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Links from GEO DataSets

Items: 20

1.

RNA-sequencing of human post-mortem brain tissues

(Submitter supplied) RNA-seq profiling was conducted on clinically-annotated human post-mortem brain tissues
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
281 Samples
Download data: TXT
2.

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
3.

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
4.

Transcriptomic profiles of skin fibroblasts from patients affected by schizophrenia and controls

(Submitter supplied) Whole-genome expression studies in peripheral tissues of patients affected by schizophrenia (SCZ) can provide new insights into the molecular basis of the disorder and innovative biomarkers that may be of great usefulness in the clinical practice. Recent evidence suggests that skin fibroblasts could represent a non-neural peripheral model useful to investigate molecular alterations in psychiatric disorders. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL11532
40 Samples
Download data: CEL
Series
Accession:
GSE62333
ID:
200062333
5.

Gene expression of L3 and L5 pyramidal neurons in the DLPFC comparing schizophrenia from bipolar major depressive disorders and unaffected subjects.

(Submitter supplied) Impairments in certain cognitive processes (e.g., working memory) are typically most pronounced in schizophrenia (SZ), intermediate in bipolar disorder (BP) and least in major depressive disorder (MDD). Given that working memory depends, in part, on neural circuitry that includes pyramidal neurons in layer 3 (L3) and layer 5 (L5) of the dorsolateral prefrontal cortex (DLPFC), we sought to determine if transcriptome alterations in these neurons were shared or distinctive for each diagnosis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13667
286 Samples
Download data: CEL
Series
Accession:
GSE87610
ID:
200087610
6.

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
7.
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
8.

Expression profiling of human adult postmortem brain tissue from subjects with bipolar disorder and healthy controls

(Submitter supplied) Bipolar affective disorder is a severe psychiatric disorder with a strong genetic component but unknown pathophysiology. We used microarray technology (Affymetrix HG-U133A GeneChips) to determine the expression of approximately 22 000 mRNA transcripts in post-mortem brain tissue (dorsolateral prefrontal cortex and orbitofrontal cortex) from patients with bipolar disorder and matched healthy controls. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
82 Samples
Download data: CEL
Series
Accession:
GSE5392
ID:
200005392
9.

Adult postmortem brain tissue (orbitofrontal cortex) from subjects with bipolar disorder and healthy controls

(Submitter supplied) Bipolar affective disorder is a severe psychiatric disorder with a strong genetic component but unknown pathophysiology. We used microarray technology (Affymetrix HG-U133A GeneChips) to determine the expression of approximately 22 000 mRNA transcripts in post-mortem brain tissue (orbitofrontal cortex) from patients with bipolar disorder and matched healthy controls. Orbitofrontal cortex tissue from a cohort of 30 subjects was investigated and the final analysis included 10 bipolar and 11 control subjects. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2191
Platform:
GPL96
21 Samples
Download data: CEL
Series
Accession:
GSE5389
ID:
200005389
10.

Adult postmortem brain tissue (dorsolateral prefrontal cortex) from subjects with bipolar disorder and healthy controls

(Submitter supplied) Bipolar affective disorder is a severe psychiatric disorder with a strong genetic component but unknown pathophysiology. We used microarray technology (Affymetrix HG-U133A GeneChips) to determine the expression of approximately 22 000 mRNA transcripts in post-mortem brain tissue (dorsolateral prefrontal cortex) from patients with bipolar disorder and matched healthy controls. A cohort of 70 subjects was investigated and the final analysis included 30 bipolar and 31 control subjects. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2190
Platform:
GPL96
61 Samples
Download data: CEL
Series
Accession:
GSE5388
ID:
200005388
11.
Full record GDS2191

Bipolar disorder: orbitofrontal cortex

Analysis of postmortem orbitofrontal cortex from 10 adults with bipolar disorder. Results provide insight into the pathophysiology of the disease.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state sets
Platform:
GPL96
Series:
GSE5389
21 Samples
Download data: CEL
DataSet
Accession:
GDS2191
ID:
2191
12.
Full record GDS2190

Bipolar disorder: dorsolateral prefrontal cortex

Analysis of postmortem dorsolateral prefrontal cortex from 30 adults with bipolar disorder. Results provide insight into the pathophysiology of the disease.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state sets
Platform:
GPL96
Series:
GSE5388
61 Samples
Download data: CEL
DataSet
Accession:
GDS2190
ID:
2190
13.

Whole transcriptome analysis of postmortem human hippocampus dentate gyrus granlule cells

(Submitter supplied) We investigated the transcriptome of dentate gyrus (DG) granule cells in postmortem hippocampus from 79 subjects with mental illness (schizophrenia, bipolar disorder, major depression) or non-psychiatric controls.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13393
79 Samples
Download data: TXT
Series
Accession:
GSE42546
ID:
200042546
14.

