Cited by 1,832Neurobiology of Language and BilingualismAdvanced Neuroimaging Techniques and ApplicationsHemispheric Asymmetry in Neuroscience

The DOI matches its Crossref record; 58 of the 58 references it cites were found in a registry or an index.

Perisylvian language networks of the human brain

Open access

Catani, Marco, Jones, Derek K., ffytche, Dominic H.·2005·Annals of Neurology

DOI 10.1002/ana.20319

Open this paper in CoChat — free account Open PDF

Abstract

Early anatomically based models of language consisted of an arcuate tract connecting Broca's speech and Wernicke's comprehension centers; a lesion of the tract resulted in conduction aphasia. However, the heterogeneous clinical presentations of conduction aphasia suggest a greater complexity of perisylvian anatomical connections than allowed for in the classical anatomical model. This article re-explores perisylvian language connectivity using in vivo diffusion tensor magnetic resonance imaging tractography. Diffusion tensor magnetic resonance imaging data from 11 right-handed healthy male subjects were averaged, and the arcuate fasciculus of the left hemisphere reconstructed from this data using an interactive dissection technique. Beyond the classical arcuate pathway connecting Broca's and Wernicke's areas directly, we show a previously undescribed, indirect pathway passing through inferior parietal cortex. The indirect pathway runs parallel and lateral to the classical arcuate fasciculus and is composed of an anterior segment connecting Broca's territory with the inferior parietal lobe and a posterior segment connecting the inferior parietal lobe to Wernicke's territory. This model of two parallel pathways helps explain the diverse clinical presentations of conduction aphasia. The anatomical findings are also relevant to the evolution of language, provide a framework for Lichtheim's symptom-based neurological model of aphasia, and constrain, anatomically, contemporary connectionist accounts of language.

Integrity signals

Registry

Crossref · 10.1002/ana.20319

Cites

58 of 58 references verified0 citation errors · 0 not checkable

Statistics

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

Claims the paper makes

We couldn’t retrieve this paper’s full text, 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?

MR diffusion tensor spectroscopy and imaging
Basser, P. J., Mattiello, J., & LeBihan, D. (1994) · Biophysical Journal · doi:10.1016/s0006-3495(94)80775-1 · Cited by 5,970
Microstructural and physiological features of tissues elucidated by quantitative-diffusion-tensor MRI
Basser, P. J., & Pierpaoli, C. (1996) · Journal of Magnetic Resonance, Series B · doi:10.1006/jmrb.1996.0086 · Cited by 4,306
Three-dimensional tracking of axonal projections in the brain by magnetic resonance imaging
Mori, S., Crain, B. J., Chacko, V. P., & van Zijl, P. C. M. (1999) · Annals of Neurology · doi:10.1002/1531-8249(199902)45:2 · Cited by 3,513
DISCONNEXION SYNDROMES IN ANIMALS AND MAN
Geschwind, N. (1965) · Brain · doi:10.1093/brain/88.2.237 · Cited by 3,419
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
Non-invasive mapping of connections between human thalamus and cortex using diffusion imaging
Behrens, T. E. J., Johansen-Berg, H., Woolrich, M. W., Smith, S. M., Wheeler-Kingshott, C. A. M., Boulby, P. A., Barker, G. J., Sillery, E. L., Sheehan, K., Ciccarelli, O., et al. (2003) · Nature Neuroscience · doi:10.1038/nn1075 · Cited by 2,330
Speech and Brain‐Mechanisms
(1960) · Medical Journal of Australia · doi:10.5694/j.1326-5377.1960.tb76238.x · Cited by 2,178
Tracking neuronal fiber pathways in the living human brain
Conturo, T. E., Lori, N. F., Cull, T. S., Akbudak, E., Snyder, A. Z., Shimony, J. S., McKinstry, R. C., Burton, H., & Raichle, M. E. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.18.10422 · Cited by 1,774
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
Sex differences in the functional organization of the brain for language
Shaywitz, B. A., Shaywltz, S. E., Pugh, K. R., Constable, R. T., Skudlarski, P., Fulbright, R. K., Bronen, R. A., Fletcher, J. M., Shankweiler, D., Katz, L., et al. (1995) · Nature · doi:10.1038/373607a0 · Cited by 1,372

