Olivia J. Veatch

The paper identifies MEIS1 as a gene involved in sleep abnormalities and cerebellar development using cross-species variant-to-function analyses in zebrafish.

This study shows that a favorable lifestyle reduces ADRD risk even in individuals with high polygenic risk, but APOE ε4 genotype remains a strong risk factor.

This study identifies 14 genome-wide significant loci for obstructive sleep apnea, including three independent of BMI, and highlights genetic pathways involving obesity, neurological, and craniofacial factors.

The paper identifies conserved genes at insomnia GWAS loci using zebrafish CRISPR screens and chromatin interaction data, finding that MEIS1 and SKIV2L mutations produce insomnia-like behaviors.

This study evaluates sleep disturbances in children with Rett, Angelman, and Prader-Willi syndromes compared to typically developing controls, identifying common sleep issues and their associations.

The paper identifies genetic variants associated with obstructive sleep apnea using electronic health records and links them to comorbidities.

The paper identifies clinically relevant genetic dysfunction in ASD risk genes by analyzing whole-exome data from 2,381 individuals, finding associations between specific variants and cognitive symptoms.