Neal S. Peachey

This study identifies ten genetic loci associated with dry eye disease and finds significant genetic correlations with several comorbidities.

The paper identifies a rare variant in VE-PTP associated with CSC, varicose veins, and glaucoma using genome-wide data from multiple cohorts.

This study identifies 240 novel genetic loci associated with mosaic loss of chromosome Y through a multi-ancestry GWAS of the Million Veteran Program and UK Biobank.

This paper introduces SLED, a splicing-based method to control gene expression in specific cell types, demonstrating its utility in targeting neurons, photoreceptors, and cancer cells.

This study investigates RS1 deficiency in mice, identifying aberrant neuro-glial activity and signaling disruptions that may inform therapeutic strategies for XLRS.

This study shows that deleting Ptbp1 in adult retinal Muller glia and brain astrocytes does not convert glia into neurons, using genetic lineage tracing, scRNA-Seq, and electrophysiology.

This paper investigates the effects of Ranbp2 loss in retinal ganglion neurons and motoneurons in an ALS-like model, revealing distinct paracrine signaling and immune responses.