arXiv subjects

Neda Jahanshad

Publications and source records attributed to Neda Jahanshad.

22 records · Page 2Linked to original sources

arXiv2017

Structural Connectome Validation Using Pairwise Classification

In this work, we study the extent to which structural connectomes and topological derivative measures are unique to individual changes within human brains. To do so, we classify structural connectome pairs from two large longitudinal datasets as either belonging to the same individual or not. Our data is comprised of 227 individuals from the Alzheimer's Disease Neuroimaging Initiative (ADNI) and 226 from the Parkinson's Progression Markers Initiative (PPMI). We achieve 0.99 area under the ROC curve score for features which represent either weights or network structure of the connectomes (node degrees, PageRank and local efficiency). Our approach may be useful for eliminating noisy features as a preprocessing step in brain aging studies and early diagnosis classification problems.

q-bio.NC↗

arXiv2016

An Empirical Study of Continuous Connectivity Degree Sequence Equivalents

In the present work we demonstrate the use of a parcellation free connectivity model based on Poisson point processes. This model produces for each subject a continuous bivariate intensity function that represents for every possible pair of points the relative rate at which we observe tracts terminating at those points. We fit this model to explore degree sequence equivalents for spatial continuum graphs, and to investigate the local differences between estimated intensity functions for two different tractography methods. This is a companion paper to Moyer et al. (2016), where the model was originally defined.

q-bio.NC↗

arXiv2016

Large-scale Collaborative Imaging Genetics Studies of Risk Genetic Factors for Alzheimer's Disease Across Multiple Institutions

Genome-wide association studies (GWAS) offer new opportunities to identify genetic risk factors for Alzheimer's disease (AD). Recently, collaborative efforts across different institutions emerged that enhance the power of many existing techniques on individual institution data. However, a major barrier to collaborative studies of GWAS is that many institutions need to preserve individual data privacy. To address this challenge, we propose a novel distributed framework, termed Local Query Model (LQM) to detect risk SNPs for AD across multiple research institutions. To accelerate the learning process, we propose a Distributed Enhanced Dual Polytope Projection (D-EDPP) screening rule to identify irrelevant features and remove them from the optimization. To the best of our knowledge, this is the first successful run of the computationally intensive model selection procedure to learn a consistent model across different institutions without compromising their privacy while ranking the SNPs that may collectively affect AD. Empirical studies are conducted on 809 subjects with 5.9 million SNP features which are distributed across three individual institutions. D-EDPP achieved a 66-fold speed-up by effectively identifying irrelevant features.

cs.LG↗

arXiv2015

Unifying inference on brain network variations in neurological diseases: The Alzheimer's case

There is growing interest in understanding how the structural interconnections among brain regions change with the occurrence of neurological diseases. Diffusion weighted MRI imaging has allowed researchers to non-invasively estimate a network of structural cortical connections made by white matter tracts, but current statistical methods for relating such networks to the presence or absence of a disease cannot exploit this rich network information. Standard practice considers each edge independently or summarizes the network with a few simple features. We enable dramatic gains in biological insight via a novel unifying methodology for inference on brain network variations associated to the occurrence of neurological diseases. The key of this approach is to define a probabilistic generative mechanism directly on the space of network configurations via dependent mixtures of low-rank factorizations, which efficiently exploit network information and allow the probability mass function for the brain network-valued random variable to vary flexibly across the group of patients characterized by a specific neurological disease and the one comprising age-matched cognitively healthy individuals.

stat.AP↗