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Abstract In this paper, we consider the fractional Hardy–Hénon equations with an isolated singularity. If the isolated singularity is located at the origin, we give a classification of solutions to this equation. If the isolated singularity is located at infinity, in the case of exterior domains, we provide decay estimates of solutions and their gradients at infinity. Our results are an extension of the classical work by Caffarelli, Gidas et al. [ABSTRACT FROM AUTHOR]

Longitudinal neuroimaging data plays an important role in mapping the neural developmental profile of major neuropsychiatric and neurodegenerative disorders and normal brain. The development of such developmental maps is critical for the prevention, diagnosis, and treatment of many brain-related diseases. The aim of this paper is to develop a spatio-temporal Gaussian process (STGP) framework to accurately delineate the developmental trajectories of brain structure and function, while achieving better prediction by explicitly incorporating the spatial and temporal features of longitudinal neuroimaging data. Our STGP integrates a functional principal component model (FPCA) and a partition parametric space–time covariance model to capture the medium-to-large and small-to-medium spatio-temporal dependence structures, respectively. We develop a three-stage efficient estimation procedure as well as a predictive method based on a kriging technique. Two key novelties of STGP are that it can efficiently use a small number of parameters to capture complex non-stationary and non-separable spatio-temporal dependence structures and that it can accurately predict spatio-temporal changes. We illustrate STGP using simulated data sets and two real data analyses including longitudinal positron emission tomography data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) and longitudinal lateral ventricle surface data from a longitudinal study of early brain development. [ABSTRACT FROM AUTHOR]

Abstract: The aim of this paper is to develop a spatial Gaussian predictive process (SGPP) framework for accurately predicting neuroimaging data by using a set of covariates of interest, such as age and diagnostic status, and an existing neuroimaging data set. To achieve a better prediction, we not only delineate spatial association between neuroimaging data and covariates, but also explicitly model spatial dependence in neuroimaging data. The SGPP model uses a functional principal component model to capture medium-to-long-range (or global) spatial dependence, while SGPP uses a multivariate simultaneous autoregressive model to capture short-range (or local) spatial dependence as well as cross-correlations of different imaging modalities. We propose a three-stage estimation procedure to simultaneously estimate varying regression coefficients across voxels and the global and local spatial dependence structures. Furthermore, we develop a predictive method to use the spatial correlations as well as the cross-correlations by employing a cokriging technique, which can be useful for the imputation of missing imaging data. Simulation studies and real data analysis are used to evaluate the prediction accuracy of SGPP and show that SGPP significantly outperforms several competing methods, such as voxel-wise linear model, in prediction. Although we focus on the morphometric variation of lateral ventricle surfaces in a clinical study of neurodevelopment, it is expected that SGPP is applicable to other imaging modalities and features. [Copyright &y& Elsevier]

Abstract: Many large-scale longitudinal imaging studies have been or are being widely conducted to better understand the progress of neuropsychiatric and neurodegenerative disorders and normal brain development. The goal of this article is to develop a multiscale adaptive generalized estimation equation (MAGEE) method for spatial and adaptive analysis of neuroimaging data from longitudinal studies. MAGEE is applicable to making statistical inference on regression coefficients in both balanced and unbalanced longitudinal designs and even in twin and familial studies, whereas standard software platforms have several major limitations in handling these complex studies. Specifically, conventional voxel-based analyses in these software platforms involve Gaussian smoothing imaging data and then independently fitting a statistical model at each voxel. However, the conventional smoothing methods suffer from the lack of spatial adaptivity to the shape and spatial extent of region of interest and the arbitrary choice of smoothing extent, while independently fitting statistical models across voxels does not account for the spatial properties of imaging observations and noise distribution. To address such drawbacks, we adapt a powerful propagation–separation (PS) procedure to sequentially incorporate the neighboring information of each voxel and develop a new novel strategy to solely update a set of parameters of interest, while fixing other nuisance parameters at their initial estimators. Simulation studies and real data analysis show that MAGEE significantly outperforms voxel-based analysis. [Copyright &y& Elsevier]

Abstract Heterogeneous longitudinal data have become prevalent in medical, biological, and social studies. This paper proposes a finite mixture of varying coefficient models for handling heterogeneous populations. Each component of the mixture is modeled by a varying coefficient mixed-effect model that characterizes the longitudinal relations among variables. The identifiability of the mixture model is studied. Regression splines with equally spaced knots are used to approximate the varying coefficient functions, and a nested expectation maximization algorithm is developed to obtain the maximum likelihood estimation. We propose a penalized likelihood method based on the smoothly clipped absolute deviation (SCAD) penalty for the component selection of finite mixture of varying coefficient model. A modified BIC-based criterion based on the SCAD penalty, the BIC SCAD , is proposed for selecting the penalty parameter and spline space simultaneously. The asymptotic properties of parameter estimation and component selection consistency are studied under mild conditions. Simulation studies are conducted to illustrate the component selection, parameter estimation, and inference of the proposed method. The model is then applied to a heterogeneous longitudinal data set from a study of the treatment effect on the use of heroin in the California Civil Addict Program. [ABSTRACT FROM AUTHOR]