The Role of the Cerebellum in Schizophrenia

Dementia Praecox or the Group of Schizophrenias

(1951) · Journal of the American Medical Association · doi:10.1001/jama.1951.02920270079043 · Cited by 4,407

J Neuropsychiatry Clin Neurosci

Yudofsky, S. C., & Hales, R. E. (1992) · The Journal of Neuropsychiatry and Clinical Neurosciences · doi:10.1176/jnp.4.4.359 · Cited by 3,818

Developmental and regional expression in the rat brain and functional properties of four NMDA receptors

Monyer, H., Burnashev, N., Laurie, D. J., Sakmann, B., & Seeburg, P. H. (1994) · Neuron · doi:10.1016/0896-6273(94)90210-0 · Cited by 3,535

A theory of cerebellar cortex

Marr, D. (1969) · The Journal of Physiology · doi:10.1113/jphysiol.1969.sp008820 · Cited by 3,253

The cerebellar cognitive affective syndrome

Schmahmann, J. (1998) · Brain · doi:10.1093/brain/121.4.561 · Cited by 3,230

Recent advances in the phencyclidine model of schizophrenia

(1991) · American Journal of Psychiatry · doi:10.1176/ajp.148.10.1301 · Cited by 2,904

A theory of cerebellar function

Albus, J. S. (1971) · Mathematical Biosciences · doi:10.1016/0025-5564(71)90051-4 · Cited by 2,539

Remission in Schizophrenia: Proposed Criteria and Rationale for Consensus

Andreasen, N. C., Carpenter, W. T., Kane, J. M., Lasser, R. A., Marder, S. R., & Weinberger, D. R. (2005) · American Journal of Psychiatry · doi:10.1176/appi.ajp.162.3.441 · Cited by 2,350

A review of MRI findings in schizophrenia

Shenton, M. E., Dickey, C. C., Frumin, M., & McCarley, R. W. (2001) · Schizophrenia Research · doi:10.1016/s0920-9964(01)00163-3 · Cited by 2,346

The cerebellum and neural control

Ito, M. (1984) · Cited by 2,314

Volumetric differences in gray and white matter of cerebellar Crus I/ II across the different clinical stages of schizophrenia

Morimoto, C., Uematsu, A., Nakatani, H., Takano, Y., Iwashiro, N., Abe, O., Yamasue, H., Kasai, K., & Koike, S. (2021) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.13277 · Cited by 20

A Characterization of the Effects of Minocycline Treatment During Adolescence on Structural, Metabolic, and Oxidative Stress Parameters in a Maternal Immune Stimulation Model of Neurodevelopmental Brain Disorders

Romero‐Miguel, D., Casquero‐Veiga, M., MacDowell, K. S., Torres-Sánchez, S., Garcia-Partida, J. A., Lamanna‐Rama, N., Romero‐Miranda, A., Berrocoso, E., Leza, J. C., Desco, M., et al. (2021) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyab036 · Cited by 21

Gray Matter Alterations in First-Admission Adolescents with Schizophrenia

Henze, R., Brunner, R. M., Thiemann, U., Parzer, P., Richterich, A., Essig, M., Resch, F., & Stieltjes, B. (2010) · Journal of Neuroimaging · doi:10.1111/j.1552-6569.2010.00504.x · Cited by 21

Involvement of the primate specific gene G72 in schizophrenia: From genetic studies to pathomechanisms

Drews, E., Otte, D.-M., & Zimmer, A. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.10.009 · Cited by 24

Superior size–weight illusion performance in patients with schizophrenia: Evidence for deficits in forward models

Williams, L. E., Ramachandran, V. S., Hubbard, E. M., BRAFF, D. L., & Light, G. A. (2009) · Schizophrenia Research · doi:10.1016/j.schres.2009.10.021 · Cited by 24

Altered brain connectivity in patients with schizophrenia is consistent across cognitive contexts

Orban, P., Desseilles, M., Mendrek, A., Bourque, J., Bellec, P., & Stip, É. (2016) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.150247 · Cited by 21

