The Cerebellum: Adaptive Prediction for Movement and Cognition

Trends in Cognitive Sciences

Volumn 21, Issue 5, 2017, Pages 313-332

  Sokolov, Arseny A ^a,b   Miall, R Chris ^c   Ivry, Richard B ^d  

^a LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

cerebellum; cognition; language; learning; prediction; social cognition

Indexed keywords

FORECASTING; MOTION ESTIMATION; NEUROIMAGING;

CEREBELLUM; COGNITION; LANGUAGE; LEARNING; SOCIAL COGNITION;

BRAIN;

ADAPTIVE BEHAVIOR; ANALYTICAL ERROR; CEREBELLUM; COGNITION; COORDINATION; DEFAULT MODE NETWORK; HUMAN; LONG TERM DEPRESSION; META ANALYSIS (TOPIC); MOVEMENT (PHYSIOLOGY); NEUROANATOMY; PREDICTION; REVIEW; SENSORIMOTOR CORTEX; SOCIAL COGNITION; ATTENTION; EXECUTIVE FUNCTION; LANGUAGE; NEUROIMAGING; PHYSIOLOGY;

ATTENTION; CEREBELLUM; COGNITION; EXECUTIVE FUNCTION; HUMANS; LANGUAGE; MOVEMENT; NEUROIMAGING;

EID: 85017370408     PISSN: 13646613     EISSN: 1879307X     Source Type: Journal    
DOI: 10.1016/j.tics.2017.02.005     Document Type: Review

References (202)

1. 1 Petersen, S.E., et al. Positron emission tomographic studies of the processing of single words. J. Cogn. Neurosci. 1 (1989), 153–170.
2. 2 Fiez, J.A., et al. Impaired non-motor learning and error detection associated with cerebellar damage. A single case study. Brain 115 (1992), 155–178.
3. 3 Ivry, R.B., Fiez, J.A., Cerebellar contributions to cognition and imagery. Gazzaniga, M., (eds.) The Cognitive Neurosciences, 2nd edn, 2000, MIT Press, 999–1011.
4. 4 Ishikawa, T., et al. The cerebro-cerebellum: could it be loci of forward models?. Neurosci. Res. 104 (2016), 72–79.
5. 5 Middleton, F.A., Strick, P.L., Cerebellar projections to the prefrontal cortex of the primate. J. Neurosci. 21 (2001), 700–712.
6. 6 Strick, P.L., et al. Cerebellum and nonmotor function. Annu. Rev. Neurosci. 32 (2009), 413–434.
7. 7 Salmi, J., et al. Cognitive and motor loops of the human cerebro-cerebellar system. J. Cogn. Neurosci. 22 (2010), 2663–2676.
8. 8 Grodd, W., et al. Sensorimotor mapping of the human cerebellum: fMRI evidence of somatotopic organization. Hum. Brain Mapp. 13 (2001), 55–73.
9. 9 Rijntjes, M., et al. Multiple somatotopic representations in the human cerebellum. Neuroreport 10 (1999), 3653–3658.
10. 10 Nitschke, M.F., et al. Somatotopic motor representation in the human anterior cerebellum. A high-resolution functional MRI study. Brain 119 (1996), 1023–1029.
11. 11 Habas, C., et al. Distinct cerebellar contributions to intrinsic connectivity networks. J. Neurosci. 29 (2009), 8586–8594.
12. 12 Buckner, R.L., et al. The organization of the human cerebellum estimated by intrinsic functional connectivity. J. Neurophysiol. 106 (2011), 2322–2345.
13. 13 Dobromyslin, V.I., Distinct functional networks within the cerebellum and their relation to cortical systems assessed with independent component analysis. Neuroimage 60 (2012), 2073–2085.
14. 14 O'Reilly, J.X., et al. Distinct and overlapping functional zones in the cerebellum defined by resting state functional connectivity. Cereb. Cortex 20 (2010), 953–965.
15. 15 Stoodley, C.J., Schmahmann, J.D., Functional topography in the human cerebellum: a meta-analysis of neuroimaging studies. Neuroimage 44 (2009), 489–501.
16. 16 Hawkes, R., Leclerc, N., Antigenic map of the rat cerebellar cortex: the distribution of parasagittal bands as revealed by monoclonal anti-Purkinje cell antibody mabQ113. J. Comp. Neurol. 256 (1987), 29–41.
