Area of research
Molecular Biology · Genetics
Research interest
Research interests include Genetic Associations and Epidemiology, Epigenetics and DNA Methylation, Genetics and Neurodevelopmental Disorders, and Genomics and Chromatin Dynamics.
Major-depressive-disorder-associated dysregulation of ZBTB7A in orbitofrontal cortex promotes astrocyte-mediated stress susceptibility
ZBTB7A regulates MDD-specific chromatin signatures and astrocyte-mediated stress vulnerability in orbitofrontal cortex
Common variants contribute to intrinsic human brain functional networks
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups
Chromatin domain alterations linked to 3D genome organization in a large cohort of schizophrenia and bipolar disorder brains
The three-dimensional landscape of cortical chromatin accessibility in Alzheimer’s disease
Common genetic variation influencing human white matter microstructure
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders
The three-dimensional landscape of chromatin accessibility in Alzheimer’s disease
Author Correction: Brain Cell Type Specific Gene Expression and Co-expression Network Architectures
Identification of shared and differentiating genetic risk for autism spectrum disorder, attention deficit hyperactivity disorder and case subgroups
Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions
Common schizophrenia risk variants are enriched in open chromatin regions of human glutamatergic neurons
Functional annotation of rare structural variation in the human brain
Chromatin accessibility mapping of the striatum identifies tyrosine kinase FYN as a therapeutic target for heroin use disorder
Common genetic variation influencing human white matter microstructure
Identification of common genetic risk variants for autism spectrum disorder
CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder
Comprehensive functional genomic resource and integrative model for the human brain
The Mount Sinai cohort of large-scale genomic, transcriptomic and proteomic data in Alzheimer's disease
Brain Cell Type Specific Gene Expression and Co-expression Network Architectures
A Bayesian framework for multiple trait colocalization from summary association statistics
An atlas of chromatin accessibility in the adult human brain
Cell-specific histone modification maps in the human frontal lobe link schizophrenia risk to the neuronal epigenome
Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls
Discovery of the first genome-wide significant risk loci for ADHD
Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression
Common risk variants identified in autism spectrum disorder