Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence. - Wikidata - thesis-toulmin - TriplyDB

Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.

Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.

http://www.wikidata.org/entity/Q33581309

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Extracellular and Intracellular Signaling for Neuronal Polarity Neural Signature of DCD: A Critical Review of MRI Neuroimaging Studies Genetic Counseling for Autism Spectrum Disorder in an Evolving Theoretical Landscape The role of sex-differential biology in risk for autism spectrum disorder The future of human cerebral cartography: a novel approach Reconciling evidence-based medicine and precision medicine in the era of big data: challenges and opportunities Learning delays in a mouse model of Autism Spectrum Disorder.Heterogeneity within Autism Spectrum Disorders: What have We Learned from Neuroimaging Studies?Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery.The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.A Comparison of Structural Brain Imaging Findings in Autism Spectrum Disorder and Attention-Deficit Hyperactivity Disorder.Definition of a visuospatial dimension as a step forward in the diagnostic puzzle of nonverbal learning disability.Mutations in the BLOC-1 subunits dysbindin and muted generate divergent and dosage-dependent phenotypes.Neurodevelopmental disorders: mechanisms and boundary definitions from genomes, interactomes and proteomes.Examining the Overlap between Autism Spectrum Disorder and 22q11.2 Deletion Syndrome.The EU-AIMS Longitudinal European Autism Project (LEAP): design and methodologies to identify and validate stratification biomarkers for autism spectrum disorders.Loss of X-linked Protocadherin-19 differentially affects the behavior of heterozygous female and hemizygous male mice Personality and self-insight in individuals with autism spectrum disorder.A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders.Opposing brain differences in 16p11.2 deletion and duplication carriers.The scaffold protein Nde1 safeguards the brain genome during S phase of early neural progenitor differentiation.Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.Autism traits in the RASopathies.High-resolution copy number variation analysis of schizophrenia in Japan.MeCP2 regulates the synaptic expression of a Dysbindin-BLOC-1 network component in mouse brain and human induced pluripotent stem cell-derived neurons.Gene dosage in the dysbindin schizophrenia susceptibility network differentially affect synaptic function and plasticity A different view on the checkerboard? Alterations in early and late visually evoked EEG potentials in Asperger observers Adaptive and maladaptive correlates of repetitive behavior and restricted interests in persons with down syndrome and developmentally-matched typical children: a two-year longitudinal sequential design Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.An assessment of sex bias in neurodevelopmental disorders.Incorporating Functional Information in Tests of Excess De Novo Mutational Load.Pooling Bio-Specimens in the Presence of Measurement Error and Non-Linearity in Dose-Response: Simulation Study in the Context of a Birth Cohort Investigating Risk Factors for Autism Spectrum Disorders Genetics and genomics of autism spectrum disorder: embracing complexity.Annual Research Review: Discovery science strategies in studies of the pathophysiology of child and adolescent psychiatric disorders--promises and limitations.Molecular subtyping and improved treatment of neurodevelopmental disease.The genetics and neurobiology of ESSENCE: The third Birgit Olsson lecture Shift happens: family background influences clinical variability in genetic neurodevelopmental disorders Autism spectrum disorder causes, mechanisms, and treatments: focus on neuronal synapses.Pluripotent stem cells as a model to study non-coding RNAs function in human neurogenesis.Integrating precision medicine in the study and clinical treatment of a severely mentally ill person

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Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.

http://www.wikidata.org/entity/Q33581309

description

2013 nî lūn-bûn

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2013 թուականի Մարտին հրատարակուած գիտական յօդուած

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2013 թվականի մարտին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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Developmental brain dysfunctio ...... based on new genetic evidence.

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Developmental brain dysfunctio ...... based on new genetic evidence.

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Developmental brain dysfunctio ...... based on new genetic evidence.

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Developmental brain dysfunctio ...... based on new genetic evidence.

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Developmental brain dysfunctio ...... based on new genetic evidence.

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Developmental brain dysfunctio ...... based on new genetic evidence.

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Developmental brain dysfunctio ...... based on new genetic evidence.

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Developmental brain dysfunctio ...... based on new genetic evidence.

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Developmental brain dysfunctio ...... based on new genetic evidence.

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Lancet Neurology

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Developmental brain dysfunctio ...... based on new genetic evidence.

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Andres Moreno-De-Luca

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Daniel Moreno-De-Luca

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David H Ledbetter

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David W Evans

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Scott M Myers

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Thomas D Challman

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P2860

Understanding the impact of 1q21.1 copy number variant

Childhood developmental disorders: an academic and clinical convergence point for psychiatry, neurology, psychology and pediatrics

Rare chromosomal deletions and duplications increase risk of schizophrenia

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila

Large recurrent microdeletions associated with schizophrenia

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

Practical guidelines for managing patients with 22q11.2 deletion syndrome

Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders

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4

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Daniel Moreno-De-Luca

Andres Moreno-De-Luca

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23518333

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