Flagged first, then by citations

Show all 57 references

Research works printed but not linked: 2

Broca P, 1861, Perte de la parole, ramollissement chronique et destruction partielle du lobe antérieur gauche, Bull Soc Anthropol, 2, 235
Wernicke C, 1874, Der aphasische Symptomencomplex

Sorted by citations

Items 801–900 of 1,003

Neural substrate differences in language networks and associated language-related behavioral impairments in children with TBI: A preliminary fMRI investigation
Karunanayaka, P., Holland, S. K., Yuan, W., Altaye, M., Jones, B. V., Michaud, L. J., Walz, N. C., & Wade, S. L. (2007) · Neurorehabilitation · doi:10.3233/nre-2007-22503 · Cited by 33
Meta-analytic connectivity modeling of the left and right inferior frontal gyri
Bulut, T. (2022) · Cortex · doi:10.1016/j.cortex.2022.07.003 · Cited by 31
Distinct neural signatures of cognitive subtypes of dyslexia with and without phonological deficits
van Ermingen‐Marbach, M., Grande, M., Pape‐Neumann, J., Saß, K., & Heim, S. (2013) · NeuroImage Clinical · doi:10.1016/j.nicl.2013.03.010 · Cited by 32
Rapid and Minimum Invasive Functional Brain Mapping by Real-Time Visualization of High Gamma Activity During Awake Craniotomy
Ogawa, H., Kamada, K., Kapeller, C., Hiroshima, S., Prueckl, R., & Guger, C. (2014) · World Neurosurgery · doi:10.1016/j.wneu.2014.08.009 · Cited by 32
Similarities and differences in neuroplasticity mechanisms between brain gliomas and nonlesional epilepsy
Bourdillon, P., Apra, C., Guénot, M., & Duffau, H. (2017) · Epilepsia · doi:10.1111/epi.13935 · Cited by 32
Left frontotemporal effective connectivity during semantic feature judgments in patients with chronic aphasia and age-matched healthy controls
Meier, E. L., Johnson, J. P., & Kiran, S. (2018) · Cortex · doi:10.1016/j.cortex.2018.08.006 · Cited by 33
Perisylvian epileptic network revisited
Halász, P., Kelemen, A., Rosdy, B., Rásonyi, G., Clemens, B., & Szűcs, A. (2018) · Seizure · doi:10.1016/j.seizure.2018.12.003 · 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
A Review on Treatment-Related Brain Changes in Aphasia
Schevenels, K., Price, C. J., Zink, I., Smedt, B. D., & Vandermosten, M. (2020) · Neurobiology of Language · doi:10.1162/nol_a_00019 · Cited by 32
RAN training in dyslexia: Behavioral and brain correlates
Stappen, C. V., Dricot, L., & Reybroeck, M. V. (2020) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2020.107566 · Cited by 38
The Evolution of Language Systems in the Human Brain
Deacon, T. W. (2007) · Elsevier eBooks · doi:10.1016/b0-12-370878-8/00020-3 · Cited by 32
Increased left hemisphere impairment in high-functioning autism: A tract based spatial statistics study
Perkins, T. J., Stokes, M. A., McGillivray, J., Mussap, A. J., Cox, I. A., Maller, J. J., & Bittar, R. G. (2014) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2014.08.003 · Cited by 33
Generalization of the effects of phonological training for anomia using structural equation modelling: A multiple single-case study
Vitali, P., Tettamanti, M., Abutalebi, J., Ansaldo, A. I., Perani, D., Cappa, S. F., & Joanette, Y. (2009) · Neurocase · doi:10.1080/13554790903329117 · Cited by 32
Presurgical Mapping of Verbal Language in Brain Tumors with Functional MR Imaging and MR Tractography
Bizzi, A. (2009) · Neuroimaging Clinics of North America · doi:10.1016/j.nic.2009.08.010 · Cited by 32
The Neuroanatomical Pathway Model of Language
Friederici, A. D. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-407794-2.00029-8 · Cited by 35
Microsurgical Anatomy of the White Matter Tracts in Hemispherotomy
Küçükyürük, B., Yağmurlu, K., Tanrıöver, N., Uzan, M., & Rhoton, A. L. (2014) · Operative Neurosurgery · doi:10.1227/neu.0000000000000288 · Cited by 31
Beyond the word and image: II- Structural and functional connectivity of a common semantic system
