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Genetic Association study of Autism in Saudi Females using SNP array

NIAID Data Ecosystem2026-03-14 收录

自闭症遗传关联分析

SNP基因分型研究

数据链接：

https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE221098 数据链接链接失效反馈

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资源简介：

Multiple variations in olfactory receptor genes are contributing to ASD in females of Arab origin case control study

应用场景：

创建时间：

2023-03-23

自闭症遗传关联分析

外显子组测序变异检测

We report on results from whole-exome sequencing (WES) of 1,039 subjects diagnosed with autism spectrum disorders (ASD) and 870 controls selected from the NIMH repository to be of similar ancestry to

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Social development QTL associated with ASD subtypes.

自闭症遗传关联分析

神经发育数量性状位点

ap-value adjusted using Benjamini-Hochberg False Discovery Rate method; bBonferroni-adjusted p-value. *CNV located in Chromosomal band as reported by Pinto et al. [15].

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Case-control association test results for 4 runs of homozygosity (ROH) regions nominally associated with the risk of autism (unadjusted p-value <0.01) in the discovery sample.

自闭症遗传关联分析

病例对照关联研究

*RCase = prevalence rate of the ROH marker in cases; RCtrl = prevalence rate of the ROH marker in controls; ΔUnadjusted p-values based on the Fisher’s exact tests.

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Association of oligodendrocytes differentiation regulator gene DUSP15 with autism

自闭症遗传关联分析

候选基因研究

Objectives: Autism is a pervasive neurodevelopmental disorder with high heritability. Genetic factors play crucial roles in the aetiology of autism. Dual specificity phosphatase 15 (DUSP15) has been r

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Additional file 3 of Association between rare, genetic variants linked to autism and ultrasonography fetal anomalies in children with autism spectrum disorder

自闭症遗传关联分析

产前超声异常检测

Supplementary Material 3

Figshare2024-10-01 更新40