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Atlas of Human Brain Connections
Abstract
This atlas capitalises on novel diffusion MRI tractography methods to provide a comprehensive overview of connections derived from virtual in vivo tractography dissections of the human brain.
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In the citing paper
“This ground truth data set included association, projection, and commissural tracts that have been previously described using post-mortem anatomical and electrophysiological methods41.”
From Tractography-based connectomes are dominated by false-positive connections (2016) · cites this paper as [41]
In the citing paper
“A great many studies clearly distinguish the 2 bundles as distinct entities, both anatomically and functionally (56, 59, 70, 71, 75, 76).”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [70]
In the citing paper
“the anterior segment of the AF appears to somehow correspond to the SLF III, and the two terms are used interchangeably.”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [70]
In the citing paper
“some of their subcomponents appear to overlap as if they each share a subdivision: the SLF III and the anterior segment of the AF (Figure 4).”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [70]
In the citing paper
“this bundle can be divided into three segments (a long, anterior, and posterior segment), each connecting two regions of either Broca, Wernicke, or the territory of Geschwind (inferior parietal lobule).”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [70]
In the citing paper
“These parietal connections include the precuneus and may also include more dorsal parts of the superior parietal lobule (areas PE and PM) and the inferior parietal lobule (PG) (Catani and Thiebaut de Schotten, 2012; Schmahmann and Pandya, 2006).”
From The cingulum bundle: Anatomy, function, and dysfunction (2018) · cites this paper as Catani and Thiebaut de Schotten, 2012
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BackgroundCabrera, D. V., Stobbe, R., Smyth, P. S., et al. (2019) · Brain and Behavior · doi:10.1002/brb3.1514 · Cited by 20
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Kurki, T. J. I., Himanen, L., Vuorinen, E., Myllyniemi, A., Saarenketo, A.-R., Kauko, T., Brandstack, N., & Tenovuo, O. S. (2014) · Neuroradiology · doi:10.1007/s00234-014-1410-7 · Cited by 20
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“These regions are associated with visual function and include the lateral areas of V3A (hOc4d), according to the studies by Catani and Thiebaut de Schotten (2012) and Malikovic et al. (2016).”
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“Based on its distinct anatomical connections in the cortical areas, the SLF can be divided into three subcomponents (SLF I, II and III) (Catani and Mesulam 2008; Catani and Thiebaut de Schotten 2012).”
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Ricchi, M., Campani, G., Nagmutdinova, A., Bortolotti, V., Greco, D., Golini, C., Grist, J. T., Brizi, L., & Testa, C. M. (2025) · European Radiology Experimental · doi:10.1186/s41747-025-00570-5 · Cited by 10
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“…into projection pathways, which transmit sensory-motor information; association pathways, which integrate information from different brain regions within the same hemisphere; and commissural pathways, which facilitate information transfer between the two hemispheres (Catani & de Schotten, 2015).”
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Presson, N., Krishnaswamy, D., Wagener, L., Bird, W., Jarbo, K., Pathak, S., Puccio, A. M., Borrasso, A. J., Benso, S., Okonkwo, D. O., et al. (2015) · Military Medicine · doi:10.7205/milmed-d-14-00413 · Cited by 10
Bykanov, A., Pitskhelauri, D. I., Batalov, A. I., et al. (2017) · Burdenko s Journal of Neurosurgery · doi:10.17116/neiro201780726-38 · Cited by 10
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“…purposes, t-maps of functional activations during the reading task were further characterised by measuring the average level of activations in subcortical areas (Catani and Thiebaut de Schotten, 2012) as well as in areas derived from a multimodal atlas of the brain surface (Glasser et al., 2016).”
BackgroundMethodInfluentialSelf-citationWhite matter integrity as a mediator between socioeconomic status and executive function
Shaked, D., Katzel, L. I., Davatzikos, C. A., Gullapalli, R. P., Seliger, S. L., Erus, G., Evans, M. K., Zonderman, A. B., & Waldstein, S. R. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.1021857 · Cited by 9
“These tracts are considered multicomponent bundles with distinct functional and anatomical subdomains (Catani and Thiebaut de Schotten, 2012).”
