A primed immune transcriptional program is activated in oligodendroglia in multiple sclerosis [Cut&Run IFNgvsCtr]

DHX9 suppresses spurious RNA processing defects originating from the Alu invasion of the human genome [uvCLAP CLIP-seq]

Liebenberg syndrome severity arises from variations in Pitx1 locus topology and ectopically transcribing cells

Temporal constraints on enhancer usage and enhancer-promoter connectivity shape the regulation of limb gene transcription

Integration of 3D genome architecture and local chromatin features uncovers enhancers underlying craniofacial-specific cartilage defects

Re-configuration of Chromatin Structure During the Mitosis-G1 Phase Progression

Multi-scale 3D genome rewiring during mouse neural development

Direct neuronal reprogramming of mouse astrocytes is associated with multiscale epigenome remodeling and requires Yy1

AgRP neuron epigenomes across hunger states reveal that IRF3 mediates leptin's effects

A long noncoding RNA lincRNA-EPS acts as a transcriptional brake to restrain inflammation

Promoter of lncRNA gene *PVT1* is a tumor suppressor DNA element

Nuclear Organization of Lens Epithelium and Fiber Cells in Newborn Lens

Estrogen-induced NETs promote aseptic inflammation via NKCC1

Drosha loss drives pineoblastoma by upregulating Ccnd2

Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms

Aberrant homeodomain-DNA cooperative dimerization underlies distinct developmental defects in two dominant CRX retinopathy models

Direct DNA crosslinking with CAP-C uncovers transcription-dependent chromatin organization at high resolution

Global examination of LncMyoD binding sites using ChIRP-seq

Sequencing of N6-methyl-deoxyadenosine at single-base resolution across the mammalian genome

MEF2B C-terminal mutations enhance transcriptional activity and stability to drive B cell lymphomagenesis