Jouen, A.-L., Ellmore, T. M., Madden-Lombardi, C., Pallier, C., Dominey, P. F., & Ventre‐Dominey, J. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.10.039 · Cited by 30
Microsurgical Anatomy of the Vertical Rami of the Superior Longitudinal Fasciculus: An Intraparietal Sulcus Dissection Study
Monroy-Sosa, A., Jennings, J. E., Chakravarthi, S. S., Fukui, M. B., Celix, J. M., Kojis, N., Lindsay, M., Walia, S., Rovin, R., & Kassam, A. B. (2018) · Operative Neurosurgery · doi:10.1093/ons/opy077 · Cited by 32
Right Structural and Functional Reorganization in Four-Year-Old Children with Perinatal Arterial Ischemic Stroke Predict Language Production
Clément, F., Ripollés, P., Ferreri, L., Muchart, J., Sierpowska, J., Fons, C., Solé, J., Rebollo, M., Zatorre, R. J., Garcı́a-Alix, A., et al. (2019) · eNeuro · doi:10.1523/eneuro.0447-18.2019 · Cited by 29
A network underlying human higher-order motor control: Insights from machine learning-based lesion-behaviour mapping in apraxia of pantomime
Sperber, C., Wiesen, D., Goldenberg, G., & Karnath, H. (2019) · Cortex · doi:10.1016/j.cortex.2019.08.023 · Cited by 32
Microstructural Injury to Left-Sided Perisylvian White Matter Predicts Language Decline After Brain Radiation Therapy
Tibbs, M. D., Huynh‐Le, M., Karunamuni, R. A., Reyes, A., Macari, A. C., Tringale, K. R., Salans, M. A., Yip, A. T., Liu, E. Y., Simon, A. B., et al. (2020) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2020.07.032 · Cited by 31
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
The genetic architecture of language functional connectivity
Mekki, Y., Guillemot, V., Lemaître, H., Carrión-Castillo, A., Forkel, S. J., Frouin, V., & Philippe, C. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118795 · Cited by 31
Functional MRI in children: clinical and research applications
Leach, J. L., & Holland, S. K. (2009) · Pediatric Radiology · doi:10.1007/s00247-009-1452-x · Cited by 32
The Contribution of Neuroimaging to the Study of Language and Aphasia
Lee, A. H., Kannan, V. C., & Hillis, A. E. (2006) · Neuropsychology Review · doi:10.1007/s11065-006-9014-6 · Cited by 31
Mapping a lateralization gradient within the ventral stream for auditory speech perception
Specht, K. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00629 · Cited by 37
Reliability of the corticospinal tract and arcuate fasciculus reconstructed with DTI-based tractography: implications for clinical practice
Kristo, G., Leemans, A., de Gelder, B., Raemaekers, M. A. H., Rutten, G.-J. M., & Ramsey, N. F. (2012) · European Radiology · doi:10.1007/s00330-012-2589-9 · Cited by 31
Neuroanatomical correlates of childhood apraxia of speech: A connectomic approach
Fiori, S., Guzzetta, A., Mitra, J., Pannek, K., Pasquariello, R., Cipriani, P., Tosetti, M., Cioni, G., Rose, S., & Chilosi, A. M. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.11.003 · Cited by 36
Task- and stimulus-related cortical networks in language production: Exploring similarity of MEG- and fMRI-derived functional connectivity
Liljeström, M., Stevenson, C. M., Kujala, J., & Salmelin, R. H. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.07.017 · Cited by 34
Development of effective connectivity for narrative comprehension in children
Schmithorst, V. J., Holland, S. K., & Plante, E. (2007) · Neuroreport · doi:10.1097/wnr.0b013e3282e9a4ef · Cited by 32
Functional relevance of interhemispheric fiber tracts in speech processing
Steinmann, S., & Mulert, C. (2011) · Journal of Neurolinguistics · doi:10.1016/j.jneuroling.2011.07.003 · Cited by 30
Intra– and inter–hemispheric network dynamics supporting object recognition and speech production
Kitazawa, Y., Sonoda, M., Sakakura, K., Mitsuhashi, T., Firestone, E., Ueda, R., Kambara, T., Iwaki, H., Luat, A. F., Marupudi, N. I., et al. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.119954 · Cited by 29
