Publications by authors named "Fabrice Heitz"

In the field of forensic anthropology, researchers aim to identify anonymous human remains and determine the cause and circumstances of death from skeletonized human remains. Sex determination is a fundamental step of this procedure because it influences the estimation of other traits, such as age and stature. Pelvic bones are especially dimorphic, and are thus the most useful bones for sex identification.

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Article Synopsis
  • Patients with type 2 diabetes experience a decline in pancreatic beta cell function, leading to insulin production issues and blood glucose regulation problems.
  • The deterioration of these cells is linked to the buildup of toxic forms of islet amyloid polypeptide (IAPP), including both soluble and insoluble aggregates.
  • A newly developed human monoclonal antibody targets the harmful IAPP oligomers, demonstrating protective effects on beta cells and improved glucose control in animal models, indicating a potential therapeutic approach for enhancing beta cell function in type 2 diabetes.
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Whether in medical imaging, astronomy or remote sensing, the data are increasingly complex. In addition to the spatial dimension, the data may contain temporal or spectral information that characterises the different sources present in the image. The compromise between spatial resolution and temporal/spectral resolution is often at the expense of spatial resolution, resulting in a potentially large mixing of sources in the same pixel/voxel.

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Purpose: We address the automatic segmentation of healthy and cancerous liver tissues (parenchyma, active and necrotic parts of hepatocellular carcinoma (HCC) tumor) on multiphase CT images using a deep learning approach.

Methods: We devise a cascaded convolutional neural network based on the U-Net architecture. Two strategies for dealing with multiphase information are compared: Single-phase images are concatenated in a multi-dimensional features map on the input layer, or output maps are computed independently for each phase before being merged to produce the final segmentation.

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Purpose: Toward an efficient clinical management of hepatocellular carcinoma (HCC), we propose a classification framework dedicated to tumor necrosis rate estimation from dynamic contrast-enhanced CT scans. Based on machine learning, it requires weak interaction efforts to segment healthy, active and necrotic liver tissues.

Methods: Our contributions are two-fold.

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Memory formation is associated with activity-dependent changes in synaptic plasticity. The mechanisms underlying these processes are complex and involve multiple components. Recent work has implicated the protein KIBRA in human memory, but its molecular functions in memory processes remain not fully understood.

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There is a real need in the neuroscience community for efficient tools to compare Diffusion Tensor Magnetic Resonance Imaging across cohorts of subjects. Most studies focus on the comparison of scalar images such as fractional anisotropy or mean diffusivity. Although different statistical frameworks have been proposed to compare the whole diffusion tensor information, they are still seldom used in neuroimaging studies.

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Gene knockout by homologous recombination is a popular method to study gene functions in the mouse in vivo. However, its lack of temporal control has limited the interpretation of knockout studies because the complete elimination of a gene product often alters developmental processes, and can induce severe malformations or lethality. Conditional gene knockdown has emerged as a compelling alternative to gene knockout, an approach well-established in vitro but that remains challenging in vivo, especially in the adult brain.

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Brain atrophy is considered an important marker of disease progression in many chronic neuro-degenerative diseases such as multiple sclerosis (MS). A great deal of attention is being paid toward developing tools that manipulate magnetic resonance (MR) images for obtaining an accurate estimate of atrophy. Nevertheless, artifacts in MR images, inaccuracies of intermediate steps and inadequacies of the mathematical model representing the physical brain volume change, make it rather difficult to obtain a precise and unbiased estimate.

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Diffusion weighted magnetic resonance imaging (DW-MRI) makes it possible to probe brain connections in vivo. This paper presents a change detection framework that relies on white matter pathways with application to neuromyelitis optica (NMO). The objective is to detect local or global fiber diffusion property modifications between two longitudinal DW-MRI acquisitions of a patient.

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Leber's hereditary optic neuropathy (LHON) is an inherited disease caused by mutations in complex I of the mitochondrial respiratory chain. The disease is characterized by loss of central vision due to retinal ganglion cell (RGC) dysfunction and optic nerve atrophy. Despite progress towards a better understanding of the disease, no therapeutic treatment is currently approved for this devastating disease.

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An imbalance between pro-survival and pro-death pathways in brain cells can lead to neuronal cell death and neurodegeneration. While such imbalance is known to be associated with alterations in glutamatergic and Ca(2+) signaling, the underlying mechanisms remain undefined. We identified the protein Ser/Thr phosphatase protein phosphatase-1 (PP1), an enzyme associated with glutamate receptors, as a key trigger of survival pathways that can prevent neuronal death and neurodegeneration in the adult hippocampus.

