The application of nonlinear dynamic causal modelling for fMRI in subjects at high genetic risk of schizophrenia
Abstract
Nonlinear Dynamic Causal Modelling (DCM) for fMRI provides computational modelling of gating mechanisms at the neuronal population level. It allows for estimations of connection strengths with nonlinear modulation within task-dependent networks. This paper presents an application of nonlinear DCM in subjects at high familial risk of schizophrenia performing the Hayling Sentence Completion Task (HSCT). We analysed scans of 19 healthy controls and 46 subjects at high familial risk of schizophrenia, which included 26 high risk subjects without psychotic symptoms and 20 subjects with psychotic symptoms. The activity-dependent network consists of the intra parietal cortex (IPS), inferior frontal gyrus (IFG), middle temporal gyrus (MTG), anterior cingulate cortex (ACC) and the mediodorsal (MD) thalamus. The connections between the MD thalamus and the IFG were gated by the MD thalamus. We used DCM to investigate altered connection strength of these connections. Bayesian Model Selection (BMS) at the group and family level was used to compare the optimal bilinear and nonlinear models. Bayesian Model Averaging (BMA) was used to assess the connection strengths with the gating from the MD thalamus and the IFG. The nonlinear models provided the better explanation of the data. Furthermore, the BMA analysis showed significantly lower connection strength of the thalamocortical connection with nonlinear modulation from the MD thalamus in high risk subjects with psychotic symptoms and those who subsequently developed schizophrenia. These findings demonstrate that nonlinear DCM provides a method to investigate altered connectivity at the level of neural circuits. The reduced connection strength with thalamic gating may be a neurobiomarker implicated in the development of psychotic symptoms. This study suggests that nonlinear DCM could lead to new insights into functional and effective dysconnection at the network level in subjects at high familial risk.
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DCM studies in schizophrenia demonstrated differences in functional network architecture and effective connectivity compared to healthy controls across various tasks.
“These studies demonstrated differences in functional network architecture and effective connectivity compared to healthy controls across various tasks.”
From Can Bayesian Theories of Autism Spectrum Disorder Help Improve Clinical Practice? (2016) · cites this paper as [131]
Cites
Statistical Power Analysis for the Behavioral Sciences
Muller, K. E., & Cohen, J. (1989) · Technometrics · doi:10.2307/1270020 · Cited by 99,588 · see citing works
Statistical power analysis for the behavioral sciences
Cohen, J. (1990) · Computers Environment and Urban Systems · doi:10.1016/0198-9715(90)90050-4 · Cited by 65,406 · see citing works
An Introduction to the Bootstrap
Efron, B., & Tibshirani, R. J. (1994) · doi:10.1201/9780429246593 · Cited by 40,500 · see citing works
The Positive and Negative Syndrome Scale (PANSS) for schizophrenia.
Kay, S. R., Fiszbein, A., & Opler, L. A. (1987) · Schizophrenia Bulletin · doi:10.1093/schbul/13.2.261 · Cited by 21,378 · see citing works
Talairach, J., Tournoux, P., & Rayport, M. (1988) · Thieme eBooks · Cited by 5,058 · see citing works
Friston, K. J., Harrison, L., & Penny, W. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00202-7 · Cited by 4,583 · see citing works
Neurophysiological and Computational Principles of Cortical Rhythms in Cognition
Wang, X.-J. (2010) · Physiological Reviews · doi:10.1152/physrev.00035.2008 · Cited by 1,939 · see citing works
Moghaddam, B., Adams, B., Verma, A., & Daly, D. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-08-02921.1997 · Cited by 1,793 · see citing works
Synaptic depression and cortical gain control
Abbott, L. F., Varela, J. A., Sen, K., & Nelson, S. B. (1997) · Science · doi:10.1126/science.275.5297.221 · Cited by 1,690 · see citing works
Abbott, L. F., & Regehr, W. G. (2004) · Nature · doi:10.1038/nature03010 · Cited by 1,684 · see citing works
Bayesian model selection for group studies
Stephan, K. E., Penny, W. D., Daunizeau, J., Moran, R. J., & Friston, K. J. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.03.025 · Cited by 1,423 · see citing works
Sleep and arousal: thalamocortical mechanisms
McCormick, D. A., & Bal, T. (1997) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.20.1.185 · Cited by 1,267 · see citing works
An Introduction to the Bootstrap.
