ArticleNeuroImage2013
Guided exploration of genomic risk for gray matter abnormalities in schizophrenia using parallel independent component analysis with reference.
Article in NeuroImage, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
35 citing papers in PubMed, 54 citations in OpenAlex.
- Imaging-genomic spatial-modality attentive fusion for studying neuropsychiatric disorders.Human brain mapping · 2024Article
- A spatially constrained independent component analysis jointly informed by structural and functional network connectivity.bioRxiv : the preprint server for biology · 2024Article
- Multi-modal deep learning from imaging genomic data for schizophrenia classification.Frontiers in psychiatry · 2024Article
- A spatially constrained independent component analysis jointly informed by structural and functional network connectivity.Network neuroscience (Cambridge, Mass.) · 2024Article
- Deep multimodal predictome for studying mental disorders.Human brain mapping · 2023Article
- Three-way parallel group independent component analysis: Fusion of spatial and spatiotemporal magnetic resonance imaging data.Human brain mapping · 2022Article
- Sparse deep neural networks on imaging genetics for schizophrenia case-control classification.Human brain mapping · 2021Article
- Distinct structural brain circuits indicate mood and apathy profiles in bipolar disorder.NeuroImage. Clinical · 2020Article
- Parallel group ICA+ICA: Joint estimation of linked functional network variability and structural covariation with application to schizophrenia.Human brain mapping · 2019Article
- Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa.Molecular neurobiology · 2019Article
- A method for building a genome-connectome bipartite graph model.Journal of neuroscience methods · 2019Article
- The Translational Potential of Neuroimaging Genomic Analyses To Diagnosis And Treatment In The Mental Disorders.Proceedings of the IEEE. Institute of Electrical and Electronics Engineers · 2019Article
- Shared Genetic Risk of Schizophrenia and Gray Matter Reduction in 6p22.1.Schizophrenia bulletin · 2019Article
- A framework for linking resting-state chronnectome/genome features in schizophrenia: A pilot study.NeuroImage · 2019Article
- Imaging Genetics Towards a Refined Diagnosis of Schizophrenia.Frontiers in psychiatry · 2019Review
- A Schizophrenia-Related Genetic-Brain-Cognition Pathway Revealed in a Large Chinese Population.EBioMedicine · 2018Article
- Multimodal Fusion With Reference: Searching for Joint Neuromarkers of Working Memory Deficits in Schizophrenia.IEEE transactions on medical imaging · 2018Article
- Variability in Resting State Network and Functional Network Connectivity Associated With Schizophrenia Genetic Risk: A Pilot Study.Frontiers in neuroscience · 2018Article
- Neuroimaging genomics in psychiatry-a translational approach.Genome medicine · 2017Review
- Multimodal Neuroimaging in Schizophrenia: Description and Dissemination.Neuroinformatics · 2017Article
Corrections and comments
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Authors and funding
12 authors at 7 institutions in 2 countries.
Funding
Abstract
One application of imaging genomics is to explore genetic variants associated with brain structure and function, presenting a new means of mapping genetic influences on mental disorders. While there is growing interest in performing genome-wide searches for determinants, it remains challenging to identify genetic factors of small effect size, especially in limited sample sizes. In an attempt to address this issue, we propose to take advantage of a priori knowledge, specifically to extend parallel independent component analysis (pICA) to incorporate a reference (pICA-R), aiming to better reveal relationships between hidden factors of a particular attribute. The new approach was first evaluated on simulated data for its performance under different configurations of effect size and dimensionality. Then pICA-R was applied to a 300-participant (140 schizophrenia (SZ) patients versus 160 healthy controls) dataset consisting of structural magnetic resonance imaging (sMRI) and single nucleotide polymorphism (SNP) data. Guided by a reference SNP set derived from ANK3, a gene implicated by the Psychiatric Genomic Consortium SZ study, pICA-R identified one pair of SNP and sMRI components with a significant loading correlation of 0.27 (p=1.64×10(-6)). The sMRI component showed a significant group difference in loading parameters between patients and controls (p=1.33×10(-15)), indicating SZ-related reduction in gray matter concentration in prefrontal and temporal regions. The linked SNP component also showed a group difference (p=0.04) and was predominantly contributed to by 1030 SNPs. The effect of these top contributing SNPs was verified using association test results of the Psychiatric Genomic Consortium SZ study, where the 1030 SNPs exhibited significant SZ enrichment compared to the whole genome. In addition, pathway analyses indicated the genetic component majorly relating to neurotransmitter and nervous system signaling pathways. Given the simulation and experiment results, pICA-R may prove a promising multivariate approach for use in imaging genomics to discover reliable genetic risk factors under a scenario of relatively high dimensionality and small effect size.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.