Skip to content
naulon

No retraction, correction or concern found when last checked on Nov 1, 2026.

TAPAS: An Open-Source Software Package for Translational Neuromodeling and Computational Psychiatry

Stefan Frässle, Eduardo A. Aponte, Saskia Bollmann and 18 more

Frontiers in Psychiatry · 2021 · Review · CC BY

doi:10.3389/fpsyt.2021.680811

Abstract

Psychiatry faces fundamental challenges with regard to mechanistically guided differential diagnosis, as well as prediction of clinical trajectories and treatment response of individual patients. This has motivated the genesis of two closely intertwined fields: (i) Translational Neuromodeling (TN), which develops “computational assays” for inferring patient-specific disease processes from neuroimaging, electrophysiological, and behavioral data; and (ii) Computational Psychiatry (CP), with the goal of incorporating computational assays into clinical decision making in everyday practice. In order to serve as objective and reliable tools for clinical routine, computational assays require end-to-end pipelines from raw data (input) to clinically useful information (output). While these are yet to be established in clinical practice, individual components of this general end-to-end pipeline are being developed and made openly available for community use. In this paper, we present the T ranslational A lgorithms for P sychiatry- A dvancing S cience (TAPAS) software package, an open-source collection of building blocks for computational assays in psychiatry. Collectively, the tools in TAPAS presently cover several important aspects of the desired end-to-end pipeline, including: (i) tailored experimental designs and optimization of measurement strategy prior to data acquisition, (ii) quality control during data acquisition, and (iii) artifact correction, statistical inference, and clinical application after data acquisition. Here, we review the different tools within TAPAS and illustrate how these may help provide a deeper understanding of neural and cognitive mechanisms of disease, with the ultimate goal of establishing automatized pipelines for predictions about individual patients. We hope that the openly available tools in TAPAS will contribute to the further development of TN/CP and facilitate the translation of advances in computational neuroscience into clinically relevant computational assays.

References 230

  1. 1.

    American Psychiatric Association. (2013 ). Diagnostic and Statistical Manual of Mental Disorders (DSM-5 R). Arlington, VA: American Psychiatric Publishing.

    Not in our library10.1176/appi.journals.9780890425596

  2. 2.

    World Health Organization (1990). International Classification of Diseases. Geneva: World Health Organization Press.

    Not in our library

  3. 3.

    Cuthbert B Insel T. Toward new approaches to psychotic disorders: the NIMH research domain criteria project. Schizophrenia Bull. (2010 ) 36:1061–2.

    Not in our library10.1093/schbul/sbq108

  4. 4.

    Kapur S Phillips AG Insel TR. Why has it taken so long for biological psychiatry to develop clinical tests and what to do about it? Mol Psychiatry. (2012 ) 17:1174–9.

    Not in our library10.1038/mp.2012.105

  5. 5.

    Krystal JH State MW. Psychiatric disorders: diagnosis to therapy. Cell. (2014 ) 157:201–14.

    Not in our library10.1016/j.cell.2014.02.042

  6. 6.

    Owen MJ. New approaches to psychiatric diagnostic classification. Neuron. (2014 ) 84:564–71.

    Not in our library10.1016/j.neuron.2014.10.028

  7. 7.

    Stephan KE Bach DR Fletcher PC Flint J Frank MJ Friston KJ. Charting the landscape of priority problems in psychiatry, part 1: classification and diagnosis. Lancet Psychiatry. (2016 ) 3:77–83.

    Not in our library10.1016/s2215-0366(15)00361-2

  8. 8.

    Stephan KE Binder EB Breakspear M Dayan P Johnstone EC Meyer-Lindenberg A. Charting the landscape of priority problems in psychiatry, part 2: pathogenesis and aetiology. Lancet Psychiatry. (2016 ) 3:84–90.

    Not in our library10.1016/s2215-0366(15)00360-0

  9. 9.

    Moran RJ Jung F Kumagai T Endepols H Graf R Dolan RJ. Dynamic causal models and physiological inference: a validation study using isoflurane anaesthesia in rodents. PLoS ONE. (2011 ) 6:e22790.

    Not in our library10.1371/journal.pone.0022790

  10. 10.

    Deco G Kringelbach ML. Great expectations: using whole-brain computational connectomics for understanding neuropsychiatric disorders. Neuron. (2014 ) 84:892–905.

    Not in our library10.1016/j.neuron.2014.08.034

  11. 11.

    Gilbert JR Symmonds M Hanna MG Dolan RJ Friston KJ Moran RJ. Profiling neuronal ion channelopathies with non-invasive brain imaging and dynamic causal models: Case studies of single gene mutations. Neuroimage. (2016 ) 124:43–53.

    Not in our library10.1016/j.neuroimage.2015.08.057

  12. 12.

    Symmonds M Moran CH Leite MI Buckley C Irani SR Stephan KE. Ion channels in EEG: isolating channel dysfunction in NMDA receptor antibody encephalitis. Brain. (2018 ) 141:1691–702.

    Not in our library10.1093/brain/awy107

  13. 13.

    Frässle S Yao Y Schöbi D Aponte EA Heinzle J Stephan KE. Generative models for clinical applications in computational psychiatry. Wiley Interdiscip Rev Cogn Sci. (2018 ) 9:e1460.

    Not in our library10.1002/wcs.1460

  14. 14.

    Adams NE Hughes LE Phillips HN Shaw AD Murley AG Nesbitt D. GABA-ergic dynamics in human frontotemporal networks confirmed by pharmaco-magnetoencephalography. J. Neurosci. (2020 ) 40:1640–9.

    Not in our library10.1523/jneurosci.1689-19.2019

  15. 15.

    Maia T Frank M. From reinforcement learning models to psychiatric and neurological disorders. Nat Neurosci. (2011 ) 14:154–62.

    Not in our library10.1038/nn.2723

  16. 16.

    Stephan K Mathys C. Computational approaches to psychiatry. Curr Opin Neurobiol. (2014 ) 25:85–92.

    Not in our library10.1016/j.conb.2013.12.007

  17. 17.

    Iglesias S Tomiello S Schneebeli M Stephan KE. Models of neuromodulation for computational psychiatry. Wiley Interdiscip Rev Cogn Sci. (2016 ) 8:e1420.

    Not in our library10.1002/wcs.1420

  18. 18.

    Lawson RP Mathys C Rees G. Adults with autism overestimate the volatility of the sensory environment. Nat Neurosci. (2017 ) 20:1293–9.

    Not in our library10.1038/nn.4615

  19. 19.

    Powers AR Mathys C Corlett PR. Pavlovian conditioning-induced hallucinations result from overweighting of perceptual priors. Science. (2017 ) 357:596–600.

    Not in our library10.1126/science.aan3458

  20. 20.

    Cole DM Diaconescu AO Pfeiffer UJ Brodersen KH Mathys CD Julkowski D. Atypical processing of uncertainty in individuals at risk for psychosis. Neuroimage Clin. (2020 ) 26:102239.

    Not in our library10.1016/j.nicl.2020.102239

  21. 21.

