The DOI matches its Crossref record; 53 of the 54 references it cites were found in a registry or an index.
The contribution of the insula to motor aspects of speech production: A review and a hypothesis
Abstract
Based on clinical and functional imaging data, the left anterior insula has been assumed to support prearticulatory functions of speech motor control such as the "programming" of vocal tract gestures. In order to further elucidate this model, a recent functional magnetic resonance imaging (fMRI) study of our group (Riecker, Ackermann, Wildgruber, Dogil, & Grodd, 200) investigated both overt (aloud) and covert (silent) production of highly overlearned word strings ("automatic speech"), based on the suggestion that "inner speech" might provide a "window" into preparatory motor activities (Jeannerod, 1994). As a control condition, subjects were asked to reproduce a nonlyrical tune. In contrast to hemodynamic responses within motor cortex and cerebellum, activation of the intrasylvian cortex turned out to be bound to overt task performance. Rather than prearticulatory processes, these findings suggest the left insula to contribute to the actual coordination of the up to 100 muscles engaged in articulation and phonation. Conceivably, the association of speech production with intrasylvian cortex might have evolved within the framework of phylogenetically older connections between the insula and limbic structures, on the one hand, and nonspeech functions of the upper midline musculature such as swallowing, on the other. Whereas (overt) speech tasks predominantly elicit activation within left anterior insula, reproduction of a nonlyrical tune yielded an opposite response pattern. Conceivably, the opposite distributional pattern of speaking and singing at the level of intrasylvian cortex reflects operation of the two hemispheres across different time domains ("double filtering by frequency theory": left hemisphere=segmental information, right hemisphere=intonation contours of verbal utterances and musical melodies; ). In line with this suggestion, a further study of our group (Ackermann et al., 2001) provided first evidence that differential hemispheric filtering might be bound to insular cortex.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“The notion that the AIC may govern the engagement of specialized brain networks to which it is connected finds support in evidence that activation of the AIC precedes, and directly influences, activation of prefrontal regions during response inhibition [44] and activation of the striatum during reward anticipation [27].”
From The role of the anterior insula in adolescent decision making (2014) · cites this paper as [27]
In the citing paper
“Specifically, the AIC has been shown to act in cooperation with several reward-processing areas (ACC, striatum and thalamus [27, 67–69]) and, importantly, its involvement with these regions appears to be dependent on age [69].”
From The role of the anterior insula in adolescent decision making (2014) · cites this paper as [27]
In the citing paper
“For example, Cho et al. [27] (2013) found that, already by adolescence, activation of the AIC is able to evoke subsequent activation within the striatum during anticipation of reward.”
From The role of the anterior insula in adolescent decision making (2014) · cites this paper as [27]
In the citing paper
“Task-dependent connectivity findings also point to developmental changes in the relationship between the AIC and the striatum, but suggest that this connection may have reached a state of maturity by midadolescence that is adequate to support adult-like functions [27, 67].”
From The role of the anterior insula in adolescent decision making (2014) · cites this paper as [27]
In the citing paper
“Not only is the relationship between the AIC and striatum established by adolescence, but the strength of connectivity (as indexed by co-activation) between the insula and the striatum during reward anticipation did not differ from that of adults.”
From The role of the anterior insula in adolescent decision making (2014) · cites this paper as [27]
In the citing paper
“These two studies, which both show age-dependent differences in AIC (and striatal) activation during reward processing, illustrate that even if connectivity between the AIC and the striatum reaches an adult-like state by adolescence [27, 67], reward opportunities may still evoke stronger recruitment of both regions during adolescence.”
From The role of the anterior insula in adolescent decision making (2014) · cites this paper as [27]
In the citing paper
“It is possible that both the structural and functional connectivity between the AIC and reward processing regions is adequately mature during adolescence [27] and that the AIC therefore exhibits adult-like engagement during anticipation of reward.”
From The role of the anterior insula in adolescent decision making (2014) · cites this paper as [27]
In the citing paper
“The association of the left insula with motor processing rather than articulatory planning was emphasized again following observations that left anterior insula activation was higher for overt than covert speech (Ackermann and Riecker, 2004; Shuster and Lemieux, 2005) and unaffected by the demands on motor planning (Shuster and Lemieux, 2005; Blank et al., 2002).”
