Cited by 467Advanced Neuroimaging Techniques and ApplicationsFunctional Brain Connectivity StudiesClassical Anatomy and Histology

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Atlas of Human Brain Connections

Catani, Marco, Thiebaut de Schotten, Michel·2012·Oxford University Press eBooks

DOI 10.1093/med/9780199541164.001.0001

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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.

Integrity signals

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Crossref · 10.1093/med/9780199541164.001.0001

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Items 301–400 of 467

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A prospective study of MRI biomarkers in the brain and lower limb muscles for prediction of lower limb motor recovery following stroke
Elameer, M., Lumley, H., Moore, S. A., Marshall, K., Alton, A., Smith, F. E., Gani, A., Blamire, A. M., Rodgers, H., Price, C., et al. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1229681 · Cited by 7
Impact of non-invasive brain stimulation on transcallosal modulation in mild traumatic brain injury: a multimodal pilot investigation
Ansado, J., Blunt, A., Chen, J., Koski, L. M., & Ptito, A. (2019) · Brain Injury · doi:10.1080/02699052.2019.1605620 · Cited by 6
“Parasagittal ROIs were drawn in the left and right hemispheres to better map the real anatomical boundaries of the CC (38,39) in keeping with the new diffusion MRI tractography atlas (40).”
Method
Brain Structural Abnormalities of Major Depressive Disorder
Wu, H., Melicher, T., Bauer, I. E., Sanches, M., & Soares, J. C. (2019) · Elsevier eBooks · doi:10.1016/b978-0-323-58131-8.00003-3 · Cited by 6
Can reduced leftward asymmetry of white matter integrity be a marker of transition to psychosis in at-risk mental state?
Saito, J., Nemoto, T., Katagiri, N., Hori, M., Tagata, H., Funatogawa, T., Yamaguchi, T., Tsujino, N., & Mizuno, M. (2020) · Asian Journal of Psychiatry · doi:10.1016/j.ajp.2020.102450 · Cited by 6
Bayesian stroke modeling details sex biases in the white matter substrates of aphasia
Kernbach, J. M., Hartwigsen, G., Lim, J., Bae, H., Yu, K., Schlaug, G., Bonkhoff, A. K., Rost, N. S., & Bzdok, D. (2023) · Communications Biology · doi:10.1038/s42003-023-04733-1 · Cited by 7
Thalamic Nuclei Segmentation Using Tractography, Population-Specific Priors and Local Fibre Orientation
Semedo, C., Cardoso, M. J., Vos, S. B., Sudre, C. H., Bocchetta, M., Ribbens, A., Smeets, D., Rohrer, J. D., & Sebastien Ourselin, A. (2018) · Lecture notes in computer science · doi:10.1007/978-3-030-00931-1_44 · Cited by 5
“The resulting segmentations were in agreement with previous known anatomy, with anterior thalamic regions preferentially connected to prefrontal, motor and sensory cortices, whereas posterior clusters had mainly WM projections towards parietal, occipital and temporal regions [14].”
Result
Age-related differences in white matter: Comparing fixel based and tensor based analysesPreprint
Kelley, S., Plass, J., Bender, A. R., & Polk, T. (2019) · bioRxiv · doi:10.1101/751628 · Cited by 7
Decoding Brain Interstitial Transport In Vivo: A Fully Validated Bottom-Up Mechanistic Prediction FrameworkPreprint
Tian, Y., Pecco, N., Zhan, W., Galvan, S., Secoli, R., Riva, M., Bello, L., Falini, A., y Baena, F. R., Castellano, A., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.22.643151 · Cited by 6
“This dual role makes FO a crucial component in the brain’s connectivity and function [66, 67].”
Relation Between Reading Performance and White-Matter Alteration and Reorganization in Neurosurgical Patients
Cargnelutti, E., Maieron, M., Ius, T., Škrap, M., & Tomasino, B. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.563259 · Cited by 5
“In case of disagreement, fibers were tracked again based on the anatomical atlas (31, 32) and starting from accurate detection by the same neuroradiologists of the above-mentioned reference points; finally, a further comparison was performed to check fascicle matching with the atlas.”