Localization of specific language pathways using diffusion‐weighted imaging tractography for presurgical planning of children with intractable epilepsy
Jeong, J., Asano, E., Juhász, C., & Chugani, H. T. (2014) · Epilepsia · doi:10.1111/epi.12863 · Cited by 30
Surgical Approaches to the Temporal Horn: An Anatomic Analysis of White Matter Tract Interruption
Kadri, P. A. S., de Oliveira, J. G., Krayenbühl, N., Türe, U., de Oliveira, E. P. L., Al‐Mefty, O., & Ribas, G. C. (2016) · Operative Neurosurgery · doi:10.1093/ons/opw011 · Cited by 30
Functional connectivity of language networks after perinatal stroke
Carlson, H. L., Sugden, C., Brooks, B. L., & Kirton, A. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.101861 · Cited by 30
What you learn & when you learn it: Impact of early bilingual & music experience on the structural characteristics of auditory-motor pathways
Vaquero, L., Rousseau, P.-N., Vozian, D., Klein, D., & Penhune, V. B. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116689 · Cited by 36
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
Intraoperative Brain Mapping by Cortico-Cortical Evoked Potential
Yamao, Y., Matsumoto, R., Kikuchi, T., Yoshida, K., Kunieda, T., & Miyamoto, S. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.635453 · Cited by 31
The Microstructural Plasticity of the Arcuate Fasciculus Undergirds Improved Speech in Noise Perception in Musicians
Li, X., Zatorre, R. J., & Du, Y. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab063 · Cited by 28
Modularity and granularity across the language network-A primary progressive aphasia perspective
Mesulam, M. M., Coventry, C., Rader, B. M., Kuang, A., Sridhar, J., Martersteck, A., Zhang, H., Thompson, C. K., Weıntraub, S., & Rogalski, E. J. (2021) · Cortex · doi:10.1016/j.cortex.2021.05.002 · Cited by 29
Bidirectional Connectivity Between Broca's Area and Wernicke's Area During Interactive Verbal Communication
Ono, Y., Zhang, X., Noah, J. A., Dravida, S., & Hirsch, J. (2021) · Brain Connectivity · doi:10.1089/brain.2020.0790 · Cited by 35
Increased microstructural white matter correlations in left, but not right, temporal lobe epilepsy
Pustina, D., Doucet, G. E., Sperling, M. R., Sharan, A. D., & Tracy, J. I. (2014) · Human Brain Mapping · doi:10.1002/hbm.22614 · Cited by 30
Callosal degeneration topographically correlated with cognitive function in amnestic mild cognitive impairment and alzheimer's disease dementia
Wang, P., Chou, K., Chang, N., Lin, K., Chen, W., Lan, G., Lin, C., & Lirng, J. (2013) · Human Brain Mapping · doi:10.1002/hbm.22271 · Cited by 30
Cortical plasticity induced by rapid Hebbian learning of novel tonal word-forms: Evidence from mismatch negativity
Yue, J., Bastiaanse, R., & Alter, K. (2014) · Brain and Language · doi:10.1016/j.bandl.2014.09.007 · Cited by 31
The neural basis of aphasia rehabilitation: Evidence from neuroimaging and neurostimulation
Cappa, S. F. (2011) · Neuropsychological Rehabilitation · doi:10.1080/09602011.2011.614724 · Cited by 30
Evidence from cognitive neuroscience for the role of graphical and algebraic representations in understanding function
Thomas, M. O. J., Wilson, A. J. C., Corballis, M. C., Lim, V. K., & Yoon, C. (2010) · ZDM · doi:10.1007/s11858-010-0272-7 · Cited by 33
Vulnerability of the ventral language network in children with focal epilepsy
Croft, L. J., Baldeweg, T., Sepeta, L. N., Zimmaro, L. A., Berl, M. M., & Gaillard, W. D. (2014) · Brain · doi:10.1093/brain/awu154 · Cited by 30
Pragmatic abilities in multiple sclerosis: The contribution of the temporo-parietal junction
Carotenuto, A., Cocozza, S., Quarantelli, M., Arcara, G., Lanzillo, R., Morra, V. B., Cerillo, I., Tedeschi, E., Orefice, G., Bambini, V., et al. (2018) · Brain and Language · doi:10.1016/j.bandl.2018.08.003 · Cited by 32
