Sort   by:  
 Page size 
UnknownSubcortical Brain Alterations in Carriers of Genomic Copy Number Variants.
Not available
S-EPMC10885337 | biostudies-literature
UnknownPrioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics.
Not available
S-EPMC8196250 | biostudies-literature
UnknownChallenges in multi-task learning for fMRI-based diagnosis: Benefits for psychiatric conditions and CNVs would likely require thousands of patients
Not available
S-EPMC12290746 | biostudies-literature
UnknownAltered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study.
Not available
S-EPMC6986984 | biostudies-literature
UnknownSubcortical brain alterations in carriers of genomic copy number variants.
Not available
S-EPMC9980268 | biostudies-literature
UnknownLarge-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size.
Not available
S-EPMC6292748 | biostudies-literature
UnknownMapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness.
Not available
S-EPMC7419015 | biostudies-literature
Unknown1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
Not available
S-EPMC7985307 | biostudies-literature
UnknownAssociation of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
Not available
S-EPMC6822096 | biostudies-literature
UnknownEffects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.
Not available
S-EPMC8675420 | biostudies-literature
Sort   by:  
 Page size