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Showing papers by "Olivier Commowick published in 2019"


Journal ArticleDOI
TL;DR: The need to move forward to a symptom-based research area of biomarkers, which help to understand the pathophysiology of mood depressive disorders and to stratify precise phenotypes of depression with targeted therapeutic strategies is underlined.

57 citations


Proceedings ArticleDOI
08 Apr 2019
TL;DR: Novel geometric statistics are proposed to measure the alignment of the reconstructed diffusion model with the apparent centerline of the spine to study and evaluate the impact of distortion correction by comparing 3 distortion correction methods from reversed gradient polarity strategy.
Abstract: Acquiring and processing Diffusion MRI in spinal cord present inherent challenges. Differences in magnetic susceptibility between soft tissues, air and bone make the magnetic field of spinal cord non-uniform and inhomogeneous. In this context various procedures were proposed for correcting this distortion. In this work, we propose novel geometric statistics to measure the alignment of the reconstructed diffusion model with the apparent centerline of the spine. In parallel of the correlation with an anatomical T2-weighted image, we show the utility of these statistics to study and evaluate the impact of distortion correction by comparing 3 distortion correction methods from reversed gradient polarity strategy.

9 citations


Proceedings ArticleDOI
08 Apr 2019
TL;DR: This work presents a new method to create a diffeomorphic longitudinal (4D) atlas composed of a set of 3D atlases each representing an average model at a given age by generalizing atlasing methods to produce atlased unbiased with respect to the initial reference up to a rigid transformation and ensuring Diffeomorphic deformations thanks to the Baker-Campbell-Hausdorff formula and the log-Euclidean framework for diffeomorphisms.
Abstract: We present a new method to create a diffeomorphic longitudinal (4D) atlas composed of a set of 3D atlases each representing an average model at a given age. This is achieved by generalizing atlasing methods to produce atlases unbiased with respect to the initial reference up to a rigid transformation and ensuring diffeomorphic deformations thanks to the Baker-Campbell-Hausdorff formula and the log-Euclidean framework for diffeomorphisms. Subjects are additionally weighted using an asymmetric function to closely match specified target ages. Creating a longitudinal atlas also implies dealing with subjects with large brain differences that can lead to registration errors. This is overcome by a robust rigid registration based on polar decomposition. We illustrate these techniques for the creation of a 4D pediatric atlas, showing their ability to create a temporally consistent atlas.

7 citations


Book ChapterDOI
13 Oct 2019
TL;DR: This work proposes a new diffeomorphic online atlasing method that integrates new subjects following an iterative procedure gradually shifting the centroid of the images to its final position, making it computationally cheap to update regularly an atlas as new images are acquired.
Abstract: Online atlasing, i.e. incrementing an atlas with new images as they are acquired, is key when performing studies on databases very large or still being gathered. We propose to this end a new diffeomorphic online atlasing method without having to perform again the atlasing process from scratch. New subjects are integrated following an iterative procedure gradually shifting the centroid of the images to its final position, making it computationally cheap to update regularly an atlas as new images are acquired (only needing a number of registrations equal to the number of new subjects). We evaluate this iterative centroid approach through the analysis of the sharpness and variance of the resulting atlases, and the transformations of images, comparing their deviations from a conventional method. We demonstrate that the transformations divergence between the two approaches is small and stable and that both atlases reach equivalent levels of image quality.

4 citations


Proceedings Article
08 Apr 2019
TL;DR: An improved CNN framework for the segmentation of Multiple Sclerosis lesions from multimodal MRI using a two-step intensity normalization and a cascaded network with cost sensitive learning is presented.
Abstract: We present an improved CNN framework for the segmentation of Multiple Sclerosis (MS) lesions from multimodal MRI. It uses a two-step intensity normalization and a cascaded network with cost sensitive learning. Performance was assessed on a public multi-site dataset.

3 citations


Posted ContentDOI
11 Mar 2019-bioRxiv
TL;DR: A novel method to quantify brain growth in 3 arbitrary orthogonal directions of the brain or its sub-regions through linear registration is proposed by introducing a 9 degrees of freedom (dof) transformation called anisotropic similarity which is an affine transformation with constrained scaling directions along arbitrarily chosen Orthogonal vectors.
Abstract: We propose a novel method to quantify brain growth in 3 arbitrary orthogonal directions of the brain or its sub-regions through linear registration. This is achieved by introducing a 9 degrees of freedom (dof) transformation called anisotropic similarity which is an affine transformation with constrained scaling directions along arbitrarily chosen orthogonal vectors. This gives the opportunity to extract scaling factors describing brain growth along those directions by registering a database of subjects onto a common reference. This information about directional growth brings insights that are not usually available in longitudinal volumetry analysis. The interest of this method is illustrated by studying the anisotropic regional and global brain development of 308 healthy subjects betwen 0 and 19 years old. A gender comparison of those scaling factors is also performed for 4 classes of age. We demonstrate through these applications the stability of the method to the chosen reference and its ability to highlight growth differences accros regions and gender.