Language as shaped by social interaction
Enfield, N. J. (2008) · Behavioral and Brain Sciences · doi:10.1017/s0140525x08005104 · Cited by 28
Proficiency Predictors in Sequential Bilinguals
Austin, L., Hernández, A. E., & Schwieter, J. W. (2019) · Cambridge University Press eBooks · doi:10.1017/9781108641395 · Cited by 28
Mapping the cortical representation of speech sounds in a syllable repetition task
Markiewicz, C. J., & Bohland, J. W. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.07.023 · Cited by 35
Apparently competing motivations in morphosyntactic variation
Mondorf, B. (2014) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198709848.003.0013 · Cited by 29
A lesion and connectivity-based hierarchical model of chronic aphasia recovery dissociates patients and healthy controls
Meier, E. L., Johnson, J. P., Pan, Y., & Kiran, S. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.101919 · Cited by 29
Functional Connectivity of Language Regions of Stroke Patients with Expressive Aphasia During Real-Time Functional Magnetic Resonance Imaging Based Neurofeedback
Sreedharan, S., Arun, K., Sylaja, P., Kesavadas, C., & Sitaram, R. (2019) · Brain Connectivity · doi:10.1089/brain.2019.0674 · Cited by 31
Isolating the white matter circuitry of the dorsal language stream: Connectome‐Symptom Mapping in stroke induced aphasia
Baboyan, V. G., Basilakos, A., Yourganov, G., Rorden, C., Bonilha, L., Fridriksson, J., & Hickok, G. S. (2021) · Human Brain Mapping · doi:10.1002/hbm.25647 · Cited by 26
Effects of melodic intonation therapy in patients with chronic nonfluent aphasia
Marchina, S., Norton, A. C., & Gottfried Schlaug, A. (2022) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14927 · Cited by 29
Correlation between language function and the left arcuate fasciculus detected by diffusion tensor imaging tractography after brain tumor surgery
Hayashi, Y., Kinoshita, M., Nakada, M., & Hamada, J. (2012) · Journal of neurosurgery · doi:10.3171/2012.8.jns12348 · Cited by 29
Effect of Action Verbs on the Performance of a Complex Movement
Rabahi, T., Fargier, P., Sarraj, A. R., Clouzeau, C., & Massarelli, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068687 · Cited by 33
Whole-Brain Haemodynamic After-Effects of 1-Hz Magnetic Stimulation of the Posterior Superior Temporal Cortex During Action Observation
Arfeller, C., Schwarzbach, J. V., Ubaldi, S., Ferrari, P., Barchiesi, G., & Cattaneo, L. (2012) · Brain Topography · doi:10.1007/s10548-012-0239-9 · 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
Lateralization of Brain Networks and Clinical Severity in Toddlers with Autism Spectrum Disorder: A HARDI Diffusion MRI Study
Conti, E., Calderoni, S., Gaglianese, A., Pannek, K., Mazzotti, S., Rose, S., Scelfo, D., Tosetti, M., Muratori, F., Cioni, G., et al. (2015) · Autism Research · doi:10.1002/aur.1533 · Cited by 29
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
Deixis and the Interactional Foundations of Reference
Sidnell, J., & Enfield, N. J. (2016) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780199697960.013.27 · Cited by 30
Can language-action links explain language laterality?: An ERP study of perceptual and articulatory learning of novel pseudowords
Friedemann Pulvermüller, A., Kiff, J. D., & Юрьевич, Ш. Ю. (2011) · Cortex · doi:10.1016/j.cortex.2011.02.006 · Cited by 31
Current challenges in the practice of epilepsy surgery
Wrench, J. M., Matsumoto, R., Inoue, Y., & Wilson, S. J. (2011) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2011.02.011 · Cited by 28
Using in vivo probabilistic tractography to reveal two segregated dorsal ‘language-cognitive’ pathways in the human brain
Cloutman, L. L., Binney, R. J., Morris, D. M., Parker, G. J. M., & Ralph, M. A. L. (2013) · Brain and Language · doi:10.1016/j.bandl.2013.06.005 · Cited by 29
