Related references
Note: Only part of the references are listed.Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue
Chloe C. Y. Wong et al.
HUMAN MOLECULAR GENETICS (2019)
Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes
Erfan Aref-Eshghi et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
Communicating complex genomic information: A counselling approach derived from research experience with Autism Spectrum Disorder
Ny Hoang et al.
PATIENT EDUCATION AND COUNSELING (2018)
Peripheral blood epi-signature of Claes-Jensen syndrome enables sensitive and specific identification of patients and healthy carriers with pathogenic mutations in KDM5C
Laila C. Schenkel et al.
CLINICAL EPIGENETICS (2018)
The defining DNA methylation signature of Kabuki syndrome enables functional assessment of genetic variants of unknown clinical significance
Erfan Aref-Eshghi et al.
EPIGENETICS (2017)
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
Ryan K. C. Yuen et al.
NATURE NEUROSCIENCE (2017)
Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome
Laila C. Schenkel et al.
EPIGENETICS & CHROMATIN (2017)
CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in cerebral organoids derived from iPS cells
Ping Wang et al.
MOLECULAR AUTISM (2017)
Environmental enrichment attenuates behavioral abnormalities in valproic acid-exposed autism model mice
Hiroshi Yamaguchi et al.
BEHAVIOURAL BRAIN RESEARCH (2017)
CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions
Darci T. Butcher et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2017)
Improvement by Methylphenidate and Atomoxetine of Social Interaction Deficits and Recognition Memory Impairment in a Mouse Model of Valproic Acid-Induced Autism
Yuta Hara et al.
AUTISM RESEARCH (2016)
A De Novo Frameshift Mutation in Chromodomain Helicase DNA-Binding Domain 8 (CHD8): A Case Report and Literature Review
Nancy Merner et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2016)
Histone Acetylome-wide Association Study of Autism Spectrum Disorder
Wenjie Sun et al.
CELL (2016)
Withdrawn/Depressed Behaviors and Error-Related Brain Activity in Youth With Obsessive-Compulsive Disorder
Gregory L. Hanna et al.
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY (2016)
Can we identify meaningful epigenetic effects on human brain function and related risk for mental illness?
Yuliya S. Nikolova et al.
EPIGENOMICS (2016)
Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy
Kristin D. Kernohan et al.
CLINICAL EPIGENETICS (2016)
Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23
Emma Strong et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2015)
The Cognitive and Behavioral Phenotype of the 16p11.2 Deletion in a Clinically Ascertained Population
Ellen Hanson et al.
BIOLOGICAL PSYCHIATRY (2015)
An evaluation of statistical methods for DNA methylation microarray data analysis
Dongmei Li et al.
BMC BIOINFORMATICS (2015)
Paternal sperm DNA methylation associated with early signs of autism risk in an autism-enriched cohort
Jason I. Feinberg et al.
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY (2015)
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder
Kristiina Tammimies et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2015)
Whole-genome sequencing of quartet families with autism spectrum disorder
Ryan K. C. Yuen et al.
NATURE MEDICINE (2015)
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Stephan J. Sanders et al.
NEURON (2015)
NSD1 mutations generate a genome-wide DNA methylation signature
S. Choufani et al.
NATURE COMMUNICATIONS (2015)
CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment
Ping Wang et al.
MOLECULAR AUTISM (2015)
Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology
Rebecca A. Barnard et al.
FRONTIERS IN NEUROSCIENCE (2015)
DNA Extracted From Saliva for Methylation Studies of Psychiatric Traits: Evidence for Tissue Specificity and Relatedness to Brain
Alicia K. Smith et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2015)
De novo identification of differentially methylated regions in the human genome
Timothy J. Peters et al.
EPIGENETICS & CHROMATIN (2015)
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
Dalila Pinto et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2014)
The 22q11.2 Deletion Syndrome as a Window into Complex Neuropsychiatric Disorders Over the Lifespan
Rachel K. Jonas et al.
BIOLOGICAL PSYCHIATRY (2014)
Immune dysregulation in autism spectrum disorder
Daniela Briceno Noriega et al.
EUROPEAN JOURNAL OF PEDIATRICS (2014)
Methylomic analysis of monozygotic twins discordant for autism spectrum disorder and related behavioural traits
C. C. Y. Wong et al.
MOLECULAR PSYCHIATRY (2014)
Common DNA methylation alterations in multiple brain regions in autism
C. Ladd-Acosta et al.
MOLECULAR PSYCHIATRY (2014)
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis et al.