Cerebellar transcranial direct current stimulation interacts with BDNF Val66Met in motor learning

van der Vliet, R., Jonker, Z. D., Louwen, S. C., Heuvelman, M., de Vreede, L., Ribbers, G. M., Zeeuw, C. I. D., Donchin, O., Selles, R. W., van der Geest, J. N., et al. (2018) · Brain stimulation · doi:10.1016/j.brs.2018.04.009 · Cited by 24

Expression of mutant DISC1 in Purkinje cells increases their spontaneous activity and impairs cognitive and social behaviors in mice

Shevelkin, A. V., Terrillion, C. E., Abazyan, B. N., Kajstura, T. J., Jouroukhin, Y., Rudow, G. L., Troncoso, J. C., Linden, D. J., & Pletnikov, M. V. (2017) · Neurobiology of Disease · doi:10.1016/j.nbd.2017.04.008 · Cited by 21

Early Celastrol Administration Prevents Ketamine-Induced Psychotic-Like Behavioral Dysfunctions, Oxidative Stress and IL-10 Reduction in The Cerebellum of Adult Mice

Schiavone, S., Tucci, P., Trabace, L., & Morgese, M. G. (2019) · Molecules · doi:10.3390/molecules24213993 · Cited by 20

Intrinsic cerebellar functional connectivity of social cognition and theory of mind in first-episode psychosis patients

Park, S. H., Kim, T., Ha, M., Moon, S., Lho, S. K., Kim, M., & Kwon, J. S. (2021) · Schizophrenia · doi:10.1038/s41537-021-00193-w · Cited by 22

Ca2+-stimulated adenylyl cyclases as therapeutic targets for psychiatric and neurodevelopmental disorders

Chen, J., Ding, Q., An, L., & Wang, H. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.949384 · Cited by 21

Impaired saccadic adaptation in schizophrenic patients with high neurological soft sign scores

Picard, H., Séac’h, A. L., Amado, I., Raphaël Gaillard, B., Krebs, M., & Beauvillain, C. (2012) · Psychiatry Research · doi:10.1016/j.psychres.2012.04.039 · Cited by 20

Impaired Cerebellar-Dependent Eyeblink Conditioning in First-Degree Relatives of Individuals With Schizophrenia

Bolbecker, A. R., Kent, J. S., Petersen, I. T., Klaunig, M. J., Forsyth, J. K., Howell, J. M., Westfall, D. R., O’Donnell, B. F., & Hetrick, W. P. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt112 · Cited by 20

Alcohol-induced psychotic disorder: brain perfusion and psychopathology—before and after anti-psychotic treatment

Jordaan, G. P., Warwick, J., Nel, D. G., Hewlett, R. H., & Emsley, R. A. (2011) · Metabolic Brain Disease · doi:10.1007/s11011-011-9273-7 · Cited by 20

The p75NTR Influences Cerebellar Circuit Development and Adult Behavior via Regulation of Cell Cycle Duration of Granule Cell Progenitors

Zanin, J. P., Verpeut, J. L., Li, Y., Shiflett, M. W., Wang, S. S. ‐., Santhakumar, V., & Friedman, W. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0990-19.2019 · Cited by 20

The Optogenetic Revolution in Cerebellar Investigations

Prestori, F., Montagna, I., D'Angelo, E. U., & Mapelli, L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21072494 · Cited by 20

Sparse deep neural networks on imaging genetics for schizophrenia case–control classification

Chen, J., Li, X., Calhoun, V. D., Turner, J. A., van Erp, T. G. M., Wang, L., Andreassen, O. A., Agartz, I., Westlye, L. T., Jönsson, E. G., et al. (2021) · Human Brain Mapping · doi:10.1002/hbm.25387 · Cited by 19

The cerebellum and learning of non-motor associations in individuals at clinical-high risk for psychosis

Bernard, J. A., Orr, J. M., Dean, D. J., & Mittal, V. A. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.03.023 · Cited by 20

An Association Study on the Cognitive Function and the Cerebral Grey Matter Volume of Patients with First-Episode Schizophrenia.

