The CHD8 overgrowth syndrome: A detailed evaluation of an emerging overgrowth phenotype in 27 patients
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Title
The
CHD8
overgrowth syndrome: A detailed evaluation of an emerging overgrowth phenotype in 27 patients
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
Volume 181, Issue 4, Pages 557-564
Publisher
Wiley
Online
2019-11-13
DOI
10.1002/ajmg.c.31749
References
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Related references
Note: Only part of the references are listed.- A distinct neurodevelopmental syndrome with intellectual disability, autism spectrum disorder, characteristic facies, and macrocephaly is caused by defects in CHD8
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- The clinical presentation caused by truncating CHD8 variants
- (2019) Sofia Douzgou et al. CLINICAL GENETICS
- Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion
- (2018) Ahmad N. Abou Tayoun et al. HUMAN MUTATION
- Sexually dimorphic behavior, neuronal activity, and gene expression in Chd8-mutant mice
- (2018) Hwajin Jung et al. NATURE NEUROSCIENCE
- A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review
- (2016) Nancy Merner et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- CHD8 intragenic deletion associated with autism spectrum disorder
- (2016) Elliot S. Stolerman et al. European Journal of Medical Genetics
- Identification of a rare variant in CHD8 that contributes to schizophrenia and autism spectrum disorder susceptibility
- (2016) Hiroki Kimura et al. SCHIZOPHRENIA RESEARCH
- Long term follow-up in a patient with a de novo microdeletion of 14q11.2 involvingCHD8
- (2015) Jana Drabova et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment
- (2015) Ping Wang et al. Molecular Autism
- Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involvingCHD8gene, is associated with autism and macrocephaly
- (2014) Paolo Prontera et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development
- (2014) Raphael Bernier et al. CELL
- Prevalence and incidence rates of autism in the UK: time trend from 2004–2010 in children aged 8 years
- (2013) Brent Taylor et al. BMJ Open
- Patterns and rates of exonic de novo mutations in autism spectrum disorders
- (2012) Benjamin M. Neale et al. NATURE
- Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
- (2012) Brian J. O’Roak et al. NATURE
- Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
- (2012) B. J. O'Roak et al. SCIENCE
- The Deciphering Developmental Disorders (DDD) study
- (2011) HELEN V FIRTH et al. DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
- Histone H1 Recruitment by CHD8 Is Essential for Suppression of the Wnt- -Catenin Signaling Pathway
- (2011) M. Nishiyama et al. MOLECULAR AND CELLULAR BIOLOGY
- CHD8 Is an ATP-Dependent Chromatin Remodeling Factor That Regulates -Catenin Target Genes
- (2008) B. A. Thompson et al. MOLECULAR AND CELLULAR BIOLOGY
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