Publications

(2022). Placental methylome reveals a 22q13.33 brain regulatory gene locus associated with autism. Genome Biology.
DOI
(2022). Long-term effects of wildfire smoke exposure during early life on the nasal epigenome in rhesus macaques. Environment International.
DOI
(2021). Stable DNMT3L overexpression in SH-SY5Y neurons recreates a facet of the genome-wide Down syndrome DNA methylation signature. Epigenetics and Chromatin.
(2021). Epigenetic Impacts of Early Life Stress in Fetal Alcohol Spectrum Disorders Shape the Neurodevelopmental Continuum. Frontiers in Molecular Neuroscience.
DOI
(2020). Low-pass whole genome bisulfite sequencing of neonatal dried blood spots identifies a role for RUNX1 in down syndrome DNA methylation profiles. Human Molecular Genetics.
DOI
(2020). Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes. Genome Medicine.
DOI
(2019). Whole genome bisulfite sequencing of Down syndrome brain reveals regional DNA hypermethylation and novel disorder insights. Epigenetics.
(2019). Epigenomic Convergence of Neural-Immune Risk Factors in Neurodevelopmental Disorder Cortex. Cerebral Cortex.
(2019). Imprinting effects of UBE3A loss on synaptic gene networks and Wnt signaling pathways. Human Molecular Genetics.
DOI
(2018). Snord116-dependent diurnal rhythm of DNA methylation in mouse cortex. Nature Communications.