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Links from GEO DataSets

Items: 13

1.

Gene expression from human prefrontal cortex (BA46)

(Submitter supplied) Accumulating evidence suggests that mitochondrial dysfunction underlies the pathophysiology of bipolar disorder (BD) and schizophrenia (SZ). We performed large-scale DNA microarray analysis of postmortem brains of patients with BD or SZ, and examined expression patterns of mitochondria-related genes. We found a global down-regulation of mitochondrial genes, such as those encoding respiratory chain components, in BD and SZ samples, even after the effect of sample pH was controlled. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
102 Samples
Download data: CEL
Series
Accession:
GSE12649
ID:
200012649
2.

Gene expression profiles of patients with schizophrenia, bipolar disorder and healthy controls

(Submitter supplied) Schizophrenia (SZ) and bipolar disorder (BD) are severe psychiatric conditions, with a lifetime prevalence of about 1%. Both disorders have a neurodevelopment component, with onset of symptoms occurring most frequently during late adolescence or early adulthood. Genetic findings indicate the existence of an overlap in genetic susceptibility across the disorders. These gene expression profiles were used to identify the molecular mechanisms that differentiate SZ and BP from healthy controls but also that distinguish both from healthy individuals. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
88 Samples
Download data: TXT
Series
Accession:
GSE62191
ID:
200062191
3.

Gene expression from human prefrontal cortex (BA10)

(Submitter supplied) We performed the oligonucleotide microarray analysis in bipolar disorder, major depression, schizophrenia, and control subjects using postmortem prefrontal cortices provided by the Stanley Foundation Brain Collection. By comparing the gene expression profiles of similar but distinctive mental disorders, we explored the uniqueness of bipolar disorder and its similarity to other mental disorders at the molecular level. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3345
Platform:
GPL8300
50 Samples
Download data: CEL
Series
Accession:
GSE12654
ID:
200012654
4.
Full record GDS3345

Various mental disorders: postmortem brains

Analysis of postmortem prefrontal cortices from subjects with bipolar disorder, depression, and schizophrenia. Results provide insight into the molecular pathophysiology of these mental disorders.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 4 disease state sets
Platform:
GPL8300
Series:
GSE12654
50 Samples
Download data: CEL
DataSet
Accession:
GDS3345
ID:
3345
5.

Correlation between DNA methylation and gene expression in the brains of patients with bipolar disorder and schizophrenia

(Submitter supplied) Aberrant DNA methylation and gene expression have been reported in postmortem brain tissues of psychotic patients, but until now there has been no systematic evaluation of synergistic changes in methylation and expression on a genome-wide scale in brain tissue. In this study, genome-wide methylation and expression analyses were performed on cerebellum samples from 39 patients with schizophrenia, 36 patients with bipolar disorder, and 43 unaffected controls, to screen for a correlation between gene expression and CpG methylation. more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL8490
168 Samples
Download data: TXT
Series
Accession:
GSE38873
ID:
200038873
6.

Microarray profiling of PFC, HPC and STR from subjects with schizophrenia, bipolar, MDD or control

(Submitter supplied) Schizophrenia is a complex psychiatric disorder encompassing a range of symptoms and etiology dependent upon the interaction of genetic and environmental factors. Several risk genes, such as DISC1, have been associated with schizophrenia as well as bipolar disorder (BPD) and major depressive disorder (MDD), consistent with the hypothesis that a shared genetic architecture could contribute to divergent clinical syndromes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
205 Samples
Download data: CEL
Series
Accession:
GSE53987
ID:
200053987
7.

Gene expression alterations in the postmortem hippocampus from older patients with bipolar disorder – a hypothesis generating study

(Submitter supplied) Gene expression of samples from the postmortem hippocampus of older bipolar disorder subjects and controls. Gene expression data was generated using the SurePrint G3 Human Gene Expression v3 microarray. Rank feature selection was performed to identify a subset of features that can optimally differentiate BD and controls.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL20844
22 Samples
Download data: TXT
Series
Accession:
GSE210064
ID:
200210064
8.

Aberrant transcriptomes and DNA methylomes define pathways that drive pathogenesis and loss of brain laterality/asymmetry in schizophrenia and bipolar disorder

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL8490 GPL16311
41 Samples
Download data: CEL, IDAT
Series
Accession:
GSE120342
ID:
200120342
9.

Aberrant transcriptomes and DNA methylomes define pathways that drive pathogenesis and loss of brain laterality/asymmetry in schizophrenia and bipolar disorder [Illumina]

(Submitter supplied) Although the loss or reversal of brain laterality is one of the most consistent modalities in schizophrenia (SCZ) and bipolar disorder (BD), its molecular basis remains elusive. Our limited previous studies indicated that epigenetic modifications are key to the asymmetric transcriptomes of brain hemispheres. We used whole-genome expression microarrays to profile post-mortem brain samples from subjects with SCZ, psychotic BD [BD(+)] or non-psychotic BD [BD(-)], or matched controls (n=10/group, corresponding to different brain hemispheres) and performed whole-genome DNA methylation (DNAM) profiling of the same samples (n=3-4/group) to identify pathways associated with SCZ or BD(+) and genes/sites susceptible to epigenetic regulation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8490
11 Samples
Download data: IDAT
Series
Accession:
GSE120341
ID:
200120341
10.

Aberrant transcriptomes and DNA methylomes define pathways that drive pathogenesis and loss of brain laterality/asymmetry in schizophrenia and bipolar disorder [Affymetrix]

(Submitter supplied) Although the loss or reversal of brain laterality is one of the most consistent modalities in schizophrenia (SCZ) and bipolar disorder (BD), its molecular basis remains elusive. Our limited previous studies indicated that epigenetic modifications are key to the asymmetric transcriptomes of brain hemispheres. We used whole-genome expression microarrays to profile post-mortem brain samples from subjects with SCZ, psychotic BD [BD(+)] or non-psychotic BD [BD(-)], or matched controls (n=10/group, corresponding to different brain hemispheres) and performed whole-genome DNA methylation (DNAM) profiling of the same samples (n=3-4/group) to identify pathways associated with SCZ or BD(+) and genes/sites susceptible to epigenetic regulation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16311
30 Samples
Download data: CEL
Series
Accession:
GSE120340
ID:
200120340
11.

Systematically characterizing dysfunctional long intergenic non-coding RNAs in multiple brain regions of major psychosis

(Submitter supplied) Schizophrenia (SZ) and bipolar disorder (BD) are severe neuropsychiatric disorders with serious impact on patients, together termed “major psychosis”. Recently, long intergenic non-coding RNAs (lincRNAs) were reported to play important roles in mental diseases. However, little was known about their molecular mechanism in pathogenesis of SZ and BD. Here, we performed RNA sequencing on 82 post-mortem brain tissues from three brain regions (orbitofrontal cortex (BA11), anterior cingulate cortex (BA24) and dorsolateral prefrontal cortex (BA9)) of patients with SZ and BD and control subjects, generating over one billion reads. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
82 Samples
Download data: TXT
12.

Total RNA sequecing for human induced pluripotent derived cerebral organoids

(Submitter supplied) Total RNA sequecing for human induced pluripotent derived cerebral organoids from healthy controls and Bipolar disorder
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
22 Samples
Download data: TXT
13.

RNA sequencing for human induced pluripotent derived cerebral organoids

(Submitter supplied) Total RNA sequecing for human induced pluripotent derived cerebral organoids from healthy controls and schizophrenia (SCZ) patients
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
21 Samples
Download data: TXT
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