From A review and synthesis of the first 20years of PET and fMRI studies of heard speech, spoken language and reading (2012) · cites this paper as Ackermann and Riecker, 2004
In the citing paper
“The association of the left insula with motor processing rather than articulatory planning was emphasized again following observations that left anterior insula activation was higher for overt than covert speech (Ackermann and Riecker, 2004; Shuster and Lemieux, 2005) and unaffected by the demands on motor planning (Shuster and Lemieux, 2005; Blank et al., 2002).”
From A review and synthesis of the first 20years of PET and fMRI studies of heard speech, spoken language and reading (2012) · cites this paper as Ackermann and Riecker, 2004
Citations
Cites
A theory of lexical access in speech production
Levelt, W. J. M., Roelofs, A., & Meyer, A. S. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99001776 · Cited by 5,295
Speaking: from intention to articulation
(1989) · Choice Reviews Online · doi:10.5860/choice.27-1947 · Cited by 5,017
Speaking. From Intention to Articulation
Caplan, D. N. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90151-y · Cited by 4,036
The representing brain: Neural correlates of motor intention and imagery
Jeannerod, M. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00034026 · Cited by 2,652
Positron emission tomographic studies of the cortical anatomy of single-word processing
Petersen, S. E., Fox, P. T., Posner, M. I., Mintun, M., & Raichle, M. E. (1988) · Nature · doi:10.1038/331585a0 · Cited by 2,593
Gazzaniga, M. S., & Bizzi, E. (2000) · Cited by 2,547
(1960) · Medical Journal of Australia · doi:10.5694/j.1326-5377.1960.tb76238.x · Cited by 2,178
Circuitry and functional aspects of the insular lobe in primates including humans
AUGUSTINE, J. (1996) · Brain Research Reviews · doi:10.1016/s0165-0173(96)00011-2 · Cited by 1,776
Lateralization of Phonetic and Pitch Discrimination in Speech Processing
Zatorre, R. J., Evans, A. C., Meyer, E., & GJEDDE, A. H. (1992) · Science · doi:10.1126/science.1589767 · Cited by 1,499
Positron Emission Tomographic Studies of the Processing of Singe Words
Petersen, S. E., Fox, P. T., Posner, M. I., Mintun, M. A., & Raichle, M. E. (1989) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1989.1.2.153 · Cited by 1,298
Cited by
Sorted by citations
How do you feel — now? The anterior insula and human awareness
(Bud) Craig, A. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2555 · Cited by 6,657
Price, C. J. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.04.062 · Cited by 2,159
Investigating emotion with music: An fMRI study
Koelsch, S., Fritz, T., v. Cramon, D. Y., Müller, K., & Friederici, A. D. (2006) · Human Brain Mapping · doi:10.1002/hbm.20180 · Cited by 1,037
Legrain, V., Iannetti, G. D., Plaghki, L., & Mouraux, A. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.10.005 · Cited by 854
The hidden island of addiction: the insula
Naqvi, N. H., & Bechara, A. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2008.09.009 · Cited by 833
Inner Speech: Development, Cognitive Functions, Phenomenology, and Neurobiology
Alderson-Day, B., & Fernyhough, C. (2015) · Psychological Bulletin · doi:10.1037/bul0000021 · Cited by 864
The Spatial and Temporal Signatures of Word Production Components: A Critical Update
Indefrey, P. (2011) · Frontiers in Psychology · doi:10.3389/fpsyg.2011.00255 · Cited by 767
“, 2001; and more recently Ackermann and Riecker, 2004, for the absence of Broca’s area activation in direct comparisons of overt and covert responses). The somewhat indirect conclusion that Broca’s area is the most likely candidate area for syllabification has more recently been challenged for different reasons. First…”