Mathematical Difficulties and White Matter Abnormalities in Subacute Pediatric Mild Traumatic Brain Injury
Beek, L. V., Ghesquière, P., Lagae, L. G., & Smedt, B. D. (2015) · Journal of Neurotrauma · doi:10.1089/neu.2014.3809 · Cited by 34
Altered topological properties of brain networks in the early MS patients revealed by cognitive task-related fMRI and graph theory
Ashtiani, S. N. M., Daliri, M. R., Behnam, H., Hossein‐Zadeh, G., Mehrpour, M., Motamed, M. R., & Fadaie, F. (2017) · Biomedical Signal Processing and Control · doi:10.1016/j.bspc.2017.10.006 · Cited by 28
Challenge to Unity: Relationship Between Hemispheric Asymmetry of the Default Mode Network and Mind Wandering
Kajimura, S., Kochiyama, T., Abe, N., & Nomura, M. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy086 · Cited by 32
The human connectome from an evolutionary perspective
Ardesch, D. J., Scholtens, L. H., & van den Heuvel, M. P. (2019) · Progress in brain research · doi:10.1016/bs.pbr.2019.05.004 · Cited by 33
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
Chapter 14 Aphasia
ALEXANDER, M. P., & Hillis, A. E. (2008) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)88014-6 · Cited by 31
Diffusion tensor imaging in the study of language and aphasia
Geva, S., Correia, M., & Warburton, E. A. (2011) · Aphasiology · doi:10.1080/02687038.2010.534803 · Cited by 28
White matter microstructure of 6-year old children born preterm and full term
Dodson, C. K., Travis, K. E., Ben‐Shachar, M., & Feldman, H. M. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.08.005 · Cited by 28
Diffusion tractography reveals pervasive asymmetry of cerebral white matter tracts in the bottlenose dolphin (Tursiops truncatus)
Wright, A. K., Theilmann, R. J., Ridgway, S. H., & Scadeng, M. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1525-9 · Cited by 27
Attenuated resting-state functional connectivity in patients with childhood- and adult-onset schizophrenia
Watsky, R. E., Gotts, S. J., Berman, R. A., McAdams, H. M., Zhou, X., Greenstein, D. K., Lalonde, F. M., Gochman, P., CLASEN, L. S., Shora, L., et al. (2018) · Schizophrenia Research · doi:10.1016/j.schres.2018.01.003 · Cited by 26
Hyperactivation of left inferior parietal lobule and left temporal gyri shortens resting EEG microstate in schizophrenia
Soni, S., Muthukrishnan, S. P., Sood, M., Kaur, S., & Sharma, R. (2018) · Schizophrenia Research · doi:10.1016/j.schres.2018.06.020 · Cited by 28
Arcuate fasciculus tractography integrated into Gamma Knife surgery
Maruyama, K., Koga, T., Kamada, K., Ota, T., Itoh, D., Ino, K., Igaki, H., Aoki, S., Masutani, Y., Shin, M., et al. (2008) · Journal of neurosurgery · doi:10.3171/2008.4.17521 · Cited by 28
Merging of Phonological and Gestural Circuits in Early Language Evolution
Aboitiz, F., & Garcia, R. A. (2009) · Reviews in the Neurosciences · doi:10.1515/revneuro.2009.20.1.71 · Cited by 29
From Tones in Tinnitus to Sensed Social Interaction in Schizophrenia: How Understanding Cortical Organization Can Inform the Study of Hallucinations and Psychosis
Ffytche, D. H., & Wible, C. G. (2014) · Schizophrenia Bulletin · doi:10.1093/schbul/sbu041 · Cited by 27
Context
Fetzer, A. (2015) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780199697960.013.15 · Cited by 28
Comprehension of reversible constructions in semantic aphasia
Dragoy, O., Bergelson, M. B., Вячеславовна, И. Е., Laurinavichyute, A., Mannova, E., Skvortsov, A. A., & Statnikov, A. I. (2015) · Aphasiology · doi:10.1080/02687038.2015.1063582 · Cited by 27
Topographical relationships between arcuate fasciculus connectivity and cortical thickness
Phillips, O. R., Clark, K. A., Woods, R. P., Subotnik, K. L., Asarnow, R. F., Nuechterlein, K. H., Toga, A. W., & Narr, K. L. (2010) · Human Brain Mapping · doi:10.1002/hbm.21147 · 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
