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2020-07-20
相关数据集
Genomic evidence for multifactorial inheritance in autism
Autism spectrum disorder (ASD) is a common highly heritable disorder with multifactorial influences.
DataCite Commons2023-05-16 更新70
Coordinates of Xp11.22 deletions and Xp11.22 genes previously implicated or proposed to be involved in the development of intellectual disability/developmental delay/autism.
Coordinates of Xp11.22 deletions and Xp11.22 genes previously implicated or proposed to be involved in the development of intellectual disability/developmental delay/autism.
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Enrichment of rare functional variants in mGluR pathway genes in autism cases detected by high-throughput sequencing.
SNVs in mGluR pathway genes were identified in pools of AGRE or control samples and classified based on allele frequency and predicted functional impact. The values shown represent the numbers of dist
NIAID Data Ecosystem20
Characteristics of CNVs identified in 105 autism patients and 267 healthy controls.
Characteristics of CNVs identified in 105 autism patients and 267 healthy controls.
NIAID Data Ecosystem60
Participant demographics (N = 14).
Several professional organizations recommend conducting genetic testing as part of the autism diagnosis process, as it can provide additional information and benefits for autistic people and their fam
NIAID Data Ecosystem20



