Mapping cortical thickness in children with 22q11.2 deletions. - Wikidata - awgldk - TriplyDB

Mapping cortical thickness in children with 22q11.2 deletions.

Mapping cortical thickness in children with 22q11.2 deletions.

http://www.wikidata.org/entity/Q33644926

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Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndrome Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development Single nucleotide polymorphism in the neuroplastin locus associates with cortical thickness and intellectual ability in adolescents The Center for Computational Biology: resources, achievements, and challenges The Insight ToolKit image registration framework.The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory.Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes Regional cortical volumes and congenital heart disease: a MRI study in 22q11.2 deletion syndrome Structural brain atlases: design, rationale, and applications in normal and pathological cohorts.Animal models of psychiatric disorders that reflect human copy number variation.Developmental changes in multivariate neuroanatomical patterns that predict risk for psychosis in 22q11.2 deletion syndrome Mapping cortical morphology in youth with velocardiofacial (22q11.2 deletion) syndrome.Mapping the stability of human brain asymmetry across five sex-chromosome aneuploidies.Typical and atypical brain development: a review of neuroimaging studies.Cortical mapping of genotype-phenotype relationships in schizophrenia.Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome Incidental radiologic findings in the 22q11.2 deletion syndrome Aberrant Cortical Morphometry in the 22q11.2 Deletion Syndrome.Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.Cortical gyrification in velo-cardio-facial (22q11.2 deletion) syndrome: a longitudinal study Cortical Morphology Differences in Subjects at Increased Vulnerability for Developing a Psychotic Disorder: A Comparison between Subjects with Ultra-High Risk and 22q11.2 Deletion Syndrome.Neural phenotypes of common and rare genetic variants.Prenatal Alcohol Exposure is Associated with Regionally Thinner Cortex During the Preadolescent Period Functional significance of atypical cortical organization in spina bifida myelomeningocele: relations of cortical thickness and gyrification with IQ and fine motor dexterity.Disrupted anatomic networks in the 22q11.2 deletion syndrome.Genetic contributions to changes of fiber tracts of ventral visual stream in 22q11.2 deletion syndrome.Alterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletions.Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome.Age, plasticity, and homeostasis in childhood brain disorders Mapping genetic influences on ventricular structure in twins.Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion.Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome.White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging.Do children with congenital hypothyroidism exhibit abnormal cortical morphology?Visual perception skills: a comparison between patients with Noonan syndrome and 22q11.2 deletion syndrome.Autism spectrum disorder: neuropathology and animal models.

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P2860

Mapping cortical thickness in children with 22q11.2 deletions.

http://www.wikidata.org/entity/Q33644926

description

2006 nî lūn-bûn

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2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2006 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

Mapping cortical thickness in children with 22q11.2 deletions.

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Mapping cortical thickness in children with 22q11.2 deletions.

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type

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Mapping cortical thickness in children with 22q11.2 deletions.

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Mapping cortical thickness in children with 22q11.2 deletions.

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Mapping cortical thickness in children with 22q11.2 deletions.

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Mapping cortical thickness in children with 22q11.2 deletions.

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Cerebral Cortex

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Mapping cortical thickness in children with 22q11.2 deletions.

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Beverly S Emanuel

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Carrie E Bearden

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Daqiang Sun

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David C Glahn

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Helen Tran

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Jennifer A Geaga

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Lara Zimmermann

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Rebecca A Dutton

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Theo G M van Erp

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Tony J Simon

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P2860

Dynamic mapping of human cortical development during childhood through early adulthood.

Early asymmetry of gene transcription in embryonic human left and right cerebral cortex

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

Anomalous asymmetry of fusiform and parahippocampal gyrus gray matter in schizophrenia: A postmortem study

Interactions between number and space in parietal cortex

MR of the cerebral operculum: abnormal opercular formation in infants and children

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia

BrainSuite: An automated cortical surface identification tool

Associations between prepulse inhibition and executive visual attention in children with the 22q11 deletion syndrome

The neuropathology of schizophrenia. A critical review of the data and their interpretation.

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1889-1898

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10.1093/CERCOR/BHL097

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Paul M. Thompson

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cortical thickness

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2819929

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