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Function Over Form: Modeling Groups of Inherited Neurological Conditions in ZebrafishRELN Mutations in Autism Spectrum DisorderGenetics of Autism Spectrum Disorder: Current Status and Possible Clinical ApplicationsMicroRNAs: Not "Fine-Tuners" but Key Regulators of Neuronal Development and FunctionNeuroimaging endophenotypes in autism spectrum disorderChannelopathy pathogenesis in autism spectrum disordersSerotonin transporter variant drives preventable gastrointestinal abnormalities in development and function.Using Gene Ontology to describe the role of the neurexin-neuroligin-SHANK complex in human, mouse and rat and its relevance to autismMitochondrial dysfunction as a neurobiological subtype of autism spectrum disorder: evidence from brain imaging.Neural signatures of autism spectrum disorders: insights into brain network dynamicsAutism in the Son of a Woman with Mitochondrial Myopathy and Dysautonomia: A Case Report.Bio-collections in autism research.Serum microRNA profiles in children with autism.Genetic variation in the oxytocin receptor (OXTR) gene is associated with Asperger SyndromeMTHFR Gene C677T Polymorphism in Autism Spectrum DisordersCerebellar oxidative DNA damage and altered DNA methylation in the BTBR T+tf/J mouse model of autism and similarities with human post mortem cerebellum.Maternal thyroid autoantibody and elevated risk of autism in a national birth cohort.A Pooled Genome-Wide Association Study of Asperger Syndrome.Endocannabinoid Signaling in AutismPlatelet studies in autism spectrum disorder patients and first-degree relatives3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances.Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder.Candidate Biomarkers in Children with Autism Spectrum Disorder: A Review of MRI Studies.Pediatric asthma and autism-genomic perspectives.Does the cognitive architecture of simplex and multiplex ASD families differ?Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability.Monogenic mouse models of autism spectrum disorders: Common mechanisms and missing links.Paternal HLA-C and Maternal Killer-Cell Immunoglobulin-Like Receptor Genotypes in the Development of AutismIdentifying essential cell types and circuits in autism spectrum disorders.Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism.A developmental, longitudinal investigation of autism phenotypic profiles in fragile X syndrome.Autism, Mitochondria and Polybrominated Diphenyl Ether Exposure.Executive Functioning Mediates the Effect of Behavioral Problems on Depression in Mothers of Children With Developmental Disabilities.Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome.Lipid rafts: a signaling platform linking cholesterol metabolism to synaptic deficits in autism spectrum disorders.A 9-year-old-girl with Phelan McDermid Syndrome, who had been diagnosed with an autism spectrum disorder.Glutathione metabolism in the prefrontal brain of adults with high-functioning autism spectrum disorder: an MRS study.Biomarkers in autism spectrum disorder: the old and the new.The contribution of platelet studies to the understanding of disease mechanisms in complex and monogenetic neurological disorders.Involvement of synaptic genes in the pathogenesis of autism spectrum disorders: the case of synapsins
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Autism genetics.
@en
type
label
Autism genetics.
@en
prefLabel
Autism genetics.
@en
P1476
Autism genetics
@en
P2093
Valerio Napolioni
P304
P356
10.1016/J.BBR.2013.06.012
P407
P577
2013-06-13T00:00:00Z