BackgroundInfluentialDuffau, H. (2005) · The Lancet Neurology · doi:10.1016/s1474-4422(05)70140-x · Cited by 702
Conjoint activity of anterior insular and anterior cingulate cortex: awareness and response
Medford, N., & Critchley, H. D. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0265-x · Cited by 627
Duffau, H. (2005) · Brain · doi:10.1093/brain/awh423 · Cited by 641
Craig, A. D. (. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0248-y · Cited by 600
The image of time: A voxel-wise meta-analysis
Wiener, M., Turkeltaub, P., & Coslett, H. B. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.09.064 · Cited by 594
An fMRI investigation of syllable sequence production
Bohland, J. W., & Guenther, F. H. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.04.173 · Cited by 561
Contrasting acute and slow-growing lesions: a new door to brain plasticity
Desmurget, M., Bonnetblanc, F., & Duffau, H. (2006) · Brain · doi:10.1093/brain/awl300 · Cited by 531
Emotional moments across time: a possible neural basis for time perception in the anterior insula
Craig, A. D. (. (2009) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2009.0008 · Cited by 499
Speech Production as State Feedback Control
Houde, J. F., & Nagarajan, S. S. (2011) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00082 · Cited by 463
Stuttered and fluent speech production: An ALE meta‐analysis of functional neuroimaging studies
Brown, S., Ingham, R. J., Ingham, J. C., Laird, A. R., & Fox, P. T. (2005) · Human Brain Mapping · doi:10.1002/hbm.20140 · Cited by 449
Alterations in brain structure and functional connectivity in prescription opioid-dependent patients
Upadhyay, J., Maleki, N., Potter, J. S., Elman, I., Rudrauf, D., Knudsen, J., Wallin, D. J., Pendse, G., McDonald, L., Griffin, M. L., et al. (2010) · Brain · doi:10.1093/brain/awq138 · Cited by 403
Naturalizing aesthetics: Brain areas for aesthetic appraisal across sensory modalities
Brown, S., Gao, X., Tisdelle, L., Eickhoff, S. B., & Liotti, M. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.06.012 · Cited by 376
The anatomo-functional connectivity of language revisited
Duffau, H. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.10.025 · Cited by 350
Age of acquisition: Its neural and computational mechanisms.
Hernández, A. E., & Li, P. (2007) · Psychological Bulletin · doi:10.1037/0033-2909.133.4.638 · Cited by 345
Interoception and emotion: A neuroanatomical perspective.
Craig, A. D. (2008) · Cited by 289
Song and speech: brain regions involved with perception and covert production
Callan, D. E., Tsytsarev, V., Hanakawa, T., Callan, A. M., Katsuhara, M., Fukuyama, H., & Turner, R. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.036 · Cited by 287
In Your Right Mind: Right Hemisphere Contributions to Language Processing and Production
Lindell, A. K. (2006) · Neuropsychology Review · doi:10.1007/s11065-006-9011-9 · Cited by 307
Cerliani, L., Thomas, R. M., Jbabdi, S., Siero, J. C. W., Nanetti, L., Crippa, A., Gazzola, V., D'Arceuil, H. E., & Keysers, C. (2011) · Human Brain Mapping · doi:10.1002/hbm.21338 · Cited by 299
Experience-dependent neural substrates involved in vocal pitch regulation during singing
Zarate, J. M., & Zatorre, R. J. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.01.026 · Cited by 257
Neural correlates of verbal feedback processing: an fMRI study employing overt speech
Christoffels, I. K., Formisano, E., & Schiller, N. O. (2007) · Human Brain Mapping · doi:10.1002/hbm.20315 · Cited by 254
A systems perspective on the effective connectivity of overt speech production
Eickhoff, S. B., Heim, S., Zilles, K., & Amunts, K. (2009) · Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences · doi:10.1098/rsta.2008.0287 · Cited by 259