    Jirsa VK Sporns O Breakspear M Deco G McIntosh AR. Towards the virtual brain: network modeling of the intact and the damaged brain. Arch Ital Biol. (2010 ) 148:189–205.

    Not in our library10.4449/aib.v148i3.1223

  22. 22.

    Montague P Dolan R Friston K Dayan P. Computational psychiatry. Trends Cogn Sci. (2012 ) 16:72–80.

    Not in our library10.1016/j.tics.2011.11.018

  23. 23.

    Friston KJ Stephan KE Montague R Dolan RJ. Computational psychiatry: the brain as a phantastic organ. Lancet Psychiatry. (2014 ) 1:148–58.

    Not in our library10.1016/s2215-0366(14)70275-5

  24. 24.

    Wang XJ Krystal JH. Computational psychiatry. Neuron. (2014 ) 84:638–54.

    Not in our library10.1016/j.neuron.2014.10.018

  25. 25.

    Stephan KE Iglesias S Heinzle J Diaconescu AO. Translational perspectives for computational neuroimaging. Neuron. (2015 ) 87:716–32.

    Not in our library10.1016/j.neuron.2015.07.008

  26. 26.
  27. 27.

    Huys QJ Maia TV Frank MJ. Computational psychiatry as a bridge from neuroscience to clinical applications. Nat Neurosci. (2016 ) 19:404–13.

    Not in our library10.1038/nn.4238

  28. 28.

    Paulus MP Huys QJ Maia TV. A roadmap for the development of applied computational psychiatry. Biol Psychiatry Cogn Neurosci Neuroimaging. (2016 ) 1:386–92.

    Not in our library10.1016/j.bpsc.2016.05.001

  29. 29.

    Browning M Carter CS Chatham C Den Ouden H Gillan CM Baker JT. Realizing the clinical potential of computational psychiatry: report from the Banbury Center Meeting, February 2019. Biol Psychiatry. (2020 ) 88:e5–e10.

    Not in our library10.1016/j.biopsych.2019.12.026

  30. 30.
  31. 31.

    Stephan K Baldeweg T Friston K. Synaptic plasticity and dysconnection in schizophrenia. Biol Psychiatry. (2006 ) 59:929–39.

    Not in our library10.1016/j.biopsych.2005.10.005

  32. 32.

    Friston KJ Ashburner JT Kiebel SJ Nichols TE Penny WD. (2006 ) Statistical Parametric Mapping: the Analysis of Functional Brain Images. Burlington: Elsevier.

    Not in our library

  33. 33.

    Smith SM Jenkinson M Woolrich MW Beckmann CF Behrens TEJ Johansen-Berg H. Advances in functional and structural MR image analysis and implementation as FSL. Neuroimage. (2004 ) 23:S208–19.

    Not in our library10.1016/j.neuroimage.2004.07.051

  34. 34.

    Cox RW. AFNI: software for analysis and visualization of functional magnetic resonance neuroimages. Comput Biomed Res. (1996 ) 29:162–73.

    Not in our library10.1006/cbmr.1996.0014

  35. 35.
  36. 36.
  37. 37.

    Helske J. KFAS: exponential family state space models in R. J Statistical Software. (2017 ) 78:1–39.

    Not in our library10.18637/jss.v078.i10

  38. 38.

    Yousefi A Paulk AC Basu I Mirsky JL Dougherty DD Eskandar EN. COMPASS: an open-source, general-purpose software toolkit for computational psychiatry. Front Neurosci. (2018 ) 12:957.

    Not in our library10.1101/377556

  39. 39.
  40. 40.

    Maxwell SE. The persistence of underpowered studies in psychological research: causes, consequences, and remedies. Psychol Methods. (2004 ) 9:147–63.

    Not in our library10.1037/1082-989x.9.2.147

  41. 41.

    Carter CS Perlstein W Ganguli R Brar J Mintun M Cohen JD. Functional hypofrontality and working memory dysfunction in schizophrenia. Am J Psychiatry. (1998 ) 155:1285–7.

    Not in our library10.1176/ajp.155.9.1285

  42. 42.

    Van Snellenberg JX Torres IJ Thornton AE. Functional neuroimaging of working memory in schizophrenia: task performance as a moderating variable. Neuropsychology. (2006 ) 20:497–510.

    Not in our library10.1037/0894-4105.20.5.497

  43. 43.

    Van Horn JD Grethe JS Kostelec P Woodward JB Aslam JA Rus D. The Functional Magnetic Resonance Imaging Data Center (fMRIDC): the challenges and rewards of large-scale databasing of neuroimaging studies. Philos Trans R Soc Lond B Biol Sci. (2001 ) 356:1323–39.

    Not in our library10.1098/rstb.2001.0916

  44. 44.

    Poline JB Breeze JL Ghosh S Gorgolewski K Halchenko YO Hanke M. Data sharing in neuroimaging research. Front Neuroinform. (2012 ) 6:9.

    Not in our library10.3389/fninf.2012.00009

  45. 45.

    Poldrack RA Gorgolewski KJ. Making big data open: data sharing in neuroimaging. Nat Neurosci. (2014 ) 17:1510–7.

    Not in our library10.1038/nn.3818

  46. 46.

    Van Essen DC Smith SM Barch DM Behrens TEJ Yacoub E Ugurbil K. The WU-minn human connectome project: an overview. Neuroimage. (2013 ) 80:62–79.

    Not in our library10.1016/j.neuroimage.2013.05.041

  47. 47.

    Petzschner FH Weber LA Wellstein KV Paolini G Do CT Stephan KE. Focus of attention modulates the heartbeat evoked potential. Neuroimage. (2019 ) 186:595–606.

    Not in our library10.1016/j.neuroimage.2018.11.037

  48. 48.

    Khalsa SS Adolphs R Cameron OG Critchley HD Davenport PW Feinstein JS. Interoception and mental health: a roadmap. Biol Psychiatry Cogn Neurosci Neuroimaging. (2018 ) 3:501–13.

    Not in our library10.1016/j.bpsc.2017.12.004

  49. 49.

    Poser BA Setsompop K. Pulse sequences and parallel imaging for high spatiotemporal resolution MRI at ultra-high field. Neuroimage. (2018 ) 168:101–18.

    Not in our library10.1016/j.neuroimage.2017.04.006

  50. 50.

    Bollmann S Barth M. New acquisition techniques and their prospects for the achievable resolution of fMRI. Prog Neurobiol. (2020 ) 101936.

    Not in our library10.1016/j.pneurobio.2020.101936

  51. 51.

    Weldon KB Olman CA. Forging a path to mesoscopic imaging success with ultra-high field functional magnetic resonance imaging. Philos Trans R Soc Lond B Biol Sci. (2021 ) 376:20200040.

    Not in our library10.1098/rstb.2020.0040

  52. 52.

    Bellon EM Haacke EM Coleman PE Sacco DC Steiger DA Gangarosa RE. MR artifacts: a review. AJR Am J Roentgenol. (1986 ) 147:1271–81.