Zhang, X., Yao, J., Lv, Y., Zhao, X., Li, Y., Sui, Y., & Zhiping, D. (2018) · Europe PMC (PubMed Central) · doi:10.11919/j.issn.1002-0829.217138 · Cited by 18

Altered functional connectivity of cerebellar networks in first-episode schizophrenia

Feng, S., Zheng, S., Zou, H., Dong, L., Zhu, H., Liu, S., Wang, D., Ning, Y., & Jia, H. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1024192 · Cited by 19

Gene expression of glutamate transporters SLC1A1, SLC1A3 and SLC1A6 in the cerebellar subregions of elderly schizophrenia patients and effects of antipsychotic treatment

von Wilmsdorff, M., Blaich, C., Zink, M., Treutlein, J., Bauer, M., Schulze, T. G., Schneider-Axmann, T., Gruber, O., Rietschel, M., Schmitt, A., et al. (2012) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2011.645877 · Cited by 19

Visuospatial Organization and Recall in Cerebellar Ataxia

Slapik, M. B., Kronemer, S. I., Morgan, O. P., Bloes, R., Lieberman, S., Mandel, J. A., Rosenthal, L. S., & Marvel, C. L. (2018) · The Cerebellum · doi:10.1007/s12311-018-0948-z · Cited by 19

Brain function, structure and genomic data are linked but show different sensitivity to duration of illness and disease stage in schizophrenia

Luo, N., Tian, L., Calhoun, V. D., Chen, J., Lin, D., Vergara, V. M., Rao, S., Yang, J., Zhuo, C., Xu, Y. J., et al. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.101887 · Cited by 20

Timing dysfunction and cerebellar resting state functional connectivity abnormalities in youth at clinical high-risk for psychosis

Osborne, K. J., Damme, K. S. F., Gupta, T., Dean, D. J., Bernard, J. A., & Mittal, V. A. (2020) · Psychological Medicine · doi:10.1017/s0033291719004161 · Cited by 21

Weaker Cerebellocortical Connectivity Within Sensorimotor and Executive Networks in Schizophrenia Compared to Healthy Controls: Relationships with Processing Speed

Clark, S., Tannahill, A., Calhoun, V. D., Bernard, J. A., Bustillo, J., & Turner, J. A. (2020) · Brain Connectivity · doi:10.1089/brain.2020.0792 · Cited by 20

Family history of depression is associated with alterations in task‐dependent connectivity between the cerebellum and ventromedial prefrontal cortex

Tepfer, L. J., Alloy, L. B., & Smith, D. V. (2021) · Depression and Anxiety · doi:10.1002/da.23143 · Cited by 19

Reduction of gyrification index in the cerebellar vermis in schizophrenia: A post-mortem study

Schmitt, A., Schulenberg, W., Bernstein, H., Steiner, J. H., Schneider-Axmann, T., Yeganeh-Doost, P., Malchow, B., Hasan, A., Gruber, O., Bogerts, B., et al. (2011) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2011.598379 · Cited by 19

ErbB4 in Laminated Brain Structures: A Neurodevelopmental Approach to Schizophrenia

Pérez‐García, C. G. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00472 · Cited by 21

Dentate Nucleus: Connectivity-Based Anatomic Parcellation Based on Superior Cerebellar Peduncle Projections

Taçyıldız, A. E., Bilgin, B., Güngör, A., Üçer, M., Karadağ, A., & Tanrıöver, N. (2021) · World Neurosurgery · doi:10.1016/j.wneu.2021.05.102 · Cited by 18

Altered Coupling of Cerebral Blood Flow and Functional Connectivity Strength in First-Episode Schizophrenia Patients With Auditory Verbal Hallucinations

Chen, J.-L., Xue, K.-K., Yang, M., Wang, K.-F., Xu, Y.-H., Wen, B.-H., Cheng, J.-L., Han, S.-Q., & Wei, Y.-R. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.821078 · Cited by 15

Role of cerebellum in sleep-dependent memory processes

Jackson, A., & Xu, W. (2023) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2023.1154489 · Cited by 21