BackgroundInfluentialBanihashemi, L., Schmithorst, V. J., Bertocci, M. A., Samolyk, A., Zhang, Y., Santos, J. P. L., Versace, A., Taylor, M., English, G. E., Northrup, J. B., et al. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.03.004 · Cited by 9
Development and Developmental Disorders of the Cerebral Cortex
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De-Torres, I., Dávila, G., Berthier, M. L., Froudist‐Walsh, S., Moreno‐Torres, I., & Ruiz‐Cruces, R. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00675 · Cited by 9
“ORIGINAL RESEARCH ARTICLE published: 18 October 2013 doi: 10.3389/fnhum.2013.00675 Repeating with the right hemisphere: reduced interactions between phonological and lexical-semantic systems in crossed aphasia?”
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BackgroundRôle du cortex préfrontal dans l’adaptation comportementale chez l’homme
Volle, E., & Lévy, R. (2014) · médecine/sciences · doi:10.1051/medsci/20143002016 · Cited by 13
“Cette distinction fonctionnelle correspondrait aux aires de projections des connexions anatomiques du CPFL avec les régions associatives postérieures, elles-mêmes dépendantes des domaines [17].”
BackgroundSingle-digit arithmetic processing—anatomical evidence from statistical voxel-based lesion analysis
Mihulowicz, U., Willmes, K., Karnath, H., & Klein, E. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00286 · Cited by 10
“…reported a diverging finding in a patient with severe Frontiers in Human Neuroscience www.frontiersin.org May 2014 | Volume 8 | Article 286 | 6 multiplication fact-retrieval deficits, although his brain lesion did not involve the left AG (see also Van Harskamp et al., 2005 for a similar case).”
BackgroundKaneko, F., Shibata, E., Okawada, M., & Nagamine, T. (2019) · Brain stimulation · doi:10.1016/j.brs.2019.10.016 · Cited by 9
López-Barroso, D., Paredes-Pacheco, J., Torres-Prioris, M. J., Dávila, G., & Berthier, M. (2023) · Brain Structure and Function · doi:10.1007/s00429-023-02655-6 · Cited by 7
“Finally, P4 showed hypometabolic activity in the SMA, SMG, IFG pTr, superior parietal cortex, and MTG. P2, P3, and P4 did not show hypometabolic activity in the right hemisphere.”
MethodInfluentialNozais, V., Theaud, G., Descoteaux, M., et al. (2023) · Brain Structure and Function · doi:10.1007/s00429-023-02714-y · Cited by 7
“1 below.”
BackgroundMethodInfluentialSelf-citationDirect Inside-Out Observation of Superficial White Matter Fasciculi in the Human Brain
Dannhoff, G., Morichon, A., Smirnov, M., Barantin, L., Destrieux, C., & Maldonado, I. L. (2024) · Brain Connectivity · doi:10.1089/brain.2023.0050 · Cited by 8
“This has led to the establishment of WM atlases for humans (Catani and Thiebaut de Schotten, 2012; Guevara et al., 2017) and the proposition of a complex, 3D model of SWM arrangement within the frontal lobe, termed the ‘‘poppy flower’’ arrangement (Catani et al., 2012).”
A prominent vertical occipital white matter fasciculus unique to primate brains
Takemura, H., Kaneko, T., Sherwood, C. C., et al. (2024) · Current Biology · doi:10.1016/j.cub.2024.06.034 · Cited by 8
Supratentorial White Matter Tracts
Ramos‐Fresnedo, A., Segura-Duran, I., Chaichana, K. L., & Pillai, J. J. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-811783-5.00002-1 · Cited by 9
Debarle, C., Perlbarg, V., Jacquens, A., et al. (2021) · Annals of Physical and Rehabilitation Medicine · doi:10.1016/j.rehab.2020.08.002 · Cited by 8
Anatomical bases of fast parietal grasp control in humans: A diffusion-MRI tractography study
Richard, N., Desmurget, M., Teillac, A., Beuriat, P.-A., Bardi, L., Coudé, G., Szathmári, A., Mottolèse, C., Sirigu, A., & Hiba, B. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118002 · Cited by 9
Corpus callosum in schizophrenia with deficit and non‐deficit syndrome: a statistical shape analysis
Türk, Y., Ercan, İ., Şahin, İ., Gürsel, B. E., Uzunoglu, A., Öge, C., Beyazyüz, E., & Albayrak, Y. (2021) · General Psychiatry · doi:10.1136/gpsych-2021-100635 · Cited by 8
“Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not- for-profit sectors.”
