Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.
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Synaptic Wnt/GSK3β Signaling Hub in AutismLearning and behavioral deficits associated with the absence of the fragile X mental retardation protein: what a fly and mouse model can teach us.Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and BackA Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.An evo-devo approach to thyroid hormones in cerebral and cerebellar cortical development: etiological implications for autismGestational and early postnatal hypothyroidism alters VGluT1 and VGAT bouton distribution in the neocortex and hippocampus, and behavior in rats.Excitation-Transcription Coupling in Parvalbumin-Positive Interneurons Employs a Novel CaM Kinase-Dependent Pathway Distinct from Excitatory NeuronsNew insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes.Delineating the Common Biological Pathways Perturbed by ASD's Genetic Etiology: Lessons from Network-Based StudiesThe fragile X syndrome-autism comorbidity: what do we really know?A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus.Altered gene expression in early postnatal monoamine oxidase A knockout mice.Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders.Unifying Views of Autism Spectrum Disorders: A Consideration of Autoregulatory Feedback Loops.Autism genetics - an overview.Autism Symptoms in Fragile X Syndrome.The role of ASTN2 variants in childhood and adult ADHD, comorbid disorders and associated personality traits.Common Regulatory Variants of CYFIP1 Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism.Conditional Loss of Hoxa5 Function Early after Birth Impacts on Expression of Genes with Synaptic Function.Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities.Lack of replication of previous autism spectrum disorder GWAS hits in European populations.Modeling Fragile X Syndrome in Drosophila.Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population
P2860
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P2860
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.
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name
Common variants in genes of th ...... for autism spectrum disorders.
@en
Common variants in genes of th ...... for autism spectrum disorders.
@nl
type
label
Common variants in genes of th ...... for autism spectrum disorders.
@en
Common variants in genes of th ...... for autism spectrum disorders.
@nl
prefLabel
Common variants in genes of th ...... for autism spectrum disorders.
@en
Common variants in genes of th ...... for autism spectrum disorders.
@nl
P2093
P2860
P50
P1433
P1476
Common variants in genes of th ...... for autism spectrum disorders.
@en
P2093
Andreas G Chiocchetti
Anette Voran
Christine M Freitag
Eftichia Duketis
Gabriele Schmötzer
Guillaume Huguet
Jobst Meyer
Laura M Kämpfer
Michael Knapp
P2860
P2888
P304
P356
10.1007/S00439-013-1416-Y
P577
2014-01-19T00:00:00Z