Prioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics.

Cereb Cortex · 2021 · PMC8196250 · PMID 33638978

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Regional AIFM3 expression was significantly correlated with ΔSA severity among children ( r = 0.41, P AHBA = 0.029) and adults ( r = 0.42, P AHBA = 0.034), and approached significance in adolescents ( r = 0.39, P AHBA = 0.062; Supplementary Table 9 ).

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