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 (Q33717278)

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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	scientific article

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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)

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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

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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

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Europe PubMed Central

PubMed publication ID

28 July 2017

21

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Europe PubMed Central

PubMed publication ID

28 July 2017

Patterns of Nonrandom Mating Within and Across 11 Major Psychiatric Disorders

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

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

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An atlas of genetic correlations across human diseases and traits

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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

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CNVs in neuropsychiatric disorders

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

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

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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?

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The contribution of de novo coding mutations to autism spectrum disorder

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Synaptic, transcriptional and chromatin genes disrupted in autism

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

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Biological insights from 108 schizophrenia-associated genetic loci

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Most genetic risk for autism resides with common variation

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The familial risk of autism

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Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

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

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A de novo convergence of autism genetics and molecular neuroscience

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

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

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

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

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

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Identification of candidate intergenic risk loci in autism spectrum disorder

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

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

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

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

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

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

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

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

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

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Genome-wide association study identifies five new schizophrenia loci

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

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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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