RNA-sequencing of the brain transcriptome implicates dysregulation of neuroplasticity, circadian rhythms, and GTPase binding in bipolar disorder

(Submitter supplied) See "Akula et al., Molecular Psychiatry in Press". RNA-sequencing (RNA-seq) is a powerful technique to investigate the complexity of gene expression in the human brain. We used RNA-seq to survey the brain transcriptome in high-quality post-mortem dorsolateral prefrontal cortex from 11 individuals diagnosed with bipolar disorder (BD) and from 11 age- and gender-matched controls. Deep sequencing was performed, with over 350 million reads per specimen. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL15433 GPL9115
22 Samples
Download data: TXT
15.

Building a schizophrenia genetic network: Transcription Factor 4 regulates genes involved in neuronal development and schizophrenia risk

(Submitter supplied) The transcription factor 4 (TCF4) locus is a robust association finding with schizophrenia (SZ), but little is known about the genes regulated by the encoded transcription factor. Therefore, we conducted chromatin immunoprecipitation sequencing (ChIP-seq) of TCF4 in neural-derived (SH-SY5Y) cells to identify genome-wide TCF4 binding sites, followed by data integration with SZ association findings. We identified 11,322 TCF4 binding sites overlapping in two ChIP-seq experiments. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20148
5 Samples
Download data: TAGALIGN, TXT
Series
Accession:
GSE112704
ID:
200112704
16.

Common schizophrenia risk variants are implicated in the function of glutamatergic neurons

(Submitter supplied) The epigenome of human brain cells encompasses key information in understanding brain function in both healthy and diseased states. To further explore this, we used ATAC-seq to profile chromatin structure in four distinct populations of cells (glutamatergic neurons, GABAergic neurons, oligodendrocytes, and microglia/astrocytes), from three different regions of the brain. Chromatin accessibility was found to vary vastly by cell type and, more moderately, by brain region, with glutamatergic neurons showing the greatest regional variability. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
47 Samples
Download data: TSV
Series
Accession:
GSE143666
ID:
200143666
17.

An Atlas of Chromatin Accessibility in the Adult Human Brain

(Submitter supplied) The majority of common genetic risk variants associated with neuropsychiatric disease are non-coding and are thought to exert their effects by disrupting the function of cis regulatory elements (CREs), including promoters and enhancers. Within each cell, chromatin is arranged in specific patterns to expose the repertoire of CREs required for optimal spatiotemporal regulation of gene expression. To further our understanding of the complex mechanisms that modulate transcription in the brain, we utilized frozen postmortem samples to generate the largest human brain and cell type-specific open chromatin dataset to date. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
115 Samples
Download data: BW
Series
Accession:
GSE96949
ID:
200096949
18.

Cell-type specific transcriptomics of the the dlPFC in females with MDD [single-nucleus RNA-seq]

(Submitter supplied) We performed high-throughput snRNA-seq using the 10X Genomics Chromium platform on archived post-mortem dorsolateral prefrontal cortex (BA9) tissue in female MDD subjects who died by suicide and in female control subjects to identify cell-type specific differentially expressed genes. We further re-processed in parallel a previously generated snRNA-seq dataset in males with or without MDD to generate comparable differential expression results and compare the cell-type specific MDD-associated differences between the sexes.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL28038 GPL24676
38 Samples
Download data: CSV, MTX
Series
Accession:
GSE213982
ID:
200213982
19.

Transcriptional signatures of schizophrenia in hiPSC-derived NPCs and neurons are concordant with signatures from post mortem adult brains

(Submitter supplied) Whereas highly penetrant variants have proven well-suited to human induced pluripotent stem cell (hiPSC)-based models, the power of hiPSC-based studies to resolve the much smaller effects of common variants within the size of cohorts that can be realistically assembled remains uncertain. In developing a large case/control schizophrenia (SZ) hiPSC-derived cohort of neural progenitor cells and neurons, we identified and accounted for a variety of technical and biological sources of variation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
94 Samples
Download data: CSV
20.

Sex-specific Transcriptional Signatures in Human Depression

(Submitter supplied) Rational: Major depressive disorder (MDD) is a leading cause of disease burden worldwide. While the incidence, symptoms and treatment of MDD all point toward major sex differences, the molecular mechanisms underlying this sexual dimorphism remain largely unknown. Methods: Here, combining differential expression and gene coexpression network analyses, we provide a comprehensive characterization of male and female transcriptional profiles associated with MDD across 6 brain regions. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL13112 GPL11154
341 Samples
Download data: TXT
Series
Accession:
GSE102556
ID:
200102556
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