Method
Alcohol-induced deficits in reactive control of response selection and inhibition are counteracted by a seemingly paradox increase in proactive control
Stock, A., Wendiggensen, P., Ghin, F., & Beste, C. (2023) · Scientific Reports · doi:10.1038/s41598-023-28012-5 · Cited by 5
Effects of Damage to the Integrity of the Left Dual-Stream Frontotemporal Network Mediated by the Arcuate Fasciculus and Uncinate Fasciculus on Acute/Subacute Post-Stroke Aphasia
Yu, Q., Jiang, Y., Sun, Y., Ju, X., Ye, T., Liu, N., Qian, S., & Liu, K. (2023) · Brain Sciences · doi:10.3390/brainsci13091324 · Cited by 5
“To date, the MdLF is one of the least studied and poorly understood association tracts connecting the temporal and parietal regions [2,12,13].”
Background
Revealing the confusion of the evolution of the term sagittal stratum. Historical overview and systematic literature review
Gülsuna, B., Güngör, A., Börcek, A. Ö., et al. (2023) · Cortex · doi:10.1016/j.cortex.2023.10.010 · Cited by 5
The correlation between brain structure characteristics and emotion regulation ability in children at high risk of autism spectrum disorder
Ding, N., Fu, L., Qian, L., Sun, B., Li, C., Gao, H., Lei, T., & Ke, X. (2024) · European Child & Adolescent Psychiatry · doi:10.1007/s00787-024-02369-y · Cited by 6
Structural and functional connectivity associations with anterior cingulate sulcal variability
Harper, L., Strandberg, O. T., Spotorno, N., Nilsson, M., Lindberg, O. E., Hansson, O., & Santillo, A. F. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02812-5 · Cited by 7
“…the PCS was highly connected to regions of the cin-gulum, insula, frontal, temporal, and parietal cortex as well as the thalamus, caudate, pallidum, putamen, hippocampus, and amygdala, key components of the DMN and SN, in accordance with standard literature (Catani and Thiebaut de Schotten 2012).”
Result
Dissecting white matter pathways: A neuroanatomical approach
Forkel, S. J., Bortolami, C., Dulyan, L., Barrett, R. L. C., & Beyh, A. (2025) · Elsevier eBooks · doi:10.1016/b978-0-12-818894-1.00012-4 · Cited by 6
White matter fiber tracking directed by interpolating splines and a methodological framework for evaluation
Losnegård, A., Lundervold, A., & Hodneland, E. (2013) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2013.00013 · Cited by 4
Mechanism of Corpus Callosum Infarction Associated with Acute Hydrocephalus: Clinical, Surgical, and Radiological Evaluations for Pathophysiology
Hirono, S., Kawauchi, D., Kobayashi, M., et al. (2019) · World Neurosurgery · doi:10.1016/j.wneu.2019.03.288 · Cited by 5
Altered functional connectivity between primary and secondary somatosensory areas in panic disorder
Cheng, C., Liu, C.-Y., & Hsu, S. (2020) · Psychiatry Research · doi:10.1016/j.psychres.2020.112808 · Cited by 5
Cerebral White Matter Mediation of Age-Related Differences in Picture Naming Across Adulthood
Troutman, S. B. W., Madden, D. J., & Diaz, M. T. (2022) · Neurobiology of Language · doi:10.1162/nol_a_00065 · Cited by 5
Visual alertness and brain diffusion tensor imaging at term age predict neurocognitive development at preschool age in extremely preterm‐born children
Aho, L., Sairanen, V., Lönnberg, P., Wolford, E., Lano, A., & Metsäranta, M. (2023) · Brain and Behavior · doi:10.1002/brb3.3048 · Cited by 5
“Both IFOF and SLF white matter tracts have cortical terminations in the parietal lobe (Catani et al., 2013).”
Polyaesthetic sights and sounds: media aesthetics in The Fantastic Flying Books of Mr. Morris Lessmore, Upgrade Soul and The Vampyre of Time and Memory
Engberg, M. (2014) · SoundEffects - An Interdisciplinary Journal of Sound and Sound Experience · doi:10.7146/se.v4i1.20370 · Cited by 5
An Introduction to Human Brain Anatomy
Forstmann, B. U., Keuken, M. C., & Alkemade, A. (2015) · Springer eBooks · doi:10.1007/978-1-4939-2236-9_4 · Cited by 6
Functional Organization of the Brain and Psychic Activity: A View Beyond Luria (With Luria)
Peña‐Casanova, J. (2018) · KnE Life Sciences · doi:10.18502/kls.v4i8.3329 · Cited by 5
“The model should include the role of connection pathways of the brain (hodology) [5]: intrahemispheric and interhemispheric pathways (see [6]).”