17. 17 Sugihara, I., Shinoda, Y., Molecular, topographic, and functional organization of the cerebellar cortex: a study with combined aldolase C and olivocerebellar labeling. J. Neurosci. 24 (2004), 8771–8785.
18. 18 Buono, P., et al. Differential distribution of aldolase A and C in the human central nervous system. J. Neurocytol. 30 (2001), 957–965.
19. 19 Diedrichsen, J., Zotow, E., Surface-based display of volume-averaged cerebellar imaging data. PLoS One, 10, 2015, e0133402.
20. 20 Wadiche, J.I., Jahr, C.E., Patterned expression of Purkinje cell glutamate transporters controls synaptic plasticity. Nat. Neurosci. 8 (2005), 1329–1334.
21. 21 Zhou, H., et al. Cerebellar modules operate at different frequencies. Elife, 3, 2014, e02536.
22. 22 Marzban, H., Hawkes, R., On the architecture of the posterior zone of the cerebellum. Cerebellum 10 (2011), 422–434.
23. 23 Stoodley, C.J., et al. Location of lesion determines motor vs. cognitive consequences in patients with cerebellar stroke. Neuroimage Clin. 12 (2016), 765–775.
24. 24 Dum, R.P., Strick, P.L., An unfolded map of the cerebellar dentate nucleus and its projections to the cerebral cortex. J. Neurophysiol. 89 (2003), 634–639.
25. 25 Ramnani, N., et al. The evolution of prefrontal inputs to the cortico-pontine system: diffusion imaging evidence from macaque monkeys and humans. Cereb. Cortex 16 (2006), 811–818.
26. 26 Brodal, P., The corticopontine projection in the rhesus monkey. Origin and principles of organization. Brain 101 (1978), 251–283.
27. 27 Glickstein, M., et al. Visual pontocerebellar projections in the macaque. J. Comp. Neurol. 349 (1994), 51–72.
28. 28 Schmahmann, J.D., Pandya, D.N., Projections to the basis pontis from the superior temporal sulcus and superior temporal region in the rhesus monkey. J. Comp. Neurol. 308 (1991), 224–248.
29. 29 Jack, A., et al. Subcortical contributions to effective connectivity in brain networks supporting imitation. Neuropsychologia 49 (2011), 3689–3698.
30. 30 Sokolov, A.A., et al. Biological motion processing: the left cerebellum communicates with the right superior temporal sulcus. Neuroimage 59 (2012), 2824–2830.
31. 31 Sokolov, A.A., et al. Structural loop between the cerebellum and the superior temporal sulcus: evidence from diffusion tensor imaging. Cereb. Cortex 24 (2014), 626–632.
32. 32 Booth, J.R., et al. The role of the basal ganglia and cerebellum in language processing. Brain Res. 1133 (2007), 136–144.
33. 33 Kellermann, T., et al. Effective connectivity of the human cerebellum during visual attention. J. Neurosci. 32 (2012), 11453–11460.
34. 34 Allen, G., et al. Attentional activation of the cerebellum independent of motor involvement. Science 275 (1997), 1940–1943.
35. 35 Ide, J.S., Li, C.S., A cerebellar thalamic cortical circuit for error-related cognitive control. Neuroimage 54 (2011), 455–464.
36. 36 Ivry, R.B., Keele, S.W., Timing functions of the cerebellum. J. Cogn. Neurosci. 1 (1989), 136–152.
37. 37 Ravizza, S.M., et al. Cerebellar damage produces selective deficits in verbal working memory. Brain 129 (2006), 306–320.
38. 38 Ito, M., Control of mental activities by internal models in the cerebellum. Nat. Rev. Neurosci. 9 (2008), 304–313.
39. 39 Hore, J., et al. Cerebellar dysmetria at the elbow, wrist, and fingers. J. Neurophysiol. 65 (1991), 563–571.
40. 40 Bastian, A.J., et al. Cerebellar ataxia: abnormal control of interaction torques across multiple joints. J. Neurophysiol. 76 (1996), 492–509.
41. 41 Lisberger, S.G., Visual guidance of smooth-pursuit eye movements: sensation, action, and what happens in between. Neuron 66 (2010), 477–491.
42. 42 Doya, K., What are the computations of the cerebellum, the basal ganglia and the cerebral cortex?. Neural Netw. 12 (1999), 961–974.
43. 43 Kawato, M., Gomi, H., The cerebellum and VOR/OKR learning models. Trends Neurosci. 15 (1992), 445–453.
44. 44 Ito, M., Cerebellar circuitry as a neuronal machine. Prog. Neurobiol. 78 (2006), 272–303.