Subcortical contributions to the sense of body ownership

Crucianelli, L., Reader, A. T., & Ehrsson, H. H. (2023) · Brain · doi:10.1093/brain/awad359 · Cited by 22

Mapping cerebellar anatomical heterogeneity in mental and neurological illnesses

Kim, M., Leonardsen, E. H., Rutherford, S. E., Selbæk, G., Persson, K., Steen, N. E., Smeland, O. B., Ueland, T., Richard, G., Beckmann, C. F., et al. (2024) · Nature Mental Health · doi:10.1038/s44220-024-00297-z · Cited by 15

Emotion Processing in Women with Schizophrenia Is Menstrual Cycle Phase and Affective Valence Dependent: An fMRI Study

Mendrek, A., Bourque, J., Dubé, A., Lakis, N., & Champagne, J. (2012) · ISRN Psychiatry · doi:10.5402/2012/656274 · Cited by 19

Psychiatric Manifestations Associated With Mega Cisterna Magna

Pandurangi, S. A., Pandurangi, A., Matkar, A., Shetty, N., & Patil, P. (2014) · Journal of Neuropsychiatry · doi:10.1176/appi.neuropsych.13040097 · Cited by 18

Dandy-Walker Malformation-Like Condition Revealed by Refractory Schizophrenia: A Case Report and Literature Review

Tréhout, M., Zhang, N., Blouet, M., Borha, A., & Dollfus, S. (2018) · Neuropsychobiology · doi:10.1159/000494695 · Cited by 18

The Implementation of Predictions During Sequencing

Molinari, M., & Masciullo, M. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00439 · Cited by 19

Increased grey matter volume and associated resting-state functional connectivity in chronic spontaneous urticaria: A structural and functional MRI study

Wang, Y., Gao, D., Cui, B., Yu, B., Fang, J., Wang, Z., Tang, R., Cao, Z., Song, W., Song, P., et al. (2021) · Journal of Neuroradiology · doi:10.1016/j.neurad.2021.01.011 · Cited by 18

A Deep Learning Model for Data-Driven Discovery of Functional Connectivity

Mahmood, U., Fu, Z., Calhoun, V. D., & Plis, S. (2021) · Algorithms · doi:10.3390/a14030075 · Cited by 21

Anti-brain autoantibodies in the serum of schizophrenic patients: A case-control study

Margari, F., Petruzzelli, M. G., Mianulli, R., Toto, M., Pastore, A., Bizzaro, N., & Tampoia, M. (2013) · Psychiatry Research · doi:10.1016/j.psychres.2013.09.006 · Cited by 18

Discrimination of motor and sensorimotor effects of phencyclidine and MK-801: Involvement of GluN2C-containing NMDA receptors in psychosis-like models

Tarrés-Gatius, M., López‐Hill, X., Miquel-Rio, L., Castarlenas, L., Fabius, S., Santana, N., Vilaró, M. T., Artigas, F., Scorza, C., & Castañé, A. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109079 · Cited by 17

Dysconnection and cognition in schizophrenia: A spectral dynamic causal modeling study

Zarghami, T. S., Zeidman, P., Razi, A., Bahrami, F., & Hossein‐Zadeh, G. (2023) · Human Brain Mapping · doi:10.1002/hbm.26251 · Cited by 16

Computer-assisted cognitive remediation therapy for patients with schizophrenia induces microstructural changes in cerebellar regions involved in cognitive functions

Matsuoka, K., Morimoto, T., Matsuda, Y., Yasuno, F., Taoka, T., Miyasaka, T., Yoshikawa, H., Takahashi, M., Kitamura, S., Kichikawa, K., et al. (2019) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2019.09.001 · Cited by 19

Systematic elucidation and in vivo validation of sequences enriched in hindbrain transcriptional controlPreprint

Burzynski, G. M., Reed, X., Taher, L., Stine, Z. E., Matsui, T., Ovcharenko, I., & McCallion, A. S. (2012) · Genome Research · doi:10.1101/gr.139717.112 · Cited by 17

