Roman Kosoy

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Chromatin accessibility provides a window into the genetic etiology of human brain disease
Lineage specific 3D genome structure in the adult human brain and neurodevelopmental changes in the chromatin interactome
Activity-Dependent Transcriptional Program in NGN2+ Neurons Enriched for Genetic Risk for Brain-Related Disorders
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups
Genetics of the human microglia regulome refines Alzheimer’s disease risk loci