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Roman Kosoy*

Single-nucleus transcriptome-wide association study of human brain disorders
Plasticity of human microglia and brain perivascular macrophages in aging and Alzheimer’s disease
Alzheimer’s disease transcriptional landscape in ex vivo human microglia
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

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