Kimber, A., Efron, B., & Tibshirani, R. J. (1994) · Journal of the Royal Statistical Society Series D (The Statistician) · doi:10.2307/2348146 · Cited by 1,246 · see citing works
Dysconnection in schizophrenia: from abnormal synaptic plasticity to failures of self-monitoring
Stephan, K. E., Friston, K. J., & Frith, C. D. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn176 · Cited by 1,134 · see citing works
McCormick, D. A. (1992) · Progress in Neurobiology · doi:10.1016/0301-0082(92)90012-4 · Cited by 1,117 · see citing works
Gain Modulation from Background Synaptic Input
Chance, F. S., Abbott, L. F., & Reyes, A. D. (2002) · Neuron · doi:10.1016/s0896-6273(02)00820-6 · Cited by 1,012 · see citing works
Multiple Roles of Calcium Ions in the Regulation of Neurotransmitter Release
Neher, E., & Sakaba, T. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.019 · Cited by 933 · see citing works
Glutamate and Schizophrenia: Beyond the Dopamine Hypothesis
Coyle, J. T. (2006) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-006-9062-8 · Cited by 917 · see citing works
The Emerging Role of Glutamate in the Pathophysiology and Treatment of Schizophrenia
GOFF, D. C., & Coyle, J. T. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.9.1367 · Cited by 914 · see citing works
Comparing dynamic causal models.
Penny, W. D., Stephan, K. E., Mechelli, A., & Friston, K. J. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.03.026 · Cited by 848 · see citing works
Synaptic plasticity and dysconnection in schizophrenia
Stephan, K. E., Baldeweg, T., & Friston, K. J. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.10.005 · Cited by 841 · see citing works
Comparing families of dynamic causal models
Penny, W. D., Stephan, K. E., Daunizeau, J., Rosa, M. J., Friston, K. J., Schofield, T. M., & Leff, A. P. (2010) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000709 · Cited by 688 · see citing works
Frith, C. D., Friston, K. J., Liddle, P. F., & Frackowiak, R. S. J. (1991) · Neuropsychologia · doi:10.1016/0028-3932(91)90029-8 · Cited by 656 · see citing works
Hypofrontality in schizophrenia: distributed dysfunctional circuits in neuroleptic-naïve patients
Andreasen, N. C., OʼLeary, D. S., Flaum, M. A., Nopoulos, P., Watkins, G. L., Ponto, L. L. B., & Hichwa, R. D. (1997) · The Lancet · doi:10.1016/s0140-6736(96)08258-x · Cited by 597 · see citing works
Krystal, J. H., D'Souza, D. C., Mathalon, D., Perry, E., Belger, A., & Hoffman, R. (2003) · Psychopharmacology · doi:10.1007/s00213-003-1582-z · Cited by 530 · see citing works
Lawrie, S. M., Buechel, C., Whalley, H. C., Frith, C. D., Friston, K. J., & Johnstone, E. C. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(02)01316-1 · Cited by 529 · see citing works
Impact of Correlated Synaptic Input on Output Firing Rate and Variability in Simple Neuronal Models
Salinas, E., & Sejnowski, T. J. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-16-06193.2000 · Cited by 472 · see citing works
Causal Modelling and Brain Connectivity in Functional Magnetic Resonance Imaging
Friston, K. J. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000033 · Cited by 439 · see citing works
Frith, C., Friston, K. J., Herold, S., Silbersweig, D., Fletcher, P. C., Cahill, C., Dolan, R. J., Frackowiak, R. S. J., & Liddle, P. F. (1995) · The British Journal of Psychiatry · doi:10.1192/bjp.167.3.343 · Cited by 424 · see citing works
Nonlinear dynamic causal models for fMRI
Stephan, K. E., Kasper, L., Harrison, L. M., Daunizeau, J., den Ouden, H. E. M., Breakspear, M., & Friston, K. J. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.04.262 · Cited by 416 · see citing works
Generalized and Specific Neurocognitive Deficits in Prodromal Schizophrenia
Lencz, T., Smith, C. W., McLaughlin, D., Auther, A. M., Nakayama, E. Y., Hovey, L. S., & Cornblatt, B. A. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.09.005 · Cited by 402 · see citing works
Neuroplasticity of Neocortical Circuits in Schizophrenia
Lewis, D. A., & González‐Burgos, G. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301563 · Cited by 362 · see citing works
Glutamate receptor dynamics in dendritic microdomains.