Flowers, H. L., Silver, F. L., Fang, J., Rochon, E., & Martino, R. (2013) · Journal of Communication Disorders · doi:10.1016/j.jcomdis.2013.04.001 · Cited by 249
Duffau, H. (2006) · Journal of Neuro-Oncology · doi:10.1007/s11060-005-9109-6 · Cited by 250
Functional organization of the human anterior insular cortex
Mutschler, I., Wieckhorst, B., Kowalevski, S., Derix, J., Wentlandt, J., Schulze‐Bonhage, A., & Ball, T. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.03.101 · Cited by 238
Brain activity varies with modulation of dynamic pitch variance in sentence melody
Meyer, M., Steinhauer, K., Alter, K., Friederici, A. D., & von Cramon, D. Y. (2004) · Brain and Language · doi:10.1016/s0093-934x(03)00350-x · Cited by 228
Coello, A. F., Moritz‐Gasser, S., Martino, J., Martinoni, M., Matsuda, R., & Duffau, H. (2013) · Journal of neurosurgery · doi:10.3171/2013.6.jns122470 · Cited by 222
Ackermann, H., Hage, S. R., & Ziegler, W. (2014) · Behavioral and Brain Sciences · doi:10.1017/s0140525x13003099 · Cited by 224
Self-citationThe somatotopy of speech: phonation and articulation in the human motor cortex
Brown, S., Laird, A. R., Pfordresher, P. Q., Thelen, S. M., Turkeltaub, P., & Liotti, M. (2009) · Brain and Cognition · doi:10.1016/j.bandc.2008.12.006 · Cited by 210
An fMRI investigation of covertly and overtly produced mono- and multisyllabic words
SHUSTER, L., & LEMIEUX, S. (2005) · Brain and Language · doi:10.1016/j.bandl.2004.07.007 · Cited by 205
“Aha!”: The neural correlates of verbal insight solutions
Aziz‐Zadeh, L., Kaplan, J., & Iacoboni, M. (2008) · Human Brain Mapping · doi:10.1002/hbm.20554 · Cited by 199
Cloutman, L. L., Binney, R. J., Drakesmith, M., Parker, G. J. M., & Ralph, M. A. L. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.11.016 · Cited by 213
Similar cerebral networks in language, music and song perception
Schön, D., Gordon, R. L., Campagne, A., Magne, C., Astésano, C., Anton, J., & Besson, M. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.02.023 · Cited by 228
Overt and imagined singing of an Italian aria
Kleber, B., Birbaumer, N., Veit, R., Trevorrow, T., & Lotze, M. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.02.053 · Cited by 186
Ackermann, H., & Riecker, A. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0257-x · Cited by 191
Self-citationMechanisms and neural basis of object and pattern recognition: A study with chess experts.
Bilalić, M., Langner, R., Erb, M., & Grodd, W. (2010) · Journal of Experimental Psychology General · doi:10.1037/a0020756 · Cited by 187
L1 and L2 processing in the bilingual brain: A meta-analysis of neuroimaging studies
Liu, H., & Cao, F. (2016) · Brain and Language · doi:10.1016/j.bandl.2016.05.013 · Cited by 178
Role of the precentral gyrus of the insula in complex articulation
Baldo, J. V., Wilkins, D. P., Ogar, J., Willock, S., & Dronkers, N. F. (2011) · Cortex · doi:10.1016/j.cortex.2010.07.001 · Cited by 175
RESECTION OF WORLD HEALTH ORGANIZATION GRADE II GLIOMAS INVOLVING BROCA'S AREA
Benzagmout, M., Gatignol, P., & Duffau, H. (2007) · Neurosurgery · doi:10.1227/01.neu.0000298902.69473.77 · Cited by 176
FMRI Study of Emotional Speech Comprehension
Beaucousin, V., Lacheret-Dujour, A., Turbelin, M., Morel, M., Mazoyer, B. M., & Tzourio‐Mazoyer, N. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhj151 · Cited by 173
Rethinking the neurological basis of language
Stowe, L. A., Haverkort, M., & Zwarts, F. (2004) · Lingua · doi:10.1016/j.lingua.2004.01.013 · Cited by 175
Halai, A. D., Woollams, A. M., & Ralph, M. A. L. (2016) · Cortex · doi:10.1016/j.cortex.2016.04.016 · Cited by 183
Grabski, K., Lamalle, L., Vilain, C., Schwartz, J., Vallée, N., Troprés, I., Baciu, M., Bas, J. L., & Sato, M. (2011) · Human Brain Mapping · doi:10.1002/hbm.21363 · Cited by 181
