Area of research
Molecular Biology · Genetics
Research interest
Research interests include Epigenetics and DNA Methylation, Genomics and Chromatin Dynamics, Single-cell and spatial transcriptomics, and Genetics and Neurodevelopmental Disorders.
Heterogeneous epigenetic variation converges on splicing dysregulation in opioid addiction
Single chromatin fiber profiling and nucleosome position mapping in the human brain
Chromatin domain alterations linked to 3D genome organization in a large cohort of schizophrenia and bipolar disorder brains
Population-level variation in enhancer expression identifies disease mechanisms in the human brain
Targeting histone demethylase LSD1 for treatment of deficits in autism mouse models
HIV integration in the human brain is linked to microglial activation and 3D genome remodeling
Convergence of case-specific epigenetic alterations identify a confluence of genetic vulnerabilities tied to opioid overdose
HIV integration in the human brain is linked to microglial activation and 3D genome remodeling
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders
Common Genetic Variation in Humans Impacts In Vitro Susceptibility to SARS-CoV-2 Infection
Convergence of case-specific epigenetic alterations identify a confluence of genetic vulnerabilities tied to opioid dependence
Acetylated Chromatin Domains Link Chromosomal Organization to Cell- and Circuit-level Dysfunction in Schizophrenia and Bipolar Disorder
Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions
Functional annotation of rare structural variation in the human brain
A chromosomal connectome for psychiatric and metabolic risk variants in adult dopaminergic neurons
Neuronal and glial 3D chromatin architecture illustrates cellular etiology of brain disorders
Common genetic variation in humans impacts <i>in vitro</i> susceptibility to SARS-CoV-2 infection
Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder
Comprehensive functional genomic resource and integrative model for the human brain
Integrative functional genomic analysis of human brain development and neuropsychiatric risks
Neuron-specific signatures in the chromosomal connectome associated with schizophrenia risk
Cell-specific histone modification maps in the human frontal lobe link schizophrenia risk to the neuronal epigenome
The methyltransferase SETDB1 regulates a large neuron-specific topological chromatin domain
The epigenomics of schizophrenia, in the mouse
Practical Guidelines for High-Resolution Epigenomic Profiling of Nucleosomal Histones in Postmortem Human Brain Tissue
Neuronal Deletion of Kmt2a/Mll1 Histone Methyltransferase in Ventral Striatum is Associated with Defective Spike-Timing-Dependent Striatal Synaptic Plasticity, Altered Response to Dopaminergic Drugs, and Increased Anxiety