(Q33717278)

English

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

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scholarly article

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Europe PubMed Central

PubMed publication ID

28 July 2017

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Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

genome-wide association study

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autism spectrum disorder

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based on heuristic

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Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

publication date

22 May 2017

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Europe PubMed Central

PubMed publication ID

28 July 2017

Molecular Autism

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Europe PubMed Central

PubMed publication ID

28 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

21

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Patterns of Nonrandom Mating Within and Across 11 Major Psychiatric Disorders

1 reference

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Disease and Polygenic Architecture: Avoid Trio Design and Appropriately Account for Unscreened Control Subjects for Common Disease

1 reference

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Heritability of autism spectrum disorders: a meta-analysis of twin studies

1 reference

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An atlas of genetic correlations across human diseases and traits

1 reference

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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

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21 June 2018

From the genetic architecture to synaptic plasticity in autism spectrum disorder

1 reference

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CNVs in neuropsychiatric disorders

1 reference

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Relative performance of gene- and pathway-level methods as secondary analyses for genome-wide association studies

1 reference

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Second-generation PLINK: rising to the challenge of larger and richer datasets

1 reference

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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

1 reference

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A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

1 reference

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The contribution of de novo coding mutations to autism spectrum disorder

1 reference

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Synaptic, transcriptional and chromatin genes disrupted in autism

1 reference

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Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour

1 reference

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DNA methylation analysis of the autistic brain reveals multiple dysregulated biological pathways

1 reference

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Biological insights from 108 schizophrenia-associated genetic loci

1 reference

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21 June 2018

Most genetic risk for autism resides with common variation

1 reference

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21 June 2018

The familial risk of autism

1 reference

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21 June 2018

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

1 reference

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A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism

1 reference

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A de novo convergence of autism genetics and molecular neuroscience

1 reference

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21 June 2018

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

1 reference

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21 June 2018

Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism

1 reference

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21 June 2018

Genome-wide association study of autistic-like traits in a general population study of young adults.

1 reference

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Recurrence of autism spectrum disorders in full- and half-siblings and trends over time: a population-based cohort study

1 reference

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21 June 2018

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

1 reference

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21 June 2018

Identification of candidate intergenic risk loci in autism spectrum disorder

1 reference

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21 June 2018

Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder

1 reference

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21 June 2018

Meta-analysis methods for genome-wide association studies and beyond

1 reference

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The evidence for association of ATP2B2 polymorphisms with autism in Chinese Han population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5441062

21 June 2018

A discovery resource of rare copy number variations in individuals with autism spectrum disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5441062

21 June 2018

Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5441062

21 June 2018

Individual common variants exert weak effects on the risk for autism spectrum disorders

1 reference

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Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5441062

21 June 2018

INRICH: interval-based enrichment analysis for genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5441062

21 June 2018

Gastrointestinal dysfunction in autism: parental report, clinical evaluation, and associated factors

1 reference

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Autism-like socio-communicative deficits and stereotypies in mice lacking heparan sulfate

1 reference

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21 June 2018

The Study to Explore Early Development (SEED): a multisite epidemiologic study of autism by the Centers for Autism and Developmental Disabilities Research and Epidemiology (CADDRE) network

1 reference

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1 reference

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Genome-wide association study identifies five new schizophrenia loci

1 reference

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Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

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Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study

1 reference

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Gene expression in blood is associated with risperidone response in children with autism spectrum disorders

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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

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21 June 2018

Do common variants play a role in risk for autism? Evidence and theoretical musings

1 reference

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Changing the landscape of autism research: the autism genetic resource exchange

1 reference

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De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment

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Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits

1 reference

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Pilot study of the effect of methyl B12 treatment on behavioral and biomarker measures in children with autism

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

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Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland

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

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21 June 2018

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

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Practical aspects of imputation-driven meta-analysis of genome-wide association studies

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Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

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Association between microdeletion and microduplication at 16p11.2 and autism

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

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The CHARGE study: an epidemiologic investigation of genetic and environmental factors contributing to autism

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PDZ domain proteins of synapses

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Genome-wide scan for loci of Asperger syndrome

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A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

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The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

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Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

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Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

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Astrotactin provides a receptor system for CNS neuronal migration

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Autism spectrum disorder diagnoses in Stockholm preschoolers

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Including known covariates can reduce power to detect genetic effects in case-control studies

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VEGAS2: Software for More Flexible Gene-Based Testing

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Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression.

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21 January 2018

Association of autism in two patients with hereditary multiple exostoses caused by novel deletion mutations of EXT1.

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Converging evidence for an association of ATP2B2 allelic variants with autism in male subjects.

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Independent replication and initial fine mapping of 3p21-24 in Asperger syndrome.

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FOXP1mutations cause intellectual disability and a recognizable phenotype

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21 January 2018

Identifiers

10.1186/S13229-017-0137-9

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Dimensions Publication ID

1 reference

https://scigraph.springernature.com/pub.10.1186/s13229-017-0137-9

9 September 2019

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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