45. 45 Requarth, T., Sawtell, N.B., Plastic corollary discharge predicts sensory consequences of movements in a cerebellum-like circuit. Neuron 82 (2014), 896–907.
46. 46 Tomatsu, S., et al. Information processing in the hemisphere of the cerebellar cortex for control of wrist movement. J. Neurophysiol. 115 (2016), 255–270.
47. 47 Green, A.M., et al. A reevaluation of the inverse dynamic model for eye movements. J. Neurosci. 27 (2007), 1346–1355.
48. 48 Hewitt, A.L., et al. Representation of limb kinematics in Purkinje cell simple spike discharge is conserved across multiple tasks. J. Neurophysiol. 106 (2011), 2232–2247.
49. 49 Laurens, J., et al. Computation of linear acceleration through an internal model in the macaque cerebellum. Nat. Neurosci. 16 (2013), 1701–1708.
50. 50 Herzfeld, D.J., et al. Encoding of action by the Purkinje cells of the cerebellum. Nature 526 (2015), 439–442.
51. 51 Kawato, M., Gomi, H., A computational model of four regions of the cerebellum based on feedback-error learning. Biol. Cybern. 68 (1992), 95–103.
52. 52 Shidara, M., et al. Inverse-dynamics model eye movement control by Purkinje cells in the cerebellum. Nature 365 (1993), 50–52.
53. 53 Lisberger, S.G., Internal models of eye movement in the floccular complex of the monkey cerebellum. Neuroscience 162 (2009), 763–776.
54. 54 Ebner, T.J., et al. What features of limb movements are encoded in the discharge of cerebellar neurons?. Cerebellum 10 (2011), 683–693.
55. 55 Liu, X., et al. Neuronal activity related to the visual representation of arm movements in the lateral cerebellar cortex. J. Neurophysiol. 89 (2003), 1223–1237.
56. 56 Wolpert, D.M., Kawato, M., Multiple paired forward and inverse models for motor control. Neural Netw. 11 (1998), 1317–1329.
57. 57 Frens, M.A., Donchin, O., Forward models and state estimation in compensatory eye movements. Front. Cell. Neurosci., 3, 2009, 13.
58. 58 Brooks, J.X., Cullen, K.E., The primate cerebellum selectively encodes unexpected self-motion. Curr. Biol. 23 (2013), 947–955.
59. 3H]leucine and wheat germ agglutinin coupled horseradish peroxidase anterograde tracing. Neuroscience 34 (1990), 645–655.
60. 60 De Zeeuw, C.I., et al. Microcircuitry and function of the inferior olive. Trends Neurosci., 21, 1998, 391400.
61. 61 Marr, D., A theory of cerebellar cortex. J. Physiol. 202 (1969), 437–470.
62. 62 Albus, J.S., A theory of cerebellar function. Math. Biosci. 10 (1971), 25–61.
63. 63 Brooks, J.X., et al. Learning to expect the unexpected: rapid updating in primate cerebellum during voluntary self-motion. Nat. Neurosci. 18 (2015), 1310–1317.
64. 64 Ohmae, S., Medina, J.F., Climbing fibers encode a temporal-difference prediction error during cerebellar learning in mice. Nat. Neurosci. 18 (2015), 1798–1803.
65. 65 Gibson, A.R., et al. Activation of climbing fibers. Cerebellum 3 (2004), 212–221.
66. 66 Apps, R., Movement-related gating of climbing fibre input to cerebellar cortical zones. Prog. Neurobiol. 57 (1999), 537–562.
67. 67 Lang, E.J., et al. The roles of the olivocerebellar pathway in motor learning and motor control. A consensus paper. Cerebellum 16 (2016), 230–252.
68. 68 Suvrathan, A., et al. Timing rules for synaptic plasticity matched to behavioral function. Neuron 92 (2016), 959–967.
69. 69 Marien, P., Beaton, A., The enigmatic linguistic cerebellum: clinical relevance and unanswered questions on nonmotor speech and language deficits in cerebellar disorders. Cerebellum Ataxias, 1, 2014, 12.
70. 70 Chein, J.M., Fiez, J.A., Dissociation of verbal working memory system components using a delayed serial recall task. Cereb. Cortex 11 (2001), 1003–1014.
71. 71 Justus, T., et al. Reduced phonological similarity effects in patients with damage to the cerebellum. Brain Lang. 95 (2005), 304–318.
