Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology
出版年份 2015 全文链接
标题
Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology
作者
关键词
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出版物
Frontiers in Neuroscience
Volume 9, Issue -, Pages -
出版商
Frontiers Media SA
发表日期
2015-12-17
DOI
10.3389/fnins.2015.00477
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies
- (2015) Jianling Ji et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A
- (2015) Lucas M Bronicki et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Gene hunting in autism spectrum disorder: on the path to precision medicine
- (2015) Daniel H Geschwind et al. LANCET NEUROLOGY
- The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
- (2015) Justin Cotney et al. Nature Communications
- Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample
- (2015) Emma Colvert et al. JAMA Psychiatry
- The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes
- (2015) B Wilkinson et al. Translational Psychiatry
- Familial Recurrence of Autism Spectrum Disorder: Evaluating Genetic and Environmental Contributions
- (2014) Neil Risch et al. AMERICAN JOURNAL OF PSYCHIATRY
- Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development
- (2014) Raphael Bernier et al. CELL
- The discovery of integrated gene networks for autism and related disorders
- (2014) Fereydoun Hormozdiari et al. GENOME RESEARCH
- De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability
- (2014) S E McCarthy et al. MOLECULAR PSYCHIATRY
- Synaptic, transcriptional and chromatin genes disrupted in autism
- (2014) Silvia De Rubeis et al. NATURE
- Discovery and saturation analysis of cancer genes across 21 tumour types
- (2014) Michael S. Lawrence et al. NATURE
- The contribution of de novo coding mutations to autism spectrum disorder
- (2014) Ivan Iossifov et al. NATURE
- A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP
- (2014) Céline Helsmoortel et al. NATURE GENETICS
- CHD8regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors
- (2014) Aarathi Sugathan et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Recurrent de novo mutations implicate novel genes underlying simplex autism risk
- (2014) B. J. O'Roak et al. Nature Communications
- DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics
- (2014) Li Liu et al. Molecular Autism
- Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
- (2013) A. Jeremy Willsey et al. CELL
- Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism
- (2013) Neelroop N. Parikshak et al. CELL
- Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
- (2013) Gemma L Carvill et al. NATURE GENETICS
- From neural development to cognition: unexpected roles for chromatin
- (2013) Jehnna L. Ronan et al. NATURE REVIEWS GENETICS
- The chromatin remodeller CHD8 is required for E2F-dependent transcription activation of S-phase genes
- (2013) Alicia Subtil-Rodríguez et al. NUCLEIC ACIDS RESEARCH
- Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes
- (2013) Xin He et al. PLoS Genetics
- Global Prevalence of Autism and Other Pervasive Developmental Disorders
- (2012) Mayada Elsabbagh et al. Autism Research
- Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries
- (2012) Michael E. Talkowski et al. CELL
- Patterns and rates of exonic de novo mutations in autism spectrum disorders
- (2012) Benjamin M. Neale et al. NATURE
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism
- (2012) Stephan J. Sanders et al. NATURE
- Rate of de novo mutations and the importance of father’s age to disease risk
- (2012) Augustine Kong et al. NATURE
- Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
- (2012) Brian J. O’Roak et al. NATURE
- De novo mutations in human genetic disease
- (2012) Joris A. Veltman et al. NATURE REVIEWS GENETICS
- De Novo Gene Disruptions in Children on the Autistic Spectrum
- (2012) Ivan Iossifov et al. NEURON
- Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
- (2012) B. J. O'Roak et al. SCIENCE
- The Allen Human Brain Atlas
- (2012) Elaine H. Shen et al. TRENDS IN NEUROSCIENCES
- Pten Knockdown In Vivo Increases Excitatory Drive onto Dentate Granule Cells
- (2011) B. W. Luikart et al. JOURNAL OF NEUROSCIENCE
- Transcriptomic analysis of autistic brain reveals convergent molecular pathology
- (2011) Irina Voineagu et al. NATURE
- Exome sequencing supports a de novo mutational paradigm for schizophrenia
- (2011) Bin Xu et al. NATURE GENETICS
- Increased exonic de novo mutation rate in individuals with schizophrenia
- (2011) Simon L Girard et al. NATURE GENETICS
- Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
- (2011) Brian J O'Roak et al. NATURE GENETICS
- Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders
- (2010) Jill A Rosenfeld et al. GENETICS IN MEDICINE
- The NIH Roadmap Epigenomics Mapping Consortium
- (2010) Bradley E Bernstein et al. NATURE BIOTECHNOLOGY
- A de novo paradigm for mental retardation
- (2010) Lisenka E L M Vissers et al. NATURE GENETICS
- Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size
- (2009) M. Shinawi et al. JOURNAL OF MEDICAL GENETICS
- CHD8 suppresses p53-mediated apoptosis through histone H1 recruitment during early embryogenesis
- (2009) Masaaki Nishiyama et al. NATURE CELL BIOLOGY
- Exome sequencing identifies the cause of a mendelian disorder
- (2009) Sarah B Ng et al. NATURE GENETICS
- The chromatin remodeling factor CHD8 interacts with elongating RNA polymerase II and controls expression of the cyclin E2 gene
- (2009) M. Rodríguez-Paredes et al. NUCLEIC ACIDS RESEARCH
- WGCNA: an R package for weighted correlation network analysis
- (2008) Peter Langfelder et al. BMC BIOINFORMATICS
- Advances in autism genetics: on the threshold of a new neurobiology
- (2008) Brett S. Abrahams et al. NATURE REVIEWS GENETICS
- AutDB: a gene reference resource for autism research
- (2008) Saumyendra N. Basu et al. NUCLEIC ACIDS RESEARCH
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