Yunin Ludeña

This study identifies sex-specific DNA methylation signatures of autism spectrum disorder in newborn blood, showing replication and enrichment for ASD-risk genes and neurodevelopmental processes.

This paper identifies 35 genome-wide significant ASD risk genes in admixed Latin American populations, showing consistency with European cohorts and supporting the universality of ASD biology.

The paper identifies two methylation-based episignatures in ADNP syndrome but finds limited correlation with clinical phenotypes.

This study identifies 99 genes associated with autism spectrum disorder through large-scale exome sequencing, showing differences in mutation frequencies between ASD and severe neurodevelopmental delay groups.