https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:41878 Tue 16 Aug 2022 10:04:26 AEST ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:36040 Thu 22 Jun 2023 10:07:54 AEST ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:37069 Thu 13 Aug 2020 12:12:43 AEST ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:1927 Sat 24 Mar 2018 08:33:12 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:1288 Sat 24 Mar 2018 08:32:45 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:2955 Sat 24 Mar 2018 08:31:00 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:9881 Sat 24 Mar 2018 08:12:48 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:17127 Sat 24 Mar 2018 08:02:31 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:20776 Sat 24 Mar 2018 08:00:21 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:19895 Sat 24 Mar 2018 07:57:03 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:29913 Sat 24 Mar 2018 07:40:55 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:25812 postmortem brain tissue, and later in studies of peripheral blood. The collective body of schizophrenia microarray literature contains apparent inconsistencies between studies, with failures to replicate top hits, in part due to small sample sizes, cohort-specific effects, differences in array types, and other confounders. In an attempt to summarize existing studies of schizophrenia cases and non-related comparison subjects, we performed two mega-analyses of a combined set of microarray data from postmortem prefrontal cortices (n = 315) and from ex-vivo blood tissues (n = 578). We adjusted regression models per gene to remove non-significant covariates, providing best-estimates of transcripts dysregulated in schizophrenia. We also examined dysregulation of functionally related gene sets and gene co-expression modules, and assessed enrichment of cell types and genetic risk factors. The identities of the most significantly dysregulated genes were largely distinct for each tissue, but the findings indicated common emergent biological functions (e.g. immunity) and regulatory factors (e.g., predicted targets of transcription factors and miRNA species across tissues). Our network-based analyses converged upon similar patterns of heightened innate immune gene expression in both brain and blood in schizophrenia. We also constructed generalizable machine-learning classifiers using the blood-based microarray data. Our study provides an informative atlas for future pathophysiologic and biomarker studies of schizophrenia.]]> Sat 24 Mar 2018 07:34:35 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:27390 Sat 24 Mar 2018 07:34:09 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:23767 Sat 24 Mar 2018 07:13:20 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:23440 Sat 24 Mar 2018 07:12:55 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:54757 Mon 11 Mar 2024 15:01:56 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:33406 Fri 26 Oct 2018 16:06:18 AEDT ]]>