数据链接:
官方服务:
资源简介:
Association of DCDC2 with reading development.
应用场景:
创建时间:
2016-04-25
相关数据集
Overexpression of Dyrk1A is implicated in several cognitive, electrophysiological and neuromorphological alterations found in a mouse model of Down syndrome
Down syndrome (DS) phenotypes result from the overexpression of several dosage-sensitive genes. The DYRK1A (dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A) gene, which has been impl
NIAID Data Ecosystem90
Analysis of targeted exons by selector technology enrichment and SOLID sequencing of DNA from 100 individuals from Finland with dyslexia.. Targeted sequencing of 11 candidate genes for dyslexia
Genetic analyses of common traits have lately been focused on genome-wide association analysis using known markers at varying genomic resolution. Detection of rare and novel variants, however, require
NIAID Data Ecosystem40
Table_1_Genetic Structure of IQ, Phonemic Decoding Skill, and Academic Achievement.pdf
The aim of this study was to examine whether phonemic decoding skill (deficits of which characterize dyslexia) shares genetic and/or environmental covariance with scholastic abilities independent of g
NIAID Data Ecosystem30
Common variant tests VIQADJ.
Dyslexia is a common learning impairment with a genetic basis that affects word reading and spelling. An increasing list of loci and genes have been implicated, but analyses to-date have investigated
Figshare2025-05-27 更新40
Genetic risk for neurodegenerative disorders, and its overlap with cognitive ability and physical function
Neurodegenerative disorders are associated with impaired cognitive function and worse physical health outcomes. This study aims to test whether polygenic risk for Alzheimer’s disease, Amyotrophic Late
NIAID Data Ecosystem40



