Similar studies for GEO DataSets (Select 200221098) - GEO DataSets

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Items: 3

Select item 2002210981.

Genetic Association study of Autism in Saudi Females using SNP array

(Submitter supplied) Multiple variations in olfactory receptor genes are contributing to ASD in females of Arab origin

Organism:: Homo sapiens

Type:: Genome variation profiling by SNP array

Platform:: GPL31039
73 Samples

Download data: IDAT, TXT

Series

Accession:: GSE221098

ID:: 200221098

PubMed Full text in PMC Similar studies

Select item 2001139672.

Functional DNA methylation signatures for genomic loci that confer an increased risk for autism spectrum disorder: 16p11.2 deletions and CHD8 variants

(Submitter supplied) Autism spectrum disorder (ASD) is a common and etiologically heterogeneous neurodevelopmental disorder. Although many genetic causes have been identified (>200 ASD-risk genes), no single gene mutation accounts for >1% of all ASD cases. A role for epigenetic mechanisms in ASD etiology is supported by the fact that many ASD-risk genes function as epigenetic regulators and evidence that epigenetic dysregulation can interrupt normal brain development. more...

Organism:: Homo sapiens

Type:: Methylation profiling by genome tiling array

Platform:: GPL13534
134 Samples

Download data: IDAT

Series

Accession:: GSE113967

ID:: 200113967

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 2002222593.

Convergent coexpression of autism associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies

(Submitter supplied) Autism spectrum disorder (ASD) is a highly heritable neurodevelopmental disorder characterized by deficits in social interactions and communication. Protein function altering variants in many genes have been shown to contribute to ASD risk; however, understanding the biological convergence across so many genes has been difficult and genetic studies depending on presence of deleterious variation may be limited in implicating highly intolerant genes with shorter coding sequences. more...