Background
Structural Neuroimaging
Forkel, S. J., & Catani, M. (2017) · Wiley eBooks · doi:10.1002/9781394259762.ch15 · Cited by 9
Self-citation
Short-range human cortico-cortical white matter fibers have thinner axons and are less myelinated compared to long-range fibers despite a similar g-ratio
Ruthig, P., Planitz, D. E. V. D., Morozova, M., Reimann, K., Jäger, C., Reinert, T., Mohammadi, S., Weiskopf, N., Kirilina, E. P., & Morawski, M. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3002906 · Cited by 5
“These connections are crucial for various functions, including sensory-motor integration [1,2], language perception [3], and inter-hemispheric information transfer [4].”
A speech fluency brain network derived from gliomas
Sun, C., Zhang, J., Bu, L., Lu, J., Yao, Y., & Wu, J. (2024) · Brain Communications · doi:10.1093/braincomms/fcae153 · Cited by 5
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The fiber-density-coreset for redundancy reduction in huge fiber-sets
Alexandroni, G., Moreno, G. Z., Sochen, N., & Greenspan, H. K. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.11.027 · Cited by 4
MRI volumetry and diffusion tensor imaging for diagnosis and follow-up of late post-traumatic injuries
Jacquens, A., Delmotte, P.-R., Gourbeix, C., Farny, N., Liaudet, B. P., Hijazi, D., Batisti, V., Torkomian, G., Cassereau, D., Debarle, C., et al. (2023) · Annals of Physical and Rehabilitation Medicine · doi:10.1016/j.rehab.2023.101783 · Cited by 4
The Cerebral Cortex and Complex Cerebral Functions
ten Donkelaar, H. J., Catani, M., van Domburg, P., Eling, P., Küsters, B., & Hori, A. (2020) · Springer eBooks · doi:10.1007/978-3-030-41878-6_15 · Cited by 4
Self-citation
Functional Approaches to the Surgery of Brain Gliomas
Giampiccolo, D., Nunes, S., Cattaneo, L., & Sala, F. (2022) · Advances and technical standards in neurosurgery · doi:10.1007/978-3-030-99166-1_2 · Cited by 4
Behavioral inhibition corresponds to white matter fiber bundle integrity in older adults
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Notes on Techniques
ten Donkelaar, H. J. (2011) · Springer eBooks · doi:10.1007/978-3-642-19134-3_3 · Cited by 4
Localization of Brain Function
Weis, S., Sonnberger, M., Dunzinger, A., Voglmayr, E., Aichholzer, M., Kleiser, R., & Strasser, P. (2019) · Springer eBooks · doi:10.1007/978-3-7091-1544-2_14 · Cited by 4
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Self-citation
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An MRI Deep Brain Adult Template With An Advanced Atlas-Based Tool For Diffusion Tensor Imaging Analysis
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“Fiber tracing was labelled 10,56,61,64 , otherwise described and affixed with FT (e.g. thalamo-striatal FT).”
Method
Preoperative interhemispheric coherence as a potential predictive marker for seizure outcome after total corpus callosotomy in nonlesional generalized epilepsy: a scalp EEG study
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“Insights into the neurobiological abnormalities associated with STBs are important as they encourage greater efforts to examine treatments to normalise these morphological alterations and reduce suicide deaths.”
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“18 At the same time, functional neuroimaging methods, such as resting-state 19,20 and task-based 21,22 functional connectivity, reveal how brain areas interact within these networks.”
Full interhemispheric integration sustained by a fraction of posterior callosal fibers
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“Finally, full splits appeared to show conserved bilateral FC across limbic regions like the orbitofrontal cortex and temporal poles, which are known to be structurally coupled through the preserved anterior commissure as well as the CC 22,23,24 .”
