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Links from GEO DataSets

Items: 20

1.
Full record GDS2824

Autism, fragile X syndrome, and 15q11-q13 duplication: lymphoblastoid cells

Analysis of lymphoblastoid cells from males with autism due to a fragile X mutation or a 15q11-q13 duplication. Results provide insight into the pathogenesis of autism spectrum disorders.
Organism:
Homo sapiens
Type:
Expression profiling by array, log ratio, 2 disease state, 3 genotype/variation sets
Platform:
GPL1708
Series:
GSE7329
30 Samples
Download data: TXT
DataSet
Accession:
GDS2824
ID:
2824
2.

Gene expression profiles of lymphoblastoid cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2824
Platform:
GPL1708
30 Samples
Download data: TXT
Series
Accession:
GSE7329
ID:
200007329
3.

control males

(Submitter supplied) gene expression profiles of lymphoblastoid cells from control males without autism Keywords: control males
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1708
15 Samples
Download data: TXT
Series
Accession:
GSE7317
ID:
200007317
4.

autism with FMR1FM

(Submitter supplied) gene expression profiles of lymphoblastoid cells from individuals with autism and full mutation of FMR1 Keywords: autism with FMR1-FM
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1708
8 Samples
Download data: TXT
Series
Accession:
GSE7316
ID:
200007316
5.

autism with dup(15q)

(Submitter supplied) gene expression profiles of lymphoblastoid cells from individuals with autism and duplication of 15q11-13 Keywords: autism with dup(15q)
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1708
7 Samples
Download data: TXT
Series
Accession:
GSE7315
ID:
200007315
6.

Expression data from brain tissue of Rattus norvegicus treated with D-Serine

(Submitter supplied) d-serine is naturally present throughout the human body. It is also used as add-on therapy for treatment-refractory schizophrenia. d-Serine interacts with the strychnine-insensitive glycine binding site of NMDA receptor, and this interaction could lead to potentially toxic activity (i.e., excitotoxicity) in brain tissue. The transcriptomic changes that occur in the brain after d-serine exposure have not been fully explored. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS3643
Platform:
GPL1355
24 Samples
Download data: CEL
Series
Accession:
GSE10748
ID:
200010748
7.
Full record GDS3643

D-serine effect on the brain: dose response

Analysis of forebrains of animals treated with up to 500 mg/kg D-serine for 96 hours. D-serine is involved in many physiological processes through its interaction with the glycine binding site of the NMDA receptor. Results provide insight into the impact of D-serine exposure on neuronal functions.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 agent, 6 dose sets
Platform:
GPL1355
Series:
GSE10748
24 Samples
Download data: CEL
DataSet
Accession:
GDS3643
ID:
3643
8.

Overexpression of disease-associated CYFIP1 alters cellular and synaptic morphology through mTOR dysregulation of mTOR signaling

(Submitter supplied) Rare genomic gains at 15q11-q13 are observed in 1-2% of individuals with an Autism Spectrum Disorder (ASD). Because many genes are included here and breakpoints vary between cases, the potential contribution of specific genes is unclear. Cytoplasmic FMR1 interacting protein 1 (CYFIP1) is interesting in this regard given the association of smaller overlapping deletions with each of schizophrenia and intellectual disability. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
6 Samples
Download data: TXT
Series
Accession:
GSE40852
ID:
200040852
9.

Gene expression profiling of lymphoblastoid cell lines from monozygotic twins discordant in severity of autism

(Submitter supplied) Background: The autism spectrum includes a set of complex multigenic developmental disorders that severely impact the development of language, non-verbal communication, and social skills, and are associated with odd, stereotyped, repetitive behavior and restricted interests. To date, diagnosis of these neurologically based disorders relies predominantly upon behavioral observations often prompted by delayed speech or aberrant behavior, and there are no known genes that can serve as definitive biomarkers for the disorders. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL3427
19 Samples
Download data
Series
Accession:
GSE4187
ID:
200004187
10.

Gene Expression Signature Shared in Autoimmune Diseases Not in Unaffected Family Members

(Submitter supplied) Even though autoimmune diseases are heterogeneous, believed to result from the interaction between genetic and environmental components, patients with these disorders exhibit reproducible patterns of gene expression in their peripheral blood mononuclear cells. A portion of this gene expression profile reflects family resemblance rather than the actual presence of an autoimmune disease. Here we wanted to identify that portion of this gene expression pattern that is independent of family resemblance and determine if it is a product of disease duration, disease onset, or other factors. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL538
67 Samples
Download data
Series
Accession:
GSE3447
ID:
200003447
11.

Gene expression profiling of lymphoblastoid cell lines from autistic and nonaffected sib pairs

(Submitter supplied) Despite the identification of numerous autism susceptibility genes, the pathobiology of autism remains unknown. The present “case-control” study takes a global approach to understanding the molecular basis of autism spectrum disorders based upon large-scale gene expression profiling. DNA microarray analyses were conducted on lymphoblastoid cell lines from over 20 sib pairs in which one sibling had a diagnosis of autism and the other was not affected in order to identify biochemical and signaling pathways which are differentially regulated in cells from autistic and nonautistic siblings. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL3427
38 Samples
Download data: MEV
Series
Accession:
GSE15451
ID:
200015451
12.