72. 72 Lesage, E., et al. Cerebellar BOLD signal during the acquisition of a new lexicon predicts its early consolidation. Brain Lang. 161 (2015), 33–44.
73. 73 Raboyeau, G., et al. Lexical learning of the English language: a PET study in healthy French subjects. Neuroimage 22 (2004), 1808–1818.
74. 74 Arasanz, C.P., et al. The cerebellum and its role in word generation: a cTBS study. Cortex 48 (2012), 718–724.
75. 75 Argyropoulos, G.P., et al. θ-Burst stimulation of the right neocerebellar vermis selectively disrupts the practice-induced acceleration of lexical decisions. Behav. Neurosci. 125 (2011), 724–734.
76. 76 Argyropoulos, G.P., Muggleton, N.G., Effects of cerebellar stimulation on processing semantic associations. Cerebellum 12 (2013), 83–96.
77. 77 Oliveri, M., et al. Motor and linguistic linking of space and time in the cerebellum. PLoS One, 4, 2009, e7933.
78. 78 Nicolson, R.I., et al. Developmental dyslexia: the cerebellar deficit hypothesis. Trends Neurosci. 24 (2001), 508–511.
79. 79 Marien, P., et al. Cognitive, linguistic and affective disturbances following a right superior cerebellar artery infarction: a case study. Cortex 45 (2009), 527–536.
80. 80 Moberget, T., Ivry, R.B., Cerebellar contributions to motor control and language comprehension: searching for common computational principles. Ann. N. Y. Acad. Sci. 1369 (2016), 154–171.
81. 81 Pickering, M.J., Clark, A., Getting ahead: forward models and their place in cognitive architecture. Trends Cogn. Sci. 18 (2014), 451–456.
82. 82 Moberget, T., et al. Generalized role for the cerebellum in encoding internal models: evidence from semantic processing. J. Neurosci. 34 (2014), 2871–2878.
83. 83 Lesage, E., et al. Cerebellar BOLD response to linguistic stimuli is modulated by predictability. Neuroscience 2014, 2014, Society for Neuroscience.
84. 84 Lesage, E., et al. Cerebellar rTMS disrupts predictive language processing. Curr. Biol. 22 (2012), R794–R795.
85. 85 Miall, R.C., et al. Modulation of linguistic prediction by TDCS of the right lateral cerebellum. Neuropsychologia 86 (2016), 103–109.
86. 86 Imamizu, H., et al. Human cerebellar activity reflecting an acquired internal model of a new tool. Nature 403 (2000), 192–195.
87. 87 Koster-Hale, J., Saxe, R., Theory of mind: a neural prediction problem. Neuron 79 (2013), 836–848.
88. 88 Pavlova, M.A., Biological motion processing as a hallmark of social cognition. Cereb. Cortex 22 (2012), 981–995.
89. 89 Frith, C.D., Frith, U., Mechanisms of social cognition. Annu. Rev. Psychol. 63 (2012), 287–313.
90. 90 Olsson, A., Ochsner, K.N., The role of social cognition in emotion. Trends Cogn. Sci. 12 (2008), 65–71.
91. 91 Weightman, M.J., et al. A review of the role of social cognition in major depressive disorder. Front. Psychiatry, 5, 2014, 179.
92. 92 de Waal, F.B., Putting the altruism back into altruism: the evolution of empathy. Annu. Rev. Psychol. 59 (2008), 279–300.
93. 93 Davis, M., Empathy: A Social Psychological Approach. 1996, Westview Press.
94. 94 Shamay-Tsoory, S.G., Two systems for empathy: a double dissociation between emotional and cognitive empathy in inferior frontal gyrus versus ventromedial prefrontal lesions. Brain 132 (2009), 617–627.
95. 95 Schmahmann, J.D., Sherman, J.C., The cerebellar cognitive affective syndrome. Brain 121 (1998), 561–579.
96. 96 D'Agata, F., et al. The recognition of facial emotions in spinocerebellar ataxia patients. Cerebellum 10 (2011), 600–610.
97. 97 Adamaszek, M., et al. Impairment of emotional facial expression and prosody discrimination due to ischemic cerebellar lesions. Cerebellum 13 (2014), 338–345.
98. 98 Sokolovsky, N., et al. A preliminary characterisation of cognition and social cognition in spinocerebellar ataxia types 2, 1, and 7. Behav Neurol. 23 (2010), 17–29.
99. 99 Parvizi, J., et al. Pathological laughter and crying: a link to the cerebellum. Brain 124 (2001), 1708–1719.