Newpher, T. M., & Ehlers, M. D. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.030 · Cited by 356 · see citing works
Schizophrenia and the disconnection hypothesis
Friston, K. J. (1999) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.1999.tb05985.x · Cited by 321 · see citing works
Barrages of Synaptic Activity Control the Gain and Sensitivity of Cortical Neurons
Shu, Y., Hasenstaub, A., Badoual, M., Bal, T., & McCormick, D. A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-32-10388.2003 · Cited by 298 · see citing works
Biophysical Mechanisms of Multistability in Resting-State Cortical Rhythms
Freyer, F., Roberts, J. A., Becker, R., Robinson, P. A., Ritter, P., & Breakspear, M. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6693-10.2011 · Cited by 289 · see citing works
Completion norms for 329 sentence contexts
Bloom, P. A., & Fischler, I. (1980) · Memory & Cognition · doi:10.3758/bf03213783 · Cited by 279 · see citing works
Emerging views of corticothalamic function
Briggs, F., & Usrey, W. M. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.09.002 · Cited by 268 · see citing works
Salinas, E., & B, T. J. S. A. (2001) · The Neuroscientist · doi:10.1177/107385840100700512 · Cited by 264 · see citing works
The thalamus and schizophrenia: current status of research
Byne, W. M., Hazlett, E. A., Buchsbaum, M. S., & Kemether, E. M. (2008) · Acta Neuropathologica · doi:10.1007/s00401-008-0404-0 · Cited by 250 · see citing works
Attenuated Frontal Activation During a Verbal Fluency Task in Patients With Schizophrenia
Curtis, V. A., Bullmore, E. T., Brammer, M. J., Wright, I. C., Williams, S., Morris, R. G., Sharma, T. S., Murray, R. M., & McGuire, P. K. (1998) · American Journal of Psychiatry · doi:10.1176/ajp.155.8.1056 · Cited by 249 · see citing works
Glutamatergic theories of schizophrenia.
Javitt, D. C. (2010) · PubMed · Cited by 248 · see citing works
Dose-finding trial of D-cycloserine added to neuroleptics for negative symptoms in schizophrenia
GOFF, D. C., Tsai, G. E., Manoach, D. S., & Coyle, J. T. (1995) · American Journal of Psychiatry · doi:10.1176/ajp.152.8.1213 · Cited by 243 · see citing works
Synaptic depression enables neuronal gain control
Rothman, J. S., Cathala, L., Steuber, V., & Silver, R. A. (2009) · Nature · doi:10.1038/nature07604 · Cited by 243 · see citing works
Kolluri, N., Sun, Z., Sampson, A. R., & Lewis, D. A. (2005) · American Journal of Psychiatry · doi:10.1176/appi.ajp.162.6.1200 · Cited by 241 · see citing works
Santana, N., Mengod, G., & Artigas, F. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn134 · Cited by 231 · see citing works
Alain Destexhe, A. (2009) · Journal of Computational Neuroscience · doi:10.1007/s10827-009-0164-4 · Cited by 231 · see citing works
Molecular Targets for Treating Cognitive Dysfunction in Schizophrenia
Gray, J. A., & Roth, B. L. (2007) · Schizophrenia Bulletin · doi:10.1093/schbul/sbm074 · Cited by 225 · see citing works
Cortical Development and Thalamic Pathology in Schizophrenia
Jones, E. G. (1997) · Schizophrenia Bulletin · doi:10.1093/schbul/23.3.483 · Cited by 223 · see citing works
Dynamic causal models of neural system dynamics: current state and future extensions
Stephan, K. E., Harrison, L. M., Kiebel, S. J., Olivier David, A., Penny, W. D., & Friston, K. J. (2007) · Journal of Biosciences · doi:10.1007/s12038-007-0012-5 · Cited by 222 · see citing works
Cognitive Functioning in the Schizophrenia Prodrome