White matter anatomy of the human deep brain revisited with high resolution DTI fibre tracking
Lemaire, J., Cosnard, G., Sakka, L. J., Nuti, C., Gradkowski, W., Mori, S., & Hermoye, L. (2011) · Neurochirurgie · doi:10.1016/j.neuchi.2011.04.001 · Cited by 27
Temporally and spatially distinct theta oscillations dissociate a language-specific from a domain-general processing mechanism across the age trajectory
Beese, C., Meyer, L., Vassileiou, B., & Friederici, A. D. (2017) · Scientific Reports · doi:10.1038/s41598-017-11632-z · Cited by 30
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
The connectional anatomy of visual mental imagery: evidence from a patient with left occipito-temporal damage
Hajhajate, D., Kaufmann, B. C., Liu, J., Siuda-Krzywicka, K., & Bartolomeo, P. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02505-x · Cited by 29
Architecture and connectivity of the human angular gyrus and of its homolog region in the macaque brain
Niu, M., & Palomero‐Gallagher, N. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02509-7 · Cited by 27
Deficits in naming pictures of objects are associated with glioma infiltration of the inferior longitudinal fasciculus: A study with diffusion MRI tractography, volumetric MRI , and neuropsychology
Papagno, C., Pascuzzo, R., Ferrante, C., Casarotti, A., Riva, M., Antelmi, L., Gennari, A. G., Mattavelli, G. C., & Bizzi, A. (2023) · Human Brain Mapping · doi:10.1002/hbm.26325 · Cited by 27
L2-Proficiency-Dependent Laterality Shift in Structural Connectivity of Brain Language Pathways
Xiang, H., van Leeuwen, T. M., Dediu, D., Roberts, L., Norris, D. G., & Peter Hagoort, A. (2015) · Brain Connectivity · doi:10.1089/brain.2013.0199 · Cited by 27
Microstructural anatomical differences between bilinguals and monolinguals
Singh, N. C., Rajan, A., Malagi, A., Ramanujan, K., Canini, M., Rosa, P. A. D., Raghunathan, P., Weekes, B., & Abutalebi, J. (2017) · Bilingualism Language and Cognition · doi:10.1017/s1366728917000438 · Cited by 30
Component deficits of visual neglect: “Magnetic” attraction of attention vs. impaired spatial working memory
Toba, M. N., Rabuffetti, M., Duret, C., Pradat-Diehl, P., Gainotti, G., & Bartolomeo, P. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.11.034 · Cited by 27
Vocabulary growth rate from preschool to school‐age years is reflected in the connectivity of the arcuate fasciculus in 14‐year‐old children
Su, M., de Schotten, M. T., Zhao, J., Song, S., Zhou, W., Gong, G., McBride, C. A., Ramus, F., & Shu, H. (2018) · Developmental Science · doi:10.1111/desc.12647 · Cited by 30
Developmental conduction aphasia after neonatal stroke
Northam, G. B., Adler, S., Eschmann, K. C. J., Chong, W. K., Cowan, F. M., & Baldeweg, T. (2018) · Annals of Neurology · doi:10.1002/ana.25218 · Cited by 27
A Comparison of Evoked and Non-evoked Functional Networks
Hebbink, J., van Blooijs, D., Huiskamp, G. J. M., Leijten, F. S. S., van Gils, S. A., & Meijer, H. G. E. (2018) · Brain Topography · doi:10.1007/s10548-018-0692-1 · Cited by 27
Fifty years of disconnexion syndromes and the Geschwind legacy
Mesulam, M. M. (2015) · Brain · doi:10.1093/brain/awv198 · Cited by 27
Orconstructions: Monosemy vs. polysemy
Ariel, M. (2014) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198709848.003.0020 · Cited by 27
The role of language-related functional brain regions and white matter tracts in network plasticity of post-stroke aphasia
Han, Y., Jing, Y., Shi, Y., Mo, H., Wan, Y., Zhou, H.-W., & Deng, F. (2024) · Journal of Neurology · doi:10.1007/s00415-024-12358-5 · Cited by 27
The Misnomer of Attention-Deficit Hyperactivity Disorder
Wasserman, T. H., & Wasserman, L. D. (2015) · Applied Neuropsychology Child · doi:10.1080/21622965.2015.1005487 · Cited by 27