100. 100 Parvizi, J., et al. Pathological laughter and crying in patients with multiple system atrophy-cerebellar type. Mov. Disord. 22 (2007), 798–803.
101. 101 Schutter, D.J., van Honk, J., The cerebellum in emotion regulation: a repetitive transcranial magnetic stimulation study. Cerebellum 8 (2009), 28–34.
102. 102 Adamaszek, M., et al. Neural correlates of impaired emotional face recognition in cerebellar lesions. Brain Res. 1613 (2015), 1–12.
103. 103 Schmahmann, J.D., The neuropsychiatry of the cerebellum – insights from the clinic. Cerebellum 6 (2007), 254–267.
104. 104 Stoodley, C.J., Schmahmann, J.D., Evidence for topographic organization in the cerebellum of motor control versus cognitive and affective processing. Cortex 46 (2010), 831–844.
105. 105 Heath, R.G., Harper, J.W., Ascending projections of the cerebellar fastigial nucleus to the hippocampus, amygdala, and other temporal lobe sites: evoked potential and histological studies in monkeys and cats. Exp. Neurol. 45 (1974), 268–287.
106. 106 Bernard, J.A., et al. Resting state cortico-cerebellar functional connectivity networks: a comparison of anatomical and self-organizing map approaches. Front. Neuroanat., 6, 2012, 31.
107. 107 Sang, L., et al. Resting-state functional connectivity of the vermal and hemispheric subregions of the cerebellum with both the cerebral cortical networks and subcortical structures. Neuroimage 61 (2012), 1213–1225.
108. 108 Van Overwalle, F., Social cognition and the cerebellum: a meta-analysis of over 350 fMRI studies. Neuroimage 86 (2014), 554–572.
109. 109 Hoche, F., et al. Cerebellar contribution to social cognition. Cerebellum 15 (2016), 732–743.
110. 110 Parente, A., et al. Selective theory of mind impairment and cerebellar atrophy: a case report. J. Neurol. 260 (2013), 2166–2169.
111. 111 Garrard, P., et al. Cognitive and social cognitive functioning in spinocerebellar ataxia: a preliminary characterization. J. Neurol. 255 (2008), 398–405.
112. 112 Frith, C., Frith, U., Theory of mind. Curr. Biol. 15 (2005), R644–R646.
113. 113 Nawrot, M., Rizzo, M., Motion perception deficits from midline cerebellar lesions in human. Vision Res. 35 (1995), 723–731.
114. 114 Ivry, R.B., Diener, H.C., Impaired velocity perception in patients with lesions to the cerebellum. J. Cogn. Neurosci. 3 (1991), 355–366.
115. 115 Jokisch, D., et al. Differential involvement of the cerebellum in biological and coherent motion perception. Eur. J. Neurosci. 21 (2005), 3439–3446.
116. 116 Sokolov, A.A., et al. Cerebellar engagement in an action observation network. Cereb. Cortex 20 (2010), 486–491.
117. 117 Jack, A., Pelphrey, K.A., Neural correlates of animacy attribution include neocerebellum in healthy adults. Cereb. Cortex 25 (2015), 4240–4247.
118. 118 Gobbini, M.I., et al. Two takes on the social brain: a comparison of theory of mind tasks. J. Cogn. Neurosci. 19 (2007), 1803–1814.
119. 119 Barsalou, L.W., Simulation, situated conceptualization, and prediction. Philos. Trans. R. Soc. Lond. B Biol. Sci. 364 (2009), 1281–1289.
120. 120 Brown, E.C., Brune, M., The role of prediction in social neuroscience. Front. Hum. Neurosci., 6, 2012, 147.
121. 121 Gazzola, V., Keysers, C., The observation and execution of actions share motor and somatosensory voxels in all tested subjects: single-subject analyses of unsmoothed fMRI data. Cereb. Cortex 19 (2009), 1239–1255.
122. 122 Fuentes, C.T., Bastian, A.J., ‘Motor cognition’ – what is it and is the cerebellum involved?. Cerebellum 6 (2007), 232–236.
123. 123 Rizzolatti, G., Sinigaglia, C., The functional role of the parieto-frontal mirror circuit: interpretations and misinterpretations. Nat. Rev. Neurosci 11 (2010), 264–274.
124. 124 Miall, R.C., Connecting mirror neurons and forward models. Neuroreport 14 (2003), 2135–2137.
125. 125 Wolpert, D.M., et al. A unifying computational framework for motor control and social interaction. Philos. Trans. R. Soc. Lond. B Biol. Sci. 358 (2003), 593–602.