26th Annual Computational Neuroscience Meeting (CNS*2017): Part 2

Rubchinsky, L. L., Ahn, S., Klijn, W., Cumming, B., Yates, S., Karakasis, V., Peyser, A., Woodman, M., Diaz-Pier, S., Deraeve, J., et al. (2017) · BMC Neuroscience · doi:10.1186/s12868-017-0371-2 · Cited by 17

The Cerebellum Links to Positive Symptoms of Psychosis: A Systematic Review and Meta-analysis

Pinheiro, A. P., Johnson, J. F., Amorim, M., Roberto, M. S., Schwartze, M., Kotz, S. A., & Shenton, M. E. (2021) · Schizophrenia Bulletin Open · doi:10.1093/schizbullopen/sgab039 · Cited by 17

Reconfiguration of Functional Dynamics in Cortico-Thalamo-Cerebellar Circuit in Schizophrenia Following High-Frequency Repeated Transcranial Magnetic Stimulation

Huang, H., Zhang, B., Mi, L., Liu, M., Chang, X., Luo, Y., Li, C., He, H., Zhou, J., Yang, R., et al. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.928315 · Cited by 16

Brain Hemispheric Asymmetry in Schizophrenia and Bipolar Disorder

Pinto, D., Martins, R., Macedo, A., Castelo-Branco, M. S., Duarte, J. V., & Madeira, N. G. G. F. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12103421 · Cited by 16

Progressive brain structural changes after the first year of treatment in first-episode treatment-naive patients with deficit or nondeficit schizophrenia

Lei, W., Kirkpatrick, B. W., Wang, Q., Deng, W., Li, M., Guo, W., Liang, S., Li, Y., Zhang, C., Li, X., et al. (2019) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2019.04.009 · Cited by 16

Higher Body-Mass Index and Lower Gray Matter Volumes in First Episode of Psychosis

Kolenič, M., Španiel, F., Hlinka, J., Matějka, M., Knytl, P., Šebela, A., Renka, J., & Hájek, T. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.556759 · Cited by 17

Detecting abnormal connectivity in schizophrenia via a joint directed acyclic graph estimation model

Zhang, G., Cai, B., Zhang, A., Tu, Z., Xiao, L., Stephen, J. M., Wilson, T. W., Calhoun, V. D., & Wang, Y. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119451 · Cited by 16

Disassociated and concurrent structural and functional abnormalities in the drug-naïve first-episode early onset schizophrenia

Li, Q., Liu, S., Cao, X., Li, Z., Fan, Y., Wang, Y., Wang, J., & Xu, Y. J. (2022) · Brain Imaging and Behavior · doi:10.1007/s11682-021-00608-3 · Cited by 16

Involvement of cerebellar and subcortical connector hubs in schizophrenia

Yamamoto, M., Bagarinao, E., Shimamoto, M., Iidaka, T., & Ozaki, N. (2022) · NeuroImage Clinical · doi:10.1016/j.nicl.2022.103140 · Cited by 16

Effective Treatment With Clozapine and Valproate for Refractory Schizophrenia-Like Psychosis After Cerebellar Hemorrhage

Almeida, J., Serrao, E., Almeida, A., & Afonso, J. (2011) · Clinical neuropharmacology · doi:10.1097/wnf.0b013e31821f4d91 · Cited by 17

A Comprehensive Analysis of Cerebellar Volumes in the 22q11.2 Deletion Syndrome

Schmitt, J. E., DeBevits, J. J., Roalf, D. R., Ruparel, K., Gallagher, R. S., Gur, R. C., Alexander‐Bloch, A. F., Eom, T.-Y., Alam, S., Steinberg, J., et al. (2021) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2021.11.008 · Cited by 16

Correlates between neurological soft signs and saccadic parameters in schizophrenia

Picard, H., Amado, I., Bourdel, M., Landgraf, S., Olié, J., & Krebs, M. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.03.012 · Cited by 15

State-Dependent Entrainment of Prefrontal Cortex Local Field Potential Activity Following Patterned Stimulation of the Cerebellar Vermis

