Genetic contributions to changes of fiber tracts of ventral visual stream in 22q11.2 deletion syndrome
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Genetic contributions to changes of fiber tracts of ventral visual stream in 22q11.2 deletion syndrome
Authors
Keywords
22q11.2 deletion syndrome (22q11.2DS,VCFS), Diffusion Tensor MRI (DT-MRI), Fractional anisotropy (FA), Axial diffusivity (AD), Inferior fronto-occipital fasciculus (IFOF), Inferior longitudinal fasciculus (ILF), High-risk schizophrenia
Journal
Brain Imaging and Behavior
Volume 7, Issue 3, Pages 316-325
Publisher
Springer Nature
Online
2013-04-23
DOI
10.1007/s11682-013-9232-5
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Atlas-based white matter analysis in individuals with velo-cardio-facial syndrome (22q11.2 deletion syndrome) and unaffected siblings
- (2012) Petya D Radoeva et al. Behavioral and Brain Functions
- Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome?
- (2012) Kate Baker et al. CURRENT OPINION IN NEUROLOGY
- Reduced fractional anisotropy and axial diffusivity in white matter in 22q11.2 deletion syndrome: A pilot study
- (2012) Z. Kikinis et al. SCHIZOPHRENIA RESEARCH
- Resting-state networks in adolescents with 22q11.2 deletion syndrome: Associations with prodromal symptoms and executive functions
- (2012) Martin Debbané et al. SCHIZOPHRENIA RESEARCH
- Neuropsychological Profile of Italian Children and Adolescents with 22q11.2 Deletion Syndrome with and Without Intellectual Disability
- (2011) Stefano Vicari et al. BEHAVIOR GENETICS
- Frontal terminations for the inferior fronto-occipital fascicle: anatomical dissection, DTI study and functional considerations on a multi-component bundle
- (2011) Silvio Sarubbo et al. Brain Structure & Function
- Proline and COMT Status Affect Visual Connectivity in Children with 22q11.2 Deletion Syndrome
- (2011) Maurice J. C. M. Magnée et al. PLoS One
- White matter abnormalities in adults with 22q11 deletion syndrome with and without schizophrenia
- (2011) Fabiana da Silva Alves et al. SCHIZOPHRENIA RESEARCH
- White matter microstructure in 22q11 deletion syndrome: a pilot diffusion tensor imaging and voxel-based morphometry study of children and adolescents
- (2010) Frederick Sundram et al. Journal of Neurodevelopmental Disorders
- Positive symptoms and white matter microstructure in never-medicated first episode schizophrenia
- (2010) V. Cheung et al. PSYCHOLOGICAL MEDICINE
- Insights into brain development from neurogenetic syndromes: evidence from fragile X syndrome, Williams syndrome, Turner syndrome and velocardiofacial syndrome
- (2009) E. Walter et al. NEUROSCIENCE
- Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome
- (2009) D. W. Meechan et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome
- (2008) Tony J Simon et al. Behavioral and Brain Functions
- Neuropathologic Features in Adults with 22q11.2 Deletion Syndrome
- (2008) T. R. Kiehl et al. CEREBRAL CORTEX
- A diffusion tensor imaging tractography atlas for virtual in vivo dissections
- (2008) M CATANI et al. CORTEX
- Velo-cardio-facial syndrome: 30 Years of study
- (2008) Robert J. Shprintzen Developmental Disabilities Research Reviews
- Age-related deficits in fronto-temporal connections in schizophrenia: A diffusion tensor imaging study
- (2008) G ROSENBERGER et al. SCHIZOPHRENIA RESEARCH
- Abnormal white matter microstructure in schizophrenia: A voxelwise analysis of axial and radial diffusivity
- (2008) Marc L. Seal et al. SCHIZOPHRENIA RESEARCH
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started