Simon, A. E., Cattapan-Ludewig, K., Zmilacher, S., Arbach, D., Gruber, K., Dvorsky, D. N., Roth, B., Isler, E., Zimmer, A., & Umbricht, D. (2007) · Schizophrenia Bulletin · doi:10.1093/schbul/sbm018 · Cited by 220 · see citing works
Dynamic causal modelling for fMRI: A two-state model
Marreiros, A. C., Kiebel, S. J., & Friston, K. J. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.08.019 · Cited by 199 · see citing works
Variational Bayesian identification and prediction of stochastic nonlinear dynamic causal models
Jean Daunizeau, A., Friston, K. J., & Kiebel, S. J. (2009) · Physica D Nonlinear Phenomena · doi:10.1016/j.physd.2009.08.002 · Cited by 198 · see citing works
Generalised filtering and stochastic DCM for fMRI
Baojuan Li, A., Jean Daunizeau, A., Stephan, K. E., Penny, W. D., Hu, D., & Friston, K. J. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.01.085 · Cited by 198 · see citing works
A General Model of Synaptic Transmission and Short-Term Plasticity
Pan, B., & Zucker, R. S. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.025 · Cited by 195 · see citing works
Neuroplasticity signaling pathways linked to the pathophysiology of schizophrenia
Balu, D. T., & Coyle, J. T. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.10.005 · Cited by 182 · see citing works
Low-frequency BOLD fluctuations demonstrate altered thalamocortical connectivity in schizophrenia
Welsh, R. C., Chen, A. C., & Taylor, S. F. (2010) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn145 · Cited by 181 · see citing works
Generative embedding for model-based classification of fMRI data
Brodersen, K. H., Schofield, T. M., Leff, A. P., Ong, C. S., Lomakina, E. I., Buhmann, J. M., & Stephan, K. E. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002079 · Cited by 165 · see citing works
Fu, C. H. Y., Morgan, K. D., John Suckling, A., Williams, S., Andrew, C., Vythelingum, G. N., & McGuire, P. K. (2002) · NeuroImage · doi:10.1006/nimg.2002.1189 · Cited by 164 · see citing works
The Functional Anatomy of Inhibition Processes Investigated with the Hayling Task
Collette, F., der Linden, M. V., Delfiore, G., Degueldre, C., Luxen, A., & Salmon, É. (2001) · NeuroImage · doi:10.1006/nimg.2001.0846 · Cited by 162 · see citing works
Glutamatergic transmission in schizophrenia
Kantrowitz, J. T., & Javitt, D. C. (2012) · Current Opinion in Psychiatry · doi:10.1097/yco.0b013e32835035b2 · Cited by 155 · see citing works
Clinton, S., & Meador-Woodruff, J. (2004) · Schizophrenia Research · doi:10.1016/j.schres.2003.09.017 · Cited by 153 · see citing works
A 4.0-T fMRI study of brain connectivity during word fluency in first-episode schizophrenia
Boksman, K., Théberge, J., Williamson, P., Drost, D. J., MALLA, A. K., Densmore, M., Takhar, J., Pavlosky, W. F., Menon, R. S., & Neufeld, R. W. J. (2004) · Schizophrenia Research · doi:10.1016/j.schres.2004.09.025 · Cited by 144 · see citing works
Multiplicative Gain Changes Are Induced by Excitation or Inhibition Alone
Murphy, B. K., & Miller, K. D. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-31-10040.2003 · Cited by 144 · see citing works
fMRI correlates of state and trait effects in subjects at genetically enhanced risk of schizophrenia
Whalley, H. C. (2003) · Brain · doi:10.1093/brain/awh070 · Cited by 143 · see citing works
Self-citationThe functional anatomy of verbal initiation and suppression using the Hayling Test.