Transcriptomic analysis of autistic brain reveals convergent molecular pathology [high-throughput sequence data]

(Submitter supplied) Autism spectrum disorder (ASD) is a common, highly heritable neurodevelopmental condition characterized by marked genetic heterogeneity. Thus, a fundamental question is whether autism represents an aetiologically heterogeneous disorder in which the myriad genetic or environmental risk factors perturb common underlying molecular pathways in the brain. Here, we demonstrate consistent differences in transcriptome organization between autistic and normal brain by gene co-expression network analysis. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9115
6 Samples
Download data: TXT
13.

Transcriptomic Analysis of Autism Brain Reveals Convergent Molecular Pathology [array data]

(Submitter supplied) Autism spectrum disorder (ASD) is a common, highly heritable neuro-developmental condition characterized by marked genetic heterogeneity. Thus, a fundamental question is whether autism represents an etiologically heterogeneous disorder in which the myriad genetic or environmental risk factors perturb common underlying molecular pathways in the brain. Here, we demonstrate consistent differences in transcriptome organization between autistic and normal brain by gene co-expression network analysis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6883
79 Samples
Download data: TXT
Series
Accession:
GSE28521
ID:
200028521
14.

Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders

(Submitter supplied) Autism spectrum disorders (ASD) are neurodevelopmental disorders characterized by delayed/abnormal language development, deficits in social interaction, repetitive behaviors and restricted interests. The heterogeneity in clinical presentation of ASD, likely due to different etiologies, complicates genetic/biological analyses of these disorders. DNA microarray analyses were conducted on 116 lymphoblastoid cell lines (LCL) from individuals with idiopathic autism who are divided into 3 phenotypic subgroups according to severity scores from the commonly used Autism Diagnostic Interview-Revised questionnaire and age-matched, nonautistic controls. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL3427
116 Samples
Download data: MEV
Series
Accession:
GSE15402
ID:
200015402
15.

Brain transcriptional and epigenetic associations with the autistic phenotype

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Methylation profiling by array
Platforms:
GPL10558 GPL8490
72 Samples
Download data
Series
Accession:
GSE38609
ID:
200038609
16.

Brain transcriptional and epigenetic associations with the autistic phenotype (methylation data)

(Submitter supplied) Autism is a common neurodevelopmental syndrome. Numerous rare genetic etiologies are reported; most cases are idiopathic. To uncover important gene dysregulation in autism, we analyzed carefully selected idiopathic autistic and control cerebellar and BA19 (occipital) brain tissues using high-resolution whole genome gene expression and DNA methylation microarrays. No changes in DNA methylation were identified in autistic brain but gene expression abnormalities in two areas of metabolism were apparent: down-regulation of genes of mitochondrial oxidative phosphorylation and of protein translation. more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL8490
36 Samples
Download data: TXT
Series
Accession:
GSE38608
ID:
200038608
17.

Brain transcriptional and epigenetic associations with the autistic phenotype (expression data)

(Submitter supplied) Autism is a common neurodevelopmental syndrome. Numerous rare genetic etiologies are reported; most cases are idiopathic. To uncover important gene dysregulation in autism we analyzed carefully selected idiopathic autistic and control cerebellar and BA19 (occipital) brain tissues using high resolution whole genome gene expression and DNA methylation microarrays. No changes in DNA methylation were identified in autistic brain but gene expression abnormalities in two areas of metabolism were apparent: down-regulation of genes of mitochondrial oxidative phosphorylation and of protein translation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
36 Samples
Download data: TXT
Series
Accession:
GSE38322
ID:
200038322
18.

Gene expression in blood of children with autism spectrum disorder

(Submitter supplied) Gene expression in blood of children with autism spectrum disorder (ASD) was studied. Transcriptional profiles were compared with age and gender matched, typically developing children from the general population (GP) or IQ matched children with mental retardation or developmental delay (MR/DD). Keywords: autism analysis
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
56 Samples
Download data: CEL
Series
Accession:
GSE6575
ID:
200006575
19.

Modeling the functional genomics of autism using human neurons.

(Submitter supplied) We examined whether a human neuronal culture system could be used to assess the transcriptional program involved in human neural differentiation and in modeling some of the molecular features of a neurodevelopmental disorder such as autism.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6883
16 Samples
Download data: TXT
Series
Accession:
GSE28046
ID:
200028046
20.

The Disruption of Celf6, a Gene Identified by Translational Profiling of Serotonergic Neurons, Results in Autism-Related Behaviors

(Submitter supplied) The immense molecular diversity of neurons challenges our ability to deconvolve the relationship between the genetic and the cellular underpinnings of neuropsychiatric disorders. We suspected that comprehensive approaches to parsing this complexity may inform human genetics studies. The serotonergic system has long been suspected in disorders that involve repetitive behaviors and resistance to change, including autism. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE36068
ID:
200036068
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