Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome. - Vandana Shashi; Srirangam Muddasani; Cesar C. Santos; Margaret N. Berry; Thomas R. Kwapil; Kathryn E. Lewandowski; Matcheri S. Keshavan (NeuroImage, 2004)

Enriched phenotypes in rare variant carriers suggest pathogenic mechanisms in rare disease patients. - Lane Fitzsimmons; Maria T. Acosta; David R. Adams; Ben Afzali; Ali Al-Beshri; Eric Allenspach; Aimee Allworth; Raquel L. Alvarez; Justin Alvey; Ashley Andrews; Euan A. Ashley; Carlos A. Bacino; et al. (BioData Min., 2025)