Right hemisphere activation in recovery from aphasia
Raboyeau, G., Boissezon, X. D., Marie, N., Balduyck, S., Puel, M., Bézy, C., Démonet, J., & Cardebat, D. (2008) · Neurology · doi:10.1212/01.wnl.0000287115.85956.87 · Cited by 165
Anterior insula degeneration in frontotemporal dementia
Seeley, W. W. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0263-z · Cited by 162
Towards a neurocomputational model of speech production and perception
Kröger, B. J., Kannampuzha, J., & Neuschaefer‐Rube, C. (2008) · Speech Communication · doi:10.1016/j.specom.2008.08.002 · Cited by 163
Duffau, H., Moritz‐Gasser, S., & Gatignol, P. (2009) · Neurosurgical FOCUS · doi:10.3171/2009.5.focus0938 · Cited by 160
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
Effect of word and syllable frequency on activation during lexical decision and reading aloud
Carreiras, M., Mechelli, A., & Price, C. J. (2006) · Human Brain Mapping · doi:10.1002/hbm.20236 · Cited by 155
Afif, A., Minotti, L., Kahane, P., & Hoffmann, D. (2010) · Epilepsia · doi:10.1111/j.1528-1167.2010.02755.x · Cited by 156
Dual Neural Network Model for the Evolution of Speech and Language
Hage, S. R., & Nieder, A. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.10.006 · Cited by 151
The Margins of the Language Network in the Brain
Hertrich, I., Dietrich, S., & Ackermann, H. (2020) · Frontiers in Communication · doi:10.3389/fcomm.2020.519955 · Cited by 165
Self-citationFunctional MRI reveals the existence of modality and coordination-dependent timing networks
Jantzen, K. J., Steinberg, F. L., & Kelso, J. A. S. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.12.029 · Cited by 150
Cineradiography of Monkey Lip-Smacking Reveals Putative Precursors of Speech Dynamics
Ghazanfar, A. A., Takahashi, D. Y., Mathur, N., & Fitch, W. T. (2012) · Current Biology · doi:10.1016/j.cub.2012.04.055 · Cited by 148
Neural networks involved in voluntary and involuntary vocal pitch regulation in experienced singers
Zarate, J. M., Wood, S., & Zatorre, R. J. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.10.025 · Cited by 131
Lesion correlates of conversational speech production deficits
Borovsky, A., Saygın, A. P., Bates, E. A., & Dronkers, N. F. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.03.023 · Cited by 138
Janes, A. C., Nickerson, L. D. H., Frederick, B. B., & Kaufman, M. J. (2012) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2012.02.020 · Cited by 127
Speech errors in progressive non-fluent aphasia
Ash, S., McMillan, C. T., Gunawardena, D., Avants, B., Morgan, B. E., Khan, A., Moore, P., Gee, J. C., & Grossman, M. (2010) · Brain and Language · doi:10.1016/j.bandl.2009.12.001 · Cited by 136
Anatomical Correlates of Foreign Speech Sound Production
Golestani, N., & Pallier, C. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhl003 · Cited by 130
Abstract Grammatical Processing of Nouns and Verbs in Broca's Area: Evidence from FMRI
Sahin, N. T., Pinker, S. A., & Halgren, E. (2006) · Cortex · doi:10.1016/s0010-9452(08)70394-0 · Cited by 129
Renier, L. A., Anurova, I., Volder, A. D., Carlson, S., VanMeter, J. W., & Rauschecker, J. P. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0910-09.2009 · Cited by 124
The insular lobe and brain plasticity: Lessons from tumor surgery
Duffau, H., Taillandier, L., Gatignol, P., & Capelle, L. (2005) · Clinical Neurology and Neurosurgery · doi:10.1016/j.clineuro.2005.09.004 · Cited by 127
Brain regions recruited for the effortful comprehension of noise-vocoded words
Hervais‐Adelman, A., Carlyon, R. P., Johnsrude, I. S., & Davis, M. H. (2012) · Language and Cognitive Processes · doi:10.1080/01690965.2012.662280 · Cited by 128