Authors: Catani, M., Jones, D. K., & ffytche, D. H.
Affiliations: King's College London (GB)
National Institutes of Health (US)
Corresponding author: Catani, Marco
ORCID: Catani, Marco
Jones, Derek K.
ffytche, Dominic H.
Venue: Annals of Neurology
Publisher: Wiley
Published: 2004-12-13
Volume: 57
Issue: 1
Pages: 8-16
ISSN: 0364-5134 (ISSN-L)
1531-8249
DOI: 10.1002/ana.20319
OpenAlex: W2072923434
Cited by: 1,832
References: 57
Citations by year: 2026: 54 · 2025: 57 · 2024: 81 · 2023: 65 · 2022: 88 · 2021: 100 · 2020: 94 · 2019: 81 · 2018: 96 · 2017: 114 · 2016: 107 · 2015: 117 · 2014: 127 · 2013: 109 · 2012: 106
FWCI: 18.10
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations: Annals of Neurology (publishedVersion)
PubMed (publishedVersion)
Research Portal (King's College London) (submittedVersion)
Funders: Wellcome Trust
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Neurobiology of Language and Bilingualism
Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
Life Sciences › Neuroscience › Cognitive Neuroscience › Hemispheric Asymmetry in Neuroscience
Keywords: arcuate fasciculus, conduction aphasia, Broca's area, Wernicke's area, inferior parietal lobule, diffusion tractography, language evolution
MeSH terms: Adult, Brain, Brain Mapping, Frontal Lobe, Humans, Language, Male, Neural Pathways, Temporal Lobe, Neural Networks, Computer, Imaging, Three-Dimensional, Diffusion Magnetic Resonance Imaging

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

Perisylvian language networks of the human brain

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