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This paper presents a longitudinal change detection framework for detecting relevant modifications in diffusion MRI, with application to neuromyelitis optica (NMO) and multiple sclerosis (MS). The core problem is to identify image regions that are significantly different between two scans. The proposed method is based on multivariate statistical testing which was initially introduced for tensor population comparison.

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Diffusion tensor magnetic resonance imaging (DT-MRI) tractography allows to probe brain connections in vivo. This paper presents a change detection framework that relies on white-matter pathways with application to neuromyelitis optica (NMO). The objective is to detect global or local fiber diffusion property modifications between two longitudinal DT-MRI acquisitions of a patient.

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The automatic analysis of subtle changes between MRI scans is an important tool for monitoring disease evolution. Several methods have been proposed to detect changes in serial conventional MRI but few works have considered Diffusion Tensor Imaging (DTI), which is a promising modality for monitoring neurodegenerative disease and particularly Multiple Sclerosis (MS). In this paper, we introduce a comprehensive framework for detecting changes between two DTI acquisitions by considering different levels of representation of diffusion imaging, namely the Apparent Diffusion Coefficient (ADC) images, the diffusion tensor fields, and scalar images characterizing diffusion properties such as the fractional anisotropy and the mean diffusivity.

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This paper presents a longitudinal change detection framework for detecting relevant modifications in diffusion MRI, with application to Multiple Sclerosis (MS). The proposed method is based on multivariate statistical testings which were initially introduced for tensor population comparison. We use these methods in the context of longitudinal change detection by considering several strategies to build sets of tensors characterizing the variability of each voxel.

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Chromatin remodeling through histone posttranslational modifications (PTMs) and DNA methylation has recently been implicated in cognitive functions, but the mechanisms involved in such epigenetic regulation remain poorly understood. Here, we show that protein phosphatase 1 (PP1) is a critical regulator of chromatin remodeling in the mammalian brain that controls histone PTMs and gene transcription associated with long-term memory. Our data show that PP1 is present at the chromatin in brain cells and interacts with enzymes of the epigenetic machinery including HDAC1 (histone deacetylase 1) and histone demethylase JMJD2A (jumonji domain-containing protein 2A).

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In this paper, we study the performance of popular brain atrophy estimation algorithms using a simulated gold standard. The availability of a gold standard facilitates a sound evaluation of the measures of atrophy estimation, which is otherwise complicated. Firstly, we propose an approach for the construction of a gold standard.

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The automatic analysis of longitudinal changes between Diffusion Tensor Imaging (DTI) acquisitions is a promising tool for monitoring disease evolution. However, few works address this issue and existing methods are generally limited to the detection of changes between scalar images characterizing diffusion properties, such as Fractional Anisotropy or Mean Diffusivity, while richer information can be exploited from the whole set of Apparent Diffusion Coefficient (ADC) images that can be derived from a DTI acquisition. In this paper, we present a general framework for detecting changes between two sets of ADC images and we investigate the performance of four statistical tests.

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Image registration aims at estimating a consistent mapping between two images. Common techniques consist in choosing arbitrarily one image as a reference image and the other one as a floating image, thus leading to the estimation of inconsistent mappings. We present a symmetric formulation of the registration problem that maps the two images in a common coordinate system halfway between them.

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This correspondence addresses the inversion of 3-D transformation fields, which is a problem that typically arises in image warping problems. A topology preserving parametric B-spline-based representation of the deformation field is considered. Topology preservation ensures that the transformation is a one-to-one mapping and consequently that it is invertible.

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We present an original appearance model that generalizes the usual Gaussian visual subspace model to non-Gaussian and nonparametric distributions. It can be useful for the modeling and recognition of images under difficult conditions such as large occlusions and cluttered backgrounds. Inference under the model is efficiently solved using the mean shift algorithm.

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We present a new way of constraining the evolution of a region-based active contour with respect to a reference shape. Minimizing a shape prior, defined as a distance between shape descriptors based on the Legendre moments of the characteristic function, leads to a geometric flow that can be used with benefits in a two-class segmentation application. The shape model includes intrinsic invariance with regard to pose and affine deformations.

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This paper deals with topology preservation in three-dimensional (3-D) deformable image registration. This work is a nontrivial extension of, which addresses the case of two-dimensional (2-D) topology preserving mappings. In both cases, the deformation map is modeled as a hierarchical displacement field, decomposed on a multiresolution B-spline basis.

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In this paper, a novel functional magnetic resonance imaging (fMRI) brain mapping method is presented within the statistical modeling framework of hidden semi-Markov event sequence models (HSMESMs). Neural activation detection is formulated at the voxel level in terms of time coupling between the sequence of hemodynamic response onsets (HROs) observed in the fMRI signal, and an HSMESM of the hidden sequence of task-induced neural activations. The sequence of HRO events is derived from a continuous wavelet transform (CWT) of the fMRI signal.

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