María Claudia Lattig

The paper identifies 253 autism-associated genes using rare variation from 62,429 individuals and finds pleiotropy across physiological systems and developmental disorders.

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.

This study identifies novel genetic risk loci for COVID-19 hospitalization in admixed American populations through a large GWAS.

This study identifies neuronal-specific DNA methylation and hydroxymethylation changes in the orbitofrontal cortex associated with alcohol use disorder, replicating prior findings and uncovering novel loci.