Common genetic variants, acting additively, are a major source of risk for autism
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Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architectureGluten- and casein-free dietary intervention for autism spectrum conditionsehavioral GeneticsThe ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic dataA novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism.The Evolving Diagnostic and Genetic Landscapes of Autism Spectrum DisorderGenetics of Autism Spectrum Disorder: Current Status and Possible Clinical ApplicationsMoving from capstones toward cornerstones: successes and challenges in applying systems biology to identify mechanisms of autism spectrum disordersThe developmental transcriptome of the human brain: implications for neurodevelopmental disordersA genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Advancing the understanding of autism disease mechanisms through geneticsThe role of sex-differential biology in risk for autism spectrum disorderSynaptic, transcriptional and chromatin genes disrupted in autismGenetic relationship between five psychiatric disorders estimated from genome-wide SNPsA comprehensive meta-analysis of common genetic variants in autism spectrum conditionsAn Overview of Autism Spectrum Disorder, Heterogeneity and Treatment Options.Folic acid and autism: What do we know?Environmental Enrichment Therapy for Autism: Outcomes with Increased Access.Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders.Dopaminergic variants in siblings at high risk for autism: Associations with initiating joint attention.Neural signatures of autism spectrum disorders: insights into brain network dynamicsDAWN: a framework to identify autism genes and subnetworks using gene expression and genetics.Genomic diagnosis for children with intellectual disability and/or developmental delayA de novo convergence of autism genetics and molecular neuroscience.Prioritization of neurodevelopmental disease genes by discovery of new mutations.Age of onset and family history as indicators of polygenic risk for major depression.Measuring shared variants in cohorts of discordant siblings with applications to autismBio-collections in autism research.Gene × Environment interactions in autism spectrum disorders: role of epigenetic mechanisms.Most genetic risk for autism resides with common variation.A candidate gene association study further corroborates involvement of contactin genes in autismResearch review: Polygenic methods and their application to psychiatric traits.Increasing our understanding of human cognition through the study of Fragile X Syndrome.Peptide sharing between influenza A H1N1 hemagglutinin and human axon guidance proteins.Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.The evidence for association of ATP2B2 polymorphisms with autism in Chinese Han populationIntegrated model of de novo and inherited genetic variants yields greater power to identify risk genes.Performance comparison of bench-top next generation sequencers using microdroplet PCR-based enrichment for targeted sequencing in patients with autism spectrum disorderSynergistic interactions between Drosophila orthologues of genes spanned by de novo human CNVs support multiple-hit models of autism
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P2860
Common genetic variants, acting additively, are a major source of risk for autism
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2012 nî lūn-bûn
@nan
2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
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2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Common genetic variants, acting additively, are a major source of risk for autism
@ast
Common genetic variants, acting additively, are a major source of risk for autism
@en
type
label
Common genetic variants, acting additively, are a major source of risk for autism
@ast
Common genetic variants, acting additively, are a major source of risk for autism
@en
prefLabel
Common genetic variants, acting additively, are a major source of risk for autism
@ast
Common genetic variants, acting additively, are a major source of risk for autism
@en
P2093
P2860
P50
P356
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Common genetic variants, acting additively, are a major source of risk for autism
@en
P2093
A Jeremy Willsey
Bernie Devlin
Christopher A Walsh
Daniel Geschwind
Daniel Moreno-De-Luca
David H Ledbetter
Dorothy E Grice
James S Sutcliffe
Jennifer K Lowe
Matthew W State
P2860
P2888
P356
10.1186/2040-2392-3-9
P50
P577
2012-10-15T00:00:00Z
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P6179
1015660824