Ilaria D’Atri

Mutations in TYR and OCA2 associated with oculocutaneous albinism in Pakistani families

E. Baple, S. Ennis, A. Crosby, 2018, Meta Gene.

Tyrosinase (TYR) gene sequencing and literature review reveals recurrent mutations and multiple population founder gene mutations as causative of oculocutaneous albinism (OCA) in Pakistani families

S. Mahmood, E. Baple, A. Crosby, 2019, Eye.

The Dlx5 and Foxg1 transcription factors, linked via miRNA-9 and -200, are required for the development of the olfactory and GnRH system

C. Peano, D. Conte, G. Merlo, 2015, Molecular and Cellular Neuroscience.

Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa

J. Lupski, P. Sieving, S. Jhangiani, 2018, PLoS genetics.

Interference with the Cannabinoid Receptor CB1R Results in Miswiring of GnRH3 and AgRP1 Axons in Zebrafish Embryos

K. Mackie, G. Merlo, P. Provero, 2019, International journal of molecular sciences.

STIM1 Is Required for Remodeling of the Endoplasmic Reticulum and Microtubule Cytoskeleton in Steering Growth Cones

Ethan K. Scott, E. Scott, J. Chilton, 2019, The Journal of Neuroscience.