{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["13"],"submitter":["Liu Y"],"pubmed_abstract":["It is widely accepted, given the complex nature of schizophrenia (SCZ) gene networks, that a few or a small number of genes are unlikely to represent the underlying functional pathways responsible for SCZ pathogenesis. Several studies from large cohorts have been performed to search for key SCZ network genes using different analytical approaches, such as differential expression tests, genome-wide association study (GWAS), copy number variations, and differential methylations, or from the analysis of mutations residing in the coding regions of the genome. However, only a small portion (<10%) of candidate genes identified in these studies were considered SCZ disease-associated genes in SCZ pathways. RNA sequencing (RNA-seq) has been a powerful method to detect functional signals. In this stu"],"journal":["Frontiers in psychiatry"],"pagination":["797329"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8978801"],"repository":["biostudies-literature"],"pubmed_title":["Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data."],"pmcid":["PMC8978801"],"pubmed_authors":["Liu Y","Sleiman PAM","Tian L","Hakonarson H","Qu HQ","Chang X","Glessner J"],"additional_accession":[]},"is_claimable":false,"name":"Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data.","description":"It is widely accepted, given the complex nature of schizophrenia (SCZ) gene networks, that a few or a small number of genes are unlikely to represent the underlying functional pathways responsible for SCZ pathogenesis. Several studies from large cohorts have been performed to search for key SCZ network genes using different analytical approaches, such as differential expression tests, genome-wide association study (GWAS), copy number variations, and differential methylations, or from the analysis of mutations residing in the coding regions of the genome. However, only a small portion (<10%) of candidate genes identified in these studies were considered SCZ disease-associated genes in SCZ pathways. RNA sequencing (RNA-seq) has been a powerful method to detect functional signals. In this stu","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022","modification":"2025-04-04T19:10:34.259Z","creation":"2025-04-04T19:10:34.259Z"},"accession":"S-EPMC8978801","cross_references":{"pubmed":["35386517"],"doi":["10.3389/fpsyt.2022.797329"]}}