    Not in our library10.2214/ajr.147.6.1271

  53. 53.

    Kirilina E Lutti A Poser BA Blankenburg F Weiskopf N. The quest for the best: The impact of different EPI sequences on the sensitivity of random effect fMRI group analyses. Neuroimage. (2016 ) 126:49–59.

    Not in our library10.1016/j.neuroimage.2015.10.071

  54. 54.

    Bright MG Murphy K. Cleaning up the fMRI time series: mitigating noise with advanced acquisition and correction strategies. Neuroimage. (2017 ) 154:1–3.

    Not in our library10.1016/j.neuroimage.2017.03.056

  55. 55.

    Volz S Callaghan MF Josephs O Weiskopf N. Maximising BOLD sensitivity through automated EPI protocol optimisation. Neuroimage. (2019 ) 189:159–70.

    Not in our library10.1016/j.neuroimage.2018.12.052

  56. 56.

    Bollmann S Kasper L Pruessmann KP Barth M Stephan KE. Interactive and flexible quality control in fMRI sequence evaluation: the uniQC toolbox. In: 26th Annual Meeting of the International Society for Magnetic Resonance Imaging in Medicine. Paris (2018 ). p. 2842. Available online at: https://archive.ismrm.org/2018/2842.html

    Not in our library

  57. 57.

    Hesselmann V Girnus R Wedekind C Hunsche S Bunke J Schulte O. Functional MRI using multiple receiver coils: BOLD signal changes and signal-to-noise ratio for three-dimensional-PRESTO vs. single shot EPI in comparison to a standard quadrature head coil. J Magn Reson Imaging. (2004 ) 20:321–6.

    Not in our library10.1002/jmri.20101

  58. 58.

    Posse S Wiese S Gembris D Mathiak K Kessler C Grosse-Ruyken ML. Enhancement of BOLD-contrast sensitivity by single-shot multi-echo functional MR imaging. Magn Reson Med. (1999 ) 42:87–97.

    Not in our library10.1002/(sici)1522-2594(199907)42:1<87::aid-mrm13>3.0.co;2-o

  59. 59.

    Poser BA Versluis MJ Hoogduin JM Norris DG. BOLD contrast sensitivity enhancement and artifact reduction with multiecho EPI: parallel-acquired inhomogeneity-desensitized fMRI. Magn Reson Med. (2006 ) 55:1227–35.

    Not in our library10.1002/mrm.20900

  60. 60.

    Menon RS. Postacquisition suppression of large-vessel BOLD signals in high-resolution fMRI. Magn Reson Med. (2002 ) 47:1–9.

    Not in our library10.1002/mrm.10041

  61. 61.

    Rowe DB. Parameter estimation in the magnitude-only and complex-valued fMRI data models. Neuroimage. (2005 ) 25:1124–32.

    Not in our library10.1016/j.neuroimage.2004.12.048

  62. 62.

    Kundu P Voon V Balchandani P Lombardo MV Poser BA Bandettini PA. Multi-echo fMRI: a review of applications in fMRI denoising and analysis of BOLD signals. Neuroimage. (2017 ) 154:59–80.

    Not in our library10.1016/j.neuroimage.2017.03.033

  63. 63.

    Huber L Handwerker DA Jangraw DC Chen G Hall A Stuber C. High-Resolution CBV-fMRI allows mapping of laminar activity and connectivity of cortical input and output in human M1. Neuron. (2017 ) 96:1253–63 e1257.

    Not in our library10.1016/j.neuron.2017.11.005

  64. 64.

    Lu H Hua J van Zijl. P. C. Noninvasive functional imaging of cerebral blood volume with vascular-space-occupancy (VASO) MRI. NMR Biomed. (2013 ) 26:932–48.

    Not in our library10.1002/nbm.2905

  65. 65.

    Alsop DC Detre JA Golay X Gunther M Hendrikse J Hernandez-Garcia L. Recommended implementation of arterial spin-labeled perfusion MRI for clinical applications: a consensus of the ISMRM perfusion study group and the European consortium for ASL in dementia. Magn Reson Med. (2015 ) 73:102–16.

    Not in our library10.1002/mrm.25197

  66. 66.

    Koretsky AP. Early development of arterial spin labeling to measure regional brain blood flow by MRI. Neuroimage. (2012 ) 62:602–7.

    Not in our library10.1016/j.neuroimage.2012.01.005

  67. 67.

    Glover GH Li TQ Ress D. Image-based method for retrospective correction of physiological motion effects in fMRI: RETROICOR. Magn Reson Med. (2000 ) 44:162–7.

    Not in our library10.1002/1522-2594(200007)44:1<162::aid-mrm23>3.0.co;2-e

  68. 68.

    Kruger G Glover GH. Physiological noise in oxygenation-sensitive magnetic resonance imaging. Magn Reson Med. (2001 ) 46:631–7.

    Not in our library10.1002/mrm.1240

  69. 69.

    Power JD Barnes KA Snyder AZ Schlaggar BL Petersen SE. Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion. Neuroimage. (2012 ) 59:2142–54.

    Not in our library10.1016/j.neuroimage.2011.10.018

  70. 70.

    Yendiki A Koldewyn K Kakunoori S Kanwisher N Fischl B. Spurious group differences due to head motion in a diffusion MRI study. Neuroimage. (2014 ) 88:79–90.

    Not in our library10.1016/j.neuroimage.2013.11.027

  71. 71.

    Reuter M Tisdall MD Qureshi A Buckner RL van der Kouwe AJW Fischl B. Head motion during MRI acquisition reduces gray matter volume and thickness estimates. Neuroimage. (2015 ) 107:107–15.

    Not in our library10.1016/j.neuroimage.2014.12.006

  72. 72.

    Gardner EA Ellis JH Hyde RJ Aisen AM Quint DJ Carson PL. Detection of degradation of magnetic resonance (MR) images: comparison of an automated MR image-quality analysis system with trained human observers. Acad Radiol. (1995 ) 2:277–81.

    Not in our library10.1016/s1076-6332(05)80184-9

  73. 73.
  74. 74.

    Woodard JP Carley-Spencer MP. No-reference image quality metrics for structural MRI. Neuroinformatics. (2006 ) 4:243–62.

    Not in our library10.1385/ni:4:3:243

  75. 75.

    Gedamu EL Collins DL Arnold DL. Automated quality control of brain MR images. J Magn Reson Imaging. (2008 ) 28:308–19.

    Not in our library10.1002/jmri.21434

  76. 76.

    Mortamet B Bernstein MA Jack CR Jr Gunter JL Ward C. Automatic quality assessment in structural brain magnetic resonance imaging. Magn Reson Med. (2009 ) 62:365–72.

    Not in our library10.1002/mrm.21992

  77. 77.

    Pizarro RA Cheng X Barnett A Lemaitre H Verchinski BA Goldman AL. Automated quality assessment of structural magnetic resonance brain images based on a supervised machine learning algorithm. Front Neuroinform. (2016 ) 10:52.

    Not in our library10.3389/fninf.2016.00052

  78. 78.
  79. 79.
  80. 80.