Tremblay, S. A., Chapman, C. A., & Courtemanche, R. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2019.00060 · Cited by 15

Cognitive correlates of gray matter abnormalities in adolescent siblings of patients with childhood-onset schizophrenia

Wagshal, D., Knowlton, B. J., Cohen, J. R., Bookheimer, S. Y., Bilder, R. M., Fernandez, V. G., & Asarnow, R. F. (2014) · Schizophrenia Research · doi:10.1016/j.schres.2014.12.006 · Cited by 15

Differential patterns of age‐related cortical and subcortical functional connectivity in 6‐to‐10 year old children: A connectome‐wide association study

Langen, C. D., Muetzel, R. L., Blanken, L. M. E., van der Lugt, A., Tiemeier, H. W., Verhulst, F. C., Niessen, W. J., & White, T. J. H. (2018) · Brain and Behavior · doi:10.1002/brb3.1031 · Cited by 18

Transcriptional signatures of the whole-brain voxel-wise resting-state functional network centrality alterations in schizophrenia

Guo, L., Ma, J., Cai, M., Zhang, M., Xu, Q., Wang, H., Zhang, Y., Yao, J., Sun, Z., Chen, Y., et al. (2023) · Schizophrenia · doi:10.1038/s41537-023-00422-4 · Cited by 15

Overview on cognitive impairment in psychotic disorders: From impaired microcircuits to dysconnectivity

Mana, L., Schwartz-Palleja, M., Vila‐Vidal, M., & Deco, G. (2024) · Schizophrenia Research · doi:10.1016/j.schres.2024.05.008 · Cited by 13

Decoding Schizophrenia: How AI-Enhanced fMRI Unlocks New Pathways for Precision Psychiatry

Stefano, V. D., D’Angelo, M., Monaco, F., Vignapiano, A., Martiadis, V., Barone, E., Fornaro, M., Steardo, L., Solmi, M., Manchia, M., et al. (2024) · Brain Sciences · doi:10.3390/brainsci14121196 · Cited by 20

Circadian Clock Proteins and Melatonin Receptors in Neurons and Glia of the Sapajus apella Cerebellum

Campos, L. M. G., Hataka, A., Vieira, I. Z. [., Buchaim, R. L., Robalinho, I. F., Arantes, G. E. P. S., Viégas, J. S., Bosso, H., Bravos, R. M., & Pinato, L. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00005 · Cited by 14

[Comorbidity between obsessive-compulsive disorder and schizophrenia: prevalence, explanatory theories, and nosological status].

Frías, Á., Palma, C., & Farriols, N. (2014) · Actas Españolas de Psiquiatría · Cited by 14

Rack1 Controls Parallel Fiber–Purkinje Cell Synaptogenesis and Synaptic Transmission

Yang, H., Yang, C., Zhu, Q., Wei, M., Li, Y., Cheng, J., Liu, F., Wu, Y., Zhang, J., Zhang, C., et al. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00539 · Cited by 14

Epigenetic analysis suggests aberrant cerebellum brain aging in old-aged adults with autism spectrum disorder and schizophrenia

Liu, L., Qi, X., Cheng, S., Meng, P., Yang, X., Pan, C., Zhang, N., Chen, Y., Li, C., Zhang, H., et al. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02233-6 · Cited by 14

Impairments of cerebellar structure and function in a zebrafish KO of neuropsychiatric risk gene znf536

Kim, T.-Y., Roychaudhury, A., Kim, H.-T., Choi, T., Baek, S. T., Thyme, S. B., & Kim, C. (2024) · Translational Psychiatry · doi:10.1038/s41398-024-02806-1 · Cited by 13

Dose-dependent LSD effects on cortical/thalamic and cerebellar activity: brain oxygen level–dependent fMRI study in awake rats

Ghaw, A., Chunduri, A., Chang, A., Ortiz, R. J., Kozlowska, M., Kulkarni, P. P., & Ferris, C. F. (2024) · Brain Communications · doi:10.1093/braincomms/fcae194 · Cited by 13

Gray matters: ViT-GAN framework for identifying schizophrenia biomarkers linking structural MRI and functional network connectivity

Bi, Y.-D., Abrol, A., Jia, S., Sui, J., & Calhoun, V. (2024) · NeuroImage · doi:10.1016/j.neuroimage.2024.120674 · Cited by 15

The cerebellar connectome

Boonstra, J. T. (2025) · Behavioural Brain Research · doi:10.1016/j.bbr.2025.115457 · Cited by 14

Cerebellar hypoactivation is associated with impaired sensory integration in schizophrenia.

