Autism Spectrum Disorders
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
Like chromodomain helicase DNA binding protein 8 (CHD8), the most frequently mutated gene in individuals with ASD, the candidate gene <i>AT-rich interaction domain 1B</i> (<i>ARID1B</i>) encodes a chromatin remodeling factor.
|
28867767 |
2017 |
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
CLINGEN |
Histone H1 recruitment by CHD8 is essential for suppression of the Wnt-β-catenin signaling pathway.
|
22083958 |
2012 |
Autism Spectrum Disorders
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
As demonstrated in our patients, along with other previously reported studies support that disruption of the CHD8 gene represents a specific genetic sub-type of ASD.
|
30376831 |
2018 |
Autism Spectrum Disorders
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
Loss of function alleles of human chd8 are correlated with autism spectrum disorder.
|
29079199 |
2018 |
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
CLINGEN |
Our findings indicate that CHD8 disruptions define a distinct ASD subtype and reveal unexpected comorbidities between brain development and enteric innervation.
|
24998929 |
2014 |
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
MGD |
|
|
|
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
BEFREE |
Mutations in chromodomain helicase DNA-binding domain 8 (CHD8) have been identified in independent genotyping studies of autism spectrum disorder.
|
26789910 |
2016 |
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
CLINGEN |
Mutations in chromodomain helicase DNA-binding domain 8 (CHD8) have been identified in independent genotyping studies of autism spectrum disorder.
|
26789910 |
2016 |
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
CLINGEN |
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
|
22495309 |
2012 |
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
CTD_human |
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.
|
28191889 |
2017 |
Autism Spectrum Disorders
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
Notably, recent studies also disclosed CHD8 heterozygous loss-of-function mutations in patients with ASD and macrocephaly.
|
25257502 |
2014 |
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
BEFREE |
Our findings indicate that CHD8 disruptions define a distinct ASD subtype and reveal unexpected comorbidities between brain development and enteric innervation.
|
24998929 |
2014 |
Autism Spectrum Disorders
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
Our data support associations between specific genes and reciprocal subphenotypes (CHD8-macrocephaly and DYRK1A-microcephaly) and replicate the importance of a β-catenin-chromatin-remodeling network to ASD etiology.
|
23160955 |
2012 |
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
CLINGEN |
De novo genic mutations among a Chinese autism spectrum disorder cohort.
|
27824329 |
2016 |
Autism Spectrum Disorders
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
Genes associated with ASD were strongly enriched among indirectly down-regulated loci (P < 10(-8)) and CHD8-bound genes (P = 0.0043), which align with previously identified coexpression modules during fetal development.
|
25294932 |
2014 |
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
BEFREE |
Because identification of novel CHD7 and CHD8 interacting partners will provide further insights into the pathogenesis of CHARGE syndrome and ASD/NDD, we searched for additional associated polypeptides using the method of stable isotope labeling by amino acids in cell culture (SILAC) in combination with mass spectrometry.
|
23285124 |
2012 |
Autism Spectrum Disorders
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
We sequenced 136 microcephaly or macrocephaly (Mic-Mac)-related genes and 158 possible ASD-risk genes in 536 Chinese ASD probands and detected 22 damaging de novo mutations (DNMs) in 20 genes, including CHD8 and SCN2A, with recurrent events.
|
28831199 |
2017 |
Autism Spectrum Disorders
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
We characterized sexually dimorphic changes in mice carrying a heterozygous mutation in Chd8 (Chd8<sup>+/N2373K</sup>) that was first identified in human CHD8 (Asn2373LysfsX2), a strong ASD-risk gene that encodes a chromatin remodeler.
|
30104731 |
2018 |
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
BEFREE |
These results suggest that CHD8 insufficiency may be a central hub in neuronal development and ASD risk.
|
25989142 |
2015 |
Autism Spectrum Disorders
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
Heterozygous mutations in CHD8 give rise to ASD that is often accompanied by macrocephaly, gastrointestinal complaints, and slender habitus.
|
29768199 |
2018 |
Autism Spectrum Disorders
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
Genome-wide DNA methylation (DNAm) was assessed using the Illumina Infinium HumanMethylation450 and MethylationEPIC arrays in blood from individuals with ASD of heterogeneous, undefined etiology (n = 52), and individuals with 16p11.2 deletions (16p11.2del, n = 9) or pathogenic variants in the chromatin modifier CHD8 (CHD8<sup>+/-</sup>, n = 7).
|
31311581 |
2019 |
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
BEFREE |
We explore the field through the lens of Chd3, Chd4, and Chd5 proteins, which incorporate into the nucleosome remodeling and deacetylase (NuRD) complex, and the related proteins Chd7 and Chd8, implicated in the pathogenesis of intellectual disability and autism spectrum disorders.
|
31146125 |
2019 |
Autism Spectrum Disorders
|
0.800 |
Biomarker
|
disease |
BEFREE |
The mechanism by which deficiency of CHD8 causes ASD has not been fully elucidated.
|
30574290 |
2018 |
Autism Spectrum Disorders
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
We investigated 25 individuals with CHD8 protein truncating variants (PTVs), including 10 previously unreported patients and found a male to female ratio of 2.7:1 (19:7) and a pattern of common features: macrocephaly (62.5%), tall stature (47%), developmental delay and/or intellectual disability (81%), ASDs (84%), sleep difficulties (50%), gastrointestinal problems (40%), and distinct facial features.
|
31001818 |
2019 |
Autism Spectrum Disorders
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
The most interesting genes included in this deletion are CHD8, a chromodomain helicase DNA binding protein that is associated with autism spectrum disorders, and MMP14, a matrix metalloproteinase that has been linked to obesity and type 2 diabetes.
|
24243641 |
2014 |