126. 126 Barsalou, L.W., Perceptual symbol systems. Behav. Brain Sci. 22 (1999), 577–609 discussion 610–560.
127. 127 Mahon, B.Z., Caramazza, A., A critical look at the embodied cognition hypothesis and a new proposal for grounding conceptual content. J. Physiol. Paris 102 (2008), 59–70.
128. 128 Berthoz, S., et al. An fMRI study of intentional and unintentional (embarrassing) violations of social norms. Brain 125 (2002), 1696–1708.
129. 129 Courchesne, E., et al. Hypoplasia of cerebellar vermal lobules VI and VII in autism. N. Engl. J. Med. 318 (1988), 1349–1354.
130. 130 D'Mello, A.M., Stoodley, C.J., Cerebro-cerebellar circuits in autism spectrum disorder. Front. Neurosci., 9, 2015, 408.
131. 131 Igelstrom, K.M., et al. Functional connectivity between the temporoparietal cortex and cerebellum in autism spectrum disorder. Cereb. Cortex, 2016, 10.1093/cercor/bhw079 Published online April 12, 2016.
132. 132 Olivito, G., et al. Resting-state functional connectivity changes between dentate nucleus and cortical social brain regions in autism spectrum disorders. Cerebellum 16 (2017), 283–292.
133. 133 Jack, A., Morris, J.P., Neocerebellar contributions to social perception in adolescents with autism spectrum disorder. Dev. Cogn. Neurosci. 10 (2014), 77–92.
134. 134 Catani, M., et al. Altered cerebellar feedback projections in Asperger syndrome. Neuroimage 41 (2008), 1184–1191.
135. 135 Blake, R., et al. Visual recognition of biological motion is impaired in children with autism. Psychol. Sci. 14 (2003), 151–157.
136. 136 Klin, A., et al. Two-year-olds with autism orient to non-social contingencies rather than biological motion. Nature 459 (2009), 257–261.
137. 137 Koldewyn, K., et al. The psychophysics of visual motion and global form processing in autism. Brain 133 (2010), 599–610.
138. 138 Nackaerts, E., et al. Recognizing biological motion and emotions from point-light displays in autism spectrum disorders. PLoS One, 7, 2012, e44473.
139. 139 Tager-Flusberg, H., A psychological approach to understanding the social and language impairments in autism. Int. Rev. Psychiatry 11 (1999), 325–334.
140. 140 Roman-Urrestarazu, A., Brain structure in different psychosis risk groups in the northern Finland 1986 birth cohort. Schizophr. Res. 153 (2014), 143–149.
141. 141 Laidi, C., et al. Cerebellar volume in schizophrenia and bipolar I disorder with and without psychotic features. Acta Psychiatr. Scand. 131 (2015), 223–233.
142. 142 Levitt, J.J., et al. Quantitative volumetric MRI study of the cerebellum and vermis in schizophrenia: clinical and cognitive correlates. Am. J. Psychiatry 156 (1999), 1105–1107.
143. 143 Guo, W., et al. Resting-state cerebellar-cerebral networks are differently affected in first-episode, drug-naive schizophrenia patients and unaffected siblings. Sci. Rep., 5, 2015, 17275.
144. 144 Anticevic, A., et al. Mediodorsal and visual thalamic connectivity differ in schizophrenia and bipolar disorder with and without psychosis history. Schizophr. Bull. 40 (2014), 1227–1243.
145. 145 Shinn, A.K., et al. Aberrant cerebellar connectivity in motor and association networks in schizophrenia. Front. Hum. Neurosci., 9, 2015, 134.
146. 146 Kanaan, R.A., et al. Microstructural organization of cerebellar tracts in schizophrenia. Biol. Psychiatry 66 (2009), 1067–1069.
147. 147 Kim, D.J., et al. Disrupted modular architecture of cerebellum in schizophrenia: a graph theoretic analysis. Schizophr. Bull. 40 (2014), 1216–1226.
148. 148 Kim, J., et al. Impaired visual recognition of biological motion in schizophrenia. Schizophr. Res. 77 (2005), 299–307.
149. 149 Kim, J., et al. Deficient biological motion perception in schizophrenia: results from a motion noise paradigm. Front. Psychol., 4, 2013, 391.
150. 150 Pedersen, A., et al. Theory of mind in patients with schizophrenia: is mentalizing delayed?. Schizophr. Res. 137 (2012), 224–229.