Nathaniel-James, D., Fletcher, P. C., & Frith, C. (1997) · Neuropsychologia · doi:10.1016/s0028-3932(96)00104-2 · Cited by 142 · see citing works
Johnstone, E. C. (2000) · Schizophrenia Research · doi:10.1016/s0920-9964(99)00225-x · Cited by 137 · see citing works
Self-citationROMANIDES, A., Duffy, P., & Kalivas, P. W. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00747-7 · Cited by 136 · see citing works
Functional disconnectivity in subjects at high genetic risk of schizophrenia
Whalley, H. C., Simonotto, E., Marshall, I., Owens, D. G. C., Goddard, N., Johnstone, E. C., & Lawrie, S. M. (2005) · Brain · doi:10.1093/brain/awh556 · Cited by 134 · see citing works
Self-citationNathaniel-James, D., & Frith, C. (2002) · NeuroImage · doi:10.1006/nimg.2002.1167 · Cited by 131 · see citing works
Abnormal Glucose Metabolism in the Mediodorsal Nucleus of the Thalamus in Schizophrenia
Hazlett, E. A., Buchsbaum, M. S., Kemether, E. M., Bloom, R. F., Platholi, J., Brickman, A. M., Shihabuddin, L., Tang, C. Y., & Byne, W. M. (2004) · American Journal of Psychiatry · doi:10.1176/appi.ajp.161.2.305 · Cited by 121 · see citing works
Harris, J. M., Moorhead, T. W. J., Miller, P., McIntosh, A. M., Bonnici, H. M., Owens, D. G. C., Johnstone, E. C., & Lawrie, S. M. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.11.027 · Cited by 119 · see citing works
Self-citationPeople at risk of schizophrenia
Hodges, A., Byrne, M., Grant, L., & Johnstone, E. C. (1999) · The British Journal of Psychiatry · doi:10.1192/bjp.174.6.547 · Cited by 118 · see citing works
Self-citationFusar‐Poli, P. (2011) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2011.46 · Cited by 117 · see citing works
Dysfunctional Thalamus-Related Networks in Schizophrenia
Pinault, D. (2011) · Schizophrenia Bulletin · doi:10.1093/schbul/sbq165 · Cited by 105 · see citing works
An Integrated Microcircuit Model of Attentional Processing in the Neocortex
Ardid, S., Wang, X., & Compte, A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1145-07.2007 · Cited by 105 · see citing works
Molecular Abnormalities of the Glutamate Synapse in the Thalamus in Schizophrenia
Meador‐Woodruff, J. H., Clinton, S. M., Beneyto, M., & McCullumsmith, R. E. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1300.005 · Cited by 101 · see citing works
Thermenos, H. W., Seidman, L. J., Breiter, H., Goldstein, J. M., Goodman, J. M., Poldrack, R. A., Faraone, S. V., & Tsuang, M. T. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2003.11.014 · Cited by 100 · see citing works
Cingulate activity and fronto-temporal connectivity in people with prodromal signs of psychosis
Allen, P., Stephan, K., Mechelli, A., Day, F., Ward, N., Dalton, J., Williams, S. C. R., & McGuire, P. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.08.038 · Cited by 92 · see citing works
Thalamo‐frontal white matter alterations in chronic schizophrenia
Oh, J. S., Kubicki, M. R., Rosenberger, G., Sylvain Bouix, A., Levitt, J. J., McCarley, R. W., Westin, C., & Shenton, M. E. (2009) · Human Brain Mapping · doi:10.1002/hbm.20809 · Cited by 84 · see citing works
Seghier, M. L., Josse, G., Leff, A. P., & Price, C. J. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq203 · Cited by 79 · see citing works
The mediodorsal thalamic nucleus and schizophrenia
Alelú‐Paz, R., & Giménez‐Amaya, J. M. (2008) · Journal of Psychiatry and Neuroscience · doi:10.1139/jpn.0846 · Cited by 75 · see citing works
Beyond the dopamine receptor: novel therapeutic targets for treating schizophrenia
Coyle, J. T., Balu, D. T., Benneyworth, M. A., Basu, A. C., & Roseman, A. S. (2010) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2010.12.3/jcoyle · Cited by 75 · see citing works
Synapses with short-term plasticity are optimal estimators of presynaptic membrane potentials
Pfister, J.-P., Dayan, P., & Lengyel, M. (2010) · Nature Neuroscience · doi:10.1038/nn.2640 · Cited by 74 · see citing works
Catching up on schizophrenia: natural history and neurobiology.
