventral language pathways in individuals with and without developmental language disorder (DLD)
Lee, J. C., Dick, A. S., & Tomblin, J. B. (2020) · Brain Imaging and Behavior · doi:10.1007/s11682-019-00209-1 · Cited by 39
Brain white matter fibre tracts: a review of functional neuro-oncological relevance
Voets, N., Bartsch, A., & Plaha, P. (2017) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2017-316170 · Cited by 38

Authors: Martino, J., De Witt Hamer, P. C., Berger, M. S., Lawton, M. T., Arnold, C. M., de Lucas, E. M., & Duffau, H.
Affiliations: Marqués de Valdecilla University Hospital (ES)
University of California, San Francisco (US)
Inserm (FR)
Corresponding author: Martino, Juan
ORCID: Martino, Juan
Berger, Mitchel S.
Lawton, Michael T.
Arnold, Christine M.
Duffau, Hugues
Venue: Brain Structure and Function
Publisher: Springer Science and Business Media LLC
Published: 2012-03-16
Volume: 218
Issue: 1
Pages: 105-121
ISSN: 1863-2653 (ISSN-L)
1863-2661
DOI: 10.1007/s00429-012-0386-5
OpenAlex: W2038327846
Cited by: 280
References: 81
Citations by year: 2026: 9 · 2025: 10 · 2024: 13 · 2023: 15 · 2022: 22 · 2021: 35 · 2020: 19 · 2019: 28 · 2018: 19 · 2017: 17 · 2016: 22 · 2015: 26 · 2014: 23 · 2013: 20 · 2012: 2
FWCI: 17.14
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Brain Structure and Function (publishedVersion)
PubMed (publishedVersion)
Pure Amsterdam UMC (publishedVersion)
Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
Data Archiving and Networked Services (DANS) (submittedVersion)
Topics: Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
Health Sciences › Medicine › Anatomy › Classical Anatomy and Histology
Life Sciences › Neuroscience › Cognitive Neuroscience › Neurobiology of Language and Bilingualism
Keywords: superior longitudinal fasciculus, arcuate fasciculus, fiber dissection, diffusion tensor tractography, supramarginal gyrus, superior temporal gyrus, middle temporal gyrus, angular gyrus, precentral gyrus, inferior frontal gyrus, inferior temporal gyrus, white matter anatomy
MeSH terms: Adult, Aged, Cadaver, Cerebral Cortex, Dissection, Frontal Lobe, Humans, Middle Aged, Neural Pathways, Parietal Lobe, Temporal Lobe, Young Adult, Diffusion Tensor Imaging, Neuroanatomical Tract-Tracing Techniques

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Analysis of the subcomponents and cortical terminations of the perisylvian superior longitudinal fasciculus: a fiber dissection and DTI tractography study

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks