A probabilistic MR atlas of the human cerebellum

Advances in functional and structural MR image analysis and implementation as FSL

Smith, S. M., Jenkinson, M., Woolrich, M. W., Beckmann, C. F., Behrens, T. E. J., Johansen-Berg, H., Bannister, P. R., De Luca, M., Drobnjak, I., Flitney, D. E., et al. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.07.051 · Cited by 13,630

Improved Optimization for the Robust and Accurate Linear Registration and Motion Correction of Brain Images

Jenkinson, M., Bannister, P., Brady, M., & Smith, S. (2002) · NeuroImage · doi:10.1006/nimg.2002.1132 · Cited by 11,888

Voxel-Based Morphometry—The Methods

Ashburner, J., & Friston, K. J. (2000) · NeuroImage · doi:10.1006/nimg.2000.0582 · Cited by 8,676

A new SPM toolbox for combining probabilistic cytoarchitectonic maps and functional imaging data

Eickhoff, S. B., Stephan, K. E., Mohlberg, H., Grefkes, C., Fink, G. R., Amunts, K., & Zilles, K. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.12.034 · Cited by 4,033

The cerebellum and cognition

Schmahmann, J. D. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2018.07.005 · Cited by 1,625

Evolution of the cerebellar cortex: The selective expansion of prefrontal-projecting cerebellar lobules

Balsters, J. H., Cussans, E., Diedrichsen, J., Phillips, K. A., Preuss, T. M., Rilling, J. K., & Ramnani, N. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.045 · Cited by 241

Dissociating timing and coordination as functions of the cerebellum

Diedrichsen, J., Criscimagna-Hemminger, S. E., & Shadmehr, R. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0061-07.2007 · Cited by 127

The organization of the human cerebellum estimated by intrinsic functional connectivity

Buckner, R. L., Krienen, F. M., Castellanos, A., Diaz, J. C., & Yeo, B. T. T. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00339.2011 · Cited by 7,304

Functional topography of the cerebellum for motor and cognitive tasks: An fMRI study

Stoodley, C. J., Valera, E. M., & Schmahmann, J. D. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.065 · Cited by 1,106

The Dynamics of Functional Brain Networks: Integrated Network States during Cognitive Task Performance

Shine, J. M., Bissett, P. G., Bell, P. T., Koyejo, O., Balsters, J. H., Gorgolewski, K. J., Moodie, C. A., & Poldrack, R. A. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.018 · Cited by 886

Sustaining attention to simple tasks: A meta-analytic review of the neural mechanisms of vigilant attention.

Langner, R., & Eickhoff, S. B. (2013) · Psychological Bulletin · doi:10.1037/a0030694 · Cited by 746

Functional boundaries in the human cerebellum revealed by a multi-domain task battery

King, M., Hernandez-Castillo, C. R., Poldrack, R. A., Ivry, R. B., & Diedrichsen, J. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0436-x · Cited by 673

Learning-induced autonomy of sensorimotor systems

Bassett, D. S., Yang, M., Wymbs, N. F., & Grafton, S. T. (2015) · Nature Neuroscience · doi:10.1038/nn.3993 · Cited by 603

Prospective longitudinal atrophy in Alzheimer’s disease correlates with the intensity and topography of baseline tau-PET

La Joie, R., Visani, A. V., Baker, S. L., Brown, J. A., Bourakova, V., Cha, J., Chaudhary, K., Edwards, L., Iaccarino, L., Janabi, M., et al. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.aau5732 · Cited by 612

Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis

Rohrer, J. D., Nicholas, J. M., Cash, D. M., van Swieten, J., Dopper, E., Jiskoot, L., van Minkelen, R., Rombouts, S. A., Cardoso, M. J., Clegg, S., et al. (2015) · The Lancet Neurology · doi:10.1016/s1474-4422(14)70324-2 · Cited by 538

Functional gradients of the cerebellum

Guell, X., Schmahmann, J. D., Gabrieli, J. D., & Ghosh, S. S. (2018) · eLife · doi:10.7554/elife.36652 · Cited by 472

Comprehensive cellular‐resolution atlas of the adult human brain

Ding, S., Royall, J. J., Sunkin, S. M., Ng, L., Facer, B. A. C., Lesnar, P., Guillozet‐Bongaarts, A., McMurray, B., Szafer, A., Dolbeare, T. A., et al. (2016) · Journal of Comparative Neurology · doi:10.1002/cne.24080 · Cited by 447

Microglial activation and tau propagate jointly across Braak stages

Pascoal, T. A., Benedet, A. L., Ashton, N. J., Kang, M. S., Therriault, J., Chamoun, M., Savard, M., Lussier, F. Z., Tissot, C., Karikari, T. K., et al. (2021) · Nature Medicine · doi:10.1038/s41591-021-01456-w · Cited by 490

Cognitive Network Neuroscience

Medaglia, J. D., Lynall, M.-E., & Bassett, D. S. (2015) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00810 · Cited by 419

Altered cerebellar connectivity in autism and cerebellar-mediated rescue of autism-related behaviors in mice

Stoodley, C. J., D’Mello, A. M., Ellegood, J., Jakkamsetti, V., Liu, P., Nebel, M. B., Gibson, J. M., Kelly, E., Meng, F., Cano, C. A., et al. (2017) · Nature Neuroscience · doi:10.1038/s41593-017-0004-1 · Cited by 387

Biomarker modeling of Alzheimer’s disease using PET-based Braak staging

Therriault, J., Pascoal, T. A., Lussier, F. Z., Tissot, C., Chamoun, M., Bezgin, G., Servaes, S., Benedet, A. L., Ashton, N. J., Karikari, T. K., et al. (2022) · Nature Aging · doi:10.1038/s43587-022-00204-0 · Cited by 308

Universal transform or multiple functionality? Understanding the contribution of the human cerebellum across task domains

Diedrichsen, J., King, M., Hernandez-Castillo, C., Sereno, M., & Ivry, R. B. (2019) · Neuron · doi:10.1016/j.neuron.2019.04.021 · Cited by 281

Cerebellar gray matter and lobular volumes correlate with core autism symptoms

D'Mello, A. M., Crocetti, D., Mostofsky, S. H., & Stoodley, C. J. (2015) · NeuroImage: Clinical · doi:10.1016/j.nicl.2015.02.007 · Cited by 281

Functional alignment with anatomical networks is associated with cognitive flexibility

Medaglia, J. D., Huang, W., Karuza, E. A., Kelkar, A., Thompson-Schill, S. L., Ribeiro, A., & Bassett, D. S. (2017) · Nature Human Behaviour · doi:10.1038/s41562-017-0260-9 · Cited by 223

Evolution of the cerebellar cortex: The selective expansion of prefrontal-projecting cerebellar lobules

Balsters, J. H., Cussans, E., Diedrichsen, J., Phillips, K. A., Preuss, T. M., Rilling, J. K., & Ramnani, N. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.045 · Cited by 241

Encoding of sensory prediction errors in the human cerebellum

Schlerf, J., Ivry, R. B., & Diedrichsen, J. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4504-11.2012 · Cited by 168

Disruption of thalamic functional connectivity is a neural correlate of dexmedetomidine-induced unconsciousness

Akeju, O., Loggia, M. L., Catana, C., Pavone, K. J., Vazquez, R., Rhee, J., Contreras Ramirez, V., Chonde, D. B., Izquierdo-Garcia, D., Arabasz, G., et al. (2014) · eLife · doi:10.7554/elife.04499 · Cited by 168

18F‐flortaucipir tau positron emission tomography distinguishes established progressive supranuclear palsy from controls and Parkinson disease: A multicenter study

Schonhaut, D. R., McMillan, C. T., Spina, S., Dickerson, B. C., Siderowf, A., Devous, M. D., Tsai, R., Winer, J., Russell, D. S., Litvan, I., et al. (2017) · Annals of Neurology · doi:10.1002/ana.25060 · Cited by 175

Meta-analysis of neural systems underlying placebo analgesia from individual participant fMRI data

Zunhammer, M., Spisák, T., Wager, T. D., Bingel, U., The Placebo Imaging Consortium, Atlas, L., Benedetti, F., Büchel, C., Choi, J. C., Colloca, L., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21179-3 · Cited by 171

Cerebellar transcranial magnetic stimulation: the role of coil geometry and tissue depth

Hardwick, R. M., Lesage, E., & Miall, R. C. (2014) · Brain Stimulation · doi:10.1016/j.brs.2014.04.009 · Cited by 169

The “What” and “When” of Self-Initiated Movements

Hoffstaedter, F., Grefkes, C., Zilles, K., & Eickhoff, S. B. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhr391 · Cited by 166

Functional segregation of the human dorsomedial prefrontal cortex

Eickhoff, S. B., Laird, A. R., Fox, P. T., Bzdok, D., & Hensel, L. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhu250 · Cited by 159

Functional neuroanatomy of peripheral inflammatory physiology: A meta-analysis of human neuroimaging studies

Kraynak, T. E., Marsland, A. L., Wager, T. D., & Gianaros, P. J. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.07.013 · Cited by 165

18F-flortaucipir (AV-1451) tau PET in frontotemporal dementia syndromes

Tsai, R. M., Bejanin, A., Lesman-Segev, O., LaJoie, R., Visani, A., Bourakova, V., O’Neil, J. P., Janabi, M., Baker, S., Lee, S. E., et al. (2019) · Alzheimer's Research & Therapy · doi:10.1186/s13195-019-0470-7 · Cited by 164

Evidence of a novel somatopic map in the human neocerebellum during complex actions

Schlerf, J. E., Verstynen, T. D., Ivry, R. B., & Spencer, R. M. C. (2010) · Journal of Neurophysiology · doi:10.1152/jn.01117.2009 · Cited by 155

Advanced MRI techniques to improve our understanding of experience-induced neuroplasticity

Tardif, C. L., Gauthier, C. J., Steele, C. J., Bazin, P.-L., Schäfer, A., Schaefer, A., Turner, R., & Villringer, A. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.08.047 · Cited by 127

Cerebellar asymmetry and its relation to cerebral asymmetry estimated by intrinsic functional connectivity

Wang, D., Buckner, R. L., & Liu, H. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00598.2012 · Cited by 124

Cerebellar contributions to visuomotor adaptation and motor sequence learning: an ALE meta-analysis

Bernard, J. A., & Seidler, R. D. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00027 · Cited by 122

The Role of Dopamine in Value-Based Attentional Orienting

Anderson, B. A., Kuwabara, H., Wong, D. F., Gean, E. G., Rahmim, A., Brašić, J. R., George, N., Frolov, B., Courtney, S. M., & Yantis, S. (2016) · Current Biology · doi:10.1016/j.cub.2015.12.062 · Cited by 118

Bridging the gap between functional and anatomical features of cortico-cerebellar circuits using meta-analytic connectivity modeling: Meta-Analytic Connectivity Modeling of Cortico-Cerebellar Circuits

Balsters, J. H., Laird, A. R., Fox, P. T., & Eickhoff, S. B. (2014) · Human Brain Mapping · doi:10.1002/hbm.22392 · Cited by 113

Cerebellar-motor dysfunction in schizophrenia and psychosis-risk: The importance of regional cerebellar analysis approaches

Bernard, J. A., & Mittal, V. A. (2014) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2014.00160 · Cited by 100

Metabolic and Haemodynamic Resting-State Connectivity of the Human Brain: A High-Temporal Resolution Simultaneous BOLD-FMRI and FDG-FPET Multimodality Study

Jamadar, S. D., Ward, P. G., Liang, E. X., Orchard, E. R., Chen, Z., & Egan, G. F. (2020) · doi:10.1101/2020.05.01.071662 · Cited by 98

Functional connectivity between the temporoparietal cortex and cerebellum in autism spectrum disorder

Igelström, K. M., Webb, T. W., & Graziano, M. S. A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw079 · Cited by 93

Same Genes, Different Brains: Neuroanatomical Differences Between Monozygotic Twins Discordant for Musical Training

de Manzano, Ö., & Ullén, F. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhx299 · Cited by 92

Mapping Human Laryngeal Motor Cortex during Vocalization

Eichert, N., Papp, D., Mars, R. B., & Watkins, K. E. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa182 · Cited by 89

Functional connectivity gradients as a common neural architecture for predictive processing in the human brain.

Katsumi, Y., Kamona, N., Zhang, J., Bunce, J. G., Hutchinson, J. B., Yarossi, M., Tunik, E., Quigley, K. S., Dickerson, B. C., & Barrett, L. F. (2021) · doi:10.1101/2021.09.01.456844 · Cited by 89

Correspondence of functional connectivity gradients across human isocortex, cerebellum, and hippocampus

(2023) · doi:10.1038/s42003-023-04796-0 · Cited by 89

The effects of trauma on brain and body: A unifying role for the midbrain periaqueductal gray

Terpou, B. A., Harricharan, S., McKinnon, M. C., Frewen, P., Jetly, R., & Lanius, R. A. (2019) · Journal of Neuroscience Research · doi:10.1002/jnr.24447 · Cited by 82

Activation of the cerebellar cortex and the dentate nucleus in a prism adaptation fMRI study

Küper, M., Wünnemann, M. J. S., Thürling, M., Stefanescu, R. M., Maderwald, S., Elles, H. G., Göricke, S., Ladd, M. E., & Timmann, D. (2014) · Human Brain Mapping · doi:10.1002/hbm.22274 · Cited by 81

Scaling of Neural Responses to Visual and Auditory Motion in the Human Cerebellum

Baumann, O., & Mattingley, J. B. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5661-09.2010 · Cited by 78

Longitudinal structural and metabolic changes in frontotemporal dementia

Bejanin, A., Tammewar, G., Marx, G., Cobigo, Y., Iaccarino, L., Kornak, J., Staffaroni, A. M., Dickerson, B. C., Boeve, B. F., Knopman, D. S., et al. (2020) · Neurology · doi:10.1212/wnl.0000000000009760 · Cited by 70

