Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
about
Language development in rural and urban Russian-speaking children with and without developmental language disorder.Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairmentThe intergenerational multiple deficit model and the case of dyslexia.A novel relationship for schizophrenia, bipolar and major depressive disorder Part 5: a hint from chromosome 5 high density association screen.Reading and language disorders: the importance of both quantity and quality.Genome-wide screening for DNA variants associated with reading and language traitsExome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language ImpairmentCommon Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language DevelopmentLack of replication for the myosin-18B association with mathematical ability in independent cohorts.Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.Nop9 is a PUF-like protein that prevents premature cleavage to correctly process pre-18S rRNA.Insights into the genetic foundations of human communication.Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3.Increased Power for Detection of Parent-of-Origin Effects via the Use of Haplotype Estimation.CTNND2-a candidate gene for reading problems and mild intellectual disability.Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.Genome-Wide Studies of Specific Language Impairment.Interhemispheric gene expression differences in the cerebral cortex of humans and macaque monkeys.Evaluation of results from genome-wide studies of language and reading in a novel independent dataset.Parent-of-Origin Dependent Gene Expression in Male and Female Schistosome Parasites.What aDNA can (and cannot) tell us about the emergence of language and speech
P2860
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P2860
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
description
2014 nî lūn-bûn
@nan
2014 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մարտին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Genome-wide association analys ...... specific language impairment.
@ast
Genome-wide association analys ...... specific language impairment.
@en
type
label
Genome-wide association analys ...... specific language impairment.
@ast
Genome-wide association analys ...... specific language impairment.
@en
prefLabel
Genome-wide association analys ...... specific language impairment.
@ast
Genome-wide association analys ...... specific language impairment.
@en
P2093
P2860
P50
P356
P1476
Genome-wide association analys ...... n specific language impairment
@en
P2093
E R Hennessy
G Conti-Ramsden
P F Bolton
SLI Consortium
P2860
P304
P356
10.1111/GBB.12127
P407
P50
P577
2014-03-24T00:00:00Z