Related references
Note: Only part of the references are listed.Germline Chd8 haploinsufficiency alters brain development in mouse
Andrea L. Gompers et al.
NATURE NEUROSCIENCE (2017)
Arid1b haploinsufficient mice reveal neuropsychiatric phenotypes and reversible causes of growth impairment
Cemre Celen et al.
ELIFE (2017)
Etiological influences on the stability of autistic traits from childhood to early adulthood: evidence from a twin study
Mark J. Taylor et al.
MOLECULAR AUTISM (2017)
Transcriptomic immaturity of the hippocampus and prefrontal cortex in patients with alcoholism
Tomoyuki Murano et al.
SCIENTIFIC REPORTS (2017)
Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism
Thomas C. Jaramillo et al.
AUTISM RESEARCH (2016)
CHD8 haploinsufficiency results in autistic-like phenotypes in mice
Yuta Katayama et al.
NATURE (2016)
Chd8 mediates cortical neurogenesis via transcriptional regulation of cell cycle and Wnt signaling
Omer Durak et al.
NATURE NEUROSCIENCE (2016)
Pallidum and lateral ventricle volume enlargement in autism spectrum disorder
Andia H. Turner et al.
PSYCHIATRY RESEARCH-NEUROIMAGING (2016)
Reduced Personal Space in Individuals with Autism Spectrum Disorder
Kosuke Asada et al.
PLOS ONE (2016)
Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms
Alissa M. D'Gama et al.
NEURON (2015)
Trimmomatic: a flexible trimmer for Illumina sequence data
Anthony M. Bolger et al.
BIOINFORMATICS (2014)
Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development
Raphael Bernier et al.
CELL (2014)
Strong Genetic Influences on the Stabiliiy of Autistic Traits in Childhood
Karla Holmboe et al.
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY (2014)
De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability
S. E. McCarthy et al.
MOLECULAR PSYCHIATRY (2014)
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis et al.
NATURE (2014)
Intellectual disability and autism spectrum disorders: Causal genes and molecular mechanisms
Anand K. Srivastava et al.
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS (2014)
Validation of microinjection methods for generating knockout mice by CRISPR/Cas-mediated genome engineering
Takuro Horii et al.
SCIENTIFIC REPORTS (2014)
Transcriptomic evidence for immaturity of the prefrontal cortex in patients with schizophrenia
Hideo Hagihara et al.
MOLECULAR BRAIN (2014)
Contextual and Cued Fear Conditioning Test Using a Video Analyzing System in Mice
Hirotaka Shoji et al.
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS (2014)
Double Nicking by RNA-Guided CRISPR Cas9 for Enhanced Genome Editing Specificity
F. Ann Ran et al.
CELL (2013)
Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries
Michael E. Talkowski et al.
CELL (2012)
Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B
C. Halgren et al.
CLINICAL GENETICS (2012)
Patterns and rates of exonic de novo mutations in autism spectrum disorders
Benjamin M. Neale et al.
NATURE (2012)
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
Brian J. O'Roak et al.
NATURE (2012)
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome
Gijs W. E. Santen et al.
NATURE GENETICS (2012)
Fast gapped-read alignment with Bowtie 2
Ben Langmead et al.
NATURE METHODS (2012)
Brain Transcriptional and Epigenetic Associations with Autism
Matthew R. Ginsberg et al.
PLOS ONE (2012)
Measuring the Maturity of the Fast-Spiking Interneuron Transcriptional Program in Autism, Schizophrenia, and Bipolar Disorder
Michael J. Gandal et al.
PLOS ONE (2012)
Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
Brian J. O'Roak et al.
SCIENCE (2012)
Reduced transcript expression of genes affected by inherited and de novo CNVs in autism
Alex S. Nord et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2011)
Ontology-Based Meta-Analysis of Global Collections of High-Throughput Public Data
Ilya Kupershmidt et al.
PLOS ONE (2010)
Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability
Abdul Noor et al.
SCIENCE TRANSLATIONAL MEDICINE (2010)
A scaling normalization method for differential expression analysis of RNA-seq data
Mark D. Robinson et al.
GENOME BIOLOGY (2010)
Abnormal Behavior in a Chromosome-Engineered Mouse Model for Human 15q11-13 Duplication Seen in Autism
Jin Nakatani et al.
CELL (2009)
Transcriptional and Electrophysiological Maturation of Neocortical Fast-Spiking GABAergic Interneurons
Benjamin W. Okaty et al.
JOURNAL OF NEUROSCIENCE (2009)
Abnormal fear conditioning and amygdala processing in an animal model of autism
Kamila Markram et al.
NEUROPSYCHOPHARMACOLOGY (2008)
The effects of intellectual functioning on the range of core symptoms of autism spectrum disorders
Johnny L. Matson et al.
RESEARCH IN DEVELOPMENTAL DISABILITIES (2008)
Designing mouse behavioral tasks relevant to autistic-like behaviors
JN Crawley
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS (2004)
Share Paper
