Facial phenotypes in subgroups of prepubertal boys with autism spectrum disorders are correlated with clinical phenotypesSex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priorityTranscriptional and functional complexity of Shank3 provides a molecular framework to understand the phenotypic heterogeneity of SHANK3 causing autism and Shank3 mutant miceDecreased tryptophan metabolism in patients with autism spectrum disordersGenome-wide linkage using the Social Responsiveness Scale in Utah autism pedigreesPolymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestryPCR and serology find no association between xenotropic murine leukemia virus-related virus (XMRV) and autismHaploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communicationSex differences in structural organization of motor systems and their dissociable links with repetitive/restricted behaviors in children with autismConstrained spherical deconvolution-based tractography and tract-based spatial statistics show abnormal microstructural organization in Asperger syndromeThe association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysisFrom molecules to neural morphology: understanding neuroinflammation in autism spectrum conditionGazefinder as a clinical supplementary tool for discriminating between autism spectrum disorder and typical development in male adolescents and adultsGenes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression.Sex differences in the association between infant markers and later autistic traits.Brinp1(-/-) mice exhibit autism-like behaviour, altered memory, hyperactivity and increased parvalbumin-positive cortical interneuron densityOverexpression of Homer1a in the basal and lateral amygdala impairs fear conditioning and induces an autism-like social impairmentCortical morphological markers in children with autism: a structural magnetic resonance imaging study of thickness, area, volume, and gyrificationAltered gaze following during live interaction in infants at risk for autism: an eye tracking study.Auditory encoding abnormalities in children with autism spectrum disorder suggest delayed development of auditory cortex.A neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in miceMeasuring autistic traits in the general population: a systematic review of the Autism-Spectrum Quotient (AQ) in a nonclinical population sample of 6,900 typical adult males and femalesLoci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait lociHistopathologic characterization of the BTBR mouse model of autistic-like behavior reveals selective changes in neurodevelopmental proteins and adult hippocampal neurogenesisAutism-associated gene Dlgap2 mutant mice demonstrate exacerbated aggressive behaviors and orbitofrontal cortex deficitsSerum and cerebrospinal fluid immune mediators in children with autistic disorder: a longitudinal studyAltered social behavior and ultrasonic communication in the dystrophin-deficient mdx mouse model of Duchenne muscular dystrophy.A comprehensive meta-analysis of common genetic variants in autism spectrum conditionsIdentification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control populationRecurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders.SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)Whole-genome sequencing in an autism multiplex familyPlacental methylome analysis from a prospective autism studyUltrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice.Elevated cortisol during play is associated with age and social engagement in children with autism.Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.Name recognition in autism: EEG evidence of altered patterns of brain activity and connectivityAssessment of olfactory detection thresholds in children with autism spectrum disorders using a pulse ejection system.Enhanced olfactory sensitivity in autism spectrum conditionsReduced isolation-induced pup ultrasonic communication in mouse pups lacking brain serotonin.
P1433
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P1433
description
revista científica
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rivista scientifica
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scientific journal
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vědecký časopis
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wetenschappelijk tijdschrift van BioMed Central
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wissenschaftliche Fachzeitschrift
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науковий журнал
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مجلة
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वैज्ञानिक पत्रिका
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name
Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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Molecular Autism
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P31
P921
P243
P3181
P4616
P6366
P1055
P1156
19700177555
P1159
P1160
Mol. Autism
P123
P1277
P1476
Molecular Autism
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