Li, Z., Huang, J., Hung, K. S. Y., Deng, Y. M., Wang, Y., Wang, Y., Lui, S. S. Y., Mak, H. K., Sham, P. C., Cheung, E. F. C., et al. (2020) · Journal of Abnormal Psychology · doi:10.1037/abn0000636 · Cited by 13

Cerebellar Cortex and Cerebellar White Matter Volume in Normal Cognition, Mild Cognitive Impairment, and Dementia

Zdanovskis, N., Platkājis, A., Kostiks, A., Grigorjeva, O., & Karelis, G. (2021) · Brain Sciences · doi:10.3390/brainsci11091134 · Cited by 11

Association between aerobic fitness and the functional connectome in patients with schizophrenia

Roell, L., Maurus, I., Keeser, D., Karali, T., Papazov, B., Hasan, A., Schmitt, A., Papazova, I., Lembeck, M., Hirjak, D., et al. (2022) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-022-01411-x · Cited by 13

Modified climbing fiber/Purkinje cell synaptic connectivity in the cerebellum of the neonatal phencyclidine model of schizophrenia

Veleanu, M., Urrieta-Chávez, B., Sigoillot, S. M., Paul, M. A., Usardi, A., Iyer, K., Delagrange, M., Doyle, J., Heintz, N., Bécamel, C., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2122544119 · Cited by 16

Cerebellar dysconnectivity in schizophrenia and bipolar disorder is associated with cognitive and clinical variables

Cattarinussi, G., Giorgio, A. D., & Sambataro, F. (2024) · Schizophrenia Research · doi:10.1016/j.schres.2024.03.039 · Cited by 13

The Optic Radiation and the Cerebellar Peduncles in Adolescents with First‐Admission Schizophrenia —A Diffusion Tensor Imaging Study

Henze, R., Brunner, R. M., Thiemann, U., Parzer, P., Klein, J., Resch, F., & Stieltjes, B. (2012) · Journal of Neuroimaging · doi:10.1111/j.1552-6569.2011.00668.x · Cited by 13

Classical eyeblink conditioning and schizophrenia: A short review

Lubow, R. E. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.03.006 · Cited by 13

Dandy Walker Variant and Bipolar I Disorder with Graphomania

Can, S. S., Uğurlu, G. K., & Çakmak, S. (2014) · Psychiatry Investigation · doi:10.4306/pi.2014.11.3.336 · Cited by 13

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Wilber, A. A., Lin, G. L., & Wellman, C. L. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.01.010 · Cited by 13

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Wang, S., Ouyang, W.-C., Wu, M.-Y., & Kuo, L. (2019) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-019-01004-1 · Cited by 12

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Kulkarni, J., Gavrilidis, E., Hayes, E., Heaton, V., & Worsley, R. (2012) · Expert Review of Neurotherapeutics · doi:10.1586/ern.12.62 · Cited by 12

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Mundorf, A., Merklein, S. A., Rice, L. C., Desmond, J. E., & Peterburs, J. (2024) · Developmental Psychobiology · doi:10.1002/dev.22556 · Cited by 13

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Picard, H., Amado, I., Mouchet-Mages, S., Olié, J., & Krebs, M. (2007) · Schizophrenia bulletin · doi:10.1093/schbul/sbm049 · Cited by 290

Schizophrenia Bulletin doi:10.1093/schbul/sbm049 Schizophrenia Bulletin Advance Access published June 11, 2007 The Role of the Cerebellum in Schizophrenia: an Update of Clinical, Cognitive, and Functional Evidences

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김문두, & 강병조 (1999) · Cited by 4