Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior. - Wikidata - awgldk - TriplyDB

Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.

Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.

http://www.wikidata.org/entity/Q31143422

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Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.Conceptualizing neurodevelopmental disorders through a mechanistic understanding of fragile X syndrome and Williams syndrome A human neurodevelopmental model for Williams syndrome Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndrome Association of mouse Dlg4 (PSD-95) gene deletion and human DLG4 gene variation with phenotypes relevant to autism spectrum disorders and Williams' syndrome A dual comparative approach: integrating lines of evidence from human evolutionary neuroanatomy and neurodevelopmental disorders Musicality Correlates With Sociability and Emotionality in Williams Syndrome Social functioning and autonomic nervous system sensitivity across vocal and musical emotion in Williams syndrome and autism spectrum disorder.Cross-modal influences of affect across social and non-social domains in individuals with Williams syndrome.Oxytocin and vasopressin are dysregulated in Williams Syndrome, a genetic disorder affecting social behavior Sensitivity of the autonomic nervous system to visual and auditory affect across social and non-social domains in williams syndrome Atypical hemispheric asymmetry in the perception of negative human vocalizations in individuals with Williams syndrome.Induced chromosome deletion in a Williams-Beuren syndrome mouse model causes cardiovascular abnormalities.Cortisol reactivity and performance abilities in social situations in adults with Williams syndrome.Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome Abnormal structure or function of the amygdala is a common component of neurodevelopmental disorders.Toward a deeper characterization of the social phenotype of Williams syndrome: The association between personality and social drive Affiliative behavior in Williams syndrome: social perception and real-life social behavior Characterizing associations and dissociations between anxiety, social, and cognitive phenotypes of Williams syndrome.The Drosophila agnostic Locus: Involvement in the Formation of Cognitive Defects in Williams Syndrome Longitudinal course of anxiety in children and adolescents with Williams syndrome Cognitive and behavioral characteristics of children with Williams syndrome: implications for intervention approaches.Genetic counseling of adults with Williams syndrome: a first study The social phenotype of Williams syndrome.Altered microstructure within social-cognitive brain networks during childhood in Williams syndrome.Williams syndrome as a model for elucidation of the pathway genes - the brain - cognitive functions: genetics and epigenetics Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content.A preliminary study of orbitofrontal activation and hypersociability in Williams Syndrome Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders Adaptive behavior in Chinese children with Williams syndrome Individual differences in social behavior predict amygdala response to fearful facial expressions in Williams syndrome Contrasting patterns of language-associated brain activity in autism and Williams syndrome.Language and sociability: insights from Williams syndrome.Relations between social-perceptual ability in multi- and unisensory contexts, autonomic reactivity, and social functioning in individuals with Williams syndrome.Children with Williams Syndrome: Language, Cognitive, and Behavioral Characteristics and their Implications for Intervention.Neural processing of race by individuals with Williams syndrome: do they show the other-race effect? (And why it matters)Autonomic response to approachability characteristics, approach behavior, and social functioning in Williams syndrome Morphological differences in the mirror neuron system in Williams syndrome.The fusiform face area is enlarged in Williams syndrome.Toddlers with Williams syndrome process upright but not inverted faces holistically.

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P2860

Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.

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2008年の論文

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Defining the social phenotype ...... gene, the brain, and behavior.

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Defining the social phenotype ...... gene, the brain, and behavior.

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Defining the social phenotype ...... gene, the brain, and behavior.

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Albert Galaburda

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Anna Järvinen-Pasley

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Debra L Mills

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P2860

The murine CYLN2 gene: genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region

Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23

The tortuous route from genes to behavior: A neuroconstructivist approach

GTF2IRD1 in craniofacial development of humans and mice

Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval

Development itself is the key to understanding developmental disorders

Increased gyrification in Williams syndrome: evidence using 3D MRI methods.

Relative sparing of primary auditory cortex in Williams Syndrome.

Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome.

The Observer Video-Pro: new software for the collection, management, and presentation of time-structured data from videotapes and digital media files.

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