151. 151 Andreasen, N.C., et al. Theory of mind and schizophrenia: a positron emission tomography study of medication-free patients. Schizophr. Bull. 34 (2008), 708–719.
152. 152 Frith, C.D., et al. Explaining the symptoms of schizophrenia: abnormalities in the awareness of action. Brain Res. Brain Res. Rev. 31 (2000), 357–363.
153. 153 Ford, J.M., Mathalon, D.H., Anticipating the future: automatic prediction failures in schizophrenia. Int. J. Psychophysiol. 83 (2012), 232–239.
154. 154 Knolle, F., et al. Cerebellar contribution to the prediction of self-initiated sounds. Cortex 49 (2013), 2449–2461.
155. 155 Ford, J.M., et al. Did I do that? Abnormal predictive processes in schizophrenia when button pressing to deliver a tone. Schizophr. Bull. 40 (2014), 804–812.
156. 156 Leggio, M.G., et al. Cognitive sequencing impairment in patients with focal or atrophic cerebellar damage. Brain 131 (2008), 1332–1343.
157. 157 Keele, S.W., et al. The cognitive and neural architecture of sequence representation. Psychol. Rev. 110 (2003), 316–339.
158. 158 Balsters, J.H., et al. Cerebellum and cognition: evidence for the encoding of higher order rules. Cereb. Cortex 23 (2013), 1433–1443.
159. 159 Friston, K., The free-energy principle: a unified brain theory?. Nat. Rev. Neurosci. 11 (2010), 127–138.
160. 160 Levinson, S.C., Turn-taking in human communication – origins and implications for language processing. Trends Cogn. Sci. 20 (2016), 6–14.
161. 161 Schoenenberg, K., et al. On interaction behaviour in telephone conversations under transmission delay. Speech Commun. 63–64 (2014), 1–14.
162. 162 Kitazawa, S., et al. Effects of delayed visual information on the rate and amount of prism adaptation in the human. J. Neurosci. 15 (1995), 7644–7652.
163. 163 Brudner, S.N., et al. Delayed feedback during sensorimotor learning selectively disrupts adaptation but not strategy use. J. Neurophysiol. 115 (2016), 1499–1511.
164. 164 Fiorillo, C.D., et al. The temporal precision of reward prediction in dopamine neurons. Nat. Neurosci. 11 (2008), 966–973.
165. 165 De Zeeuw, C.I., Ten Brinke, M.M., Motor learning and the cerebellum. Cold Spring Harb. Perspect. Biol., 7, 2015, a021683.
166. 166 Watson, T.C., et al. Electrophysiological mapping of novel prefrontal–cerebellar pathways. Front. Integr. Neurosci., 3, 2009, 18.
167. 167 Kuypers, H.G., Lawrence, D.G., Cortical projections to the red nucleus and the brain stem in the rhesus monkey. Brain Res. 4 (1967), 151–188.
168. 168 Sasaki, K., et al. Electrophysiological studies of the projections from the parietal association area to the cerebellar cortex. Exp. Brain Res. 23 (1975), 91–102.
169. 169 D'Angelo, E., et al. Distributed circuit plasticity: new clues for the cerebellar mechanisms of learning. Cerebellum 15 (2016), 139–151.
170. 170 Akshoomoff, N.A., Attention coordination and anticipatory control. Int. Rev. Neurobiol. 41 (1997), 575–598.
171. 171 Desmond, J.E., et al. Dissociation of frontal and cerebellar activity in a cognitive task: evidence for a distinction between selection and search. Neuroimage 7 (1998), 368–376.
172. 172 Andreasen, N.C., Pierson, R., The role of the cerebellum in schizophrenia. Biol. Psychiatry 64 (2008), 81–88.
173. 173 Andreasen, N.C., et al. “Cognitive dysmetria” as an integrative theory of schizophrenia: a dysfunction in cortical–subcortical–cerebellar circuitry?. Schizophr. Bull. 24 (1998), 203–218.
174. 174 Schmahmann, J.D., Dysmetria of thought: clinical consequences of cerebellar dysfunction on cognition and affect. Trends Cogn. Sci. 2 (1998), 362–371.
175. 175 Alexander, M.P., et al. Cognitive impairments due to focal cerebellar injuries in adults. Cortex 48 (2012), 980–990.
176. 176 Malm, J., et al. Cognitive impairment in young adults with infratentorial infarcts. Neurology 51 (1998), 433–440.
177. 177 Sokolov, A.A., et al. Recovery of biological motion perception and network plasticity after cerebellar tumor removal. Cortex 59 (2014), 146–152.