    Di Martino A Yan CG Li Q Denio E Castellanos FX Alaerts K. The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism. Mol. Psychiatry. (2014 ) 19:659–67.

    Not in our library10.1038/mp.2013.78

  81. 81.
  82. 82.

    Keil B Wald LL. Massively parallel MRI detector arrays. J Magnetic Resonance. (2013 ) 229:75–89.

    Not in our library10.1016/j.jmr.2013.02.001

  83. 83.

    Hendriks AD D'Agata F Raimondo L Schakel T Geerts L Luijten PR. Pushing functional MRI spatial and temporal resolution further: high-density receive arrays combined with shot-selective 2D CAIPIRINHA for 3D echo-planar imaging at 7 T. NMR Biomed. (2020 ) 33:e4281.

    Not in our library10.1002/nbm.4281

  84. 84.

    Dymerska B Poser BA Barth M Trattnig S Robinson SD. A method for the dynamic correction of B0-related distortions in single-echo EPI at 7T. Neuroimage. (2018 ) 168:321–31.

    Not in our library10.1016/j.neuroimage.2016.07.009

  85. 85.

    Jezzard P Balaban RS. Correction for geometric distortion in echo planar images from B0 field variations. Magn Reson Med. (1995 ) 34:65–73.

    Not in our library10.1002/mrm.1910340111

  86. 86.

    Jezzard P Clare S. Sources of distortion in functional MRI data. Hum Brain Mapp. (1999 ) 8:80–5.

    Not in our library10.1002/(sici)1097-0193(1999)8:2/3<80::aid-hbm2>3.0.co;2-c

  87. 87.
  88. 88.

    Murphy K Birn RM Bandettini PA. Resting-state fMRI confounds and cleanup. Neuroimage. (2013 ) 80:349–59.

    Not in our library10.1016/j.neuroimage.2013.04.001

  89. 89.

    Brosch JR Talavage TM Ulmer JL Nyenhuis JA. Simulation of human respiration in fMRI with a mechanical model. IEEE Trans Biomed Eng. (2002 ) 49:700–7.

    Not in our library10.1109/tbme.2002.1010854

  90. 90.

    Raj D Anderson AW Gore JC. Respiratory effects in human functional magnetic resonance imaging due to bulk susceptibility changes. Phys Med Biol. (2001 ) 46:3331–40.

    Not in our library10.1088/0031-9155/46/12/318

  91. 91.

    Birn RM Diamond JB Smith MA Bandettini PA. Separating respiratory-variation-related fluctuations from neuronal-activity-related fluctuations in fMRI. Neuroimage. (2006 ) 31:1536–48.

    Not in our library10.1016/j.neuroimage.2006.02.048

  92. 92.

    Dagli MS Ingeholm JE Haxby JV. Localization of cardiac-induced signal change in fMRI. Neuroimage. (1999 ) 9:407–15.

    Not in our library10.1006/nimg.1998.0424

  93. 93.

    Huettel SA Song AW McCarthy G. Functional Magnetic Resonance Imaging. Sunderland, MA: Sinauer Associates (2009 ).

    Not in our library

  94. 94.

    Chang C Cunningham JP Glover GH. Influence of heart rate on the BOLD signal: the cardiac response function. Neuroimage. (2009 ) 44:857–69.

    Not in our library10.1016/j.neuroimage.2008.09.029

  95. 95.

    Hirsch JA Bishop B. Respiratory sinus arrhythmia in humans - how breathing pattern modulates heart-rate. Am J Physiol. (1981 ) 241:H620–9.

    Not in our library10.1152/ajpheart.1981.241.4.h620

  96. 96.

    Kasper L Bollmann S Diaconescu AO Hutton C Heinzle J Iglesias S. The PhysIO toolbox for modeling physiological noise in fMRI data. J Neurosci Methods. (2017 ) 276:56–72.

    Not in our library10.1016/j.jneumeth.2016.10.019

  97. 97.

    Brooks JC Beckmann CF Miller KL Wise RG Porro CA Tracey I. Physiological noise modelling for spinal functional magnetic resonance imaging studies. Neuroimage. (2008 ) 39:680–92.

    Not in our library10.1016/j.neuroimage.2007.09.018

  98. 98.

    Verstynen TD Deshpande V. Using pulse oximetry to account for high and low frequency physiological artifacts in the BOLD signal. Neuroimage. (2011 ) 55:1633–44.

    Not in our library10.1016/j.neuroimage.2010.11.090

  99. 99.

    Chang C Glover GH. Effects of model-based physiological noise correction on default mode network anti-correlations and correlations. Neuroimage. (2009 ) 47:1448–59.

    Not in our library10.1016/j.neuroimage.2009.05.012

  100. 100.

    Harrison SJ Bianchi S Heinzle J Stephan KE Iglesias S Kasper L. A Hilbert-based method for processing respiratory timeseries. bioRxiv [Preprint]. (2020 ).

    Not in our library10.1101/2020.09.30.321562

  101. 101.

    Friston KJ Williams S Howard R Frackowiak RS Turner R. Movement-related effects in fMRI time-series. Magn Reson Med. (1996 ) 35:346–55.

    Not in our library10.1002/mrm.1910350312

  102. 102.

    Ashburner J. Preparing fMRI Data for Statistical Analysis. Fmri Techniques and Protocols, 2nd Edition. (2016 ) 119:155–81.

    Not in our library10.1007/978-1-4939-5611-_61

  103. 103.

    Carp J. The secret lives of experiments: methods reporting in the fMRI literature. Neuroimage. (2012 ) 63:289–300.

    Not in our library10.1016/j.neuroimage.2012.07.004

  104. 104.

    Power JD Mitra A Laumann TO Snyder AZ Schlaggar BL Petersen SE. Methods to detect, characterize, and remove motion artifact in resting state fMRI. Neuroimage. (2014 ) 84:320–41.

    Not in our library10.1016/j.neuroimage.2013.08.048

  105. 105.

    Jenkinson M Beckmann CF Behrens TE Woolrich MW Smith SM. Fsl. Neuroimage. (2012 ) 62:782–90.

    Not in our library10.1016/j.neuroimage.2011.09.015

  106. 106.

    Fischl B. FreeSurfer. Neuroimage. (2012 ) 62:774–81.

    Not in our library10.1016/j.neuroimage.2012.01.021

  107. 107.
  108. 108.

    Strother SC. Evaluating fMRI preprocessing pipelines. IEEE Eng Med Biol Mag. (2006 ) 25:27–41.

    Not in our library10.1109/memb.2006.1607667

  109. 109.
  110. 110.

    Power JD Plitt M Laumann TO Martin A. Sources and implications of whole-brain fMRI signals in humans. Neuroimage. (2017 ) 146:609–25.

    Not in our library10.1016/j.neuroimage.2016.09.038

  111. 111.

    Glasser MF Sotiropoulos SN Wilson JA Coalson TS Fischl B Andersson JL. The minimal preprocessing pipelines for the Human Connectome Project. Neuroimage. (2013 ) 80:105–24.

    Not in our library10.1016/j.neuroimage.2013.04.127

  112. 112.

    Esteban O Markiewicz CJ Blair RW Moodie CA Isik AI Erramuzpe A. fMRIPrep: a robust preprocessing pipeline for functional MRI. Nat. Methods. (2019 ) 16:111–16.

    Not in our library10.1038/s41592-018-0235-4

  113. 113.

    Filiou MD Turck CW. General overview: biomarkers in neuroscience research. Int Rev Neurobiol. (2011 ) 101:1–17.

    Not in our library10.1016/b978-0-12-387718-5.00001-8

  114. 114.

    Jirsa VK Proix T Perdikis D Woodman MM Wang H Gonzalez-Martinez J. The virtual epileptic patient: individualized whole-brain models of epilepsy spread. Neuroimage. (2016 ) 145:377–88.

    Not in our library10.1016/j.neuroimage.2016.04.049

  115. 115.

    Petzschner FH Weber LAE Gard T Stephan KE. Computational psychosomatics and computational psychiatry: toward a joint framework for differential diagnosis. Biol Psychiatry. (2017 ) 82:421–30.

    Not in our library10.1016/j.biopsych.2017.05.012

  116. 116.

    Friston KJ Redish AD Gordon JA. Computational nosology and precision psychiatry. Comput Psychiatr. (2017 ) 1:2–23.

    Not in our library10.1162/cpsy_a_00001

  117. 117.

    Bishop CM. Pattern Recognition and Machine Learning. New York, NY: Springer. (2006 ).

    Not in our library

  118. 118.

    Penny WD Stephan KE Mechelli A Friston KJ. Comparing dynamic causal models. Neuroimage. (2004 ) 22:1157–72.

    Not in our library10.1016/j.neuroimage.2004.03.026

  119. 119.

    Stephan KE Schlagenhauf F Huys QJ Raman S Aponte EA Brodersen KH. Computational neuroimaging strategies for single patient predictions. Neuroimage. (2017 ) 145:180–99.

    Not in our library10.1016/j.neuroimage.2016.06.038

  120. 120.

    Friston KJ. Functional and effective connectivity: a review. Brain Connect. (2011 ) 1:13–6.

    Not in our library10.1089/brain.2011.0008

  121. 121.
  122. 122.

    Menon V. Large-scale brain networks and psychopathology: a unifying triple network model. Trends Cogn Sci. (2011 ) 15:483–506.

    Not in our library10.1016/j.tics.2011.08.003

  123. 123.

    Friston KJ Frith CD. Schizophrenia: a disconnection syndrome? Clin. Neurosci. (1995 ) 3:89–97.

    Not in our library

  124. 124.

    Bullmore ET Frangou S Murray RM. The dysplastic net hypothesis: an integration of developmental and dysconnectivity theories of schizophrenia. Schizophr Res. (1997 ) 28:143–56.

    Not in our library10.1016/s0920-9964(97)00114-x

  125. 125.
  126. 126.

    Kennedy DP Redcay E Courchesne E. Failing to deactivate: resting functional abnormalities in autism. Proc Natl Acad Sci USA. (2006 ) 103:8275–80.

    Not in our library10.1073/pnas.0600674103

  127. 127.

    Courchesne E Pierce K Schumann CM Redcay E Buckwalter JA Kennedy DP. Mapping early brain development in autism. Neuron. (2007 ) 56:399–413.

    Not in our library10.1016/j.neuron.2007.10.016

  128. 128.

    Muller RA. The study of autism as a distributed disorder. Ment Retard Dev Disabil Res Rev. (2007 ) 13:85–95.

    Not in our library10.1002/mrdd.20141

  129. 129.

    Mayberg HS. Limbic-cortical dysregulation: a proposed model of depression. J Neuropsychiatry Clin Neurosci. (1997 ) 9:471–81.

    Not in our library10.1176/jnp.9.3.471

  130. 130.

    Greicius MD Flores BH Menon V Glover GH Solvason HB Kenna H. Resting-state functional connectivity in major depression: abnormally increased contributions from subgenual cingulate cortex and thalamus. Biol Psychiatry. (2007 ) 62:429–37.

    Not in our library10.1016/j.biopsych.2006.09.020

  131. 131.

    Wang L Hermens DF Hickie IB Lagopoulos J. A systematic review of resting-state functional-MRI studies in major depression. J Affect Disord. (2012 ) 142:6–12.

    Not in our library10.1016/j.jad.2012.04.013

  132. 132.

    Friston K Harrison L Penny W. Dynamic causal modelling. Neuroimage. (2003 ) 19:1273–302.

    Not in our library10.1016/s1053-8119(03)00202-7

  133. 133.

    David O Kiebel SJ Harrison LM Mattout J Kilner JM Friston KJ. Dynamic causal modeling of evoked responses in EEG and MEG. Neuroimage. (2006 ) 30:1255–72.

    Not in our library10.1016/j.neuroimage.2005.10.045

  134. 134.

    Daunizeau J David O Stephan K. Dynamic causal modelling: a critical review of the biophysical and statistical foundations. Neuroimage. (2011 ) 58:312–22.

    Not in our library10.1016/j.neuroimage.2009.11.062

  135. 135.
  136. 136.
  137. 137.

    Dima D Roiser JP Dietrich DE Bonnemann C Lanfermann H Emrich HM. Understanding why patients with schizophrenia do not perceive the hollow-mask illusion using dynamic causal modelling. Neuroimage. (2009 ) 46:1180–6.

    Not in our library10.1016/j.neuroimage.2009.03.033

  138. 138.

    Deserno L Sterzer P Wüstenberg T Heinz A Schlagenhauf F. Reduced prefrontal-parietal effective connectivity and working memory deficits in schizophrenia. J. Neurosci. (2012 ) 32:12–20.

    Not in our library10.1523/jneurosci.3405-11.2012

  139. 139.
  140. 140.

    Lefebvre S Demeulemeester M Leroy A Delmaire C Lopes R Pins D. Network dynamics during the different stages of hallucinations in schizophrenia. Hum Brain Mapp. (2016 ) 37:2571–86.

    Not in our library10.1002/hbm.23197

  141. 141.

    Li B Cui LB Xi YB Friston KJ Guo F Wang HN. Abnormal effective connectivity in the brain is involved in auditory verbal hallucinations in schizophrenia. Neurosci Bull. (2017 ) 33:281–91.

    Not in our library10.1007/s12264-017-0101-x

  142. 142.

    Grèzes J Wicker B Berthoz S de Gelder. B. A failure to grasp the affective meaning of actions in autism spectrum disorder subjects. Neuropsychologia. (2009 ) 47:1816–25.

    Not in our library10.1016/j.neuropsychologia.2009.02.021

  143. 143.

    Radulescu E Minati L Ganeshan B Harrison NA Gray MA Beacher FD. Abnormalities in fronto-striatal connectivity within language networks relate to differences in grey-matter heterogeneity in Asperger syndrome. Neuroimage Clin. (2013 ) 2:716–26.

    Not in our library10.1016/j.nicl.2013.05.010

  144. 144.

    Schlösser RG Wagner G Koch K Dahnke R Reichenbach JR Sauer H. Fronto-cingulate effective connectivity in major depression: a study with fMRI and dynamic causal modeling. Neuroimage. (2008 ) 43:645–55.

    Not in our library10.1016/j.neuroimage.2008.08.002

  145. 145.

    Almeida JR Versace A Mechelli A Hassel S Quevedo K Kupfer DJ. Abnormal amygdala-prefrontal effective connectivity to happy faces differentiates bipolar from major depression. Biol Psychiatry. (2009 ) 66:451–9.

    Not in our library10.1016/j.biopsych.2009.03.024

  146. 146.

    Woolrich MW Stephan KE. Biophysical network models and the human connectome. Neuroimage. (2013 ) 80:330–8.

    Not in our library10.1016/j.neuroimage.2013.03.059

  147. 147.

    Friston K Mattout J Trujillo-Barreto N Ashburner J Penny W. Variational free energy and the Laplace approximation. Neuroimage. (2007 ) 34:220–34.

    Not in our library10.1016/j.neuroimage.2006.08.035

  148. 148.

    Wipf D Nagarajan S. A unified Bayesian framework for MEG/EEG source imaging. Neuroimage. (2009 ) 44:947–66.

    Not in our library10.1016/j.neuroimage.2008.02.059

  149. 149.

    Calderhead B Girolami M. Estimating Bayes factors via thermodynamic integration and population MCMC. Comp Statistics Data Analysis. (2009 ) 53:4028–45.

    Not in our library10.1016/j.csda.2009.07.025

  150. 150.

    Kirkwood JG. Statistical mechanics of fluid mixtures. J Chem Phys. (1935 ) 3:300–13.

    Not in our library10.1063/1.1749657

  151. 151.

    Lartillot N Philippe H. Computing Bayes factors using thermodynamic integration. Systematic Biol. (2006 ) 55:195–207.

    Not in our library10.1080/10635150500433722

  152. 152.

    Aponte EA Raman S Sengupta B Penny WD Stephan KE Heinzle J. mpdcm: a toolbox for massively parallel dynamic causal modeling. J Neurosci Methods. (2016 ) 257:7–16.

    Not in our library10.1016/j.jneumeth.2015.09.009

  153. 153.

    Sengupta B Friston KJ Penny WD. Gradient-free MCMC methods for dynamic causal modelling. Neuroimage. (2015 ) 112:375–81.

    Not in our library10.1016/j.neuroimage.2015.03.008

  154. 154.

    Frässle S Stephan KE Friston KJ Steup M Krach S Paulus FM. Test-retest reliability of dynamic causal modeling for fMRI. Neuroimage. (2015 ) 117:56–66.

    Not in our library10.1016/j.neuroimage.2015.05.040

  155. 155.

    Banerjee S Carlin BP Gelfand AE. Hierarchical Modeling and Analysis for Spatial Data, Second edition. ed. Boca Raton: CRC Press, Taylor and Francis Group (2015 ).

    Not in our library

  156. 156.

    Efron B Morris C. Stein's estimation rule and its competitors - empirical bayes approach. J Am Stat Assoc. (1973 ) 68:117–30.

    Not in our library10.1080/01621459.1973.10481350

  157. 157.

    Kass R Steffey D. Aproximate Bayesian inference in conditionally indepedent hierarchical models (parametric empirical Bayes models). J Am Stat Assoc. (1989 ) 84:717–26.

    Not in our library10.1080/01621459.1989.10478825

  158. 158.

    Gelman A Charlin JB Stern HS Rubin DB. Bayesian Data Analysis. Chapman and Hall (2004 ).

    Not in our library10.1201/9780429258480

  159. 159.

    Maritz JS Lwin T. Empirical Bayes Methods, 2nd ed. London; New York, NY: Chapman and Hall (1989 ).

    Not in our library

  160. 160.
  161. 161.

    Raman S Deserno L Schlagenhauf F Stephan KE. A hierarchical model for integrating unsupervised generative embedding and empirical Bayes. J Neurosci Methods. (2016 ) 269:6–20.

    Not in our library10.1016/j.jneumeth.2016.04.022

  162. 162.

    Yao Y Raman SS Schiek M Leff A Frassle S Stephan KE. Variational Bayesian inversion for hierarchical unsupervised generative embedding (HUGE). Neuroimage. (2018 ) 179:604–19.

    Not in our library10.1016/j.neuroimage.2018.06.073

  163. 163.

    Yao Y Stephan KE. Markov chain Monte Carlo methods for hierarchical clustering of dynamic causal models. arXiv. (2020 ) 2012.05744.

    Not in our library10.1002/hbm.25431

  164. 164.

    Stephan K Friston K Frith C. Dysconnection in schizophrenia: from abnormal synaptic plasticity to failures of self-monitoring. Schizophrenia Bull. (2009 ) 35:509–27.

    Not in our library10.1093/schbul/sbn176

  165. 165.

    Frässle S Lomakina EI Kasper L Manjaly ZM Leff A Pruessmann KP. A generative model of whole-brain effective connectivity. Neuroimage. (2018 ) 179:505–29.

    Not in our library10.1016/j.neuroimage.2018.05.058

  166. 166.

    Frässle S Lomakina EI Razi A Friston KJ Buhmann JM Stephan KE. Regression DCM for fMRI. Neuroimage. (2017 ) 155:406–21.

    Not in our library10.1016/j.neuroimage.2017.02.090

  167. 167.

    Frässle S Manjaly ZM Do CT Kasper L Pruessmann KP Stephan KE. Whole-brain estimates of directed connectivity for human connectomics. Neuroimage. (2021 ) 225:117491.

    Not in our library10.1016/j.neuroimage.2020.117491

  168. 168.

    Frässle S Harrison SJ Heinzle J Clementz B Tamminga C Sweeney J. Regression dynamic causal modeling for resting-state fMRI. bioRxiv. (2020 ).

    Not in our library10.1101/2020.08.12.247536

  169. 169.

    Heinzle J Koopmans PJ den Ouden HEM Raman S Stephan KE. A hemodynamic model for layered BOLD signals. Neuroimage. (2016 ) 125:556–70.

    Not in our library10.1016/j.neuroimage.2015.10.025

  170. 170.

    Rao RP Ballard DH. Predictive coding in the visual cortex: a functional interpretation of some extra-classical receptive-field effects. Nat Neurosci. (1999 ) 2:79–87.

    Not in our library10.1038/4580

  171. 171.

    Friston K. A theory of cortical responses. Philos Trans R Soc Lond B Biol Sci. (2005 ) 360:815–36.

    Not in our library10.1098/rstb.2005.1622

  172. 172.

    Buxton R Wong E Frank L. Dynamics of blood flow and oxygenation changes during brain activation: the balloon model. Magn Reson Med. (1998 ) 39:855–64.

    Not in our library10.1002/mrm.1910390602

  173. 173.

    Friston KJ Mechelli A Turner R Price CJ. Nonlinear responses in fMRI: the Balloon model, Volterra kernels, other hemodynamics. Neuroimage. (2000 ) 12:466–77.

    Not in our library10.1006/nimg.2000.0630

  174. 174.
  175. 175.

    Havlicek M Roebroeck A Friston K Gardumi A Ivanov D Uludag K. Physiologically informed dynamic causal modeling of fMRI data. Neuroimage. (2015 ) 122:355–72.

    Not in our library10.1016/j.neuroimage.2015.07.078

  176. 176.

    Havlicek M Uludag K. A dynamical model of the laminar BOLD response. Neuroimage. (2020 ) 204:116209.

    Not in our library10.1016/j.neuroimage.2019.116209

  177. 177.
  178. 178.

    Mathys C Daunizeau J Friston KJ Stephan KE. A bayesian foundation for individual learning under uncertainty. Front Hum Neurosci. (2011 ) 5:39.

    Not in our library10.3389/fnhum.2011.00039

  179. 179.
  180. 180.
  181. 181.

    Rescorla RA Wagner AR. A theory of Pavlovian conditioning: variations in the effectiveness of reinforcement and nonreinforcement. In: Black AH. Prokasy WF, editors. Classical Conditioning II: Current Research and Theory. New York, NY: Appleton Century Crofts (1972 ). p. 64–99.

    Not in our library

  182. 182.

    Sutton RS. Gain adaptation beats least squares. In: Proceedings of the 7th Yale Workshop on Adaptive and Learning Systems (1992 ).

    Not in our library

  183. 183.

    Baum LE Petrie T. Statistical inference for probabilistic functions of finite state markov chains. Annals Mathematical Statistics. (1966 ) 37:1554.

    Not in our library10.1214/aoms/1177699147

  184. 184.

    Stephan K Penny W Daunizeau J Moran R Friston K. Bayesian model selection for group studies. Neuroimage. (2009 ) 46:1004–17.

    Not in our library10.1016/j.neuroimage.2009.03.025

  185. 185.

    Iglesias S Mathys C Brodersen KH Kasper L Piccirelli M den Ouden HE. Hierarchical prediction errors in midbrain and basal forebrain during sensory learning. Neuron. (2013 ) 80:519–30.

    Not in our library10.1016/j.neuron.2013.09.009

  186. 186.

    Weber LA Diaconescu AO Mathys C Schmidt A Kometer M Vollenweider FX. Ketamine affects prediction errors about statistical regularities: a computational single-trial analysis of the mismatch negativity. J Neurosci. (2020 ) 40:5658–68.

    Not in our library10.1523/jneurosci.3069-19.2020

  187. 187.

    Heinzle J Aponte EA Stephan KE. Computational models of eye movements and their application to schizophrenia. Current Opinion Behav Sci. (2016 ) 11:21–9.

    Not in our library10.1016/j.cobeha.2016.03.008

  188. 188.

    Hutton SB Ettinger U. The antisaccade task as a research tool in psychopathology: A critical review. Psychophysiology. (2006 ) 43:302–13.

    Not in our library10.1111/j.1469-8986.2006.00403.x

  189. 189.

    Rommelse NNJ Van der Stigchel S Sergeant JA. A review on eye movement studies in childhood and adolescent psychiatry. Brain Cognition. (2008 ) 68:391–414.

    Not in our library10.1016/j.bandc.2008.08.025

  190. 190.

    Hallett PE. Primary and secondary saccades to goals defined by instructions. Vision Res. (1978 ) 18:1279–96.

    Not in our library10.1016/0042-6989(78)90218-3

  191. 191.

    Fukushima J Fukushima K Chiba T Tanaka S Yamashita I Kato M. Disturbances of voluntary control of saccadic eye-movements in schizophrenic-patients. Biol Psychiatry. (1988 ) 23:670–7.

    Not in our library10.1016/0006-3223(88)90050-9

  192. 192.

    Curtis CE Calkins ME Grove WM Feil KJ Lacono WG. Saccadic disinhibition in patients with acute and remitted schizophrenia and their first-degree biological relatives. Am J Psychiatry. (2001 ) 158:100–6.

    Not in our library10.1176/appi.ajp.158.1.100

  193. 193.

    Reilly JL Frankovich K Hill S Gershon ES Keefe RSE Keshavan MS. Elevated Antisaccade Error Rate as an Intermediate Phenotype for Psychosis Across Diagnostic Categories. Schizophrenia Bull. (2014 ) 40:1011–21.

    Not in our library10.1093/schbul/sbt132

  194. 194.

    Aponte EA Schöbi D Stephan KE Heinzle J. Computational dissociation of dopaminergic and cholinergic effects on action selection and inhibitory control. Biol Psychiatry Cogn Neurosci Neuroimaging. (2020 ) 5:364–72.

    Not in our library10.1016/j.bpsc.2019.10.011

  195. 195.

    Cooray GK Sengupta B Douglas P Englund M Wickstrom R Friston K. Characterising seizures in anti-NMDA-receptor encephalitis with dynamic causal modelling. Neuroimage. (2015 ) 118:508–19.

    Not in our library10.1016/j.neuroimage.2015.05.064

  196. 196.

    Dalmau J Tuzun E Wu HY Masjuan J Rossi JE Voloschin A. Paraneoplastic anti-N-methyl-D-aspartate receptor encephalitis associated with ovarian teratoma. Ann Neurol. (2007 ) 61:25–36.

    Not in our library10.1002/ana.21050

  197. 197.

    Shawe-Taylor J Cristianini N. Kernel Methods for Pattern Analysis. Cambridge: Cambridge University Press (2004 ).

    Not in our library

  198. 198.

    Frässle S Marquand AF Schmaal L Dinga R Veltman DJ van der Wee NJA. Predicting individual clinical trajectories of depression with generative embedding. Neuroimage Clin. (2020 ) 26:102213.

    Not in our library10.1016/j.nicl.2020.102213

  199. 199.

    Pedregosa F Varoquaux G Gramfort A Michel V Thirion B Grisel O. Scikit-learn: machine learning in python. J Machine Learn Res. (2011 ) 12:2825–30. Available online at: https://dl.acm.org/doi/10.5555/1953048.2078195

    Not in our library

  200. 200.

    Snoek L Miletic S Scholte HS. How to control for confounds in decoding analyses of neuroimaging data. Neuroimage. (2019 ) 184:741–60.

    Not in our library10.1016/j.neuroimage.2018.09.074

  201. 201.

    Varoquaux G Raamana PR Engemann DA Hoyos-Idrobo A Schwartz Y Thirion B. Assessing and tuning brain decoders: cross-validation, caveats, and guidelines. Neuroimage. (2017 ) 145:166–79.

    Not in our library10.1016/j.neuroimage.2016.10.038

  202. 202.

    Varoquaux G. Cross-validation failure: Small sample sizes lead to large error bars. Neuroimage. (2018 ) 180:68–77.

    Not in our library10.1016/j.neuroimage.2017.06.061

  203. 203.

    Friston K. The free-energy principle: a rough guide to the brain? Trends Cogn Sci. (2009 ) 13:293–301.

    Not in our library10.1016/j.tics.2009.04.005

  204. 204.

    Yu AJ Dayan P. Uncertainty, neuromodulation, and attention. Neuron. (2005 ) 46:681–92.

    Not in our library10.1016/j.neuron.2005.04.026

  205. 205.

    Iglesias S Kasper L Harrison SJ Manka R Mathys C Stephan KE. Cholinergic and dopaminergic effects on prediction error and uncertainty responses during sensory associative learning. Neuroimage. (2020 ) 226:117590.

    Not in our library10.1016/j.neuroimage.2020.117590

  206. 206.

    Takahashi YK Batchelor HM Liu B Khanna A Morales M Schoenbaum G. Dopamine neurons respond to errors in the prediction of sensory features of expected rewards. Neuron. (2017 ) 95:1395–405 e1393.

    Not in our library10.1016/j.neuron.2017.08.025

  207. 207.

    Stalnaker TA Howard JD Takahashi YK Gershman SJ Kahnt T Schoenbaum G. Dopamine neuron ensembles signal the content of sensory prediction errors. Elife. (2019 ) 8:e49315.

    Not in our library10.7554/elife.49315.010

  208. 208.

    Suarez JA Howard JD Schoenbaum G Kahnt T. Sensory prediction errors in the human midbrain signal identity violations independent of perceptual distance. Elife. (2019 ) 8:e43962.

    Not in our library10.7554/elife.43962.032

  209. 209.

    Friston KJ. Hallucinations and perceptual inference. Behav Brain Sci. (2005 ) 28:764.

    Not in our library10.1017/s0140525x05290131

  210. 210.

    Pellicano E Burr D. When the world becomes 'too real': a Bayesian explanation of autistic perception. Trends Cognitive Sci. (2012 ) 16:504–10.

    Not in our library10.1016/j.tics.2012.08.009

  211. 211.

    Schofield TM Penny WD Stephan KE Crinion JT Thompson AJ Price CJ. Changes in auditory feedback connections determine the severity of speech processing deficits after stroke. J Neurosci. (2012 ) 32:4260–70.

    Not in our library10.1523/jneurosci.4670-11.2012

  212. 212.
  213. 213.

    Harrison OK Garfinkel SN Marlow L Finnegan S Marino S Nanz L. The Filter Detection Task for measurement of breathing-related interoception and metacognition. bioRxiv [Preprint]. (2020 ).

    Not in our library10.1101/2020.06.29.176941

  214. 214.

    Rieger SW Stephan KE Harrison OK. Remote, automated, and MRI-compatible administration of interoceptive inspiratory resistive loading. Front Hum Neurosci. (2020 ) 14:161.

    Not in our library10.3389/fnhum.2020.00161

  215. 215.

    Aponte EA Stephan KE Heinzle J. Switch costs in inhibitory control and voluntary behaviour: a computational study of the antisaccade task. Eur J Neurosci. (2019 ) 50:3205–20.

    Not in our library10.1111/ejn.14435

  216. 216.

    Aponte EA Tschan DG Stephan KE Heinzle J. Inhibition failures and late errors in the antisaccade task: influence of cue delay. J Neurophysiol. (2018 ) 120:3001–16.

    Not in our library10.1152/jn.00240.2018

  217. 217.

    Aponte EA Yao Y Raman S Frässle S Heinzle J Penny WD. An introduction to thermodynamic integration and application to dynamic causal models. bioRxiv. (2020 ).

    Not in our library10.1101/2020.12.21.423807

  218. 218.

    Birn RM Smith MA Jones TB Bandettini PA. The respiration response function: the temporal dynamics of fMRI signal fluctuations related to changes in respiration. Neuroimage. (2008 ) 40:644–54.

    Not in our library10.1016/j.neuroimage.2007.11.059

  219. 219.

    Brazil IA Mathys CD Popma A Hoppenbrouwers SS Cohn MD. Representational uncertainty in the brain during threat conditioning and the link with psychopathic traits. Biol Psychiatry Cogn Neurosci Neuroimaging. (2017 ) 2:689–95.

    Not in our library10.1016/j.bpsc.2017.04.005

  220. 220.

    Daunizeau J den Ouden HE Pessiglione M Kiebel SJ Friston KJ Stephan KE. Observing the observer (II): deciding when to decide. PLoS ONE. (2010 ) 5:e15555.

    Not in our library10.1371/journal.pone.0015555

  221. 221.
  222. 222.

    Durstewitz D Koppe G Meyer-Lindenberg A. Deep neural networks in psychiatry. Mol. Psychiatry. (2019 ) 24:1583–98.

    Not in our library10.1038/s41380-019-0365-9

  223. 223.

    Dwyer DB Falkai P Koutsouleris N. Machine learning approaches for clinical psychology and psychiatry. Annu Rev Clin Psychol. (2018 ) 14:91–118.

    Not in our library10.1146/annurev-clinpsy-032816-045037

  224. 224.

    Gillan CM Whelan R. What big data can do for treatment in psychiatry. Current Opinion Behav Sci. (2017 ) 18:34–42.

    Not in our library10.1016/j.cobeha.2017.07.003

  225. 225.
  226. 226.

    Mourao-Miranda J Reinders AATS Rocha-Rego V Lappin J Rondina J. Individualized prediction of illness course at the first psychotic episode: a support vector machine MRI study. Psychol Med. (2012 ) 42:1037–47.

    Not in our library10.1017/s0033291711002005

  227. 227.

    Portugal LCL Schrouff J Stiffler R Bertocci M Bebko G Chase H. Predicting anxiety from wholebrain activity patterns to emotional faces in young adults: a machine learning approach. Neuroimage-Clinical. (2019 ) 23:101813.

    Not in our library10.1016/j.nicl.2019.101813

  228. 228.

    Schmaal L Marquand AF Rhebergen D van Tol MJ Ruh é HG van der Wee NJ. Predicting the naturalistic course of major depressive disorder using clinical and multimodal neuroimaging information: a multivariate pattern recognition study. Biol Psychiatry. (2015 ) 78:278–86.

    Not in our library10.1016/j.biopsych.2014.11.018

  229. 229.

    Sengupta B Friston KJ Penny WD. Gradient-based MCMC samplers for dynamic causal modelling. Neuroimage. (2016 ) 125:1107–18.

    Not in our library10.1016/j.neuroimage.2015.07.043

  230. 230.

    Vossel S Bauer M Mathys C Adams RA Dolan RJ Stephan KE. Cholinergic stimulation enhances Bayesian belief updating in the deployment of spatial attention. J Neurosci. (2014 ) 34:15735–42.

    Not in our library10.1523/jneurosci.0091-14.2014

Cited by papers we hold 3

Reads

Read by people on this page

None yet.

Checked or read by AI through naulon

None yet.

A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.

Are you an author?

Is this your paper?

Claim it to add your note and be paid when agents cite it. Free.