Kumfor, F., Miller, L. A., Lah, S. S., Hsieh, S., Savage, S. A., Hodges, J. R., & Piguet, O. (2011) · Social Neuroscience · doi:10.1080/17470919.2011.620779 · Cited by 124
Riecker, A., Kassubek, J., Gröschel, K., Grodd, W., & Ackermann, H. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.03.046 · Cited by 114
Self-citationZarate, J. M. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00237 · Cited by 125
The Neural Correlate of Speech Rhythm as Evidenced by Metrical Speech Processing
Geiser, E., Zaehle, T., Jäncke, L., & Meyer, M. E. (2007) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.20029 · Cited by 118
Involvement of Insula and Cingulate Cortices in Control and Suppression of Natural Urges
Lerner, A., Bagic, A., Hanakawa, T., Boudreau, E. A., Pagan, F., Mari, Z., Bara-Jimenez, W., Aksu, M., Sato, S., Murphy, D. L., et al. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn074 · Cited by 112
The role of the anterior insula in adolescent decision making
Smith, A. R., Steinberg, L., & Chein, J. (2014) · Developmental Neuroscience · doi:10.1159/000358918 · Cited by 110
Re-establishing Broca's initial findings
Richardson, J. D., Fillmore, P., Rorden, C., LaPointe, L. L., & Fridriksson, J. (2012) · Brain and Language · doi:10.1016/j.bandl.2012.08.007 · Cited by 109
Surgery of Insular Nonenhancing Gliomas
Škrap, M., Mondani, M., Tomasino, B., Weis, L., Budai, R., Pauletto, G., Eleopra, R., Fadiga, L., & Ius, T. (2011) · Neurosurgery · doi:10.1227/neu.0b013e31823f5be5 · Cited by 110
Functional connectivity between brain regions involved in learning words of a new language
Veroude, K., Norris, D. G., Shumskaya, E., Gullberg, M., & Indefrey, P. (2010) · Brain and Language · doi:10.1016/j.bandl.2009.12.005 · Cited by 114
Duffau, H., Leroy, M., & Gatignol, P. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.07.017 · Cited by 112
Kleber, B., Zeitouni, A. G., Friberg, A., & Zatorre, R. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4418-12.2013 · Cited by 116
Converging Evidence for Triple Word Form Theory in Children With Dyslexia
Richards, T. L., Aylward, E., Field, K. M., Grimme, A. C., Raskind, W. H., Richards, A. L., Nagy, W. E., Eckert, M. A., Leonard, C. M., Abbott, R. D., et al. (2006) · Developmental Neuropsychology · doi:10.1207/s15326942dn3001_3 · Cited by 110
Word Retrieval Failures in Old Age: The Relationship between Structure and Function
Shafto, M. A., Stamatakis, E. A., Tam, P. P., & TYLER, L. K. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21321 · Cited by 102
Dissociating stimulus-driven semantic and phonological effect during reading and naming
Mechelli, A., Josephs, O., Lambon Ralph, M. A., McClelland, J. L., & Price, C. J. (2007) · Human Brain Mapping · doi:10.1002/hbm.20272 · Cited by 97
Anterior insular cortex is a bottleneck of cognitive control
Wu, T., Wang, X., Wu, Q., Spagna, A., Yang, J., Yuan, C., Wu, Y., Gao, Z., Hof, P. R., & Fan, J. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.02.042 · Cited by 104
Pugnaghi, M., Meletti, S., Castana, L., Francione, S., Nobili, L., Mai, R., & Tassi, L. (2011) · Clinical Neurophysiology · doi:10.1016/j.clinph.2011.03.013 · Cited by 102
The neural substrates for atypical planning and execution of word production in stuttering
Lu, C., Chen, C., Ning, N., Ding, G., Guo, T., Peng, D., Yang, Y., Li, K., & Lin, C. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.10.016 · Cited by 97
Monkey lipsmacking develops like the human speech rhythm
Morrill, R. J., Paukner, A., Ferrari, P. F., & Ghazanfar, A. A. (2012) · Developmental Science · doi:10.1111/j.1467-7687.2012.01149.x · Cited by 99
Central Nervous System Control of Voice and Swallowing
Ludlow, C. L. (2015) · Journal of Clinical Neurophysiology · doi:10.1097/wnp.0000000000000186 · Cited by 105
Speech and song: The role of the cerebellum
