Connecting genes to brain in the autism spectrum disorders - Test2 - elhamkhani - TriplyDB

Connecting genes to brain in the autism spectrum disorders

Connecting genes to brain in the autism spectrum disorders

http://www.wikidata.org/entity/Q28705565

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The shock of the new: progress in schizophrenia genomics Chemicals, Nutrition, and Autism Spectrum Disorder: A Mini-Review The role of cerebellar circuitry alterations in the pathophysiology of autism spectrum disorders Consensus paper: pathological role of the cerebellum in autism Coronin 1 regulates cognition and behavior through modulation of cAMP/protein kinase A signaling Advancing the understanding of autism disease mechanisms through genetics Aberrant Development of Speech Processing in Young Children with Autism: New Insights from Neuroimaging Biomarkers.Circuit-specific intracortical hyperconnectivity in mice with deletion of the autism-associated Met receptor tyrosine kinase Mild dermatoglyphic deviations in adolescents with autism spectrum disorders and average intellectual abilities as compared to typically developing boys Modeling autistic features in animals Applying machine learning to facilitate autism diagnostics: pitfalls and promises.Sex differences in the cerebellum and frontal cortex: roles of estrogen receptor alpha and sex chromosome genes Influence of stimulant-induced hyperactivity on social approach in the BTBR mouse model of autism Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice Autism as early neurodevelopmental disorder: evidence for an sAPPα-mediated anabolic pathway Distinct regions of the cerebellum show gray matter decreases in autism, ADHD, and developmental dyslexia Are maternal social networks and perceptions of trust associated with suspected autism spectrum disorder in offspring? A population-based study in Japan Expression profiling of autism candidate genes during human brain development implicates central immune signaling pathways.Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?A comparison of pragmatic language in boys with autism and fragile X syndrome.Genetic insights into the functional elements of language.Comparative RNA editing in autistic and neurotypical cerebella.Consistency between research and clinical diagnoses of autism among boys and girls with fragile X syndrome.Saccade adaptation abnormalities implicate dysfunction of cerebellar-dependent learning mechanisms in Autism Spectrum Disorders (ASD).Cardiac autonomic regulation in autism and Fragile X syndrome: a review.Modifier genes and non-genetic factors reshape anatomical deficits in Zfp423-deficient mice.Genetic effects on cerebellar structure across mouse models of autism using a magnetic resonance imaging atlas Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity.The Role of Epigenetic Change in Autism Spectrum Disorders.Predictable enriched environment prevents development of hyper-emotionality in the VPA rat model of autism Caregiver strain and sensory features in children with autism spectrum disorder and other developmental disabilities Oxytocin receptor and Mecp2 308/Y knockout mice exhibit altered expression of autism-related social behaviors.CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment.Abnormal glutamate release in aged BTBR mouse model of autism.A Two-Hit Model of Autism: Adolescence as the Second Hit The importance of autism research.Lighting a path: genetic studies pinpoint neurodevelopmental mechanisms in autism and related disorders.Environmental factors in autism.Relationship Between Cortical Gyrification, White Matter Connectivity, and Autism Spectrum Disorder.Intrinsic gray-matter connectivity of the brain in adults with autism spectrum disorder.

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Connecting genes to brain in the autism spectrum disorders

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2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2010 թվականի ապրիլին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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Connecting genes to brain in the autism spectrum disorders

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Connecting genes to brain in the autism spectrum disorders

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Functional and anatomical cortical underconnectivity in autism: evidence from an FMRI study of an executive function task and corpus callosum morphometry

Advances in autism genetics: on the threshold of a new neurobiology

Mapping Early Brain Development in Autism

Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria.

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

Minicolumnar pathology in autism

AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders

Association of tuberous sclerosis of temporal lobes with autism and atypical autism

Language-related Cntnap2 gene is differentially expressed in sexually dimorphic song nuclei essential for vocal learning in songbirds

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

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