Lewis, D. A., & Lieberman, J. A. (2000) · Neuron · doi:10.1016/s0896-6273(00)00111-2 · Cited by 71 · see citing works
Stochastic Differential Equation Model for Cerebellar Granule Cell Excitability
Saarinen, A. J., Linne, M., & Yli-Harja, O. P. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000004 · Cited by 71 · see citing works
Kiss, T., Hoffmann, W. E., Scott, L., Kawabe, T. T., Milici, A. J., Nilsen, E. A., & Hajós, M. (2011) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2011.00014 · Cited by 70 · see citing works
The diverse functions of short-term plasticity components in synaptic computations
Deng, P., & Klyachko, V. A. (2011) · Communicative & Integrative Biology · doi:10.4161/cib.15870 · Cited by 69 · see citing works
Excess of Neurons in the Human Newborn Mediodorsal Thalamus Compared with That of the Adult
Abitz, M., Nielsen, R., Jones, E. G., Laursen, H. B., Græm, N., & Pakkenberg, B. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl163 · Cited by 66 · see citing works
Fronto-temporal Interactions during Overt Verbal Initiation and Suppression
Allen, P., Mechelli, A., Stephan, K., Day, F., Dalton, J., Williams, S. C. R., & McGuire, P. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.20107 · Cited by 57 · see citing works
Glutamatergic abnormalities of the thalamus in schizophrenia: a systematic review
Watis, L., Chen, S. H., Chua, H.-C., Chong, S. A., & Sim, K. (2008) · Journal of Neural Transmission · doi:10.1007/s00702-007-0859-5 · Cited by 56 · see citing works
Mitelman, S. A., Brickman, A. M., Shihabuddin, L., et al. (2004) · Schizophrenia Research · doi:10.1016/j.schres.2004.10.014 · Cited by 54 · see citing works
Pakkenberg, B., Scheel‐Krüger, J., & Kristiansen, L. V. (2009) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.2009.01447.x · Cited by 52 · see citing works
Sodhi, M., Simmons, M. S., McCullumsmith, R. E., Haroutunian, V. H., & Meador‐Woodruff, J. H. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.02.022 · Cited by 52 · see citing works
Dauvermann, M. R., Mukherjee, P., Moorhead, W. T., Stanfield, A. C., Fusar‐Poli, P., Lawrie, S. M., & Whalley, H. C. (2012) · Current Pharmaceutical Design · doi:10.2174/138161212799316235 · Cited by 47 · see citing works
Self-citationLee, C.-M. J., Chang, W., Chang, K., & Shyu, B. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05485.x · Cited by 44 · see citing works
State-Dependent Firing Determines Intrinsic Dendritic Ca2+Signaling in Thalamocortical Neurons
Errington, A. C., Renger, J. J., Uebele, V. N., & Crunelli, V. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2968-10.2010 · Cited by 42 · see citing works
Local Dendrodendritic Inhibition Regulates Fast Synaptic Transmission in Visual Thalamus
Crandall, S. R., & Cox, C. L. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4402-11.2012 · Cited by 33 · see citing works
Augustinaite, S., & Heggelund, P. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.131540 · Cited by 30 · see citing works
Négyessy, L., & Goldman-Rakic, P. S. (2005) · Experimental Brain Research · doi:10.1007/s00221-005-2237-6 · Cited by 30 · see citing works
Onn, S., & Wang, X. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04122.x · Cited by 29 · see citing works
Receptor saturation controls short-term synaptic plasticity at corticothalamic synapses
Sun, Y.-G., & Beierlein, M. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00942.2010 · Cited by 24 · see citing works
The Edinburgh High Risk Study: current status and future prospects.