Callan, D. E., Kawato, M., Parsons, L. M., & Turner, R. (2007) · The Cerebellum · doi:10.1080/14734220601187733 · Cited by 97
Acquired and congenital disorders of sung performance: A review
Berkowska, M., & Bella, S. D. (2009) · Advances in Cognitive Psychology · doi:10.2478/v10053-008-0068-2 · Cited by 97
Language and Visual Perception Associations: Meta-Analytic Connectivity Modeling of Brodmann Area 37
Ardila, A., Bernal, B., & Rosselli, M. (2015) · Behavioural Neurology · doi:10.1155/2015/565871 · Cited by 93
Apraxia in progressive nonfluent aphasia
Rohrer, J. D., Rossor, M. N., & Warren, J. D. (2009) · Journal of Neurology · doi:10.1007/s00415-009-5371-4 · Cited by 93
How reading acquisition changes children’s spoken language network
Monzalvo, K., & Dehaene‐Lambertz, G. (2013) · Brain and Language · doi:10.1016/j.bandl.2013.10.009 · Cited by 103
Participation of the insula in language revisited: A meta-analytic connectivity study
Ardila, A., Bernal, B., & Rosselli, M. (2014) · Journal of Neurolinguistics · doi:10.1016/j.jneuroling.2014.02.001 · Cited by 97
Age of acquisition modulates neural activity for both regular and irregular syntactic functions
Hernández, A. E., Hofmann, J., & Kotz, S. A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.02.055 · Cited by 91
Neuronal basis of speech comprehension
Specht, K. (2013) · Hearing Research · doi:10.1016/j.heares.2013.09.011 · Cited by 91
Regional Cortical Thinning Associated with Detectable Levels of HIV DNA
Kallianpur, K. J., Kirk, G. R., Sailasuta, N., Valcour, V., Shiramizu, B., Nakamoto, B. K., & Shikuma, C. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr285 · Cited by 76
Neural correlates of Eureka moment
Sprugnoli, G., Rossi, S., Emmendorfer, A. K., Rossi, A., Liew, S., Tatti, E., Lorenzo, G. D., Pascual‐Leone, Á., & Santarnecchi, E. (2017) · Intelligence · doi:10.1016/j.intell.2017.03.004 · Cited by 85
Voice and Fluency Changes as a Function of Speech Task and Deep Brain Stimulation
Sidtis, D. V. L., Rogers, T. D., Godier, V., Tagliati, M., & Sidtis, J. J. (2010) · Journal of Speech Language and Hearing Research · doi:10.1044/1092-4388(2010/09-0154 · Cited by 75
Ray, D., Bezmaternykh, D., Mel’nikov, M., Friston, K. J., & Das, M. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2105730118 · Cited by 73
Metadata
- Authors
- Ackermann, H., & Riecker, A.
- Affiliations
- University of Tübingen (DE)
- Corresponding author
- Ackermann, Hermann
- ORCID
- Ackermann, Hermann
- Venue
- Brain and Language
- Publisher
- Elsevier BV
- Published
- 2004-05
- Volume
- 89
- Issue
- 2
- Pages
- 320-328
- ISSN
- 0093-934X (ISSN-L)
- OpenAlex
- W1981179822
- Cited by
- 343
- References
- 54
- Citations by year
- 2026: 9 · 2025: 9 · 2024: 6 · 2023: 8 · 2022: 9 · 2021: 9 · 2020: 12 · 2019: 14 · 2018: 14 · 2017: 9 · 2016: 16 · 2015: 21 · 2014: 24 · 2013: 17 · 2012: 26
- FWCI
- 5.54
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Brain and Language (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neurobiology of Language and Bilingualism
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Phonetics and Phonology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neuroscience and Music Perception
- Keywords
- speech motor control, inner speech, covert speech, overt speech, hemispheric lateralization, singing, phonation, swallowing, speech evolution
- MeSH terms
- Brain Mapping, Cerebral Cortex, Dominance, Cerebral, Facial Muscles, Humans, Image Processing, Computer-Assisted, Imagination, Laryngeal Muscles, Limbic System, Magnetic Resonance Imaging, Motor Cortex, Music, Pharyngeal Muscles, Phonation, Sound Spectrography, Speech, Speech Perception, Voice, Imaging, Three-Dimensional
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