Genetics of brain networks and connectivity
Dennis, E. L., Thompson, P. M., & Jahanshad, N. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813838-0.00008-x · Cited by 3
Volumetric asymmetry of the major association white fibers in healthy young adults
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“For example, the Atlas of Human Brain Connections by Catani and Thiebaut de Schotten (2012) and other similar publications that summarize neuroimaging connectomics to clinical disorders (see Cohen et al., 2021; Perovnik et al., 2022; Schirmer et al., 2021) provide the kind of background needed.”
A rare case of ispilateral hemiparesis in a patient with uncrossed pyramidal tract shown by tractography
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Wang, L., Wang, J., Liu, B.-H., Tuo, D., Lui, S. S. Y., Wan, W., Huang, J., & Chan, R. C. K. (2024) · Behavioural Brain Research · doi:10.1016/j.bbr.2024.114979 · Cited by 2
The brain and its pathways
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Self-citation
Neurobiologically informed graph theory analysis of the language system
Morishima, Y., van den Heuvel, M. P., Strik, W. K., & Dierks, T. (2025) · Network Neuroscience · doi:10.1162/netn_a_00443 · Cited by 3
“We exploit existing neurobiological knowledge of domain-specific brain network systems (Catani & De Schotten, 2012; K. L. Campbell & Tyler, 2018; Kim et al., 2012; Mahon, 2022; Morey et al., 2019; Yeo et al., 2011) and apply graph network analysis to how the domain-specific brain network systems…”
RETRACTED: Unraveling the link between brain injury and enhanced artistic skills
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Retracted
Pathophysiological Divergence Between Vascular and Post-Stroke Dementia: Bridging Human and Experimental Perspectives
Ahn, J. H., Shin, M. C., Kim, D. W., Yoo, K., & Won, M. (2025) · Journal of Integrative Neuroscience · doi:10.31083/jin45565 · Cited by 2
“These structures support interhemispheric communication, thalamocortical relay, and memory consolidation, respectively [30–32].”
Features of white matter development in very preterm children from infancy to late childhood
Gilchrist, C. P., & Thompson, D. K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-817986-4.00029-8 · Cited by 2
Funktionelle Neuroanatomie
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Development and Developmental Disorders of the Cerebral Cortex
ten Donkelaar, H. J., Vasung, L., Molnár, Z., Aronica, E., Lammens, M. M. Y., van Bokhoven, H., Ulzen, K. K.-V., & Hori, A. (2023) · Springer eBooks · doi:10.1007/978-3-031-26098-8_10 · Cited by 3
Associative white matter tracts selectively predict sensorimotor learning
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“…tractsthatallowforatleasttwodifferentcommunicationpathways, includingalongsegment(connectingtemporalandfrontalcortices),an anteriorindirectsegment(connectingparietalandfrontalcortices),anda posteriorsegment(connectingparietalandtemporalcortices) 40,41 .”
Background
Associations among white matter microstructural changes and the development of emotional reactivity and regulation in infancy
Zhang, Y., Banihashemi, L., Versace, A., Samolyk, A., Abdelkader, M., Taylor, M., English, G. E., Schmithorst, V. J., Lee, V., Stiffler, R. S., et al. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03025-w · Cited by 2
“In infancy, the microstructural development of white matter (WM) tracts integrating several emotion-related neural networks is critical for the development of emotional reactivity and regulation during this period [33 – 36].”
The third branch of the superior longitudinal system
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Diffusion parameters of the core of cingulum are associated with age-related ventricular enlargement: a diffusion tensor tractography study
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Overview of the Human Brain and Spinal Cord
ten Donkelaar, H. J. (2011) · Springer eBooks · doi:10.1007/978-3-642-19134-3_1 · Cited by 2
Pseudoneglect in visual search: Behavioral evidence and connectional constraints in simulated neural circuitryPreprint
Gigliotta, O., Malkinson, T. S., Miglino, O., & Bartolomeo, P. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/129171 · Cited by 2
Interhemispheric Connectivity of the Human Temporal LobesPreprint
Binder, J. R., Giraldo‐Chica, M., Mathis, J. R., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.01.601568 · Cited by 2
“Lateral to the anterior commissure, fiber tracts traverse the Gratiolet canal in a posterolaterally oriented arc at the ventral aspect of the putamen/globus pallidus border and enter the temporal stem, as previously described (Baudo, Colombo et al. 2022; Catani and Thiebaut de Schotten 2012).”