178. 178 Yeo, B.T., et al. The organization of the human cerebral cortex estimated by intrinsic functional connectivity. J. Neurophysiol. 106 (2011), 1125–1165.
179. 179 Pavlova, M., et al. Recognition of point-light biological motion displays by young children. Perception 30 (2001), 925–933.
180. 180 Pavlova, M., et al. Cortical response to social interaction is affected by gender. Neuroimage 50 (2010), 1327–1332.
181. 181 Brodal, P., The pontocerebellar projection in the rhesus monkey: an experimental study with retrograde axonal transport of horseradish peroxidase. Neuroscience 4 (1979), 193–208.
182. 182 Brown, J.T., et al. A study of afferent input to the inferior olivary complex in the rat by retrograde axonal transport of horseradish peroxidase. J. Comp. Neurol. 176 (1977), 1–22.
183. 183 Berkley, K.J., Worden, I.G., Projections to the inferior olive of the cat. I. Comparisons of input from the dorsal column nuclei, the lateral cervical nucleus, the spino-olivary pathways, the cerebral cortex and the cerebellum. J. Comp. Neurol. 180 (1978), 237–251.
184. 184 Oka, H., et al. The parieto-rubro-olivary pathway in the cat. Exp. Brain Res. 37 (1979), 115–125.
185. 185 Monakow, K.H., et al. Projections of precentral and premotor cortex to the red nucleus and other midbrain areas in Macaca fascicularis. Exp. Brain Res. 34 (1979), 91–105.
186. 186 Sakai, S.T., Cerebellar thalamic and thalamocortical projections. Manto, M., et al. (eds.) Handbook of Cerebellum and Cerebellar Disorders, 2013, Springer, 529–547.
187. 187 Arakaki, T.L., et al. Structure of human brain fructose 1,6-(bis)phosphate aldolase: linking isozyme structure with function. Protein Sci. 13 (2004), 3077–3084.
188. 188 Voogd, J., Glickstein, M., The anatomy of the cerebellum. Trends Cogn. Sci. 2 (1998), 307–313.
189. 189] Voogd, J., et al. The distribution of climbing and mossy fiber collateral branches from the copula pyramidis and the paramedian lobule: congruence of climbing fiber cortical zones and the pattern of zebrin banding within the rat cerebellum. J. Neurosci. 23 (2003), 4645–4656.
190. 190 Pakan, J.M., et al. Climbing fiber projections in relation to zebrin stripes in the ventral uvula in pigeons. J. Comp. Neurol. 522 (2014), 3629–3643.
191. 191 Tsutsumi, S., et al. Structure–function relationships between aldolase C/zebrin II expression and complex spike synchrony in the cerebellum. J. Neurosci. 35 (2015), 843–852.
192. 192 Koziol, L.F., et al. Consensus paper: the cerebellum's role in movement and cognition. Cerebellum 13 (2014), 151–177.
193. 193 Marien, P., et al. Consensus paper: language and the cerebellum: an ongoing enigma. Cerebellum 13 (2014), 386–410.
194. 194 Ackermann, H., et al. The contribution of the cerebellum to speech production and speech perception: clinical and functional imaging data. Cerebellum 6 (2007), 202–213.
195. 195 Baumann, O., et al. Consensus paper: the role of the cerebellum in perceptual processes. Cerebellum 14 (2015), 197–220.
196. 196 Aarsen, F.K., et al. Long-term sequelae in children after cerebellar astrocytoma surgery. Neurology 62 (2004), 1311–1316.
197. 197 Steinlin, M., Cerebellar disorders in childhood: cognitive problems. Cerebellum 7 (2008), 607–610.
198. 198 Tavano, A., et al. Disorders of cognitive and affective development in cerebellar malformations. Brain 130 (2007), 2646–2660.
199. 199 Timmann, D., Daum, I., How consistent are cognitive impairments in patients with cerebellar disorders?. Behav. Neurol. 23 (2010), 81–100.
200. 200 Zecevic, N., Rakic, P., Differentiation of Purkinje cells and their relationship to other components of developing cerebellar cortex in man. J. Comp. Neurol. 167 (1976), 27–47.
201. 201 ten Donkelaar, H.J., Development and developmental disorders of the human cerebellum. J. Neurol. 250 (2003), 1025–1036.
202. 202 Wang, S.S., et al. The cerebellum, sensitive periods, and autism. Neuron 83 (2014), 518–532.