Johnstone, E. C., Russell, K. D., Harrison, L. K., et al. (2003) · PubMed · Cited by 22 · see citing works
Self-citationVolman, V., Levine, H., & B, T. J. S. A. (2010) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000973 · Cited by 14 · see citing works
Javitt, D. C., Frusciante, M. J., & Zukin, S. R. (1994) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)22395-3 · Cited by 7 · see citing works
The Effect of NMDA Receptors on Gain Modulation
Berends, M., Maex, R., & Schutter, E. D. (2005) · Neural Computation · doi:10.1162/089976605774320520 · Cited by 7 · see citing works
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Computational approaches to psychiatry
Stephan, K. E., & Mathys, C. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.12.007 · Cited by 260 · see citing works
Can Bayesian Theories of Autism Spectrum Disorder Help Improve Clinical Practice?
Haker, H., Schneebeli, M., & Stephan, K. E. (2016) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2016.00107 · Cited by 130 · see citing works
Charting the landscape of priority problems in psychiatry, part 2: pathogenesis and aetiology
Stephan, K. E., Binder, E. B., Breakspear, M., Dayan, P., Johnstone, E. C., Meyer-Lindenberg, A., Schnyder, U., Wang, X.-J., Bach, D. R., Fletcher, P. C., et al. (2016) · The Lancet Psychiatry · doi:10.1016/s2215-0366(15)00360-0 · Cited by 64 · see citing works
Self-citationOculomotor prediction: A window into the psychotic mind
Thakkar, K. N., Diwadkar, V. A., & Rolfs, M. (2017) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2017.02.001 · Cited by 66 · see citing works
- Authors
- Dauvermann, M. R., Whalley, H. C., Romaniuk, L., Valton, V., Owens, D. G. C., Johnstone, E. C., Lawrie, S. M., & Moorhead, T. W. J.
- Affiliations
- Royal Edinburgh Hospital (GB)
- University of Edinburgh (GB)
- Corresponding author
- Dauvermann, Maria R.
- ORCID
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2013-06
- Volume
- 73
- Pages
- 16-29
- ISSN
- 1053-8119 (ISSN-L)
- OpenAlex
- W2043735337
- Cited by
- 49
- References
- 106
- Citations by year
- 2025: 1 · 2024: 1 · 2023: 4 · 2022: 1 · 2021: 4 · 2020: 1 · 2019: 2 · 2018: 2 · 2017: 7 · 2016: 7 · 2015: 5 · 2014: 7 · 2013: 7
- FWCI
- 4.73
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Research Portal (King's College London) (submittedVersion)
- University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
- Funders
- Dr Mortimer and Theresa Sackler Foundation
- Dorothy Hodgkin Fellowship from the Royal Society (DH080018)
- EPSRC
- BBSRC
- MRC
- TMRC
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- schizophrenia, familial risk, high genetic risk, mediodorsal thalamus, inferior frontal gyrus, thalamocortical connections, nonlinear modulation, Bayesian model averaging, Bayesian model selection, psychotic symptoms, neurobiomarkers, effective connectivity
- MeSH terms
- Adolescent, Algorithms, Bayes Theorem, Brain, Delusions, Female, Hallucinations, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Male, Models, Neurological, Neural Pathways, Neuronal Plasticity, Psychomotor Performance, Risk, Schizophrenia, Schizophrenic Psychology, Thalamus, Linear Models, Nonlinear Dynamics, Genetic Predisposition to Disease, Young Adult
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.
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