Identification of De Novo JAK2 and MAPK7 Mutations Related to Autism Spectrum Disorder Using Whole-Exome Sequencing in a Chinese Child and Adolescent Trio-Based Sample

ELMO Domain Containing 1 (ELMOD1) Gene Mutation Is Associated with Mental Retardation and Autism Spectrum Disorder

(2019) Mohammad Miryounesi et al.   JOURNAL OF MOLECULAR NEUROSCIENCE

Synaptic and brain-expressed gene sets relate to the shared genetic risk across five psychiatric disorders

(2019) Anke R. Hammerschlag et al.   PSYCHOLOGICAL MEDICINE

The ASD Living Biology: from cell proliferation to clinical phenotype

(2018) Eric Courchesne et al.   MOLECULAR PSYCHIATRY

Delineation of early brain development from fetuses to infants with diffusion MRI and beyond

(2018) Minhui Ouyang et al.   NEUROIMAGE

Whole-Exome Sequencing Identifies One De Novo Variant in the FGD6 Gene in a Thai Family with Autism Spectrum Disorder

(2018) Chuphong Thongnak et al.   International Journal of Genomics

Autism spectrum disorder

(2018) Catherine Lord et al.   LANCET

A large-scale integrative analysis of GWAS and common meQTLs across whole life course identifies genes, pathways and tissue/cell types for three major psychiatric disorders

(2018) Yan Zhao et al.   NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS

MAPK3 at the Autism-Linked Human 16p11.2 Locus Influences Precise Synaptic Target Selection at Drosophila Larval Neuromuscular Junctions

(2017) Sang Mee Park et al.   MOLECULES AND CELLS

Upregulation of IL-9 and JAK-STAT signaling pathway in children with autism

(2017) Sheikh F. Ahmad et al.   PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY

An autism spectrum disorder-related de novo mutation hotspot discovered in the GEF1 domain of Trio

(2017) Anastasiia Sadybekov et al.   Nature Communications

Identification of autism-related MECP2 mutations by whole-exome sequencing and functional validation

(2017) Zhu Wen et al.   Molecular Autism

Altered neurite morphology and cholinergic function of induced pluripotent stem cell-derived neurons from a patient with Kleefstra syndrome and autism

(2017) J Nagy et al.   Translational Psychiatry

Cortical thickness change in autism during early childhood

(2016) Elizabeth Smith et al.   HUMAN BRAIN MAPPING

Whole-exome sequencing identifies a novel heterozygous missense variant of the EN2 gene in two unrelated patients with autism spectrum disorder

(2016) Areerat Hnoonual et al.   PSYCHIATRIC GENETICS

Recent Advances in Autism Spectrum Disorders: Applications of Whole Exome Sequencing Technology

(2016) Elif Funda Sener et al.   Psychiatry Investigation

Pathway Network Analyses for Autism Reveal Multisystem Involvement, Major Overlaps with Other Diseases and Convergence upon MAPK and Calcium Signaling

(2016) Ya Wen et al.   PLoS One

Gene hunting in autism spectrum disorder: on the path to precision medicine

(2015) Daniel H Geschwind et al.   LANCET NEUROLOGY

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database

(2015) Jinchen Li et al.   MOLECULAR PSYCHIATRY

Phenolyzer: phenotype-based prioritization of candidate genes for human diseases

(2015) Hui Yang et al.   NATURE METHODS

Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample

(2015) Emma Colvert et al.   JAMA Psychiatry

Sera from Children with Autism Induce Autistic Features Which Can Be Rescued with a CNTF Small Peptide Mimetic in Rats

(2015) Syed Faraz Kazim et al.   PLoS One

Transcriptional Consequences of 16p11.2 Deletion and Duplication in Mouse Cortex and Multiplex Autism Families

(2014) Ian Blumenthal et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genomic and genetic aspects of autism spectrum disorder

(2014) Xiaoxi Liu et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Variants of the CNTNAP2 5′ promoter as risk factors for autism spectrum disorders: a genetic and functional approach

(2014) A G Chiocchetti et al.   MOLECULAR PSYCHIATRY

Synaptic, transcriptional and chromatin genes disrupted in autism

(2014) Silvia De Rubeis et al.   NATURE

The contribution of de novo coding mutations to autism spectrum disorder

(2014) Ivan Iossifov et al.   NATURE

Most genetic risk for autism resides with common variation

(2014) Trent Gaugler et al.   NATURE GENETICS

The Cerebellum, Sensitive Periods, and Autism

(2014) Samuel S.-H. Wang et al.   NEURON

Economic Burden of Childhood Autism Spectrum Disorders

(2014) T. A. Lavelle et al.   PEDIATRICS

Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder

(2014) Donna M Werling et al.   Molecular Autism

Autism

(2013) Meng-Chuan Lai et al.   LANCET

Co-expression Profiling of Autism Genes in the Mouse Brain

(2013) Idan Menashe et al.   PLoS Computational Biology

Exome versus transcriptome sequencing in identifying coding region variants

(2012) Chee-Seng Ku et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits

(2012) Melanie Lacaria et al.   HUMAN MOLECULAR GENETICS

Early Brain Overgrowth in Autism Associated With an Increase in Cortical Surface Area Before Age 2 Years

(2011) Heather Cody Hazlett et al.   ARCHIVES OF GENERAL PSYCHIATRY

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

(2011) Joachim Hallmayer   ARCHIVES OF GENERAL PSYCHIATRY

Quantitative in vivo MRI measurement of cortical development in the fetus

(2011) Cédric Clouchoux et al.   Brain Structure & Function

ERK2 Contributes to the Control of Social Behaviors in Mice

(2011) Y. Satoh et al.   JOURNAL OF NEUROSCIENCE

Solving the Autism Puzzle a Few Pieces at a Time

(2011) Christian P. Schaaf et al.   NEURON

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

(2011) Stephan J. Sanders et al.   NEURON

Cytoscape 2.8: new features for data integration and network visualization

(2010) M. E. Smoot et al.   BIOINFORMATICS

A genome-wide scan for common alleles affecting risk for autism

(2010) R. Anney et al.   HUMAN MOLECULAR GENETICS

MutationTaster evaluates disease-causing potential of sequence alterations

(2010) Jana Marie Schwarz et al.   NATURE METHODS

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function

(2010) David Warde-Farley et al.   NUCLEIC ACIDS RESEARCH

Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample

(2010) Katri Kantojärvi et al.   PSYCHIATRIC GENETICS

Identifying a High Fraction of the Human Genome to be under Selective Constraint Using GERP++

(2010) Eugene V. Davydov et al.   PLoS Computational Biology

Characteristics and Concordance of Autism Spectrum Disorders Among 277 Twin Pairs

(2009) Rebecca E. Rosenberg et al.   ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE

A genome-wide linkage and association scan reveals novel loci for autism

(2009) Lauren A. Weiss et al.   NATURE

Common genetic variants on 5p14.1 associate with autism spectrum disorders

(2009) Kai Wang et al.   NATURE

Brain‐derived neurotrophic factor stimulates the neural differentiation of human umbilical cord blood‐derived mesenchymal stem cells and survival of differentiated cells through MAPK/ERK and PI3K/Akt‐dependent signaling pathways

(2008) Jung Yeon Lim et al.   JOURNAL OF NEUROSCIENCE RESEARCH

AutDB: a gene reference resource for autism research

(2008) Saumyendra N. Basu et al.   NUCLEIC ACIDS RESEARCH