Picketts Lab

The ATRXt Protein Represses rDNA Transcription While Mirroring ATRX Interactions and Heterochromatin Localization

Pathogenic variants in the SMARCA1 gene cause a novel neurodevelopmental disorder

Interferon dependent immune memory during HSV-1 neuronal latency via increased H3K9me3 and restriction by ATRX

The SMARCA5–DMRT1 Pioneer Complex Establishes Epigenetic Priming to Direct Male Germline Development

It Takes a Village of Chromatin Remodelers to Regulate rDNA Expression

The chromatin remodeler ADNP regulates neurodevelopmental disorder risk genes and neocortical neurogenesis

The ChAHP chromatin remodelling complex regulates neurodevelopmental disorder risk genes to scale the production of neocortical layers

Conditional c-MYC activation in catecholaminergic cells drives distinct neuroendocrine tumors: neuroblastoma vs somatostatinoma

PHF6-mediated transcriptional control of NSC via Ephrin receptors is impaired in the intellectual disability syndrome BFLS

Personal journeys to and in human genetics and dysmorphology

A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition