Pasi Jylänki
Radboud University Nijmegen
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Publication
Featured researches published by Pasi Jylänki.
NeuroImage | 2015
Ronald J. Janssen; Pasi Jylänki; R.P.C. Kessels; M.A.J. van Gerven
The striatum is involved in many different aspects of behaviour, reflected by the variety of cortical areas that provide input to this structure. This input is topographically organized and is likely to result in functionally specific signals. Such specificity can be examined using functional clustering approaches. Here, we propose a Bayesian model-based functional clustering approach applied solely to resting state striatal functional MRI timecourses to identify intrinsic striatal functional modules. Data from two sets of ten participants were used to obtain parcellations and examine their robustness. This stable clustering was used to initialize a more constrained model in order to obtain individualized parcellations in 57 additional participants. Resulting cluster time courses were used to examine functional connectivity between clusters and related to the rest of the brain in a GLM analysis. We find six distinct clusters in each hemisphere, with clear inter-hemispheric correspondence and functional relevance. These clusters exhibit functional connectivity profiles that further underscore their homologous nature and are consistent with existing notions on segregation and integration in parallel cortico-basal ganglia loops. Our findings suggest that multiple territories within both the affective and motor regions can be distinguished solely using resting state functional MRI from these regions.
international workshop on machine learning for signal processing | 2014
Ville Tolvanen; Pasi Jylänki; Aki Vehtari
This paper presents a novel approach for approximate integration over the uncertainty of noise and signal variances in Gaussian process (GP) regression. Our efficient and straightforward approach can also be applied to integration over input dependent noise variance (heteroscedasticity) and input dependent signal variance (non-stationarity) by setting independent GP priors for the noise and signal variances. We use expectation propagation (EP) for inference and compare results to Markov chain Monte Carlo in two simulated data sets and three empirical examples. The results show that EP produces comparable results with less computational burden.
Clinical Neurophysiology | 2016
Haiteng Jiang; T. Popov; Pasi Jylänki; Kun Bi; Zhijian Yao; Qing Lu; Ole Jensen; M.A.J. van Gerven
OBJECTIVEnWe aimed to integrate neural data and an advanced machine learning technique to predict individual major depressive disorder (MDD) patient severity.nnnMETHODSnMEG data was acquired from 22 MDD patients and 22 healthy controls (HC) resting awake with eyes closed. Individual power spectra were calculated by a Fourier transform. Sources were reconstructed via beamforming technique. Bayesian linear regression was applied to predict depression severity based on the spatial distribution of oscillatory power.nnnRESULTSnIn MDD patients, decreased theta (4-8 Hz) and alpha (8-14 Hz) power was observed in fronto-central and posterior areas respectively, whereas increased beta (14-30 Hz) power was observed in fronto-central regions. In particular, posterior alpha power was negatively related to depression severity. The Bayesian linear regression model showed significant depression severity prediction performance based on the spatial distribution of both alpha (r=0.68, p=0.0005) and beta power (r=0.56, p=0.007) respectively.nnnCONCLUSIONSnOur findings point to a specific alteration of oscillatory brain activity in MDD patients during rest as characterized from MEG data in terms of spectral and spatial distribution.nnnSIGNIFICANCEnThe proposed model yielded a quantitative and objective estimation for the depression severity, which in turn has a potential for diagnosis and monitoring of the recovery process.
PLOS ONE | 2017
D. Benozzo; Pasi Jylänki; E. Olivetti; P. Avesani; M.A.J. van Gerven
In many fields of science, there is the need of assessing the causal influences among time series. Especially in neuroscience, understanding the causal interactions between brain regions is of primary importance. A family of measures have been developed from the parametric implementation of the Granger criteria of causality based on the linear autoregressive modelling of the signals. We propose a new Bayesian method for linear model identification with a structured prior (GMEP) aiming to apply it as linear regression method in the context of the parametric Granger causal inference. GMEP assumes a Gaussian scale mixture distribution for the group sparsity prior and it enables flexible definition of the coefficient groups. Approximate posterior inference is achieved using Expectation Propagation for both the linear coefficients and the hyperparameters. GMEP is investigated both on simulated data and on empirical fMRI data in which we show how adding information on the sparsity structure of the coefficients positively improves the inference process. In the same simulation framework, GMEP is compared with others standard linear regression methods. Moreover, the causal inferences derived from GMEP estimates and from a standard Granger method are compared across simulated datasets of different dimensionality, density connection and level of noise. GMEP allows a better model identification and consequent causal inference when prior knowledge on the sparsity structure are integrated in the structured prior.
PLOS ONE | 2016
Ronald J. Janssen; Pasi Jylänki; M.A.J. van Gerven
We have proposed a Bayesian approach for functional parcellation of whole-brain FMRI measurements which we call Clustered Activity Estimation with Spatial Adjacency Restrictions (CAESAR). We use distance-dependent Chinese restaurant processes (dd-CRPs) to define a flexible prior which partitions the voxel measurements into clusters whose number and shapes are unknown a priori. With dd-CRPs we can conveniently implement spatial constraints to ensure that our parcellations remain spatially contiguous and thereby physiologically meaningful. In the present work, we extend CAESAR by using Gaussian process (GP) priors to model the temporally smooth haemodynamic signals that give rise to the measured FMRI data. A challenge for GP inference in our setting is the cubic scaling with respect to the number of time points, which can become computationally prohibitive with FMRI measurements, potentially consisting of long time series. As a solution we describe an efficient implementation that is practically as fast as the corresponding time-independent non-GP model with typically-sized FMRI data sets. We also employ a population Monte-Carlo algorithm that can significantly speed up convergence compared to traditional single-chain methods. First we illustrate the benefits of CAESAR and the GP priors with simulated experiments. Next, we demonstrate our approach by parcellating resting state FMRI data measured from twenty participants as taken from the Human Connectome Project data repository. Results show that CAESAR affords highly robust and scalable whole-brain clustering of FMRI timecourses.
Archive | 2012
Jarno Vanhatalo; Jaakko Riihimäki; Jouni Hartikainen; Pasi Jylänki; Ville Tolvanen; Aki Vehtari
arXiv: Applications | 2016
Arno Solin; Pasi Jylänki; Jaakko Kauramäki; Tom Heskes; Marcel A. J. van Gerven; Simo Särkkä
international conference on artificial intelligence and statistics | 2014
Tomi Peltola; Pasi Jylänki; Aki Vehtari
Archive | 2008
Ville-Petteri Mäkinen; Pasi Soininen; T. Tukiainen; J. Niemi; Pasi Jylänki; Antti J. Kangas; Tomi Peltola; J. Hokkanen; Linda S. Kumpula; J. Ojanen; N. Sandholm; Carol Forsblom; Aki Vehtari; Per-Henrik Groop; Kimmo Kaski; Mika Ala-Korpela
Archive | 2007
Pasi Jylänki; Jaakko Niemi; Ville-Petteri Mäkinen; Aino Salminen; Lauri Vanhatalo; Pasi Soininen; Petri Ingman; Kimmo Kaski; Per-Henrik Groop; Aki Vehtari; Mika Ala-Korpela