Intermittent theta burst stimulation of cerebellar vermis enhances fronto-cerebellar resting state functional connectivity in schizophrenia with predominant negative symptoms: A randomized controlled trial

Basavaraju, R., Ithal, D., Thanki, M. V., Ramalingaiah, A. H., Thirthalli, J., Reddy, R. P., Brady, R. O., Halko, M. A., Bolo, N. R., Keshavan, M. S., et al. (2021) · Schizophrenia Research · doi:10.1016/j.schres.2021.10.005 · Cited by 70

Tau PET imaging predicts cognition in atypical variants of Alzheimer's disease

Phillips, J. S., Das, S. R., McMillan, C. T., Irwin, D. J., Roll, E. E., Da Re, F., Nasrallah, I. M., Wolk, D. A., & Grossman, M. (2018) · Human Brain Mapping · doi:10.1002/hbm.23874 · Cited by 68

Poly(GP), neurofilament and grey matter deficits in C9orf72 expansion carriers

Meeter, L. H. H., Gendron, T. F., Sias, A. C., Jiskoot, L. C., Russo, S. P., Donker Kaat, L., Papma, J. M., Panman, J. L., van der Ende, E. L., Dopper, E. G., et al. (2018) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.559 · Cited by 61

Linking dopaminergic reward signals to the development of attentional bias: A positron emission tomographic study

Anderson, B. A., Kuwabara, H., Wong, D. F., Roberts, J., Rahmim, A., Brašić, J. R., & Courtney, S. M. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.05.062 · Cited by 55

The Sensory and Motor Components of the Cortical Hierarchy Are Coupled to the Rhythm of the Stomach during Rest

Rebollo, I., & Tallon-Baudry, C. (2022) · The Journal of Neuroscience · doi:10.1523/jneurosci.1285-21.2021 · Cited by 46

APOEε4 potentiates amyloid β effects on longitudinal tau pathology

Ferrari-Souza, J. P., Bellaver, B., Ferreira, P. C. L., Benedet, A. L., Povala, G., Lussier, F. Z., Leffa, D. T., Therriault, J., Tissot, C., Soares, C., et al. (2023) · Nature Aging · doi:10.1038/s43587-023-00490-2 · Cited by 43

Effects of Emotional Contexts on Cerebello-Thalamo-Cortical Activity during Action Observation

Mazzola, V., Vuilleumier, P., Latorre, V., Petito, A., Gallese, V., Popolizio, T., Arciero, G., & Bondolfi, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075912 · Cited by 34

Associations of perceived adverse lifetime experiences with brain structure in UK Biobank participants

Gheorghe, D. A., Li, C., Gallacher, J., & Bauermeister, S. (2021) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.13298 · Cited by 34

Deep Cerebellar Transcranial Direct Current Stimulation of the Dentate Nucleus to Facilitate Standing Balance in Chronic Stroke Survivors—A Pilot Study

Rezaee, Z., Kaura, S., Solanki, D., Dash, A., Srivastava, M. V. P., Lahiri, U., & Dutta, A. (2020) · Brain Sciences · doi:10.3390/brainsci10020094 · Cited by 31

The threatful self: midbrain functional connectivity to cortical midline and parietal regions during subliminal trauma-related processing in PTSD.

Terpou, B. A., Densmore, M., Théberge, J., Thome, J., Frewen, P., McKinnon, M. C., & Lanius, R. A. (2019) · Chronic Stress · doi:10.1177/2470547019871369 · Cited by 26

Cerebellar volume deficits in medication-naive obsessive compulsive disorder

Narayanaswamy, J. C., Jose, D., Kalmady, S. V., Agarwal, S. M., Venkatasubramanian, G., & Janardhan Reddy, Y. C. (2016) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2016.07.005 · Cited by 25

A dual larynx motor networks hypothesis

Belyk, M., Eichert, N., & McGettigan, C. (2021) · Philosophical Transactions of the Royal Society B · doi:10.1098/rstb.2020.0392 · Cited by 17

Early Adversity Affects Cerebellar Structure and Function—A Systematic Review of Human and Animal Studies

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

Theory of mind profile and cerebellar alterations in remitted bipolar disorder 1 and 2: a comparison study

Olivito, G., Lupo, M., Siciliano, L., Gragnani, A., Saettoni, M., Pancheri, C., Panfili, M., Pignatelli, F., Delle Chiaie, R., & Leggio, M. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.971244 · Cited by 12

Untitled work

(n.d.) · Progress in Neuro-Psychopharmacology and Biological Psychiatry / PsyPost · doi:10.1016/j.pnpbp.2026.111679