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Links from GEO DataSets

Items: 17

1.

Major depression MDD suicide brain study

(Submitter supplied) Background: Major Depressive Disorder (MDD) represents a major social and economic health issue and constitutes a major risk factor for MDD suicide. The molecular pathology of suicidal depression remains poorly understood, although it has been hypothesized that regulatory genomic processes are involved in the pathology of both MDD and suicidality. Methods: Genome-wide patterns of DNA methylation were assessed in depressed MDD suicide completers (n=20) and compared to non-psychiatric, sudden-death controls (n=20) using tissue from two cortical brain regions (Brodmann Area 11 (BA11) and Brodmann Area 25 (BA25)). more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
75 Samples
Download data: CSV
Series
Accession:
GSE88890
ID:
200088890
2.

Genome-Wide DNA Methylation Meta-analysis in the Brains of Suicide Completers I

(Submitter supplied) Suicide is the second leading cause of death globally among young people representing a significant global health burden. Although the molecular pathology of suicide remains poorly understood, it has been hypothesised that epigenomic processes may play a role. The objective of this study was to identify suicide-associated DNA methylation changes in the human brain by utilising previously published and unpublished methylomic datasets. more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL23976
58 Samples
Download data: CSV
Series
Accession:
GSE137222
ID:
200137222
3.

Whole-transcriptome brain expression and exon-usage profiling in major depression and suicide

(Submitter supplied) Brain gene expression profiling studies of suicide and depression using oligonucleotide microarrays have often failed to distinguish these two phenotypes. Moreover, next generation sequencing approaches are more accurate in quantifying gene expression and can detect alternative splicing. Using RNA-seq, we examined whole-exome gene and exon expression in non-psychiatric controls (CON, N=29), DSM-IV major depressive disorder suicides (MDD-S, N=21) and MDD non-suicides (MDD, N=9) in the dorsal lateral prefrontal cortex (Brodmann Area 9) of sudden death medication-free individuals post mortem. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL16791 GPL15520
86 Samples
Download data: CSV
4.

DNA methylation and inflammation marker profiles associated with a history of depression.

(Submitter supplied) Depression is a common and disabling disorder, representing a major social and economic health issue. Moreover, depression is associated with the progression of diseases with an inflammatory etiology including many inflammatory-related disorders. At the molecular level, the mechanisms by which depression might promote the onset of these diseases and associated immune-dysfunction are not well understood. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
194 Samples
Download data: CSV
Series
Accession:
GSE113725
ID:
200113725
5.

Schizophrenia-associated methylomic variation: molecular signatures of disease and polygenic risk burden across multiple brain regions

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
142 Samples
Download data
Series
Accession:
GSE89707
ID:
200089707
6.

Schizophrenia-associated methylomic variation: molecular signatures of disease and polygenic risk burden across multiple brain regions (striatum LNDBB).

(Submitter supplied) Genetic association studies provide evidence for a substantial polygenic component to schizophrenia, although the neurobiological mechanisms underlying the disorder remain largely undefined. Building on recent studies supporting a role for developmentally regulated epigenetic variation in the molecular etiology of schizophrenia, this study aimed to identify epigenetic variation associated with both a diagnosis of schizophrenia and elevated polygenic risk burden for the disease across multiple brain regions. more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
49 Samples
Download data: CSV
Series
Accession:
GSE89706
ID:
200089706
7.

Schizophrenia-associated methylomic variation: molecular signatures of disease and polygenic risk burden across multiple brain regions (striatum DBCBB).

(Submitter supplied) Genetic association studies provide evidence for a substantial polygenic component to schizophrenia, although the neurobiological mechanisms underlying the disorder remain largely undefined. Building on recent studies supporting a role for developmentally regulated epigenetic variation in the molecular etiology of schizophrenia, this study aimed to identify epigenetic variation associated with both a diagnosis of schizophrenia and elevated polygenic risk burden for the disease across multiple brain regions. more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
33 Samples
Download data: CSV
Series
Accession:
GSE89705
ID:
200089705
8.

Schizophrenia-associated methylomic variation: molecular signatures of disease and polygenic risk burden across multiple brain regions (hippocampus LNDBB).

(Submitter supplied) Genetic association studies provide evidence for a substantial polygenic component to schizophrenia, although the neurobiological mechanisms underlying the disorder remain largely undefined. Building on recent studies supporting a role for developmentally regulated epigenetic variation in the molecular etiology of schizophrenia, this study aimed to identify epigenetic variation associated with both a diagnosis of schizophrenia and elevated polygenic risk burden for the disease across multiple brain regions. more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
27 Samples
Download data: CSV
Series
Accession:
GSE89703
ID:
200089703
9.

Schizophrenia-associated methylomic variation: molecular signatures of disease and polygenic risk burden across multiple brain regions (cerebellum DBCBB).