BackgroundMethod
Human brain connections
Voogd, J. (2014) · Brain · doi:10.1093/brain/awu047 · Cited by 1
Impact of follow ups, time interval and study duration in diffusion & myelin MRI clinical study in MS
Edde, M., Houde, F., Theaud, G., Dumont, M., Gilbert, G., Houde, J., Maltais, L., Théberge, A., Doumbia, M., Beaudoin, A., et al. (2023) · NeuroImage Clinical · doi:10.1016/j.nicl.2023.103529 · Cited by 2
The connected hemispheres—the role of the corpus callosum for hemispheric asymmetries
Ocklenburg, S., & Güntürkün, O. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-99737-9.00007-0 · Cited by 1
Age-related white matter alterations in children with neurofibromatosis type 1: a diffusion MRI tractography study
Bruckert, L., Travis, K. E., Tam, L. T., Yeom, K. W., & Campen, C. J. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1542957 · Cited by 1
Functional cortical mapping and structural subcortical anatomy predicts intra-operative speech arrest: a nTMS-tractography study
Jung, J., Rajwani, K., Mirallave-Pescador, A., et al. (2025) · Clinical Neurophysiology · doi:10.1016/j.clinph.2025.2110995 · Cited by 1
Surgical treatment of glial tumors of the frontal lobe. Current state of the problem. Part I: motor functional system
Bykanov, A., Bezbabicheva, T. S., & Pitskhelauri, D. I. (2025) · Burdenko s Journal of Neurosurgery · doi:10.17116/neiro202589051115 · Cited by 1
The enigma of reflex eating epilepsy: A cohort study of 50 patients with insights from multimodal evaluation
Asranna, A., Chatterjee, A., Duble, S. N., Mundlamuri, R. C., Kenchaiah, R., Mariyappa, N., Bhargava, G. K., Viswanathan, L. G., Sangeeth, T. A., James, N., et al. (2025) · Epileptic Disorders · doi:10.1002/epd2.70132 · Cited by 1
The role of crossmodal interaction in psychological and brain organization of mathematical abilities
Khokhlov, N. A., & Kovyazina, M. S. (2016) · National Psychological Journal · doi:10.11621/npj.2016.0408 · Cited by 1
Anatomy of the Sagittal Stratum Revisited
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Functional Systems
Weis, S., Sonnberger, M., Dunzinger, A., Voglmayr, E., Aichholzer, M., Kleiser, R., & Strasser, P. (2019) · Springer eBooks · doi:10.1007/978-3-7091-1544-2_12 · Cited by 1
Language and Cognitive Tests: A Target-Guided Protocol
Verst, S. M., Alves, T. V., & de Oliveira, L. D. (2022) · Springer eBooks · doi:10.1007/978-3-030-95730-8_18 · Cited by 2
Quantitative and Qualitative Aspects of Factors and Forms of Aphasia: Clinical Data
Peña‐Casanova, J., Hernandez, J., & Diéguez-Vide, F. (2022) · Lurian Journal · doi:10.15826/lurian.2021.2.4.3 · Cited by 1
“Moreover, the current hodological and parallel processing approach adds to the possibilities of interpretation of aphasia mechanisms (e. g., Catani & Thiebaut de Schotten, 2012).”
Possible Integrations Between Sociology, Social Psychology and Social Neuroscience
Auriemma, V. (2023) · Springer eBooks · doi:10.1007/978-3-031-38860-6_4 · Cited by 1
Neurobiologically Informed Phenomenology of the Schizophrenia Spectrum
Walther, S., & Strik, W. K. (2024) · Springer eBooks · doi:10.1007/978-3-031-38391-5_25 · Cited by 1
Functional MRI for stereoscopic vision analysis: an experimental design
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Foundations for an ontology of brain areas, circuits and functions
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Authors: Catani, M., & Thiebaut de Schotten, M.
ORCID: Catani, Marco
Venue: Oxford University Press eBooks
Publisher: Oxford University Press
Published: 2012-03
DOI: 10.1093/med/9780199541164.001.0001
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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