Cited by 290Bioinformatics and Genomic NetworksFunctional Brain Connectivity StudiesGene Regulatory Network Analysis

The DOI matches its Crossref record; 105 of the 105 references it cites were found in a registry or an index.

Beyond modules and hubs: the potential of gene coexpression networks for investigating molecular mechanisms of complex brain disorders

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Gaiteri, C., Ding, Y., French, B., Tseng, G. C., Sibille, E.·2014·Genes, Brain and Behavior

Abstract

In a research environment dominated by reductionist approaches to brain disease mechanisms, gene network analysis provides a complementary framework in which to tackle the complex dysregulations that occur in neuropsychiatric and other neurological disorders. Gene–gene expression correlations are a common source of molecular networks because they can be extracted from high‐dimensional disease data and encapsulate the activity of multiple regulatory systems. However, the analysis of gene coexpression patterns is often treated as a mechanistic black box, in which looming ‘hub genes’ direct cellular networks, and where other features are obscured. By examining the biophysical bases of coexpression and gene regulatory changes that occur in disease, recent studies suggest it is possible to use coexpression networks as a multi‐omic screening procedure to generate novel hypotheses for disease mechanisms. Because technical processing steps can affect the outcome and interpretation of coexpression networks, we examine the assumptions and alternatives to common patterns of coexpression analysis and discuss additional topics such as acceptable datasets for coexpression analysis, the robust identification of modules, disease‐related prioritization of genes and molecular systems and network meta‐analysis. To accelerate coexpression research beyond modules and hubs, we highlight some emerging directions for coexpression network research that are especially relevant to complex brain disease, including the centrality–lethality relationship, integration with machine learning approaches and network pharmacology .

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  1. 10.1038/nature10166 · DOI · Paper page
  2. E.M. Izhikevich 2007 The MIT press Cambridge

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Metadata

Authors
Gaiteri, C., Ding, Y., French, B., Tseng, G. C., & Sibille, E.
Affiliations
  • Allen Institute for Brain Science (US)
  • University of Pittsburgh (US)
Corresponding author
Sibille, E.
Venue
Genes, Brain and Behavior
Publisher
Wiley
Published
2013-12-10
Volume
13
Issue
1
Pages
13-24
ISSN
  • 1601-183X (ISSN-L)
  • 1601-1848
OpenAlex
W1823837540
Cited by
289
References
105
Citations by year
2026: 9 · 2025: 20 · 2024: 14 · 2023: 14 · 2022: 25 · 2021: 38 · 2020: 21 · 2019: 24 · 2018: 29 · 2017: 32 · 2016: 34 · 2015: 20 · 2014: 9
FWCI
1.97
Type
journal article
Language
en
Open access
Locations
  • Genes Brain & Behavior (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institutes of Health
  • National Institute of Mental Health (MH084060, R01MH093723, R01MH077159, K02MH084060)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
Keywords
gene co-expression network, neuropsychiatric disorders, hub genes, network modules, network meta-analysis, gene prioritization, network pharmacology, machine learning integration
MeSH terms
Animals, Humans, Nervous System Diseases, Transcription, Genetic, Gene Regulatory Networks

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