NATURE (2014)
The contribution of de novo coding mutations to autism spectrum disorder
Ivan Iossifov et al.
NATURE (2014)
Recurrent de novo mutations implicate novel genes underlying simplex autism risk
B. J. O'Roak et al.
NATURE COMMUNICATIONS (2014)
Mosaic Epigenetic Dysregulation of Ectodermal Cells in Autism Spectrum Disorder
Esther R. Berko et al.
PLOS GENETICS (2014)
DNA methylation analysis of the autistic brain reveals multiple dysregulated biological pathways
S. Nardone et al.
TRANSLATIONAL PSYCHIATRY (2014)
On the Outside, Looking In: A Review and Evaluation of the Comparability of Blood and Brain -omes
Daniel S. Tylee et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2013)
The Genetic Landscapes of Autism Spectrum Disorders
Guillaume Huguet et al.
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 14 (2013)
Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5C
Daria Grafodatskaya et al.
BMC MEDICAL GENOMICS (2013)
Autism spectrum disorder in the genetics clinic: a review
M. T. Carter et al.
CLINICAL GENETICS (2013)
Converging pathways in autism spectrum disorders: interplay between synaptic dysfunction and immune responses
Irina Voineagu et al.
FRONTIERS IN HUMAN NEUROSCIENCE (2013)
In utero exposure to valproic acid and autism - A current review of clinical and animal studies
Florence I. Roullet et al.
NEUROTOXICOLOGY AND TERATOLOGY (2013)
DNA methylation arrays as surrogate measures of cell mixture distribution
Eugene Andres Houseman et al.
BMC BIOINFORMATICS (2012)
Tissue type is a major modifier of the 5-hydroxymethylcytosine content of human genes
Colm E. Nestor et al.
GENOME RESEARCH (2012)
Bump hunting to identify differentially methylated regions in epigenetic epidemiology studies
Andrew E. Jaffe et al.
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY (2012)
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
Flore Zufferey et al.
JOURNAL OF MEDICAL GENETICS (2012)
A review of research trends in physiological abnormalities in autism spectrum disorders: immune dysregulation, inflammation, oxidative stress, mitochondrial dysfunction and environmental toxicant exposures
D. A. Rossignol et al.
MOLECULAR PSYCHIATRY (2012)
Human-Specific Transcriptional Networks in the Brain
Genevieve Konopka et al.
NEURON (2012)
Differential DNA Methylation in Purified Human Blood Cells: Implications for Cell Lineage and Studies on Disease Susceptibility
Lovisa E. Reinius et al.
PLOS ONE (2012)
Brain Transcriptional and Epigenetic Associations with Autism
Matthew R. Ginsberg et al.
PLOS ONE (2012)
Modeling human cortical development in vitro using induced pluripotent stem cells
Jessica Mariani et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Global methylation profiling of lymphoblastoid cell lines reveals epigenetic contributions to autism spectrum disorders and a novel autism candidate gene, RORA, whose protein product is reduced in autistic brain
AnhThu Nguyen et al.
FASEB JOURNAL (2010)
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
Bridget A. Fernandez et al.
JOURNAL OF MEDICAL GENETICS (2010)
Independent filtering increases detection power for high-throughput experiments
Richard Bourgon et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals
E. K. Bijlsma et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2009)
CHD8 is an ATP-dependent chromatin remodeling factor that regulates beta-catenin target genes
Brandi A. Thompson et al.
MOLECULAR AND CELLULAR BIOLOGY (2008)
Advances in autism genetics: on the threshold of a new neurobiology
Brett S. Abrahams et al.
NATURE REVIEWS GENETICS (2008)
Association between microdeletion and microduplication at 16p11.2 and autism
Lauren A. Weiss et al.
NEW ENGLAND JOURNAL OF MEDICINE (2008)
Plexin-B2, but not Plexin-B1, critically modulates neuronal migration and patterning of the developing nervous system in vivo
Suhua Deng et al.
JOURNAL OF NEUROSCIENCE (2007)
Abnormal neurodevelopment, neurosignaling and behaviour in Npas3-deficient mice
EW Brunskill et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2005)
Disruption of a brain transcription factor, NPAS3, is associated with schizophrenia and learning disability
BS Pickard et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2005)