Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome

Published:2015-04 Issue:1 Volume:232 Page:106-114
ISSN:0925-4927
Container-title:Psychiatry Research: Neuroimaging
language:en
Short-container-title:Psychiatry Research: Neuroimaging

Author:

Deng Yi,Goodrich-Hunsaker Naomi J.,Cabaral Margarita,Amaral David G.,Buonocore Michael H.,Harvey Danielle,Kalish Kristopher,Carmichael Owen T.,Schumann Cynthia M.,Lee Aaron,Dougherty Robert F.,Perry Lee M.,Wandell Brian A.,Simon Tony J.

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Psychiatry and Mental health,Radiology, Nuclear Medicine and imaging,Neuroscience (miscellaneous)

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1. Interhemispheric CA1 projections support spatial cognition and are affected in a mouse model of the 22q11.2 deletion syndrome;2024-09-06

2. DWI Hyperintensity in the Fornix Fimbria on MRI in Children;American Journal of Neuroradiology;2022-02-24

3. Opposing white matter microstructure abnormalities in 22q11.2 deletion and duplication carriers;Translational Psychiatry;2021-11-10

4. Tbx1, a gene encoded in 22q11.2 copy number variant, is a link between alterations in fimbria myelination and cognitive speed in mice;Molecular Psychiatry;2021-11-05

5. Brain microstructural abnormalities in 22q11.2 deletion syndrome: A systematic review of diffusion tensor imaging studies;European Neuropsychopharmacology;2021-11