BackgroundAwake surgery versus VEP in tumors of visual pathway: Case report
Verst, S. M., de Melo, M. N., Caivano, A. B. S., et al. (2020) · Interdisciplinary Neurosurgery · doi:10.1016/j.inat.2020.100675 · Cited by 8
Connectivity defines the distinctive anatomy and function of the hand-knob area
Beyh, A., Howells, H., Giampiccolo, D., et al. (2024) · Brain Communications · doi:10.1093/braincomms/fcae261 · Cited by 7
“51”
Self-citationFunctional Systems and Brain Functional Units Beyond Luria, With Luria: Anatomical Aspects
Peña‐Casanova, J., & Sigg-Alonso, J. (2020) · Lurian Journal · doi:10.15826/lurian.2020.1.1.6 · Cited by 7
Kimura, I., Oishi, H., Hayashi, M. J., & Amano, K. (2021) · Cerebral Cortex Communications · doi:10.1093/texcom/tgab065 · Cited by 6
Overview of the Development of the Human Brain and Spinal Cord
ten Donkelaar, H. J., Takakuwa, T., Vasung, L., Yamada, S., Shiota, K., & van der Vliet, T. (2023) · Springer eBooks · doi:10.1007/978-3-031-26098-8_1 · Cited by 8
Contribution of Diffusion Tractography to the Anatomy of Language
Catani, M., & Budisavljević, S. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-396460-1.00022-6 · Cited by 8
Self-citationAnsado, J., Collins, D. L., Fonov, V., Garon, M., Alexandrov, L., Karama, S., Evans, A. C., Beauchamp, M. H., & Brain Development Cooperative Group (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12869 · Cited by 7
Heaps‐Woodruff, J. M., Joska, J. A., Cabeen, R. P., Baker, L. M., Salminen, L. E., Hoare, J., Laidlaw, D. H., Wamser‐Nanney, R. A., Peng, C.-Z., Engelbrecht, S., et al. (2017) · Brain Imaging and Behavior · doi:10.1007/s11682-017-9769-9 · Cited by 7
Farah, R., Dudley, J. A., Hutton, J., & Horowitz‐Kraus, T. (2020) · Brain and Cognition · doi:10.1016/j.bandc.2020.105532 · Cited by 7
Sociology and Neuroscience: An Emerging Dialogue
Tibbetts, P. E. (2015) · The American Sociologist · doi:10.1007/s12108-015-9268-7 · Cited by 7
Metadata
- Authors
- Catani, M., & Thiebaut de Schotten, M.
- ORCID
- Catani, Marco
- Venue
- Oxford University Press eBooks
- Publisher
- Oxford University Press
- Published
- 2012-03
- OpenAlex
- W574584042
- Cited by
- 467
- References
- 0
- Citations by year
- 2026: 10 · 2025: 33 · 2024: 33 · 2023: 32 · 2022: 32 · 2021: 35 · 2020: 41 · 2019: 37 · 2018: 34 · 2017: 38 · 2016: 41 · 2015: 35 · 2014: 34 · 2013: 20 · 2012: 5
- FWCI
- 21.99
- Type
- book
- Language
- en
- Open access
- closed
- Locations
- Oxford University Press eBooks (publishedVersion)
- Research Portal (King's College London) (submittedVersion)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Anatomy › Classical Anatomy and Histology
- Keywords
- human brain connectivity, diffusion MRI tractography, white matter tracts, brain dissection, virtual dissection, human brain atlas, neuroanatomy
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