(Submitter supplied) Genetic association studies provide evidence for a substantial polygenic component to schizophrenia, although the neurobiological mechanisms underlying the disorder remain largely undefined. Building on recent studies supporting a role for developmentally regulated epigenetic variation in the molecular etiology of schizophrenia, this study aimed to identify epigenetic variation associated with both a diagnosis of schizophrenia and elevated polygenic risk burden for the disease across multiple brain regions. more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
33 Samples
Download data: CSV
Series
Accession:
GSE89702
ID:
200089702
10.

lncRNA and mRNA expression data in peripheral blood sampled from MDD patients

(Submitter supplied) Long noncoding RNAs (lncRNAs) are pervasively transcribed and have a direct role in the regulation of genes involved in neural plasticity and cognitive function. Moreover, alterations in the expression of several lncRNAs have been observed in some psychiatric disorders. However, changes in the expression of regulatory lncRNAs in MDD have not yet been reported. Using microarrays, we profiled the expression of 51513 lncRNAs and 35123 mRNAs in peripheral blood sampled from MDD patients as well as demographically-matched controls.
Organism:
Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platform:
GPL17976
22 Samples
Download data: CEL, CHP
Series
Accession:
GSE52790
ID:
200052790
11.

Methylomic profiling of human brain tissue supports a neurodevelopmental origin for schizophrenia.

(Submitter supplied) Background: Schizophrenia is a severe neuropsychiatric disorder that is hypothesized to result from disturbances in early brain development, and there is mounting evidence to support a role for developmentally-regulated epigenetic variation in the molecular etiology of the disorder. Here, we describe a systematic study of schizophrenia-associated methylomic variation in the adult brain and its relationship to changes in DNA methylation across human fetal brain development. more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
87 Samples
Download data: CSV, TXT
Series
Accession:
GSE61431
ID:
200061431
12.

Methylomic profiling of human brain tissue supports a neurodevelopmental origin for schizophrenia.

(Submitter supplied) Background: Schizophrenia is a severe neuropsychiatric disorder that is hypothesized to result from disturbances in early brain development, and there is mounting evidence to support a role for developmentally-regulated epigenetic variation in the molecular etiology of the disorder. Here, we describe a systematic study of schizophrenia-associated methylomic variation in the adult brain and its relationship to changes in DNA methylation across human fetal brain development. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
33 Samples
Download data: TXT
Series
Accession:
GSE61380
ID:
200061380
13.

Meta-analysis of Epigenome Wide Association Studies of Major Depressive Disorder

(Submitter supplied) EPIC array data were generated from 2 MDD case control cohorts. EWAS was performed in each cohort, followed by meta-analysis between the 2 cohort. Cohort 1: A total of 191 blood samples from 112 patients with MDD was collected up till the interim analysis (wave 1 samples) from an observational clinical study OBSERVEMDD0001 (ClinicalTrials.gov Identifier: NCT02489305) compared to 32 healthy controls; Cohort 2: The MDD cases (N = 359) were drawn from the Molecular Biomarkers of Antidepressant Response study compared to 68 healthy controls.
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL21145
655 Samples
Download data: TXT
Series
Accession:
GSE198904
ID:
200198904
14.

Integrative transcriptome- and DNA methylation analysis of brain tissue from the temporal pole in suicide decedents and their controls (RNA-Seq)

(Submitter supplied) To investige gene expression and methylation changes in the suicide decedents group from postmortem brain tissues
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
61 Samples
Download data: CSV
Series
Accession:
GSE243356
ID:
200243356
15.

Immunological subtypes of depression: insights from monocyte gene expression III

(Submitter supplied) 32 genes of a previously established inflammation-related gene signature were assessed in 197 patients with MDD and 151 controls collected during the EU-MOODINFLAME project. Monocyte gene expression data were related to age, gender, BMI, depression severity, Childhood Adversity (CA), and Suicide Risk (SR) data studycenter 3
Organism:
Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL28312
136 Samples
Download data: TXT
Series
Accession:
GSE147584
ID:
200147584
16.

Immunological subtypes of depression: insights from monocyte gene expression

(Submitter supplied) 32 genes of a previously established inflammation-related gene signature were assessed in 197 patients with MDD and 151 controls collected during the EU-MOODINFLAME project. Monocyte gene expression data were related to age, gender, BMI, depression severity, Childhood Adversity (CA), and Suicide Risk (SR) data studycenter 1
Organism:
Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL28312
136 Samples
Download data: TXT
Series
Accession:
GSE147582
ID:
200147582
17.

Postmortem gene expression profiles in the habenulae of suicides: Implication of endothelial dysfunction in the neurovascular system

(Submitter supplied) The habenula (Hb) is an epithalamic structure that links multiple forebrain areas with the mid/hindbrain monoaminergic systems. As an anti-reward center, it has been implicated in the etiology of various neuropsychiatric disorders, particularly those associated with dysregulated reward circuitry. In this regard, Hb has been proposed as a therapeutic target for treatment-resistant depression associated with a higher risk of suicide. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
20 Samples
Download data: CEL
Series
Accession:
GSE199536
ID:
200199536
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