4.8 Article

Synaptic, transcriptional and chromatin genes disrupted in autism

Related references

Note: Only part of the references are listed.
Article Genetics & Heredity

Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

Dalila Pinto et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2014)

Article Genetics & Heredity

A Higher Mutational Burden in Females Supports a Female Protective Model in Neurodevelopmental Disorders

Sebastien Jacquemont et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2014)

Article Multidisciplinary Sciences

De novo mutations in schizophrenia implicate synaptic networks

Menachem Fromer et al.

NATURE (2014)

Article Genetics & Heredity

A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP

Celine Helsmoortel et al.

NATURE GENETICS (2014)

Article Genetics & Heredity

A framework for the interpretation of de novo mutation in human disease

Kaitlin E. Samocha et al.

NATURE GENETICS (2014)

Article Genetics & Heredity

Most genetic risk for autism resides with common variation

Trent Gaugler et al.

NATURE GENETICS (2014)

Article Biotechnology & Applied Microbiology

Chronic cocaine-regulated epigenomic changes in mouse nucleus accumbens

Jian Feng et al.

GENOME BIOLOGY (2014)

Article Genetics & Heredity

Identification of Small Exonic CNV from Whole-Exome Sequence Data and Application to Autism Spectrum Disorder

Christopher S. Poultney et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2013)

Article Genetics & Heredity

Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder

Santhosh Girirajan et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2013)

Article Biochemical Research Methods

Network2Canvas: network visualization on a canvas with enrichment analysis

Christopher M. Tan et al.

BIOINFORMATICS (2013)

Article Neurosciences

Myo9b and RICS Modulate Dendritic Morphology of Cortical Neurons

Hui Long et al.

CEREBRAL CORTEX (2013)

Article Genetics & Heredity

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Stephan Ripke et al.

NATURE GENETICS (2013)

Review Genetics & Heredity

From neural development to cognition: unexpected roles for chromatin

Jehnna L. Ronan et al.

NATURE REVIEWS GENETICS (2013)

Article Neurosciences

Using Whole-Exome Sequencing to Identify Inherited Causes of Autism

Timothy W. Yu et al.

NEURON (2013)

Article Multidisciplinary Sciences

Examining and interpreting the female protective effect against autistic behavior

Elise B. Robinson et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)

Article Multidisciplinary Sciences

FMRP targets distinct mRNA sequence elements to regulate protein expression

Manuel Ascano et al.

NATURE (2012)

Article Multidisciplinary Sciences

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Benjamin M. Neale et al.

NATURE (2012)

Article Multidisciplinary Sciences

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

Stephan J. Sanders et al.

NATURE (2012)

Article Multidisciplinary Sciences

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

Brian J. O'Roak et al.

NATURE (2012)

Article Neurosciences

De Novo Gene Disruptions in Children on the Autistic Spectrum

Ivan Iossifov et al.

NEURON (2012)

Article Biochemistry & Molecular Biology

HIstome-a relational knowledgebase of human histone proteins and histone modifying enzymes

Satyajeet P. Khare et al.

NUCLEIC ACIDS RESEARCH (2012)

Article Genetics & Heredity

Common genetic variants, acting additively, are a major source of risk for autism

Lambertus Klei et al.

MOLECULAR AUTISM (2012)

Review Genetics & Heredity

Autism Spectrum Disorders and Autistic Traits: A Decade of New Twin Studies

Angelica Ronald et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2011)

Article Biochemistry & Molecular Biology

FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism

Jennifer C. Darnell et al.

Article Neurosciences

Nav1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome

Linda Volkers et al.

EUROPEAN JOURNAL OF NEUROSCIENCE (2011)

Article Multidisciplinary Sciences

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

Irina Voineagu et al.

NATURE (2011)

Article Genetics & Heredity

A framework for variation discovery and genotyping using next-generation DNA sequencing data

Mark A. DePristo et al.

NATURE GENETICS (2011)

Review Neurosciences

Dendritic spine pathology in neuropsychiatric disorders

Peter Penzes et al.

NATURE NEUROSCIENCE (2011)

Article Biochemical Research Methods

ChEA: transcription factor regulation inferred from integrating genome-wide ChIP-X experiments

Alexander Lachmann et al.

BIOINFORMATICS (2010)

Article Multidisciplinary Sciences

Functional impact of global rare copy number variation in autism spectrum disorders

Dalila Pinto et al.

NATURE (2010)

Letter Biochemical Research Methods

A method and server for predicting damaging missense mutations

Ivan A. Adzhubei et al.

NATURE METHODS (2010)

Article Cell & Tissue Engineering

MicroRNA miR-137 Regulates Neuronal Maturation by Targeting Ubiquitin Ligase Mind Bomb-1

Richard D. Smrt et al.

STEM CELLS (2010)

Article Multidisciplinary Sciences

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Joseph T. Glessner et al.

NATURE (2009)

Article Multidisciplinary Sciences

Strong association of de novo copy number mutations with autism

Jonathan Sebat et al.

SCIENCE (2007)

Article Biochemistry & Molecular Biology

Molecular characterization and comparison of the components and multiprotein complexes in the postsynaptic proteome

MO Collins et al.

JOURNAL OF NEUROCHEMISTRY (2006)

Article Multidisciplinary Sciences

Postnatal neurodevelopmental disorders: Meeting at the synapse?

HY Zoghbi

SCIENCE (2003)